TCF-1: a maverick in T cell development and function

被引:44
作者
Gounari, Fotini [1 ,2 ]
Khazaie, Khashayarsha [2 ]
机构
[1] Univ Chicago, Dept Med, Knapp Res Ctr, Sect Rheumatol, 5841 S Maryland Ave, Chicago, IL 60637 USA
[2] Mayo Clin, Dept Immunol, Scottsdale, AZ 85259 USA
基金
美国国家卫生研究院;
关键词
EDGE BETA-CATENIN; TRANSCRIPTION FACTORS; HMG DOMAIN; FACTOR-I; DIFFERENTIATION; EFFECTOR; LINEAGE; LEF-1; SPECIFICATION; CHROMATIN;
D O I
10.1038/s41590-022-01194-2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The T cell-specific DNA-binding protein TCF-1 is a central regulator of T cell development and function along multiple stages and lineages. Because it interacts with beta-catenin, TCF-1 has been classically viewed as a downstream effector of canonical Wnt signaling, although there is strong evidence for beta-catenin-independent TCF-1 functions. TCF-1 co-binds accessible regulatory regions containing or lacking its conserved motif and cooperates with other nuclear factors to establish context-dependent epigenetic and transcription programs that are essential for T cell development and for regulating immune responses to infection, autoimmunity and cancer. Although it has mostly been associated with positive regulation of chromatin accessibility and gene expression, TCF-1 has the potential to reduce chromatin accessibility and thereby suppress gene expression. In addition, the binding of TCF-1 bends the DNA and affects the chromatin conformation genome wide. This Review discusses the current understanding of the multiple roles of TCF-1 in T cell development and function and their mechanistic underpinnings. The transcription factor TCF-1 has multiple roles during T cell development and in mature T cells. Gounari and Khazaie review the potential mechanisms by which TCF-1 regulates gene expression.
引用
收藏
页码:671 / 678
页数:8
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