1. Neuroscience

The tetraspanin TSPAN5 regulates AMPAR exocytosis by interacting with the AP4 complex

  1. Edoardo Moretto  Is a corresponding author
  2. Federico Miozzo
  3. Anna Longatti
  4. Caroline Bonnet
  5. Francoise Coussen
  6. Fanny Jaudon
  7. Lorenzo A Cingolani
  8. Maria Passafaro  Is a corresponding author
  1. Institute of Neuroscience, CNR, Italy
  2. NeuroMI Milan Center for Neuroscience, University of Milano-Bicocca, Italy
  3. University of Bordeaux, Interdisciplinary Institute for Neuroscience, France
  4. Department of Life Sciences, University of Trieste, Italy
  5. IRCCS Ospedale Policlinico San Martino, Italy
  6. Center for Synaptic Neuroscience and Technology (NSYN), Istituto Italiano di Tecnologia (IIT), Italy
https://doi.org/10.7554/eLife.76425
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Cite this article
  1. Edoardo Moretto
  2. Federico Miozzo
  3. Anna Longatti
  4. Caroline Bonnet
  5. Francoise Coussen
  6. Fanny Jaudon
  7. Lorenzo A Cingolani
  8. Maria Passafaro
(2023)
The tetraspanin TSPAN5 regulates AMPAR exocytosis by interacting with the AP4 complex
eLife 12:e76425.
https://doi.org/10.7554/eLife.76425
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Abstract

Intracellular trafficking of AMPA receptors is a tightly regulated process which involves several adaptor proteins, and is crucial for the activity of excitatory synapses both in basal conditions and during synaptic plasticity. We found that, in rat hippocampal neurons, an intracellular pool of the tetraspanin TSPAN5 promotes exocytosis of AMPA receptors without affecting their internalisation. TSPAN5 mediates this function by interacting with the adaptor protein complex AP4 and Stargazin and possibly using recycling endosomes as a delivery route. This work highlights TSPAN5 as a new adaptor regulating AMPA receptor trafficking.

Editor's evaluation

Glutamate receptor trafficking to synapses plays a crucial role in adjusting the efficacy of information flow in the nervous system. Here the authors show in hippocampal neurons that TSPAN5, a tetraspanin family protein facilitates the delivery of AMPA-type glutamate receptors to the cell surface by interacting with adaptor proteins, AP-4, and stargazin. The work provides evidence supporting a novel mechanism that contributes to the regulation of AMPA receptor traffic and is of interest to the molecular neuroscience and cell biology community.

https://doi.org/10.7554/eLife.76425.sa0

Introduction

Tetraspanins are transmembrane proteins conserved in metazoans that present four transmembrane domains, a small and a large extracellular loop, and intracellular N- and C-termini (Berditchevski, 2001). Tetraspanins have the peculiar ability to organise tetraspanin enriched microdomains, membrane domains in which they accumulate (Charrin et al., 2002). Tetraspanins have been proposed to function as molecular facilitators by promoting physical proximity between proteins that belong to signalling complexes (Charrin et al., 2014). To date, 33 tetraspanins have been described in mammals, with functions in cell-cell adhesion, sperm-egg fusion, cell motility, and proliferation (Hemler, 2005). TSPAN5 is part of the C8 subgroup of tetraspanins and was previously shown to regulate the intracellular trafficking and activity of the protease ADAM-10 (Dornier et al., 2012; Eschenbrenner et al., 2020; Haining et al., 2012; Jouannet et al., 2016; Noy et al., 2016; Saint-Pol et al., 2017).

A previous study from our laboratory showed that, in hippocampal pyramidal neurons, TSPAN5 is enriched in dendritic spines and promotes their morphological maturation during synaptogenesis (Moretto et al., 2019). This action is mediated by controlling the surface mobility of the postsynaptic adhesion molecule neuroligin-1 via an interaction occurring on the plasma membrane. A few other studies have investigated the function of tetraspanins at the synapse identifying their role in intracellular trafficking of neurotransmitter receptors in neurons (Bassani et al., 2012; Lee et al., 2017; Murru et al., 2018; Murru et al., 2017).

Here, we report a significant increase in the intracellular pool of TSPAN5 in dendritic spines upon neuronal maturation. We demonstrate that in mature neurons TSPAN5 does not participate in dendritic spine maturation but has the main function of controlling surface delivery of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors (AMPARs). AMPARs are tetrameric complexes that mediate most of the fast excitatory transmission in response to the neurotransmitter glutamate in neurons (Henley and Wilkinson, 2016). AMPAR surface levels are directly responsible for synapse weakening or strengthening during synaptic plasticity (Huganir and Nicoll, 2013); their intracellular trafficking is an extremely complex phenomenon involving several auxiliary proteins (Anggono and Huganir, 2012; Moretto and Passafaro, 2018) that can be impaired in neurological and neurodevelopmental disorders (Henley and Wilkinson, 2016; Moretto et al., 2016; Moretto et al., 2018).

Importantly, we found that TSPAN5 exerts this function by interacting with AP4, a member of the adaptor protein complex family (Boehm and Bonifacino, 2001; Bonifacino, 2014; Robinson and Bonifacino, 2001), which coding genes are mutated in a syndrome characterised by spastic paraplegia and intellectual disability (Sanger et al., 2019). AP4 was previously found to regulate the intracellular trafficking and sorting of several transmembrane proteins in neurons including the stargazin-AMPARs complex (Matsuda et al., 2008), the glutamate receptor δ2 (Yap et al., 2003), the autophagy regulator ATG9 (Ivankovic et al., 2020), and DAGLB, an enzyme involved in the production of the endocannabinoid 2-AG (Davies et al., 2022).

Our data identify a novel function of TSPAN5 at the synapse and highlight AMPARs defective trafficking as a possible mechanism for intellectual disability symptoms in the AP4 deficiency syndrome.

Results

TSPAN5 intracellular pool interacts with the AP4 complex

In our previous work (Moretto et al., 2019), we observed the existence of a substantial intracellular pool of TSPAN5 in mature neurons. We thus performed crosslinking experiments using bis(sulfosuccinimidyl)suberate (BS3) on rat cultured hippocampal neurons. This crosslinker is not permeable to membranes and, as such, if applied to living cells will only crosslink plasma membrane proteins which will appear as high molecular weight bands upon western blot analysis. In contrast, the intracellular pool will not be crosslinked, thereby running at the expected molecular weight. We analysed TSPAN5 levels in BS3 experiments and looked at DIV12 and DIV19. At DIV12 synaptogenesis is prominent in rat cultured neurons (Chanda et al., 2017) while at DIV19, primary neurons are considered functionally mature. As shown in Figure 1A, TSPAN5 appears as a complex pattern of bands. This is probably due to the association of this protein with cholesterol-rich membranes which makes it poorly soluble in standard lysis buffers (Charrin et al., 2014). We previously demonstrated that all these bands are specific (Moretto et al., 2019) and thus they were all included in the quantification. We observed an increase in the intracellular levels of TSPAN5 from DIV12 to DIV19, which was not accompanied by a concomitant increase in plasma membrane levels (Figure 1A), suggesting that increased intracellular levels of TSPAN5 do not necessarily imply increased delivery of this protein to the plasma membrane. The transferrin receptor showed a more stable distribution across these time points. It needs to be mentioned that it is possible that a fraction of TSPAN5 present on the plasma membrane does not interact with any other protein. This fraction would not be crosslinked and run as a monomer. However, this eventuality is quite unlikely, especially considering that the main function of tetraspanins is exerted by homo- and heterotypic interactions (Charrin et al., 2014). To test if the increase in intracellular TSPAN5 could be related to a different function compared to its previously described role in dendritic spines maturation (Moretto et al., 2019), we transfected cultured hippocampal neurons at DIV13 with scrambled, Sh-TSPAN5, and rescue (coding for the Sh-TSPAN5 and an ShRNA-resistant form of TSPAN5) constructs. A reduction of TSPAN5 at this time point is unlikely to affect dendritic spine maturation as synaptogenesis is already underway. We analysed dendritic spine density and morphology at DIV21 (Figure 1B) and observed that dendritic spine density was reduced, but to a lower extent compared to our previous observations when knocking down TSPAN5 at DIV5 (20% compared to more than 65% reduction, respectively) (Moretto et al., 2019). Even more interestingly, the morphology of dendritic spines was completely unaffected by TSPAN5 knockdown at this time point. In contrast, our previous results had shown a strong reduction (50%) in mature mushroom dendritic spines in favour of less mature thin dendritic spines when TSPAN5 levels were downregulated from DIV5 (Moretto et al., 2019). These data support a more prominent role of TSPAN5 for dendritic spine maturation at early stages of development and suggest that TSPAN5 might be involved in other functions at more mature stages. We decided to explore whether the intracellular pool of TSPAN5 could have a role in regulating intracellular trafficking given previous evidence on the role of this and other tetraspanins (Dornier et al., 2012; Haining et al., 2012; Jouannet et al., 2016; Noy et al., 2016; Saint-Pol et al., 2017; Bassani et al., 2012).

Figure 1
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TSPAN5 intracellular levels increase with neuronal maturation.

(A) Bis(sulfosuccinimidyl)suberate (BS3) crosslinking experiment on cultured rat hippocampal neurons at DIV12 and -19 blotted for TSPAN5, transferrin receptor (TfR), and tubulin. Arrows indicate the higher molecular weight bands present in the BS3+lanes that represent the plasma membrane pool of the proteins. Tubulin was used as a loading control; TfR was used as a crosslinking positive control (TSPAN5: total/tubulin: DIV12 2.599±0.38, DIV19 3.357±0.25; intra/tubulin: DIV12 2.643±0.14, DIV19 3.582±0.16; extra/tubulin: DIV12 2.552±0.70, DIV19 2.871±1.01; TfR: total/tubulin: DIV12 4.87±0.81, DIV19 4.48±1.05; intra/tubulin: DIV12 4.18±1.61, DIV19 4.73±1.53; extra/tubulin: DIV12 4.94±0.6, DIV19 6.44±0.95). n = 3–4 independent cultures per condition. Unpaired Student T test. (B) Left panels: Confocal images of DIV20 cultured rat hippocampal neurons transfected at DIV13 with either scrambled, Sh-TSPAN5, or rescue (expressing simultaneously both the Sh-TSPAN5 and an ShRNA-resistant form of TSPAN5) constructs, all co-expressing GFP. Scale bar = 20 μm. Inserts (25 μm wide) show higher magnification of the dendrites highlighted in white. Right panel: Quantification of dendritic spine density represented as histograms. Dendritic spine density (no. of dendritic spines/μm: scrambled 0.51±0.02; Sh-TSPAN5 0.41±0.03; rescue 0.67±0.03). Pie charts (bottom panels) show quantification of dendritic spine morphology. Dendritic spine morphology (%: stubby: scrambled 31.20±1.52, Sh-TSPAN5 30.25±2.02, rescue 29.46±1.38; thin: scrambled 40.10±2.45, Sh-TSPAN5 40.51±1.96, rescue 38.07±2.5; mushroom: scrambled 27.15±2.25, Sh-TSPAN5 29.24, rescue 32.49±2.44). n = scrambled, 14; Sh-TSPAN5, 16; rescue, 17 neurons. One Way ANOVA, Newman-Kulspost hoc multiplecomparison test.

Values represent the mean ± SEM. *=p < 0.05, **=p < 0.01, ***=p < 0.001.

Figure 1—source data 1

individual data values for the bar graphs and pie charts in panels A and B.

https://cdn.elifesciences.org/articles/76425/elife-76425-fig1-data1-v1.xlsx
Figure 1—source data 2

Raw images and images with cropped areas highlighted of the blots in panel A.

https://cdn.elifesciences.org/articles/76425/elife-76425-fig1-data2-v1.zip

The only portions of TSPAN5 exposed to the cytosol are the N- and C-termini (Berditchevski, 2001). The C-terminus of other tetraspanins has been shown to regulate the intracellular trafficking of other proteins (Bassani et al., 2012). We thus decided to perform a yeast two-hybrid screen using the C-terminal tail of TSPAN5 as a bait. Among the clones identified (the full list is presented in Figure 2—source data 1), four of them coded for amino acids 1–102 of the protein AP4σ, one of the subunits of the adaptor protein complex AP4 (Boehm and Bonifacino, 2001; Bonifacino, 2014; Robinson and Bonifacino, 2001). This complex is an obligate tetramer of four different subunits (β, µ, ε, and σ), which readily assemble and are almost undetectable as single subunits (Hirst et al., 2013). The AP4 complex has been previously shown to participate in intracellular trafficking of transmembrane proteins, including AMPARs via direct interaction of its epsilon subunit with the auxiliary AMPAR subunit Stargazin (Matsuda et al., 2008). We validated the interaction between TSPAN5 and AP4 by GST pulldown on rat brain lysates (cortices and hippocampi) using the C-terminus of TSPAN5 fused to GST (GST-Ct) which precipitated AP4ε (Figure 2A), one of the subunits of the AP4 complex. In addition, we confirmed the interaction via co-immunoprecipitation experiments by immunoprecipitating TSPAN5, AP4σ, or AP4ε from rat brain lysates (cortices and hippocampi) and found that all three proteins were associated (Figure 2B).

Figure 2 with 1 supplement see all
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TSPAN5 interacts with AP4 and forms a complex with GluA2 and Stargazin.

(A) GST-pulldown experiment on adult rat hippocampus and cortex lysates using empty GST or GST fused to TSPAN5 C-terminus (GST-Ct). Input: 2.5% of pulldown volume. Blots probed for AP4ε. Red Ponceau shows the GST-bound fragments. (B) Co-immunoprecipitation experiment on adult rat hippocampus and cortex lysates. Input: 2.5% of the immunoprecipitated volume. Immunoprecipitation: α-rabbit IgG, α-TSPAN5, α-AP4σ, or α-AP4ε. Blots probed for TSPAN5, AP4σ, and AP4ε. (C) GST-pulldown experiments on adult rat hippocampus and cortex lysates using empty-GST or GST fused to the C-terminus of TSPAN5 (GST-Ct). Input: 2.5% of pulldown volume. Blots probed for GluA2/3, GluA1, Stargazin, and NMDAR subunit GluN2A. n = 3 independent experiments. Unpaired Student T test. (D) Quantification of experiment in panel C: intensity of the pulldown band for GluA2/3 and GluA1 each normalised on their input (pulldown/input: GluA2, 1.09±0.07; GluA1, 0.63±0.09). (E) GST-pulldown experiments on adult rat hippocampus and cortex lysates using empty-GST or GST-fused to the C-terminal of Stargazin (GST-Ct Stargazin). Input: 2.5% of pulldown volume. Blots probed for GluA2/3, TSPAN5, and CD81.

Values represent the mean ± SEM. *=p < 0.05, **=p < 0.01, ***=p < 0.001.

Figure 2—source data 1

List of the proteins identified with the yeast two-hybrid screening performed with full-length or C-terminal tail of TSPAN5 and individual data values for the bar graphs in panel D.

https://cdn.elifesciences.org/articles/76425/elife-76425-fig2-data1-v1.xlsx
Figure 2—source data 2

Raw images and images with cropped areas highlighted of the blots in panels A, B, C, and E.

https://cdn.elifesciences.org/articles/76425/elife-76425-fig2-data2-v1.zip

TSPAN5 can form a complex with GluA2 and Stargazin and localises in recycling endosomes

Given the previously shown interaction of AP4 with Stargazin and AMPARs (Matsuda et al., 2008), we performed GST-pulldown experiments to investigate whether TSPAN5 could be part of the same protein complex. By using the C-terminus of TSPAN5 for GST-pulldown experiments on rat brain lysates, we were able to confirm that the C-terminal tail of TSPAN5 is sufficient to precipitate Stargazin, GluA1, and GluA2/3 (Figure 2C). The NMDA receptor subunit GluN2A instead was not detected in the precipitates, supporting the specificity of the interaction. Interestingly, GluA2/3 appeared to be pulled down more efficiently than GluA1, suggesting a preferential association between TSPAN5 and GluA2/3-containing AMPARs (Figure 2D). To further characterise the interaction, we performed GST pulldown using the C-terminal tail of Stargazin, which was previously identified to be the region responsible for the interaction with AP4 (Matsuda et al., 2008). With this experiment, we detected GluA2/3 and TSPAN5 in the precipitate (Figure 2E). As a negative control, CD81, another member of the tetraspanin family, was not precipitated by the GST-Ct-Stargazin.

The formation of the complex was also confirmed in immunoprecipitation experiments in Hela cells, which endogenously express AP4, transfected with TSPAN5-GFP, Stargazin-HA, and GluA2 (Figure 2—figure supplement 1).

AP4, Stargazin, and AMPARs were previously shown to interact in heterologous cells, which have little to no expression of TSPAN5 (Matsuda et al., 2008). This suggests that TSPAN5 is not necessary for the formation of the complex, and we hypothesised that it could be participating in directing these proteins to a specific cellular compartment.

Thus, we next addressed where this association takes place. Given that the intracellular pool of TSPAN5 must reside in intracellular vesicles, we prepared synaptosomes from rat brains (cortices and hippocampi) and loaded their content on a linear sucrose gradient to separate different populations of vesicles (Rao et al., 2011; Figure 3A and B). We observed that AP4ε, TSPAN5, Stargazin, GluA1, and GluA2/3 are all present at significant levels in the heaviest fractions which are positive for the recycling endosomes marker transferrin receptor (Figure 3A and B). This experiment suggests that the intracellular pool of TSPAN5 could associate with AP4, Stargazin, GluA1, and GluA2 in recycling endosomes. We also analysed the localisation of TSPAN5 in cultured hippocampal neurons by evaluating its colocalisation with overexpressed GFP-tagged Rabs: Rab4, Rab7, and Rab11, markers of early, late, and recycling endosomes, respectively (Figure 3C). TSPAN5 showed a high level of colocalisation with all three Rabs. This is not surprising as TSPAN5 is likely to be transported in the endolysosomal pathway, similarly to many other transmembrane proteins that can localise in the plasma membrane. However, colocalisation with Rab11-positive endosomes was significantly higher than with the other two Rabs. To further clarify the location where the complex forms, we transfected DIV12 rat hippocampal neurons with dsRed-tagged Rab5, Rab7, or Rab11 and performed proximity ligation assay (PLA) using antibodies directed against TSPAN5 and GluA2 (Figure 3D). We then measured the colocalisation of the PLA signal, corresponding to sites of proximity between TSPAN5 and GluA2, with each of the Rabs. Although some level of colocalisation was visible with all three Rabs, this was more pronounced with Rab11 (Figure 3D), strongly pointing towards Rab11-positive organelles as the location in which the complex between TSPAN5, AP4, Stargazin, and AMPARs preferentially forms. Control experiments with only one or the other antibody are shown in Figure 3—figure supplement 1.

Figure 3 with 1 supplement see all
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TSPAN5 complex with AP4, Stargazin, and α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors (AMPARs) localises in recycling endosomes.

(A) Vesicles fractionation from synaptosomes obtained from adult rat hippocampus and cortex. Ten isovolumetric fractions were isolated. Blots were probed for: EEA1 for early endosomes, Rab7 for late endosomes, VGLUT1 for synaptic vesicles, TfR for recycling endosomes, AP4ε, GluA1, GluA2/3, Stargazin, and TSPAN5. (B) Quantification of the experiment in panel A: the intensity of each band was normalised over the sum of the intensity of the bands in the 10 fractions. n = 3 separate experiments. (C) Top panel: Confocal images of DIV20 cultured rat hippocampal neurons transfected at DIV12 with plasmids encoding either Rab4-GFP, Rab7-GFP, or Rab11-GFP and immunolabelled for TSPAN5 (magenta). Colocalising puncta are highlighted by white arrowheads. Scale bar = 10 µm. Bottom panel: Quantification of TSPAN5 colocalisation (Mander’s M1 coefficient) with RAB4-GFP, RAB7-GFP, and RAB11-GFP (Mander’s M1 coefficient: Rab4, 0.77±0.02; Rab7, 0.79±0.06; 0.94±0.02). n = 6 neurons per condition. One Way ANOVA, Newman-Kulspost hoc multiple comparison test. (D) Left panel: Confocal images of DIV20 cultured mouse hippocampal neurons transfected at DIV12 with plasmids encoding either Rab5-DsRed, Rab7-DsRed, or Rab11-DsRed, immunolabelled for MAP2 (green) and subjected to proximity ligation assay (PLA) on TSPAN5 and GluA2 antibodies, with far red detection probe (magenta). DsRed signal is shown in cyan. Scale bar = 10 µm. Right panel: Quantification of PLA signal colocalisation with Rab5-DsRed, Rab7-DsRed, and Rab11-DsRed (Mander’s M1 coefficient: Rab5, 0.44±0.07; Rab7, 0.37±0.07; Rab11, 0.91±0.03). n = 16-18 neurons. One Way ANOVA, Newman-Kulspost hoc multiple comparison test.

Values represent the mean ± SEM. *=p < 0.05, **=p < 0.01, ***=p < 0.001.

Figure 3—source data 1

Individual data values for the graphs in panels B, C, and D.

https://cdn.elifesciences.org/articles/76425/elife-76425-fig3-data1-v1.xlsx
Figure 3—source data 2

Raw images and images with cropped areas highlighted of the blots in panel A.

https://cdn.elifesciences.org/articles/76425/elife-76425-fig3-data2-v1.zip

TSPAN5 depletion affects surface and total levels of AMPAR subunits GluA2 and GluA1

Our data so far suggest that TSPAN5 could participate in the intracellular trafficking of AMPARs, a tightly regulated process that is crucial to maintain a correct level of receptors at the synapse membrane and to ensure efficient synaptic transmission (Anggono and Huganir, 2012).

