1. Neuroscience

TrpML-mediated astrocyte microdomain Ca2+ transients regulate astrocyte–tracheal interactions

  1. Zhiguo Ma  Is a corresponding author
  2. Marc R Freeman  Is a corresponding author
  1. Vollum Institute, Oregon Health and Science University, United States
https://doi.org/10.7554/eLife.58952
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  1. Zhiguo Ma
  2. Marc R Freeman
(2020)
TrpML-mediated astrocyte microdomain Ca2+ transients regulate astrocyte–tracheal interactions
eLife 9:e58952.
https://doi.org/10.7554/eLife.58952
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Abstract

Astrocytes exhibit spatially-restricted near-membrane microdomain Ca2+transients in their fine processes. How these transients are generated and regulate brain function in vivo remains unclear. Here we show that Drosophila astrocytes exhibit spontaneous, activity-independent microdomain Ca2+ transients in their fine processes. Astrocyte microdomain Ca2+ transients are mediated by the TRP channel TrpML, stimulated by reactive oxygen species (ROS), and can be enhanced in frequency by the neurotransmitter tyramine via the TyrRII receptor. Interestingly, many astrocyte microdomain Ca2+ transients are closely associated with tracheal elements, which dynamically extend filopodia throughout the central nervous system (CNS) to deliver O2 and regulate gas exchange. Many astrocyte microdomain Ca2+ transients are spatio-temporally correlated with the initiation of tracheal filopodial retraction. Loss of TrpML leads to increased tracheal filopodial numbers, growth, and increased CNS ROS. We propose that local ROS production can activate astrocyte microdomain Ca2+ transients through TrpML, and that a subset of these microdomain transients promotes tracheal filopodial retraction and in turn modulate CNS gas exchange.

Introduction

Astrocytes exhibit two major types of Ca2+ signaling events, whole-cell fluctuations and near-membrane microdomain Ca2+ transients (Khakh and McCarthy, 2015). Whole-cell transients are coordinated across astrocyte networks and regulated by adrenergic receptor signaling. Emerging data suggests these transients are important for state-dependent changes (Ding et al., 2013; Ma et al., 2016; Paukert et al., 2014; Srinivasan et al., 2015), and involve TRPA1 channels that regulate the insertion of neurotransmitter transporters like GAT-3 into astrocyte membranes to alter neurophysiology (Shigetomi et al., 2011). Whole-cell astrocyte Ca2+ transients in the Drosophila CNS are also stimulated by the invertebrate equivalents of adrenergic transmitters, octopamine (Oct) and tyramine (Tyr). Octopamine and tyramine stimulate cell-wide astrocyte Ca2+ increase through the dual-specificity Octopamine-Tyramine Receptor (Oct-TyrR) and the TRP channel Water witch (Wtrw). This astrocyte-mediated signaling event downstream of octopamine and tyramine is critical for in vivo neuromodulation: astrocyte-specific elimination of Oct-TyrR or Wtrw in larvae blocks the ability of octopamine and tyramine to silence downstream dopaminergic neurons, and alters both simple chemosensory behavior and a touch-induced startle response (Ma et al., 2016). Adrenergic regulation of whole-cell astrocyte Ca2+ transients is therefore an ancient and broadly conserved feature of metazoan astrocytes.

The mechanisms that generate astrocyte microdomain Ca2+ transients are not understood, nor are the precise in vivo roles for this type of astrocyte signaling (Bazargani and Attwell, 2016; Khakh and McCarthy, 2015). In mammals, astrocyte microdomain Ca2+ transients occur spontaneously, do not require neuronal activity (Nett et al., 2002), depend on extracellular Ca2+ (Rungta et al., 2016; Srinivasan et al., 2015), and persist in cultured astrocytes, which has been used to argue they are cell-autonomous (Khakh and McCarthy, 2015; Nett et al., 2002). A recent study described close association of astrocyte microdomain Ca2+ transients with mitochondria, and found that pharmacological blockade of the mPTP led to a suppression of transients, while ROS led to an enhancement of transients. These observations led to the proposal that astrocyte microdomain Ca2+ transients were generated by opening of the mPTP during oxidative phosphorylation, perhaps as a means to balance mitochondrial function and ongoing astrocyte support with local metabolic needs (Agarwal et al., 2017).

In this study, we report that Drosophila astrocytes exhibit spontaneous, activity-independent microdomain Ca2+ transients, and show they are mediated by the TRP channel TrpML. Many astrocyte microdomain Ca2+ transients are associated with branches and filopodia extending from CNS trachea, an interconnected set of tubules that allow for gas exchange in the larval CNS, and astrocyte microdomain Ca2+ transients precede the onset of filopodial retraction. Astrocyte microdomain Ca2+ transients are regulated by ROS and loss of TrpML leads to tracheal overgrowth and increased CNS ROS. We propose that one in vivo role for tracheal–astrocyte interactions is to regulate CNS gas exchange, with tracheal filopodia-dependent local hyperoxia resulting in increased production of ROS, which gates TrpML to generate local astrocyte microdomain Ca2+ transients, ultimately promoting tracheal retraction and reducing local O2 delivery.

Results

Drosophila astrocytes exhibit microdomain Ca2+ transients

To monitor the near-membrane Ca2+ activity in astrocytes, we expressed myristoylated GCaMP5a (myr-GCaMP5a) in astrocytes using the astrocyte-specific alrm-Gal4 driver. We acutely dissected 3rd instar larval CNS and live-imaged myr-GCaMP5a signals in the ventral nerve cord (VNC) (Ma et al., 2016). We collected images at the midpoint of the neuropil along the dorsoventral axis for 6 min time windows (Figure 1A). We found that astrocyte microdomain Ca2+ transients exhibited diverse waveforms, with variable durations and frequencies (Figure 1A; Figure 1—video 1). The average full width at half maximum (FWHM) for these Ca2+ transients was 5.5 ± 2.26 (mean ± SD) seconds (Figure 1B). Microdomain Ca2+ transients frequently occurred at the same location, suggesting there are hotspots where microdomains repeatedly occur for a given astrocyte. The majority of foci exhibited 1–3 events during the 6 min imaging window (Figure 1C), and Ca2+ transients at different sites did not exhibit obvious synchrony with one another. We also observed microdomain Ca2+ transients of a similar rise-and-fall pattern, although with a slightly shorter duration (FWHM, 1.7 ± 0.08 s, mean ± SD) in the astrocytes of intact L1 (1st instar) larvae (Figure 1- Figure 1—figure supplement 1A and B; Figure 1—video 2), suggesting the microdomain Ca2+ transients in the acute CNS preparations we observed largely reflect in vivo astrocyte activity, although with some differences in duration. Blockade of action potential firing with tetrodotoxin did not alter astrocyte microdomain Ca2+ transients, although they were eliminated by removal of extracellular Ca2+ and were sensitive to the Ca2+ channel blocker lanthanum chloride (LaCl3) (Figure 1D), suggesting Ca2+ entry from extracellular space is essential for generation of astrocyte microdomain Ca2+ transients.

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Characterization of microdomain Ca2+ transients in Drosophila astrocytes.

