表观遗传学
生物
细胞分化
DNA甲基化
细胞毒性T细胞
CD8型
组蛋白
效应器
神经发生的表观遗传调控
细胞生物学
T细胞
免疫学
遗传学
免疫系统
基因表达
DNA
组蛋白甲基转移酶
基因
体外
作者
Avik Dutta,Harini Venkataganesh,Paul E. Love
出处
期刊:Cells
[Multidisciplinary Digital Publishing Institute]
日期:2021-12-08
卷期号:10 (12): 3459-3459
被引量:38
标识
DOI:10.3390/cells10123459
摘要
Immature CD4− CD8− thymocytes progress through several developmental steps in the thymus, ultimately emerging as mature CD4+ (helper) or CD8+ (cytotoxic) T cells. Activation of naïve CD4+ and CD8+ T cells in the presence of specific cytokines results in the induction of transcriptional programs that result in their differentiation into effector or memory cells and in the case of CD4+ T cells, the adoption of distinct T-helper fates. Previous studies have shown that histone modification and DNA methylation play important roles in each of these events. More recently, the roles of specific epigenetic regulators in T cell differentiation have been clarified. The identification of the epigenetic modifications and modifiers that control mature T cell differentiation and specification has also provided further insights into how dysregulation of these processes can lead to cancer or autoimmune diseases. In this review, we summarize recent findings that have provided new insights into epigenetic regulation of T cell differentiation in both mice and humans.
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