Wang Chao, Collins Mary, Kuchroo Vijay K
Evergrande Center for Immunological Diseases, Harvard Medical School, Brigham and Women's Hospital, 77 Avenue Louis Pasteur, Boston, MA 02115, USA.
Evergrande Center for Immunological Diseases, Harvard Medical School, Brigham and Women's Hospital, 77 Avenue Louis Pasteur, Boston, MA 02115, USA.
Curr Opin Immunol. 2015 Dec;37:6-10. doi: 10.1016/j.coi.2015.08.001. Epub 2015 Aug 27.
Effector CD4 T cell lineages have been implicated as potent inducers of autoimmune diseases. Tbet, Gata3 and Rorgt are master transcriptional regulators of Th1, Th2 and Th17 lineages respectively and promote the distinct expression of signature cytokines. Significant progress has been made in understanding the transcriptional network that drives CD4 T cell differentiation, revealing novel points of regulation mediated by transcription factors, cell surface receptors, cytokines and chemokines. Epigenetic modifications and metabolic mediators define the transcriptional landscape in which master transcription factors operate and collaborate with a network of transcriptional modifiers to guide lineage specification, plasticity and function.
效应性CD4 T细胞谱系被认为是自身免疫性疾病的强效诱导因子。Tbet、Gata3和Rorgt分别是Th1、Th2和Th17谱系的主要转录调节因子,并促进特征性细胞因子的不同表达。在理解驱动CD4 T细胞分化的转录网络方面已经取得了重大进展,揭示了由转录因子、细胞表面受体、细胞因子和趋化因子介导的新的调控点。表观遗传修饰和代谢介质定义了主要转录因子发挥作用并与转录修饰因子网络协作以指导谱系特化、可塑性和功能的转录格局。