生物
细胞生物学
CD8型
免疫系统
染色质免疫沉淀
T细胞
转录调控
染色质
祖细胞
免疫学
转录因子
基因
干细胞
基因表达
遗传学
发起人
作者
Xueyang Bao,Yingyu Qin,Linrong Lu,Mingzhu Zheng
标识
DOI:10.3389/fimmu.2022.884569
摘要
T-lymphocytes play crucial roles for maintaining immune homeostasis by fighting against various pathogenic microorganisms and establishing self-antigen tolerance. They will go through several stages and checkpoints in the thymus from progenitors to mature T cells, from CD4-CD8- double negative (DN) cells to CD4+CD8+ double positive (DP) cells, finally become CD4+ or CD8+ single positive (SP) cells. The mature SP cells then emigrate out of the thymus and further differentiate into distinct subsets under different environment signals to perform specific functions. Each step is regulated by various transcriptional regulators downstream of T cell receptors (TCRs) that have been extensively studied both in vivo and vitro via multiple mouse models and advanced techniques, such as single cell RNA sequencing (scRNA-seq) and Chromatin Immunoprecipitation sequencing (ChIP-seq). This review will summarize the transcriptional regulators participating in the early stage of T cell development reported in the past decade, trying to figure out cascade networks in each process and provide possible research directions in the future.
科研通智能强力驱动
Strongly Powered by AbleSci AI