The Runx1 transcription factor inhibits the differentiation of naive CD4+ T cells into the Th2 lineage by repressing GATA3 expression

被引:110
作者
Komine, O
Hayashi, K
Natsume, W
Watanabe, T
Seki, Y
Seki, N
Yagi, R
Sukzuki, W
Tamuchi, H
Hozumi, K
Habu, S
Kubo, M
Satake, M
机构
[1] Tohoku Univ, Inst Dev Aging & Canc, Dept Mol Immunol, Aoba Ku, Sendai, Miyagi 9808575, Japan
[2] Sci Univ Tokyo, Res Inst Biol Sci, Noda, Chiba 2780022, Japan
[3] Kitasato Univ, Sch Med, Dept Microbiol & Parasitol, Sagamihara, Kanagawa 2288555, Japan
[4] Tokai Univ, Sch Med, Dept Immunol, Isehara, Kanagawa 2591193, Japan
关键词
GATA3; Runx1; Th2; T lymphocytes; Transcription factor;
D O I
10.1084/jem.20021200
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Differentiation of naive CD4(+) T cells into helper T (Th) cells is controlled by a combination of several transcriptional factors. In this study, we examined the functional role of the Runx1 transcription factor in Th cell differentiation. Naive T cells from transgenic mice expressing a dominant interfering form of Runx1 exhibited enhanced interleukin 4 production and efficient Th2 differentiation. In contrast, transduction of Runx1 into wild-type T cells caused a complete attenuation of Th2 differentiation and was accompanied by the cessation of GATA3 expression. Furthermore, endogenous expression of Runx1 in naive T cells declined after T cell receptor stimulation, at the same time that expression of GATA3 increased. We conclude that Runx1 plays a novel role as a negative regulator of GATA3 expression, thereby inhibiting the Th2 cell differentiation.
引用
收藏
页码:51 / 61
页数:11
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