Center of Gallbladder Disease, Shanghai East Hospital, Institute of Gallstone Disease, Tongji University School of Medicine, Shanghai, China.
State Key Laboratory of Reproductive Medicine, School of Public Health, Nanjing Medical University, Nanjing, Jiangsu, China.
Nat Commun. 2022 Jan 11;13(1):252. doi: 10.1038/s41467-021-27758-8.
Cholesterol gallstone disease is a worldwide common disease. Cholesterol supersaturation in gallbladder bile is the prerequisite for its pathogenesis, while the mechanism is not completely understood. In this study, we find enrichment of gut microbiota (especially Desulfovibrionales) in patients with gallstone disease. Fecal transplantation of gut microbiota from gallstone patients to gallstone-resistant strain of mice can induce gallstone formation. Carrying Desulfovibrionales is associated with enhanced cecal secondary bile acids production and increase of bile acid hydrophobicity facilitating intestinal cholesterol absorption. Meanwhile, the metabolic product of Desulfovibrionales, HS increase and is shown to induce hepatic FXR and inhibit CYP7A1 expression. Mice carrying Desulfovibrionales present induction of hepatic expression of cholesterol transporters Abcg5/g8 to promote biliary secretion of cholesterol as well. Our study demonstrates the role of gut microbiota, Desulfovibrionales, as an environmental regulator contributing to gallstone formation through its influence on bile acid and cholesterol metabolism.
胆固醇结石病是一种全球性的常见病。胆囊胆汁中胆固醇的过饱和是其发病的前提,但其发病机制尚不完全清楚。在这项研究中,我们发现胆结石患者的肠道微生物群(特别是脱硫弧菌)富集。将胆结石患者的肠道微生物群粪便移植到胆结石抗性的小鼠中,可诱导胆结石形成。携带脱硫弧菌与增强的盲肠次级胆汁酸产生和增加胆汁酸疏水性,促进肠道胆固醇吸收相关。同时,脱硫弧菌的代谢产物 HS 增加,并显示出诱导肝脏 FXR 并抑制 CYP7A1 表达。携带脱硫弧菌的小鼠表现出诱导肝脏胆固醇转运蛋白 Abcg5/g8 的表达,以促进胆固醇的胆汁分泌。我们的研究表明,肠道微生物群,脱硫弧菌,作为一种环境调节剂,通过影响胆汁酸和胆固醇代谢,在胆结石形成中起作用。