MicroRNA-103 contributes to osteoarthritis development by targeting Sox6

被引:28
作者
Chen, Jian [1 ]
Wu, Xing [1 ]
机构
[1] Tongji Univ, Shanghai Peoples Hosp 10, Dept Orthoped, Sch Med, Shanghai 200040, Peoples R China
基金
中国国家自然科学基金;
关键词
miR-103; Sox6; Osteoarthritis; CANCER-CELLS; EXPRESSION; CHONDROCYTE; DIFFERENTIATION; PROLIFERATION; INHIBITOR; INVASION; GROWTH;
D O I
10.1016/j.biopha.2019.109186
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Osteoarthritis is a degenerative joint disease, worldwide, and its underlying molecular mechanisms are still poorly understood. MicroRNAs are important regulators of diverse biological processes, including osteoarthritis. In this study, we showed that miR-103 was deregulated in osteoarthritis patients. We performed CCK8 and colony formation assay and found that miR-103 inhibited chondrocyte proliferation. We also found that miR-103 inhibited chondrocyte formation and maturation by RT-PCR, western blotting, and immunocytochemistry. Inhibition of miR-103 suppressed production of the catabolic factors and pro-inflammatory cytokines induced by IL-15 in chondrocytes. Finally, we found that Sox6 was a direct target of miR-103 and participated in osteoarthritis development. In summary, we demonstrated that miR-103 contributed to osteoarthritis development by directly targeting and inhibiting the expression of Sox6. Regulation of miR-103 expression in human chondrocytes may be an effective treatment for osteoarthritis.
引用
收藏
页数:7
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