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A cerebellar-thalamocortical pathway drives behavioral context-dependent movement initiation

Executing learned motor behaviors often requires the transformation of sensory cues into patterns of motor commands that generate appropriately timed actions. The cerebellum and thalamus are two key areas involved in shaping cortical output and movement, but the contribution of a cerebellar-thalamoc...

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Autores principales: Dacre, Joshua, Colligan, Matt, Clarke, Thomas, Ammer, Julian J., Schiemann, Julia, Chamosa-Pino, Victor, Claudi, Federico, Harston, J. Alex, Eleftheriou, Constantinos, Pakan, Janelle M.P., Huang, Cheng-Chiu, Hantman, Adam W., Rochefort, Nathalie L., Duguid, Ian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8315304/
https://www.ncbi.nlm.nih.gov/pubmed/34146469
http://dx.doi.org/10.1016/j.neuron.2021.05.016
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author Dacre, Joshua
Colligan, Matt
Clarke, Thomas
Ammer, Julian J.
Schiemann, Julia
Chamosa-Pino, Victor
Claudi, Federico
Harston, J. Alex
Eleftheriou, Constantinos
Pakan, Janelle M.P.
Huang, Cheng-Chiu
Hantman, Adam W.
Rochefort, Nathalie L.
Duguid, Ian
author_facet Dacre, Joshua
Colligan, Matt
Clarke, Thomas
Ammer, Julian J.
Schiemann, Julia
Chamosa-Pino, Victor
Claudi, Federico
Harston, J. Alex
Eleftheriou, Constantinos
Pakan, Janelle M.P.
Huang, Cheng-Chiu
Hantman, Adam W.
Rochefort, Nathalie L.
Duguid, Ian
author_sort Dacre, Joshua
collection PubMed
description Executing learned motor behaviors often requires the transformation of sensory cues into patterns of motor commands that generate appropriately timed actions. The cerebellum and thalamus are two key areas involved in shaping cortical output and movement, but the contribution of a cerebellar-thalamocortical pathway to voluntary movement initiation remains poorly understood. Here, we investigated how an auditory “go cue” transforms thalamocortical activity patterns and how these changes relate to movement initiation. Population responses in dentate/interpositus-recipient regions of motor thalamus reflect a time-locked increase in activity immediately prior to movement initiation that is temporally uncoupled from the go cue, indicative of a fixed-latency feedforward motor timing signal. Blocking cerebellar or motor thalamic output suppresses movement initiation, while stimulation triggers movements in a behavioral context-dependent manner. Our findings show how cerebellar output, via the thalamus, shapes cortical activity patterns necessary for learned context-dependent movement initiation.
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spelling pubmed-83153042021-07-31 A cerebellar-thalamocortical pathway drives behavioral context-dependent movement initiation Dacre, Joshua Colligan, Matt Clarke, Thomas Ammer, Julian J. Schiemann, Julia Chamosa-Pino, Victor Claudi, Federico Harston, J. Alex Eleftheriou, Constantinos Pakan, Janelle M.P. Huang, Cheng-Chiu Hantman, Adam W. Rochefort, Nathalie L. Duguid, Ian Neuron Article Executing learned motor behaviors often requires the transformation of sensory cues into patterns of motor commands that generate appropriately timed actions. The cerebellum and thalamus are two key areas involved in shaping cortical output and movement, but the contribution of a cerebellar-thalamocortical pathway to voluntary movement initiation remains poorly understood. Here, we investigated how an auditory “go cue” transforms thalamocortical activity patterns and how these changes relate to movement initiation. Population responses in dentate/interpositus-recipient regions of motor thalamus reflect a time-locked increase in activity immediately prior to movement initiation that is temporally uncoupled from the go cue, indicative of a fixed-latency feedforward motor timing signal. Blocking cerebellar or motor thalamic output suppresses movement initiation, while stimulation triggers movements in a behavioral context-dependent manner. Our findings show how cerebellar output, via the thalamus, shapes cortical activity patterns necessary for learned context-dependent movement initiation. Cell Press 2021-07-21 /pmc/articles/PMC8315304/ /pubmed/34146469 http://dx.doi.org/10.1016/j.neuron.2021.05.016 Text en © 2021 The Authors https://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
Dacre, Joshua
Colligan, Matt
Clarke, Thomas
Ammer, Julian J.
Schiemann, Julia
Chamosa-Pino, Victor
Claudi, Federico
Harston, J. Alex
Eleftheriou, Constantinos
Pakan, Janelle M.P.
Huang, Cheng-Chiu
Hantman, Adam W.
Rochefort, Nathalie L.
Duguid, Ian
A cerebellar-thalamocortical pathway drives behavioral context-dependent movement initiation
title A cerebellar-thalamocortical pathway drives behavioral context-dependent movement initiation
title_full A cerebellar-thalamocortical pathway drives behavioral context-dependent movement initiation
title_fullStr A cerebellar-thalamocortical pathway drives behavioral context-dependent movement initiation
title_full_unstemmed A cerebellar-thalamocortical pathway drives behavioral context-dependent movement initiation
title_short A cerebellar-thalamocortical pathway drives behavioral context-dependent movement initiation
title_sort cerebellar-thalamocortical pathway drives behavioral context-dependent movement initiation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8315304/
https://www.ncbi.nlm.nih.gov/pubmed/34146469
http://dx.doi.org/10.1016/j.neuron.2021.05.016
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