FOXP3型
RAR相关孤儿受体γ
孤儿受体
转录因子
白细胞介素2受体
免疫系统
维甲酸
生物
Treg细胞
免疫学
细胞生物学
调节性T细胞
T细胞
癌症研究
遗传学
基因
作者
Zuojia Chen,Fang Lin,Yayi Gao,Zhiyuan Li,Jing Zhang,Yue Xing,Zongwu Deng,Zhengju Yao,Andy Tsun,Bin Li
标识
DOI:10.1016/j.intimp.2010.11.008
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 RORγt 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 RORγt expressing Th17 cells. These may provide new insights into therapeutic intervention and targeting of human immune-deficient diseases.
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