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Splicing factor SRSF1 is indispensable for regulatory T cell homeostasis and function

The ability of regulatory T (Treg) cells to control the immune response and limit the development of autoimmune diseases is determined by distinct molecular processes, which are not fully understood. We show here that serine/arginine-rich splicing factor 1 (SRSF1), which is decreased in T cells from...

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Detalles Bibliográficos
Autores principales: Katsuyama, Takayuki, Moulton, Vaishali R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8476088/
https://www.ncbi.nlm.nih.gov/pubmed/34233194
http://dx.doi.org/10.1016/j.celrep.2021.109339
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author Katsuyama, Takayuki
Moulton, Vaishali R.
author_facet Katsuyama, Takayuki
Moulton, Vaishali R.
author_sort Katsuyama, Takayuki
collection PubMed
description The ability of regulatory T (Treg) cells to control the immune response and limit the development of autoimmune diseases is determined by distinct molecular processes, which are not fully understood. We show here that serine/arginine-rich splicing factor 1 (SRSF1), which is decreased in T cells from patients with systemic lupus erythematosus, is necessary for the homeostasis and proper function of Treg cells, because its conditional absence in these cells leads to profound autoimmunity and organ inflammation by elevating the glycolytic metabolism and mTORC1 activity and the production of proinflammatory cytokines. Our data reveal a molecular mechanism that controls Treg cell plasticity and offer insights into the pathogenesis of autoimmune disease.
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spelling pubmed-84760882021-09-27 Splicing factor SRSF1 is indispensable for regulatory T cell homeostasis and function Katsuyama, Takayuki Moulton, Vaishali R. Cell Rep Article The ability of regulatory T (Treg) cells to control the immune response and limit the development of autoimmune diseases is determined by distinct molecular processes, which are not fully understood. We show here that serine/arginine-rich splicing factor 1 (SRSF1), which is decreased in T cells from patients with systemic lupus erythematosus, is necessary for the homeostasis and proper function of Treg cells, because its conditional absence in these cells leads to profound autoimmunity and organ inflammation by elevating the glycolytic metabolism and mTORC1 activity and the production of proinflammatory cytokines. Our data reveal a molecular mechanism that controls Treg cell plasticity and offer insights into the pathogenesis of autoimmune disease. 2021-07-06 /pmc/articles/PMC8476088/ /pubmed/34233194 http://dx.doi.org/10.1016/j.celrep.2021.109339 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ).
spellingShingle Article
Katsuyama, Takayuki
Moulton, Vaishali R.
Splicing factor SRSF1 is indispensable for regulatory T cell homeostasis and function
title Splicing factor SRSF1 is indispensable for regulatory T cell homeostasis and function
title_full Splicing factor SRSF1 is indispensable for regulatory T cell homeostasis and function
title_fullStr Splicing factor SRSF1 is indispensable for regulatory T cell homeostasis and function
title_full_unstemmed Splicing factor SRSF1 is indispensable for regulatory T cell homeostasis and function
title_short Splicing factor SRSF1 is indispensable for regulatory T cell homeostasis and function
title_sort splicing factor srsf1 is indispensable for regulatory t cell homeostasis and function
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8476088/
https://www.ncbi.nlm.nih.gov/pubmed/34233194
http://dx.doi.org/10.1016/j.celrep.2021.109339
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