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Synaptic representation of locomotion in single cerebellar granule cells

The cerebellum plays a crucial role in the regulation of locomotion, but how movement is represented at the synaptic level is not known. Here, we use in vivo patch-clamp recordings to show that locomotion can be directly read out from mossy fiber synaptic input and spike output in single granule cel...

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Detalles Bibliográficos
Autores principales: Powell, Kate, Mathy, Alexandre, Duguid, Ian, Häusser, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4499793/
https://www.ncbi.nlm.nih.gov/pubmed/26083712
http://dx.doi.org/10.7554/eLife.07290
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author Powell, Kate
Mathy, Alexandre
Duguid, Ian
Häusser, Michael
author_facet Powell, Kate
Mathy, Alexandre
Duguid, Ian
Häusser, Michael
author_sort Powell, Kate
collection PubMed
description The cerebellum plays a crucial role in the regulation of locomotion, but how movement is represented at the synaptic level is not known. Here, we use in vivo patch-clamp recordings to show that locomotion can be directly read out from mossy fiber synaptic input and spike output in single granule cells. The increase in granule cell spiking during locomotion is enhanced by glutamate spillover currents recruited during movement. Surprisingly, the entire step sequence can be predicted from input EPSCs and output spikes of a single granule cell, suggesting that a robust gait code is present already at the cerebellar input layer and transmitted via the granule cell pathway to downstream Purkinje cells. Thus, synaptic input delivers remarkably rich information to single neurons during locomotion. DOI: http://dx.doi.org/10.7554/eLife.07290.001
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spelling pubmed-44997932015-07-14 Synaptic representation of locomotion in single cerebellar granule cells Powell, Kate Mathy, Alexandre Duguid, Ian Häusser, Michael eLife Neuroscience The cerebellum plays a crucial role in the regulation of locomotion, but how movement is represented at the synaptic level is not known. Here, we use in vivo patch-clamp recordings to show that locomotion can be directly read out from mossy fiber synaptic input and spike output in single granule cells. The increase in granule cell spiking during locomotion is enhanced by glutamate spillover currents recruited during movement. Surprisingly, the entire step sequence can be predicted from input EPSCs and output spikes of a single granule cell, suggesting that a robust gait code is present already at the cerebellar input layer and transmitted via the granule cell pathway to downstream Purkinje cells. Thus, synaptic input delivers remarkably rich information to single neurons during locomotion. DOI: http://dx.doi.org/10.7554/eLife.07290.001 eLife Sciences Publications, Ltd 2015-06-17 /pmc/articles/PMC4499793/ /pubmed/26083712 http://dx.doi.org/10.7554/eLife.07290 Text en © 2015, Powell et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Powell, Kate
Mathy, Alexandre
Duguid, Ian
Häusser, Michael
Synaptic representation of locomotion in single cerebellar granule cells
title Synaptic representation of locomotion in single cerebellar granule cells
title_full Synaptic representation of locomotion in single cerebellar granule cells
title_fullStr Synaptic representation of locomotion in single cerebellar granule cells
title_full_unstemmed Synaptic representation of locomotion in single cerebellar granule cells
title_short Synaptic representation of locomotion in single cerebellar granule cells
title_sort synaptic representation of locomotion in single cerebellar granule cells
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4499793/
https://www.ncbi.nlm.nih.gov/pubmed/26083712
http://dx.doi.org/10.7554/eLife.07290
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AT duguidian synapticrepresentationoflocomotioninsinglecerebellargranulecells
AT haussermichael synapticrepresentationoflocomotioninsinglecerebellargranulecells