To investigate this possibility, we transfected rat hippocampal neurons at DIV12 with either scrambled, Sh-TSPAN5, or rescue constructs and measured the surface levels of the two most abundant subunits of AMPARs GluA2 (Figure 4A) and GluA1 (Figure 4B) at DIV20. We observed that knockdown of TSPAN5 induced a reduction of surface GluA2 levels that was reversed in the rescue condition (Figure 4A). In contrast, GluA1 appeared to be increased upon TSPAN5 knockdown (Figure 4B), an effect that was reversed in the rescue condition. We also analysed surface levels of both GluA2 and GluA1 specifically in the postsynaptic compartment, by restricting the analysis on dendritic spines or dendritic shafts as identified in the GFP channel by morphological criteria. The reduction of GluA2 and the increase in GluA1 were present in both compartments (Figure 4A and B), suggesting that these effects are not restricted to dendritic spines.

Figure 4 with 1 supplement see all
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TSPAN5 depletion affects surface and total levels of the AMPAR subunits GluA2 and GluA1.

(A) Top panel: Confocal images of dendrites from cultured rat hippocampal neurons transfected at DIV12 with either scrambled, Sh-TSPAN5, or rescue constructs, all co-expressing GFP and immunostained at DIV20 with an antibody against an extracellular epitope of GluA2 (magenta) in non-permeabilising condition. Boxes are 20 μm wide. Full neurons are shown in Figure 4—figure supplement 1. Bottom panel: Quantification of surface GluA2 signal mean intensity on the whole GFP-positive area (GluA2 intensity [A.U.] total: scrambled 14302±1430, Sh-TSPAN5 10250±884, rescue 15476±1352); GluA2 mean intensity in dendritic spines (scrambled 14290±593; Sh-TSPAN5 11006±1055; rescue 14544±1293); GluA2 mean intensity in dendritic shafts (scrambled 14579±610; Sh-TSPAN5 9730±921; rescue 14512±1482). N = scrambled, 23; Sh-TSPAN5, 19; rescue, 18 neurons. One Way ANOVA, Newman-Kulspost hoc multiple comparison test. (B) Top panel: Confocal images of dendrites from cultured rat hippocampal neurons transfected at DIV12 with either scrambled, Sh-TSPAN, or rescue constructs, all co-expressing GFP and immunostained at DIV20 with an antibody against an extracellular epitope of GluA1 (magenta) in non-permeabilising condition. Boxes are 20 μm wide. Full neurons are shown in the Figure 4—figure supplement 1. Bottom panel: Quantification of GluA1 signal mean intensity on the whole GFP-positive area (GluA1 intensity [A.U.] total: scrambled 9404±494, Sh-TSPAN5 11492±817, rescue 9167±565); GluA1 mean intensity in dendritic spines (scrambled 11232±599; Sh-TSPAN5 13711±831; rescue 11185±634); GluA1 mean intensity in dendritic shafts (scrambled 9914±563; Sh-TSPAN5 12128±808; rescue 9610±678). N = scrambled, 35; Sh-TSPAN5, 36; rescue, 35 neurons. One Way ANOVA, Newman-Kulspost hoc multiple comparison test. (C) BS3 crosslinking on DIV20 cultured rat hippocampal neurons infected at DIV12 with lentiviral particles encoding for scrambled, Sh-TSPAN5, or rescue all co-expressing GFP. Blots probed for AMPARs subunits GluA2/3 and GluA1. Tubulin was used as a loading control, GFP was used as a control for infection. Arrowheads indicate total and intracellular bands, arrows indicate crosslinked plasma membrane bands. Full blots are shown in the Figure 4—figure supplement 1. (D) Quantification relative to panel C (GluA2/3: total/tubulin: scrambled 1±0.04, Sh-TSPAN5 0.76±0.06, rescue 0.91±0.04; intra/tubulin: scrambled 1±0.09, Sh-TSPAN5 0.71±0.09, rescue 0.91±0.14; extra/tubulin: scrambled 1±0.06, Sh-TSPAN5 0.75±0.09, rescue 1.08±0.08; GluA1: total/tubulin: scrambled 1±0.15, Sh-TSPAN5 1.65±0.22, rescue 1.14±0.0; intra/tubulin: scrambled 1±0.48, Sh-TSPAN5 0.5±0.4, rescue 0.69±0.44; extra/tubulin: scrambled 1±0.29, Sh-TSPAN5 2.06±0.14, rescue 1.21±0.23). n = 4/6 independent cultures. One Way ANOVA, Newman-Kulspost hoc multiple comparison test.

Values represent the mean ± SEM. *=p < 0.05, **=p < 0.01, ***=p < 0.001.

Figure 4—source data 1

Individual data values for the graphs in panels A, B, and D.

https://cdn.elifesciences.org/articles/76425/elife-76425-fig4-data1-v1.xlsx
Figure 4—source data 2

Raw images and images with cropped areas highlighted of the blots in panel C.

https://cdn.elifesciences.org/articles/76425/elife-76425-fig4-data2-v1.zip

We confirmed these results by BS3 crosslinking in hippocampal neurons that were transduced with lentiviral particles carrying scrambled, Sh-TSPAN5, or rescue DNA (Figure 4C and D). In these experiments, we observed a significant reduction in plasma membrane and total levels of GluA2/3, possibly suggesting an increased degradation of the receptor in addition to its reduced plasma membrane localisation. Similarly, the increase in GluA1 was observed both in the plasma membrane fraction and in the total level, suggesting a potential compensatory effect driven by increased protein synthesis or reduced degradation.

TSPAN5 and AP4 regulate surface GluA2 levels without affecting its internalisation

To investigate whether the TSPAN5-AP4 complex is responsible for the regulation of GluA2 surface levels, we evaluated the GluA2 surface levels in neurons transfected with a construct carrying the Sh-TSPAN5 and the cDNA for the human TSPAN5 lacking the C-terminus (rescue ΔC) (Figure 5A and B), since this region is the one interacting with AP4 (Figure 2A). We found that the TSPAN5- ΔC was unable to rescue the knockdown of TSPAN5, confirming the importance of the TSPAN5-AP4 interaction for maintaining the correct surface levels of GluA2.

Figure 5 with 2 supplements see all
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TSPAN5 and AP4 regulate surface GluA2 levels without affecting its internalisation.

(A) Confocal images of DIV20 cultured rat hippocampal neurons transfected with vectors coding for GFP (green) and either a scrambled ShRNA, the Sh-TSPAN5, and a construct carrying the ShTSPAN5 and the cDNA for TSPAN5 lacking the C-terminus (rescue ΔC), and surface stained at DIV20 for GluA2 (magenta). Scale bar = 10 µm. (B) Quantification of the intensity of the surface GluA2 signal: GluA2 mean intensity (scrambled 30384±1390; Sh-TSPAN5 23654±1113; rescue ΔC 26686±1116). n = 15/19 neurons. One Way ANOVA, Newman-Kulspost hoc multiple comparison test. (C) Left panel: Confocal images of DIV20 cultured rat hippocampal neurons transduced at DIV12 with lentiviral particles coding for an mCherry (magenta) and either scrambled or Sh-TSPAN5 and with lentiviral particles coding for a GFP (green), CRISPR/Cas9, and either a control guide RNA (Ctrl gRNA) or gRNAs directed against AP4B (AP4B gRNA) or AP4E (AP4E gRNA), respectively, and immunostained at DIV20 with an antibody against an extracellular epitope of GluA2 (cyan). Scale bar = 10 µm. Right panel: Quantification of the intensity of the GluA2 signal: GluA2 mean intensity (scrambled-Ctrl gRNA 24627±840; scrambled-AP4B gRNA 20737±1236; scrambled-AP4E gRNA 19339±1165; Sh-TSPAN5-Ctrl gRNA 19864±1331; Sh-TSPAN5-AP4B gRNA 19407±836; Sh-TSPAN5-AP4E gRNA 19836±1279). n = 18 neurons from three independent experiments. One Way ANOVA, Newman-Kulspost hoc multiple comparison test. (D) Left panel: Confocal images of DIV20 culture rat hippocampal neurons transfected at DIV12 with plasmid coding for a GFP (green), CRISPR/Cas9, and either a control guide RNA (Ctrl gRNA) or gRNAs directed against AP4B (AP4B gRNA) or AP4E (AP4E gRNA), respectively, immunostained for MAP2 (magenta) and subjected to proximity ligation assay (PLA) on TSPAN5 and GluA2 antibodies, with red detection probe (cyan). Scale bar = 10 µm. Right panel: Quantification of the density of PLA signal per cell (# PLA puncta/cell: Ctrl gRNA 4.1±1; AP4B gRNA 1.4±0.5; AP4E gRNA 1.8±0.5). n = 18, 15, 16 neurons, respectively from three independent experiments. One Way ANOVA, Newman-Kulspost hoc multiple comparison test.

Values represent the mean ± SEM. *=p < 0.05, **=p < 0.01, ***=p < 0.001.

Figure 5—source data 1

Individual data values for the graphs in panels B, C, and D.

https://cdn.elifesciences.org/articles/76425/elife-76425-fig5-data1-v1.xlsx

We then designed guide RNAs (gRNAs) to knock down AP4β and -ε via CRISPR/Cas9 and tested them by generating lentiviral particles and infecting cultured rat hippocampal neurons. Both RT-PCR and western blotting showed efficient reduction in the levels of AP4 (Figure 5—figure supplement 1). In line with previous findings (Matsuda et al., 2008; Hirst et al., 2013), targeting one subunit reduced the expression also of the others. We then transduced cultured rat hippocampal neurons at DIV12 with lentiviral particles coding for either a control, an APβ, or an AP4ε gRNA and simultaneously with lentiviral particles coding for scrambled or TSPAN5 shRNA. We analysed GluA2 surface levels at DIV20 and observed that the knockdown of either AP4 or TSPAN5 reduced GluA2 levels to the same extent. In addition, the simultaneous knockdown of TSPAN5 and AP4 did not induce any further reduction (Figure 5C), supporting the hypothesis that the two proteins participate in the same pathway.

According to the hypothesised complex arrangement, in which AP4 mediates the interaction between TSPAN5 and Stargazin-AMPARs, we reasoned that removal of AP4 would induce a reduction in the surface levels of GluA2 due to its impossibility to engage in the complex with TSPAN5. To demonstrate this, we performed PLA between TSPAN5 and GluA2 in rat hippocampal neurons transfected at DIV12 with the Ctrl, AP4β, or AP4ε gRNAs (Figure 5D). As expected, reducing AP4 levels compromised the interaction between TSPAN5 and GluA2.

Another tetraspanin, TSPAN7, was previously shown to regulate AMPAR internalisation (Bassani et al., 2012). To explore whether TSPAN5 could have a similar role, we evaluated the internalisation of AMPARs using an antibody-feeding assay. Rat hippocampal neurons transfected at DIV12 with either scrambled or Sh-TSPAN5 were exposed to an α-GluA2 antibody directed against a surface epitope and incubated for different time points. Both scrambled- and Sh-TSPAN5-transfected neurons exhibited a significant increase in the GluA2 intracellular/total ratio after 5 min, suggesting that AMPAR internalisation is not affected by TSPAN5 knockdown. Interestingly, in scrambled-transfected neurons, recycling of the receptor at 10 min post incubation brought GluA2 back to the surface, with levels of the intracellular/total ratio similar to those at time point 0; by contrast, the Sh-TSPAN5-transfected neurons maintained higher levels of internalised receptor at the 10 min time point. This potentially points to defects in GluA2 exocytosis.

TSPAN5 regulates exocytosis of GluA2-containing AMPARs

Given the possible localisation of the TSPAN5, AP4, Stargazin, and AMPAR complex in Rab11-positive organelles, which have been shown to mediate receptor recycling back to the plasma membrane, we decided to directly evaluate GluA2 recycling. To this end, we relied on an overexpression model as recycling levels of endogenous GluA2 receptors are too low to be detected by an antibody-feeding approach. We decided to use super-ecliptic pHluorin (SEP)-tagged GluA2, where the SEP has been inserted in the extracellular domain of GluA2 (Ashby et al., 2004; Sankaranarayanan et al., 2000; Hildick et al., 2012). SEP is extremely useful for intracellular trafficking studies as it is only fluorescent at a neutral pH, allowing for the visualisation of the receptor only when it is exposed to the neutral extracellular environment. Instead, its fluorescence is quenched in the acidic intracellular vesicles. We verified the functionality of SEP-GluA2 by exposure to imaging media at pH 6, which completely abolished the signal, or to media containing NH4Cl that alkalinise also intracellular vesicles (Figure 6—figure supplement 1). To avoid interferences from endoplasmic reticulum (ER)-contained GluA2, we only evaluated the signal in individual dendritic spines, which are virtually devoid of ER (Rathje et al., 2013; Rathje et al., 2014; Wilkinson et al., 2014). We applied a FRAP-FLIP protocol in which a portion of dendrite (ROI) is bleached and then imaged over 300 s while repetitively bleaching the flanking regions of the ROI to eliminate interference from receptors laterally diffusing into the ROI (Hildick et al., 2012; Figure 6A). This protocol allows for the selective visualisation of receptors that were present in intracellular compartments at the time of the initial bleaching. These receptors are quenched and therefore not affected by bleaching, retaining the ability to fluoresce once exposed to the neutral extracellular environment. As such, the protocol allows for the visualisation of newly synthesised receptors and internalised receptors recycling back to the plasma membrane. Application of cycloheximide before the experiment allowed us to block synthesis of new receptors, thereby restricting the analysis to recycling receptors only (Figure 5A). To our surprise, there were no differences in the levels or kinetics of SEP-GluA2 recycling between scrambled-, Sh-TSPAN5-, or rescue mCherry-transfected neurons (Figure 6B–D). Considering the reduction in GluA2 surface levels shown before (Figure 3), the absence of differences in this experiment could be either due to cycloheximide blocking the synthesis of other proteins necessary for TSPAN5-dependent recycling of AMPARs, thus masking the effect of TSPAN5 knockdown, or because TSPAN5 regulates the exocytosis of newly synthesised receptors. We thus used the same FRAP-FLIP approach but without application of cycloheximide; this experimental setup allows for the simultaneous observation of recycling receptor and exocytosis of newly synthesised receptor (Figure 6E). In this experiment, we observed a significant reduction of the recovery after photobleaching in individual dendritic spines of Sh-TSPAN5-transfected neurons compared to scrambled-transfected neurons as measured by the area under the curve (Figure 6F–H). Given this change, we decided to analyse the amplitude and kinetic of exocytosis. To do this, we fitted an exponential curve (ΔF/Fpre=A(1−e−tτ)) onto our data according to Hildick et al., 2012. We then extrapolated the values for A, corresponding to the steady state ΔF/Fpre, and τ, which represents a time constant related to the kinetic of exocytosis (Figure 6I). For both parameters the Sh-TSPAN5 neurons presented significant differences compared to the scrambled condition with smaller A and greater τ, suggesting lower steady-state recovery of GluA2 and slower kinetics (Figure 6I). These defects were completely reversed in rescue-transfected neurons, even showing a potentiation of the recovery. These data strongly suggest that exocytosis of newly synthesised GluA2 receptors is regulated by TSPAN5. However, our experiments do not exclude the possibility that TSPAN5 could also regulate the recycling of GluA2-containing AMPARs, an effect that would be masked by the application of cycloheximide in the experiment presented in Figure 6A–D which could cause the loss of rapidly turning over factors needed for this process.

Figure 6 with 1 supplement see all
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TSPAN5 regulates exocytosis of GluA2-containing α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors (AMPARs).

(A) Schematic of the FRAP-FLIP experiment presented in panel B. SEP-GluA2 in pre-bleaching condition is either fluorescent (green) if exposed to the extracellular media or quenched (light green) if in intracellular compartments. A region of the dendrite is bleached (black box). SEP-GluA2 that was fluorescent (and so extracellularly exposed) at the time of bleaching becomes bleached (light blue). Quenched SEP-GluA2 is not affected by the bleaching. During imaging, the ROI flanking regions are continuously bleached (black lateral boxes), thus lateral diffusing SEP-GluA2 will be bleached. Receptors that have been internalised and directed for recycling are exocytosed and become fluorescent. Newly synthesised receptors would not be present due to the application of cycloheximide (CHX) (crossed out receptors). Controls for pH sensitivity of the SEP signal are shown in Figure 6—figure supplement 1. (B) Live confocal images of individual dendritic spines from DIV20 cultured rat hippocampal neurons transfected at DIV12 with SEP-GluA2 and either scrambled, Sh-TSPAN5, or rescue construct co-expressing mCherry. Neurons were treated for 2 hr with 200 μg/ml of cycloheximide to inhibit protein synthesis and then imaged under a FRAP-FLIP protocol for 5 min to isolate the recycling receptors. mCherry (magenta) and SEP-GluA2 (white) images (time points: prebleach, postbleach, 10, 20, 30, 60, 120, 180, 240, and 300 s) are shown. The dendritic spine mask is depicted with white dashed line. Scale bar =1 µm. (C) Quantification of the ΔF/Fpre for SEP-GluA2 over time for scrambled-, Sh-TSPAN5-, and rescue-transfected neurons. (D) Quantification of the area under the curve relative to panel B (area under the curve [A.U.]: scrambled 15.56±0.74, Sh-TSPAN5 11.99±2.51, rescue 11.77±1.31). n = scrambled, 56; Sh-TSPAN5, 53; rescue, 53 dendritic spines. One Way ANOVA, Newman-Kulspost hoc multiple comparison test.(E) Schematic of the FRAP-FLIP experiment presented in panel F. SEP-GluA2 at basal condition is either fluorescent (green) if exposed to the extracellular media or quenched (light green) if in intracellular compartments. A region of the dendrite is bleached (black box). SEP-GluA2 that was fluorescent (and so extracellularly exposed) at the time of bleaching becomes bleached (light blue). Quenched SEP-GluA2 is not affected by the bleaching. During imaging the ROI flanking regions are continuously bleached (black box), thus lateral diffusing SEP-GluA2 will be bleached. Receptors that have been internalised and directed for recycling are exocytosed and become fluorescent. Newly synthesised receptors could also travel in intracellular vesicles to be exocytosed and become fluorescent. (F) Confocal images of individual dendritic spines from DIV20 cultured rat hippocampal neurons transfected at DIV12 with SEP-GluA2 and either scrambled, Sh-TSPAN5, or rescue construct co-expressing mCherry. Neurons were imaged under a FRAP-FLIP protocol for 5 min to analyse receptor exocytosis. mCherry (magenta) and SEP-GluA2 (white) images (time points: prebleach, postbleach, 10, 20, 30, 60, 120, 180, 240, and 300 s) are shown. The dendritic spine mask is depicted with white dashed line. Scale bar =1 µm. (G) Quantification of the ΔF/Fpre for SEP-GluA2 over time for scrambled-, Sh-TSPAN5-, and rescue-transfected neurons. (H) Quantification of the area under the curve relative to panel E (area under the curve [A.U.]: scrambled 14.85±0.89, Sh-TSPAN5 7.49±1.77, rescue 18.5±2.18). One Way ANOVA, Newman-Kulspost hoc multiple comparison test. (I) Quantification of the parameters A and τ, representative of the steady state ΔF/Fpre and of the time constant of the exocytosis kinetics, based on the fitting of the first eight time points with the exponential function (ΔF/Fpre=A(1−e−tτ) a (ΔF/Fpre): scrambled, 0.0522±0.0002; Sh-TSPAN5, 0.0388±0.0008; rescue, 0.0832±0.0003). (τ (s): scrambled, 4.5±0.2; Sh-TSPAN5, 12.2±1.2; rescue, 7.4±0.2). n = scrambled, 56; Sh-TSPAN5, 35; rescue, 29 dendritic spines. One Way ANOVA, Newman-Kulspost hoc multiple comparison test.

Values represent the mean ± SEM. *=p < 0.05, **=p < 0.01, ***=p < 0.001.

Figure 6—source data 1

Individual data values for the graphs presented in panels C and G.

https://cdn.elifesciences.org/articles/76425/elife-76425-fig6-data1-v1.xlsx

TSPAN5 regulates exocytosis of newly synthesised AMPARs possibly by avoiding their degradation via the lysosomal pathway

To further confirm the role of TSPAN5 in AMPAR exocytosis, we took advantage of an ER retention system called ARIAD (Hangen et al., 2018; Rivera et al., 2000). In this system, the ARIAD-GluA2 is synthesised in the ER similarly to endogenous GluAs, but the presence of a conditional aggregation domain (CAD) results in its retention in this compartment. The protein can be released in a controlled manner by application of the ARIAD ligand that causes the disassembly of the CAD allowing the protein to continue along the secretory pathway. The fusion protein also presents a myc tag on the extracellular side allowing detection of the exocytosed receptor. As such, by applying an anti-myc antibody in the culture media after exposing the cells to the ARIAD ligand, one can assess the levels of plasma membrane inserted ARIAD-GluA2 directly coming from the ER site of synthesis (Figure 7A, B). As expected from our previous results, TSPAN5 knockdown resulted in a reduction in the surface levels of ARIAD-GluA2 90 min after application of the ARIAD ligand, an effect that was rescued by re-expression of the Sh-resistant form of TSPAN5 (Figure 7C). We also analysed dendritic transport of ARIAD-tdTomato-GluA2 via live imaging of neurons 30 min after addition of the ARIAD ligand. Here, we did not detect any change in the average speed of transport of GluA2-containing vesicles in either the anterograde or retrograde direction (Figure 7—figure supplement 1A, B), nor in the average number of vesicles (Figure 7—figure supplement 1C). These results suggest that there is either a lower amount of GluA2 loaded into each of these vesicles directed for exocytosis or that these vesicles fail to deliver their content to the plasma membrane of dendrites and might be directed for degradation as a result.

Figure 7 with 1 supplement see all
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TSPAN5 regulates exocytosis of newly synthesised α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors (AMPARs), possibly by preventing their degradation via the lysosomal pathway.

