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Potentiation of cerebellar Purkinje cells facilitates whisker reflex adaptation through increased simple spike activity

Cerebellar plasticity underlies motor learning. However, how the cerebellum operates to enable learned changes in motor output is largely unknown. We developed a sensory-driven adaptation protocol for reflexive whisker protraction and recorded Purkinje cell activity from crus 1 and 2 of awake mice....

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Autores principales: Romano, Vincenzo, De Propris, Licia, Bosman, Laurens WJ, Warnaar, Pascal, ten Brinke, Michiel M, Lindeman, Sander, Ju, Chiheng, Velauthapillai, Arthiha, Spanke, Jochen K, Middendorp Guerra, Emily, Hoogland, Tycho M, Negrello, Mario, D'Angelo, Egidio, De Zeeuw, Chris I
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6326726/
https://www.ncbi.nlm.nih.gov/pubmed/30561331
http://dx.doi.org/10.7554/eLife.38852
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author Romano, Vincenzo
De Propris, Licia
Bosman, Laurens WJ
Warnaar, Pascal
ten Brinke, Michiel M
Lindeman, Sander
Ju, Chiheng
Velauthapillai, Arthiha
Spanke, Jochen K
Middendorp Guerra, Emily
Hoogland, Tycho M
Negrello, Mario
D'Angelo, Egidio
De Zeeuw, Chris I
author_facet Romano, Vincenzo
De Propris, Licia
Bosman, Laurens WJ
Warnaar, Pascal
ten Brinke, Michiel M
Lindeman, Sander
Ju, Chiheng
Velauthapillai, Arthiha
Spanke, Jochen K
Middendorp Guerra, Emily
Hoogland, Tycho M
Negrello, Mario
D'Angelo, Egidio
De Zeeuw, Chris I
author_sort Romano, Vincenzo
collection PubMed
description Cerebellar plasticity underlies motor learning. However, how the cerebellum operates to enable learned changes in motor output is largely unknown. We developed a sensory-driven adaptation protocol for reflexive whisker protraction and recorded Purkinje cell activity from crus 1 and 2 of awake mice. Before training, simple spikes of individual Purkinje cells correlated during reflexive protraction with the whisker position without lead or lag. After training, simple spikes and whisker protractions were both enhanced with the spiking activity now leading behavioral responses. Neuronal and behavioral changes did not occur in two cell-specific mouse models with impaired long-term potentiation at their parallel fiber to Purkinje cell synapses. Consistent with cerebellar plasticity rules, increased simple spike activity was prominent in cells with low complex spike response probability. Thus, potentiation at parallel fiber to Purkinje cell synapses may contribute to reflex adaptation and enable expression of cerebellar learning through increases in simple spike activity.
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spelling pubmed-63267262019-01-11 Potentiation of cerebellar Purkinje cells facilitates whisker reflex adaptation through increased simple spike activity Romano, Vincenzo De Propris, Licia Bosman, Laurens WJ Warnaar, Pascal ten Brinke, Michiel M Lindeman, Sander Ju, Chiheng Velauthapillai, Arthiha Spanke, Jochen K Middendorp Guerra, Emily Hoogland, Tycho M Negrello, Mario D'Angelo, Egidio De Zeeuw, Chris I eLife Neuroscience Cerebellar plasticity underlies motor learning. However, how the cerebellum operates to enable learned changes in motor output is largely unknown. We developed a sensory-driven adaptation protocol for reflexive whisker protraction and recorded Purkinje cell activity from crus 1 and 2 of awake mice. Before training, simple spikes of individual Purkinje cells correlated during reflexive protraction with the whisker position without lead or lag. After training, simple spikes and whisker protractions were both enhanced with the spiking activity now leading behavioral responses. Neuronal and behavioral changes did not occur in two cell-specific mouse models with impaired long-term potentiation at their parallel fiber to Purkinje cell synapses. Consistent with cerebellar plasticity rules, increased simple spike activity was prominent in cells with low complex spike response probability. Thus, potentiation at parallel fiber to Purkinje cell synapses may contribute to reflex adaptation and enable expression of cerebellar learning through increases in simple spike activity. eLife Sciences Publications, Ltd 2018-12-18 /pmc/articles/PMC6326726/ /pubmed/30561331 http://dx.doi.org/10.7554/eLife.38852 Text en © 2018, Romano 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
Romano, Vincenzo
De Propris, Licia
Bosman, Laurens WJ
Warnaar, Pascal
ten Brinke, Michiel M
Lindeman, Sander
Ju, Chiheng
Velauthapillai, Arthiha
Spanke, Jochen K
Middendorp Guerra, Emily
Hoogland, Tycho M
Negrello, Mario
D'Angelo, Egidio
De Zeeuw, Chris I
Potentiation of cerebellar Purkinje cells facilitates whisker reflex adaptation through increased simple spike activity
title Potentiation of cerebellar Purkinje cells facilitates whisker reflex adaptation through increased simple spike activity
title_full Potentiation of cerebellar Purkinje cells facilitates whisker reflex adaptation through increased simple spike activity
title_fullStr Potentiation of cerebellar Purkinje cells facilitates whisker reflex adaptation through increased simple spike activity
title_full_unstemmed Potentiation of cerebellar Purkinje cells facilitates whisker reflex adaptation through increased simple spike activity
title_short Potentiation of cerebellar Purkinje cells facilitates whisker reflex adaptation through increased simple spike activity
title_sort potentiation of cerebellar purkinje cells facilitates whisker reflex adaptation through increased simple spike activity
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6326726/
https://www.ncbi.nlm.nih.gov/pubmed/30561331
http://dx.doi.org/10.7554/eLife.38852
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