The mammalian cerebellum is a highly multimodal structure, receiving inputs from multiple sensory modalities and integrating them during complex sensorimotor coordination tasks. Previously, using cell-type-specific anatomical projection mapping, it was shown that multimodal pathways converge onto individual cerebellar granule cells (Huang et al., 2013). Here we directly measure synaptic currents using in vivo patch-clamp recordings and confirm that a subset of single granule cells receive convergent functional multimodal (somatosensory, auditory, and visual) inputs via separate mossy fibers. Furthermore, we show that the integration of multimodal signals by granule cells can enhance action potential output. These recordings directly demonstrate functional convergence of multimodal signals onto single granule cells.https://doi.org/10.7554/eLife.12916.001
Integrating multimodal sensory signals is one of the fundamental operations performed by the brain. The midbrain and cerebral association cortex (Stein and Stanford, 2008), and the cerebellum receive and process sensory signals of various modalities (Snider and Stowell, 1944; Azizi and Woodward, 1990; Gao et al., 1996; Sobel et al., 1998). Although it is well known that each granule cell in the mammalian cerebellum receives excitatory synaptic inputs from on average four mossy fibers (Eccles et al., 1967; Jakab and Hamori, 1988), it is important to determine whether multisensory integration takes place already on the level of the granule cells, which form the input layer, or only in the downstream neurons, including Purkinje cells. A recent study using projection mapping has shown that some granule cells receive mossy fibers from two areas in the brainstem (the basilar pontine nucleus and the external cuneate nucleus), providing morphological evidence of multimodal convergence in single granule cells (Huang et al., 2013; see also Chabrol et al., 2015). However, in vivo single cerebellar granule cells in cats have been shown to only respond to stimulation of a single modality (Jörntell and Ekerot, 2006; Spanne and Jörntell, 2015). Therefore, to determine whether functional multimodal convergence is common we made whole-cell patch-clamp recordings in vivo from single granule cells and directly tested responsiveness to sensory stimulation of different modalities.
We made patch-clamp recordings from single cerebellar granule cells of rats in vivo to examine their responses to auditory, visual and somatosensory stimulation. We selected crus I and II and the dorsal paraflocculus of the cerebellum because previous studies suggested that these areas might receive multisensory inputs (Azizi and Woodward, 1990; Huang et al., 2013). The high quality of voltage clamp recordings in granule cells in vivo enabled detection of individual sensory-evoked EPSCs (Chadderton et al., 2004; Rancz et al., 2007; Arenz et al., 2008), thus providing exquisite sensitivity for detection of responses to a sensory stimulus. 45% of granule cells (60/133 cells) in crus I and II and 10% of those (3/30 cells) in the dorsal paraflocculus responded to somatosensory stimulation with a burst of EPSCs (Figure 1A–E left column and Figure 1F–G), as described previously (Chadderton et al., 2004; Rancz et al., 2007). In contrast, auditory stimulation (white noise, 81–91 dB SPL, Figure 1A–E middle column) evoked EPSCs in 25% of granule cells in crus I and II (33/133 cells) and 10% (3/30 cells) of granule cells in the dorsal paraflocculus (Figure 1F–G). When different sound levels were systematically tested, the number of evoked EPSC events increased with increasing sound levels (from 75 dB to 94 dB), while the mean amplitude of evoked EPSCs remained constant (Figure 1—figure supplement 1). Finally, visual stimulation (binocular LED flash; Figure 1A–E right column) evoked EPSCs in 87% of granule cells (26/30 cells) in the dorsal paraflocculus, while visual responses in crus I and II were rare (Figure 1F–G). When visual stimulation was delivered monocularly, ipsilateral stimulation evoked the predominant response (Figure 1—figure supplement 2). In summary, auditory and visual stimulation evoked bursts of EPSCs in granule cells that were comparable to those evoked by somatosensory stimulation (Figure 1—figure supplement 3).
A subpopulation of granule cells responded to multiple sensory modalities (Figure 1F,G). In dorsal paraflocculus 20% (6/30 cells) of granule cells were multisensory, and in crus I and II 14% (18/133 cells) were multisensory. In both regions, we found individual granule cells that responded to stimulation of three separate sensory modalities. Figure 2 shows a representative granule cell in crus II that responded to auditory stimulation, somatosensory stimulation and a combination of these two stimuli.