(A) Schematic of the ARIAD-GluA2 construct. (B) In basal conditions (Berditchevski, 2001), ARIAD-GluA2 is retained in the endoplasmic reticulum (ER) due to the self-assembly properties of the conditional aggregation domain (CAD). Upon application (Charrin et al., 2002), the ARIAD ligand binds to CAD, inhibits self-assembly and allows the ARIAD-GluA2 to move to the Golgi where the endogenous Furin protease cleaves the CAD. ARIAD-GluA2 can now be loaded onto secretory vesicles (Charrin et al., 2014), transported along the dendrites, and subsequently exocytosed (Hemler, 2005). Application of an anti-myc antibody in the culture medium allows for the detection of the plasma membrane pool of GluA2 that was released from the ER after application of the ARIAD ligand. (C) Left panel: Confocal images of DIV20 rat cultured hippocampal neurons transfected at DIV12 with the ARIAD-myc-GluA2 construct and with a plasmid coding for GFP (green) and either scrambled, Sh-TSPAN5, or rescue, and immunostained with an anti-myc antibody in live staining conditions (magenta) 90 min after the application of the ARIAD ligand. Scale bar = 5 µm. Right panel: Quantification of the surface anti-myc mean intensity normalised to scrambled (scrambled 100±7.14; Sh-TSPAN5 71.44±6.81; rescue 101.4±7.92). n = 27–31 neurons per condition. One Way ANOVA, Newman-Kulspost hoc multiple comparison test.(D) Confocal images of secondary dendrites from DIV20 rat cultured hippocampal neurons transfected at DIV12 with either scrambled or Sh-TSPAN5 constructs, both co-expressing GFP. Neurons were treated for 90 min with either vehicle (H2O) or leupeptin (100 μM), fixed and immunostained for GLUA2/3 (magenta). Scale bar = 5 μm. (E) Relative quantification of GluA2/3 staining mean intensity (GluA2/3 mean intensity: scrambled vehicle 31.25±2.43; scrambled leupeptin: 36.95±2.25: Sh-TSPAN5 vehicle: 24.51±1.35; Sh-TSPAN5 leupeptin 33.3±2.22). n = scrambled vehicle, 20; scrambled leupeptin, 20; Sh-TSPAN5 vehicle, 20; Sh-TSPAN5 leupeptin, 20 neurons. One Way ANOVA, Newman-Kulspost hoc multiple comparison test. (F) Left panel: Confocal images of DIV20 rat cultured hippocampal neurons transfected at DIV12 with the ARIAD-myc-GluA1 construct and with a plasmid coding for GFP (green) and either scrambled, Sh-TSPAN5, or rescue, and immunostained with an anti-myc antibody in live staining conditions (magenta) 90 min after the application of the ARIAD ligand. Scale bar = 5 µm. Right panel: Quantification of the surface anti-myc mean intensity normalised to scrambled (scrambled 95.32±5.07; Sh-TSPAN5 52.49±4.95; rescue 81.064±6.2). n = 27–29 neurons per condition. One Way ANOVA, Newman-Kulspost hoc multiple comparison test.

Values represent the mean ± SEM. *=p < 0.05, **=p < 0.01, ***=p < 0.001.

Figure 7—source data 1

Individual data values for the graphs presented in panels C, E, and F.

https://cdn.elifesciences.org/articles/76425/elife-76425-fig7-data1-v1.zip

To test this second possibility, we assessed the total levels of GluA2/3 via immunofluorescence in DIV20 neurons transfected at DIV12 with either scrambled or Sh-TSPAN5 and treated with the lysosomal inhibitor leupeptin (Figure 7D and E), since AMPARs are mostly degraded via this pathway (Ehlers, 2000). Leupeptin treatment increased GluA2/3 to similar levels in scrambled- and Sh-TSPAN5-transfected neurons, suggesting that AMPARs degradation is increased in the absence of TSPAN5 (Figure 7D and E). However, this experiment does not directly demonstrate that GluA2-containing AMPARs are rerouted towards degradation. We also tested whether the exocytosis of newly synthesised GluA1 is regulated by TSPAN5 by using the same ARIAD system (Figure 7F). Silencing TSPAN5 also reduced the surface levels of newly synthesised GluA1, which was rescued by re-expressing an ShRNA-resistant TSPAN5. This strengthen the hypothesis that the overall increase in the surface GluA1 levels (Figure 4B–D) is a compensatory mechanism.

It is important to note that these experiments still do not exclude a possible regulation of TSPAN5 on recycling AMPARs.

Altogether, our data support a model whereby the association of TSPAN5 with GluA2, occurring via AP4 and Stargazin, promotes the exocytosis of AMPARs, potentially via Rab11/TfR-positive recycling endosomes (Figure 8).

Figure 8
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TSPAN5 regulates α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors (AMPARs) exocytosis through recycling endosomes by the formation of a tetrameric complex with AP4 and Stargazin.

Working model of TSPAN5 function in mature neurons (left) and TSPAN5 silencing effects (right). TSPAN5 forms a complex with Stargazin and AMPARs in the endoplasmic reticulum or in endoplasmic reticulum-Golgi intermediate compartment (ERGIC) vesicles. The presence of TSPAN5 is necessary to direct the GluA2 and Stargazin complex to the plasma membrane. TSPAN5 silencing in neurons induces the redirection of GluA2-containing vesicles to lysosomal degradation.

Discussion

In this work, we have identified an intracellular pool of TSPAN5 that participates in the delivery of newly synthesised AMPARs to the plasma membrane. We showed that TSPAN5 forms a complex with AP4, Stargazin, and AMPARs and that this interaction could take place in recycling endosomes. Although the main function of recycling endosomes is to redirect endocytosed receptors back to the plasma membrane, they have also been shown to participate in a non-canonical secretory pathway. Proteins synthesised in the dendritic ER are trafficked to an ER-Golgi intermediate compartment before being loaded to recycling endosomes for insertion in the plasma membrane (Bowen et al., 2017; Hirling, 2009). As a result, the receptors would bypass the Golgi compartment, which is poorly present in dendrites and dendritic spines. The molecular regulators of this process are not well defined. However, our data do not fully identify the nature of the organelles involved, therefore further investigations are required.

In addition, our experiments cannot fully exclude that TSPAN5 could also regulate the recycling of AMPARs. It is thus possible that TSPAN5 could modulate the delivery to the plasma membrane of both newly synthesised and recycling AMPARs.

Although our experiments show a differential effect of TSPAN5 knockdown on surface levels of GluA2 and GluA1 at the steady state, TSPAN5 appears to regulate the exocytosis of both GluA2 and GluA1. This is in line with the fact that both can interact with Stargazin (Chen et al., 2000), and thus with AP4 and TSPAN5 (Figure 2). The differences at the steady state could be due to a compensatory potentiation of a secretory pathway that does not rely on TSPAN5 and that is responsible for GluA1-containing AMPAR delivery exploited to maintain normal synaptic activity. The trafficking of GluA2 and GluA1 was previously shown to be partially regulated by separate mechanisms for example with GluA2 delivery and recycling being a constitutive process, whereas GluA1 exocytosis to the plasma membrane is more dependent on synaptic plasticity (Passafaro et al., 2001; Shi et al., 2001). Our findings do not elucidate whether AMPARs exhibit a different subunit composition upon TSPAN5 knockdown. However, the fact that we observe a reduction in GluA2 and GluA3 and an increase in GluA1 potentially suggests that there could be an overall reduction in GluA2/3 tetramers and that the remaining GluA2 could potentially be redirected to GluA1/2 tetramers. In addition, an increase of GluA1 homomers could also occur. This could partially explain our previous observation that AMPAR-mediated mEPSCs are not affected by TSPAN5 knockdown in either their amplitude or frequency, but display altered kinetics (Moretto et al., 2019) which can be due to a change in the receptor subunit composition (Lu et al., 2009).

Our results also shed new light on AP4 function. AP complexes select transmembrane proteins via interaction through typical sorting motifs and promote their insertion into specific vesicles (Robinson, 2004). A role for AP4 in AMPARs intracellular trafficking was previously shown (Matsuda et al., 2008; Matsuda et al., 2013): AP4 was found to restrict AMPARs from being directed towards the axonal compartment. AP4β knockout mice presented with mislocalisation of AMPARs to the axon, which accumulated in autophagosomes. The authors did not detect a reduction of dendritic AMPARs in AP4β knockout neurons, however this could have been due to compensatory mechanisms arising in vivo upon constitutive knockout of the AP4 complex or because only levels of overexpressed AMPARs were analysed. It remains possible that other AP complexes could compensate for the loss of AP4. In particular, AP1 was found to regulate sorting and exocytosis of membrane proteins (Bonifacino, 2014). Interestingly, the involvement of AP4 in AMPAR exocytosis could potentially explain the intellectual disability phenotype of AP4 deficiency syndrome; an imbalance between GluA2 and GluA1 subunits in the composition of AMPARs was previously shown to cause changes in how neurons respond to synaptic plasticity events, thus impacting on learning and memory functions (Moretto et al., 2018).

As the association between AP4, Stargazin, and AMPARs was shown to occur in heterologous cells, with little to no expression of TSPAN5 (Matsuda et al., 2008), we believe that TSPAN5 is not necessary for the formation of the complex but that it could rather be involved in directing the complex to the correct organelle for its delivery to the plasma membrane.

Together with our previous work, these data highlight the importance of TSPAN5 for neuronal function. TSPAN5 appears to act on two independent pathways; on the one hand, its localisation at the plasma membrane is crucial for the maturation of dendritic spines during neuronal development (Moretto et al., 2019); on the other hand, TSPAN5 localisation in intracellular vesicles in mature neurons regulates exocytosis of AMPARs enabling correct synaptic function.

Experimental models

Animal procedures were performed in accordance with the European Community Council Directive of November 24, 1986 (86/609/EEC) on the care and use of animals. Animal procedures were approved by the Italian Ministry of Health (Protocol Number N° 2D46AN.463).

The HEK293 cell line (293 [HEK-293] CRL-1573 from ATCC, confirmed by STR profiling) used to generate the lentiviruses and the HeLa cells (HeLa CCL-2 from ATCC, confirmed by STR profiling) were grown in DMEM supplemented with 10% FBS, 1% L-glutamine, 0.1% gentamycin. All cell lines were tested for mycoplasma and confirmed negative.

Primary hippocampal neurons were prepared from Wistar E18 rat brains or form C57/BL6 E16 mouse brains (Folci et al., 2014; Zapata et al., 2017; Valnegri et al., 2011). Neurons were plated onto coverslips coated overnight with 0.25 mg/ml poly-D-lysine (Sigma-Aldrich) at 75,000 per well and grown in Neurobasal medium supplemented with 2% B27 prepared as in Chen et al., 2008, 0.25% L-glutamine, 1% penicillin/streptomycin, and 0.125% glutamate (Sigma-Aldrich).

Three-month-old male Wistar rats were used for hippocampus and cortex lysates.

Methods

Plasmids

pLVTHM-scrambled, pLVTHM-Sh-TSPAN5, pSicor-TSPAN5-GFP (rescue), pSicor-TSPAN5-ΔC-GFP (rescue ΔC), pSicor-scrambled-mCherry, pSicor-Sh-TSPAN5-mCherry, pSicor-TSPAN5-mCherry, pGEX4T1-TSPAN5-Ct, and TSPAN5-GFP have been characterised in our previous work (Moretto et al., 2019). Rab4-GFP, Rab7-GFP, and Rab11-GFP are kind gifts from Prof. G Schiavo. pCl-SEP-GluA2 was obtained from Addgene #24001 (Kopec et al., 2006). DsRed-Rab5, DsRed-Rab7, and DsRed-Rab11 were obtained from Addgene (#13050, #12661, #12679) (Sharma et al., 2003; Choudhury et al., 2002). Stargazin-HA and GluA2-myc plasmids were kind gifts of Dr Francoise Coussen. The pLenti-U6-(BsmBI)-hSyn-SaCas9-P2A-EGFP vector allowing the expression of Staphylococcus aureus Cas9 and a gRNA for the knockdown of AP4β and AP4ε were constructed by replacing the EF-1α promoter in the pLenti_SaCRISPR-EGFP plasmid (gift from Christopher Vakoc; Addgene #118636) with the hSyn promoter from the pAAV-hSyn-EGFP plasmid (gift from Bryan Roth; Addgene #50465). The gRNA sequences were designed as previously described (Jaudon et al., 2020; Jaudon et al., 2022; Riccardi et al., 2022) and were inserted downstream of the U6 promoter using BsmbI cloning sites. EGFP expression was used for visualisation of the transduced neurons. The gRNAs were CCGGTAGCGCAGCCTATCAGC and TTGATGAATCCTTACGAAGAG for AP4β and -ε, respectively. The control non-targeting gRNA sequence was GTTCCGCGTTACATAACTTA.

Yeast two-hybrid screening

For yeast two-hybrid experiments, a fragment corresponding to the TSPAN5 C-terminal tail (aa 254–268) was cloned in frame with the GAL4 DNA-binding domain (pGBKT7 vector) and used as bait to screen a human adult brain cDNA library (Clonetech, Mate and Plate Library). Positives clones (3+) grew on plates containing X-α-GAL and Aureobasidin A (QDO/X/A plates) and expressed all four integrated reporter genes: HIS3, ADE2, AUR1C, and MEL1 under the control of three distinct Gal4-responsive promoters. cDNA plasmids from positive clones were recovered via DH5a Escherichia coli (E. coli) and sequenced.

Transfection and infection

For lentivirus production, HEK293FT cells were transfected using the calcium phosphate method. Briefly, DNA was mixed with 130 mM CaCl2 in H2O. One volume of HEBS buffer (280 mM NaCl, 100 mM HEPES, 1.5 mM Na2HPO4, pH 7.11) was added to the DNA and thoroughly mixed to produce air bubbles. The mix was added to the cells and left for 5 hr before washing and changing the medium.

Rat hippocampal neurons were transfected with Lipofectamine 2000 (Invitrogen) following the manufacturer’s instructions or infected with lentiviral particles produced as previously described (Lois et al., 2002).

BS3 crosslinking

Experiments were carried out according to Boudreau et al., 2012. Briefly, primary hippocampal neurons were washed twice with PBS supplemented with 0.1 mM CaCl2 (Sigma-Aldrich) and 1 mM MgCl2 (Sigma-Aldrich) at 37°C. Neurons were then exposed to PBS supplemented with 0.1 mM CaCl2 and 1 mM MgCl2 with or without the BS3 crosslinker (1 mg/ml, Thermo Fisher) at 4°C for 10 min. Neurons were then rapidly washed first with TBS supplemented with 0.1 mM CaCl2 and 1 mM MgCl2 plus 50 mM glycine (Sigma-Aldrich) at 4°C and subsequently with TBS supplemented with 0.1 mM CaCl2 and 1 mM MgCl2 at 4°C prior to lysis with BS3 buffer (50 mM Tris-HCl, 150 mM NaCl, 1 mM EDTA, pH 7.4, 1% SDS plus protease inhibitors). 3× Laemmli sample buffer was then added and samples were analysed by SDS-PAGE and western blotting. Crosslinked proteins present in the plasma membrane appeared as high molecular bands. All the other bands, which were also present in the non-crosslinked reaction, were considered as part of the intracellular pool and their intensity quantified to generate the graphs in Figure 1A, according to our previous results (Moretto et al., 2019). Extracellular and intracellular intensities were normalised on tubulin intensity.

Vesicles purification

Hippocampi and cortices were collected from adult Wistar rats and homogenised with glass-teflon homogeniser in homogenisation buffer (0.32 M sucrose, 20 mM HEPES-NaOH, protease inhibitors, pH 7.4). The total homogenate was centrifuged at 1000 × g for 10 min at 4°C. The supernatant S1 was further centrifuged at 10,000 × g for 15 min at 4°C. The resulting pellet, corresponding to crude synaptosomal fraction, was resuspended in homogenisation buffer and centrifuged again at 10,000 × g for 15 min at 4°C to wash the synaptosomes. Crude synaptosomes were lysed using hypotonic shock by resuspension in H2O. The resulting vesicles were layered on a 9 ml 50–1000 mM sucrose gradient (in H2O) and centrifuged in an SW40Ti Beckman rotor at 65,000 × g for 3 hr. After centrifugation, 10 equal fractions were collected from the top of the gradient, and protein precipitation was performed using 6% trichloroacetic acid and 0.02% deoxycholate. 3× sample buffer was then added and the samples analysed by SDS-PAGE and western blot.

Immunoprecipitation

For immunoprecipitation experiments on hippocampi and cortices, these were dissected from adult rat brains, lysed in RIPA buffer (50 mM Tris, 150 mM NaCl, 1 mM EDTA, 1% NP40, 1% Triton X-100, pH 7.4, protease inhibitor) with a tephlon-glass homogeniser, rotated for 1 hr at 4°C and centrifuged at 10,000 × g for 30 min at 4°C. Supernatants were incubated with antibodies at 4°C overnight. Protein A-agarose beads (GE Healthcare, USA) were incubated with the supernatant at 4°C for 2 hr. Beads were washed three times with RIPA buffer, resuspended in 3× Laemmli sample buffer and analysed by SDS-PAGE followed by western blotting.

For experiments on HeLa we incubated Protein G-agarose beads (GE Healthcare, USA) with antibodies at 4°C for 2 hr. Beads were washed three times with RIPA buffer. Hela lysates in RIPA were incubated with Protein G-agarose beads at 4°C for 1 hr for lysate pre-clearing. The recovered supernatant was then incubated with the antibody-conjugated beads at 4°C overnight, washed three times in RIPA buffer, and resuspended in 3× Laemmli sample buffer and analysed by SDS-PAGE followed by western blotting.

GST pulldown

GST-fusion proteins were prepared by growing transformed BL21 E. coli and inducing recombinant protein expression by adding IPTG (0.5 mM final concentration) for 2 hr. Bacteria were pelleted, and the GST-fusion protein was purified employing standard procedures using glutathione Sepharose beads (Thermo Scientific).

Hippocampi and cortices dissected from adult rat brains were pooled together, lysed in RIPA buffer by homogenisation in a tephlon-glass homogeniser, rotated for 1 hr at 4°C and then centrifuged at 10,000 × g for 30 min at 4°C. Supernatants were incubated with glutathione Sepharose beads for 3 hr at 4°C and then washed and resuspended in 3× sample buffer and analysed by SDS-PAGE followed by western blotting.

Western blots

Proteins were transferred from the acrylamide gel onto the nitrocellulose membrane (0.22 µm, GE Healthcare). Membranes were incubated with the primary antibodies (α-TSPAN5, Aviva Systems Biology #AV46640, 1:500; α-transferrin receptor, Thermo Fisher Clone H68.4, 1:500; α-tubulin, Sigma-Aldrich T5168, 1:40,000; α-AP4σ, gift from Dr Margaret Robinson, 1:500; α-AP4ε, BD Biosciences 612018, 1:1000; α-GluA1, Cell Signaling #13185, 1:1000; α-GluA2/3, gift from Dr Cecilia Gotti, 1:2000; α-Stargazin, Cell Signaling #8511, 1:1000; α-EEA1, BD Transduction Laboratories Clone 14, 1:2000; α-Rab11 BD Transduction Laboratories Clone 47, 1:1500; α-Rab7, SySy 320003, 1:700; α-Vglut1, SySy 135303, 1:2000; α-GFP, MBL #598, 1:2,500; α-GluN2A, Neuromab N327/95, 1:1000; α-CD81, Santa Cruz Biotech #166029, 1:1000; α-GFP, MBL 598, 1:1000; α-HA, Cell Signaling #3724, 1:500) at room temperature for 2–3  hr or overnight at 4°C in TBS Tween-20 (0.1%), milk (5%). After washing, the blots were incubated at room temperature for 1 hr with horseradish peroxidase-conjugated α-rabbit, α-mouse, or α-rat antibodies (1: 2000) in TBS Tween-20 (0.1%), milk (5%). Immunoreactive bands on blots were visualised by enhanced chemiluminescence (Chemidoc XRS+, Bio-Rad) or standard film development.

Immunocytochemistry

Cultured hippocampal neurons were washed in PBS supplemented with 0.1 mM CaCl2 and 1 mM MgCl2 and fixed in paraformaldehyde (PFA) (4%, Sigma-Aldrich)/sucrose (4%, Sigma-Aldrich) for 10 min at room temperature and incubated with primary antibodies (α-TSPAN5, Aviva System Biology #AV46640, 1:50; α-GluA2/3, gift of Dr Cecilia Gotti, 1:500) in GDB1X solution (2×: 0.2% gelatin, 0.6% Triton X-100, 33 mM Na2HPO4, 0.9 M NaCl, pH 7.4) for 2 hr at room temperature.

For surface staining, antibodies (α-GluA2, Merck clone 6C4, 1:200; α-GluA1, Cell Signaling #13185, 1:150, α-myc, Sigma #M5546, 1:1000) were applied to neurons for 10 min at room temperature followed by a washing step in PBS supplemented with 0.1 mM CaCl2 and 1 mM MgCl2 and PFA fixation.

After three washes with high salt buffer (500 mM NaCl, 20 mM NaPO42-, pH 7.4), coverslips were incubated with secondary antibodies (Alexa-conjugated: 1:400; DyLight-conjugated: 1:300) in GDB1X solution for 1 hr at room temperature.

Internalisation experiments were performed as described by Bassani et al., 2012. Briefly, neurons were incubated with the anti-GluA2 surface epitope antibody at 10 μg/ml in culture medium for 10 min at room temperature. Excess antibody was then removed by washing with PBS c/m. The antibody-bound receptors were then allowed to undergo internalisation for 0, 5, or 10 min in the original media at 37°C. After PFA fixation, a secondary antibody labelled with Alexa Fluor 555 was incubated in non-permeabilising condition (PBS supplemented with 10% goat serum) for 1 hr at room temperature, thus labelling receptor-antibody remained on the surface. After washing, the coverslips were incubated with a secondary antibody labelled with DyeLight-649 in permeabilising condition (GDB1X) for 1 hr at room temperature to label the internalised receptor antibody.

