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Scramblase TMEM16F terminates T cell receptor signaling to restrict T cell exhaustion

In chronic infection, T cells become hyporesponsive to antigenic stimulation to prevent immunopathology. Here, we show that TMEM16F is required to curb excessive T cell responses in chronic infection with virus. TMEM16F-deficient T cells are hyperactivated during the early phase of infection, exhibi...

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Autores principales: Hu, Yu, Kim, Ji Hyung, He, Kangmin, Wan, Qi, Kim, Jessica, Flach, Melanie, Kirchhausen, Tom, Vortkamp, Andrea, Winau, Florian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5110022/
https://www.ncbi.nlm.nih.gov/pubmed/27810927
http://dx.doi.org/10.1084/jem.20160612
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author Hu, Yu
Kim, Ji Hyung
He, Kangmin
Wan, Qi
Kim, Jessica
Flach, Melanie
Kirchhausen, Tom
Vortkamp, Andrea
Winau, Florian
author_facet Hu, Yu
Kim, Ji Hyung
He, Kangmin
Wan, Qi
Kim, Jessica
Flach, Melanie
Kirchhausen, Tom
Vortkamp, Andrea
Winau, Florian
author_sort Hu, Yu
collection PubMed
description In chronic infection, T cells become hyporesponsive to antigenic stimulation to prevent immunopathology. Here, we show that TMEM16F is required to curb excessive T cell responses in chronic infection with virus. TMEM16F-deficient T cells are hyperactivated during the early phase of infection, exhibiting increased proliferation and cytokine production. Interestingly, this overactivation ultimately leads to severe T cell exhaustion and the inability of the host to control viral burden. Mechanistically, we identify TMEM16F as the dominant lipid scramblase in T lymphocytes that transports phospholipids across membranes. TMEM16F is located in late endosomes, where it facilitates the generation of multivesicular bodies for TCR degradation and signal termination. Consequently, TMEM16F deficiency results in sustained signaling and augmented T cell activation. Our results demonstrate that scramblase restricts TCR responses to avoid overactivation, ensuring a well-balanced immune response in chronic infectious disease.
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spelling pubmed-51100222017-05-14 Scramblase TMEM16F terminates T cell receptor signaling to restrict T cell exhaustion Hu, Yu Kim, Ji Hyung He, Kangmin Wan, Qi Kim, Jessica Flach, Melanie Kirchhausen, Tom Vortkamp, Andrea Winau, Florian J Exp Med Research Articles In chronic infection, T cells become hyporesponsive to antigenic stimulation to prevent immunopathology. Here, we show that TMEM16F is required to curb excessive T cell responses in chronic infection with virus. TMEM16F-deficient T cells are hyperactivated during the early phase of infection, exhibiting increased proliferation and cytokine production. Interestingly, this overactivation ultimately leads to severe T cell exhaustion and the inability of the host to control viral burden. Mechanistically, we identify TMEM16F as the dominant lipid scramblase in T lymphocytes that transports phospholipids across membranes. TMEM16F is located in late endosomes, where it facilitates the generation of multivesicular bodies for TCR degradation and signal termination. Consequently, TMEM16F deficiency results in sustained signaling and augmented T cell activation. Our results demonstrate that scramblase restricts TCR responses to avoid overactivation, ensuring a well-balanced immune response in chronic infectious disease. The Rockefeller University Press 2016-11-14 /pmc/articles/PMC5110022/ /pubmed/27810927 http://dx.doi.org/10.1084/jem.20160612 Text en © 2016 Hu et al. 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 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Research Articles
Hu, Yu
Kim, Ji Hyung
He, Kangmin
Wan, Qi
Kim, Jessica
Flach, Melanie
Kirchhausen, Tom
Vortkamp, Andrea
Winau, Florian
Scramblase TMEM16F terminates T cell receptor signaling to restrict T cell exhaustion
title Scramblase TMEM16F terminates T cell receptor signaling to restrict T cell exhaustion
title_full Scramblase TMEM16F terminates T cell receptor signaling to restrict T cell exhaustion
title_fullStr Scramblase TMEM16F terminates T cell receptor signaling to restrict T cell exhaustion
title_full_unstemmed Scramblase TMEM16F terminates T cell receptor signaling to restrict T cell exhaustion
title_short Scramblase TMEM16F terminates T cell receptor signaling to restrict T cell exhaustion
title_sort scramblase tmem16f terminates t cell receptor signaling to restrict t cell exhaustion
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5110022/
https://www.ncbi.nlm.nih.gov/pubmed/27810927
http://dx.doi.org/10.1084/jem.20160612
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