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Layer 5 Intratelencephalic Neurons in the Motor Cortex Stably Encode Skilled Movement
The primary motor cortex (M1) and the dorsal striatum play a critical role in motor learning and the retention of learned behaviors. Motor representations of corticostriatal ensembles emerge during motor learning. In the coordinated reorganization of M1 and the dorsal striatum for motor learning, la...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for Neuroscience
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10601372/ https://www.ncbi.nlm.nih.gov/pubmed/37699714 http://dx.doi.org/10.1523/JNEUROSCI.0428-23.2023 |
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author | Shinotsuka, Takanori Tanaka, Yasuhiro R. Terada, Shin-Ichiro Hatano, Natsuki Matsuzaki, Masanori |
author_facet | Shinotsuka, Takanori Tanaka, Yasuhiro R. Terada, Shin-Ichiro Hatano, Natsuki Matsuzaki, Masanori |
author_sort | Shinotsuka, Takanori |
collection | PubMed |
description | The primary motor cortex (M1) and the dorsal striatum play a critical role in motor learning and the retention of learned behaviors. Motor representations of corticostriatal ensembles emerge during motor learning. In the coordinated reorganization of M1 and the dorsal striatum for motor learning, layer 5a (L5a) which connects M1 to the ipsilateral and contralateral dorsal striatum, should be a key layer. Although M1 L5a neurons represent movement-related activity in the late stage of learning, it is unclear whether the activity is retained as a memory engram. Here, using Tlx3-Cre male transgenic mice, we conducted two-photon calcium imaging of striatum-projecting L5a intratelencephalic (IT) neurons in forelimb M1 during late sessions of a self-initiated lever-pull task and in sessions after 6 d of nontraining following the late sessions. We found that trained male animals exhibited stable motor performance before and after the nontraining days. At the same time, we found that M1 L5a IT neurons strongly represented the well-learned forelimb movement but not uninstructed orofacial movements. A subset of M1 L5a IT neurons consistently coded the well-learned forelimb movement before and after the nontraining days. Inactivation of M1 IT neurons after learning impaired task performance when the lever was made heavier or when the target range of the pull distance was narrowed. These results suggest that a subset of M1 L5a IT neurons continuously represent skilled movement after learning and serve to fine-tune the kinematics of well-learned movement. SIGNIFICANCE STATEMENT Motor memory persists even when it is not used for a while. IT neurons in L5a of the M1 gradually come to represent skilled forelimb movements during motor learning. However, it remains to be determined whether these changes persist over a long period and how these neurons contribute to skilled movements. Here, we show that a subset of M1 L5a IT neurons retain information for skilled forelimb movements even after nontraining days. Furthermore, suppressing the activity of these neurons during skilled forelimb movements impaired behavioral stability and adaptability. Our results suggest the importance of M1 L5a IT neurons for tuning skilled forelimb movements over a long period. |
format | Online Article Text |
id | pubmed-10601372 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Society for Neuroscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-106013722023-10-27 Layer 5 Intratelencephalic Neurons in the Motor Cortex Stably Encode Skilled Movement Shinotsuka, Takanori Tanaka, Yasuhiro R. Terada, Shin-Ichiro Hatano, Natsuki Matsuzaki, Masanori J Neurosci Research Articles The primary motor cortex (M1) and the dorsal striatum play a critical role in motor learning and the retention of learned behaviors. Motor representations of corticostriatal ensembles emerge during motor learning. In the coordinated reorganization of M1 and the dorsal striatum for motor learning, layer 5a (L5a) which connects M1 to the ipsilateral and contralateral dorsal striatum, should be a key layer. Although M1 L5a neurons represent movement-related activity in the late stage of learning, it is unclear whether the activity is retained as a memory engram. Here, using Tlx3-Cre male transgenic mice, we conducted two-photon calcium imaging of striatum-projecting L5a intratelencephalic (IT) neurons in forelimb M1 during late sessions of a self-initiated lever-pull task and in sessions after 6 d of nontraining following the late sessions. We found that trained male animals exhibited stable motor performance before and after the nontraining days. At the same time, we found that M1 L5a IT neurons strongly represented the well-learned forelimb movement but not uninstructed orofacial movements. A subset of M1 L5a IT neurons consistently coded the well-learned forelimb movement before and after the nontraining days. Inactivation of M1 IT neurons after learning impaired task performance when the lever was made heavier or when the target range of the pull distance was narrowed. These results suggest that a subset of M1 L5a IT neurons continuously represent skilled movement after learning and serve to fine-tune the kinematics of well-learned movement. SIGNIFICANCE STATEMENT Motor memory persists even when it is not used for a while. IT neurons in L5a of the M1 gradually come to represent skilled forelimb movements during motor learning. However, it remains to be determined whether these changes persist over a long period and how these neurons contribute to skilled movements. Here, we show that a subset of M1 L5a IT neurons retain information for skilled forelimb movements even after nontraining days. Furthermore, suppressing the activity of these neurons during skilled forelimb movements impaired behavioral stability and adaptability. Our results suggest the importance of M1 L5a IT neurons for tuning skilled forelimb movements over a long period. Society for Neuroscience 2023-10-25 /pmc/articles/PMC10601372/ /pubmed/37699714 http://dx.doi.org/10.1523/JNEUROSCI.0428-23.2023 Text en Copyright © 2023 Shinotsuka et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Articles Shinotsuka, Takanori Tanaka, Yasuhiro R. Terada, Shin-Ichiro Hatano, Natsuki Matsuzaki, Masanori Layer 5 Intratelencephalic Neurons in the Motor Cortex Stably Encode Skilled Movement |
title | Layer 5 Intratelencephalic Neurons in the Motor Cortex Stably Encode Skilled Movement |
title_full | Layer 5 Intratelencephalic Neurons in the Motor Cortex Stably Encode Skilled Movement |
title_fullStr | Layer 5 Intratelencephalic Neurons in the Motor Cortex Stably Encode Skilled Movement |
title_full_unstemmed | Layer 5 Intratelencephalic Neurons in the Motor Cortex Stably Encode Skilled Movement |
title_short | Layer 5 Intratelencephalic Neurons in the Motor Cortex Stably Encode Skilled Movement |
title_sort | layer 5 intratelencephalic neurons in the motor cortex stably encode skilled movement |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10601372/ https://www.ncbi.nlm.nih.gov/pubmed/37699714 http://dx.doi.org/10.1523/JNEUROSCI.0428-23.2023 |
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