Coverslips were washed with high salt buffer and mounted with Mowiol (Sigma-Aldrich).

Quantification was performed as signal measured in the 649 channel (corresponding to internalised AMPARs, IAMPARs) divided by the sum between the signal in the 649 channel and the signal in the 555 channel (corresponding to the extracellular AMPARs E AMPARs): IAMPARs/(IAMPARs + EAMPARs).

PLA was performed according to the manufacturer’s protocol (DuoLink In Situ PLA, Merck Millipore) using DNA probes-conjugated secondary antibodies and DuoLink Fluorescent Detection reagents red or far red.

Colocalisation of the PLA signal and different DsRed-Rabs in Figure 3 was performed using the ImageJ plugin JACOP.

Fluorescence images were acquired with an LSM800 Meta confocal microscope (Carl Zeiss) and a 63× oil-immersion objective (numerical aperture 1.4) with sequential acquisition settings, at 1024×1024 pixels resolution. Images were collected as Z-stack series projections of approximately 6–10 images, each averaged four times and taken at depth intervals of 0.75 μm.

Dendritic spines were counted on all GFP-positive neuronal dendritic arbor excluding the soma and classified with NeuronStudio software (NeuronStudio) according to the following parameters: general parameters for spine identification: length >0.2 μm and <3.0 μm, max width 3.0 μm, stubby spines size >10 voxels, non-stubby spines size >5 voxels. For spine-type classifications, the following logical tests were used: if neck ratio (head/neck diameter)>1.100 then a spine was classified as thin (if also spine length/head diameter >2.5) or mushroom (if also head diameter was >0.35 μm). A spine is classified as stubby if it fails any of the precedent logical tests.

For quantification, a mask was drawn on the GFP or mCherry channel and the immunofluorescence signal for the different antibodies was quantified as mean intensity. For the analysis of surface GluA2 or GluA1 in Figure 4, dendritic spine regions were identified via NeuronStudio as stated above and the quantification performed only on the corresponding areas.

FRAP-FLIP imaging of SEP-GluA2

Neurons transfected with pCl-SEP-GluA2 and either scrambled, Sh-TSPAN5, or rescue mCherry constructs were incubated for 15 min in equilibrated Tyrode’s buffer (15 mM D-glucose, 108 mM NaCl, 5 mM KCl, 2 mM MgCl2, 2 mM CaCl2, and 25 mM HEPES-NaOH, pH 7.4) and coverslips were mounted in an open Inox chamber (Life Imaging Services). For recycling only experiments, neurons were previously incubated with 200 µg/ml cycloheximide (Life Technologies) for 2 hr with cycloheximide also present in the recording Tyrode’s buffer. An LSM800 confocal microscope equipped with an environmental chamber (37°C, 5% CO2) was used. A secondary dendrite from neurons positive for both mCherry and SEP signal was selected and a portion of the dendrite (ROI) was initially bleached with high 488 nm laser power (80%) and then sequentially bleached at the extremities of the ROI and imaged every 500 ms. The fluorescence intensity of SEP-GluA2 on individual dendritic spines was measured for individual time points and normalised as Fn−F0 (∆F)/Fprebleach. The area under the curve was measured via GraphPad Prism 8 as area below a curve fitted by regression on the average values. For the experiment in Figure 6E–I, the exponential curve ΔF/Fpre=A(1−e−tτ) was fitted on the first eight time points and then the values of A and τ were extrapolated from the fitted curve.

Real-time PCR

mRNA was extracted from cultured rat hippocampal neurons using Nucleozol Reagent following the manufacturer’s instructions (Macherey Nagel).

For each condition, 1.5 μg of extracted mRNA was used to synthetise cDNA using SuperScript VILO cDNA Synthesis Kit (Thermo Fisher).

The target sequences of AP4B, AP4E, and β-actin (endogenous control) were amplified from 60 ng of cDNA in the presence of SYBR Green PCR Master Mix (Applied Biosystems) using Applied Biosystems 7000 Real-Time thermocycler. Primer sequences were as follows: AP4B Fw (AGTTGCTGGGACTTCGACAA), AP4B Rv (CCGTGGACCCCAAGTAACC), AP4E Fw (TTCTGGATGGTTTTGTGGCTG), AP4E Rv (CCAGTGAAGCCAGATGAAGAAAA), β-actin Fw (AGATGACCCAGATCATGTTTGAGA), β-actin Rev (CCTCGTAGATGGGCACAGTGT).

Each sample was run in triplicate, and results were calculated using the ΔΔCT method to allow normalisation of each sample to the internal standard and comparison with the calibrator of each experiment.

Experiments with ARIAD constructs

Ninety min after addition of the ARIAD ligand (2 µM), anti-myc antibody (Sigma, #M5546, 1:1000) was added to the media. Neurons were directly fixed with 4% PFA, 4% sucrose, and then incubated with a secondary antibody anti-mouse Alexa Fluor 565. Images were taken with a Leica DM5000 microscope with a 40× objective. Quantification was performed with ImageJ to quantify the surface receptor mean intensity.

Intracellular transport videos were acquired on an inverted Leica microscope (DMI6000B) at the Bordeaux Imaging Center at DIV18–19. This microscope, controlled with Metamorph (Molecular Devices, Sunnyvale, CA, USA), is equipped with a confocal spinning-disk system (Yokogawa CSU-X1, laser: 491 nm, 561 nm), an EMCCD camera (Photometrics Quantem 512), a FRAP scanner (Roper Scientific, Evry, France, 561 nm), and an oil objective HCX PL Apo 100X1.4 NA. The coverslips were mounted in a Ludin chamber with 1 ml of Tyrode medium (15 mM glucose, 100 mM NaCl, 5 mM KCl, 2 mM MgCl2, 2 mM CaCl2, 10 mM HEPES, 247 mosm/l) with 2 µM of ARIAD ligand to release the proteins of interest from the ER, and placed at 37°C in a Life Imaging Services chamber. Videos were acquired between 30 and 60 min of incubation with the ligand using the following acquisition sequence (Hangen et al., 2018): 10 images are acquired (100 ms exposure), followed by the photobleaching of ~60 µm² of proximal dendrite (5 repetitions, 70% laser), followed by video acquisition (1 min at 1 Hz, 300 images, 100 ms exposure). Co-transfection with the sh-RNAs or control was confirmed by the acquisition of an image in the green channel (488 nm) prior to the video recording.

The videos were analysed by generating kymographs, thanks to the ImageJ plugin KymoToolBox (Hangen et al., 2018). The vesicles’ pathways were traced by the deep learning software KymoButler (Jakobs et al., 2019). From those traces, the number of vesicles and mean speed were calculated.

Schematic figure

The schematics in Figures 6A, E—8 were prepared using BioRender software (https://biorender.com/).

Quantification

All statistical analyses were done with GraphPad Prism 8 software.

Two-tailed unpaired t-test was performed to assess statistical significance between two independent groups (Figures 1A and 2D). One-way ANOVA, followed by Newman-Kuls post hoc multiple comparison test, was used to assess statistical significance between three or more groups (Figures 1B, 3C, D—7C, E and F, Figure 5—figure supplement 1; Figure 5—figure supplement 2, Figure 6—figure supplement 1, Figure 7—figure supplement 1).

Statistical details of the experiments can be found in the figure legends (exact mean values, standard errors of the mean [SEM], and n).

Western blots were repeated at least three times from three independent experiments. Imaging experiments on cultured neurons were performed on at least three independent cultures.

Data availability

All data generated during this study are included in the manuscript and supporting files. Source data files have been provided for all figures.

References

  39. Book
    1. Moretto E
    2. Passafaro M
    3. Bassani S
    (2016) X-linked asds and ID gene mutations
    In: Sala C, Verpelli C, editors. Neuronal and Synaptic Dysfunction in Autism Spectrum Disorder and Intellectual Disability. Netherlands: Elsevier. pp. 129–150.
    https://doi.org/10.1016/B978-0-12-800109-7.00009-1

Decision letter

  1. Yukiko Goda
    Reviewing Editor; Okinawa Institute of Science and Technology, Japan
  2. Richard W Aldrich
    Senior Editor; The University of Texas at Austin, United States

In the interests of transparency, eLife publishes the most substantive revision requests and the accompanying author responses.

Decision letter after peer review:

[Editors’ note: the authors submitted for reconsideration following the decision after peer review. What follows is the decision letter after the first round of review.]

Thank you for submitting your work entitled "The tetraspanin TSPAN5 regulates AMPARs exocytosis by interacting with AP-4 complex" for consideration by eLife. Your article has been reviewed by 3 peer reviewers, and the evaluation has been overseen by a Reviewing Editor and a Senior Editor. The reviewers have opted to remain anonymous.

Our decision has been reached after consultation between the reviewers. Based on these discussions and the individual reviews below, we regret to inform you that your work will not be considered further for publication in eLife.

All three reviewers agree that the intracellular regulatory mechanisms underlying the cell surface delivery of AMPAR is an important problem. However, the present study raises more questions than answers, and much further experimental work is required in support of the claimed model. We hope you find the reviewer comments constructive.

Reviewer #1:

Moretto et al. have recently reported a developmental role for a member of tetraspanins TSPAN5, in morphological maturation of dendritic spines. Here, in a follow up study the authors identify an additional role for TSPAN5 in trafficking of GluA2 to the cell surface in mature synapses. TSPAN5 interacts with AP-4 and also with stargazin and GluA1 and GluA2/3 that can be found in the recycling endosomes. Knocking down TSPAN5 reduces cell surface GluA2 as well as total levels of GluA2 while cell surface GluA1 is increased along with its total levels. TSPAN5 knock-down also compromises exocytosis of GluA2 to the spine surface, an effect which is lost upon blocking protein synthesis. Based on these observations, it is concluded that TSPAN5 specifically regulates exocytosis of newly synthesized GluA2 from recycling endosomes. While the findings are potentially interesting, as the manuscript stands, the conclusions are not compellingly supported by the data shown. Additional experiments will be needed in support of the model presented, and further insights into the mechanism by which the interaction of TSPAN5 with AP-4 and stargazin control the surface delivery specifically of GluA2-AMPAR will enhance the impact of the study.

1. Lines 66, 69, 149 and elsewhere. The use of the term "extracellular" is confusing. It should be referred to as the plasma membrane or the cell surface pool.

2. Figure 2C. The sucrose gradient separation analysis appears incomplete in that the information is limited to the relative efficiency in separating early, late and recycling endosomes and synaptic vesicles. The purity of the indicated fractions remain unclear. Other potential membrane sources, such as the Golgi membranes, lysosomes and autophagosomes should be assessed using suitable markers.

3. Figure 2D. The representative images are not of sufficient resolution and raise questions about the quantification shown. What is the scale bar? Also, it would be more meaningful to assess the degree of co-localization of endogenous proteins.

4. Figure 3A,B. Given that TSPAN5 knock-down and rescue have significant effects on spine density (Figure 1B), the changes in surface AMPAR distribution should be assessed by discriminating non-synaptic and synaptic AMPARs. To this end, it would be important to show the changes in GluA1 and GluA2 levels at synapses by confining the analysis to GluA1 and GluA2 puncta that are associated with presynaptic markers (and ideally also associated with a postsynaptic marker such as PSD-95 or Homer). Again, the image quality should be improved. Moreover, given that biochemical experiments (Figure 3C,D) show a change in total levels of GluA1 and GluA2 upon TSPAN5 knock-down, such an observation should also be supported by immunofluorescence labelling experiments to discriminate intracellular and cell surface pools of GluA1 and GluA2. Such experiments (synaptic/non-synaptic, intracellular/cell surface) are crucial for interpreting the single spine targeted FRAP-FLIP experiments shown in Figure 5.

5. Figure 4A. How does leupeptin treatment affect the total GluA1 and GluA2 measured biochemically? The labelling for GluA2/3 is so weak that the quantification is not convincing.

6. Figure 4B. Given that the experiment shown here monitors the fate of surface labelled GluA2 after washing of excess unbound antibodies and then incubating the neurons at 37C for 0, 5 and 10 min, it is not clear why 0 min time point does not show strong surface labelling. In fact, the 10 min time point shows much stronger surface signal, and it is not clear what the source is. Again, the signal quality needs to be improved to support the claim of impaired cell surface recycling of GluA2 upon knock-down of TSPAN5.

7. Figure 5. The design of the FRAP-FLIP protocol is not explained in sufficient detail in the methods, and it is difficult to interpret the figure. The very weak SEP-GluA2 signal poses an issue. Could the authors confirm the presence of intracellular SEP-GluA2 by applying preventing acidification? In addition, it would be helpful to include a control using a cell surface protein whose exo-endocytic recycling is not affected by TSPAN5 knock-down. No evidence is provided here that the relative reduction in GluA2 exocytosis observed upon TSPAN5 knock-down is due to the newly synthesized GluA2. If such were the case, then it is expected that for the scrambled group, the fluorescence intensity measurements representing GluA2 exocytosis should be higher in the absence of cycloheximide compared to cycloheximide treated group, but that is not observed. Moreover, there could be other translated proteins that participate in TSPAN5-dependent regulation of GluA2 traffic, whose activity is compromised by cycloheximide.

Reviewer #2:

Moretto, Longatti et al. found a significant fraction of TSPAN5 exists in the intracellular membrane compartment. There, it interacts directly with AP-4 sigma subunit. TSPAN5 regulates the surface amount of GluR2/3 and GluR1 differently. While TSPAN5 downregulation by shRNA reduces the surface amount of GluR2/3, the same manipulation increases GluR1. The endocytosed GluR2/3 undergo degradation pathway that can be inhibited by leupeptin. Finally, they tested if the recycled and newly synthesized receptors are affected by live imaging. They found that only newly synthesized receptor population was affected by the downregulation of TSPAN5.

Overall, this work is a bit piecemeal. I even feel that it is just a collection of the data they did not publish in their earlier work. They initially made an interesting observation that TSPAN5 interacts with AP-4. But in the rest of study, they did not study about it at all. The data have some ambiguity and often the differences are small to argue anything. They used only single treatment (for example, cycloheximide and leupeptin) to make conclusion. This is also weak.

Another serious concern is that the TSPAN5 antibody they used has multiple extra bands on western blotting on brain tissue (Figure S1 of Moretto et al., 2019). The immunostaining with such antibody cannot be trusted.

English must be edited by a native speaker. I see a lot of grammatical mistakes.

Specific comments.

Figure 1A. The authors should describe in detail how they quantified the extracellular proportion. I see an increase in high-molecular weight population in the presence of the cross-linker. However, strangely, there is no reduction in the monomer band (~35 kd). If the top band is truly cross-linked population, there should be a reduction in the monomer but this is not the case here. Also, it is not clear how they obtained the numbers in graph. Why total is less than Intra+Extra?

Line 86. SEL and LEL domain. "domain" should be plural. But "domain" is often used to refer a protein region which has solid structure but not flexible structure, such as loop between transmembrane domain. I would say "SEL and LEL" is sufficient. Besides the meaning of this sentence of not clear. What do the authors mean by "rely"? Need to rewrite.

Figure 1C. This is not useful. 3+ is not informative. What was the overall result? What genes were identified for how many clones? Among them how many were independent clones? Which domain of AP-4 sigma was identified?

Figure 1D. Add blotting with sigma subunit antibody.

Figure 1E. Something strange in this result. Generally, in a coimmunoprecipitation experiment, the immunoprecipitated protein (for which antibody is used) is much more than coimmunoprecipitated protein. But if one look at the blot, IP with TSPAN5 antibody did not recover more than TSPAN5 protein than IP with AP-4 epsilon antibody. Indeed, there is more TSPAN5 in IP with AP-4epsilon antibody. Also, in the TSPAN5 blot, do not cut the top portion of the band.

Figure 2A. In TSPAN5 blot, there is a clear band in IgG control lane. The authors put an asterisk in IP Stargazin lane. Do they mean this thin band is TSPAN5? It is hard to convince the readers.

Figure 2C. Blotting with Rab4 should be included as it was used in the next panel.

Figure 2D. I have no idea why they could see statistical significance between Rab4 and Rab7. There is only n = 6. Even it is statistically significant, I do not think the authors can make a strong argument as the average is almost the same. Also, they should test significance between Rab4 and Rab11. The authors should explain why TSPAN5 shows a significant colocalization with Rab4 comparable to Rab7 while it was not recovered in early endosome fraction in Figure 2C.

Figure 3. The authors found opposing results for GluR1 and GluR2/3. However, their finding indicates both GluR1 and GluR2/3 equally interacts with TSPAN5. Indeed, the most of GluR1 in hippocampal tissue has both GluR1/2 or GluR2/3 heterooligomer. Only ~8% is GluR1 homomer (Wenthold, 1996). This quantification include interneurons which does not express GluR2 so the amount of GluR1 homomer in pyramidal neurons is even less. The authors seem to have some explanation but merely speculation. This should be experimentally addressed. Here the involvement of AP-4 must be experimentally tested, for example, with Crispr/CAS9 or shRNA.

Figure 3C. The entire blot should be shown for GluR1 and 2/3, not just a part of it.

Figure 5. When comparing the condition with and without cycloheximide, the amount of recovery is almost the same in scrambled control. It is strange because in the absence of cycloheximide, both newly synthesized and recycled receptors are inserted at the synapse while in the presence, only the latter contributes. Also, cycloheximide stops all protein synthesis so the observed difference may or may not be due to newly synthesized GluR2/3. This should be experimentally addressed or the authors should tone down their argument.

Reviewer #3:

This manuscript reports the potential roles of intracellular TSPAN5 in dendritic spines upon neuronal maturation. The authors asked whether the intracellular TSPAN5 that is associated with AP-4 and recycling endosomes regulates AMPARs trafficking with different sets of experiments. In support of this, the authors used ShRNA already characterized to show that acute TSPAN5 downregulation in mature neurons affects the surface and total levels of GluA1 or GluA2. The authors also claimed that the intracellular pool of the tetraspanin TSPAN5 specifically promotes exocytosis of newly synthesized GluA2-containing AMPA receptor without affecting internalization or recycling.

Overall, this is an interesting study. However, I have some concerns which should be thoroughly addressed given that TSPAN5 involvement in dendritic spine maturation has been linked to its membrane clustering with neuroligin-1.

1) The annotation and the quantification of crosslinking experiment are not clear to me. "Intra" means "intracellular not crosslinked" and "extra" means "plasma membrane bound and crosslinked", I guess. Line 68-69, The sentence "here the vast majority of TSPAN5 is extracellular" is not correct.

Quantifications do show an increase in the intracellular pool at DIV19 that is not at all clear on the blots. The last panel in Figure 1A is not commented in the text. Can the authors discuss these points?

A negative control like another TSPAN should be used to show that not all TSPAN have the same profile.

The blots at DIV19 are strangely similar to those published in Figure S1C of Moretto et al., Cell Reports.

The sentence line 71 "This observation suggested that the intracellular pool of TSPAN5 could have a completely unrelated function" seems also misleading. Of course, the intracellular pool is different from the surface one but it can just mean that before being at the surface the TSPAN5 is in intracellular vesicles.

2) Two-hybrid results should be added in supplemental section

3) It would have been nice to illustrate the two different pools using confocal imaging in complement of the ShRNA experiment Figure 1B.

4) In Figure 1E, blots are cut short. Can the authors include a different TSPAN for IP? A negative control for Western blot should be included. I would have been nice to have a comparison with TSPAN7.

5) The interaction or complex between TSPAN5, GluA2 and Stargazin is a quite important point. Is the interaction between TSPAN5 and GluAs or between Stargazin and TSPAN? The co-immunoprecipitation of TSPAN with Stargazin is not convincing. Blots need to be ran a bit longer to separate bands. Alternatively, TSPAN5 antibodies should be used for immunoprecipitation. Can the authors test other antibodies like AMPAR ones? Again, negative controls should be included like NMDAR.

6) Figure 1D, Figure 3A and 3B and Figure 4A and 4B. I am not sure what we should see but images are not convincing. Authors should better illustrate what they are quantifying. How the analysis was done? Details need to be included in the method section

7) Why blots are cut in Figure 3C for GluA2/3 and GluA1? Intra and extra – as define – cannot be quantified in D if blots are developed the same way.

8) In the FRAP-FLIP protocol, neurons are treated with "with cycloheximide to remove newly synthesized receptor". However, in the abstract, the author mentioned that "TSPAN5 specifically promotes exocytosis of newly synthesized GluA2-containing AMPA receptor without affecting its internalization or recycling." This sounds not logical. How can the authors study newly synthetized receptors if they block their synthesis? What about lateral diffusion? Moreover, I do not see in the paper any experiment showing a specific role of TSPAN5 on newly synthesized receptors. GluA1 should be included as a control experiment since it does not behave the same way.

9) Graphs in all figures should be scatter plots or whisker-plots to let the readers see the distribution of the data. Combining column scatter plot and a box-and-whiskers plot on the same graph is a good way to display data.

10) The last paragraph of the discussion is very speculative and the authors should at least include data showing the effect of AP-4 loss on AMPAR exocytosis and trafficking process to claim that the paper "provides a possible mechanism for the intellectual disability symptoms that occur in AP-4 deficiency syndrome."

[Editors’ note: further revisions were suggested prior to acceptance, as described below.]

Thank you for resubmitting your work entitled "The tetraspanin TSPAN5 regulates AMPARs exocytosis by interacting with the AP-4 complex" for further consideration by eLife. Your revised article has been evaluated by Richard Aldrich (Senior Editor) and a Reviewing Editor and consultations with three reviewers. Please note that two reviewers have been newly invited.

