Deciphering the epigenetic code of T lymphocytes

被引:13
作者
Allan, Rhys S. [1 ,2 ]
Nutt, Stephen L. [1 ,2 ]
机构
[1] Walter & Eliza Hall Inst Med Res, Parkville, Vic 3052, Australia
[2] Univ Melbourne, Dept Med Biol, Parkville, Vic 3052, Australia
基金
英国医学研究理事会; 澳大利亚研究理事会;
关键词
histone modification; T cell; gene expression; epigenetic; HISTONE H3; CELL-DIFFERENTIATION; LYSINE; 9; CHROMATIN-STRUCTURE; ACTIVE CHROMATIN; GENE-EXPRESSION; CYTOKINE GENES; PERICENTRIC HETEROCHROMATIN; CONDITIONAL DELETION; AIRWAY INFLAMMATION;
D O I
10.1111/imr.12207
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The multiple lineages and differentiation states that constitute the T-cell compartment all derive from a common thymic precursor. These distinct transcriptional states are maintained both in time and after multiple rounds of cell division by the concerted actions of a small set of lineage-defining transcription factors that act in conjunction with a suite of chromatin-modifying enzymes to activate, repress, and fine-tune gene expression. These chromatin modifications collectively provide an epigenetic code that allows the stable and heritable maintenance of the T-cell phenotype. Recently, it has become apparent that the epigenetic code represents a therapeutic target for a variety of immune cell disorders, including lymphoma and acute and chronic inflammatory diseases. Here, we review the recent advances in epigenetic regulation of gene expression, particularly as it relates to the T-cell differentiation and function.
引用
收藏
页码:50 / 61
页数:12
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