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肥胖相关的肠道微生物会降解肌醇并促进脂质吸收。

Obesity-enriched gut microbe degrades myo-inositol and promotes lipid absorption.

机构信息

Department of Endocrine and Metabolic Diseases, Shanghai Institute of Endocrine and Metabolic Diseases, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China; Shanghai National Clinical Research Center for Metabolic Diseases, Key Laboratory for Endocrine and Metabolic Diseases of the National Health Commission of the PR China, Shanghai Key Laboratory for Endocrine Tumor, State Key Laboratory of Medical Genomics, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

BGI Research, Shenzhen 518083, China; Institute of Intelligent Medical Research (IIMR), BGI Genomics, Shenzhen 518083, China.

出版信息

Cell Host Microbe. 2024 Aug 14;32(8):1301-1314.e9. doi: 10.1016/j.chom.2024.06.012. Epub 2024 Jul 11.

Abstract

Numerous studies have reported critical roles for the gut microbiota in obesity. However, the specific microbes that causally contribute to obesity and the underlying mechanisms remain undetermined. Here, we conducted shotgun metagenomic sequencing in a Chinese cohort of 631 obese subjects and 374 normal-weight controls and identified a Megamonas-dominated, enterotype-like cluster enriched in obese subjects. Among this cohort, the presence of Megamonas and polygenic risk exhibited an additive impact on obesity. Megamonas rupellensis possessed genes for myo-inositol degradation, as demonstrated in vitro and in vivo, and the addition of myo-inositol effectively inhibited fatty acid absorption in intestinal organoids. Furthermore, mice colonized with M. rupellensis or E. coli heterologously expressing the myo-inositol-degrading iolG gene exhibited enhanced intestinal lipid absorption, thereby leading to obesity. Altogether, our findings uncover roles for M. rupellensis as a myo-inositol degrader that enhances lipid absorption and obesity, suggesting potential strategies for future obesity management.

摘要

许多研究报告指出肠道微生物群在肥胖中起着关键作用。然而,导致肥胖的特定微生物以及潜在的机制仍未确定。在这里,我们对中国的 631 名肥胖受试者和 374 名正常体重对照者进行了鸟枪法宏基因组测序,发现了一个以 Megamonas 为主导的、类似于肠型的聚类,在肥胖受试者中富集。在这个队列中,Megamonas 的存在和多基因风险对肥胖表现出附加影响。正如在体外和体内所证明的,Megamonas rupellensis 具有肌醇降解的基因,并且添加肌醇可有效抑制肠类器官中的脂肪酸吸收。此外,用 M. rupellensis 或表达肌醇降解基因 iolG 的 E. coli 定植的小鼠表现出增强的肠道脂质吸收,从而导致肥胖。总的来说,我们的研究结果揭示了 M. rupellensis 作为一种肌醇降解物的作用,可增强脂质吸收和肥胖,这为未来的肥胖管理提供了潜在的策略。

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