The reviewers find the study to be potentially interesting although further extensive revisions with new data are requested:

Essential revisions

1) The precise nature of TSPAN5 interaction with AP-4, especially the binding sites and the intracellular compartment where they interact, and the requirement of the TSPAN5-AP-4 interaction for AMPAR trafficking need to be compellingly shown with additional experiments. In particular, please address the comments below:

Reviewer 1, points 2, 3;

Reviewer 2, under weaknesses – points 6-8

Reviewer 3, points 1, 2

2) The claim for the exclusive regulation of newly synthesized GluA2-AMPARs by TSPAN5 should be removed unless the authors are able to provide concrete experimental evidence. The western blot data in Figure 2A should be quantified, and along with the quantification results, if in vitro interaction experiments in point 1 above provide some insights into possible specificity for GluA2 regulation by TSPAN5, the authors are welcome to speculate in the discussion.

3) For experiments involving fluorescence imaging, image quality needs to be improved.

4) In addition to the above points (1)-(3), the individual reviewer concerns that involve data re-analysis and editing of the text should be carefully addressed.

The individual reviewer comments are appended below.

Reviewer #1 (Recommendations for the authors):

The revised manuscript has been substantially improved with additional control experiments, new experiments, and careful editing. In particular, the monitoring newly synthesized GluA2 using the ARIAD system is elegant. However, several issues remain that require consideration as listed below.

Specific points

P 3, lines 64-69, and discussion. What other proteins do AP-4 interact with? Is TSPAN5 a major interactor or are there others? What is the basis for claiming that AP-4 interaction with TSPAN5 is the crucial one representing the intellectual disability associated with AP-4 deficiency?

Figure 2C. Biochemical fractionation – in the Western blot, TSPAN5 level seems to be the highest in late endosomes enriched for Rab7, along with stargazing, GluA1 and GluA2/3, but clearly devoid of AP-4. This point requires an explanation.

Figure 2D. Representative images of co-localization are difficult to see, which raises questions about the quantification. Higher resolution images should be shown. (This point has been raised in the previous version.)

Figure 5. That the requirement for TSPAN5 in controlling surface levels of GluA2 via exocytosis is likely limited to newly synthesized GluA2 should be confirmed also using bulk surface labelling experiments using surface antibody labelling and/or BS3 cross linking.

P 10, lines 267-270. The logic for the statement is not clear. That a lack of change in the speed or the number of newly ER-exited GluA2 containing vesicles traversing along the dendrite upon KD of TSPAN5 suggest for a lower amount of vesicles containing newly synthesized GluA2 being targeted for exocytosis or they are directed for degradation do not seem to match with the claim that less than 20-30% of total exocytosis is due to recycling GluA2.

Figure 6G,H. To support the conclusion that in the absence of TSPAN5 newly synthesized GluA2 is rerouted for degradation, one should compare the effect of leupeptin treatment on surface vs. intracellular ARIAD-tdTomato-GluA2 with or without TSPAN5. The experiment shown here is limited to demonstrating the effect of leupeptin treatment on the steady-state levels of total GluA2/3, whose reduction in the absence of TSPAN5 is recovered by blocking proteolysis. The pool of GluA2/3 (i.e. newly synthesized GluA2/3 destined for surface delivery) being examined is not clear.

Reviewer #2 (Recommendations for the authors):

Strengths: The authors provide solid data for some of their conclusions.

Figure 1C: GST pulldown of TSPAN5 C-terminus provides further evidence of Y2H interaction with AP-4.

Figure 2A: Greater TSPAN5 pulldown of GluA2 vs. GluA1, but this result should be quantified as this result would improve their argument for a specificity for GluA2.

Figure 3A & 3B Knock down of TSPAN5 decreases GluA2 while increases GluA1 surface intensity via imaging. Figure 3C & 3D uses BS3 crosslinking and qualitatively obtains the same result. However, BS3 cross-linking is a non-standard approach to measure surface receptor (see Weaknesses below).

Figure 4C: The lack of additive/synergistic effect of double knockdown of TSPAN5 and AP-4 implies these molecules act in the same pathway.

Figure 5: TSPAN5 influences surface expression of *newly synthesized* GluA2.

Figure 6: Surface expression is lower in shRNA TSPAN5 using Ariad drug which releases newly synthesized GluA2 from ER (Figure 6C) but this is not due to alterations in rate of trafficking (Figures6D-F), thus the authors use leupeptin to inhibit degradation and see a (modest) change. Thus, the authors suggest that TSPAN5 may increase GluA2 expression by preventing lysosomal degradation (model).

Weaknesses: The strengths above are diminished by significant weaknesses described below. Some conclusions are not supported by experimental evidence.

Figure 1A: the authors use a cross-linking approach with a membrane impermeant cross-linker to distinguish between intracellular and surface TSPAN5. This is a non-standard method as it assumes that there is no monomeric surface TSPAN5 (which would not be subject to cross-linking). A more standard approach to distinguish intracellular from surface protein is using biotinylation studies, which relies on the same chemical properties (ie., formation of stable amide bonds through reactive primary amines). At minimum, caveats of the approach should be stated because the fraction referred to as 'intracellular' is likely an over-estimation. In addition, an explanation of the multiple bands in the immunoblots should be provided as well as which specific bands were included in the graphs shown at right.

Alternatively, this result could be eliminated as attempting to demonstrate an increase in the intracellular pool at DIV 19 does not add significantly to the impact, and in fact, the issues raised above reduce impact. For example, the authors go on to state that, "To test if the increase of intracellular TSPAN5 could be related to a different function compared to its previously described role in dendritic spines maturation (Moretto et al., 2019a)." However, there is no way to distinguish between the intracellular and extracellular pools with the knock-down approach as this would target all TSPAN5.

Figure 1B: The rescue condition appears to be over-expression as the result is above baseline.

Figure 1D: the immunoprecipitation results are not convincing as only AP-4e was pulled down by GST (Figure 1C) and it is highly abundant in the input and not enriched in the co-IP with antibodies for TSPAN5.

Lin 105-108: The statement that the C-terminal region of TSPAN5 present in intracellular vesicles is facing the cytosol is confusing as all TSPAN5 C-terminal regions would face the cytosol regardless of whether present in vesicles, the plasma membrane or along the secretory pathway.

Figure 2A: Is the pull-down through AP-4? Figure 1 implies an interaction of TSPAN5 with AP-4 thus one would expect that AP-4 is present in the pull-down.

Figure 2B: the results are not convincing as the amount pull-downed is very small (much less than 2.5% of the input) and the Ponceau staining indicates more GST-Ct Stargazin protein present compared with GST alone.

Figure 2C: Blots should be quantified to support the conclusion that TSPAN5 is enriched with recycling endosomes as the blot appears to indicate a continuous amount of protein in all of the heavier fractions that overlaps with multiple markers. Indeed, the sucrose gradient fractionation suggests that TSPAN5 could be most highly enriched with Rab7 (late endosomes), which would necessitate revising the model proposed.

Figure 4D: The graph indicates 'GluA2 intracellular/Total mean intensity' as a function of time but the Methods section indicate that primary antibodies were used to label surface receptors followed by 0, 5 or 10 min of internalizaiton followed by non-permeable labeling of secondary antibodies. Thus, it is not at all clear how this methods labels intracellular GluA2 as indicated.

Line 148: The statement that, "As expected for a transmembrane protein that also localises to the plasma membrane, TSPAN5 had a high degree of colocalisation with all three Rabs analyzed" is confusing as the Rab proteins are intracellular proteins. The results in Figure 2D also indicate a modest increase in colocalization with Rab11 compared with the other Rabs, and together with the fractionation experiment in Figure 2C.

The authors should consider eliminating the focus on an intracellular pool of TSPAN5 being the dominant mechanism as the experimental approach does not distinguish between these two pools and the evidence for an increase in the intracellular pool is weak. Identifying the binding motif in the C-terminus of TSPAN5 that binds to AP-4 would strengthen the conclusions. In addition, the study could be improved if the authors can demonstrate a direct link with the AP-4 deficiency syndrome associated with intellectual disability symptoms.

Reviewer #3 (Recommendations for the authors):

In this manuscript, Moretto and Longatti et al. report a new role for TSPAN5 in regulating the trafficking of AMPA receptors. Specifically, the authors claimed that TSPAN5 promotes the exocytosis of the GluA2-containing AMPA receptors through its interaction with AP-4 and stargazin. The study is novel and is of interest to the general neuroscience and cell biology community. However, I have several major concerns, many of which are related to experimental design and data quality/analysis.

• By using GST pull-down assays, the authors showed that TSPAN-5 C-tail interacts with components of the AP-4 subunits, the GluA1 and GluA2 subunits and stargazin. A previous study by the Yuzaki lab (Matsuda et al., Neuron 2008) has reported the interaction between AP-4 and GluA1 through stargazin. However, the contribution of TSPAN-5 on the complex formation is not clear. Co-immunoprecipitation experiments in the heterologous system by overexpressing components of these complex, or if possible, direct binding assays with purified proteins, should provide a better understanding of the relationship between TSPAN5, AP-4, stargazing and AMPA receptors. Importantly, does TSPAN5 knockdown uncouple AMPA receptors-stargazin from the AP-4 complex in neurons? This could be done through proximity ligation assay (PLA – between GluA2/3 with AP-4) in wild-type vs TSPAN5 knockdown neurons.

• The authors have demonstrated using various assays that TSPAN5 is required for efficient trafficking of AMPA receptors, and that TSPAN5 and AP-4 are likely to operate on the same pathway. However, it is not clear if the interaction between TSPAN5 and AP-4 is required for AMPA receptor trafficking. This can be done by performing the rescue experiment with a TSPAN5 mutant that fails to bind to AP-4 (which requires further refinement of AP-4 binding on TSPAN5), or at the very least with TSPAN5 that lacks the C-terminal tail (δ C-tail).

• I am not convinced by the data presented in Figure 3 that TSPAN5 specifically regulates GluA2-AMPARs. In Figure 3B, I can't really see any differences in the levels of surface GluA1 between wild-type and knock-down neurons. Furthermore, the quantification of GluA1 bands from the cross-linking experiments contains only 3-4 data points with large variations among groups. It will be better if the authors consider performing the ARIAD assay or the FRAP-FLIP assay (no CHX) using the GluA1 construct.

• The localisation of TSPAN-5 requires refinement. The images in Figure 3D do not really match the quantitation on the graph that shows a high level of colocalisation between TSPAN5 and endosomal markers. Importantly, where do TSPAN5 interact with AMPARs? These can be performed with PLA assay in neurons co-expressing those Rabs.

• I suggest that the authors re-analyse the FRAP/FLIP data by measuring the amplitude and the kinetics of fluorescence recovery, instead of measuring the area under the curve. For example, data shown in Figure 5G show that the extent of SEP-GluA2 recovery (amplitude) is comparable between wild-type and TSPAN5 knockdown cells, although slightly slower. Importantly, the fluorescent of SEP-GluA2 drops quickly in TSPAN5 knockdown neurons, suggesting a defect of receptor stabilisation post-exocytosis. Not simply a defect in the rate of receptor exocytosis.

• Also, the experiments performed in the presence of cycloheximide cannot rule out the potential involvement of other newly translated proteins that are required for SEP-GluA2 exocytosis. Other experiments are required to conclude that TSPAN5 is required for the trafficking of newly synthesised GluA2 in neurons.

[Editors’ note: further revisions were suggested prior to acceptance, as described below.]

Thank you for resubmitting your work entitled "The tetraspanin TSPAN5 regulates AMPARs exocytosis by interacting with the AP-4 complex" for further consideration by eLife. Your revised article has been evaluated by Richard Aldrich (Senior Editor) and a Reviewing Editor.

The manuscript has been improved but there are some remaining issues that need to be addressed, as outlined below:

1. As the authors acknowledge, the present findings do not directly address whether the interaction of AP-4 with Stargazin and TSPAN5 and its regulation of AMPA receptor traffic is involved in intellectual disability associated with AP-4 deficiency syndrome. The final sentence should be removed from the abstract.

2. Figure 5B, Lines 203-205: The statistical comparison between scrambled and rescue with deltaC TSPAN5 shows only a weak difference, which is quite noticeable compared to the comparison between scrambles and sh-TSPAN5 knock-down. One could argue that there is a considerable recovery of GluA2 intensity. How do sh-TSPAN5 and rescue with deltaC TSPAN5 conditions compare?

3. Figure 6, Lines 281-282. The experiments shown here do not strongly support the claim that the exocytosis of newly synthesized GluA2 receptors is regulated by TSPAN5. The authors should indicate the possibility that rather, factors that are rapidly turned over are needed to promote GluA2 exocytosis.

4. Figure 7, while the ARIAD experiment shows that trafficking of newly synthesized GluA2 is dependent on TSPAN5, the possibility that TSPAN5 also facilitates the recycling of pre-existing GluA2-containing AMPA receptors is not excluded here.

5. Combining the points raised in 3 and 4 above, the authors should tone down the claim that TSPAN5 promotes exocytosis of newly synthesized AMPA receptors or rephrase such that it may not be selective for newly synthesized AMPA receptors. This could be a general mechanism for targeting both new and recycling AMPA receptors to the plasma membrane.

https://doi.org/10.7554/eLife.76425.sa1

Author response

[Editors’ note: the authors resubmitted a revised version of the paper for consideration. What follows is the authors’ response to the first round of review.]

Our decision has been reached after consultation between the reviewers. Based on these discussions and the individual reviews below, we regret to inform you that your work will not be considered further for publication in eLife.

All three reviewers agree that the intracellular regulatory mechanisms underlying the cell surface delivery of AMPAR is an important problem. However, the present study raises more questions than answers, and much further experimental work is required in support of the claimed model. We hope you find the reviewer comments constructive.

Reviewer #1:

Moretto et al. have recently reported a developmental role for a member of tetraspanins TSPAN5, in morphological maturation of dendritic spines. Here, in a follow up study the authors identify an additional role for TSPAN5 in trafficking of GluA2 to the cell surface in mature synapses. TSPAN5 interacts with AP-4 and also with stargazin and GluA1 and GluA2/3 that can be found in the recycling endosomes. Knocking down TSPAN5 reduces cell surface GluA2 as well as total levels of GluA2 while cell surface GluA1 is increased along with its total levels. TSPAN5 knock-down also compromises exocytosis of GluA2 to the spine surface, an effect which is lost upon blocking protein synthesis. Based on these observations, it is concluded that TSPAN5 specifically regulates exocytosis of newly synthesized GluA2 from recycling endosomes. While the findings are potentially interesting, as the manuscript stands, the conclusions are not compellingly supported by the data shown. Additional experiments will be needed in support of the model presented, and further insights into the mechanism by which the interaction of TSPAN5 with AP-4 and stargazin control the surface delivery specifically of GluA2-AMPAR will enhance the impact of the study.

We thank the reviewer for the interest in our findings. As suggested, in addition to further controls for the experiments that were already presented, we have included new experiments directly demonstrating the involvement of AP-4 and TSPAN5 in mediating exocytosis of newly synthesised GluA2-containing AMPARs.

1. Lines 66, 69, 149 and elsewhere. The use of the term "extracellular" is confusing. It should be referred to as the plasma membrane or the cell surface pool.

We agree with the reviewer. This has now been changed to “plasma membrane pool” throughout the manuscript.

2. Figure 2C. The sucrose gradient separation analysis appears incomplete in that the information is limited to the relative efficiency in separating early, late and recycling endosomes and synaptic vesicles. The purity of the indicated fractions remain unclear. Other potential membrane sources, such as the Golgi membranes, lysosomes and autophagosomes should be assessed using suitable markers.

We agree with the reviewer that this experiment does not generate pure fractions, as indicated also by the partial overlap of the different markers. However, it provides an indication of the localisation of the proteins of interest. Immuno-isolation would be the only way to obtain pure populations of organelles. The experiment presented, together with the colocalisation analysis in Figure 2D, provides an indication of the possible identity of the organelle involved. A precise characterisation of this will be the focus of future research. In this work, we aimed to identify the role of TSPAN5 and AP-4 in regulating AMPAR exocytosis.

3. Figure 2D. The representative images are not of sufficient resolution and raise questions about the quantification shown. What is the scale bar? Also, it would be more meaningful to assess the degree of co-localization of endogenous proteins.

We apologise to the reviewer for the low resolution of the uploaded figure. We have provided higher resolution images for this and the other microscopy images presented in the manuscript. The scale bar is now indicated in the figure legend.

Concerning the second point, RabGTPases are notoriously difficult to stain for as endogenous proteins, at least in neurons, hence the use of overexpression with fluorescent tags is widely used and accepted in the literature (Pavlos et al., 2010).

RabGTPases are notoriously complicated to stain as endogenous proteins, at least in neurons, hence the use of overexpression with fluorescent tags is widely used and accepted in the literature.

4. Figure 3A,B. Given that TSPAN5 knock-down and rescue have significant effects on spine density (Figure 1B), the changes in surface AMPAR distribution should be assessed by discriminating non-synaptic and synaptic AMPARs. To this end, it would be important to show the changes in GluA1 and GluA2 levels at synapses by confining the analysis to GluA1 and GluA2 puncta that are associated with presynaptic markers (and ideally also associated with a postsynaptic marker such as PSD-95 or Homer). Again, the image quality should be improved. Moreover, given that biochemical experiments (Figure 3C,D) show a change in total levels of GluA1 and GluA2 upon TSPAN5 knock-down, such an observation should also be supported by immunofluorescence labelling experiments to discriminate intracellular and cell surface pools of GluA1 and GluA2. Such experiments (synaptic/non-synaptic, intracellular/cell surface) are crucial for interpreting the single spine targeted FRAP-FLIP experiments shown in Figure 5.

We apologise to the reviewer for the low quality of the figure. We have provided enlarged, higher resolution images of the dendrites. Images of the full neurons have now been moved to the supplementary figure related to Figure 3.

We thank the reviewer for the suggested experiments. To discriminate synaptic and extrasynaptic pools of AMPARs we would need to implement super resolution microscopy techniques, to which unfortunately, we do not have direct access. As an alternative, in the revised manuscript, we have now presented an additional analysis on the same images in Figure 3 restricting the analysis on dendritic spines or dendritic shafts using the GFP channel as a mask. We observed that the changes detected upon TSPAN5 knockdown are present in both compartments for both GluA2 and GluA1, suggesting that this mechanism is not specifically restricted to synapses.

The reduction in total GluA2 levels observed biochemically in BS3 crosslinking experiments has also been confirmed by our analysis on total staining presented now in figure 6G, H.

5. Figure 4A. How does leupeptin treatment affect the total GluA1 and GluA2 measured biochemically? The labelling for GluA2/3 is so weak that the quantification is not convincing.

We apologise to the reviewer for the low quality of the uploaded figure, we have provided higher resolution images in the revised manuscript. The Leupeptin experiment has now been moved to figure 6G-H.

6. Figure 4B. Given that the experiment shown here monitors the fate of surface labelled GluA2 after washing of excess unbound antibodies and then incubating the neurons at 37C for 0, 5 and 10 min, it is not clear why 0 min time point does not show strong surface labelling. In fact, the 10 min time point shows much stronger surface signal, and it is not clear what the source is. Again, the signal quality needs to be improved to support the claim of impaired cell surface recycling of GluA2 upon knock-down of TSPAN5.

We apologise to the reviewer for the low quality of the figure. Again, we have provided higher resolution images.

In these experiments, the labelling was performed at room temperature to avoid damaging the cells (as this would occur if incubated on ice). This does not completely stop internalisation, hence the signal, although minimal, is present intracellularly even at time 0. This intracellularly labelled GluA2 will undergo recycling and contribute to the extracellular signal (e.g. in time 10). This is why in these experiments the internalisation is always shown as a ratio between the intracellular and total labelled protein, to correct for these effects.

Concerning the low intensity of the surface signal at time point 0, we have provided a more representative image of the data shown.

7. Figure 5. The design of the FRAP-FLIP protocol is not explained in sufficient detail in the methods, and it is difficult to interpret the figure. The very weak SEP-GluA2 signal poses an issue. Could the authors confirm the presence of intracellular SEP-GluA2 by applying preventing acidification? In addition, it would be helpful to include a control using a cell surface protein whose exo-endocytic recycling is not affected by TSPAN5 knock-down. No evidence is provided here that the relative reduction in GluA2 exocytosis observed upon TSPAN5 knock-down is due to the newly synthesized GluA2. If such were the case, then it is expected that for the scrambled group, the fluorescence intensity measurements representing GluA2 exocytosis should be higher in the absence of cycloheximide compared to cycloheximide treated group, but that is not observed. Moreover, there could be other translated proteins that participate in TSPAN5-dependent regulation of GluA2 traffic, whose activity is compromised by cycloheximide.

We apologise for not explaining the experiments in sufficient detail and have expanded on this in the revised manuscript, also providing a schematic in Figure 5A and E.

As suggested by the reviewer, we have now provided images showing the correct disappearance of SEP signal upon application of acidic (pH 6) imaging media and reappearance upon application of 50 mM NH4Cl to alkalinise the intracellular compartments. This is now shown in the supplementary figure related to Figure 5.

Regarding the second point; as stated in the methods section, the fluorescence recovery plots of the experiments are presented as ∆Fluorescence (Fn – F postbleach)/ F(prebleach) to normalise the overexpression levels which are inherently different among cells. In addition, the two experiments (now presented in Figure 5B-D and 5F-H) were performed separately and the SEP-GluA2 signal was acquired at different laser powers and as such, the intensities in the two experiments cannot be directly compared in their values.

