压电1
机械敏感通道
成骨细胞
细胞生物学
骨质疏松症
机械转化
基因剔除小鼠
骨重建
化学
骨形成
离子通道
内分泌学
生物
受体
体外
生物化学
作者
Weijia Sun,Shaopeng Chi,Yuheng Li,Shukuan Ling,Yingjun Tan,Youjia Xu,Fan Jiang,Jianwei Li,Caizhi Liu,Guohui Zhong,Dengchao Cao,Xiaoyan Jin,Dingsheng Zhao,Xingcheng Gao,Zizhong Liu,Bailong Xiao,Yingxian Li
出处
期刊:eLife
[eLife Sciences Publications, Ltd.]
日期:2019-07-10
卷期号:8
被引量:300
摘要
Mechanical load of the skeleton system is essential for the development, growth, and maintenance of bone. However, the molecular mechanism by which mechanical stimuli are converted into osteogenesis and bone formation remains unclear. Here we report that Piezo1, a bona fide mechanotransducer that is critical for various biological processes, plays a critical role in bone formation. Knockout of Piezo1 in osteoblast lineage cells disrupts the osteogenesis of osteoblasts and severely impairs bone structure and strength. Bone loss that is induced by mechanical unloading is blunted in knockout mice. Intriguingly, simulated microgravity treatment reduced the function of osteoblasts by suppressing the expression of Piezo1. Furthermore, osteoporosis patients show reduced expression of Piezo1, which is closely correlated with osteoblast dysfunction. These data collectively suggest that Piezo1 functions as a key mechanotransducer for conferring mechanosensitivity to osteoblasts and determining mechanical-load-dependent bone formation, and represents a novel therapeutic target for treating osteoporosis or mechanical unloading-induced severe bone loss.
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