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Molecular Determinants of Regulatory T Cell Development: The Essential Roles of Epigenetic Changes

Regulatory T (Treg) cells constitute a distinct T cell subset, which plays a key role in immune tolerance and homeostasis. The transcription factor Foxp3 controls a substantial part of Treg cell development and function. Yet its expression alone is insufficient for conferring developmental and funct...

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Detalles Bibliográficos
Autores principales: Kitagawa, Yohko, Ohkura, Naganari, Sakaguchi, Shimon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3650462/
https://www.ncbi.nlm.nih.gov/pubmed/23675373
http://dx.doi.org/10.3389/fimmu.2013.00106
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author Kitagawa, Yohko
Ohkura, Naganari
Sakaguchi, Shimon
author_facet Kitagawa, Yohko
Ohkura, Naganari
Sakaguchi, Shimon
author_sort Kitagawa, Yohko
collection PubMed
description Regulatory T (Treg) cells constitute a distinct T cell subset, which plays a key role in immune tolerance and homeostasis. The transcription factor Foxp3 controls a substantial part of Treg cell development and function. Yet its expression alone is insufficient for conferring developmental and functional characteristics of Treg cells. There is accumulating evidence that concurrent induction of Treg-specific epigenetic changes and Foxp3 expression is crucial for lineage specification and functional stability of Treg cells. This review discusses recent progress in our understanding of molecular features of Treg cells, in particular, the molecular basis of how a population of developing T cells is driven to the Treg cell lineage and how its function is stably maintained.
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spelling pubmed-36504622013-05-14 Molecular Determinants of Regulatory T Cell Development: The Essential Roles of Epigenetic Changes Kitagawa, Yohko Ohkura, Naganari Sakaguchi, Shimon Front Immunol Immunology Regulatory T (Treg) cells constitute a distinct T cell subset, which plays a key role in immune tolerance and homeostasis. The transcription factor Foxp3 controls a substantial part of Treg cell development and function. Yet its expression alone is insufficient for conferring developmental and functional characteristics of Treg cells. There is accumulating evidence that concurrent induction of Treg-specific epigenetic changes and Foxp3 expression is crucial for lineage specification and functional stability of Treg cells. This review discusses recent progress in our understanding of molecular features of Treg cells, in particular, the molecular basis of how a population of developing T cells is driven to the Treg cell lineage and how its function is stably maintained. Frontiers Media S.A. 2013-05-10 /pmc/articles/PMC3650462/ /pubmed/23675373 http://dx.doi.org/10.3389/fimmu.2013.00106 Text en Copyright © 2013 Kitagawa, Ohkura and Sakaguchi. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Immunology
Kitagawa, Yohko
Ohkura, Naganari
Sakaguchi, Shimon
Molecular Determinants of Regulatory T Cell Development: The Essential Roles of Epigenetic Changes
title Molecular Determinants of Regulatory T Cell Development: The Essential Roles of Epigenetic Changes
title_full Molecular Determinants of Regulatory T Cell Development: The Essential Roles of Epigenetic Changes
title_fullStr Molecular Determinants of Regulatory T Cell Development: The Essential Roles of Epigenetic Changes
title_full_unstemmed Molecular Determinants of Regulatory T Cell Development: The Essential Roles of Epigenetic Changes
title_short Molecular Determinants of Regulatory T Cell Development: The Essential Roles of Epigenetic Changes
title_sort molecular determinants of regulatory t cell development: the essential roles of epigenetic changes
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3650462/
https://www.ncbi.nlm.nih.gov/pubmed/23675373
http://dx.doi.org/10.3389/fimmu.2013.00106
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