(A) Schematic of larval CNS (white area, neuropil; gray, cortex). An imaging area showing membrane tethered myr-GCaMP5a (green) in astrocytes, in which microdomain Ca2+ transients during 6 min were maximally projected. Traces of 8 individual ROIs microdomains (right, a–h) are shown over the entire 6 min window. Pseudocolor grayscale of Ca2+ signals (bottom left), grayscale values ranging from 0 to 255 (scale bars, 20 µm). Representative time-lapse images (bottom right) of two indicated microdomain Ca2+ transients in 2 ROIs (1, 2). (B) Superimposed traces of individual microdomain Ca2+ transients and an average with its full width at half maximum (FWHM, mean ± SD). (C) Histogram showing the distribution of recurrent microdomain Ca2+ transients at same ROIs. (D) Responses of microdomain Ca2+ transients to tetrodotoxin, 0 extracellular Ca2+ and LaCl3 (n = 6, mean ± SEM, one-way ANOVA). (E) 2-color Ca2+ imaging in neighboring astrocytes. In presence of the flippase repo-FLP, myr-GCaMP5a expressing astrocytes switch to express myr-R-GECO1, resulting in 3 types of astrocytes: myr-GCaMP5a+ (green), myr-R-GECO1+ (red), expressing both indicators (orange) (scale bar, 20 µm). Quantification is from Ca2+ imaging of myr-GCaMP5a and myr-R-GECO1 that were exclusively expressed in adjacent astrocytes (n = 3, unpaired t-test). Time-lapse images and superimposed traces of representative microdomain Ca2+ transients at two juxtaposed ROIs between myr-GCaMP5a and myr-R-GECO1 expressing astrocytes. See source data Figure 1—source data 1.

Figure 1—source data 1

Characterization of microdomain Ca2+ transients in Drosophila astrocytes.

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Astrocytes tile with one another and occupy unique spatial domains in the CNS. We sought to determine whether microdomain Ca2+ transients spanned astrocyte-astrocyte cell boundaries, or if they appeared only within the domain of single cells. We used a flippable construct expressing either QF or Gal4 under the control of the alrm promoter, along with two genetically encoded Ca2+ indicators: QUAS::myr-GCaMP5a and UAS::myr-R-GECO1 (Figure 1—figure supplement 1 - Figure 1C). To confirm both myr-GCaMP5a and myr-R-GECO1 behaved similarly, we first examined double-positive cells and found both can detect the same microdomain Ca2+ transients (Figure 1—figure supplement 1 - Figure 1D), and in cells exclusively expressing one of these two Ca2+ indicators there were no differences in the overall frequency of the microdomain Ca2+ events detected between these sensors (Figure 1E). We then identified cell boundaries between myr-GCaMP5a/myr-R-GECO1 single-labeled cells, and examined the dynamics of astrocyte microdomains across those boundaries. We observed coincident signaling with myr-GCaMP5a and myr-R-GECO1 (Figure 1E). These data indicate that individual astrocyte microdomain Ca2+ transients can span astrocyte-astrocyte borders. Our observations support the notion that astrocyte microdomain Ca2+ transients are regulated by extrinsic cues that can simultaneously stimulate two astrocytes, or that astrocyte-astrocyte communication/coupling is sufficient to coordinate very local Ca2+ signaling events across neighboring cells.

Astrocyte microdomain Ca2+ transients are enhanced by tyramine through TyrRII and mediated by TrpML

To determine whether neurotransmitters were capable of modulating astrocyte microdomain Ca2+ transients, we bath applied several neurotransmitters and live-imaged astrocyte microdomain Ca2+ events. Application of glutamate, acetylcholine, GABA, or octopamine had no effect on the frequency of astrocyte microdomain Ca2+ transients (Figure 2A). In contrast, application of tyramine led to a significant increase in the frequency of these transients by ~40% (Figure 2B). We screened the known receptors for tyramine in Drosophila and found that astrocyte-specific depletion of TyrRII blocked the ability of tyramine to increase astrocyte microdomain Ca2+ transients. The spontaneous microdomain events were not dependent on the presence of tyramine or octopamine, as mutants that block the production of tyramine and octopamine (Tdc2RO54) or octopamine (TβhnM18) did not significantly alter the frequency of astrocyte microdomain Ca2+ transients, nor did mutations in Oct-TyrR, which we previously showed was essential for activation of whole-cell Ca2+ transients in astrocytes (Figure 2C). These data indicate that while astrocyte microdomain Ca2+ transients can be partially enhanced by tyramine through TyrRII, under basal conditions astrocytes do not require tyramine or octopamine for microdomain Ca2+ transient activity.

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Astrocyte microdomain Ca2+ transients are genetically distinct from soma transients and require TrpML.

(A) Responses of microdomain Ca2+ transients (frequency) to glutamate (Glu), acetylcholine (Ach), γ-aminobutyric acid (Gaba), tyramine (Tyr), octopamine (Oct) in presence of tetrodotoxin. (B) Effect of tyramine on Ca2+ transient frequency in genotypes indicated. Oct-TyrR mutants, and astrocyte-specific (alrm>) expression of RNAis to TyrR or TyrRII (in A and B, n = 6, mean ± SEM, paired t-test). (C) Quantification of microdomain Ca2+ transients in Tdc2RO54, TβhnM18 or Oct-TyrRhono mutants (n = 6, mean ± SEM, one-way ANOVA). (D) Maximally projected astrocyte microdomain Ca2+ transients during 6 min in control, trpml1 mutants, and astrocyte-specific trpmlRNAi (in pseudocolor, grayscale values ranging from 0 to 255. scale bar, 20 µm). Quantification of microdomain Ca2+ transients in mutants (loss-of-function mutations or astrocyte-specific RNAi driven by alrm-Gal4) of genes encoding TRP family ion channels (n = 6, mean ± SEM, one-way ANOVA). (E) trpml-myc expression in astrocytes rescues microdomain Ca2+ transients in trpml1 mutants (n = 6, mean ± SEM, one-way ANOVA). (F) Effect of tyramine treatment on controls and trpml1 mutants (n = 6, mean ± SEM, one-way ANOVA. within groups, paired t-test). Right panel, increase in transients by tyramine (subtracting the basal included) in control and trpml1 mutants. (G) Application of the antioxidant N-acetyl cysteine (NAC) or H2O2 to the larval CNS. (for F and G n = 6, mean ± SEM, across groups, one-way ANOVA; within groups, paired t-test; -, + indicate pre-, post-delivery). (H) H2O2 application to control and trpml mutants shows that H2O2-dependent increases require TrpML. See source data Figure 2—source data 1.

Figure 2—source data 1

Astrocyte microdomain Ca2+ transients require TrpML.

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Figure 2—source data 2

Astrocyte microdomain Ca2+ transients are genetically distinct from soma transients and require TrpML.

