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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...

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Autores principales: Roh, Seung-Eon, Kim, Seung Ha, Ryu, Changhyeon, Kim, Chang-Eop, Kim, Yong Gyu, Worley, Paul F, Kim, Sun Kwang, Kim, Sang Jeong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
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.
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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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