Concerning the last point, we thank the reviewer for pointing this out. To more directly address the possible role of TSPAN5 in regulating exocytosis of newly synthesised AMPA receptor, we performed experiments (presented now in Figure 6A-C) taking advantage of the ARIAD system (Rivera et al., 2000; Hangen et al., 2018). In this system, GluA2 is expressed fused to a conditional aggregation domain (CAD) that induces aggregation and trapping of GluA2 in the endoplasmic reticulum, which is the site of AMPAR synthesis. This pool can be released by application of an ariad ligand and exocytosis of this newly synthesised GluA2 can be observed by surface staining with an anti-myc antibody (myc tag inserted in the extracellular portion of GluA2). As shown in Figure 6A-C, this experiment confirms that TSPAN5 regulates exocytosis of newly synthesised GluA2.

We agree with the reviewer that blocking protein synthesis could remove other proteins involved in TSPAN5-mediated AMPAR recycling, we have now pointed this out in the manuscript. However, although possible, this is very unlikely because either the protein in question would need to be completely (or almost) degraded in the timeframe of the experiment (120 min since addition of cycloheximide) and only around 6% of all proteins have a half-life of less than 90 min (Chen et al., 2016), or such protein would need to be newly synthesised to exert its function.

Even if we were in such situation, this does not affect the main conclusion of the paper, that TSPAN5 regulates exocytosis of newly synthesised receptors. According to previous literature (e.g. Passafaro et al., 2001), in the timeframe of the experiment in Figure 5F-H (5 min), new synthesis and recycling accounts for a recovery of 15% of the total surface levels, whereas recycling alone is only between 0% (at time point 0min) and 5.7% (at time point 10 minutes). As such, even if we account for the maximum level (5.7%) and if AMPAR recycling was completely inhibited in absence of TSPAN5 (and this cannot be the case as we still observed some degree of recycling in the experiment in Figure 5A-E, roughly 5%), this could only account for a reduction of 30% (5%/15%), whereas here we observe a reduction of approximately 50% (Figure 5H).

As such, we believe our data demonstrate that TSPAN5 regulates the exocytosis of newly synthesised receptors.

Reviewer #2:

Moretto, Longatti et al. found a significant fraction of TSPAN5 exists in the intracellular membrane compartment. There, it interacts directly with AP-4 sigma subunit. TSPAN5 regulates the surface amount of GluR2/3 and GluR1 differently. While TSPAN5 downregulation by shRNA reduces the surface amount of GluR2/3, the same manipulation increases GluR1. The endocytosed GluR2/3 undergo degradation pathway that can be inhibited by leupeptin. Finally, they tested if the recycled and newly synthesized receptors are affected by live imaging. They found that only newly synthesized receptor population was affected by the downregulation of TSPAN5.

Overall, this work is a bit piecemeal. I even feel that it is just a collection of the data they did not publish in their earlier work. They initially made an interesting observation that TSPAN5 interacts with AP-4. But in the rest of study, they did not study about it at all. The data have some ambiguity and often the differences are small to argue anything. They used only single treatment (for example, cycloheximide and leupeptin) to make conclusion. This is also weak.

In the revised version of the manuscript, in addition to more control experiments, we have now provided new experiments that reinforce the evidence that TSPAN5 and AP-4 participate in regulating the exocytosis of newly synthesised GluA2-containing AMPARs.

Another serious concern is that the TSPAN5 antibody they used has multiple extra bands on western blotting on brain tissue (Figure S1 of Moretto et al., 2019). The immunostaining with such antibody cannot be trusted.

The localisation of tetraspanins in membranes and their complex interaction web produces different patterns of bands depending on the lysis condition. In our previous paper we have shown that upon lysis in RIPA buffer, only one band is detected in brain tissue which is completely lost in mice knockout for TSPAN5 (Figure S1A, Moretto et al., 2019). Upon lysis with buffers including SDS, tetraspanins are retained in oligomeric forms (Figure S1D and F, Moretto et al., 2019). These bands are all reduced in intensity by an ShRNA against TSPAN5 in neuronal cultures. In addition, the ShRNA against TSPAN5 reduces the signal of the anti TSPAN5 antibody also in immunostaining (Figure S1H, Moretto et al., 2019).

The localisation of tetraspanins in membranes and their complex interaction web produces different patterns of bands depending on the lysis condition. In our previous paper, we have shown that upon lysis in RIPA buffer, only one band is detected in brain tissue, which is completely lost in TSPAN5 knockout mice (Figure S1A, Moretto et al., 2019). Upon lysis with buffers including SDS, such as in the experiment in Figure 1A, tetraspanins are retained in oligomeric form (Figure S1D and F, Moretto et al., 2019). These bands are all reduced in intensity by an ShRNA against TSPAN5 in neuronal cultures (Figure S1D, Moretto et al., 2019), the efficiency of which was also confirmed via RT-PCR (Figure S1G, Moretto et al., 2019). In addition, the ShRNA against TSPAN5 reduces the signal of the anti-TSPAN5 antibody in immunostaining (Figure S1H, Moretto et al., 2019).

We believe this is sufficient evidence to demonstrate the specificity of the antibody.

English must be edited by a native speaker. I see a lot of grammatical mistakes.

We apologise to the reviewer for this. We have had the manuscript edited by a professional editing service.

Specific comments.

Figure 1A. The authors should describe in detail how they quantified the extracellular proportion. I see an increase in high-molecular weight population in the presence of the cross-linker. However, strangely, there is no reduction in the monomer band (~35 kd). If the top band is truly cross-linked population, there should be a reduction in the monomer but this is not the case here. Also, it is not clear how they obtained the numbers in graph. Why total is less than Intra+Extra?

We apologise to the reviewer for not clearly explaining how these experiments were quantified; we have also noticed a mistake in the quantification of these experiments.

All bands detected by the anti-TSPAN5 antibody are specific (see previous point above). Hence, they will all have to be considered; in the data we initially presented, we had only quantified the monomer, we have now re-quantified including all bands in the analysis.

The data are presented as intensity of TSPAN5 (total: all bands in the non-crosslinked lane normalised on tubulin; extracellular: intensity of the high molecular weight band that appears only in the BS3 crosslinked lane, normalised to tubulin; intracellular: intensity of all the bands except the high molecular weight crosslinked one, normalised to tubulin). This is the best way to analyse BS3 crosslinking experiments as the affinity of the antibody might be different between the crosslinked protein and the monomeric one (Boudreau et al., 2012). As such, only the different fractions can be compared between themselves (e.g. intracellular at DIV12 vs intracellular at DIV19) and it is not possible to infer what proportion of the protein is actually extracellular or intracellular. This is also likely to be the reason why the reduction in the non-crosslinked bands is not directly visible in the experiment.

Line 86. SEL and LEL domain. "domain" should be plural. But "domain" is often used to refer a protein region which has solid structure but not flexible structure, such as loop between transmembrane domain. I would say "SEL and LEL" is sufficient. Besides the meaning of this sentence of not clear. What do the authors mean by "rely"? Need to rewrite.

We apologise to the reviewer for this. We have rephrased the sentence as follows: “Given that TSPAN5 in the intracellular pool would have its SEL and LEL facing the lumen of vesicles, we hypothesised that this fraction of TSPAN5 could participate in intracellular trafficking through interactions of its cytosol-exposed C-terminus as previously shown for other tetraspanins”.

Figure 1C. This is not useful. 3+ is not informative. What was the overall result? What genes were identified for how many clones? Among them how many were independent clones? Which domain of AP-4 sigma was identified?

We apologise to the reviewers for this. We have provided the list of proteins in the supplementary figure related to Figure 1 and specified the region of AP-4 sigma identified, which corresponded to the first 102 amino acids.

Figure 1D. Add blotting with sigma subunit antibody.

Unfortunately, AP-4 sigma runs very close to the GST protein making it impossible to identify a clear signal in this experiment. However, AP-4 is an obligate tetramer and the presence of a AP-4 epsilon demonstrates that the whole complex is co-precipitated (Hirst et al., 2013).

Figure 1E. Something strange in this result. Generally, in a coimmunoprecipitation experiment, the immunoprecipitated protein (for which antibody is used) is much more than coimmunoprecipitated protein. But if one look at the blot, IP with TSPAN5 antibody did not recover more than TSPAN5 protein than IP with AP-4 epsilon antibody. Indeed, there is more TSPAN5 in IP with AP-4epsilon antibody. Also, in the TSPAN5 blot, do not cut the top portion of the band.

Immunoprecipitation experiments rely on the affinity of antibodies which is inherently different between different antibodies. The anti-AP-4 epsilon antibody looks more efficient in immunoprecipitating AP-4 than the anti-TSPAN5 antibody appears to be in immunoprecipitating TSPAN5, as we used the same amount of antibody (2µg). A comparison of the band intensities in immunoprecipitation experiments performed with different antibodies is therefore not possible.

Figure 2A. In TSPAN5 blot, there is a clear band in IgG control lane. The authors put an asterisk in IP Stargazin lane. Do they mean this thin band is TSPAN5? It is hard to convince the readers.

Unfortunately, the anti-TSPAN5 antibody detects a high signal arising from both the heavy and light chain of the anti-Stargazin antibody. To circumvent this issue, we have now provided a new, cleaner experiment where we used GST fused to the C-terminal tail of Stargazin, which was identified to interact with AP-4 (Matsuda et al., 2008). Using this GST fusion protein, we were able to show precipitation of TSPAN5 together with AMPAR subunit GluA2/3.

Figure 2C. Blotting with Rab4 should be included as it was used in the next panel.

We apologise to the reviewer for this, we have been unable to find a reliable anti-Rab4 antibody to perform this experiment. However, EEA1, which is presented in Figure 2C, is a reliable and routinely used marker of early endosomes.

Figure 2D. I have no idea why they could see statistical significance between Rab4 and Rab7. There is only n = 6. Even it is statistically significant, I do not think the authors can make a strong argument as the average is almost the same. Also, they should test significance between Rab4 and Rab11.

We apologise to the reviewer, we made a mistake in this graph. The significant difference is between Rab4 and Rab11 and there is no statistically significant difference between Rab4 and Rab7, this has been corrected in the revised manuscript.

The authors should explain why TSPAN5 shows a significant colocalization with Rab4 comparable to Rab7 while it was not recovered in early endosome fraction in Figure 2C.

Some partial overlap between EEA1 and TSPAN5 can be seen in lanes 4 and 5 of the fractionation experiment shown in Figure 2C. The high level of colocalisation observed in the imaging experiment could potentially be explained by the overexpression of Rabs, which has been previously shown to enhance their activity thus reducing the maturation of organelles through the endolysosomal pathway (Furusawa et al., 2018). This was necessary as endogenous RabGTPases are notoriously difficult to stain for, at least in neurons, hence the use of overexpression with fluorescent tags is widely used and accepted in the literature (Pavlos et al., 2010).

As such, we believe that the imaging experiment in figure 2D should mostly be considered a comparison between conditions rather than in its absolute values and the results considered together with the fractionation experiment presented in Figure 2C.

Figure 3. The authors found opposing results for GluR1 and GluR2/3. However, their finding indicates both GluR1 and GluR2/3 equally interacts with TSPAN5. Indeed, the most of GluR1 in hippocampal tissue has both GluR1/2 or GluR2/3 heterooligomer. Only ~8% is GluR1 homomer (Wenthold, 1996). This quantification include interneurons which does not express GluR2 so the amount of GluR1 homomer in pyramidal neurons is even less. The authors seem to have some explanation but merely speculation. This should be experimentally addressed.

Although we agree with the reviewer about the importance of AMPA receptor subunit composition, our experiments do not provide any evidence regarding the composition of different oligomers. With our experiments, both in staining, western blot and FRAP-FLIP we are detecting either GluA1 or GluA2 or GluA2/3 as individual proteins. They will then mainly be present in GluA1/2 or GluA2/3 heteromers with a smaller component of GluA1 homomers; however, our experiments cannot resolve this. This is a common approach in the AMPA receptor field mainly because only quite complicated experiments can address the actual abundance of the different oligomers given the presence of GluA2 in both GluA1/2 or GluA2/3.

It is likely that in our experiments, given the reduction of GluA2 and the increase in GluA1, GluA2/3 are the heteromers mainly reduced and it is possible that the remaining GluA2 is redirected to GluA1/2 heteromers and that we will have an increase of GluA1 homomers. We will expand the discussion on this part.

Here the involvement of AP-4 must be experimentally tested, for example, with Crispr/CAS9 or shRNA.

As suggested by the reviewer, we have generated CRISPR/Cas9 constructs to knockdown the expression of AP-4 and analysed the levels of surface GluA2 in this setting, identifying a reduction comparable to that observed upon knockdown of TSPAN5. In addition, the simultaneous knockdown of both TSPAN5 and AP-4 did not lead to a further reduction in GluA2 plasma membrane levels, which strongly supports the participation of these two proteins in the same pathway. This is shown in Figure 4C of the revised manuscript.

Figure 3C. The entire blot should be shown for GluR1 and 2/3, not just a part of it.

We have now added the full blots for GluA2/3 and GluA1 in the supplementary figure related to Figure 3 of the revised manuscript.

Figure 5. When comparing the condition with and without cycloheximide, the amount of recovery is almost the same in scrambled control. It is strange because in the absence of cycloheximide, both newly synthesized and recycled receptors are inserted at the synapse while in the presence, only the latter contributes.

As stated in the methods section, the fluorescence recovery plots of the experiments are presented as ∆Fluorescence (Fn – F postbleach)/ F (prebleach) to normalise the overexpression levels which are inherently different among cells. This would also normalise the levels to prebleach conditions in the presence of cycloheximide (the treatment was carried out for two hours before imaging). In addition, the two experiments (now shown in Figure 5A-D and 5E-H) were performed separately and acquired with different laser powers. Hence the two experiments cannot be directly compared in their absolute values.

Also, cycloheximide stops all protein synthesis so the observed difference may or may not be due to newly synthesized GluR2/3. This should be experimentally addressed or the authors should tone down their argument.

We thank the reviewer for pointing this out.

To more directly address the possible role of TSPAN5 in regulating exocytosis of newly synthesised AMPA receptors, we performed experiments (presented now in Figure 6A-C) taking advantage of the ARIAD system (Hangen et al., 2018; Rivera et al., 2000). In this system, GluA2 is expressed fused to a conditional aggregation domain (CAD) that induces aggregation and traps GluA2 in the endoplasmic reticulum, the site of AMPAR synthesis. This pool can be released by application of an ariad ligand and exocytosis of this newly synthesised GluA2 can be observed by surface staining with an anti-myc antibody (myc tag inserted in the extracellular portion of GluA2). As shown in Figure 6C, this experiment confirms that TSPAN5 regulates exocytosis of newly synthesised GluA2.

We agree with the reviewer that blocking protein synthesis could remove other proteins involved in TSPAN5-mediated AMPAR recycling, we have now pointed this out in the manuscript. However, although possible, this is very unlikely because either the protein in question would need to be completely (or almost) degraded in the timeframe of the experiment (120 min since addition of cycloheximide) and only around 6% of all proteins have a half-life of less than 90 min (Chen et al., 2016), or such protein would need to be newly synthesised to exert its function.

Even if we were in one of these situations, this would not affect the main conclusion of the paper, that TSPAN5 regulates exocytosis of newly synthesised receptors. According to previous literature (e.g. Passafaro et al., 2001), in the timeframe of the experiment in Figure 5F-H (5 min), new synthesis and recycling accounts for a recovery of 15% of the total surface levels, whereas recycling alone is only between 0% (at time point 0min) and 5.7% (at time point 10 minutes). As such, even if we account for the maximum level (5.7%) and if AMPAR recycling was completely inhibited in absence of TSPAN5 (and this cannot be the case as we still observed some degree of recycling in the experiment in Figure 5A-E, roughly 5%), this could only account for a reduction of 30% (5%/15%), whereas here we observe a reduction of approximately 50% (Figure 5H).

Reviewer #3:

This manuscript reports the potential roles of intracellular TSPAN5 in dendritic spines upon neuronal maturation. The authors asked whether the intracellular TSPAN5 that is associated with AP-4 and recycling endosomes regulates AMPARs trafficking with different sets of experiments. In support of this, the authors used ShRNA already characterized to show that acute TSPAN5 downregulation in mature neurons affects the surface and total levels of GluA1 or GluA2. The authors also claimed that the intracellular pool of the tetraspanin TSPAN5 specifically promotes exocytosis of newly synthesized GluA2-containing AMPA receptor without affecting internalization or recycling.

Overall, this is an interesting study. However, I have some concerns which should be thoroughly addressed given that TSPAN5 involvement in dendritic spine maturation has been linked to its membrane clustering with neuroligin-1.

1) The annotation and the quantification of crosslinking experiment are not clear to me. "Intra" means "intracellular not crosslinked" and "extra" means "plasma membrane bound and crosslinked", I guess. Line 68-69, The sentence "here the vast majority of TSPAN5 is extracellular" is not correct.

We apologise to the reviewer for the confusion, their interpretation is correct. We have explained the rationale of BS3 crosslinking experiments in the main text. Concerning the quantification, the data are presented as intensity of TSPAN5 (total: all bands in the non-crosslinked lane normalised on tubulin; extracellular: intensity of the high molecular weight band that appears only in the BS3 crosslinked lane, normalised on tubulin; intracellular: intensity of all the bands except the high molecular weight crosslinked one, normalised on tubulin). This is the best way to analyse BS3 crosslinking experiments as the affinity of the antibody might be different between the crosslinked protein and the non-crosslinked one (Boudreau et al., 2012). As such, only the different fractions can be compared between themselves (e.g. intracellular at DIV12 vs intracellular at DIV19) and it is not possible to infer what proportion of the protein is actually extracellular or intracellular.

For this reason, we agree with the reviewer that the sentence in line 68-69 is incorrect as we cannot compare extracellular and intracellular pools. We have removed it from the revised manuscript.

Quantifications do show an increase in the intracellular pool at DIV19 that is not at all clear on the blots.

We apologise to the reviewer; we have now provided a more representative image. In addition, we have noticed a mistake in the quantification of these experiments.

All bands detected by the anti-TSPAN5 antibody are specific (as seen in (Moretto et al., 2019)). Hence, they will all have to be considered in the quantification. In the data we presented we had only quantified the monomer. This new analysis makes no difference to the final results and is now provided in the revised version of the manuscript. In addition, we have changed the blot for TSPAN5 in Figure 1A for one that is more representative of the new quantification.

The last panel in Figure 1A is not commented in the text. Can the authors discuss these points?

We apologise for not mentioning the Transferrin receptor panels in the text. Transferrin is routinely used as a control cell surface protein for receptor trafficking experiments in neurons. Here, it is used as a control to show that not all plasma membrane proteins follow the same pattern of expression and localisation upon neuronal maturation.

A negative control like another TSPAN should be used to show that not all TSPAN have the same profile.

We apologize for not mentioning the panels about Transferrin receptor in the text. Transferrin is routinely used as a control cell surface protein for receptor trafficking experiments in neurons. It is here used as a control to show that not all plasma membrane proteins follow the same pattern of expression and localization upon neuronal maturation.

The blots at DIV19 are strangely similar to those published in Figure S1C of Moretto et al., Cell Reports.

We have now provided a different and more representative blot for this figure in the revised manuscript. The blots at DIV19 in Figure 1A were exactly the same blots from Figure S1C of Moretto et al., 2019, and we had reported the re-use of this in the submission process.

The sentence line 71 "This observation suggested that the intracellular pool of TSPAN5 could have a completely unrelated function" seems also misleading. Of course, the intracellular pool is different from the surface one but it can just mean that before being at the surface the TSPAN5 is in intracellular vesicles.

We have rephrased the sentence as follows: “We observed an increase in the intracellular levels of TSPAN5 from DIV12 to DIV19, which was not followed by a concomitant increase in plasma membrane levels (Figure 1A), suggesting that increased intracellular levels of TSPAN5 does not necessarily imply increased delivery of this protein to the plasma membrane. The transferrin receptor showed a more stable distribution across these time points”.

If the intracellular pool was only representing TSPAN5 trafficking towards the plasma membrane, we should have observed an increase between DIV12 and DIV19 in both the intracellular and extracellular fraction. Of course, other explanations are possible, for example the intracellular pool could be increased in order to be released in response to synaptic plasticity events, as it is the case for AMPA receptors (Passafaro et al., 2001). However, this prompted us to investigate if TSPAN5 could have another intracellular function, which we identified and described in the following experiments.

2) Two-hybrid results should be added in supplemental section

We have added the list of genes identified with the two-hybrid screen in Supplementary Figure 1. In the main text, we have also specified that the AP-4 sigma clones identified were coding for the first 102 amino acids of the protein.

3) It would have been nice to illustrate the two different pools using confocal imaging in complement of the ShRNA experiment Figure 1B.

We agree with the reviewer; unfortunately, the TSPAN5 antibody does not work for surface staining experiments, and therefore the suggested experiment cannot be performed.

4) In Figure 1E, blots are cut short. Can the authors include a different TSPAN for IP? A negative control for Western blot should be included. I would have been nice to have a comparison with TSPAN7.

We apologise to the reviewer for this, we have now provided a larger image of the blots in Figure 1D. In addition, we have inserted negative controls in the GST pulldown experiments in Figure 2A, B showing that another tetraspanin, CD81, is not precipitated by the C-terminal tail of Stargazin and that the NMDAR subunit 2A is not precipitated by the C-terminal tail of TSPAN5.

5) The interaction or complex between TSPAN5, GluA2 and Stargazin is a quite important point. Is the interaction between TSPAN5 and GluAs or between Stargazin and TSPAN? The co-immunoprecipitation of TSPAN with Stargazin is not convincing. Blots need to be ran a bit longer to separate bands. Alternatively, TSPAN5 antibodies should be used for immunoprecipitation. Can the authors test other antibodies like AMPAR ones? Again, negative controls should be included like NMDAR.

