Metabolite-sensing receptors GPR43 and GPR109A facilitate dietary fibre-induced gut homeostasis through regulation of the inflammasome

Laurence Macia(Monash University), Jian Tan(Monash University), Angélica T. Vieira(Monash University), Katie Leach(Monash University), Dragana Stanley(Australian Centre for Disease Preparedness), Suzanne Luong(Monash University), Mikako Maruya(RIKEN Center for Integrative Medical Sciences), Craig I. McKenzie(Monash University), Atsushi Hijikata(RIKEN Center for Integrative Medical Sciences), Connie H. Y. Wong(Monash University), Lauren C. Binge(Monash University), Alison N. Thorburn(Monash University), Nina Chevalier(Monash University), Caroline Ang(Monash University), Eliana Mariño(Monash University), R. Robert(Monash University), Stefan Offermanns(Max Planck Society), Mauro Martins Teixeira(Universidade Federal de Minas Gerais), Robert J. Moore(Commonwealth Scientific and Industrial Research Organisation), Richard A. Flavell(Howard Hughes Medical Institute), Sidonia Fagarasan(RIKEN Center for Integrative Medical Sciences), Charles R. Mackay(Monash University)
Nature Communications
April 1, 2015
Cited by 1,401Open Access
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Abstract

Diet and the gut microbiota may underpin numerous human diseases. A major metabolic product of commensal bacteria are short-chain fatty acids (SCFAs) that derive from fermentation of dietary fibre. Here we show that diets deficient or low in fibre exacerbate colitis development, while very high intake of dietary fibre or the SCFA acetate protects against colitis. SCFAs binding to the ‘metabolite-sensing’ receptors GPR43 and GPR109A in non-haematopoietic cells mediate these protective effects. The inflammasome pathway has hitherto been reported as a principal pathway promoting gut epithelial integrity. SCFAs binding to GPR43 on colonic epithelial cells stimulates K+ efflux and hyperpolarization, which lead to NLRP3 inflammasome activation. Dietary fibre also shapes gut bacterial ecology, resulting in bacterial species that are more effective for inflammasome activation. SCFAs and metabolite receptors thus explain health benefits of dietary fibre, and how metabolite signals feed through to a major pathway for gut homeostasis. Dietary fibre is metabolized into short-chain fatty acids by gut bacteria. Here the authors show that these metabolites activate the NLRP3 inflammasome in gut epithelial cells and protect mice from injury-induced colitis, suggesting a mechanism for the benefits of a high-fibre diet.


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