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Thalamocortical control of cell-type specificity drives circuits for processing whisker-related information in mouse barrel cortex
Excitatory spiny stellate neurons are prominently featured in the cortical circuits of sensory modalities that provide high salience and high acuity representations of the environment. These specialized neurons are considered developmentally linked to bottom-up inputs from the thalamus, however, the...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10539368/ https://www.ncbi.nlm.nih.gov/pubmed/37770450 http://dx.doi.org/10.1038/s41467-023-41749-x |
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author | Young, Timothy R. Yamamoto, Mariko Kikuchi, Satomi S. Yoshida, Aya C. Abe, Takaya Inoue, Kenichi Johansen, Joshua P. Benucci, Andrea Yoshimura, Yumiko Shimogori, Tomomi |
author_facet | Young, Timothy R. Yamamoto, Mariko Kikuchi, Satomi S. Yoshida, Aya C. Abe, Takaya Inoue, Kenichi Johansen, Joshua P. Benucci, Andrea Yoshimura, Yumiko Shimogori, Tomomi |
author_sort | Young, Timothy R. |
collection | PubMed |
description | Excitatory spiny stellate neurons are prominently featured in the cortical circuits of sensory modalities that provide high salience and high acuity representations of the environment. These specialized neurons are considered developmentally linked to bottom-up inputs from the thalamus, however, the molecular mechanisms underlying their diversification and function are unknown. Here, we investigated this in mouse somatosensory cortex, where spiny stellate neurons and pyramidal neurons have distinct roles in processing whisker-evoked signals. Utilizing spatial transcriptomics, we identified reciprocal patterns of gene expression which correlated with these cell-types and were linked to innervation by specific thalamic inputs during development. Genetic manipulation that prevents the acquisition of spiny stellate fate highlighted an important role for these neurons in processing distinct whisker signals within functional cortical columns, and as a key driver in the formation of specific whisker-related circuits in the cortex. |
format | Online Article Text |
id | pubmed-10539368 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105393682023-09-30 Thalamocortical control of cell-type specificity drives circuits for processing whisker-related information in mouse barrel cortex Young, Timothy R. Yamamoto, Mariko Kikuchi, Satomi S. Yoshida, Aya C. Abe, Takaya Inoue, Kenichi Johansen, Joshua P. Benucci, Andrea Yoshimura, Yumiko Shimogori, Tomomi Nat Commun Article Excitatory spiny stellate neurons are prominently featured in the cortical circuits of sensory modalities that provide high salience and high acuity representations of the environment. These specialized neurons are considered developmentally linked to bottom-up inputs from the thalamus, however, the molecular mechanisms underlying their diversification and function are unknown. Here, we investigated this in mouse somatosensory cortex, where spiny stellate neurons and pyramidal neurons have distinct roles in processing whisker-evoked signals. Utilizing spatial transcriptomics, we identified reciprocal patterns of gene expression which correlated with these cell-types and were linked to innervation by specific thalamic inputs during development. Genetic manipulation that prevents the acquisition of spiny stellate fate highlighted an important role for these neurons in processing distinct whisker signals within functional cortical columns, and as a key driver in the formation of specific whisker-related circuits in the cortex. Nature Publishing Group UK 2023-09-28 /pmc/articles/PMC10539368/ /pubmed/37770450 http://dx.doi.org/10.1038/s41467-023-41749-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Young, Timothy R. Yamamoto, Mariko Kikuchi, Satomi S. Yoshida, Aya C. Abe, Takaya Inoue, Kenichi Johansen, Joshua P. Benucci, Andrea Yoshimura, Yumiko Shimogori, Tomomi Thalamocortical control of cell-type specificity drives circuits for processing whisker-related information in mouse barrel cortex |
title | Thalamocortical control of cell-type specificity drives circuits for processing whisker-related information in mouse barrel cortex |
title_full | Thalamocortical control of cell-type specificity drives circuits for processing whisker-related information in mouse barrel cortex |
title_fullStr | Thalamocortical control of cell-type specificity drives circuits for processing whisker-related information in mouse barrel cortex |
title_full_unstemmed | Thalamocortical control of cell-type specificity drives circuits for processing whisker-related information in mouse barrel cortex |
title_short | Thalamocortical control of cell-type specificity drives circuits for processing whisker-related information in mouse barrel cortex |
title_sort | thalamocortical control of cell-type specificity drives circuits for processing whisker-related information in mouse barrel cortex |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10539368/ https://www.ncbi.nlm.nih.gov/pubmed/37770450 http://dx.doi.org/10.1038/s41467-023-41749-x |
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