Transcription factors Foxo3a and Foxo1 couple the E3 ligase Cbl-b to the induction of Foxp3 expression in induced regulatory T cells

被引:229
作者
Harada, Yohsuke [1 ]
Harada, Yasuyo [1 ]
Elly, Chris [1 ]
Ying, Ge [1 ]
Paik, Ji-Hye [2 ]
DePinho, Ronald A. [2 ]
Liu, Yun-Cai [1 ]
机构
[1] La Jolla Inst Allergy & Immunol, Div Cell Biol, La Jolla, CA 92037 USA
[2] Harvard Univ, Sch Med, Dana Farber Canc Inst, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
AKT; ACTIVATION; PROTEOLYSIS; DEFICIENCY; MECHANISMS; SURVIVAL; MICE; PI3K;
D O I
10.1084/jem.20100004
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 transcription factor Foxp3 is essential for optimal regulatory T (T reg) cell development and function. Here, we show that CD4(+) T cells from Cbl-b RING finger mutant knockin or Cbl-b-deficient mice show impaired TGF-beta-induced Foxp3 expression. These T cells display augmented Foxo3a phosphorylation, but normal TGF-beta signaling. Expression of Foxo3a rescues Foxp3 expression in Cbl-b-deficient T cells, and Foxo3a deficiency results in defective TGF-beta-driven Foxp3 induction. A Foxo3a-binding motif is present in a proximal region of the Foxp3 promoter, and is required for Foxo3a association. Foxo1 exerts similar effects as Foxo3a on Foxp3 expression. This study reveals that Foxo factors promote transcription of the Foxp3 gene in induced T reg cells, and thus provides new mechanistic insight into Foxo-mediated T cell regulation.
引用
收藏
页码:1381 / 1391
页数:11
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