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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2022
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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. |
format | Online Article Text |
id | pubmed-9620742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
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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