T cell factor 1 initiates the T helper type 2 fate by inducing the transcription factor GATA-3 and repressing interferon-γ

被引:170
|
作者
Yu, Qing [1 ]
Sharma, Archna [1 ]
Oh, Sun Young [2 ]
Moon, Hyung-Geun [2 ]
Hossain, M. Zulfiquer [1 ]
Salay, Theresa M. [1 ]
Leeds, Karen E. [1 ]
Du, Hansen [1 ]
Wu, Beibei [3 ]
Waterman, Marian L. [3 ]
Zhu, Zhou [2 ]
Sen, Jyoti Misra [1 ]
机构
[1] NIA, Lymphocyte Dev Unit, Immunol Lab, NIH, Baltimore, MD 21224 USA
[2] Johns Hopkins Univ, Sch Med, Div Clin Immunol & Allergy, Baltimore, MD USA
[3] Univ Calif Irvine, Irvine, CA USA
基金
美国国家卫生研究院;
关键词
BETA-CATENIN; LINEAGE COMMITMENT; PROSTAGLANDIN E-2; GENE-EXPRESSION; IMMUNE-SYSTEM; COLON-CANCER; TH2; CELLS; IN-VITRO; WNT; RESPONSES;
D O I
10.1038/ni.1762
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The differentiation of activated CD4(+) T cells into the T helper type 1 (T(H)1) or T(H)2 fate is regulated by cytokines and the transcription factors T-bet and GATA-3. Whereas interleukin 12 (IL-12) produced by antigen-presenting cells initiates the T(H)1 fate, signals that initiate the T(H)2 fate are not completely characterized. Here we show that early GATA-3 expression, required for T(H)2 differentiation, was induced by T cell factor 1 (TCF-1) and its cofactor beta-catenin, mainly from the proximal Gata3 promoter upstream of exon 1b. This activity was induced after T cell antigen receptor (TCR) stimulation and was independent of IL-4 receptor signaling through the transcription factor STAT6. Furthermore, TCF-1 blocked T(H)1 fate by negatively regulating interferon-gamma (IFN-gamma) expression independently of beta-catenin. Thus, TCF-1 initiates T(H)2 differentiation of activated CD4(+) T cells by promoting GATA-3 expression and suppressing IFN-gamma expression.
引用
收藏
页码:992 / U85
页数:10
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