State Key Laboratory of Space Medicine Fundamentals and Application, China Astronaut Research and Training Center, Beijing, China.
Nat Med. 2013 Jan;19(1):93-100. doi: 10.1038/nm.3026. Epub 2012 Dec 9.
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.
新出现的证据表明,微小 RNA(miRNA)在调节成骨分化和骨形成方面具有重要作用。到目前为止,还没有研究确定在人骨质疏松性骨标本中鉴定的 miRNA 的病理生理作用。在这里,我们发现,骨折老年患者骨标本中 miR-214 水平升高与骨形成程度较低相关。我们还发现,通过 miR-214 反义寡核苷酸处理 miR-214 转基因、去卵巢或后肢去负荷小鼠的成骨细胞特异性操纵 miR-214 水平,揭示了 miR-214 在调节骨形成中的抑制作用。此外,反义寡核苷酸-214 促进体外成骨细胞活性和基质矿化,而正义寡核苷酸-214 则降低了成骨细胞活性,miR-214 直接靶向 ATF4 抑制成骨细胞活性。这些数据表明,miR-214 在抑制骨形成中具有重要作用,而抑制成骨细胞中的 miR-214 可能是改善骨质疏松症的潜在合成代谢策略。