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Mucosal-associated invariant T cells promote inflammation and intestinal dysbiosis leading to metabolic dysfunction during obesity

Obesity is associated with low-grade chronic inflammation promoting insulin-resistance and diabetes. Gut microbiota dysbiosis is a consequence as well as a driver of obesity and diabetes. Mucosal-associated invariant T cells (MAIT) are innate-like T cells expressing a semi-invariant T cell receptor...

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Autores principales: Toubal, Amine, Kiaf, Badr, Beaudoin, Lucie, Cagninacci, Lucie, Rhimi, Moez, Fruchet, Blandine, da Silva, Jennifer, Corbett, Alexandra J., Simoni, Yannick, Lantz, Olivier, Rossjohn, Jamie, McCluskey, James, Lesnik, Philippe, Maguin, Emmanuelle, Lehuen, Agnès
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7381641/
https://www.ncbi.nlm.nih.gov/pubmed/32709874
http://dx.doi.org/10.1038/s41467-020-17307-0
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author Toubal, Amine
Kiaf, Badr
Beaudoin, Lucie
Cagninacci, Lucie
Rhimi, Moez
Fruchet, Blandine
da Silva, Jennifer
Corbett, Alexandra J.
Simoni, Yannick
Lantz, Olivier
Rossjohn, Jamie
McCluskey, James
Lesnik, Philippe
Maguin, Emmanuelle
Lehuen, Agnès
author_facet Toubal, Amine
Kiaf, Badr
Beaudoin, Lucie
Cagninacci, Lucie
Rhimi, Moez
Fruchet, Blandine
da Silva, Jennifer
Corbett, Alexandra J.
Simoni, Yannick
Lantz, Olivier
Rossjohn, Jamie
McCluskey, James
Lesnik, Philippe
Maguin, Emmanuelle
Lehuen, Agnès
author_sort Toubal, Amine
collection PubMed
description Obesity is associated with low-grade chronic inflammation promoting insulin-resistance and diabetes. Gut microbiota dysbiosis is a consequence as well as a driver of obesity and diabetes. Mucosal-associated invariant T cells (MAIT) are innate-like T cells expressing a semi-invariant T cell receptor restricted to the non-classical MHC class I molecule MR1 presenting bacterial ligands. Here we show that during obesity MAIT cells promote inflammation in both adipose tissue and ileum, leading to insulin resistance and impaired glucose and lipid metabolism. MAIT cells act in adipose tissue by inducing M1 macrophage polarization in an MR1-dependent manner and in the gut by inducing microbiota dysbiosis and loss of gut integrity. Both MAIT cell-induced tissue alterations contribute to metabolic dysfunction. Treatment with MAIT cell inhibitory ligand demonstrates its potential as a strategy against inflammation, dysbiosis and metabolic disorders.
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spelling pubmed-73816412020-07-28 Mucosal-associated invariant T cells promote inflammation and intestinal dysbiosis leading to metabolic dysfunction during obesity Toubal, Amine Kiaf, Badr Beaudoin, Lucie Cagninacci, Lucie Rhimi, Moez Fruchet, Blandine da Silva, Jennifer Corbett, Alexandra J. Simoni, Yannick Lantz, Olivier Rossjohn, Jamie McCluskey, James Lesnik, Philippe Maguin, Emmanuelle Lehuen, Agnès Nat Commun Article Obesity is associated with low-grade chronic inflammation promoting insulin-resistance and diabetes. Gut microbiota dysbiosis is a consequence as well as a driver of obesity and diabetes. Mucosal-associated invariant T cells (MAIT) are innate-like T cells expressing a semi-invariant T cell receptor restricted to the non-classical MHC class I molecule MR1 presenting bacterial ligands. Here we show that during obesity MAIT cells promote inflammation in both adipose tissue and ileum, leading to insulin resistance and impaired glucose and lipid metabolism. MAIT cells act in adipose tissue by inducing M1 macrophage polarization in an MR1-dependent manner and in the gut by inducing microbiota dysbiosis and loss of gut integrity. Both MAIT cell-induced tissue alterations contribute to metabolic dysfunction. Treatment with MAIT cell inhibitory ligand demonstrates its potential as a strategy against inflammation, dysbiosis and metabolic disorders. Nature Publishing Group UK 2020-07-24 /pmc/articles/PMC7381641/ /pubmed/32709874 http://dx.doi.org/10.1038/s41467-020-17307-0 Text en © The Author(s) 2020 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/.
spellingShingle Article
Toubal, Amine
Kiaf, Badr
Beaudoin, Lucie
Cagninacci, Lucie
Rhimi, Moez
Fruchet, Blandine
da Silva, Jennifer
Corbett, Alexandra J.
Simoni, Yannick
Lantz, Olivier
Rossjohn, Jamie
McCluskey, James
Lesnik, Philippe
Maguin, Emmanuelle
Lehuen, Agnès
Mucosal-associated invariant T cells promote inflammation and intestinal dysbiosis leading to metabolic dysfunction during obesity
title Mucosal-associated invariant T cells promote inflammation and intestinal dysbiosis leading to metabolic dysfunction during obesity
title_full Mucosal-associated invariant T cells promote inflammation and intestinal dysbiosis leading to metabolic dysfunction during obesity
title_fullStr Mucosal-associated invariant T cells promote inflammation and intestinal dysbiosis leading to metabolic dysfunction during obesity
title_full_unstemmed Mucosal-associated invariant T cells promote inflammation and intestinal dysbiosis leading to metabolic dysfunction during obesity
title_short Mucosal-associated invariant T cells promote inflammation and intestinal dysbiosis leading to metabolic dysfunction during obesity
title_sort mucosal-associated invariant t cells promote inflammation and intestinal dysbiosis leading to metabolic dysfunction during obesity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7381641/
https://www.ncbi.nlm.nih.gov/pubmed/32709874
http://dx.doi.org/10.1038/s41467-020-17307-0
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