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

机译:代谢物敏感受体GPR43和GPR109A通过调节炎症小体促进膳食纤维诱导的肠道稳态

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摘要

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.
机译:饮食和肠道菌群可能是许多人类疾病的基础。共生细菌的主要代谢产物是来源于膳食纤维发酵的短链脂肪酸(SCFA)。在这里,我们表明缺乏或低纤维的饮食会加剧结肠炎的发展,而高膳食纤维或SCFA乙酸盐的摄入可以预防结肠炎。与非造血细胞中“代谢物感应”受体GPR43和GPR109A结合的SCFA介导了这些保护作用。迄今为止,炎症小体途径已被报道为促进肠上皮完整性的主要途径。 SCFA与结肠上皮细胞上的GPR43结合会刺激K +外流和超极化,从而导致NLRP3炎性体激活。膳食纤维还可以改变肠道细菌的生态状况,从而产生对炎症小体激活更有效的细菌。因此,SCFA和代谢物受体可以解释膳食纤维对健康的好处,以及代谢物信号如何通过肠道稳态的主要途径提供营养。

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