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The gut microbiota regulates white adipose tissue inflammation and obesity via a family of microRNAs
- Source :
- Science Translational Medicine
- Publication Year :
- 2018
-
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, we show that 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.
- Subjects :
- 0301 basic medicine
Male
medicine.medical_specialty
Context (language use)
Inflammation
White adipose tissue
Gut flora
digestive system
Article
03 medical and health sciences
Mice
0302 clinical medicine
Insulin resistance
Internal medicine
microRNA
medicine
Adipocytes
Animals
Obesity
2. Zero hunger
biology
Tryptophan
food and beverages
General Medicine
biology.organism_classification
medicine.disease
Gastrointestinal Microbiome
MicroRNAs
030104 developmental biology
Endocrinology
030220 oncology & carcinogenesis
medicine.symptom
Insulin Resistance
Energy Metabolism
Function (biology)
Subjects
Details
- ISSN :
- 19466242
- Volume :
- 11
- Issue :
- 496
- Database :
- OpenAIRE
- Journal :
- Science translational medicine
- Accession number :
- edsair.doi.dedup.....675688a9c5c9d86a5712adda2cf50bee