RUNX proteins in transcription factor networks that regulate T-cell lineage choice

被引:184
作者
Collins, Amelie [1 ]
Littman, Dan R. [1 ]
Taniuchi, Ichiro [2 ]
机构
[1] NYU, Sch Med, Howard Hughes Med Inst, Kimmel Ctr Biol & Med,Skirball Inst Biomol Med, New York, NY 10016 USA
[2] RIKEN, Res Ctr Allergy & Immunol, Lab Transcript Regulat, Turumi Ku, Kanagawa 2300045, Japan
关键词
ROR-GAMMA-T; FETAL LIVER HEMATOPOIESIS; HELPER TYPE-1 CELLS; CORE BINDING-FACTOR; GENE-EXPRESSION; OSTEOBLAST DIFFERENTIATION; LYMPHOCYTE DEVELOPMENT; DEVELOPING THYMOCYTES; STOCHASTIC MECHANISM; POSITIVE SELECTION;
D O I
10.1038/nri2489
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Recent research has uncovered complex transcription factor networks that control the processes of T-cell development and differentiation. RUNX (runt-related transcription factor) proteins are among the many factors that have crucial roles in these networks. In this Review, we examine the mechanisms by which RUNX complexes act together with other transcription factors, such as Th-POK (T-helper-inducing POZ/Kruppel-like factor) and GATA-binding protein 3 (GATA3) in determining the CD4/CD8 lineage choice of developing thymocytes. In addition, we discuss evidence indicating that RUNX complexes are also involved in the differentiation of effector T-cell subsets and that the molecular mechanisms by which RUNX proteins regulate T-cell fate decisions are conserved between the thymus and periphery.
引用
收藏
页码:106 / 115
页数:10
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