To examine if responses to different sensory stimuli in a single granule cell were mediated by the same or separate mossy fibers, we analyzed the amplitude and waveform of individual EPSCs, since these characteristics reflect unique properties of distinct synapses (Silver et al., 1996; Arenz et al., 2008). When comparing EPSC amplitudes, we focused on the first EPSC of a sensory-evoked burst because the second and subsequent events are likely to be affected by synaptic facilitation and depression. In the cell shown in Figure 2A–F, the amplitude of auditory-evoked EPSCs (16.6 ± 0.8 pA, n = 23 sweeps) was significantly larger than that of somatosensory-evoked EPSCs (8.6 ± 1.2 pA, n = 23, P < 0.05), indicating that those two groups of EPSCs originate from different synapses, i.e. the signals are conveyed by different mossy fibers (Figure 4A). Across the population, 40% (8/20) of multisensory cells showed significantly different (P < 0.05) first EPSC amplitudes in response to different modalities (Figure 2G–H and Figure 2—figure supplement 1). Additionally, one cell also showed a significant difference (P < 0.05) in EPSC rise time for the different modalities. For the remaining cells that did not exhibit a significant difference in EPSC amplitudes between modalities, it is not possible to determine if their multimodal input arises from a single mossy fiber (Figure 4B) or from two mossy fibers that have indistinguishable characteristics (Figure 4A).
Combined stimulation of two modalities evoked responses that were approximately the sum of two unimodal responses (Figure 2). If the summation is perfectly linear, the linearity index (see Figure 2 legend) should fall on the unity line. For the cell shown in Figure 2, this index was close to, but slightly below unity (Figure 2C). Interestingly, the linearity index showed considerable variation across cells and indicated moderately sublinear summation on average (0.71 ± 0.23; mean ± s.d.) for 8 cells that received inputs from two separate mossy fibers ( Figure 4C, see Discussion). The same tendency was seen for cells that were not determined to have separate mossy fiber inputs for different modalities (0.70 ± 0.20, mean ± s.d., n = 12), which was confirmed when the synaptic charge was used instead of event number to calculate the linearity index.
Finally, we examined how multisensory stimulation drives action potential output. We first identified granule cells receiving multisensory inputs via different mossy fibers using voltage-clamp recordings, and then we obtained recordings in the same neurons in current-clamp mode. The resting membrane potential and the action potential threshold were −55.0 ± 4.7 mV and −39.7 ± 3.0 mV (n = 4), respectively. In the granule cell shown in Figure 3A–C, combined stimulation with two sensory modalities evoked more action potentials than the sum of two unimodal stimuli, indicating supralinear summation. Two of four cells exhibited such supralinear summation (Cell 1 and 2 in Figure 3D), while the other two cells showed sublinear summation. These findings suggest that, although there exists diversity across the population, granule cells are capable of integrating multisensory signals to generate enhanced action potential output.
We have taken advantage of the electrical compactness of cerebellar granule cells and their small number of synaptic inputs to probe how multisensory signals are integrated by single neurons at the input stage of the cerebellar cortex. Using high-resolution voltage-clamp recordings, we demonstrate directly that multisensory signals converge onto individual granule cells in vivo, and that multisensory input can enhance granule cell spike output.
Granule cells receive excitatory input from only 4 mossy fibers on average (Eccles et al., 1967; Jakab and Hamori, 1988). Electrophysiological recordings have shown that somatosensory inputs to crus I and II (Chadderton et al., 2004; Rancz et al., 2007) and vestibular signals to the flocculus (Arenz et al., 2008) can be conveyed to individual granule cells by single mossy fibers. Therefore, it has been speculated that the other three mossy fibers (on average) could conduct signals of other sensory modalities. This conjecture has been supported by the recent anatomical (Huang et al., 2013) and in vitro electrophysiological (Chabrol et al., 2015) demonstration that single granule cells can receive mossy fibers of different origins (see also [Sawtell, 2010]). Our findings in vivo provide a direct functional demonstration that single granule cells can receive inputs from up to three separate sensory modalities. Furthermore, we show that combined stimulation of two sensory modalities can produce enhanced spike output from granule cells, indicating that the result of multisensory integration can be transmitted to downstream neurons in the cerebellar network.
While the present study strongly supports the conclusions of Huang et al. (2013) regarding multimodal integration in single cerebellar granule cells, we could not directly prove the integration of sensory and motor signals in granule cells as proposed by their study, because we could test only integration of sensory modalities in anesthetized animals. Integration of sensory and motor inputs should to be tested in future studies using recordings from granule cells in awake behaving animals (Powell et al., 2015).
