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Frontal cortical control of posterior sensory and association cortices through the claustrum
The claustrum is a telencephalic gray matter nucleus that is richly interconnected with the neocortex. This structure subserves top-down executive functions that require frontal cortical control of posterior cortical regions. However, functional anatomical support for the claustrum allowing for long...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995986/ https://www.ncbi.nlm.nih.gov/pubmed/29623428 http://dx.doi.org/10.1007/s00429-018-1661-x |
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author | White, Michael G. Mathur, Brian N. |
author_facet | White, Michael G. Mathur, Brian N. |
author_sort | White, Michael G. |
collection | PubMed |
description | The claustrum is a telencephalic gray matter nucleus that is richly interconnected with the neocortex. This structure subserves top-down executive functions that require frontal cortical control of posterior cortical regions. However, functional anatomical support for the claustrum allowing for long-range intercortical communication is lacking. To test this, we performed a channelrhodopsin-assisted long-circuit mapping strategy in mouse brain slices. We find that anterior cingulate cortex input to the claustrum is transiently amplified by claustrum neurons that, in turn, project to parietal association cortex or to primary and secondary visual cortices. Additionally, we observe that claustrum drive of cortical neurons in parietal association cortex is layer-specific, eliciting action potential generation briefly in layers II/III, IV, and VI but not V. These data are the first to provide a functional anatomical substrate through claustrum that may underlie top-down functions, such as executive attention or working memory, providing critical insight to this most interconnected and enigmatic nucleus. |
format | Online Article Text |
id | pubmed-5995986 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-59959862018-06-25 Frontal cortical control of posterior sensory and association cortices through the claustrum White, Michael G. Mathur, Brian N. Brain Struct Funct Short Communication The claustrum is a telencephalic gray matter nucleus that is richly interconnected with the neocortex. This structure subserves top-down executive functions that require frontal cortical control of posterior cortical regions. However, functional anatomical support for the claustrum allowing for long-range intercortical communication is lacking. To test this, we performed a channelrhodopsin-assisted long-circuit mapping strategy in mouse brain slices. We find that anterior cingulate cortex input to the claustrum is transiently amplified by claustrum neurons that, in turn, project to parietal association cortex or to primary and secondary visual cortices. Additionally, we observe that claustrum drive of cortical neurons in parietal association cortex is layer-specific, eliciting action potential generation briefly in layers II/III, IV, and VI but not V. These data are the first to provide a functional anatomical substrate through claustrum that may underlie top-down functions, such as executive attention or working memory, providing critical insight to this most interconnected and enigmatic nucleus. Springer Berlin Heidelberg 2018-04-06 2018 /pmc/articles/PMC5995986/ /pubmed/29623428 http://dx.doi.org/10.1007/s00429-018-1661-x Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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. |
spellingShingle | Short Communication White, Michael G. Mathur, Brian N. Frontal cortical control of posterior sensory and association cortices through the claustrum |
title | Frontal cortical control of posterior sensory and association cortices through the claustrum |
title_full | Frontal cortical control of posterior sensory and association cortices through the claustrum |
title_fullStr | Frontal cortical control of posterior sensory and association cortices through the claustrum |
title_full_unstemmed | Frontal cortical control of posterior sensory and association cortices through the claustrum |
title_short | Frontal cortical control of posterior sensory and association cortices through the claustrum |
title_sort | frontal cortical control of posterior sensory and association cortices through the claustrum |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995986/ https://www.ncbi.nlm.nih.gov/pubmed/29623428 http://dx.doi.org/10.1007/s00429-018-1661-x |
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