van Nieuwenhuijze Annemarie, Liston Adrian
Translational Immunology Laboratory, VIB, Leuven, Belgium; Department of Microbiology and Immunology, University of Leuven, Leuven, Belgium.
Translational Immunology Laboratory, VIB, Leuven, Belgium; Department of Microbiology and Immunology, University of Leuven, Leuven, Belgium.
Prog Mol Biol Transl Sci. 2015;136:69-97. doi: 10.1016/bs.pmbts.2015.09.001. Epub 2015 Oct 9.
Regulatory T cells (Tregs) are characterized by the expression of the master transcription factor forkhead box P3 (Foxp3). Although Foxp3 expression is widely used as a marker of the Treg lineage, recent data show that the Treg fate is determined by a multifactorial signaling pathway, involving cytokines, nuclear factors, and epigenetic modifications. Foxp3 expression and the Treg phenotype can be acquired by T cells in the periphery, illustrating that the Treg fate is not necessarily conferred during thymic development. The two main Treg populations in vivo, thymic Tregs and peripheral Tregs, differ in the pathways followed for their maturation. This chapter discusses the molecular control of Treg induction, in the thymus as well as the periphery.
调节性T细胞(Tregs)的特征是表达主要转录因子叉头框P3(Foxp3)。尽管Foxp3表达被广泛用作Treg谱系的标志物,但最近的数据表明,Treg命运是由多因素信号通路决定的,涉及细胞因子、核因子和表观遗传修饰。外周T细胞可获得Foxp3表达和Treg表型,这表明Treg命运不一定在胸腺发育过程中赋予。体内的两个主要Treg群体,即胸腺Tregs和外周Tregs,在成熟所遵循的途径上有所不同。本章讨论胸腺和外周中Treg诱导的分子控制。