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Motor cortical output for skilled forelimb movement is selectively distributed across projection neuron classes
The interaction of descending neocortical outputs and subcortical premotor circuits is critical for shaping skilled movements. Two broad classes of motor cortical output projection neurons provide input to many subcortical motor areas: pyramidal tract (PT) neurons, which project throughout the neura...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8906739/ https://www.ncbi.nlm.nih.gov/pubmed/35263129 http://dx.doi.org/10.1126/sciadv.abj5167 |
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author | Park, Junchol Phillips, James W. Guo, Jian-Zhong Martin, Kathleen A. Hantman, Adam W. Dudman, Joshua T. |
author_facet | Park, Junchol Phillips, James W. Guo, Jian-Zhong Martin, Kathleen A. Hantman, Adam W. Dudman, Joshua T. |
author_sort | Park, Junchol |
collection | PubMed |
description | The interaction of descending neocortical outputs and subcortical premotor circuits is critical for shaping skilled movements. Two broad classes of motor cortical output projection neurons provide input to many subcortical motor areas: pyramidal tract (PT) neurons, which project throughout the neuraxis, and intratelencephalic (IT) neurons, which project within the cortex and subcortical striatum. It is unclear whether these classes are functionally in series or whether each class carries distinct components of descending motor control signals. Here, we combine large-scale neural recordings across all layers of motor cortex with cell type–specific perturbations to study cortically dependent mouse motor behaviors: kinematically variable manipulation of a joystick and a kinematically precise reach-to-grasp. We find that striatum-projecting IT neuron activity preferentially represents amplitude, whereas pons-projecting PT neurons preferentially represent the variable direction of forelimb movements. Thus, separable components of descending motor cortical commands are distributed across motor cortical projection cell classes. |
format | Online Article Text |
id | pubmed-8906739 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-89067392022-03-21 Motor cortical output for skilled forelimb movement is selectively distributed across projection neuron classes Park, Junchol Phillips, James W. Guo, Jian-Zhong Martin, Kathleen A. Hantman, Adam W. Dudman, Joshua T. Sci Adv Neuroscience The interaction of descending neocortical outputs and subcortical premotor circuits is critical for shaping skilled movements. Two broad classes of motor cortical output projection neurons provide input to many subcortical motor areas: pyramidal tract (PT) neurons, which project throughout the neuraxis, and intratelencephalic (IT) neurons, which project within the cortex and subcortical striatum. It is unclear whether these classes are functionally in series or whether each class carries distinct components of descending motor control signals. Here, we combine large-scale neural recordings across all layers of motor cortex with cell type–specific perturbations to study cortically dependent mouse motor behaviors: kinematically variable manipulation of a joystick and a kinematically precise reach-to-grasp. We find that striatum-projecting IT neuron activity preferentially represents amplitude, whereas pons-projecting PT neurons preferentially represent the variable direction of forelimb movements. Thus, separable components of descending motor cortical commands are distributed across motor cortical projection cell classes. American Association for the Advancement of Science 2022-03-09 /pmc/articles/PMC8906739/ /pubmed/35263129 http://dx.doi.org/10.1126/sciadv.abj5167 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Neuroscience Park, Junchol Phillips, James W. Guo, Jian-Zhong Martin, Kathleen A. Hantman, Adam W. Dudman, Joshua T. Motor cortical output for skilled forelimb movement is selectively distributed across projection neuron classes |
title | Motor cortical output for skilled forelimb movement is selectively distributed across projection neuron classes |
title_full | Motor cortical output for skilled forelimb movement is selectively distributed across projection neuron classes |
title_fullStr | Motor cortical output for skilled forelimb movement is selectively distributed across projection neuron classes |
title_full_unstemmed | Motor cortical output for skilled forelimb movement is selectively distributed across projection neuron classes |
title_short | Motor cortical output for skilled forelimb movement is selectively distributed across projection neuron classes |
title_sort | motor cortical output for skilled forelimb movement is selectively distributed across projection neuron classes |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8906739/ https://www.ncbi.nlm.nih.gov/pubmed/35263129 http://dx.doi.org/10.1126/sciadv.abj5167 |
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