The BTB-ZF Family of Transcription Factors: Key Regulators of Lineage Commitment and Effector Function Development in the Immune System

被引:74
作者
Beaulieu, Aimee M. [1 ]
Sant'Angelo, Derek B. [1 ,2 ,3 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Program Immunol, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc Ctr, Louis V Gerstner Jr Grad Sch Biomed Sci, New York, NY 10065 USA
[3] Cornell Univ, Weill Cornell Grad Sch Med Sci, New York, NY 10065 USA
基金
美国国家卫生研究院;
关键词
ZINC-FINGER PROTEIN; CD4(+) T-CELLS; GERMINAL-CENTER FORMATION; CORNEAL ENDOTHELIAL-CELLS; MEMORY B-CELLS; BTB/POZ DOMAIN; IN-VIVO; LYMPHOCYTE DIFFERENTIATION; REPRESSES TRANSCRIPTION; POSITIVE SELECTION;
D O I
10.4049/jimmunol.1004006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Successful immunity depends upon the activity of multiple cell types. Commitment of pluripotent precursor cells to specific lineages, such as T or B cells, is obviously fundamental to this process. However, it is also becoming clear that continued differentiation and specialization of lymphoid cells is equally important for immune system integrity. Several members of the BTB-ZF family have emerged as critical factors that control development of specific lineages and also of specific effector subsets within these lineages. For example, BTB-ZF genes have been shown to control T cell versus B cell commitment and CD4 versus CD8 lineage commitment. Others, such as PLZF for NKT cells and Bcl-6 for T follicular helper cells, are necessary for the acquisition of effector functions. In this review, we summarize current findings concerning the BTB-ZF family members with a reported role in the immune system. The Journal of Immunology, 2011, 187: 2841-2847.
引用
收藏
页码:2841 / 2847
页数:7
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