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Brain-wide connectivity map of mouse thermosensory cortices
In the thermal system, skin cooling is represented in the primary somatosensory cortex (S1) and the posterior insular cortex (pIC). Whether S1 and pIC are nodes in anatomically separate or overlapping thermal sensorimotor pathways is unclear, as the brain-wide connectivity of the thermal system has...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10110442/ https://www.ncbi.nlm.nih.gov/pubmed/36255325 http://dx.doi.org/10.1093/cercor/bhac386 |
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author | Bokiniec, Phillip Whitmire, Clarissa J Leva, Tobias M Poulet, James F A |
author_facet | Bokiniec, Phillip Whitmire, Clarissa J Leva, Tobias M Poulet, James F A |
author_sort | Bokiniec, Phillip |
collection | PubMed |
description | In the thermal system, skin cooling is represented in the primary somatosensory cortex (S1) and the posterior insular cortex (pIC). Whether S1 and pIC are nodes in anatomically separate or overlapping thermal sensorimotor pathways is unclear, as the brain-wide connectivity of the thermal system has not been mapped. We address this using functionally targeted, dual injections of anterograde viruses or retrograde tracers into the forelimb representation of S1 (fS1) and pIC (fpIC). Our data show that inputs to fS1 and fpIC originate from separate neuronal populations, supporting the existence of parallel input pathways. Outputs from fS1 and fpIC are more widespread than their inputs, sharing a number of cortical and subcortical targets. While, axonal projections were separable, they were more overlapping than the clusters of input cells. In both fS1 and fpIC circuits, there was a high degree of reciprocal connectivity with thalamic and cortical regions, but unidirectional output to the midbrain and hindbrain. Notably, fpIC showed connectivity with regions associated with thermal processing. Together, these data indicate that cutaneous thermal information is routed to the cortex via parallel circuits and is forwarded to overlapping downstream regions for the binding of somatosensory percepts and integration with ongoing behavior. |
format | Online Article Text |
id | pubmed-10110442 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-101104422023-04-19 Brain-wide connectivity map of mouse thermosensory cortices Bokiniec, Phillip Whitmire, Clarissa J Leva, Tobias M Poulet, James F A Cereb Cortex Original Article In the thermal system, skin cooling is represented in the primary somatosensory cortex (S1) and the posterior insular cortex (pIC). Whether S1 and pIC are nodes in anatomically separate or overlapping thermal sensorimotor pathways is unclear, as the brain-wide connectivity of the thermal system has not been mapped. We address this using functionally targeted, dual injections of anterograde viruses or retrograde tracers into the forelimb representation of S1 (fS1) and pIC (fpIC). Our data show that inputs to fS1 and fpIC originate from separate neuronal populations, supporting the existence of parallel input pathways. Outputs from fS1 and fpIC are more widespread than their inputs, sharing a number of cortical and subcortical targets. While, axonal projections were separable, they were more overlapping than the clusters of input cells. In both fS1 and fpIC circuits, there was a high degree of reciprocal connectivity with thalamic and cortical regions, but unidirectional output to the midbrain and hindbrain. Notably, fpIC showed connectivity with regions associated with thermal processing. Together, these data indicate that cutaneous thermal information is routed to the cortex via parallel circuits and is forwarded to overlapping downstream regions for the binding of somatosensory percepts and integration with ongoing behavior. Oxford University Press 2022-10-18 /pmc/articles/PMC10110442/ /pubmed/36255325 http://dx.doi.org/10.1093/cercor/bhac386 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Bokiniec, Phillip Whitmire, Clarissa J Leva, Tobias M Poulet, James F A Brain-wide connectivity map of mouse thermosensory cortices |
title | Brain-wide connectivity map of mouse thermosensory cortices |
title_full | Brain-wide connectivity map of mouse thermosensory cortices |
title_fullStr | Brain-wide connectivity map of mouse thermosensory cortices |
title_full_unstemmed | Brain-wide connectivity map of mouse thermosensory cortices |
title_short | Brain-wide connectivity map of mouse thermosensory cortices |
title_sort | brain-wide connectivity map of mouse thermosensory cortices |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10110442/ https://www.ncbi.nlm.nih.gov/pubmed/36255325 http://dx.doi.org/10.1093/cercor/bhac386 |
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