作者
Yu Liu,Chun‐Yuan Chen,Zheng‐Zhao Liu,Zhenguo Luo,Shan‐Shan Rao,Ling Jin,Tengfei Wan,Yue Tao,Yuyong Tan,Hao Yin,Fei Yang,Feiyu Huang,Jing Guo,Yiyi Wang,Kun Xia,Jia Cao,Zhenxing Wang,Chengyu Hong,Mingjie Luo,Xiaozhou Hu,Yiwei Liu,Wei Du,Jian Luo,Yingyao Hu,Yan Zhang,Jie Huang,Hong‐Ming Li,Ben Wu,Hao‐Ming Liu,Tuan‐Hui Chen,Yuxuan Qian,Youyou Li,Shi‐Kai Feng,Yang Chen,Luyue Qi,Ran Xu,Siyuan Tang,Hui Xie
摘要
Recently, the gut microbiota (GM) has been shown to be a regulator of bone homeostasis and the mechanisms by which GM modulates bone mass are still being investigated. Here, it is found that colonization with GM from children (CGM) but not from the elderly (EGM) prevents decreases in bone mass and bone strength in conventionally raised, ovariectomy (OVX)-induced osteoporotic mice. 16S rRNA gene sequencing reveals that CGM reverses the OVX-induced reduction of Akkermansia muciniphila (Akk). Direct replenishment of Akk is sufficient to correct the OVX-induced imbalanced bone metabolism and protect against osteoporosis. Mechanistic studies show that the secretion of extracellular vesicles (EVs) is required for the CGM- and Akk-induced bone protective effects and these nanovesicles can enter and accumulate into bone tissues to attenuate the OVX-induced osteoporotic phenotypes by augmenting osteogenic activity and inhibiting osteoclast formation. The study identifies that gut bacterium Akk mediates the CGM-induced anti-osteoporotic effects and presents a novel mechanism underlying the exchange of signals between GM and host bone.