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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2016
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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. |
format | Online Article Text |
id | pubmed-5110022 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
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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