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Multiple signals evoked by unisensory stimulation converge onto cerebellar granule and Purkinje cells in mice

The cerebellum receives signals directly from peripheral sensory systems and indirectly from the neocortex. Even a single tactile stimulus can activate both of these pathways. Here we report how these different types of signals are integrated in the cerebellar cortex. We used in vivo whole-cell reco...

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Autores principales: Shimuta, Misa, Sugihara, Izumi, Ishikawa, Taro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7363865/
https://www.ncbi.nlm.nih.gov/pubmed/32669638
http://dx.doi.org/10.1038/s42003-020-1110-2
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author Shimuta, Misa
Sugihara, Izumi
Ishikawa, Taro
author_facet Shimuta, Misa
Sugihara, Izumi
Ishikawa, Taro
author_sort Shimuta, Misa
collection PubMed
description The cerebellum receives signals directly from peripheral sensory systems and indirectly from the neocortex. Even a single tactile stimulus can activate both of these pathways. Here we report how these different types of signals are integrated in the cerebellar cortex. We used in vivo whole-cell recordings from granule cells and unit recordings from Purkinje cells in mice in which primary somatosensory cortex (S1) could be optogenetically inhibited. Tactile stimulation of the upper lip produced two-phase granule cell responses (with latencies of ~8 ms and 29 ms), for which only the late phase was S1 dependent. In Purkinje cells, complex spikes and the late phase of simple spikes were S1 dependent. These results indicate that individual granule cells combine convergent inputs from the periphery and neocortex and send their outputs to Purkinje cells, which then integrate those signals with climbing fiber signals from the neocortex.
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spelling pubmed-73638652020-07-20 Multiple signals evoked by unisensory stimulation converge onto cerebellar granule and Purkinje cells in mice Shimuta, Misa Sugihara, Izumi Ishikawa, Taro Commun Biol Article The cerebellum receives signals directly from peripheral sensory systems and indirectly from the neocortex. Even a single tactile stimulus can activate both of these pathways. Here we report how these different types of signals are integrated in the cerebellar cortex. We used in vivo whole-cell recordings from granule cells and unit recordings from Purkinje cells in mice in which primary somatosensory cortex (S1) could be optogenetically inhibited. Tactile stimulation of the upper lip produced two-phase granule cell responses (with latencies of ~8 ms and 29 ms), for which only the late phase was S1 dependent. In Purkinje cells, complex spikes and the late phase of simple spikes were S1 dependent. These results indicate that individual granule cells combine convergent inputs from the periphery and neocortex and send their outputs to Purkinje cells, which then integrate those signals with climbing fiber signals from the neocortex. Nature Publishing Group UK 2020-07-15 /pmc/articles/PMC7363865/ /pubmed/32669638 http://dx.doi.org/10.1038/s42003-020-1110-2 Text en © The Author(s) 2020 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
Shimuta, Misa
Sugihara, Izumi
Ishikawa, Taro
Multiple signals evoked by unisensory stimulation converge onto cerebellar granule and Purkinje cells in mice
title Multiple signals evoked by unisensory stimulation converge onto cerebellar granule and Purkinje cells in mice
title_full Multiple signals evoked by unisensory stimulation converge onto cerebellar granule and Purkinje cells in mice
title_fullStr Multiple signals evoked by unisensory stimulation converge onto cerebellar granule and Purkinje cells in mice
title_full_unstemmed Multiple signals evoked by unisensory stimulation converge onto cerebellar granule and Purkinje cells in mice
title_short Multiple signals evoked by unisensory stimulation converge onto cerebellar granule and Purkinje cells in mice
title_sort multiple signals evoked by unisensory stimulation converge onto cerebellar granule and purkinje cells in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7363865/
https://www.ncbi.nlm.nih.gov/pubmed/32669638
http://dx.doi.org/10.1038/s42003-020-1110-2
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