共 42 条
T-bet employs diverse regulatory mechanisms to repress transcription
被引:46
作者:

Oestreich, Kenneth J.
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h-index: 0
机构:
Univ Washington, Dept Immunol, Seattle, WA 98195 USA Univ Washington, Dept Immunol, Seattle, WA 98195 USA

Weinmann, Amy S.
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h-index: 0
机构:
Univ Washington, Dept Immunol, Seattle, WA 98195 USA Univ Washington, Dept Immunol, Seattle, WA 98195 USA
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.
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收藏
页码:78 / 83
页数:6
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