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Whole-cell astrocyte transients are regulated by the TRP channel Water witch (Wtrw) (Ma et al., 2016), and astrocyte basal Ca2+ levels in mammals are modulated by TrpA1 (Shigetomi et al., 2013). The molecular pathways that generate astrocyte microdomain Ca2+ transients have not been identified. We speculated that astrocyte microdomain Ca2+ transients might be regulated by one or more of the 13 TRP channels encoded in the Drosophila genome. We screened these for potential roles in the regulation of astrocyte microdomain Ca2+ transients in animals bearing TRP channel mutations or astrocyte-specific RNAi targeting trp family genes. While knockout of 11 of these TRP channels had no effect, we found that microdomain Ca2+ events decreased by ~70% to 80% in trpml loss-of-function mutants, in both intact 1st instar larvae (Figure 2—figure supplement 1 - Figure 2A) and acute CNS preparations from 3rd instar larvae (Figure 2D; Figure 2—video 1). Astrocyte-specific knockdown of trpml also reduced microdomain Ca2+ events by ~60% (Figure 2D), and expressing a version of myc-tagged TrpML (trpml-myc) in astrocytes rescued decreased microdomains in trpml mutants (Figure 2E; Figure 2—figure supplement 1 - Figure 2D), arguing for a cell-autonomous role of TrpML in regulating astrocyte microdomain Ca2+ transients. Although application of tyramine still increased microdomain Ca2+ events in trpml1 mutants, the enhancement above the basal level of spontaneous microdomain Ca2+ transients was significantly reduced (Figure 2F), suggesting tyramine enhances microdomains in frequency at least in part via TrpML.

We next examined whether TrpML was essential for tyramine activated Ca2+ events in astrocyte cell bodies, and found that tyramine induced comparable Ca2+ rise in astrocytes in control and trpml1 mutants (Figure 2—figure supplement 1 – Figure 2C). This argues for a specific role of TrpML in generating microdomain Ca2+ transients. While glial cells undergo apoptosis in trpml mutant adults (Venkatachalam et al., 2008), astrocyte development appears to be normal at 3rd instar larval stage (Figure 2—figure supplement 1 - Figure 2D). Interestingly, trpml1 mutants exhibit near fully penetrant lethality during later pupal stages as previously reported (Venkatachalam et al., 2008), and we found that expression of trpml-myc selectively in astrocytes rescued this lethality (Figure 2—figure supplement 1 - Figure 2E), demonstrating that TrpML plays an essential role in astrocytes. The myc-tagged version of TrpML predominantly localized at GFP-Lamp1+ endo-lysosomes in astrocytes in both fine astrocytic processes and cell bodies, as well as near the cell membrane (Figure 2—figure supplement 1 – Figure 2F). TrpML might therefore execute its regulation of astrocyte microdomains from endo-lysosomes, the plasma membrane, or both.

Previous work has shown that reactive oxygen species (ROS) can activate TrpML (Zhang et al., 2016), and astrocyte near-membrane Ca2+ events in mammals are sensitive to ROS (Agarwal et al., 2017). We therefore assayed the sensitivity of Drosophila astrocyte microdomain Ca2+ transients to ROS. We observed that bath application of the ROS generator hydrogen peroxide (H2O2) led to a TrpML-dependent increase in astrocyte microdomain Ca2+ events, while, reciprocally, addition of the antioxidant N-acetyl cysteine completely abolished them (Figure 2G and H; Figure 2—videos 2 and 3). These data indicate that astrocyte microdomain Ca2+ transients are mediated by TrpML and are highly sensitive to ROS. Furthermore, our observation that TrpML and Wtrw regulate only microdomain or whole-cell Ca2+ events, respectively, demonstrates that astrocyte microdomain Ca2+ transients and whole-cell changes in astrocyte Ca2+ are physiologically and genetically distinct signaling events, although adrenergic transmitters (tyramine in Drosophila and norepinephrine in mouse) may serve as factors to coordinate their activity.

Astrocyte microdomain Ca2+ transients are associated with trachea and precede tracheal filopodia retraction

Mammalian astrocytes make intimate contacts with blood vessels by forming endfeet to allow for gas exchange, uptake of nutrients from blood, and maintenance of the blood brain barrier. Fine astrocyte processes in Drosophila infiltrate the CNS neuropil where they associate with neural processes, synapses, and tracheal elements (Freeman, 2015). Tracheal cells serve a similar function to mammalian blood vessels, and their development and morphogenesis are molecularly similar (Ghabrial et al., 2003). Trachea are an interconnected series of gas-filled tubes that penetrate insect tissues, and gas exchange occurs through tracheal cell–tissue interactions (Ghabrial et al., 2003). Interestingly, we observed that half of all astrocyte microdomain Ca2+ transients we recorded were closely associated with CNS tracheal elements (Figure 3A). In live preparations where trachea were labeled with myristoylated tdTomato (myr-tdTom) and either Lifeact-GFP to visualize actin or Tubulin-GFP to visualize microtubules, we observed that tracheal branches dynamically extended and retracted actin-rich protrusions that are characteristic of filopodia (Figure 3B), and only very few were stabilized by microtubules (Figure 3—figure supplement 1 - Figure 3A). These observations imply tracheal branches dynamically explore their surroundings in the CNS with filopodia.

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Astrocyte microdomain Ca2+ transients are associated with tracheal branches and precede retraction onset of tracheal filopodia.

(A) Astrocyte microdomain Ca2+ transients (green) overlap with tracheal branches (red) (scale bar, 20 µm). (B) Tracheal branches extend and retract F-actin containing filopodia. Asterisks, myr-tdTomato labeled filopodia; Arrows, Lifeact-GFP labeled F-actin (scale bar, 10 µm). (C) Categorization of tracheal filopodia across the entire population (extension, retraction, extension and retraction, or stationary). w/Ca2+ indicates tracheal filopodia extended into an astrocyte microdomain Ca2+ transient; w/o Ca2+ indicates no visible astrocyte microdomain Ca2+ transient was observed. (D) Time-lapse images and superimposed traces (green trace, myr-GCaMP5a in astrocytes expressed as dF/F0; red trace, myr-tdTomato in tracheal filopodia expressed as length) of 3 pairs (p1, p2, p3) of tracheal filopodia and astrocyte microdomain Ca2+ transients (in pseudocolor, grayscale values ranging from 0 to 255. scale bar, 10 µm). Vertical dash lines, timepoints when tracheal filopodia enter astrocyte Ca2+ microdomains. Blue boxes, time windows astrocyte microdomain Ca2+ transients persist after tracheal filopodia enter. Note that prior to entering the astrocyte Ca2+ microdomain, tracheal filopodial extension is not coupled to increases in astrocyte Ca2+, but after entry, increased astrocyte Ca2+ is strongly correlated with tracheal filopodial retraction. (E) Temporal correlation between onset of filopodia retraction and timing of peak astrocyte microdomain Ca2+ transients in seconds (n = 61 filopodia from Extension and Retraction pool). (F) Time intervals between astrocyte microdomain Ca2+ transients and tracheal filopodial extension versus retraction. See source data Figure 3—source data 1.

Figure 3—source data 1

Distribution of microtubules and F-actin in larval CNS tracheal elements.

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Figure 3—source data 2

Astrocyte microdomain Ca2+ transients are associated with tracheal branches and precede retraction onset of tracheal filopodia. hea.

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We classified tracheal filopodia into four categories according to different behavior they exhibited during imaging: extension (1.7%), retraction (20.7%), extension and retraction (75.3%), or stationary (2.3%) (Figure 3C). The vast majority of tracheal filopodia dynamically extended and retracted during the imaging window of 6 min. We noted that those that exhibited only retraction did so very early in the imaging window, which could indicate that we began our imaging after extension had been initiated, however we cannot exclude the possibility that our imaging approach biases tracheal dynamics more toward retraction (e.g. by our imaging procedure generating ROS).

