基因敲除
软骨细胞
细胞凋亡
基因沉默
软骨
荧光素酶
小RNA
基因表达
阿格里坎
化学
标记法
骨关节炎
报告基因
细胞生物学
发病机制
细胞生长
分子生物学
癌症研究
免疫印迹
软骨发生
流式细胞术
信使核糖核酸
细胞
II型胶原
污渍
医学
转染
基因
生物
免疫学
病理
生物化学
解剖
替代医学
作者
Jing Wang,Lingqiang Chen,Song Jin,Jun Lin,Hongmei Zheng,Hong Zhang,Hao Fan,Fang He,Sha Ma,Qin Li
摘要
Altered expression of miRNA-98 (miR-98) has been reported in osteoarthritis (OA) patients, while its role and underlying mechanisms remain elusive. In the present study, a rat model of OA was established using modified Hulth method, and the expression level of miR-98 and its effect on cartilage degradation and cell apoptosis in OA rats were examined. The results showed that up-regulated miR-98 was observed in OA rats, and knockdown of miR-98 in OA rats resulted in an inhibitory effect on cartilage degradation and chondrocyte apoptosis. Then the potential apoptosis associated genes regulated by miR-98 were screened and examined in cartilage tissues. The target gene of miR-98 was validated by luciferase reporter assay. The data showed that the increased miR-98 was accompanied with a reduced expression of Bcl-2 at both mRNA and protein levels. Furthermore, the silencing of miR-98 in OA rats prevented the down-regulation of Bcl-2 in cartilage tissues. Finally, the luciferase reporter assay validated that Bcl-2 was the target gene of miR-98. In this study, we found that miR-98 might promote chondrocyte apoptosis and cartilage degradation by down-regulating Bcl-2 expression in the pathogenesis of OA, suggesting that miR-98 can be a potential target for the treatment of OA.
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