IL-2 and IL-15 dependent thymic development of Foxp3-expressing regulatory T lymphocytes

被引:33
|
作者
Apert, Cecile [1 ]
Romagnoli, Paola [1 ]
van Meerwijk, Joost P. M. [1 ]
机构
[1] Univ Toulouse, CPTP, CNRS, INSERM,UPS, Toulouse, France
关键词
regulatory T cells; thymus; differentiation; IL-2; IL-15; CELL-DEVELOPMENT; POSITIVE SELECTION; EPITHELIAL-CELLS; FOXP3; EXPRESSION; NEGATIVE SELECTION; CENTRAL TOLERANCE; GENE-EXPRESSION; DENDRITIC CELLS; SELF-ANTIGEN; DEVELOPING THYMOCYTES;
D O I
10.1007/s13238-017-0425-3
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Immunosuppressive regulatory T lymphocytes (Treg) expressing the transcription factor Foxp3 play a vital role in the maintenance of tolerance of the immune-system to self and innocuous non-self. Most Treg that are critical for the maintenance of tolerance to self, develop as an independent T-cell lineage from common T cell precursors in the thymus. In this organ, their differentiation requires signals from the T cell receptor for antigen, from co-stimulatory molecules, as well as from cytokine-receptors. Here we focus on the cytokines implicated in thymic development of Treg, with a particular emphasis on the roles of interleukin-2 (IL-2) and IL-15. The more recently appreciated involvement of TGF-beta in thymic Treg development is also briefly discussed. Finally, we discuss how cytokine-dependence of Treg development allows for temporal, quantitative, and potentially qualitative modulation of this process.
引用
收藏
页码:322 / 332
页数:11
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