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Interferon γ Is Required for Activation-induced Death of T Lymphocytes
The effector cytokine interferon γ (IFN-γ) may play a role in T cell homeostasis. We have examined the requirement for IFN-γ in one mechanism that regulates T cell expansion and survival, activation-induced cell death (AICD). CD4(+) T cells lacking IFN-γ or the Stat1 transcription factor are resista...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2002
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2194022/ https://www.ncbi.nlm.nih.gov/pubmed/12370261 http://dx.doi.org/10.1084/jem.20020666 |
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author | Refaeli, Yosef Van Parijs, Luk Alexander, Stephen I. Abbas, Abul K. |
author_facet | Refaeli, Yosef Van Parijs, Luk Alexander, Stephen I. Abbas, Abul K. |
author_sort | Refaeli, Yosef |
collection | PubMed |
description | The effector cytokine interferon γ (IFN-γ) may play a role in T cell homeostasis. We have examined the requirement for IFN-γ in one mechanism that regulates T cell expansion and survival, activation-induced cell death (AICD). CD4(+) T cells lacking IFN-γ or the Stat1 transcription factor are resistant to AICD. IFN-γ is required for the production of caspases, and retrovirus-mediated expression of caspase-8 restores the sensitivity of Stat1-deficient T cells to AICD. In vitro, IFN-γ limits the expansion of T cells that are stimulated through their antigen receptors. Thus, IFN-γ may function to control the expansion and persistence of T cells by promoting caspase-8–dependent apoptosis. |
format | Text |
id | pubmed-2194022 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2002 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21940222008-04-11 Interferon γ Is Required for Activation-induced Death of T Lymphocytes Refaeli, Yosef Van Parijs, Luk Alexander, Stephen I. Abbas, Abul K. J Exp Med Brief Definitive Report The effector cytokine interferon γ (IFN-γ) may play a role in T cell homeostasis. We have examined the requirement for IFN-γ in one mechanism that regulates T cell expansion and survival, activation-induced cell death (AICD). CD4(+) T cells lacking IFN-γ or the Stat1 transcription factor are resistant to AICD. IFN-γ is required for the production of caspases, and retrovirus-mediated expression of caspase-8 restores the sensitivity of Stat1-deficient T cells to AICD. In vitro, IFN-γ limits the expansion of T cells that are stimulated through their antigen receptors. Thus, IFN-γ may function to control the expansion and persistence of T cells by promoting caspase-8–dependent apoptosis. The Rockefeller University Press 2002-10-07 /pmc/articles/PMC2194022/ /pubmed/12370261 http://dx.doi.org/10.1084/jem.20020666 Text en Copyright © 2002, The Rockefeller University Press 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 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Brief Definitive Report Refaeli, Yosef Van Parijs, Luk Alexander, Stephen I. Abbas, Abul K. Interferon γ Is Required for Activation-induced Death of T Lymphocytes |
title | Interferon γ Is Required for Activation-induced Death of T Lymphocytes |
title_full | Interferon γ Is Required for Activation-induced Death of T Lymphocytes |
title_fullStr | Interferon γ Is Required for Activation-induced Death of T Lymphocytes |
title_full_unstemmed | Interferon γ Is Required for Activation-induced Death of T Lymphocytes |
title_short | Interferon γ Is Required for Activation-induced Death of T Lymphocytes |
title_sort | interferon γ is required for activation-induced death of t lymphocytes |
topic | Brief Definitive Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2194022/ https://www.ncbi.nlm.nih.gov/pubmed/12370261 http://dx.doi.org/10.1084/jem.20020666 |
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