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miR-223调控人牙周膜成纤维细胞中RANKL表达的功能初探
引用本文:杨迷芳,王珏,马兰,谢理哲,于金华.miR-223调控人牙周膜成纤维细胞中RANKL表达的功能初探[J].口腔生物医学,2016(4):183-186.
作者姓名:杨迷芳  王珏  马兰  谢理哲  于金华
作者单位:1. 南京医科大学口腔疾病研究江苏省重点实验室,江苏 南京,210029;2. 南京医科大学口腔疾病研究江苏省重点实验室,江苏 南京210029; 南京医科大学附属口腔医院儿童口腔预防科,江苏 南京210029
基金项目:江苏高校优势学科建设工程资助项目(2014-37)
摘    要:目的:探讨miR?223对人牙周膜成纤维细胞中核因子?κB受体活化因子配体( 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及实时定量RT?PCR检测人牙周膜成纤维细胞内RANKL和骨保护素( 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。

关 键 词:微小RNA-223  人牙周膜成纤维细胞  核因子-κB受体活化因子配体  骨保护素

Investigation of miR-223 on the expression of RANKL in human periodontal ligament fibroblasts cells
Abstract:Objective: To investigate the role of miR?223 on the expression of receptor activator for nuclear factor?κB ligand ( RANKL) in human periodontal ligament fibroblasts cells ( HPDLFs) . Methods:The HPDLFs over expressed with miR?223 was con?structed, the expression of RANKL and osteoprotegerin ( OPG) were detected by Western blot and real?time RT?PCR, and the change of RANKL/OPG ratio was calculated. Results:The RANKL expression 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 micro?environment of osteoclast differentiation. MiR?223 may play a regulatory role in osteoclast differentiation.
Keywords:miR-223  human periodontal ligament fibroblasts cells  RANKL  OPG
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