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

被引:253
作者
Virtue, Anthony T. [1 ,2 ,11 ]
McCright, Sam J. [1 ,2 ]
Wright, Jasmine M. [1 ,2 ]
Jimenez, Monica T. [1 ,2 ]
Mowel, Walter K. [1 ,2 ]
Kotzin, Jonathan J. [1 ,2 ]
Joannas, Leonel [1 ,2 ]
Basavappa, Megha G. [1 ,2 ,3 ]
Spencer, Sean P. [1 ,2 ]
Clark, Megan L. [1 ,2 ]
Eisennagel, Stephen H. [4 ]
Williams, Adam [5 ]
Levy, Maayan [2 ,3 ,6 ]
Manne, Sasikanth [7 ]
Henrickson, Sarah E. [2 ,8 ]
Wherry, E. John [2 ,7 ,9 ]
Thaiss, Christoph A. [2 ,3 ,6 ]
Elinav, Eran [6 ]
Henao-Mejia, Jorge [1 ,2 ,10 ]
机构
[1] Univ Penn, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Inst Immunol, Perelman Sch Med, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Microbiol, Philadelphia, PA 19104 USA
[4] GlaxoSmithKline, Core DMPK, Collegeville, PA 19426 USA
[5] Univ Connecticut, Ctr Hlth, Jackson Lab Genom Med, Dept Genet & Genome Sci, Farmington, CT 06032 USA
[6] Weizmann Inst Sci, Dept Immunol, Rehovot, Israel
[7] Perelman Sch Med, Dept Syst Pharmacol & Translat Therapeut, Philadelphia, PA 19104 USA
[8] Childrens Hosp Philadelphia, Div Allergy Immunol, Philadelphia, PA 19104 USA
[9] Univ Penn, Parker Inst Canc Immunotherapy, Perelman Sch Med, Philadelphia, PA 19104 USA
[10] Univ Penn, Childrens Hosp Philadelphia, Div Protect Immun, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[11] GlaxoSmithKline, Target Incubator DPU, Collegeville, PA 19426 USA
关键词
INSULIN-RESISTANCE; GENE-EXPRESSION; METABOLOMIC ANALYSIS; FAT; COMPLEMENTARY; EOSINOPHILS; MACROPHAGES; MODULATE; REVEALS;
D O I
10.1126/scitranslmed.aav1892
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
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.
引用
收藏
页数:13
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