Host-microbiota interactions: epigenomic regulation

被引:65
|
作者
Woo, Vivienne
Alenghat, Theresa [1 ]
机构
[1] Cincinnati Childrens Hosp Med Ctr, Div Immunobiol, Cincinnati, OH 45229 USA
基金
美国国家卫生研究院;
关键词
CHAIN FATTY-ACIDS; INNATE LYMPHOID-CELLS; INTESTINAL EPITHELIAL-CELLS; GUT MICROBIOTA; COMMENSAL-BACTERIA; METABOLITE BUTYRATE; DNA METHYLATION; INFLAMMATORY RESPONSES; EPIGENETIC REGULATION; HISTONE DEACETYLASES;
D O I
10.1016/j.coi.2016.12.001
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 coevolution of mammalian hosts and their commensal microbiota has led to the development of complex symbiotic relationships between resident microbes and mammalian cells. Epigenomic modifications enable host cells to alter gene expression without modifying the genetic code, and therefore represent potent mechanisms by which mammalian cells can transcriptionally respond, transiently or stably, to environmental cues. Advances in genome-wide approaches are accelerating our appreciation of microbial influences on host physiology, and increasing evidence highlights that epigenomics represent a level of regulation by which the host integrates and responds to microbial signals. In particular, bacterial-derived short chain fatty acids have emerged as one clear link between how the microbiota intersects with host epigenomic pathways. Here we review recent findings describing crosstalk between the microbiota and epigenomic pathways in multiple mammalian cell populations. Further, we discuss interesting links that suggest that the scope of our understanding of epigenomic regulation in the host-microbiota relationship is still in its infancy.
引用
收藏
页码:52 / 60
页数:9
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