Unfortunately, the anti-TSPAN5 antibody detects a high signal arising from both the heavy and light chain of the anti-Stargazin antibody. To circumvent this issue, we have now provided a new, cleaner experiment in Figure 2B, where we used GST fused to the C-terminal tail of Stargazin, which was identified to interact with AP-4 (Matsuda et al., 2008). Using this GST fusion protein, we were able to show precipitation of TSPAN5 together with AMPAR subunit GluA2/3, but not of the tetraspanin CD81.

In addition, we now show in Figure 2A that the GST pulldown using the C-terminal tail of TSPAN5 does not precipitate the NMDAR subunit 2A.

In general, experiments such as immunoprecipitation or GST-pull down cannot exactly assess direct interactions, but rather demonstrate association in a protein complex. As such, we cannot define the specific interactions. However, the interaction between TSPAN5 and AP-4 is likely to be direct, as we identified it in yeast two-hybrid. The interaction between AP-4 and GluAs is mediated by Stargazin and does not occur without it (Matsuda et al., 2008).

6) Figure 1D, Figure 3A and 3B and Figure 4A and 4B. I am not sure what we should see but images are not convincing. Authors should better illustrate what they are quantifying. How the analysis was done? Details need to be included in the method section

We apologise for the resolution of these images. We have provided higher resolution images in the revised version of the manuscript. The quantifications in Figure 3A, B and 4A, B were done by measuring the mean intensity of the signals in the GFP positive areas. We have added this in the revised manuscript methods section. In addition, now in figure 3A, B we have also analysed the images as suggested by Reviewer #1, restricting the analysis to dendritic spines or dendritic shafts, as isolated using the GFP channel and the NeuronStudio software.

7) Why blots are cut in Figure 3C for GluA2/3 and GluA1? Intra and extra – as define – cannot be quantified in D if blots are developed the same way.

We apologise for not explaining this properly. We have now provided the full blots in the supplementary figure related to figure 3.

Similarly to the experiment in Figure 1A, the quantification and comparison is only made between the same pool between conditions (extracellular in Scrambled vs extracellular in Sh-TSPAN5, both normalised on tubulin) to avoid confusion coming from different affinities of the antibody for crosslinked versus noncrosslinked proteins (Boudreau et al., 2012).

8) In the FRAP-FLIP protocol, neurons are treated with "with cycloheximide to remove newly synthesized receptor". However, in the abstract, the author mentioned that "TSPAN5 specifically promotes exocytosis of newly synthesized GluA2-containing AMPA receptor without affecting its internalization or recycling." This sounds not logical. How can the authors study newly synthetized receptors if they block their synthesis? What about lateral diffusion?

We apologise to the reviewer for not being clear. The rationale behind the experiments in Figure 5 can now be found in the schematic in Figure 5A and 5E. During the project, we hypothesised that TSPAN5 and AP-4 could actually participate in the recycling of AMPARs given the possible localisation in Rab11 positive organelles. As such, we performed the experiment with cycloheximide (Figure 5A-D), to restrict the analysis to recycling AMPARs but we did not observe any difference. We then repeated the FRAP-FLIP experiment without cycloheximide (Figure 5E-H) to include newly synthesised receptors and detected a significant difference. Hence, we hypothesised that the reduction of surface GluA2 in TSPAN5 knockdown is caused by defects in the exocytosis of newly synthesised receptors and not by an effect on receptor recycling. This has been further confirmed by the new experiment in Figure 6A-C (see point below).

Lateral diffusion was excluded in these experiments by using continuous bleaching at the edges of the ROI, as stated in the methods section. This is also explained in the schematics in Figure 5A and 5E.

Moreover, I do not see in the paper any experiment showing a specific role of TSPAN5 on newly synthesized receptors. GluA1 should be included as a control experiment since it does not behave the same way.

We thank the reviewer for pointing this out. To more directly address the possible role of TSPAN5 in regulating exocytosis of newly synthesised AMPA receptors we performed experiments (presented now in Figure 6A-C) taking advantage of the ARIAD system (Hangen et al., 2018; Rivera et al., 2000). In this system, GluA2 is expressed fused to a conditional aggregation domain (CAD) that induces aggregation and trapping of GluA2 in the endoplasmic reticulum, the site of synthesis for most AMPARs. This pool can be released by application of an ariad ligand and exocytosis of this newly synthesised GluA2 can be observed by surface staining with an anti-myc antibody (myc tag inserted in the extracellular portion of GluA2). As shown in Figure 6A-C, this experiment confirms that TSPAN5 regulates exocytosis of newly synthesised GluA2.

9) Graphs in all figures should be scatter plots or whisker-plots to let the readers see the distribution of the data. Combining column scatter plot and a box-and-whiskers plot on the same graph is a good way to display data.

We agree with the reviewer, we have replaced all the bar graphs with column scatter plots showing the distribution of data with the exception of the graphs in Figure 5D and H, as the Area under the curve was calculated as area under the curve fitted on the average of all replicates.

10) The last paragraph of the discussion is very speculative and the authors should at least include data showing the effect of AP-4 loss on AMPAR exocytosis and trafficking process to claim that the paper "provides a possible mechanism for the intellectual disability symptoms that occur in AP-4 deficiency syndrome."

In the revised manuscript, we have generated CRISPR/Cas9 constructs to knockdown the expression of AP-4 and analysed the levels of surface GluA2 in this setting, identifying a reduction comparable to that observed upon knockdown of TSPAN5. In addition, the simultaneous knockdown of both TSPAN5 and AP4 did not lead to a further reduction in GluA2 plasma membrane levels, which strongly supports the participation of these two proteins in the same pathway. This is shown in Figure 4C of the revised manuscript.

References

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[Editors’ note: what follows is the authors’ response to the second round of review.]

Reviewer #1 (Recommendations for the authors):

The revised manuscript has been substantially improved with additional control experiments, new experiments, and careful editing. In particular, the monitoring newly synthesized GluA2 using the ARIAD system is elegant. However, several issues remain that require consideration as listed below.

Specific points

P 3, lines 64-69, and discussion. What other proteins do AP-4 interact with? Is TSPAN5 a major interactor or are there others? What is the basis for claiming that AP-4 interaction with TSPAN5 is the crucial one representing the intellectual disability associated with AP-4 deficiency?

As suggested by the reviewer, we have included information about other interactors of AP-4 identified in neurons in the Introduction (lines 61-65). The paragraph reads as follows: “AP-4 was previously found to regulate the intracellular trafficking and sorting of several transmembrane proteins in neurons including the stargazin-AMPA receptors complex (26), the glutamate receptor δ2 (27), the autophagy regulator ATG9 (28), and DAGLB, an enzyme involved in the production of the endocannabinoid 2-AG (29).”. We do not claim that this interaction is crucial for the intellectual disability phenotype associated with AP-4 deficiency. We just point out that AMPA receptor levels are crucial for synaptic transmission and as such for neuronal functioning and that defects in AMPA receptor levels have been associated with other pathologies characterised by intellectual disability. This suggests that this pathway might be involved in the pathology but we do not demonstrate it in this work.

Figure 2C. Biochemical fractionation – in the Western blot, TSPAN5 level seems to be the highest in late endosomes enriched for Rab7, along with stargazing, GluA1 and GluA2/3, but clearly devoid of AP-4. This point requires an explanation.

As suggested by the reviewer, we have quantified the intensity of the bands of the different proteins analysed, now presented in Figure 3B of the revised manuscript.

It is true that there is a significant pool of TSPAN5, Stargazin and AMPA-Rs in the fractions with the highest signal for Rab7; this is likely the pool of these proteins that is being directed towards degradation, as normally occurring for transmembrane proteins (Vanlandingham and Ceresa, 2009). The absence of AP-4 in this fraction suggests that the complex under study in this work is not present in late endosomes.

A significant pool of TSPAN5, Stargazin and AMPA-Rs is present also in the heaviest fractions 8-10, positive for TfR, where also AP4 is visible. This, together with the new data showing TSPAN5-GluA2 PLA colocalisation being the highest with Rab11, presented in Figure 3D of the revised manuscript, strongly points at the TSPAN5-AP-4-Stargazin-AMPA-Rs complex being present in this compartment.

Figure 2D. Representative images of co-localization are difficult to see, which raises questions about the quantification. Higher resolution images should be shown. (This point has been raised in the previous version.)

We apologise to the reviewer for this. We have changed the images, now in Figure 3C, with images more representative of the quantification and shown with higher resolution (the figure was at 300ppi in the previous version, now at 600ppi). Colocalising puncta are now highlighted with white arrowheads.

Figure 5. That the requirement for TSPAN5 in controlling surface levels of GluA2 via exocytosis is likely limited to newly synthesized GluA2 should be confirmed also using bulk surface labelling experiments using surface antibody labelling and/or BS3 cross linking.

We thank the reviewer for this comment. Studying trafficking of endogenously newly synthesised AMPA-Rs would require very complicated experiments.

Although based on over expression systems, we believe that our experiments in Figures 6 and 7 clearly demonstrate that lowering TSPAN5 levels induces a reduction in the exocytosis of newly synthesised GluA2 AMPA-Rs. In particular, the experiment in figure 7 is based on surface labelling of newly synthetised AMPA receptors and clearly demonstrates that knockdown of TSPAN5 reduces their levels. Overexpressed AMPARs have been extensively used in the field to study their trafficking properties.

P 10, lines 267-270. The logic for the statement is not clear. That a lack of change in the speed or the number of newly ER-exited GluA2 containing vesicles traversing along the dendrite upon KD of TSPAN5 suggest for a lower amount of vesicles containing newly synthesized GluA2 being targeted for exocytosis or they are directed for degradation do not seem to match with the claim that less than 20-30% of total exocytosis is due to recycling GluA2.

We apologise to the reviewer for not being clear in this point. In the experiment presented in Figure 7A-C, we observed a reduction in the surface level of newly synthesised GluA2 but did not detect a change in the speed of transport of the vesicles containing GluA2 nor a change in the number of vesicles travelling. In particular, the reduction in GluA2 surface levels but a normal number of GluA2 positive vesicles could be explained in two ways: (1) these vesicles contain a lower amount of GluA2 (i.e. amount of GluA2 in each vesicle) which we were unable to measure in this experiment or (2) a portion of these vesicles reaches dendritic spines but fails to deliver their content to the plasma membrane. The sentence has been changed as follows: (lines 296-299) “These results suggest that there is either a lower amount of GluA2 loaded into each of these vesicles directed for exocytosis or that these vesicles can reach their destination but fail to deliver their content to the plasma membrane of dendrites and might be directed for degradation as a result.”

Figure 6G,H. To support the conclusion that in the absence of TSPAN5 newly synthesized GluA2 is rerouted for degradation, one should compare the effect of leupeptin treatment on surface vs. intracellular ARIAD-tdTomato-GluA2 with or without TSPAN5. The experiment shown here is limited to demonstrating the effect of leupeptin treatment on the steady-state levels of total GluA2/3, whose reduction in the absence of TSPAN5 is recovered by blocking proteolysis. The pool of GluA2/3 (i.e. newly synthesized GluA2/3 destined for surface delivery) being examined is not clear.

We agree with the reviewer on this point and have downplayed the conclusions of this experiment. The paragraph now reads as follows: (lines 300-307) “To test this second possibility, we assessed the total levels of GluA2/3 via immunofluorescence in DIV20 neurons transfected at DIV12 with either Scrambled or ShTSPAN5 and treated with the lysosomal inhibitor leupeptin (Figure 7D, E), since AMPARs are mostly degraded via this pathway (41). Leupeptin treatment increased GluA2/3 to similar levels in Scrambled and Sh-TSPAN5 transfected neurons, suggesting that AMPARs degradation is increased in the absence of TSPAN5 (Figure 7D-E).

However, this experiment does not directly demonstrate that newly synthesised GluA2 are rerouted towards degradation.”. We believe this does not diminish the importance of our findings and instead open up new studies to understand what is the fate of AMPA-Rs in the absence of TSPAN5 and/or AP-4.

Reviewer #2 (Recommendations for the authors):

Strengths: The authors provide solid data for some of their conclusions.

Figure 1C: GST pulldown of TSPAN5 C-terminus provides further evidence of Y2H interaction with AP-4.

Figure 2A: Greater TSPAN5 pulldown of GluA2 vs. GluA1, but this result should be quantified as this result would improve their argument for a specificity for GluA2.

Figure 3A & 3B Knock down of TSPAN5 decreases GluA2 while increases GluA1 surface intensity via imaging. Figure 3C & 3D uses BS3 crosslinking and qualitatively obtains the same result. However, BS3 cross-linking is a non-standard approach to measure surface receptor (see Weaknesses below).

Figure 4C: The lack of additive/synergistic effect of double knockdown of TSPAN5 and AP-4 implies these molecules act in the same pathway.

Figure 5: TSPAN5 influences surface expression of *newly synthesized* GluA2.

Figure 6: Surface expression is lower in shRNA TSPAN5 using Ariad drug which releases newly synthesized GluA2 from ER (Figure 6C) but this is not due to alterations in rate of trafficking (Figures6D-F), thus the authors use leupeptin to inhibit degradation and see a (modest) change. Thus, the authors suggest that TSPAN5 may increase GluA2 expression by preventing lysosomal degradation (model).

Weaknesses: The strengths above are diminished by significant weaknesses described below. Some conclusions are not supported by experimental evidence.

Figure 1A: the authors use a cross-linking approach with a membrane impermeant cross-linker to distinguish between intracellular and surface TSPAN5. This is a non-standard method as it assumes that there is no monomeric surface TSPAN5 (which would not be subject to cross-linking). A more standard approach to distinguish intracellular from surface protein is using biotinylation studies, which relies on the same chemical properties (ie., formation of stable amide bonds through reactive primary amines). At minimum, caveats of the approach should be stated because the fraction referred to as 'intracellular' is likely an over-estimation. In addition, an explanation of the multiple bands in the immunoblots should be provided as well as which specific bands were included in the graphs shown at right.

We agree that BS3 would fail to crosslink monomeric TSPAN5 that is not engaging in any interaction even if present on the surface. However, we hypothesise that the level of this pool is likely to be extremely low, considering that tetraspanins exert their function by homo and heterotypic interactions in the so called Tetraspanin Enriched Microdomains. We have mentioned this limitation in the main text as follows: (lines 89-93) “It needs to be mentioned that it is possible that a fraction of TSPAN5 present on the plasma membrane does not interact with any other protein. This fraction would not be crosslinked and run as a monomer. However, this eventuality is quite unlikely, especially considering that the main function of tetraspanins is exerted by homo and heterotypic interactions (Charrin et al., 2014).” Thus, we believe that our claim about an increase in the intracellular pool could still be valid.

In addition, as suggested by the reviewer, we have explained that we considered all bands that appear in the western blot as we previously demonstrated that they are all specific as they are decreased by the ShRNA against TSPAN5 (Moretto et al., 2019, supplementary Figure 1F). We have explained this in the main text which reads as follows: (lines 81-85) “As shown in Figure 1A, TSPAN5 appears as a complex pattern of bands. This is probably due to the association of this protein with cholesterol rich membranes which makes it poorly soluble in standard lysis buffers (3). We previously demonstrated that all these bands are specific (11) and thus they were all included in the quantification.”

Alternatively, this result could be eliminated as attempting to demonstrate an increase in the intracellular pool at DIV 19 does not add significantly to the impact, and in fact, the issues raised above reduce impact. For example, the authors go on to state that, "To test if the increase of intracellular TSPAN5 could be related to a different function compared to its previously described role in dendritic spines maturation (Moretto et al., 2019a)." However, there is no way to distinguish between the intracellular and extracellular pools with the knock-down approach as this would target all TSPAN5.

Although the point made by the reviewer about BS3 cannot be ruled out by our experiments, we find it extremely unlikely. We agree that this result is not crucial for the impact of the paper but it genuinely represent our thinking process during the development of the project.

This increase in the intracellular pool between DIV12 and DIV19 might suggest that the function of intracellular TSPAN5 is likely more important in more mature neurons, whereas the “extracellular” function of TSPAN5 on dendritic spine maturation that we previously described (Moretto et al., 2019) is crucial at younger stages as these are when most of synaptogenesis occurs in culture (Chanda et al., 2017).

Considering this point, we designed the strategy followed throughout the manuscript, which consisted in silencing TSPAN5 (and/or AP4) at DIV13 to reduce the protein levels when synaptogenesis is well underway, to reduce the interference of the “extracellular” synaptogenic function of TSPAN5 and better isolate the other function described in this manuscript. It is true that knockdown would reduce levels of TSPAN5 both intracellularly and extracellularly, but we are showing that TSPAN5 knockdown at DIV13 minimally impact synaptogenesis.

Although these experiments do not incontrovertibly demonstrate that the increase in TSPAN5 levels is due to the increase in the intracellular pool, they strongly suggest it, and we think are interesting and worth sharing with the scientific community, highlighting the rightful caveats raised by the reviewer (see point above).

Figure 1B: The rescue condition appears to be over-expression as the result is above baseline.

It is true that in many of our experiments, the rescue condition seems to induce a potentiation of TSPAN5 function. We believe that the importance of the rescue experiments in this work is to show the specificity of the function isolated with ShRNA-based knockdown and exclude off-target effects of this approach. This is demonstrated by the restoration of the defects induced by ShRNA expression by concomitant expression of an ShRNA-resistant form of TSPAN5.

The potentiation of TSPAN5 function is potentially linked to the fact that TSPAN5 expression in the Rescue condition is under the control of strong constitutive promoters and is not controlled by the endogenous TSPAN5 promoter and regulatory elements thus resulting in a relative overexpression.

Figure 1D: the immunoprecipitation results are not convincing as only AP-4e was pulled down by GST (Figure 1C) and it is highly abundant in the input and not enriched in the co-IP with antibodies for TSPAN5.

We respectfully disagree with this point. We only explored the presence of AP-4ε in the pulldown experiment (now shown in Figure 2A) because this is the only subunit for which good commercially available antibodies exist.

Regarding the Co-IP (now in Figure 2B), this experiment is used to demonstrate that an association exists between the analysed proteins. Using Co-Ips to judge the strength of an interaction is very complicated. Although we used the same amount (in µg) of the different antibodies for precipitation, these will have different affinities for their target proteins. In addition, each antibody might have different affinity for the protein in its native folded configuration compared to the denatured form of the protein that is detected in the western blot. As such we believe that, although the levels of AP-4 epsilon appear to be low in the TSPAN5 immunoprecipitate compared to the input, this experiment shows only that TSPAN5, AP4 epsilon and AP4 sigma (here detected with an homemade antibody from J Hirst, which was not available at the time of the pulldown experiment) are present in the same macromolecular complex. The interaction is specific as none of the proteins is present in the IgG control.

Line 105-108: The statement that the C-terminal region of TSPAN5 present in intracellular vesicles is facing the cytosol is confusing as all TSPAN5 C-terminal regions would face the cytosol regardless of whether present in vesicles, the plasma membrane or along the secretory pathway.

We agree with the reviewer that this sentence was confusing. We have changed it as follows: (lines 110113) “The only portions of TSPAN5 exposed to the cytosol are the N and C termini (1). The C-terminus of other tetraspanins have been shown to regulate the intracellular trafficking of other proteins (12). We thus decided to perform a yeast two-hybrid screen using the C-terminal tail of TSPAN5 as bait.”

Figure 2A: Is the pull-down through AP-4? Figure 1 implies an interaction of TSPAN5 with AP-4 thus one would expect that AP-4 is present in the pull-down.

The interaction shown here (now figure 2C) is indeed mediated by AP-4, as demonstrated by the reduction in PLA signal between TSPAN5 and GluA2 upon AP-4 knockdown (shown in Figure 5D). We just did not think it was necessary to show AP-4 in this blot as we show it in Figure 2A in the same experimental paradigm (pulldown with GST-C Terminus of TSPAN5).

Figure 2B: the results are not convincing as the amount pull-downed is very small (much less than 2.5% of the input) and the Ponceau staining indicates more GST-Ct Stargazin protein present compared with GST alone.

We respectfully disagree with the reviewer. In this figure (now Figure 2E), the Ponceau shows one band in the empty GST and two major bands in the GST-Ct-Stargazin. The lower band in the GST-Ct-Stargazin is likely to be GST that has lost the CT-Stargazin given that it runs at the same molecular weight as the band in the empty GST lane. This is quite common in this type of experiments (for example, a similar phenomenon can be seen in the Ponceau in Figure 2A).

Hence, only the upper of the two bands in the GST-Ct-Stargazin lane would be pulling down interactors of Stargazin. The intensity of this upper band is comparable to that in the empty GST lane. In addition, although it is true that the amount of proteins pulled down is lower than the input, we do not think this hamper our conclusions. The experiment shows that these proteins can associate and that the interactions are specific, which is demonstrated by the higher signal compared to the empty GST and the absence of pulled down CD81. In addition, GluA2/3, an extremely well characterised interactor of stargazin, is precipitated in a very similar way, with a level lower in the pulldown compared to the input, and a weak signal in the empty GST control.

Figure 2C: Blots should be quantified to support the conclusion that TSPAN5 is enriched with recycling endosomes as the blot appears to indicate a continuous amount of protein in all of the heavier fractions that overlaps with multiple markers. Indeed, the sucrose gradient fractionation suggests that TSPAN5 could be most highly enriched with Rab7 (late endosomes), which would necessitate revising the model proposed.

As suggested by the reviewer, we have quantified the intensity of the bands of the different proteins analysed, now presented in Figure 3B of the revised manuscript.

It is true that there is a significant pool of TSPAN5, Stargazin and AMPA-Rs in the fractions positive for Rab7; this is likely the pool of these proteins that is being directed towards degradation, as normally occurring for transmembrane proteins (Vanlandingham and Ceresa, 2009). The absence of AP-4 in this fraction suggests that the complex under study in this work is not present in late endosomes. Of course, this does not exclude a possible separate function for this pool, but this is not the focus of the present study.