When combining stimulation of two sensory modalities, we observed significant sublinear summation of synaptic currents in a subset of granule cells. Under the excellent voltage-clamp conditions that exist in granule cells, inputs from different synapses are expected to summate linearly. Thus, the observed sublinear summation of synaptic currents is likely to be due to inhibitory interactions between the two sensory pathways upstream from the granule cell (see Figure 4). Such interactions could occur at any point in upstream sensory pathways, including the brainstem, the thalamus and the cerebral cortex, particularly given that the relatively long latency (> 10 ms) of sensory responses in our recordings suggests that these sensory signals are mediated via the corticocerebellar pathway rather than direct projections from primary sensory neurons (Morissette and Bower, 1996). Further studies are required to understand the mechanism and significance of such inhibitory interactions.
It should also be noted that our findings do not directly contradict the absence of multimodal integration observed in granule cells in decerebrate animals in which the corticocerebellar pathway is not preserved (Jörntell and Ekerot, 2006; Spanne and Jörntell, 2015). It is likely that granule cells represent a diverse population with respect to functional multisensory input (Figure 4), with some granule cells appearing to be unimodal, some with multisensory input delivered by separate mossy fibers, and some with multisensory input delivered by a single mossy fiber.
The convergence of functionally distinct sensory signals in single granule cells at the input layer of the cerebellar cortex, predicted by Huang et al. (2013) and demonstrated directly here, is likely to be a crucial feature of cerebellar signal processing. Indeed, influential theories of cerebellar computation (Marr, 1969; Albus, 1971) have proposed that granule cells are not merely relaying signals but “recoding” multiple types of incoming signals. Our present study provides important in vivo functional evidence supporting this “recoding” hypothesis in the mammalian cerebellum. Moreover, it was hypothesized (Albus, 1971) that such “recoding” would expand the representation of population patterns because granule cells outnumber mossy fibers by a factor of 100 (due to the extensive branching of mossy fibers). Our observation that the linearity of summation (both in synaptic inputs and in spike outputs) varies across cells may reflect the diversity of coding patterns required for the computational role of the granule cell in expansion recoding. In future studies, it will be important to reveal how synaptic plasticity at the mossy fiber-granule cell synapse (Roggeri et al., 2008) may affect the representation of multiple sensory inputs at the level of a single granule cell.
All experiments were carried out in accordance with UK Home Office regulations and the guidelines of the Animal Experiment Committee of Jikei University. Lister-hooded rats (19–24 days old) were anaesthetized with a ketamine (60 mg/kg) and xylazine (4.5 mg/kg) mixture. Rats were freely breathing during surgery and recording. A peripheral anticholinergic drug, glycopyrrolate bromide (0.02 mg/kg S.C.) was administered in most of the experiments. In some early experiments, atropine (0.06 mg/kg) was used instead of glycopyrrolate. A head-post was glued onto the skull and a small craniotomy was made over the cerebellar region to be targeted. After removal of the dura, saline was used to prevent drying of the exposed brain surface.
Whole cell voltage-clamp (V-C) and current-clamp (I-C) recordings were made from granule cells in crus I and II and paraflocculus of the cerebellar cortex, using a Multiclamp 700B amplifier (Molecular Devices, Sunnyvale, CA). The internal solution contained: K-methanesulphonate 133 mM, KCl 7 mM, HEPES 10 mM, Mg-ATP 2 mM, Na2ATP 2 mM, Na2GTP 0.5 mM, EGTA 0.05 mM and biocytin 0.5%, pH 7.2, giving an estimated chloride reversal potential (ECl) of -69 mV. This allows excitatory synaptic currents to be observed in isolation by voltage clamping at −70 mV. Data were low-pass filtered at 6 kHz and acquired at 50 kHz using a Digidata interface and pClamp software (Molecular Devices). Offline box smoothing (up to 11 points) was applied for noise reduction.
The animal was placed in a sound-attenuating light-proof box during the recording. Somatosensory stimulation was delivered using an air-puff (50 ms, 20–50 psi at source) timed by a Picospritzer and aimed at the ipsilateral whiskers, perioral skin or eye regions. Audible noise caused by the airpuff apparatus was carefully minimized and did not evoke cerebellar responses by itself. Auditory stimulation was delivered with a calibrated speaker driven by an RP2.1 processor and RPdvs software (Tucker-Davis Technologies, Alachua, FL). Gaussian white noise (up to 20 kHz) was presented for 350 ms with linear ramp rise and fall (5 ms). Visual stimulation was presented using two white LEDs (approximate intensity 200 mcd, one for each eye) each placed at 10 mm from the left or right eye. Each LED was light-shielded with a black cylinder, which also surrounds the eye, in order to deliver monocular stimulation. These LEDs diffusely illuminate a wide visual field because they are out of focus for the rat’s vision. In a subset of visual experiments, a computer screen placed at 12 cm from the animal head was used to deliver a wide-field visual presentation (from 10° contralateral to 60° ipsilateral) of full screen flickering from black to white (10 frames/s).
