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Sparse and distributed cortical populations mediate sensorimotor integration
Touch information is central to sensorimotor integration, yet little is known about how cortical touch and movement representations interact. Touch- and movement-related activity is present in both somatosensory and motor cortices, making both candidate sites for touch-motor interactions. We studied...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10542548/ https://www.ncbi.nlm.nih.gov/pubmed/37790362 http://dx.doi.org/10.1101/2023.09.21.558857 |
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author | Pancholi, Ravi Sun-Yan, Andrew Laughton, Maya Peron, Simon |
author_facet | Pancholi, Ravi Sun-Yan, Andrew Laughton, Maya Peron, Simon |
author_sort | Pancholi, Ravi |
collection | PubMed |
description | Touch information is central to sensorimotor integration, yet little is known about how cortical touch and movement representations interact. Touch- and movement-related activity is present in both somatosensory and motor cortices, making both candidate sites for touch-motor interactions. We studied touch-motor interactions in layer 2/3 of the primary vibrissal somatosensory and motor cortices of behaving mice. Volumetric two-photon calcium imaging revealed robust responses to whisker touch, whisking, and licking in both areas. Touch activity was dominated by a sparse population of broadly tuned neurons responsive to multiple whiskers that exhibited longitudinal stability and disproportionately influenced interareal communication. Movement representations were similarly dominated by sparse, stable, reciprocally projecting populations. In both areas, many broadly tuned touch cells also produced robust licking or whisking responses. These touch-licking and touch-whisking neurons showed distinct dynamics suggestive of specific roles in shaping movement. Cortical touch-motor interactions are thus mediated by specialized populations of highly responsive, broadly tuned neurons. |
format | Online Article Text |
id | pubmed-10542548 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-105425482023-10-03 Sparse and distributed cortical populations mediate sensorimotor integration Pancholi, Ravi Sun-Yan, Andrew Laughton, Maya Peron, Simon bioRxiv Article Touch information is central to sensorimotor integration, yet little is known about how cortical touch and movement representations interact. Touch- and movement-related activity is present in both somatosensory and motor cortices, making both candidate sites for touch-motor interactions. We studied touch-motor interactions in layer 2/3 of the primary vibrissal somatosensory and motor cortices of behaving mice. Volumetric two-photon calcium imaging revealed robust responses to whisker touch, whisking, and licking in both areas. Touch activity was dominated by a sparse population of broadly tuned neurons responsive to multiple whiskers that exhibited longitudinal stability and disproportionately influenced interareal communication. Movement representations were similarly dominated by sparse, stable, reciprocally projecting populations. In both areas, many broadly tuned touch cells also produced robust licking or whisking responses. These touch-licking and touch-whisking neurons showed distinct dynamics suggestive of specific roles in shaping movement. Cortical touch-motor interactions are thus mediated by specialized populations of highly responsive, broadly tuned neurons. Cold Spring Harbor Laboratory 2023-09-22 /pmc/articles/PMC10542548/ /pubmed/37790362 http://dx.doi.org/10.1101/2023.09.21.558857 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Pancholi, Ravi Sun-Yan, Andrew Laughton, Maya Peron, Simon Sparse and distributed cortical populations mediate sensorimotor integration |
title | Sparse and distributed cortical populations mediate sensorimotor integration |
title_full | Sparse and distributed cortical populations mediate sensorimotor integration |
title_fullStr | Sparse and distributed cortical populations mediate sensorimotor integration |
title_full_unstemmed | Sparse and distributed cortical populations mediate sensorimotor integration |
title_short | Sparse and distributed cortical populations mediate sensorimotor integration |
title_sort | sparse and distributed cortical populations mediate sensorimotor integration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10542548/ https://www.ncbi.nlm.nih.gov/pubmed/37790362 http://dx.doi.org/10.1101/2023.09.21.558857 |
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