Based on their close association, we explored the potential relationship between tracheal filopodial dynamics and astrocyte microdomain Ca2+ transients. Interestingly, 52% of tracheal filopodial tips overlapped, at some point, with an astrocyte microdomain Ca2+ transient (Figure 3C). Overlap was defined as the tracheal filopodial tip falling within the maximum size of the domain of the astrocyte Ca2+ transient. Moreover, we observed that astrocyte microdomain Ca2+ transients preceded retraction events of tracheal filopodia within their domain. The onset of trachea filopodial retraction was tightly correlated with astrocyte microdomain Ca2+ peaks (R2 = 0.99, Figure 3D–F; Figure 3—figure supplement 1 – Figure 3B; Figure 3—video 1), with a latency time of 25.9 ± 2.18 s. In contrast, the intervals between trachea filopodial extension onset and astrocyte microdomain Ca2+ peaks were significantly larger (144.6 ± 11.65 s) and more broadly distributed (Figure 3—figure supplement 1 - Figure 3C). Correlations between astrocyte microdomains and any changes in tracheal filopodial dynamics were only observed when filopodia overlapped with astrocyte microdomain Ca2+ transients. For instance, we found no correlation between extension or retraction of filopodia and nearby non-overlapping astrocyte microdomain Ca2+ transients (‘bystanders’) within an circular area beginning 7.5 μm away from filapodial tips and extending outward (Figure 3—figure supplement 1 - Figure 3D). We noted that 46% of tracheal filopodia were not visibly associated with astrocyte microdomain Ca2+ transients. This argues that a large fraction of tracheal filopodia can extend and retract in the absence of local astrocyte microdomain Ca2+ signaling. However, we cannot exclude the possibility that astrocyte Ca2+ signaling above or below the plane of focus could be modulating the dynamics of these trachea. Together, these observations indicate that a large fraction of astrocyte microdomain Ca2+ transients are spatiotemporally correlated with the retraction of adjacent tracheal filopodia.

Blockade of astrocyte microdomain Ca2+ transients increases CNS ROS and trpml mutants exhibit increased tracheal growth

Based on their spatiotemporal association, we speculated that astrocyte microdomain Ca2+ transients promote tracheal filopodial retraction in response to ROS through TrpML. This predicts that loss of these transients would increase tracheal filopodial growth. To block astrocyte microdomain Ca2+ transients we used trpml1 mutants and labeled tracheal membranes with myr-tdTom. We found in trpml1 mutants that the overall rate of filopodial extension over time was indeed increased, which resulted in an increase in maximum length of the tracheal filopodia (Figure 4A). The increased filopodial extension rate, but not the maximum length of the filopodia, was phenocopied by knocking down trpml selectively in either astrocytes, and to some extent in trachea (Figure 4—figure supplement 1 – Figure 4A), arguing that TrpML functions in both astrocytes and trachea to control tracheal filopodial growth. Filopodial retraction rates remained unchanged in trpml1 mutants, suggesting astrocyte TrpML signaling facilitates tracheal filopodial retraction by suppressing extension. Our model further predicts that stimulating an increased number of astrocyte microdomain Ca2+ transients should promote filopodial retraction. To test this idea we bath applied tyramine, which stimulates astrocyte microdomain Ca2+ transients. We found tyramine application led to an increase in the percentage of tracheal filopodial retracting versus extending (Figure 4B), further supporting the notion that astrocyte microdomains facilitate filopodial retraction.

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Loss of TrpML leads to overgrowth of trachea and excessive reactive oxygen species (ROS) in larval CNS.

(A) Quantification of average filopodial retraction and extension rates, and maximal length of tracheal filopodia (n indicate the number of filopodia randomly selected from 6 to 8 larval CNS, mean ± SEM, t-test). (B) Comparison of changes in extension/retraction ratios after bath application of tyramine in control and trpml1 mutants (n = 6, mean ± SEM, one-way ANOVA across groups; within groups, paired t-test). (C) In control, one tracheal branch (labeled with btl >myr::tdTom, arrowhead) near the LON (Brp, blue) grows short filopodia (arrows) into the LON. In trpml1, two transverse tracheal branches grow near the LON, and they exhibit increases in filopodial extension into the LON (n = 20, mean ± SEM, t-test. scale bar, 10 µm). (D) Dihydroethidium (DHE) staining in indicated genotypes. ROS-oxidized DHE forms 2-hydroxyethidium (2-OH-E+) and ethidium (E+). Quantifications to right (n = 6, mean ± SEM, t-test. scale bar, 50 µm). NAC was added 5 min prior to DHE incubation. (E) Proposed model. Astrocyte microdomain Ca2+ transients are modulated by reactive oxygen species (ROS) and TrpML. Astrocyte Ca2+ signaling can facilitate filopodial retraction if a tracheal filopodium enters a microdomain. Cell cortex underlying membrane or lysosomal localization of TrpML regulates Ca2+ signaling in response to ROS, presumably due to increased O2 delivery, to generate astrocyte microdomain Ca2+ transients. Tyramine induces increased microdomain Ca2+ transients via TrpML. Loss of astrocyte microdomains resulted from trpml mutation leads to overgrown trachea including filopodia, and increased ROS. See source data Figure 4—source data 1.

Figure 4—source data 1

Loss of TrpML leads to overgrowth of trachea and excessive reactive oxygen species (ROS) in larval CNS.

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Figure 4—source data 2

Tracheal branches overgrow in the larval ventral nerve cord of trpml1 mutants.

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To quantify the longer term structural effect of loss of trpml (and astrocyte microdomain Ca2+ transients), we examined tracheal structure in larval CNS. We first counted the total number of protrusions from a pair of most posterior ganglion trachea (mpgTr) that innervate a few segments from A5 to A8/9 in the ventral nerve cord. We found that mpgTr in the ventral nerve cord in trpml1 mutants exhibited increased total length compared to those in control animals (Figure 4—figure supplement 1 - Figure 4B). We next examined a uniquely identifiable branch of the tracheal system in the larval optic neuropil (LON) (Sprecher et al., 2011). The LON is a simple tissue, composed of only a few dozen neurons and 1 ~ 2 tracheal branches that are surrounded by the processes from a single astrocyte (Figure 4—figure supplement 1 - Figure 4C). Compared to controls, we found that trpml1 mutants exhibited an approximate doubling of the number of tracheal branches, and also total filopodia in the LON (Figure 4C). Together these data indicate that TrpML restricts tracheal outgrowth through astrocyte microdomain Ca2+ transients.

It is plausible that such an increase in tracheal branches and filopodia might result in excessive O2 delivery to CNS tissues and result in a hyperoxia. To assay ROS status in the CNS we stained with the ROS indicator dihydroethidium (DHE). In live preparations of trpml1 mutants we found a ~ 3 fold increase in oxidized DHE+ puncta, likely in mitochondria (Bindokas et al., 1996), and when we eliminated trpml selectively from astrocytes by RNAi, we found a ~ 2.5 fold increase in oxidized DHE+ puncta (Figure 4D). We also validated our DHE staining by a 5 min period of acute pre-treatment with the ROS scavenger NAC, which reduced DHE+ puncta in trpml1 mutants (Figure 4D; Figure 4—figure supplement 1 – Figure 4D). These data support the notion that blockade of TrpML signaling, and in turn astrocyte microdomain Ca2+ transients, leads to increased ROS in the CNS, perhaps due to excessive O2 delivery from increased tracheal elements (Figure 4E).

