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A multidimensional coding architecture of the vagal interoceptive system

Interoception, the ability to timely and precisely sense changes inside the body, is critical for survival(1–4). Vagal sensory neurons (VSNs) form an important body-to-brain connection, navigating visceral organs along the rostral–caudal axis of the body and crossing the surface–lumen axis of organs...

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Autores principales: Zhao, Qiancheng, Yu, Chuyue D., Wang, Rui, Xu, Qian J., Dai Pra, Rafael, Zhang, Le, Chang, Rui B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8967724/
https://www.ncbi.nlm.nih.gov/pubmed/35296859
http://dx.doi.org/10.1038/s41586-022-04515-5
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author Zhao, Qiancheng
Yu, Chuyue D.
Wang, Rui
Xu, Qian J.
Dai Pra, Rafael
Zhang, Le
Chang, Rui B.
author_facet Zhao, Qiancheng
Yu, Chuyue D.
Wang, Rui
Xu, Qian J.
Dai Pra, Rafael
Zhang, Le
Chang, Rui B.
author_sort Zhao, Qiancheng
collection PubMed
description Interoception, the ability to timely and precisely sense changes inside the body, is critical for survival(1–4). Vagal sensory neurons (VSNs) form an important body-to-brain connection, navigating visceral organs along the rostral–caudal axis of the body and crossing the surface–lumen axis of organs into appropriate tissue layers(5,6). The brain can discriminate numerous body signals through VSNs, but the underlying coding strategy remains poorly understood. Here we show that VSNs code visceral organ, tissue layer and stimulus modality—three key features of an interoceptive signal—in different dimensions. Large-scale single-cell profiling of VSNs from seven major organs in mice using multiplexed projection barcodes reveals a ‘visceral organ’ dimension composed of differentially expressed gene modules that code organs along the body’s rostral–caudal axis. We discover another ‘tissue layer’ dimension with gene modules that code the locations of VSN endings along the surface–lumen axis of organs. Using calcium-imaging-guided spatial transcriptomics, we show that VSNs are organized into functional units to sense similar stimuli across organs and tissue layers; this constitutes a third ‘stimulus modality’ dimension. The three independent feature-coding dimensions together specify many parallel VSN pathways in a combinatorial manner and facilitate the complex projection of VSNs in the brainstem. Our study highlights a multidimensional coding architecture of the mammalian vagal interoceptive system for effective signal communication.
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spelling pubmed-89677242022-04-07 A multidimensional coding architecture of the vagal interoceptive system Zhao, Qiancheng Yu, Chuyue D. Wang, Rui Xu, Qian J. Dai Pra, Rafael Zhang, Le Chang, Rui B. Nature Article Interoception, the ability to timely and precisely sense changes inside the body, is critical for survival(1–4). Vagal sensory neurons (VSNs) form an important body-to-brain connection, navigating visceral organs along the rostral–caudal axis of the body and crossing the surface–lumen axis of organs into appropriate tissue layers(5,6). The brain can discriminate numerous body signals through VSNs, but the underlying coding strategy remains poorly understood. Here we show that VSNs code visceral organ, tissue layer and stimulus modality—three key features of an interoceptive signal—in different dimensions. Large-scale single-cell profiling of VSNs from seven major organs in mice using multiplexed projection barcodes reveals a ‘visceral organ’ dimension composed of differentially expressed gene modules that code organs along the body’s rostral–caudal axis. We discover another ‘tissue layer’ dimension with gene modules that code the locations of VSN endings along the surface–lumen axis of organs. Using calcium-imaging-guided spatial transcriptomics, we show that VSNs are organized into functional units to sense similar stimuli across organs and tissue layers; this constitutes a third ‘stimulus modality’ dimension. The three independent feature-coding dimensions together specify many parallel VSN pathways in a combinatorial manner and facilitate the complex projection of VSNs in the brainstem. Our study highlights a multidimensional coding architecture of the mammalian vagal interoceptive system for effective signal communication. Nature Publishing Group UK 2022-03-16 2022 /pmc/articles/PMC8967724/ /pubmed/35296859 http://dx.doi.org/10.1038/s41586-022-04515-5 Text en © The Author(s) 2022 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 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Zhao, Qiancheng
Yu, Chuyue D.
Wang, Rui
Xu, Qian J.
Dai Pra, Rafael
Zhang, Le
Chang, Rui B.
A multidimensional coding architecture of the vagal interoceptive system
title A multidimensional coding architecture of the vagal interoceptive system
title_full A multidimensional coding architecture of the vagal interoceptive system
title_fullStr A multidimensional coding architecture of the vagal interoceptive system
title_full_unstemmed A multidimensional coding architecture of the vagal interoceptive system
title_short A multidimensional coding architecture of the vagal interoceptive system
title_sort multidimensional coding architecture of the vagal interoceptive system
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8967724/
https://www.ncbi.nlm.nih.gov/pubmed/35296859
http://dx.doi.org/10.1038/s41586-022-04515-5
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