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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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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. |
format | Online Article Text |
id | pubmed-6374073 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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