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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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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. |
format | Online Article Text |
id | pubmed-7363865 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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