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肠道微生物群通过脆弱拟杆菌-戊酸相关途径影响骨骼。

Gut microbiota impacts bone via Bacteroides vulgatus-valeric acid-related pathways.

机构信息

Shunde Hospital of Southern Medical University (The First People's Hospital of Shunde), No.1 of Jiazi Road, Lunjiao, Shunde District, Foshan City, 528308, Guangdong Province, China.

Department of Endocrinology and Metabolism, The Third Affiliated Hospital of Southern Medical University, Guangzhou, 510630, Guangdong Province, China.

出版信息

Nat Commun. 2023 Oct 27;14(1):6853. doi: 10.1038/s41467-023-42005-y.

Abstract

Although the gut microbiota has been reported to influence osteoporosis risk, the individual species involved, and underlying mechanisms, remain largely unknown. We performed integrative analyses in a Chinese cohort of peri-/post-menopausal women with metagenomics/targeted metabolomics/whole-genome sequencing to identify novel microbiome-related biomarkers for bone health. Bacteroides vulgatus was found to be negatively associated with bone mineral density (BMD), which was validated in US white people. Serum valeric acid (VA), a microbiota derived metabolite, was positively associated with BMD and causally downregulated by B. vulgatus. Ovariectomized mice fed B. vulgatus demonstrated increased bone resorption and poorer bone micro-structure, while those fed VA demonstrated reduced bone resorption and better bone micro-structure. VA suppressed RELA protein production (pro-inflammatory), and enhanced IL10 mRNA expression (anti-inflammatory), leading to suppressed maturation of osteoclast-like cells and enhanced maturation of osteoblasts in vitro. The findings suggest that B. vulgatus and VA may represent promising targets for osteoporosis prevention/treatment.

摘要

虽然肠道微生物群已被报道会影响骨质疏松症的风险,但涉及的特定物种和潜在机制在很大程度上仍不清楚。我们在中国绝经前/后妇女队列中进行了整合分析,该队列进行了宏基因组学/靶向代谢组学/全基因组测序,以确定与骨骼健康相关的新型微生物组相关生物标志物。脆弱拟杆菌被发现与骨密度(BMD)呈负相关,这在美国白人中得到了验证。血清戊酸(VA)是一种由微生物群衍生的代谢物,与 BMD 呈正相关,并可被脆弱拟杆菌下调。喂食脆弱拟杆菌的去卵巢小鼠表现出骨吸收增加和骨微结构变差,而喂食 VA 的小鼠则表现出骨吸收减少和骨微结构改善。VA 抑制 RELA 蛋白的产生(促炎),并增强 IL10 mRNA 的表达(抗炎),从而抑制体外破骨细胞样细胞的成熟,并增强成骨细胞的成熟。这些发现表明,脆弱拟杆菌和 VA 可能是预防/治疗骨质疏松症的有前途的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac3c/10611739/71dc79cbe93d/41467_2023_42005_Fig1_HTML.jpg

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