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The interplay between regulatory T cells and metabolism in immune regulation

Regulatory T cells (Tregs) are crucial for peripheral tolerance and are intimately involved in immunological diseases and cancer. Recent studies have highlighted a key role for Tregs in metabolic disorders, for instance as they accumulate in the adipose tissue to protect against obesity-related infl...

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Detalles Bibliográficos
Autores principales: Zeng, Hu, Chi, Hongbo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3881602/
https://www.ncbi.nlm.nih.gov/pubmed/24404429
http://dx.doi.org/10.4161/onci.26586
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author Zeng, Hu
Chi, Hongbo
author_facet Zeng, Hu
Chi, Hongbo
author_sort Zeng, Hu
collection PubMed
description Regulatory T cells (Tregs) are crucial for peripheral tolerance and are intimately involved in immunological diseases and cancer. Recent studies have highlighted a key role for Tregs in metabolic disorders, for instance as they accumulate in the adipose tissue to protect against obesity-related inflammation and insulin resistance. Conversely, the generation and immunosuppressive functions of Tregs are influenced by both systemic and cellular metabolism. The nutritional status as well as metabolic cues such as those provided by leptin impinge upon the proliferation of Tregs. In addition, the mTOR-dependent lipid metabolism has a crucial role in programming the activity of Tregs under steady-state conditions as well as upon activation. This review discusses the intricate interaction between Tregs and metabolism, focusing on the roles of Tregs in systemic and local metabolic circuitries as well as on the regulation of Treg abundance and function by metabolic signals.
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spelling pubmed-38816022014-01-08 The interplay between regulatory T cells and metabolism in immune regulation Zeng, Hu Chi, Hongbo Oncoimmunology Review Regulatory T cells (Tregs) are crucial for peripheral tolerance and are intimately involved in immunological diseases and cancer. Recent studies have highlighted a key role for Tregs in metabolic disorders, for instance as they accumulate in the adipose tissue to protect against obesity-related inflammation and insulin resistance. Conversely, the generation and immunosuppressive functions of Tregs are influenced by both systemic and cellular metabolism. The nutritional status as well as metabolic cues such as those provided by leptin impinge upon the proliferation of Tregs. In addition, the mTOR-dependent lipid metabolism has a crucial role in programming the activity of Tregs under steady-state conditions as well as upon activation. This review discusses the intricate interaction between Tregs and metabolism, focusing on the roles of Tregs in systemic and local metabolic circuitries as well as on the regulation of Treg abundance and function by metabolic signals. Landes Bioscience 2013-11-01 2013-10-21 /pmc/articles/PMC3881602/ /pubmed/24404429 http://dx.doi.org/10.4161/onci.26586 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Review
Zeng, Hu
Chi, Hongbo
The interplay between regulatory T cells and metabolism in immune regulation
title The interplay between regulatory T cells and metabolism in immune regulation
title_full The interplay between regulatory T cells and metabolism in immune regulation
title_fullStr The interplay between regulatory T cells and metabolism in immune regulation
title_full_unstemmed The interplay between regulatory T cells and metabolism in immune regulation
title_short The interplay between regulatory T cells and metabolism in immune regulation
title_sort interplay between regulatory t cells and metabolism in immune regulation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3881602/
https://www.ncbi.nlm.nih.gov/pubmed/24404429
http://dx.doi.org/10.4161/onci.26586
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