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Movement-specific signaling is differentially distributed across motor cortex layer 5 projection neuron classes

Motor cortex generates descending output necessary for executing a wide range of limb movements. Although movement-related activity has been described throughout motor cortex, the spatiotemporal organization of movement-specific signaling in deep layers remains largely unknown. Here we record layer...

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Autores principales: Currie, Stephen P., Ammer, Julian J., Premchand, Brian, Dacre, Joshua, Wu, Yufei, Eleftheriou, Constantinos, Colligan, Matt, Clarke, Thomas, Mitchell, Leah, Faisal, A. Aldo, Hennig, Matthias H., Duguid, Ian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9620742/
https://www.ncbi.nlm.nih.gov/pubmed/35545038
http://dx.doi.org/10.1016/j.celrep.2022.110801
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author Currie, Stephen P.
Ammer, Julian J.
Premchand, Brian
Dacre, Joshua
Wu, Yufei
Eleftheriou, Constantinos
Colligan, Matt
Clarke, Thomas
Mitchell, Leah
Faisal, A. Aldo
Hennig, Matthias H.
Duguid, Ian
author_facet Currie, Stephen P.
Ammer, Julian J.
Premchand, Brian
Dacre, Joshua
Wu, Yufei
Eleftheriou, Constantinos
Colligan, Matt
Clarke, Thomas
Mitchell, Leah
Faisal, A. Aldo
Hennig, Matthias H.
Duguid, Ian
author_sort Currie, Stephen P.
collection PubMed
description Motor cortex generates descending output necessary for executing a wide range of limb movements. Although movement-related activity has been described throughout motor cortex, the spatiotemporal organization of movement-specific signaling in deep layers remains largely unknown. Here we record layer 5B population dynamics in the caudal forelimb area of motor cortex while mice perform a forelimb push/pull task and find that most neurons show movement-invariant responses, with a minority displaying movement specificity. Using cell-type-specific imaging, we identify that invariant responses dominate pyramidal tract (PT) neuron activity, with a small subpopulation representing movement type, whereas a larger proportion of intratelencephalic (IT) neurons display movement-type-specific signaling. The proportion of IT neurons decoding movement-type peaks prior to movement initiation, whereas for PT neurons, this occurs during movement execution. Our data suggest that layer 5B population dynamics largely reflect movement-invariant signaling, with information related to movement-type being routed through relatively small, distributed subpopulations of projection neurons.
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spelling pubmed-96207422022-11-02 Movement-specific signaling is differentially distributed across motor cortex layer 5 projection neuron classes Currie, Stephen P. Ammer, Julian J. Premchand, Brian Dacre, Joshua Wu, Yufei Eleftheriou, Constantinos Colligan, Matt Clarke, Thomas Mitchell, Leah Faisal, A. Aldo Hennig, Matthias H. Duguid, Ian Cell Rep Article Motor cortex generates descending output necessary for executing a wide range of limb movements. Although movement-related activity has been described throughout motor cortex, the spatiotemporal organization of movement-specific signaling in deep layers remains largely unknown. Here we record layer 5B population dynamics in the caudal forelimb area of motor cortex while mice perform a forelimb push/pull task and find that most neurons show movement-invariant responses, with a minority displaying movement specificity. Using cell-type-specific imaging, we identify that invariant responses dominate pyramidal tract (PT) neuron activity, with a small subpopulation representing movement type, whereas a larger proportion of intratelencephalic (IT) neurons display movement-type-specific signaling. The proportion of IT neurons decoding movement-type peaks prior to movement initiation, whereas for PT neurons, this occurs during movement execution. Our data suggest that layer 5B population dynamics largely reflect movement-invariant signaling, with information related to movement-type being routed through relatively small, distributed subpopulations of projection neurons. Cell Press 2022-05-10 /pmc/articles/PMC9620742/ /pubmed/35545038 http://dx.doi.org/10.1016/j.celrep.2022.110801 Text en © 2022 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
Currie, Stephen P.
Ammer, Julian J.
Premchand, Brian
Dacre, Joshua
Wu, Yufei
Eleftheriou, Constantinos
Colligan, Matt
Clarke, Thomas
Mitchell, Leah
Faisal, A. Aldo
Hennig, Matthias H.
Duguid, Ian
Movement-specific signaling is differentially distributed across motor cortex layer 5 projection neuron classes
title Movement-specific signaling is differentially distributed across motor cortex layer 5 projection neuron classes
title_full Movement-specific signaling is differentially distributed across motor cortex layer 5 projection neuron classes
title_fullStr Movement-specific signaling is differentially distributed across motor cortex layer 5 projection neuron classes
title_full_unstemmed Movement-specific signaling is differentially distributed across motor cortex layer 5 projection neuron classes
title_short Movement-specific signaling is differentially distributed across motor cortex layer 5 projection neuron classes
title_sort movement-specific signaling is differentially distributed across motor cortex layer 5 projection neuron classes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9620742/
https://www.ncbi.nlm.nih.gov/pubmed/35545038
http://dx.doi.org/10.1016/j.celrep.2022.110801
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