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Purkinje Cell Activity Determines the Timing of Sensory-Evoked Motor Initiation

Cerebellar neurons can signal sensory and motor events, but their role in active sensorimotor processing remains unclear. We record and manipulate Purkinje cell activity during a task that requires mice to rapidly discriminate between multisensory and unisensory stimuli before motor initiation. Neur...

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Autores principales: Tsutsumi, Shinichiro, Chadney, Oscar, Yiu, Tin-Long, Bäumler, Edgar, Faraggiana, Lavinia, Beau, Maxime, Häusser, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7773552/
https://www.ncbi.nlm.nih.gov/pubmed/33357441
http://dx.doi.org/10.1016/j.celrep.2020.108537
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author Tsutsumi, Shinichiro
Chadney, Oscar
Yiu, Tin-Long
Bäumler, Edgar
Faraggiana, Lavinia
Beau, Maxime
Häusser, Michael
author_facet Tsutsumi, Shinichiro
Chadney, Oscar
Yiu, Tin-Long
Bäumler, Edgar
Faraggiana, Lavinia
Beau, Maxime
Häusser, Michael
author_sort Tsutsumi, Shinichiro
collection PubMed
description Cerebellar neurons can signal sensory and motor events, but their role in active sensorimotor processing remains unclear. We record and manipulate Purkinje cell activity during a task that requires mice to rapidly discriminate between multisensory and unisensory stimuli before motor initiation. Neuropixels recordings show that both sensory stimuli and motor initiation are represented by short-latency simple spikes. Optogenetic manipulation of short-latency simple spikes abolishes or delays motor initiation in a rate-dependent manner, indicating a role in motor initiation and its timing. Two-photon calcium imaging reveals task-related coherence of complex spikes organized into conserved alternating parasagittal stripes. The coherence of sensory-evoked complex spikes increases with learning and correlates with enhanced temporal precision of motor initiation. These results suggest that both simple spikes and complex spikes govern sensory-driven motor initiation: simple spikes modulate its latency, and complex spikes refine its temporal precision, providing specific cellular substrates for cerebellar sensorimotor control.
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spelling pubmed-77735522021-01-05 Purkinje Cell Activity Determines the Timing of Sensory-Evoked Motor Initiation Tsutsumi, Shinichiro Chadney, Oscar Yiu, Tin-Long Bäumler, Edgar Faraggiana, Lavinia Beau, Maxime Häusser, Michael Cell Rep Article Cerebellar neurons can signal sensory and motor events, but their role in active sensorimotor processing remains unclear. We record and manipulate Purkinje cell activity during a task that requires mice to rapidly discriminate between multisensory and unisensory stimuli before motor initiation. Neuropixels recordings show that both sensory stimuli and motor initiation are represented by short-latency simple spikes. Optogenetic manipulation of short-latency simple spikes abolishes or delays motor initiation in a rate-dependent manner, indicating a role in motor initiation and its timing. Two-photon calcium imaging reveals task-related coherence of complex spikes organized into conserved alternating parasagittal stripes. The coherence of sensory-evoked complex spikes increases with learning and correlates with enhanced temporal precision of motor initiation. These results suggest that both simple spikes and complex spikes govern sensory-driven motor initiation: simple spikes modulate its latency, and complex spikes refine its temporal precision, providing specific cellular substrates for cerebellar sensorimotor control. Cell Press 2020-12-22 /pmc/articles/PMC7773552/ /pubmed/33357441 http://dx.doi.org/10.1016/j.celrep.2020.108537 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Tsutsumi, Shinichiro
Chadney, Oscar
Yiu, Tin-Long
Bäumler, Edgar
Faraggiana, Lavinia
Beau, Maxime
Häusser, Michael
Purkinje Cell Activity Determines the Timing of Sensory-Evoked Motor Initiation
title Purkinje Cell Activity Determines the Timing of Sensory-Evoked Motor Initiation
title_full Purkinje Cell Activity Determines the Timing of Sensory-Evoked Motor Initiation
title_fullStr Purkinje Cell Activity Determines the Timing of Sensory-Evoked Motor Initiation
title_full_unstemmed Purkinje Cell Activity Determines the Timing of Sensory-Evoked Motor Initiation
title_short Purkinje Cell Activity Determines the Timing of Sensory-Evoked Motor Initiation
title_sort purkinje cell activity determines the timing of sensory-evoked motor initiation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7773552/
https://www.ncbi.nlm.nih.gov/pubmed/33357441
http://dx.doi.org/10.1016/j.celrep.2020.108537
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