Discussion

Molecules required for the generation of astrocyte microdomain Ca2+ transients have remained elusive, it remains unclear how many ‘types’ of microdomain Ca2+transients exist in astrocytes, and the in vivo roles for these transients remain controversial and poorly defined (Agarwal et al., 2017; Bazargani and Attwell, 2016). Our work demonstrates that Drosophila astrocyte microdomain Ca2+ transients are mediated by the TRP channel TrpML, and can be stimulated by ROS and tyramine through the TyrRII receptor. Unexpectedly, we found that a large fraction of astrocyte microdomain Ca2+ transients are closely associated with tracheal elements, precede and are tightly coupled with tracheal filopodial retraction, and that stimulating astrocyte microdomain Ca2+ transients with tyramine can promote tracheal filopodial retraction. We propose that one important physiological role for a subset of astrocyte microdomain Ca2+ transients is to modulate CNS gas exchange through TrpML and ROS signaling.

Astrocyte microdomain Ca2+ transients in Drosophila share many features with those observed in mammals (Agarwal et al., 2017; Nett et al., 2002; Srinivasan et al., 2015; Zhang et al., 2017). They are spontaneously generated, exhibit diverse waveforms, and appear for the most part asynchronous across astrocyte populations. Their production requires the presence of extracellular Ca2+ and they are suppressed by the broad Ca2+ channel blocker LaCl3. Our analysis of adjacent astrocytes that are labeled with uniquely identifiable Ca2+ indicators (myr-GCaMP5a versus myr-R-GECO1) demonstrated individual astrocyte microdomain Ca2+ transients can span astrocyte-astrocyte boundaries, which might argue for an extrinsic mechanism regulating their production. Alternatively, it might indicate that astrocyte-astrocyte coupling of Ca2+ signaling events is strong during their production. Astrocyte microdomain Ca2+ transients are not suppressed by blockade of action potentials with tetrodotoxin, suggesting they are not activity dependent, although we also cannot formally rule out a role for spontaneous release of neurotransmitters at synapses.

Based on their persistence in Tdc2 mutants, which lack tyramine and octopamine in CNS, we conclude that spontaneous astrocyte microdomain Ca2+ transients do not require the production of tyramine or octopamine in vivo. Nevertheless, and similar to application of norepinephrine to mouse preparations (Agarwal et al., 2017), we found that tyramine was capable of stimulating a partial increase in astrocyte microdomain Ca2+ transients, and that to some extent this required the tyramine receptor TyrRII on astrocytes. Why these transients do not require tyramine for their spontaneous production, but can be stimulated by tyramine application, remains unclear, but this adrenergic regulation of astrocyte microdomain Ca2+ signaling appears to be a conserved feature in Drosophila and mouse. It is possible that adrenergic regulation may serve as a way to physiologically couple whole-cell and microdomain Ca2+ transients, as a mechanism to coordinate neuronal activity with astrocyte calcium signaling, or both. The regulation of astrocyte Ca2+ signaling in vivo by octopamine and tyramine is complex. Tyramine can stimulate increases in whole-cell Ca2+ levels in astrocytes through the Oct-TyrR, as does octopamine (Ma et al., 2016), but the latter has no effect in astrocyte microdomain Ca2+ transients. Signaling mediated by TyrRII may somehow increase the open probability of TrpML in microdomains in a way that is distinct from whole-cell Ca2+ signaling. This is consistent with our observation that TrpML is partially responsible for the tyramine-induced increase in astrocyte microdomain Ca2+ transients.

TrpML may exert its effects on astrocytic microdomain Ca2+ transients at endo-lysosomes, at the cell cortex, or both (Figure 4E). TrpML is well known to signal in the endo-lysosomal compartment as well as the plasma membrane (Feng et al., 2014). We observed localization of TrpML to endo-lysosomes and the cell surface (or cell cortex) in Drosophila astrocytes. TrpML may function in astrocytic endo-lysosomes (e.g. Ca2+ release from these compartments) to indirectly activate Ca2+ entry through other cation channels at the cell surface. Alternatively, TrpML might function at the cell surface to directly drive Ca2+ entry, or stimulate entry from the extracellular space by other channels, or release from intracellular stores. It is also important to note that while we have assayed Ca2+ entry, TrpML is also capable of passing several other cations (Feng et al., 2014), and so its role in regulating astrocyte functions could be mediated by these cations in addition to Ca2+.

Astrocyte microdomain Ca2+ transients and whole-cell changes in astrocyte Ca2+ signaling appear to be distinct, in terms of their regulation by neurotransmitters and the molecular machinery generating each type of event (Agarwal et al., 2017; Bazargani and Attwell, 2016; Srinivasan et al., 2015). In mammals, whole-cell astrocyte Ca2+ transients are modulated by norepinephrine, adrenergic receptor signaling, and startle stimuli, while microdomain Ca2+ transients are activity-independent, associated with mitochondria and are sensitive to ROS (Agarwal et al., 2017; Ding et al., 2013; Paukert et al., 2014). Similarly, whole-cell transients in Drosophila astrocytes are activated by tyramine or octopamine (the invertebrate adrenergic neurotransmitters). We previously showed either of these can activate the Oct-TyrR receptor and the TRP channel Waterwitch on astrocytes, and in turn through the adenosine receptor AdoR, mediate many of the physiological and behavioral changes exerted by tyramine and octopamine (Ma et al., 2016). In contrast, microdomain Ca2+ transients in astrocytes are not regulated directly by neural activity, are mediated by TrpML (but not Oct-TyrR or Wtrw) and they are sensitive to ROS.

In mouse, a subset of microdomain Ca2+ transients are associated with mitochondria, which have been proposed to serve as a source of ROS, potentially through transient opening of the mPTP (Agarwal et al., 2017). These events may also require mitochondria in Drosophila, however the density of mitochondria in astrocyte processes was sufficiently high in our preparations that drawing such a conclusion was not feasible—a single astrocyte microdomain Ca2+ transient appears to span domains that include many mitochondria. It is reasonable to speculate that astrocyte microdomain Ca2+ transients across species are to a significant extent functionally distinct from whole-cell fluctuations, and that they play a role in coupling astrocyte signaling with tracheal/vasculature dynamics or other metabolic changes occurring in astrocytic mitochondria (Agarwal et al., 2017). Multiple distinct functional roles for astrocyte microdomain Ca2+ signaling (i.e. in tracheal regulation versus metabolism) could explain why although only half of all observed astrocyte microdomain Ca2+ transients are associated with tracheal filopodia, all appear to be potently regulated by ROS. Perhaps the remaining half of astrocyte microdomain Ca2+ transients not associated with trachea are responding to mitochondria-based metabolic needs through ROS signaling. Finally, approximately half of tracheal filopodia we observed were not visibly associated with astrocyte microdomain Ca2+ transients, yet they were able to extend and retract. This argues that other mechanisms exist to modulate tracheal dynamics in the CNS and astrocyte microdomain Ca2+ transients only represent one regulatory mechanism.