The detection of EPSCs and action potentials was performed using a custom threshold-based algorithm programmed in Igor Pro (TaroTools: https://sites.google.com/site/tarotoolsregister/). The event number evoked by stimulation was counted (baseline-subtracted) in a time window adjusted for each cell to include all evoked events. Sensory responses were defined as positive when the post-stimulus histogram exceeded three times the standard deviation of the baseline. The synaptic charge was measured as the integral of the averaged current trace (baseline-subtracted and sign-reversed). Sensory response latency was defined as the time from the stimulus onset to the first EPSC event. In the analysis for Figure 3D, a granule cell that had an extremely large time difference (109 ms) between two unimodal responses compared to other cases (<35 ms) was excluded. Data are represented as mean ± s.e.m unless otherwise noted. Statistical significance was tested using the unpaired Student’s t-test unless otherwise noted.
We are grateful to Charlotte Arlt, Beverley Clark, Dimitar Kostadinov, Arnd Roth, Greg Stuart and Christian Wilms for helpful discussions and for comments on the manuscript. We thank Toshihiko Momiyama for his support, Hysell Oviedo and Jennifer Linden for help with setting up auditory equipment and Arifa Naeem for technical assistance. This work was supported by grants from the Wellcome Trust and the Gatsby Charitable Foundation (to MH) and Grant-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology of Japan and grants from the Uehara Memorial Foundation and the Takeda Science Foundation (to TI).
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Eve MarderReviewing Editor; Brandeis University, United States
In the interests of transparency, eLife includes the editorial decision letter and accompanying author responses. A lightly edited version of the letter sent to the authors after peer review is shown, indicating the most substantive concerns; minor comments are not usually included.
Thank you for submitting your work entitled "Multimodal sensory integration in single cerebellar granule cells in vivo" for consideration by eLife. Your article has been reviewed by three peer reviewers, and the evaluation has been overseen by Eve Marder as the Senior Editor and Reviewing Editor.
The reviewers have discussed the reviews with one another and the Reviewing Editor has drafted this decision to help you prepare a revised submission.
As you know, we usually provide a summary of the needed revisions, but instead I am providing you with the entire set of reviewer comments. The revisions needed are exclusively editorial, and many of them relatively minor, but it seems that the context provided by these full reviews will help you understand what is necessary for you to directly address.
It has long been thought that cerebellar granule cells perform multimodal integration and that such integration represents an important step in cerebellar processing, however whether or not granule cells actually perform such integration has been debated until recently. An elegant anatomical study published in eLife provided clear evidence that individual granule cells in some cerebellar regions integrate mossy fiber input from different sources. A recent study (Chabrol et al.) provides clear evidence for multimodal integration in cerebellar granule cells using both anatomy and in vitro electrophysiology. Multimodal integration has also been shown in vivo in granule cells in a cerebellum-like structure in electric fish. The present study by Ishikawa et al. provides further support for multimodal integration in cerebellar granule cells using in vivo electrophysiological recordings.
The central finding is that a subset of granule cells receive input about different sensory modalities and that in some cases these are conveyed by different mossy fibers (as indicated by distinct EPSC waveforms). This is a strong result with clear relevance to the field and provides in vivo physiological support for the results of Huang et al. (albeit in relation to different sets of inputs).
The authors also make claims regarding the important functional question of how multimodal convergence affects spiking output and about the different possible functional connectivity patterns in granule cells (unimodal, multimodal input conveyed by a single anatomical input etc). These claims are less well supported. The analysis of spiking output involves only four neurons amongst which half were suppressed and the other half enhanced by multimodal stimulation.
Discussion: …"Importantly, we show that granule cells represent a diverse population with respect to functional multisensory input, with some granule cells appearing to be unimodal, some with multisensory input delivered by separate mossy fibers, and some with multisensory input delivered by a single mossy fiber. These different anatomical and functional arrangements are illustrated schematically in Figure 3." I am not convinced that the authors have provided strong support for these claims. Some granule cells may be unimodal but the authors tested only a tiny fraction of the possible stimuli that could engage granule cells, so the appearance of unimodality does not count for much in my opinion. In the Results the authors say that for cases in which EPSCs don't differ significantly "it is not possible to determine if multimodal input arises from a single mossy fiber or from two mossy fibers that have indistinguishable characteristics." If this is true what is the support for the claim that some granule cells receive multisensory input delivered by a single mossy fiber? The statements made here need to be carefully qualified.
