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Population-scale organization of cerebellar granule neuron signaling during a visuomotor behavior

Granule cells at the input layer of the cerebellum comprise over half the neurons in the human brain and are thought to be critical for learning. However, little is known about granule neuron signaling at the population scale during behavior. We used calcium imaging in awake zebrafish during optokin...

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Autores principales: Sylvester, Sherika J. G., Lee, Melanie M., Ramirez, Alexandro D., Lim, Sukbin, Goldman, Mark S., Aksay, Emre R. F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5701187/
https://www.ncbi.nlm.nih.gov/pubmed/29176570
http://dx.doi.org/10.1038/s41598-017-15938-w
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author Sylvester, Sherika J. G.
Lee, Melanie M.
Ramirez, Alexandro D.
Lim, Sukbin
Goldman, Mark S.
Aksay, Emre R. F.
author_facet Sylvester, Sherika J. G.
Lee, Melanie M.
Ramirez, Alexandro D.
Lim, Sukbin
Goldman, Mark S.
Aksay, Emre R. F.
author_sort Sylvester, Sherika J. G.
collection PubMed
description Granule cells at the input layer of the cerebellum comprise over half the neurons in the human brain and are thought to be critical for learning. However, little is known about granule neuron signaling at the population scale during behavior. We used calcium imaging in awake zebrafish during optokinetic behavior to record transgenically identified granule neurons throughout a cerebellar population. A significant fraction of the population was responsive at any given time. In contrast to core precerebellar populations, granule neuron responses were relatively heterogeneous, with variation in the degree of rectification and the balance of positive versus negative changes in activity. Functional correlations were strongest for nearby cells, with weak spatial gradients in the degree of rectification and the average sign of response. These data open a new window upon cerebellar function and suggest granule layer signals represent elementary building blocks under-represented in core sensorimotor pathways, thereby enabling the construction of novel patterns of activity for learning.
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spelling pubmed-57011872017-11-30 Population-scale organization of cerebellar granule neuron signaling during a visuomotor behavior Sylvester, Sherika J. G. Lee, Melanie M. Ramirez, Alexandro D. Lim, Sukbin Goldman, Mark S. Aksay, Emre R. F. Sci Rep Article Granule cells at the input layer of the cerebellum comprise over half the neurons in the human brain and are thought to be critical for learning. However, little is known about granule neuron signaling at the population scale during behavior. We used calcium imaging in awake zebrafish during optokinetic behavior to record transgenically identified granule neurons throughout a cerebellar population. A significant fraction of the population was responsive at any given time. In contrast to core precerebellar populations, granule neuron responses were relatively heterogeneous, with variation in the degree of rectification and the balance of positive versus negative changes in activity. Functional correlations were strongest for nearby cells, with weak spatial gradients in the degree of rectification and the average sign of response. These data open a new window upon cerebellar function and suggest granule layer signals represent elementary building blocks under-represented in core sensorimotor pathways, thereby enabling the construction of novel patterns of activity for learning. Nature Publishing Group UK 2017-11-24 /pmc/articles/PMC5701187/ /pubmed/29176570 http://dx.doi.org/10.1038/s41598-017-15938-w Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Sylvester, Sherika J. G.
Lee, Melanie M.
Ramirez, Alexandro D.
Lim, Sukbin
Goldman, Mark S.
Aksay, Emre R. F.
Population-scale organization of cerebellar granule neuron signaling during a visuomotor behavior
title Population-scale organization of cerebellar granule neuron signaling during a visuomotor behavior
title_full Population-scale organization of cerebellar granule neuron signaling during a visuomotor behavior
title_fullStr Population-scale organization of cerebellar granule neuron signaling during a visuomotor behavior
title_full_unstemmed Population-scale organization of cerebellar granule neuron signaling during a visuomotor behavior
title_short Population-scale organization of cerebellar granule neuron signaling during a visuomotor behavior
title_sort population-scale organization of cerebellar granule neuron signaling during a visuomotor behavior
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5701187/
https://www.ncbi.nlm.nih.gov/pubmed/29176570
http://dx.doi.org/10.1038/s41598-017-15938-w
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