The molecular mechanisms of Foxp3 gene regulation

被引:63
|
作者
Maruyama, Takashi [1 ]
Konkel, Joanne E. [1 ]
Zamarron, Brian F. [1 ]
Chen, WanJun [1 ]
机构
[1] Natl Inst Dent & Craniofacial Res, Mucosal Immunol Sect, OIIB, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
Foxp3; CD4(+) T cells; TGF-beta; Id3; E2A; GATA3; c-Rel; T-CELL DEVELOPMENT; TRANSCRIPTION FACTOR FOXP3; TGF-BETA; EXPRESSION; DIFFERENTIATION; INDUCTION; RECEPTOR; BINDING; T(H)17; SMAD3;
D O I
10.1016/j.smim.2011.06.005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Induction of Foxp3 gene expression and acquisition of regulatory T cell fate is, understandably, a highly controlled process and one which many investigators want to illuminate. In studying the regulation of Foxp3 gene expression, several conserved non-coding regions have been identified and the role of various transcription factors at these sites has been explored. What emerges is that many factors, some positive, some negative, interact to collectively drive Foxp3 gene expression and then maintain its expression in Foxp3(+) regulatory T cells. TCR signaling is imperative for Foxp3 gene expression and TGF-beta is a key cytokine for initiating Foxp3 gene expression in naive T cells. But other signaling pathways are also known to play a role in properly orchestrating Foxp3 gene expression and regulatory T cell expansion. Here we review the recent progress in understanding the complex molecular events that drive Foxp3 gene expression and allow functional regulatory T cells to develop. Published by Elsevier Ltd.
引用
收藏
页码:418 / 423
页数:6
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