软骨细胞
骨关节炎
TCF4型
软骨
小RNA
细胞凋亡
细胞生物学
分解代谢
化学
基因表达
癌症研究
内科学
医学
生物
基因
病理
增强子
解剖
生物化学
替代医学
新陈代谢
作者
Huaming Xue,Yihui Tu,Tong Ma,Tao Wen,Tao Yang,Long Xue,Minwei Cai,Fangxing Wang,Mengying Guan
出处
期刊:Bone
[Elsevier BV]
日期:2019-03-28
卷期号:123: 129-136
被引量:49
标识
DOI:10.1016/j.bone.2019.03.035
摘要
MicroRNAs (miRNAs, miRs) are frequently dysregulated in osteoarthritis (OA), but the role of specific miRNAs in OA remains unclear. In this study, we found that miR-93-5p is underexpressed in human and rat OA-affected cartilage (compared with normal cartilage) as well as in IL-1β–treated chondrocytes. Overexpression of miR-93-5p promoted chondrocyte viability, suppressed chondrocyte apoptosis, and maintained the balance between anabolic and catabolic factors of the extracellular matrix in vitro. Similarly, injection of a miR-93-5p–expressing lentivirus alleviated the destruction of articular cartilage in a rat model of OA (anterior cruciate ligament transection). Furthermore, TCF4 was identified as a direct target gene of miR-93-5p. miR-93-5p directly targeted the 3′ untranslated region (3′-UTR) of TCF4 mRNA and repressed TCF4 expression. Overexpression of TCF4 attenuated the effects of miR-93-5p on chondrocyte apoptosis and functions. Finally, analyses of miR-93-5p and TCF4 in OA-affected cartilage tissues revealed that miR-93-5p expression inversely correlated with TCF4 expression. Altogether, these findings indicate that miR-93-5p slows OA progression partially by suppressing TCF4 expression, and this phenomenon may provide novel insights into the function of miRNA in OA.
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