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Mechanosensing through YAP controls T cell activation and metabolism

Upon immunogenic challenge, lymph nodes become mechanically stiff as immune cells activate and proliferate within their encapsulated environments, and with resolution, they reestablish a soft baseline state. Here we show that sensing these mechanical changes in the microenvironment requires the mech...

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Detalles Bibliográficos
Autores principales: Meng, Kevin P., Majedi, Fatemeh S., Thauland, Timothy J., Butte, Manish J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7398163/
https://www.ncbi.nlm.nih.gov/pubmed/32484502
http://dx.doi.org/10.1084/jem.20200053
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author Meng, Kevin P.
Majedi, Fatemeh S.
Thauland, Timothy J.
Butte, Manish J.
author_facet Meng, Kevin P.
Majedi, Fatemeh S.
Thauland, Timothy J.
Butte, Manish J.
author_sort Meng, Kevin P.
collection PubMed
description Upon immunogenic challenge, lymph nodes become mechanically stiff as immune cells activate and proliferate within their encapsulated environments, and with resolution, they reestablish a soft baseline state. Here we show that sensing these mechanical changes in the microenvironment requires the mechanosensor YAP. YAP is induced upon activation and suppresses metabolic reprogramming of effector T cells. Unlike in other cell types in which YAP promotes proliferation, YAP in T cells suppresses proliferation in a stiffness-dependent manner by directly restricting the translocation of NFAT1 into the nucleus. YAP slows T cell responses in systemic viral infections and retards effector T cells in autoimmune diabetes. Our work reveals a paradigm whereby tissue mechanics fine-tune adaptive immune responses in health and disease.
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spelling pubmed-73981632021-02-03 Mechanosensing through YAP controls T cell activation and metabolism Meng, Kevin P. Majedi, Fatemeh S. Thauland, Timothy J. Butte, Manish J. J Exp Med Article Upon immunogenic challenge, lymph nodes become mechanically stiff as immune cells activate and proliferate within their encapsulated environments, and with resolution, they reestablish a soft baseline state. Here we show that sensing these mechanical changes in the microenvironment requires the mechanosensor YAP. YAP is induced upon activation and suppresses metabolic reprogramming of effector T cells. Unlike in other cell types in which YAP promotes proliferation, YAP in T cells suppresses proliferation in a stiffness-dependent manner by directly restricting the translocation of NFAT1 into the nucleus. YAP slows T cell responses in systemic viral infections and retards effector T cells in autoimmune diabetes. Our work reveals a paradigm whereby tissue mechanics fine-tune adaptive immune responses in health and disease. Rockefeller University Press 2020-06-02 /pmc/articles/PMC7398163/ /pubmed/32484502 http://dx.doi.org/10.1084/jem.20200053 Text en © 2020 Meng et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Meng, Kevin P.
Majedi, Fatemeh S.
Thauland, Timothy J.
Butte, Manish J.
Mechanosensing through YAP controls T cell activation and metabolism
title Mechanosensing through YAP controls T cell activation and metabolism
title_full Mechanosensing through YAP controls T cell activation and metabolism
title_fullStr Mechanosensing through YAP controls T cell activation and metabolism
title_full_unstemmed Mechanosensing through YAP controls T cell activation and metabolism
title_short Mechanosensing through YAP controls T cell activation and metabolism
title_sort mechanosensing through yap controls t cell activation and metabolism
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7398163/
https://www.ncbi.nlm.nih.gov/pubmed/32484502
http://dx.doi.org/10.1084/jem.20200053
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