Chromatin remodeling and T helper subset differentiation

被引:0
|
作者
Miyatake, S
Arai, N
Arai, K
机构
[1] Univ Tokyo, Inst Med Sci, Dept Mol & Dev Biol, CREST,Minato Ku, Tokyo 1088639, Japan
[2] DNAX Res Inst Molec & Cellular Biol Inc, Dept Immunobiol, Palo Alto, CA 94304 USA
关键词
GATA3; IL-4; IL-5; IL-13; STAT6; T helper subset; Th2;
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The T helper subsets Th1 and Th2 regulate specific types of immune responses by producing distinct sets of cytokines. Differentiation of the T helper subsets from their common precursors, naive CD4+ T cells, is induced by antigen stimulation and controlled by various other conditions. Of these conditions, the contributions of the cytokine environment have been the best characterized. The presence of interleukin-4 (IL-4) directs the differentiation ton ards Th2 cells, whereas IL-12 induces Th1 differentiation. The Th2 signature cytokine genes encoding IL-4, IL-13, and IL-5 are clustered, and noncoding regions such as the intergenic region of the IL-4 and IL-13 genes are highly conserved from mice to humans, Alteration of the chromatin structure of this Th2 cytokine cluster region is detected as nuclease-accessible regions specific to Th2 cells, Activation of STAT6 promotes Th2 differentiation by inducing Th2-specific transcription factors, including GATA3, Expression of GATA3 induces Th2 differentiation and enhances the Th2 cell-specific chromatin accessibility, indicating that GATA3 is a key protein that regulates differentiation through chromatin remodeling, T helper subset differentiation provides a good system to study gene expression regulation at the chromatin level.
引用
收藏
页码:473 / 478
页数:6
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