›› 2016, Vol. 7 ›› Issue (4): 183-186.

• 论著 • 上一篇    下一篇

miR-223调控人牙周膜成纤维细胞中RANKL表达的功能初探

杨迷芳1,王珏2,马兰3,谢理哲2,于金华4   

  1. 1. 南京医科大学口腔医学研究所
    2. 南京医科大学
    3. 南京医科大学口腔疾病研究江苏省重点实验室
    4. 南京医科大学口腔医学院
  • 收稿日期:2016-12-08 修回日期:2016-12-23 出版日期:2016-12-25 发布日期:2017-01-09
  • 通讯作者: 杨迷芳 E-mail:yangmifang@qq.com

Investigation of miR-223 on the of RANKL in human periodontal ligament fibroblasts cells

  • Received:2016-12-08 Revised:2016-12-23 Online:2016-12-25 Published:2017-01-09
  • Contact: Mi-Fang Yang E-mail:yangmifang@qq.com

摘要: 目的:探讨miR-223对人牙周膜成纤维细胞中RANKL的调控作用。方法:构建过表达miR-223的人牙周膜成纤维细胞,western blot及real time PCR检测人牙周膜成纤维细胞内RANKL、OPG的表达,计算RANKL/OPG比值的改变。结果:过表达miR-223的人牙周膜成纤维细胞, RANKL的表达明显下调,RANKL/OPG比值下降。结论:miR-223可调控RANKL的表达,破坏RANKL/OPG比例的平衡,改变破骨细胞的微环境,影响破骨细胞分化。

Abstract: Objective: Investigate the role of miR-223 on the of RANKL in HPDLFs. Methods:The HPDLFs over expressed with miR-223 was constructed, the of RANKL and OPG were detected by western blot and real time PCR, and the change of RANKL/OPG ratio was calculated. Results: The RANKL was down-regulated in the HPDLFs with miR-223 over expressed and the RANKL/OPG ratio was decreased. Conclusions: MiR-223 could disrupt the homeostasis of RANKL/OPG, destroy the microenvironment of osteoclast differentiation. MiR-223 may play a regulatory role in osteoclast differentiation .