While the present manuscript is clearly relevant to the Huang et al. paper, the relationship between the two including the similarities/differences and advantages/limitations of both approaches could be made more explicit. This seems to warrant a separate paragraph in Discussion. For example Huang et al. looked at integration of cuneate and pontine (sensory and motor inputs) while the present paper looks at convergence of various sensory inputs.
Reviewer #2: In this manuscript, the authors accomplish the challenging task of making in vivo whole cell patch clamp recordings from cerebellar granule neurons in anesthetized rat. By doing so, they demonstrate conclusively that a subset of granule neurons can respond to two or more types of sensory stimulation (most frequently, auditory and somatosensory; 20% in the paraflocculus and14% in crus I & II). While this multisensory sensitivity is predicted from the anatomy, conflicting in vitro electrophysiological data make it important to demonstrate physiologically in an in vivo preparation. In fact, the result that the majority of cells were sensitive to just one modality (at least with the stimulus parameters tested) yet a significant minority were multisensory goes a long way toward resolving the discrepancy in the literature, although the authors (surprisingly?) don't emphasize this aspect of the work. The authors go on to show that in these multimodal cells, the EPSCs evoked by the two sensory stimuli applied together sum slightly sublinearly in voltage clamp, and evidence and reasoning are presented to suggest that this is indicative of upstream interactions in the two sensory pathways. The authors also demonstrate in current clamp that the sublinear EPSC summation can result in either more or fewer spikes than elicited by stimulation through a single modality, which is a useful additional piece of information, since it shows that multiple factors determine the nature of spike integration. The data are of high quality, and the manuscript is for the most part clearly written. It is hard not to wish for more manipulations, but given the technical difficulty of the recordings, it is not surprising that the work stops where it does. The manuscript seems well suited to eLife's description of a Research Advance, since the paper by Hantman and colleagues that precedes this study was anatomical, and the present work offers a (much needed) physiological confirmation. All my comments are stylistic.
1) Abstract: "These findings provide functional evidence for convergence of multimodal signals onto single granule cells." That is true but somehow this seems to go just beyond "providing evidence" for multimodal signals. The multimodal signals are actually measured.
2) Introduction, "Therefore, determining the extent to which multimodal convergence is functionally relevant in vivo requires direct recordings from single granule cells using sensory stimulation of different modalities." This sentence is likewise a bit oblique and off the point, as there is nothing about functional relevance here. Isn't the question that whether granule cells in the intact, functioning brain respond to multimodal inputs can only be assessed with direct in vivo measurements in the species of interest?
3) Please indicate species at the beginning of Results.
4) Suggestion if space permits: please give a hint in the results of why the sublinear summation might be interesting. On first reading, it seemed that non-linear summation of synaptic inputs would be expected, unless the idea was that the different modalities on the different dendrites would necessarily be so segregated that they would have to sum linearly. The Discussion cleared this up, but a little more extensive orienting of the reader earlier would be helpful.
Reviewer #3: The manuscript describes powerful and straightforward measurements indicating that single cerebellar granule neurons receive multimodal sensory inputs; it also shows that such multimodal inputs are summed in a simple manner to generate spike output. These are striking results given that these neurons receive input from 3-5 mossy fiber presynaptic terminals. They are also important because they provide direct evidence for a hypothesized integrative role for granule cells in sensorimotor processing.
In general the paper is clearly written and reports interesting findings that should be of interest to a general audience of neuroscientists. I have no substantive concerns and recommend that the paper be accepted with minimal revisions.
Minor comment: The last sentence of the Introduction seems indirect. The authors might consider something like, "To determine whether multimodal convergence is common we made whole cell recordings in vivo from single granule cells and tested responsiveness to sensory stimulation of different modalities."https://doi.org/10.7554/eLife.12916.010
- Michael Häusser
The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
Animal experimentation: This study was performed in strict accordance with UK Home Office regulations and under approval and supervision of the Animal Experiment Committee of Jikei University. Experiments were carried out under Project Licence 70/7833 issued by the Home Office, which was issued following local ethical review, and under the relevant Personal Licences issued by the Home Office. All surgery was performed under ketamine/xylazine anesthesia, and every effort was made to minimize suffering.
- Eve Marder, Reviewing Editor, Brandeis University, United States
© 2015, Ishikawa et al
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