T-bet employs diverse regulatory mechanisms to repress transcription

被引:46
作者
Oestreich, Kenneth J. [1 ]
Weinmann, Amy S. [1 ]
机构
[1] Univ Washington, Dept Immunol, Seattle, WA 98195 USA
关键词
INTERFERON-GAMMA; CELL-DIFFERENTIATION; GENE-EXPRESSION; BCL-6; CD4; EFFECTOR; ACTIVATION; RESPONSES; REQUIRES; BLIMP-1;
D O I
10.1016/j.it.2011.10.005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Lineage-defining transcription factors are responsible for activating the signature genes required for a given cell fate. They are also needed to repress the genetic programs associated with alternative lineage decisions. The T-box transcription factor T-bet is required for CD4(+) T helper 1 (Th1) cell differentiation. Numerous studies have explored the mechanisms by which T-bet activates the Th1 gene profile, but until recently not much was known about the mechanisms that T-bet utilizes to negatively regulate alternative T helper cell differentiation pathways such as the Th2 and Th17 fates. Here, we discuss new advances in the field that highlight the diverse mechanisms that T-bet employs to antagonize the gene programs for alternative T helper cell fates.
引用
收藏
页码:78 / 83
页数:6
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