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Long-range population dynamics of anatomically defined neocortical networks
The coordination of activity across neocortical areas is essential for mammalian brain function. Understanding this process requires simultaneous functional measurements across the cortex. In order to dissociate direct cortico-cortical interactions from other sources of neuronal correlations, it is...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4929001/ https://www.ncbi.nlm.nih.gov/pubmed/27218452 http://dx.doi.org/10.7554/eLife.14679 |
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author | Chen, Jerry L Voigt, Fabian F Javadzadeh, Mitra Krueppel, Roland Helmchen, Fritjof |
author_facet | Chen, Jerry L Voigt, Fabian F Javadzadeh, Mitra Krueppel, Roland Helmchen, Fritjof |
author_sort | Chen, Jerry L |
collection | PubMed |
description | The coordination of activity across neocortical areas is essential for mammalian brain function. Understanding this process requires simultaneous functional measurements across the cortex. In order to dissociate direct cortico-cortical interactions from other sources of neuronal correlations, it is furthermore desirable to target cross-areal recordings to neuronal subpopulations that anatomically project between areas. Here, we combined anatomical tracers with a novel multi-area two-photon microscope to perform simultaneous calcium imaging across mouse primary (S1) and secondary (S2) somatosensory whisker cortex during texture discrimination behavior, specifically identifying feedforward and feedback neurons. We find that coordination of S1-S2 activity increases during motor behaviors such as goal-directed whisking and licking. This effect was not specific to identified feedforward and feedback neurons. However, these mutually projecting neurons especially participated in inter-areal coordination when motor behavior was paired with whisker-texture touches, suggesting that direct S1-S2 interactions are sensory-dependent. Our results demonstrate specific functional coordination of anatomically-identified projection neurons across sensory cortices. DOI: http://dx.doi.org/10.7554/eLife.14679.001 |
format | Online Article Text |
id | pubmed-4929001 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-49290012016-07-05 Long-range population dynamics of anatomically defined neocortical networks Chen, Jerry L Voigt, Fabian F Javadzadeh, Mitra Krueppel, Roland Helmchen, Fritjof eLife Neuroscience The coordination of activity across neocortical areas is essential for mammalian brain function. Understanding this process requires simultaneous functional measurements across the cortex. In order to dissociate direct cortico-cortical interactions from other sources of neuronal correlations, it is furthermore desirable to target cross-areal recordings to neuronal subpopulations that anatomically project between areas. Here, we combined anatomical tracers with a novel multi-area two-photon microscope to perform simultaneous calcium imaging across mouse primary (S1) and secondary (S2) somatosensory whisker cortex during texture discrimination behavior, specifically identifying feedforward and feedback neurons. We find that coordination of S1-S2 activity increases during motor behaviors such as goal-directed whisking and licking. This effect was not specific to identified feedforward and feedback neurons. However, these mutually projecting neurons especially participated in inter-areal coordination when motor behavior was paired with whisker-texture touches, suggesting that direct S1-S2 interactions are sensory-dependent. Our results demonstrate specific functional coordination of anatomically-identified projection neurons across sensory cortices. DOI: http://dx.doi.org/10.7554/eLife.14679.001 eLife Sciences Publications, Ltd 2016-05-24 /pmc/articles/PMC4929001/ /pubmed/27218452 http://dx.doi.org/10.7554/eLife.14679 Text en © 2016, Chen et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Chen, Jerry L Voigt, Fabian F Javadzadeh, Mitra Krueppel, Roland Helmchen, Fritjof Long-range population dynamics of anatomically defined neocortical networks |
title | Long-range population dynamics of anatomically defined neocortical networks |
title_full | Long-range population dynamics of anatomically defined neocortical networks |
title_fullStr | Long-range population dynamics of anatomically defined neocortical networks |
title_full_unstemmed | Long-range population dynamics of anatomically defined neocortical networks |
title_short | Long-range population dynamics of anatomically defined neocortical networks |
title_sort | long-range population dynamics of anatomically defined neocortical networks |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4929001/ https://www.ncbi.nlm.nih.gov/pubmed/27218452 http://dx.doi.org/10.7554/eLife.14679 |
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