The gut microbiota regulates white adipose tissue inflammation and obesity via a family of microRNAs

肠道菌群 白色脂肪组织 脂肪组织 生物 炎症 小RNA 内科学 肥胖 免疫学 医学 生物信息学 遗传学 基因
作者
Anthony Virtue,Sam J. McCright,Jasmine M. Wright,Monica T. Jimenez,Walter K. Mowel,Jonathan J. Kotzin,Leonel Joannas,Megha Basavappa,Sean P. Spencer,Megan L. Clark,Stephen Eisennagel,Adam Williams,Maayan Levy,Sasikanth Manne,Sarah E. Henrickson,E. John Wherry,Christoph A. Thaiss,Eran Elinav,Jorge Henao-Mejía
出处
期刊:Science Translational Medicine [American Association for the Advancement of Science]
卷期号:11 (496) 被引量:270
标识
DOI:10.1126/scitranslmed.aav1892
摘要

The gut microbiota is a key environmental determinant of mammalian metabolism. Regulation of white adipose tissue (WAT) by the gut microbiota is a process critical to maintaining metabolic fitness, and gut dysbiosis can contribute to the development of obesity and insulin resistance (IR). However, how the gut microbiota regulates WAT function remains largely unknown. Here, we show that tryptophan-derived metabolites produced by the gut microbiota controlled the expression of the miR-181 family in white adipocytes in mice to regulate energy expenditure and insulin sensitivity. Moreover, dysregulation of the gut microbiota-miR-181 axis was required for the development of obesity, IR, and WAT inflammation in mice. Our results indicate that regulation of miR-181 in WAT by gut microbiota-derived metabolites is a central mechanism by which host metabolism is tuned in response to dietary and environmental changes. As we also found that MIR-181 expression in WAT and the plasma abundance of tryptophan-derived metabolites were dysregulated in a cohort of obese human children, the MIR-181 family may represent a potential therapeutic target to modulate WAT function in the context of obesity.
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