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MiR-214 targets ATF4 to inhibit bone formation

  • Xiaogang Wang
  • , Baosheng Guo
  • , Qi Li
  • , Jiang Peng
  • , Zhijun Yang
  • , Aiyuan Wang
  • , Dong Li
  • , Zhibo Hou
  • , Ke Lv
  • , Guanghan Kan
  • , Hongqing Cao
  • , Heng Wu
  • , Jinping Song
  • , Xiaohua Pan
  • , Qiao Sun
  • , Shukuan Ling
  • , Yuheng Li*
  • , Mu Zhu
  • , Pengfei Zhang
  • , Songlin Peng
  • Xiaoqing Xie, Tao Tang, An Hong, Zhaoxiang Bian, Yanqiang Bai, Aiping Lu, Yinghui Li*, Fuchu He, Ge Zhang, Yingxian Li*
*此作品的通讯作者
  • China Astronaut Research and Training Center
  • Hong Kong Baptist University
  • University of Jinan
  • General Hospital of People's Liberation Army
  • Academy of Military Medical Science China

科研成果: 期刊稿件文章同行评审

摘要

Emerging evidence indicates that microRNAs (miRNAs) have important roles in regulating osteogenic differentiation and bone formation. Thus far, no study has established the pathophysiological role for miRNAs identified in human osteoporotic bone specimens. Here we found that elevated miR-214 levels correlated with a lower degree of bone formation in bone specimens from aged patients with fractures. We also found that osteoblast-specific manipulation of miR-214 levels by miR-214 antagomir treatment in miR-214 transgenic, ovariectomized, or hindlimb-unloaded mice revealed an inhibitory role of miR-214 in regulating bone formation. Further, in vitro osteoblast activity and matrix mineralization were promoted by antagomir-214 and decreased by agomir-214, and miR-214 directly targeted ATF4 to inhibit osteoblast activity. These data suggest that miR-214 has a crucial role in suppressing bone formation and that miR-214 inhibition in osteoblasts may be a potential anabolic strategy for ameliorating osteoporosis.

源语言英语
页(从-至)93-100
页数8
期刊Nature Medicine
19
1
DOI
出版状态已出版 - 1月 2013
已对外发布

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