Maintaining a healthy, spatiotemporally regulated normoxic environment to prevent either hypoxia or hyperoxia in CNS is an enormous and ongoing challenge, as the O2-consuming metabolism is thought to fluctuate vigorously in response to neural activity. The close association of astrocyte microdomain Ca2+ transients with trachea, the larval breathing apparatus, and with tracheal retraction in particular, suggests a role in modulating CNS gas exchange. Increase in O2 delivery to tissues can lead to hyperoxia and elevated production of ROS. TrpML has recently been found to be a ROS sensor (Zhang et al., 2016), which would allow for a simple mechanism for ROS-mediated activation of TrpML downstream of increased O2 delivery. Consistent with such a role in regulation of gas exchange, we found an increase in ROS in the CNS of trpml mutants, and we demonstrated that bath application of tyramine to stimulate astrocyte microdomain Ca2+ transients was sufficient to promote tracheal filopodial retraction. Together our data support a model (Figure 4E) where a subset of TrpML-mediated microdomain Ca2+ transients in astrocytes facilitate tracheal retraction, likely in conjunction with TrpML in trachea. Complete loss of TrpML led to an increase in tracheal growth (e.g. an increased vascularization of neural tissues), which argues that astrocyte-tracheal signaling through TrpML can regulate long-term structural changes in the tracheal morphology. Based on these findings, we propose that an important role for a subset of astrocyte microdomain Ca2+ transients in the larval CNS is to coordinate gas exchange through regulation of tracheal dynamics, thereby balancing O2 delivery/CO2 removal according to local metabolic needs.

Materials and methods

Key resources table
Reagent type
(species) or resource		DesignationSource or referenceIdentifiersAdditional
information
Genetic reagent (D. melanogaster)trpml1Bloomington Stock CenterBDSC: 28992FlyBase symbol: w1118; Trpml1
Genetic reagent (D. melanogaster)trpml2Bloomington Stock CenterBDSC: 42230FlyBase symbol: w*; Trpml2/TM6B, Tb1
Genetic reagent (D. melanogaster)trpmlJF01239Bloomington Stock CenterBDSC: 31294FlyBase symbol: y1 v1; P{TRiP.JF01239}attP2
Genetic reagent (D. melanogaster)tyrRJF01878Bloomington Stock CenterBDSC: 25857FlyBase symbol: y1 v1; P{TRiP.JF01878}attP2
Genetic reagent (D. melanogaster)tyrRIIJF02749Bloomington Stock CenterBDSC: 27670FlyBase symbol: y1 v1; P{TRiP.JF02749}attP2
Genetic reagent (D. melanogaster)trpA11Bloomington Stock CenterBDSC: 36342FlyBase symbol:
TI{TI}TrpA11
Genetic reagent (D. melanogaster)trpm2Bloomington Stock CenterBDSC: 35527FlyBase symbol: w*; TI{TI}Trpm2/CyO
Genetic reagent (D. melanogaster)nompC3Bloomington Stock CenterBDSC: 42258FlyBase symbol: nompC3 cn1 bw1/CyO
Genetic reagent (D. melanogaster)trp1Bloomington Stock CenterBDSC: 5692FlyBase symbol: trp1
Genetic reagent (D. melanogaster)trpl302Bloomington Stock CenterBDSC: 31433FlyBase symbol: cn1 trpl302 bw1
Genetic reagent (D. melanogaster)pkd21Bloomington Stock CenterBDSC: 24495FlyBase symbol: w1118; Pkd21/CyO
Genetic reagent (D. melanogaster)trpγJF01244Bloomington Stock CenterBDSC: 31299FlyBase symbol: y1 v1; P{TRiP.JF01244}attP2
Genetic reagent (D. melanogaster)pyxJF01242Bloomington Stock CenterBDSC: 31297FlyBase symbol: y1 v1; P{TRiP.JF01242}attP2
Genetic reagent (D. melanogaster)btl-Gal4Bloomington Stock CenterBDSC: 8807FlyBase symbol:
W*; P{GAL4-btl.S}2, P{UASp-Act5C.T:GFP}2/CyO, P{lacZ.w+}276. UASp-Act5C.T:GFP was replaced with 10XUAS-IVS-myr::tdTomato by recombination in this paper.
Genetic reagent (D. melanogaster)UAS-Lifeact-GFPBloomington Stock CenterBDSC: 57326FlyBase symbol: w*; P{UAS-Lifeact.GFP.W}3
Genetic reagent (D. melanogaster)UASp-αTub-GFPBloomington Stock CenterBDSC: 7373FlyBase symbol: w*; P{UASp-GFPS65C-αTub84B}3/TM3, Sb1
Genetic reagent (D. melanogaster)10XUAS-IVS-myr::tdTomatoBloomington Stock CenterBDSC: 32222FlyBase symbol: w*; P{10XUAS-IVS-myr::tdTomato}attP40
Genetic reagent (D. melanogaster)UAS-trpml-mycBloomington Stock CenterBDSC: 57372FlyBase symbol: w*; P{UAS-Trpml.MYC}3, Trpml1/TM6B, Tb1
Genetic reagent (D. melanogaster)5XUAS-trpml-GCaMP5gBloomington Stock CenterBDSC: 80066FlyBase symbol: y1 w*; PBac{5XUAS-Trpml::GCaMP5G}VK00033
Genetic reagent (D. melanogaster)UAS-GFP-Lamp1Bloomington Stock CenterBDSC: 42714FlyBase symbol: w*; P{UAS-GFP-LAMP}2; P{nSyb-GAL4.S}3/T(2;3)TSTL, CyO: TM6B, Tb1
Genetic reagent (D. melanogaster)Oct-TyrRhonoKyoto Stock Center (DGRC)BDSC: 109038FlyBase symbol: w1118; P{lwB}Oct-TyrRhono
Genetic reagent (D. melanogaster)btl-LexARoy et al., 2014
Genetic reagent (D. melanogaster)nompC4Walker et al., 2000
Genetic reagent (D. melanogaster)painless70Im et al., 2015
Genetic reagent (D. melanogaster)nan36aKim et al., 2003
Genetic reagent (D. melanogaster)wtrwexKim et al., 2010
Genetic reagent (D. melanogaster)Tdc2RO54Cole et al., 2005
Genetic reagent (D. melanogaster)TβhnM18Monastirioti et al., 1996
Genetic reagent (D. melanogaster)alrm-Gal4Doherty et al., 2009
Genetic reagent (D. melanogaster)alrm > QF > Gal4Stork et al., 2014
Genetic reagent (D. melanogaster)repo-FLPaseStork et al., 2014
Genetic reagent (D. melanogaster)alrm-LexA::GADStork et al., 2014
Genetic reagent (D. melanogaster)UAS-myr::GCaMP5aThis papertransgenic flies harboring UAS-myr::GCaMP5a
Genetic reagent (D. melanogaster)UAS-myr::R-GECO1This papertransgenic flies harboring UAS-myr::R-GECO1
Genetic reagent (D. melanogaster)QUAS-myr::GCaMP5aThis papertransgenic flies harboring QUAS-myr::GCaMP5a
Genetic reagent (D. melanogaster)13XLexAop2-myr::GCaMP6sThis papertransgenic flies harboring 13XLexAop2-myr::GCaMP6s
Antibodymouse monoclonal anti-BrpDSHBCat# nc821:50
Antibodymouse monoclonal anti-c-MycDSHBCat# 9E101:100
Chemical compound, drugtetrodotoxinTocrisCat# 10781 µM
Chemical compound, druglanthanum chlorideSigma-AldrichCat# 2116050.1 mM, 1 mM
Chemical compound, drugacetylcholineSigma-AldrichCat# A66252.5 mM
Chemical compound, drugγ-aminobutyric acid (GABA)Sigma-AldrichCat# A21292.5 mM
Chemical compound, drugglutamateSigma-AldrichCat# G16262.5 mM
Chemical compound, drugtyramineSigma-AldrichCat# T903442.5 mM
Chemical compound, drugoctopamineSigma-AldrichCat# O02502.5 mM
Chemical compound, drugN-acetyl cysteineSigma-AldrichCat# A72502.5 mM
Chemical compound, drughydrogen peroxideSigma-AldrichCat# H10090.1 mM
Chemical compound, drughalocarbon oil 27Sigma-AldrichCat# H8773
Chemical compound, drugdihydroethidium (DHE)Sigma-AldrichCat# 30980030 µM
Recombinant DNA reagentpUAST-myr::GCaMP5aThis paperFly germline transformation plasmidGCaMP5a DNA with myristoylation sequence fused at the 5’ end
Recombinant DNA reagentpQUAST-myr::GCaMP5aThis paperFly germline transformation plasmidGCaMP5a DNA with myristoylation sequence fused at the 5’ end
Recombinant DNA reagentpUAST-myr::R-GECO1This paperFly germline transformation plasmidR-GECO1 DNA with myristoylation sequence fused at the 5’ end
Recombinant DNA reagentpJFRC19-13XLexAop2-IVS-myr::GCaMP6sThis paperFly germline transformation plasmidGCaMP6s DNA with myristoylation sequence fused at the 5’ end
Software, algorithmVolocityPerkinElmer, Inchttp://www.perkinelmer.com/lab-products-and-services/cellular-imaging/performing-advanced-image-data-analysis.html
Software, algorithmSlidebookIntelligent Imaging Innovations, Inchttps://www.intelligent-imaging.com/slidebook
Software, algorithmFijiSchindelin et al., 2012https://fiji.sc/
Software, algorithmGraphpad Prism 7GraphPad softwarehttps://www.graphpad.com/scientific-software/prism/
Software, algorithmIgor ProWaveMetrics, Inchttps://www.wavemetrics.com/products/igorpro
Software, algorithmAQuAWang et al., 2019https://github.com/yu-lab-vt/AQuA#fiji-plugin; Wang, 2019

