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Mesenchymal stromal cells alleviate depressive and anxiety-like behaviors via a lung vagal-to-brain axis in male mice

Major depressive disorder (MDD) is one of the most common and disabling mental disorders, and current strategies remain inadequate. Although mesenchymal stromal cells (MSCs) have shown beneficial effects in experimental models of depression, underlying mechanisms remain elusive. Here, using murine d...

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Autores principales: Huang, Jing, Huang, Weijun, Yi, Junzhe, Deng, Yiwen, Li, Ruijie, Chen, Jieying, Shi, Jiahao, Qiu, Yuan, Wang, Tao, Chen, Xiaoyong, Zhang, Xiaoran, Xiang, Andy Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10654509/
https://www.ncbi.nlm.nih.gov/pubmed/37973914
http://dx.doi.org/10.1038/s41467-023-43150-0
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author Huang, Jing
Huang, Weijun
Yi, Junzhe
Deng, Yiwen
Li, Ruijie
Chen, Jieying
Shi, Jiahao
Qiu, Yuan
Wang, Tao
Chen, Xiaoyong
Zhang, Xiaoran
Xiang, Andy Peng
author_facet Huang, Jing
Huang, Weijun
Yi, Junzhe
Deng, Yiwen
Li, Ruijie
Chen, Jieying
Shi, Jiahao
Qiu, Yuan
Wang, Tao
Chen, Xiaoyong
Zhang, Xiaoran
Xiang, Andy Peng
author_sort Huang, Jing
collection PubMed
description Major depressive disorder (MDD) is one of the most common and disabling mental disorders, and current strategies remain inadequate. Although mesenchymal stromal cells (MSCs) have shown beneficial effects in experimental models of depression, underlying mechanisms remain elusive. Here, using murine depression models, we demonstrated that MSCs could alleviate depressive and anxiety-like behaviors not due to a reduction in proinflammatory cytokines, but rather activation of dorsal raphe nucleus (DRN) 5-hydroxytryptamine (5-HT) neurons. Mechanistically, peripheral delivery of MSCs activated pulmonary innervating vagal sensory neurons, which projected to the nucleus tractus solitarius, inducing the release of 5-HT in DRN. Furthermore, MSC-secreted brain-derived neurotrophic factor activated lung sensory neurons through tropomyosin receptor kinase B (TrkB), and inhalation of a TrkB agonist also achieved significant therapeutic effects in male mice. This study reveals a role of peripheral MSCs in regulating central nervous system function and demonstrates a potential “lung vagal-to-brain axis” strategy for MDD.
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spelling pubmed-106545092023-11-16 Mesenchymal stromal cells alleviate depressive and anxiety-like behaviors via a lung vagal-to-brain axis in male mice Huang, Jing Huang, Weijun Yi, Junzhe Deng, Yiwen Li, Ruijie Chen, Jieying Shi, Jiahao Qiu, Yuan Wang, Tao Chen, Xiaoyong Zhang, Xiaoran Xiang, Andy Peng Nat Commun Article Major depressive disorder (MDD) is one of the most common and disabling mental disorders, and current strategies remain inadequate. Although mesenchymal stromal cells (MSCs) have shown beneficial effects in experimental models of depression, underlying mechanisms remain elusive. Here, using murine depression models, we demonstrated that MSCs could alleviate depressive and anxiety-like behaviors not due to a reduction in proinflammatory cytokines, but rather activation of dorsal raphe nucleus (DRN) 5-hydroxytryptamine (5-HT) neurons. Mechanistically, peripheral delivery of MSCs activated pulmonary innervating vagal sensory neurons, which projected to the nucleus tractus solitarius, inducing the release of 5-HT in DRN. Furthermore, MSC-secreted brain-derived neurotrophic factor activated lung sensory neurons through tropomyosin receptor kinase B (TrkB), and inhalation of a TrkB agonist also achieved significant therapeutic effects in male mice. This study reveals a role of peripheral MSCs in regulating central nervous system function and demonstrates a potential “lung vagal-to-brain axis” strategy for MDD. Nature Publishing Group UK 2023-11-16 /pmc/articles/PMC10654509/ /pubmed/37973914 http://dx.doi.org/10.1038/s41467-023-43150-0 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
Huang, Jing
Huang, Weijun
Yi, Junzhe
Deng, Yiwen
Li, Ruijie
Chen, Jieying
Shi, Jiahao
Qiu, Yuan
Wang, Tao
Chen, Xiaoyong
Zhang, Xiaoran
Xiang, Andy Peng
Mesenchymal stromal cells alleviate depressive and anxiety-like behaviors via a lung vagal-to-brain axis in male mice
title Mesenchymal stromal cells alleviate depressive and anxiety-like behaviors via a lung vagal-to-brain axis in male mice
title_full Mesenchymal stromal cells alleviate depressive and anxiety-like behaviors via a lung vagal-to-brain axis in male mice
title_fullStr Mesenchymal stromal cells alleviate depressive and anxiety-like behaviors via a lung vagal-to-brain axis in male mice
title_full_unstemmed Mesenchymal stromal cells alleviate depressive and anxiety-like behaviors via a lung vagal-to-brain axis in male mice
title_short Mesenchymal stromal cells alleviate depressive and anxiety-like behaviors via a lung vagal-to-brain axis in male mice
title_sort mesenchymal stromal cells alleviate depressive and anxiety-like behaviors via a lung vagal-to-brain axis in male mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10654509/
https://www.ncbi.nlm.nih.gov/pubmed/37973914
http://dx.doi.org/10.1038/s41467-023-43150-0
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