One genome, many cell states: epigenetic control of innate immunity

被引:8
|
作者
Fraschilla, Isabella [1 ,2 ,3 ,4 ]
Amatullah, Hajera [1 ,2 ,3 ]
Jeffrey, Kate L. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Massachusetts Gen Hosp, Div Gastroenterol, Boston, MA 02114 USA
[2] Massachusetts Gen Hosp, Ctr Study Inflammatory Bowel Dis, Dept Med, Boston, MA 02114 USA
[3] Harvard Med Sch, Boston, MA 02115 USA
[4] Harvard Med Sch, Program Immunol, Boston, MA 02115 USA
[5] MIT, Ctr Microbiome Informat & Therapeut, Cambridge, MA 02139 USA
基金
加拿大健康研究院;
关键词
B KINASE-ALPHA; WIDE ASSOCIATION; GENE-EXPRESSION; REGULATORY ELEMENTS; SUSCEPTIBILITY LOCI; CHROMATIN; TRANSCRIPTION; RNA; DISEASE; REVEALS;
D O I
10.1016/j.coi.2022.102173
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A hallmark of the innate immune system is its ability to rapidly initiate short-lived or sustained transcriptional programs in a cell-specific and pathogen-specific manner that is dependent on dynamic chromatin states. Much of the epigenetic landscape is set during cellular differentiation; however, pathogens and other environmental cues also induce changes in chromatin that can either promote tolerance or 'train' innate immune cells for amplified secondary responses. We review chromatin processes that enable innate immune cell differentiation and functional transcriptional responses in naive or experienced cells, in concert with signal transduction and cellular metabolic shifts. We discuss how immune chromatin mechanisms are maladapted in disease and novel therapeutic approaches for cellular reprogramming.
引用
收藏
页数:14
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