Cytokines, Transcription Factors, and the Initiation of T-Cell Development

被引:52
|
作者
Hosokawa, Hiroyuki [1 ]
Rothenberg, Ellen, V [1 ]
机构
[1] CALTECH, Div Biol & Biol Engn, Pasadena, CA 91125 USA
来源
关键词
INNATE LYMPHOID-CELLS; SEVERE COMBINED IMMUNODEFICIENCY; EARLIEST THYMIC PROGENITORS; GENE REGULATORY NETWORK; STAGE-SPECIFIC MANNER; ADULT-MOUSE THYMUS; LINEAGE COMMITMENT; BETA-SELECTION; B-CELL; HEMATOPOIETIC PROGENITORS;
D O I
10.1101/cshperspect.a028621
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Multipotent blood progenitor cells migrate into the thymus and initiate the T-cell differentiation program. T-cell progenitor cells gradually acquire T-cell characteristics while shedding their multipotentiality for alternative fates. This process is supported by extracellular signaling molecules, including Notch ligands and cytokines, provided by the thymic microenvironment. T-cell development is associated with dynamic change of gene regulatory networks of transcription factors, which interact with these environmental signals. Together with Notch or pre-T-cell-receptor (TCR) signaling, cytokines always control proliferation, survival, and differentiation of early T cells, but little is known regarding their cross talk with transcription factors. However, recent results suggest ways that cytokines expressed in distinct intrathymic niches can specifically modulate key transcription factors. This review discusses how stage-specific roles of cytokines and transcription factors can jointly guide development of early T cells.
引用
收藏
页数:19
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