An updated view on transcription factor GATA3-mediated regulation of Th1 and Th2 cell differentiation

被引:189
|
作者
Yagi, Ryoji [1 ]
Zhu, Jinfang [1 ]
Paul, William E. [1 ]
机构
[1] NIAID, Immunol Lab, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
cytokine; epigenetic modification; gene regulation; LOCUS-CONTROL REGION; CD4(+) T-CELLS; RANGE INTRACHROMOSOMAL INTERACTIONS; CYTOKINE GENE-CLUSTER; IFN-GAMMA PRODUCTION; DEVELOPING TH1 CELLS; LINEAGE COMMITMENT; FACTOR GATA-3; TH2-SPECIFIC EXPRESSION; CUTTING EDGE;
D O I
10.1093/intimm/dxr029
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD4 T-h are critical for orchestrating adaptive immune responses. The expression of the transcription factor GATA3 (GATA-binding protein 3) is up-regulated or down-regulated during T(h)2 or T(h)1 cell differentiation, respectively. Furthermore, GATA3 is responsible for induction of T(h)2 differentiation and represses T(h)1 differentiation. In this review, we present an updated view on the molecular mechanisms through which GATA3 regulates T(h)1/T(h)2 differentiation. During T(h)2 cell differentiation, GATA3 directly binds to the T(h)2 cytokine gene locus at several regions and regulates expression. On the other hand, GATA3 inhibits T(h)1 cell differentiation by preventing up-regulation of IL-12 receptor beta 2 and STAT4 (signal transducer and activator of transcription 4) and neutralization of Runx3 (runt-related transcription factor 3) function through protein-protein interaction. GATA3 may also directly act on the Ifng gene. In summary, GATA3 serves as a transcriptional activator or repressor through direct action on transcriptional machinery and/or affecting chromatin remodeling at many critical loci encoding cytokines, cytokine receptors, signaling molecules as well as transcription factors that are involved in the regulation of T(h)1 and T(h)2 differentiation.
引用
收藏
页码:415 / 420
页数:6
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