FOXP3 and RORγt: Transcriptional regulation of Treg and Th17

被引：128

作者：

Chen, Zuojia ^{[1
]}

Lin, Fang ^{[1
]}

Gao, Yayi ^{[1
]}

Li, Zhiyuan ^{[1
]}

Zhang, Jing ^{[1
]}

Xing, Yue ^{[1
]}

Deng, Zihou ^{[1
]}

Yao, Zhengju ^{[1
]}

Tsun, Andy ^{[1
]}

Li, Bin ^{[1
]}

机构：

[1] Chinese Acad Sci, Inst Pasteur Shanghai, Shanghai Inst Biol Sci, Key Lab Mol Virol & Immunol, Shanghai 200025, Peoples R China

来源：

INTERNATIONAL IMMUNOPHARMACOLOGY | 2011年 / 11卷 / 05期

关键词：

FOXP3; ROR gamma t; Regulatory T cell; T helper 17 cell; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; TGF-BETA; CELL-DIFFERENTIATION; GENE-EXPRESSION; HELPER-CELLS; LINEAGE DIFFERENTIATION; REG-CELLS; IN-VIVO; GENERATION; RESPONSES;

D O I：

10.1016/j.intimp.2010.11.008

中图分类号：

R392 [医学免疫学]; Q939.91 [免疫学];

学科分类号：

100102 ;

摘要：

FOXP3(+)CD4(+)CD25 Regulatory T (Treg) cells and IL-17 producing helper T cells (Th17) are critical subsets of T cells which play essential roles in immune homeostasis. The Forkhead family transcription factor FOXP3 is predominantly expressed in Treg cells, where the FOXP3 ensemble is essential for Treg cell development and function. As FOXP3 is to Treg cells, the orphan retinoic acid nuclear receptor (ROR) family transcription factor ROR gamma t is essential for Th17 development and function. In this review, we summarize recent progress of our understanding towards the molecular mechanisms underlying the differentiation and function of FOXP3(+) Treg cells and ROR gamma t expressing Th17 cells. These may provide new insights into therapeutic intervention and targeting of human immune-deficient diseases. (C) 2010 Elsevier B.V. All rights reserved.

引用

收藏

页码：536 / 542

页数：7

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