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Ets-1, a functional cofactor of T-bet, is essential for Th1 inflammatory responses
To mount an effective type 1 immune response, type 1 T helper (Th1) cells must produce inflammatory cytokines and simultaneously suppress the expression of antiinflammatory cytokines. How these two processes are coordinately regulated at the molecular level is still unclear. In this paper, we show t...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2213045/ https://www.ncbi.nlm.nih.gov/pubmed/15728239 http://dx.doi.org/10.1084/jem.20041330 |
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author | Grenningloh, Roland Kang, Bok Yun Ho, I-Cheng |
author_facet | Grenningloh, Roland Kang, Bok Yun Ho, I-Cheng |
author_sort | Grenningloh, Roland |
collection | PubMed |
description | To mount an effective type 1 immune response, type 1 T helper (Th1) cells must produce inflammatory cytokines and simultaneously suppress the expression of antiinflammatory cytokines. How these two processes are coordinately regulated at the molecular level is still unclear. In this paper, we show that the proto-oncogene E26 transformation–specific-1 (Ets-1) is necessary for T-bet to promote interferon-γ production and that Ets-1 is essential for mounting effective Th1 inflammatory responses in vivo. In addition, Ets-1–deficient Th1 cells also produce a very high level of interleukin 10. Thus, Ets-1 plays a crucial and unique role in the reciprocal regulation of inflammatory and antiinflammatory Th responses. |
format | Text |
id | pubmed-2213045 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-22130452008-03-11 Ets-1, a functional cofactor of T-bet, is essential for Th1 inflammatory responses Grenningloh, Roland Kang, Bok Yun Ho, I-Cheng J Exp Med Article To mount an effective type 1 immune response, type 1 T helper (Th1) cells must produce inflammatory cytokines and simultaneously suppress the expression of antiinflammatory cytokines. How these two processes are coordinately regulated at the molecular level is still unclear. In this paper, we show that the proto-oncogene E26 transformation–specific-1 (Ets-1) is necessary for T-bet to promote interferon-γ production and that Ets-1 is essential for mounting effective Th1 inflammatory responses in vivo. In addition, Ets-1–deficient Th1 cells also produce a very high level of interleukin 10. Thus, Ets-1 plays a crucial and unique role in the reciprocal regulation of inflammatory and antiinflammatory Th responses. The Rockefeller University Press 2005-02-21 /pmc/articles/PMC2213045/ /pubmed/15728239 http://dx.doi.org/10.1084/jem.20041330 Text en Copyright © 2005, 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 | Article Grenningloh, Roland Kang, Bok Yun Ho, I-Cheng Ets-1, a functional cofactor of T-bet, is essential for Th1 inflammatory responses |
title | Ets-1, a functional cofactor of T-bet, is essential for Th1 inflammatory responses |
title_full | Ets-1, a functional cofactor of T-bet, is essential for Th1 inflammatory responses |
title_fullStr | Ets-1, a functional cofactor of T-bet, is essential for Th1 inflammatory responses |
title_full_unstemmed | Ets-1, a functional cofactor of T-bet, is essential for Th1 inflammatory responses |
title_short | Ets-1, a functional cofactor of T-bet, is essential for Th1 inflammatory responses |
title_sort | ets-1, a functional cofactor of t-bet, is essential for th1 inflammatory responses |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2213045/ https://www.ncbi.nlm.nih.gov/pubmed/15728239 http://dx.doi.org/10.1084/jem.20041330 |
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