@article{3fd6b61cf0194ac299cedaea923d39a1,
title = "The gut microbiota regulates white adipose tissue inflammation and obesity via a family of microRNAs",
abstract = "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.",
author = "Virtue, {Anthony T.} and McCright, {Sam J.} and Wright, {Jasmine M.} and Jimenez, {Monica T.} and Mowel, {Walter K.} and Kotzin, {Jonathan J.} and Leonel Joannas and Basavappa, {Megha G.} and Spencer, {Sean P.} and Clark, {Megan L.} and Eisennagel, {Stephen H.} and Adam Williams and Maayan Levy and Sasikanth Manne and Henrickson, {Sarah E.} and Wherry, {E. John} and Thaiss, {Christoph A.} and Eran Elinav and Jorge Henao-Mejia",
note = "We thank the University of Pennsylvania DRC and J. Baur for the use of the Mouse Phenotyping, Physiology and Metabolism Core. We thank M. Tordoff of the Monell Chemical Senses Center for providing access to Buker LF50 minispec. We also thank the DRC Metabolomics Core. Funding: The work in this manuscript was supported by funds from CHOP, University of Pennsylvania IFI and IDOM pilot projects, NIH (grants R21AI128060, R21DK111755, and R01HL136572), the PEW Biomedical Scholars Award, and the Burroughs Wellcome Fund Investigator in the Pathogenesis of Infectious Diseases Award (to J.H.-M.); NIH T32AI070077-09 (to M.T.J.); NIH T32AI055428 and F31AI124538 (to W.K.M.); NIH T32DK007780 and F30HL138739 (to J.J.K.); NIH F30DK094708 (to S.P.S.); AI105343, AI108545, AI117950, AI082630, and CA210944 (to E.J.W.; E.J.W. is a member of the Parker Institute for Cancer Immunotherapy, which supported the University of Pennsylvania Cancer Immunotherapy Program); and NIH 5K12HD043245 and T32-HD043021, Pennsylvania Allergy Education Research Fund, and the University of Pennsylvania DRC (Pilot Grant) (to S.E.H.).",
year = "2019",
month = jun,
day = "12",
doi = "10.1126/scitranslmed.aav1892",
language = "الإنجليزيّة",
volume = "11",
journal = "Science Translational Medicine",
issn = "1946-6234",
publisher = "American Association for the Advancement of Science",
number = "496",
}