Drosophila stocks and husbandry

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All larvae/flies were cultured in cornmeal food at 25 ℃ under 12 hr/12 hr dark/light cycles. Female larvae were used for all experiments unless otherwise stated. The specific developmental stages studied in each experiment are indicated in the following Materials and method details. Drosophila strains used include: Bloomington stock center trpml1 (28992), trpml2 (42230), trpmlJF01239 (31294), tyrRJF01878 (25857), tyrRIIJF02749 (27670), trpA11 (36342), trpm2 (35527), nompC3 (42258), trp1 (5692), trpl302 (31433), pkd21 (24495), trpγJF01244 (31299), pyxJF01242 (31297), btl-Gal4 (8807), UAS-Lifeact-GFP (57326), UASp-αTub-GFP (7373), 10XUAS-IVS-myr::tdTomato (32222), UAS-trpml-myc (57372), UAS-GFP-Lamp1 (42714). Oct-TyrRhono (Nagaya et al., 2002), nompC4 (Walker et al., 2000), painless70 (Im et al., 2015), nan36a (Kim et al., 2003), wtrwex (Kim et al., 2010), Tdc2RO54 (Cole et al., 2005), TβhnM18 (Monastirioti et al., 1996), alrm-Gal4(Doherty et al., 2009), alrm >QF > Gal4, repo-FLPase, alrm-LexA::GAD (Stork et al., 2014), btl-LexA (Roy et al., 2014), 5XUAS-trpml-GCaMP5g (Wong et al., 2017). UAS-myr::GCaMP5a, UAS-myr::R-GECO1, QUAS-myr::GCaMP5a, 13XLexAop2-myr::GCaMP6s flies were generated in this study.

Constructs and transgenic flies

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The full-length ORFs of GCaMP5a, R-GECO1, GCaMP6s with an in-frame DNA fragment encoding the myristoylation signal peptide at 5’-end were cloned into vectors pUAST, pQUAST, pJFRC19 (harboring 13XLexAop2-IVS, referring to the plasmid Addgene Cat# 26224) to generate constructs pUAST-myr::GCaMP5a, pQUAST-myr::GCaMP5a, pUAST-myr::R-GECO1, pJFRC19-13XLexAop2-IVS-myr::GCaMP6s for injection. The transgenic flies were injected and recovered by Rainbow Transgenic Flies, Inc (California).

Ca2+ imaging and data analysis

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Ca2+ imaging in intact larvae: the 1st instar larva expressing myr-GCaMP5a in astrocytes (25℃, 24–32 hr after egg laying) was sandwiched in 30 µl halocarbon oil 27 (Cat# H8773, Sigma-Aldrich) between a slide and a 22 × 22 mm coverslip (Cat# 1404–15, Globe Scientific Inc), then a 3 min time-lapse video was taken immediately on a spinning disk confocal microscope equipped with a 40X oil immersion objective.

CNS dissection from early 3rd instar larvae expressing myr-GCaMP5a in astrocytes (larval density ~100, 25°C, 76–84 hr after egg laying) was performed in the imaging buffer (pH7.2) containing 110 mM NaCl, 5.4 mM KCl, 0.3 mM CaCl2, 0.8 mM MgCl2, 10 mM D-glucose, 10 mM HEPES, the CNS was immediately transferred to a silicone coated petri dish, immersed in 100 µl imaging buffer (1.2 mM CaCl2), and immobilized gently by sticking the attached nerves onto the silicone surface with forceps. The petri dish then was placed on the stage of a spinning disk confocal microscope equipped with a 40X water dipping objective. The focal plane was fixed around where most of the dorsal lateral astrocytes start to appear in the field of view. After 4 min acclimation and stabilization, a 6 min movie (excitation channel, 488 nm. exposure time, 300 ms. single focal plane) was taken for analysis. The 488 nm and 516 nm channels were alternated for imaging both the microdomain Ca2+ transients in astrocytes and the dynamics of tracheal filopodia. To keep the tracheal filopodia in focus during the course of extension and retraction, images spanning 5 µM in z depth were taken.

