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Motor context dominates output from purkinje cell functional regions during reflexive visuomotor behaviours

The cerebellum integrates sensory stimuli and motor actions to enable smooth coordination and motor learning. Here we harness the innate behavioral repertoire of the larval zebrafish to characterize the spatiotemporal dynamics of feature coding across the entire Purkinje cell population during visua...

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Autores principales: Knogler, Laura D, Kist, Andreas M, Portugues, Ruben
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6374073/
https://www.ncbi.nlm.nih.gov/pubmed/30681408
http://dx.doi.org/10.7554/eLife.42138
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author Knogler, Laura D
Kist, Andreas M
Portugues, Ruben
author_facet Knogler, Laura D
Kist, Andreas M
Portugues, Ruben
author_sort Knogler, Laura D
collection PubMed
description The cerebellum integrates sensory stimuli and motor actions to enable smooth coordination and motor learning. Here we harness the innate behavioral repertoire of the larval zebrafish to characterize the spatiotemporal dynamics of feature coding across the entire Purkinje cell population during visual stimuli and the reflexive behaviors that they elicit. Population imaging reveals three spatially-clustered regions of Purkinje cell activity along the rostrocaudal axis. Complementary single-cell electrophysiological recordings assign these Purkinje cells to one of three functional phenotypes that encode a specific visual, and not motor, signal via complex spikes. In contrast, simple spike output of most Purkinje cells is strongly driven by motor-related tail and eye signals. Interactions between complex and simple spikes show heterogeneous modulation patterns across different Purkinje cells, which become temporally restricted during swimming episodes. Our findings reveal how sensorimotor information is encoded by individual Purkinje cells and organized into behavioral modules across the entire cerebellum.
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spelling pubmed-63740732019-02-15 Motor context dominates output from purkinje cell functional regions during reflexive visuomotor behaviours Knogler, Laura D Kist, Andreas M Portugues, Ruben eLife Neuroscience The cerebellum integrates sensory stimuli and motor actions to enable smooth coordination and motor learning. Here we harness the innate behavioral repertoire of the larval zebrafish to characterize the spatiotemporal dynamics of feature coding across the entire Purkinje cell population during visual stimuli and the reflexive behaviors that they elicit. Population imaging reveals three spatially-clustered regions of Purkinje cell activity along the rostrocaudal axis. Complementary single-cell electrophysiological recordings assign these Purkinje cells to one of three functional phenotypes that encode a specific visual, and not motor, signal via complex spikes. In contrast, simple spike output of most Purkinje cells is strongly driven by motor-related tail and eye signals. Interactions between complex and simple spikes show heterogeneous modulation patterns across different Purkinje cells, which become temporally restricted during swimming episodes. Our findings reveal how sensorimotor information is encoded by individual Purkinje cells and organized into behavioral modules across the entire cerebellum. eLife Sciences Publications, Ltd 2019-01-25 /pmc/articles/PMC6374073/ /pubmed/30681408 http://dx.doi.org/10.7554/eLife.42138 Text en © 2019, Knogler et al http://creativecommons.org/licenses/by/4.0/ 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
Knogler, Laura D
Kist, Andreas M
Portugues, Ruben
Motor context dominates output from purkinje cell functional regions during reflexive visuomotor behaviours
title Motor context dominates output from purkinje cell functional regions during reflexive visuomotor behaviours
title_full Motor context dominates output from purkinje cell functional regions during reflexive visuomotor behaviours
title_fullStr Motor context dominates output from purkinje cell functional regions during reflexive visuomotor behaviours
title_full_unstemmed Motor context dominates output from purkinje cell functional regions during reflexive visuomotor behaviours
title_short Motor context dominates output from purkinje cell functional regions during reflexive visuomotor behaviours
title_sort motor context dominates output from purkinje cell functional regions during reflexive visuomotor behaviours
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6374073/
https://www.ncbi.nlm.nih.gov/pubmed/30681408
http://dx.doi.org/10.7554/eLife.42138
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