A significant pool of TSPAN5, Stargazin and AMPA-Rs is present also in the heaviest fractions 8-10, positive for TfR, where also AP4 is visible. This, together with the new data showing TSPAN5-GluA2 PLA colocalisation being the highest with Rab11, presented in Figure 3D of the revised manuscript, strongly points to the TSPAN5-AP-4-Stargazin-AMPA-Rs complex being present in this compartment.

Following the reviewer’s comment, we have however removed the claim that the proteins are enriched in TfR-positive fractions stating only their concomitant presence.

Figure 4D: The graph indicates 'GluA2 intracellular/Total mean intensity' as a function of time but the Methods section indicate that primary antibodies were used to label surface receptors followed by 0, 5 or 10 min of internalizaiton followed by non-permeable labeling of secondary antibodies. Thus, it is not at all clear how this methods labels intracellular GluA2 as indicated.

We apologise with the reviewer for not explaining this clearly. This has been now better explained in the method section as follows: (lines 545-564) “Internalisation experiments were performed as described by Bassani and colleagues (12). Briefly, neurons were incubated with the anti-GluA2 surface epitope antibody at 10 μg/ml in culture medium for 10 min at room temperature. Excess antibody was then removed by washing with PBS c/m. The antibody-bound receptors were then allowed to undergo internalisation for 0, 5 or 10 min in the original media at 37°C. After paraformaldehyde fixation, a secondary antibody labelled with AlexaFluor 555 was incubated in non-permeabilising condition (PBS supplemented with 10% goat serum) for 1 h at room temperature, thus labeling receptor-antibody remained on the surface. After washing, the coverslips were incubated with a secondary antibody labelled with DyeLight-649 in permeabilising condition (GDB1X containing 0.3% Triton X-100) for 1 h at room temperature to label the internalized receptor-antibody.

Coverslips were washed with high salt buffer and mounted with Mowiol (Sigma Aldrich).

Quantification was performed as signal measured in the 649 channel (corresponding to internalised AMPA receptors, I AMPARs) divided by the sum between the signal in the 649 channel and the signal in the 555 channel (corresponding to the extracellular AMPA receptors E AMPARs): I AMPARs/ (I AMPARs + E AMPARs).”

Line 148: The statement that, "As expected for a transmembrane protein that also localises to the plasma membrane, TSPAN5 had a high degree of colocalisation with all three Rabs analyzed" is confusing as the Rab proteins are intracellular proteins. The results in Figure 2D also indicate a modest increase in colocalization with Rab11 compared with the other Rabs, and together with the fractionation experiment in Figure 2C.

We agree with the reviewer that this sentence was not clear. We have changed it as follows: (lines 159-161) “TSPAN5 showed a high level of colocalisation with all three Rabs. This is not surprising as TSPAN5 is likely to be transported in the endolysosomal pathway, similarly to many other transmembrane proteins that can localise in the plasma membrane.” To strengthen the conclusion of TSPAN5 colocalisation with recycling endosomes we have quantified the levels of all the proteins analysed in the fractionation experiment, now shown in figure 3A,B which shows high level of TSPAN5 in the TfR positive fraction, and have included a Proximity ligation assay (PLA) showing that the association between TSPAN5 and GluA2 mostly takes place in Rab11 positive organelles, shown in Figure 3D of the revised manuscript.

Reviewer #3 (Recommendations for the authors):

In this manuscript, Moretto and Longatti et al. report a new role for TSPAN5 in regulating the trafficking of AMPA receptors. Specifically, the authors claimed that TSPAN5 promotes the exocytosis of the GluA2-containing AMPA receptors through its interaction with AP-4 and stargazin. The study is novel and is of interest to the general neuroscience and cell biology community. However, I have several major concerns, many of which are related to experimental design and data quality/analysis.

• By using GST pull-down assays, the authors showed that TSPAN-5 C-tail interacts with components of the AP-4 subunits, the GluA1 and GluA2 subunits and stargazin. A previous study by the Yuzaki lab (Matsuda et al., Neuron 2008) has reported the interaction between AP-4 and GluA1 through stargazin. However, the contribution of TSPAN-5 on the complex formation is not clear. Co-immunoprecipitation experiments in the heterologous system by overexpressing components of these complex, or if possible, direct binding assays with purified proteins, should provide a better understanding of the relationship between TSPAN5, AP-4, stargazing and AMPA receptors. Importantly, does TSPAN5 knockdown uncouple AMPA receptors-stargazin from the AP-4 complex in neurons? This could be done through proximity ligation assay (PLA – between GluA2/3 with AP-4) in wild-type vs TSPAN5 knockdown neurons.

We thank the reviewer for raising this point. Indeed our reasoning is that TSPAN5 binds AP-4 sigma, as identified by yeast two hybrid. As shown in Matsuda et al., 2008, AP-4 can in turn interact with Stargazin, via its cargo binding subunit AP-4µ and through this interaction form a complex with AMPA-Rs. As such, the complex would be formed by a linear interaction TSPAN5-AP4 sigma -AP4µ-Stargazin-AMPARs.

As suggested, to clarify the organisation of this interaction complex, we have performed PLA experiments in hippocampal neurons identifying interaction between TSPAN5 and GluA2 (Figure 5D of the revised manuscript). Removing AP-4 by CRISPR/Cas9 knockdown of AP-4β or ε dramatically reduced the interaction between TSPAN5 and GluA2, as it would be expected if AP-4 was required for the interaction (Figure 5D).

We did not perform PLA between AP-4 and GluA2, as suggested, because the formation of the complex AP-4-Stargazin-AMPA-Rs was shown to occur in heterologous systems with little to no expression of TSPAN5 (Matsuda et al., 2008, Figure 7A-C). As such TSPAN5 should not participate in the formation of the complex but rather allow the loading of this complex to the right organelle for its delivery to the plasma membrane. This has now also been included in the main text (line 145) and in the Discussion paragraph.

In addition, we showed the existence of this complex by co-immunoprecipitation experiments in Hela cells, transfected with TSPAN5-GFP, Stargazin-HA and GluA2, whereas AP-4 is endogenously expressed in these cells (Figure 2 —figure supplement 1).

• The authors have demonstrated using various assays that TSPAN5 is required for efficient trafficking of AMPA receptors, and that TSPAN5 and AP-4 are likely to operate on the same pathway. However, it is not clear if the interaction between TSPAN5 and AP-4 is required for AMPA receptor trafficking. This can be done by performing the rescue experiment with a TSPAN5 mutant that fails to bind to AP-4 (which requires further refinement of AP-4 binding on TSPAN5), or at the very least with TSPAN5 that lacks the C-terminal tail (δ C-tail).

We thank the reviewer for the suggestion. We have performed the suggested experiment by analysing the surface levels of GluA2 in neurons transfected with a construct carrying both the ShTSPAN5 and the ShRNAresistant cDNA of the human TSPAN5 without the C-terminus (Rescue ΔC), as this is the region we identified to be binding to AP-4. The data are presented in Figure 5A, B of the revised manuscript. TSPAN5 lacking the C-terminus was unable to rescue the levels of surface GluA2 upon endogenous TSPAN5 knockdown, demonstrating that TSPAN5-AP-4 interaction is necessary for the trafficking of GluA2 to the plasma membrane.

• I am not convinced by the data presented in Figure 3 that TSPAN5 specifically regulates GluA2-AMPARs. In Figure 3B, I can't really see any differences in the levels of surface GluA1 between wild-type and knock-down neurons. Furthermore, the quantification of GluA1 bands from the cross-linking experiments contains only 3-4 data points with large variations among groups. It will be better if the authors consider performing the ARIAD assay or the FRAP-FLIP assay (no CHX) using the GluA1 construct.

We thank the reviewer for this point. We have replaced the image of surface levels of GluA1 as assessed by immunocytochemistry with panels more representative of the quantification, and these are presented in Figure 4B and Figure 4 —figure supplement 1, panel B. In addition, although the variation is large in the western blot data, the differences reach statistical significance and are in agreement with our imaging experiments.

We have also followed the reviewer’s suggestion and performed the experiment using the ARIAD system on GluA1 to assess exocytosis of newly synthesised receptor upon modulation of TSPAN5. This experiment is now presented in Figure 7F of the revised manuscript. We found that reducing TSPAN5 levels induced lower levels of newly synthetised surface GluA1, an effect rescued by the expression of an ShRNA-resistant TSPAN5. This confirms that the role of TSPAN5 is not restricted to the exocytosis of newly synthesised GluA2 but also of newly synthesised GluA1. This is also a consequence of the fact that the interaction between TSPAN5 and GluA is mediated by Stargazin, which can interact with both GluA1 and GluA2. The increased steady state levels of surface GluA1, shown in Figure 4, is likely a compensatory mechanism which could be due to increased expression, reduced internalisation or reduced degradation.

• The localisation of TSPAN-5 requires refinement. The images in Figure 3D do not really match the quantitation on the graph that shows a high level of colocalisation between TSPAN5 and endosomal markers. Importantly, where do TSPAN5 interact with AMPARs? These can be performed with PLA assay in neurons co-expressing those Rabs.

We have changed the images showing colocalisation of TSPAN5 with the endosomal markers, now shown in Figure 3C of the revised manuscript, with images more representative of the quantification and also to provide increased resolution. Colocalising puncta are now highlighted with white arrowheads in the images.

In addition, as suggested by the reviewer we have performed PLA with antibodies against TSPAN5 and GluA2 and analysed the colocalisation of the PLA signal with endosomal markers. This experiment is shown in Figure 3D of the revised manuscript. The PLA signal shows very high level of colocalisation with Rab11 and much less so with Rab5 and Rab7, confirming that the TSPAN5-GluA2 association takes place mostly in Rab11 positive organelles.

• I suggest that the authors re-analyse the FRAP/FLIP data by measuring the amplitude and the kinetics of fluorescence recovery, instead of measuring the area under the curve. For example, data shown in Figure 5G show that the extent of SEP-GluA2 recovery (amplitude) is comparable between wild-type and TSPAN5 knockdown cells, although slightly slower. Importantly, the fluorescent of SEP-GluA2 drops quickly in TSPAN5 knockdown neurons, suggesting a defect of receptor stabilisation post-exocytosis. Not simply a defect in the rate of receptor exocytosis.

We thank the reviewer for this suggestion. By taking advantage of the previously used equation describing the recovery of fluorescence of SEP-GluA2 (Hildick et al., 2012), we fitted our data onto the equation ΔF/Fpre=A(1−etr) and extrapolated the values of A, corresponding to the steady state ΔF/Fpre, and τ, which represents a time constant related to the kinetic of exocytosis. These are now presented in Figure 6I of the revised manuscript. Both parameters are affected by silencing TSPAN5 demonstrating both reduced kinetics and steady state levels.

Although it is true that the drop in SEP GluA2 signal shown in Figure 6G could be different between conditions, this would be influenced also by the bleaching of the SEP fluorescence over continuous imaging. We thus decided to exclude the decay phase from the analysis.

• Also, the experiments performed in the presence of cycloheximide cannot rule out the potential involvement of other newly translated proteins that are required for SEP-GluA2 exocytosis. Other experiments are required to conclude that TSPAN5 is required for the trafficking of newly synthesised GluA2 in neurons.

Following the suggestion of one of the reviewer in the previous round of revision, which had raised a very similar point, with which we agree, we had included the experiment presented in figure 7A-F of the revised manuscript. In this experiment, we evaluate only the signal arising from newly synthesised GluA2, thanks to the ARIAD system. Here myc-tagged newly synthetised GluA2 is trapped in the ER, and can be released for secretion by application of the ARIAD ligand. We then measured the levels of this GluA2 in the plasma membrane by surface staining for myc. This experiment shows that knockdown of TSPAN5 reduces the levels of this pool of GluA2 in the surface, thus demonstrating its role in the exocytosis of newly synthesised receptors.

References

Charrin S, Jouannet S, Boucheix C, Rubinstein E. Tetraspanins at a glance. J Cell Sci. 2014 Sep 1;127(Pt 17):3641-8. doi: 10.1242/jcs.154906. Epub 2014 Aug 15. PMID: 25128561.

Chanda S, Hale WD, Zhang B, Wernig M, Südhof TC. Unique versus Redundant Functions of Neuroligin Genes in Shaping Excitatory and Inhibitory Synapse Properties. J Neurosci. 2017 Jul 19;37(29):6816-6836. doi: 10.1523/JNEUROSCI.0125-17.2017. Epub 2017 Jun 12. PMID: 28607166; PMCID: PMC5518416.

Hildick KL, González-González IM, Jaskolski F, Henley JM. Lateral diffusion and exocytosis of membrane proteins in cultured neurons assessed using fluorescence recovery and fluorescence-loss photobleaching. J Vis Exp. 2012 Feb 29;(60):3747. doi: 10.3791/3747. PMID: 22395448; PMCID: PMC3315441.

Matsuda S, Miura E, Matsuda K, Kakegawa W, Kohda K, Watanabe M, Yuzaki M. Accumulation of AMPA receptors in autophagosomes in neuronal axons lacking adaptor protein AP-4. Neuron. 2008 Mar 13;57(5):730-45. doi: 10.1016/j.neuron.2008.02.012. PMID: 18341993.

Moretto E, Longatti A, Murru L, Chamma I, Sessa A, Zapata J, et al. TSPAN5 Enriched Microdomains Provide a Platform for Dendritic Spine Maturation through Neuroligin-1 Clustering. Cell Rep. 2019 Oct 29;29(5):1130–1146.e8.

Vanlandingham PA, Ceresa BP. Rab7 regulates late endocytic trafficking downstream of multivesicular body biogenesis and cargo sequestration. J Biol Chem. 2009 May 1;284(18):12110-24. doi: 10.1074/jbc.M809277200. Epub 2009 Mar 5. PMID: 19265192; PMCID: PMC2673280.

[Editors’ note: what follows is the authors’ response to the third round of review.]

The manuscript has been improved but there are some remaining issues that need to be addressed, as outlined below:

1. As the authors acknowledge, the present findings do not directly address whether the interaction of AP-4 with Stargazin and TSPAN5 and its regulation of AMPA receptor traffic is involved in intellectual disability associated with AP-4 deficiency syndrome. The final sentence should be removed from the abstract.

According to the editors’ suggestion, we have removed this sentence from the abstract.

2. Figure 5B, Lines 203-205: The statistical comparison between scrambled and rescue with deltaC TSPAN5 shows only a weak difference, which is quite noticeable compared to the comparison between scrambles and sh-TSPAN5 knock-down. One could argue that there is a considerable recovery of GluA2 intensity. How do sh-TSPAN5 and rescue with deltaC TSPAN5 conditions compare?

According to the editors’ suggestion we have performed a statistical analysis between the Sh-TSPAN5 and Rescue deltaC TSPAN5. No statistically significant difference is detectable between these conditions either in the OneWay ANOVA (already shown) or in a Student T test (p = 0.0669).

3. Figure 6, Lines 281-282. The experiments shown here do not strongly support the claim that the exocytosis of newly synthesized GluA2 receptors is regulated by TSPAN5. The authors should indicate the possibility that rather, factors that are rapidly turned over are needed to promote GluA2 exocytosis.

We agree with the editors on this point. We have added the following sentence in line 275-278 at the end of the section discussing Figure 6 experiments: “However, our experiments do not exclude the possibility that TSPAN5 could also regulate the recycling of GluA2-containing AMPA-Rs, an effect that would be masked by the application of cycloheximide in the experiment presented in Figure 6A-D which could cause the loss of rapidly turning over factors needed for this process.”

4. Figure 7, while the ARIAD experiment shows that trafficking of newly synthesized GluA2 is dependent on TSPAN5, the possibility that TSPAN5 also facilitates the recycling of pre-existing GluA2-containing AMPA receptors is not excluded here.

We thank the editors for raising this point. We have added the following sentence in line 314-315 at the end of the section discussing Figure 7 experiments: “It is important to note that these experiments still do not exclude a possible regulation of TSPAN5 on recycling AMPA-Rs.“

5. Combining the points raised in 3 and 4 above, the authors should tone down the claim that TSPAN5 promotes exocytosis of newly synthesized AMPA receptors or rephrase such that it may not be selective for newly synthesized AMPA receptors. This could be a general mechanism for targeting both new and recycling AMPA receptors to the plasma membrane.

We thank the reviewer for this comment. In addition to the sentences included in the points above, we have added the following sentence in the Discussion section (lines 332-334): “In addition, our experiments cannot fully exclude that TSPAN5 could also regulate the recycling of AMPA-Rs. It thus possible that TSPAN5 could modulate the delivery to the plasma membrane of both newly synthesised and recycling AMPA-Rs.”

We have also removed “newly synthesised” from both the impact statement and the abstract (line 25), in the chapter title (line 233), in the discussion (line 342) and in the figure 6 title (line 956) to make more clear that AMPA-Rs recycling could also be regulated by TSPAN5.

https://doi.org/10.7554/eLife.76425.sa2

Article and author information

Author details

  1. Edoardo Moretto

    1. Institute of Neuroscience, CNR, Vedano al Lambro, Italy
    2. NeuroMI Milan Center for Neuroscience, University of Milano-Bicocca, Milan, Italy
    Contribution
    Conceptualization, Formal analysis, Investigation, Writing - original draft, Writing – review and editing
    For correspondence
    edoardo.moretto@in.cnr.it
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-3546-6797

  2. Federico Miozzo

    Institute of Neuroscience, CNR, Vedano al Lambro, Italy
    Contribution
    Investigation, Writing – review and editing
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0003-0818-9525

  3. Anna Longatti

    Institute of Neuroscience, CNR, Vedano al Lambro, Italy
    Contribution
    Formal analysis, Investigation, Writing – review and editing
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-1636-8550

  4. Caroline Bonnet

    University of Bordeaux, Interdisciplinary Institute for Neuroscience, Bordeaux, France
    Contribution
    Formal analysis, Investigation
    Competing interests
    No competing interests declared

  5. Francoise Coussen

    University of Bordeaux, Interdisciplinary Institute for Neuroscience, Bordeaux, France
    Contribution
    Formal analysis, Investigation, Writing – review and editing
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-3194-3058

  6. Fanny Jaudon

    1. Department of Life Sciences, University of Trieste, Trieste, Italy
    2. IRCCS Ospedale Policlinico San Martino, Genoa, Italy
    Contribution
    Formal analysis, Investigation, Writing – review and editing
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0001-7648-0977

  7. Lorenzo A Cingolani

    1. Department of Life Sciences, University of Trieste, Trieste, Italy
    2. Center for Synaptic Neuroscience and Technology (NSYN), Istituto Italiano di Tecnologia (IIT), Genoa, Italy
    Contribution
    Investigation, Writing – review and editing
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0001-9538-1659

  8. Maria Passafaro

    1. Institute of Neuroscience, CNR, Vedano al Lambro, Italy
    2. NeuroMI Milan Center for Neuroscience, University of Milano-Bicocca, Milan, Italy
    Contribution
    Conceptualization, Supervision, Funding acquisition, Writing – review and editing
    For correspondence
    maria.passafaro@in.cnr.it
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-0045-5676

Funding

Fondazione Telethon (GGP17283)

  • Maria Passafaro

Ministero dell'Università e della Ricerca (20172C9HLW)

  • Maria Passafaro

Fondazione Cariplo (2019-3438)

  • Maria Passafaro

Fondazione Telethon-Cariplo Alliance (GJC21035)

  • Maria Passafaro
  • Edoardo Moretto

Fondazione Telethon (GGP19181)

  • Lorenzo A Cingolani

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

Acknowledgements

We sincerely thank Skye Stuart for critical reading of the manuscript. We thank Robert Malinow for the pCI-SEP GluR2 (Addgene plasmid #24001). We thank Michisuke Yuzaki for the GST-Ct-Stargazin plasmid. We thank Margaret Robinson for the anti AP4σ antibody. We thank Cecilia Gotti for the anti-GluA2/3 antibody. We thank Richard Pagano for plasmids encoding DsRed-Rab5 WT (Addgene plasmid #13050), DsRed-Rab7 WT (Addgene plasmid #12661), and DsRed-Rab11 WT (Addgene plasmid #12679). Rab4-GFP, Rab7-GFP, and Rab11-GFP are kind gifts from Prof G Schiavo. The financial support of Fondazione Telethon, Italy (GGP17283) is gratefully acknowledged. Part of this work was supported by PRIN (Progetti di rilevante interesse nazionale – Bando 2017), 20172C9HLW, Fondazione Cariplo, Italy (2019-3438) and Fondazione Cariplo and Telethon Alliance (GJC21035).

Funding: Fondazione Telethon, Italy (GGP17283), PRIN (Progetti di ricerca di rilevante interesse nazionale – Bando 2017), 20172C9HLW Fondazione Cariplo, Italy (2019-3438), Fondazione Cariplo and Telethon Alliance, Italy (GJC21035)

Ethics

Animal procedures were performed in accordance with the European Community Council Directive of November 24, 1986 (86/609/EEC) on the care and use of animals. Animal procedures were approved by the Italian Ministry of Health (Protocol Number N° 2D46AN.463).

Senior Editor

  1. Richard W Aldrich, The University of Texas at Austin, United States

Reviewing Editor

  1. Yukiko Goda, Okinawa Institute of Science and Technology, Japan

Publication history

  1. Received: December 15, 2021
  2. Preprint posted: January 4, 2022 (view preprint)
  3. Accepted: January 25, 2023
  4. Version of Record published: February 16, 2023 (version 1)

Copyright

© 2023, Moretto et al.

This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.

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  1. Edoardo Moretto
  2. Federico Miozzo
  3. Anna Longatti
  4. Caroline Bonnet
  5. Francoise Coussen
  6. Fanny Jaudon
  7. Lorenzo A Cingolani
  8. Maria Passafaro
(2023)
The tetraspanin TSPAN5 regulates AMPAR exocytosis by interacting with the AP4 complex
eLife 12:e76425.
https://doi.org/10.7554/eLife.76425

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