IRF4公司
染色质免疫沉淀
生物
白细胞介素9
干扰素调节因子
下调和上调
功能(生物学)
干扰素
免疫学
T辅助细胞
转录因子
白细胞介素13
免疫沉淀
细胞生物学
白细胞介素
癌症研究
T细胞
细胞因子
基因
发起人
基因表达
遗传学
免疫系统
抗体
作者
Valérie Staudt,Evita Bothur,Matthias Klein,Karen Lingnau,Sebastian Reuter,Nadine Baumgart,Bastian Gerlitzki,Markus Hoffmann,Alexander Ulges,Christian Taube,Nina Dehzad,Marc A. Becker,Michael Stassen,Andrea Steinborn,Michael Lohoff,Hansjörg Schild,Edgar Schmitt,Tobias Bopp
出处
期刊:Immunity
[Elsevier]
日期:2010-08-01
卷期号:33 (2): 192-202
被引量:501
标识
DOI:10.1016/j.immuni.2010.07.014
摘要
Interferon-regulatory factor 4 (IRF4) is essential for the development of T helper 2 (Th2) and Th17 cells. Herein, we report that IRF4 is also crucial for the development and function of an interleukin-9 (IL-9)-producing CD4+ T cell subset designated Th9. IRF4-deficient CD4+ T cells failed to develop into IL-9-producing Th9 cells, and IRF4-specific siRNA inhibited IL-9 production in wild-type CD4+ T cells. Chromatin-immunoprecipitation (ChIP) analyses revealed direct IRF4 binding to the Il9 promoter in Th9 cells. In a Th9-dependent asthma model, neutralization of IL-9 substantially ameliorated asthma symptoms. The relevance of these findings is emphasized by the fact that the induction of IL-9 production also occurs in human CD4+ T cells accompanied by the upregulation of IRF4. Our data clearly demonstrate the central function of IRF4 in the development of Th9 cells and underline the contribution of this T helper cell subset to the pathogenesis of asthma.
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