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Direct translation of climbing fiber burst-mediated sensory coding into post-synaptic Purkinje cell dendritic calcium
Climbing fibers (CFs) generate complex spikes (CS) and Ca(2+) transients in cerebellar Purkinje cells (PCs), serving as instructive signals. The so-called 'all-or-none' character of CSs has been questioned since the CF burst was described. Although recent studies have indicated a sensory-d...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7581426/ https://www.ncbi.nlm.nih.gov/pubmed/32985976 http://dx.doi.org/10.7554/eLife.61593 |
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author | Roh, Seung-Eon Kim, Seung Ha Ryu, Changhyeon Kim, Chang-Eop Kim, Yong Gyu Worley, Paul F Kim, Sun Kwang Kim, Sang Jeong |
author_facet | Roh, Seung-Eon Kim, Seung Ha Ryu, Changhyeon Kim, Chang-Eop Kim, Yong Gyu Worley, Paul F Kim, Sun Kwang Kim, Sang Jeong |
author_sort | Roh, Seung-Eon |
collection | PubMed |
description | Climbing fibers (CFs) generate complex spikes (CS) and Ca(2+) transients in cerebellar Purkinje cells (PCs), serving as instructive signals. The so-called 'all-or-none' character of CSs has been questioned since the CF burst was described. Although recent studies have indicated a sensory-driven enhancement of PC Ca(2+) signals, how CF responds to sensory events and contributes to PC dendritic Ca(2+) and CS remains unexplored. Here, single or simultaneous Ca(2+) imaging of CFs and PCs in awake mice revealed the presynaptic CF Ca(2+) amplitude encoded the sensory input’s strength and directly influenced post-synaptic PC dendritic Ca(2+) amplitude. The sensory-driven variability in CF Ca(2+) amplitude depended on the number of spikes in the CF burst. Finally, the spike number of the CF burst determined the PC Ca(2+) influx and CS properties. These results reveal the direct translation of sensory information-coding CF inputs into PC Ca(2+), suggesting the sophisticated role of CFs as error signals. |
format | Online Article Text |
id | pubmed-7581426 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-75814262020-10-23 Direct translation of climbing fiber burst-mediated sensory coding into post-synaptic Purkinje cell dendritic calcium Roh, Seung-Eon Kim, Seung Ha Ryu, Changhyeon Kim, Chang-Eop Kim, Yong Gyu Worley, Paul F Kim, Sun Kwang Kim, Sang Jeong eLife Neuroscience Climbing fibers (CFs) generate complex spikes (CS) and Ca(2+) transients in cerebellar Purkinje cells (PCs), serving as instructive signals. The so-called 'all-or-none' character of CSs has been questioned since the CF burst was described. Although recent studies have indicated a sensory-driven enhancement of PC Ca(2+) signals, how CF responds to sensory events and contributes to PC dendritic Ca(2+) and CS remains unexplored. Here, single or simultaneous Ca(2+) imaging of CFs and PCs in awake mice revealed the presynaptic CF Ca(2+) amplitude encoded the sensory input’s strength and directly influenced post-synaptic PC dendritic Ca(2+) amplitude. The sensory-driven variability in CF Ca(2+) amplitude depended on the number of spikes in the CF burst. Finally, the spike number of the CF burst determined the PC Ca(2+) influx and CS properties. These results reveal the direct translation of sensory information-coding CF inputs into PC Ca(2+), suggesting the sophisticated role of CFs as error signals. eLife Sciences Publications, Ltd 2020-09-28 /pmc/articles/PMC7581426/ /pubmed/32985976 http://dx.doi.org/10.7554/eLife.61593 Text en © 2020, Roh 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 Roh, Seung-Eon Kim, Seung Ha Ryu, Changhyeon Kim, Chang-Eop Kim, Yong Gyu Worley, Paul F Kim, Sun Kwang Kim, Sang Jeong Direct translation of climbing fiber burst-mediated sensory coding into post-synaptic Purkinje cell dendritic calcium |
title | Direct translation of climbing fiber burst-mediated sensory coding into post-synaptic Purkinje cell dendritic calcium |
title_full | Direct translation of climbing fiber burst-mediated sensory coding into post-synaptic Purkinje cell dendritic calcium |
title_fullStr | Direct translation of climbing fiber burst-mediated sensory coding into post-synaptic Purkinje cell dendritic calcium |
title_full_unstemmed | Direct translation of climbing fiber burst-mediated sensory coding into post-synaptic Purkinje cell dendritic calcium |
title_short | Direct translation of climbing fiber burst-mediated sensory coding into post-synaptic Purkinje cell dendritic calcium |
title_sort | direct translation of climbing fiber burst-mediated sensory coding into post-synaptic purkinje cell dendritic calcium |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7581426/ https://www.ncbi.nlm.nih.gov/pubmed/32985976 http://dx.doi.org/10.7554/eLife.61593 |
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