Author:
Lin Xu,Xiao Hong-Mei,Liu Hui-Min,Lv Wan-Qiang,Greenbaum Jonathan,Yuan Si-Jie,Gong Rui,Zhang Qiang,Chen Yuan-Cheng,Peng Cheng,Xu Xue-Juan,Pan Dao-Yan,Chen Zhi,Li Zhang-Fang,Zhou Rou,Wang Xia-Fang,Lu Jun-Min,Ao Zeng-Xin,Song Yu-Qian,Zhang Yin-Hua,Su Kuan-Jui,Meng Xiang-He,Ge Chang-Li,Lv Feng-Ye,Shi Xing-Ming,Zhao Qi,Guo Bo-Yi,Yi Neng-Jun,Shen Hui,Papasian Christopher J.,Shen Jie,Deng Hong-Wen
Abstract
AbstractAlthough gut microbiota influences osteoporosis risk, the individual species involved, and underlying mechanisms, are unknown. We performed integrative analyses in a Chinese cohort with metagenomics/targeted metabolomics/whole-genome sequencing. Bacteroides vulgatus was found negatively associated with bone mineral density (BMD), this association was validated in US Caucasians. Serum valeric acid was positively associated with BMD, and B.vulgatus causally downregulated it. Ovariectomized mice fed B.vulgatus had decreased bone formation and increased bone resorption, lower BMD and poorer bone micro-structure. Valeric acid suppressed NF-κB p65 protein production (pro-inflammatory), and enhanced IL-10 mRNA expression (anti-inflammatory), leading to suppressed maturation of osteoclast-like cells, and enhanced maturation of osteoblasts in vitro. B.vulgatus and valeric acid represent promising targets for osteoporosis prevention/treatment.
Publisher
Cold Spring Harbor Laboratory
Cited by
2 articles.
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