The frequency (the number of microdomain Ca2+ transients per minute) of microdomain Ca2+ transients in each preparation was initially quantified as follows: a 100 µm X 100 µm window was cropped from each movie and resulted in nine smaller, side-to-side 100pixel X 100pixel windows (line drawing over movies) in which the number of microdomain Ca2+ transients was counted manually. The total number of microdomain Ca2+ transients in each preparation (100 µm X 100 µm) was acquired by adding up all the numbers counted in these 9 100pixel X 100pixel windows. The cutoff for defining a Ca2+ transient is 5% change in delta F/F0, which is evaluated by post hoc calculations after manually selecting active events. After the automatic Ca2+ signal analysis software Astrocyte Quantitative Analysis (AQuA)(Wang et al., 2019) became publicly available, we also compared our initial datasets of the dissected CNS from wildtype 3rd instar larvae using the above manual method to the ones obtained through AQuA (Manual vs AQuA-Source Data 8), and we didn’t find a significant difference (manual: 16.7 ± 3.69 versus AQuA: 19.8 ± 3.02, p=0.53). The intensity of microdomain Ca2+ transients was measured with software Volocity (PerkinElmer, Inc), and the amplitude of microdomain Ca2+ transients was defined by (Ft-F0)/F0 (t = 0,1,2…40, the peak amplitude was designated at t = 20, delta F = Ft-F0) as percentage. The full width at half maximum (FWHM) of astrocyte microdomains was acquired using software Igor Pro (WaveMetrics, Inc).

For bath application of compounds, halfway through the 6 min imaging window (~3 min), 100 µl imaging buffer (1.2 mM Ca2+) containing drugs (2X final concentration) was directly applied onto the preparations, then imaging continued for another 3 min. The chemicals used for bath application experiments include: Tocris, tetrodotoxin (1 µM, Cat# 1078). Sigma-Aldrich, lanthanum chloride (LaCl3, Cat# 211605), acetylcholine (2.5 mM, Cat# A6625), γ-aminobutyric acid (GABA, 2.5 mM, Cat# A2129), glutamate (2.5 mM, Cat# G1626), tyramine (2.5 mM, Cat# T90344), octopamine (2.5 mM, Cat# O0250), N-acetyl cysteine (NAC, 2.5 mM, Cat# A7250), hydrogen peroxide (H2O2, 0.1 mM, Cat# H1009).

Immunostaining and tracheal branch tracing

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The CNS dissected in PBS from 3rd instar larvae (larval density ~100, 25℃, 100–108 hr after egg laying) was immediately transferred in 4% formaldehyde for fixation for 20 min (for co-staining with tracheal filopodia, the dissection was performed in the imaging buffer with 0.3 mM Ca2+, and the CNS preparations were incubated in the imaging buffer with 1.2 mM Ca2+ for 10 min before 4% formaldehyde fixation). Washing in PBS for 3 × 10 min. Permeabilization in PBS + 0.3% Triton X-100 for 2 hr. Primary antibody (1:50 anti-Brp, DSHB, Cat# nc82 in PBS + 0.1% Triton X-100) incubation at 4 ℃ for ~72 hr. Secondary antibody incubation at room temperature for ~2 hr. Tracheal branches in ventral nerve cord were illuminated with 408 nm laser light and emitting autofluorescence was imaged. Each individual branch was then traced manually with Simple Neurite Tracer (Fiji).

Reactive oxygen species detection by DHE (dihydroethidium) staining

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The CNS preparations from 3rd instar larvae (larval density ~100, 25℃, 100–108 hr after egg laying) were made exactly in the same way for Ca2+ imaging. Incubation in 100 µl imaging buffer (1.2 mM Ca2+) containing 30 µM DHE for 8 min before imaging (30 µm in z depth, starting from the very dorsal side, was taken). The puncta were automatically counted by the segmentation tool in Slidebook.

Statistics

All statistics were performed in Graphpad. No data were excluded for analyses. 2–3 replications were successfully performed for each experiment. Comparison between groups was tested by one-way ANOVA with Tukey’s post hoc tests, or unpaired t-test. Comparison within groups was tested by paired t-test. p<0.05 was considered statistically significant. *p<0.05, **p<0.01.

Data availability

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Source data for Figure 1C–E; Figure 2A–H; Figure 3E and F; Figure 4A–D; Figure 2—figure supplement 1 – Figure 2A–C and E; Figure 3—figure supplement 1 – Figure 3D; Figure 4—figure supplement 1 - Figure 4A–B and D are included. Materials generated for this study will be freely available on request.

Data availability

All data generated or analyzed during this study are included in the manuscript and supporting files.

References

    1. Wang Y
    (2019)
    Accurate quantification of astrocyte and neurotransmitter fluorescence dynamics for single-cell and population-level physiology
    Nature Neuroscience.

Article and author information

Author details

  1. Zhiguo Ma

    Vollum Institute, Oregon Health and Science University, Portland, United States
    Contribution
    Conceptualization, Data curation, Formal analysis, Validation, Visualization, Methodology, Writing - original draft, Writing - review and editing
    For correspondence
    mzh@ohsu.edu
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0003-2250-1861

  2. Marc R Freeman

    Vollum Institute, Oregon Health and Science University, Portland, United States
    Contribution
    Conceptualization, Resources, Supervision, Funding acquisition, Writing - original draft, Project administration, Writing - review and editing
    For correspondence
    freemmar@ohsu.edu
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0003-3481-3715

Funding

National Institutes of Health (RO1 NS03538)

  • Marc Freeman

Oregon Health and Science University (NIH RO1 NS053538)

  • Marc Freeman

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

Acknowledgements

We thank Bloomington Stock Center, Kyoto Stock Center, Drs. CS Zuker, TB Kornberg, C Montell, J Hirsh and M Monastirioti for providing flies. We thank A Sheehan for making constructs. We thank Freeman lab members for feedback on the manuscript. This work was supported by NIH RO1 NS053538 (to MRF) and OHSU.

Copyright

© 2020, Ma and Freeman

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. Zhiguo Ma
  2. Marc R Freeman
(2020)
TrpML-mediated astrocyte microdomain Ca2+ transients regulate astrocyte–tracheal interactions
eLife 9:e58952.
https://doi.org/10.7554/eLife.58952

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    Katie Morris, Edita Bulovaite ... Mathew H Horrocks
    Research Article

    The concept that dimeric protein complexes in synapses can sequentially replace their subunits has been a cornerstone of Francis Crick’s 1984 hypothesis, explaining how long-term memories could be maintained in the face of short protein lifetimes. However, it is unknown whether the subunits of protein complexes that mediate memory are sequentially replaced in the brain and if this process is linked to protein lifetime. We address these issues by focusing on supercomplexes assembled by the abundant postsynaptic scaffolding protein PSD95, which plays a crucial role in memory. We used single-molecule detection, super-resolution microscopy and MINFLUX to probe the molecular composition of PSD95 supercomplexes in mice carrying genetically encoded HaloTags, eGFP, and mEoS2. We found a population of PSD95-containing supercomplexes comprised of two copies of PSD95, with a dominant 12.7 nm separation. Time-stamping of PSD95 subunits in vivo revealed that each PSD95 subunit was sequentially replaced over days and weeks. Comparison of brain regions showed subunit replacement was slowest in the cortex, where PSD95 protein lifetime is longest. Our findings reveal that protein supercomplexes within the postsynaptic density can be maintained by gradual replacement of individual subunits providing a mechanism for stable maintenance of their organization. Moreover, we extend Crick’s model by suggesting that synapses with slow subunit replacement of protein supercomplexes and long-protein lifetimes are specialized for long-term memory storage and that these synapses are highly enriched in superficial layers of the cortex where long-term memories are stored.