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Layer-specific integration of locomotion and sensory information in mouse barrel cortex

During navigation, rodents continually sample the environment with their whiskers. How locomotion modulates neuronal activity in somatosensory cortex, and how it is integrated with whisker-touch remains unclear. Here, we compared neuronal activity in layer 2/3 (L2/3) and L5 of barrel cortex using ca...

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Autores principales: Ayaz, Aslı, Stäuble, Andreas, Hamada, Morio, Wulf, Marie-Angela, Saleem, Aman B., Helmchen, Fritjof
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6565743/
https://www.ncbi.nlm.nih.gov/pubmed/31197148
http://dx.doi.org/10.1038/s41467-019-10564-8
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author Ayaz, Aslı
Stäuble, Andreas
Hamada, Morio
Wulf, Marie-Angela
Saleem, Aman B.
Helmchen, Fritjof
author_facet Ayaz, Aslı
Stäuble, Andreas
Hamada, Morio
Wulf, Marie-Angela
Saleem, Aman B.
Helmchen, Fritjof
author_sort Ayaz, Aslı
collection PubMed
description During navigation, rodents continually sample the environment with their whiskers. How locomotion modulates neuronal activity in somatosensory cortex, and how it is integrated with whisker-touch remains unclear. Here, we compared neuronal activity in layer 2/3 (L2/3) and L5 of barrel cortex using calcium imaging in mice running in a tactile virtual reality. Both layers increase their activity during running and concomitant whisking, in the absence of touch. Fewer neurons are modulated by whisking alone. Whereas L5 neurons respond transiently to wall-touch during running, L2/3 neurons show sustained activity. Consistently, neurons encoding running-with-touch are more abundant in L2/3 and they encode the run-speed better during touch. Few neurons across layers were also sensitive to abrupt perturbations of tactile flow during running. In summary, locomotion significantly enhances barrel cortex activity across layers with L5 neurons mainly reporting changes in touch conditions and L2/3 neurons continually integrating tactile stimuli with running.
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spelling pubmed-65657432019-06-21 Layer-specific integration of locomotion and sensory information in mouse barrel cortex Ayaz, Aslı Stäuble, Andreas Hamada, Morio Wulf, Marie-Angela Saleem, Aman B. Helmchen, Fritjof Nat Commun Article During navigation, rodents continually sample the environment with their whiskers. How locomotion modulates neuronal activity in somatosensory cortex, and how it is integrated with whisker-touch remains unclear. Here, we compared neuronal activity in layer 2/3 (L2/3) and L5 of barrel cortex using calcium imaging in mice running in a tactile virtual reality. Both layers increase their activity during running and concomitant whisking, in the absence of touch. Fewer neurons are modulated by whisking alone. Whereas L5 neurons respond transiently to wall-touch during running, L2/3 neurons show sustained activity. Consistently, neurons encoding running-with-touch are more abundant in L2/3 and they encode the run-speed better during touch. Few neurons across layers were also sensitive to abrupt perturbations of tactile flow during running. In summary, locomotion significantly enhances barrel cortex activity across layers with L5 neurons mainly reporting changes in touch conditions and L2/3 neurons continually integrating tactile stimuli with running. Nature Publishing Group UK 2019-06-13 /pmc/articles/PMC6565743/ /pubmed/31197148 http://dx.doi.org/10.1038/s41467-019-10564-8 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ayaz, Aslı
Stäuble, Andreas
Hamada, Morio
Wulf, Marie-Angela
Saleem, Aman B.
Helmchen, Fritjof
Layer-specific integration of locomotion and sensory information in mouse barrel cortex
title Layer-specific integration of locomotion and sensory information in mouse barrel cortex
title_full Layer-specific integration of locomotion and sensory information in mouse barrel cortex
title_fullStr Layer-specific integration of locomotion and sensory information in mouse barrel cortex
title_full_unstemmed Layer-specific integration of locomotion and sensory information in mouse barrel cortex
title_short Layer-specific integration of locomotion and sensory information in mouse barrel cortex
title_sort layer-specific integration of locomotion and sensory information in mouse barrel cortex
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6565743/
https://www.ncbi.nlm.nih.gov/pubmed/31197148
http://dx.doi.org/10.1038/s41467-019-10564-8
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