阿格里坎
软骨发生
间充质干细胞
硫氧化物9
运行x2
细胞生物学
小RNA
软骨细胞
化学
软骨
细胞分化
下调和上调
II型胶原
转录因子
骨关节炎
生物
病理
解剖
医学
基因
关节软骨
替代医学
生物化学
作者
Ziwei Luo,Jinqi Xie,Haoxiang Ye,Mingjie Zhang,Yangping Liu,Chunmei Ma,Jiahui Cao,Hao Pan,Xiaosheng Liu,Xianxi Zhou,Jiechen Kong,Dongfeng Chen,Aijun Liu
标识
DOI:10.1177/19476035231207778
摘要
Objective MicroRNAs (miRNAs) play a key role in the differentiation of bone marrow–derived mesenchymal stem cells (BMSCs) into chondrocytes. Our previous study found that novel-miR-81 can relieve osteoarthritis, but its role in chondrogenic differentiation of BMSCs remains unclear. The purpose of this study was to explore the role of novel-miR-81 in chondrogenic differentiation of BMSCs. Methods We used a model in which transforming growth factor (TGF)-β3-induced BMSCs differentiation into chondrocytes. We detected the expression Sox9, Collagen Ⅱ, Aggrecan, novel-miR-81, and Rac2 by real-time reverse transcription-quantitative polymerase chain reaction (RT-qPCR). Western blot was performed to detect the expression of Sox9, Collagen Ⅱ, and Rac2. Dual-luciferase reporter gene assay confirmed that the association between novel-miR-81 and Rac2. In addition, the ectopic chondrocyte differentiation of BMSCs was performed subcutaneously in nude mice. The effect of novel-miR-81 and Rac2 on ectopic chondrogenic differentiation of BMSCs was determined by immunohistochemical staining. Results Novel-miR-81 upregulated in chondrogenic differentiation of BMSCs. Rac2 was a key target of novel-miR-81. Mimic novel-miR-81 and siRac2 upregulated the expression of Sox9, Collagen Ⅱ, and Aggrecan. Conclusion Novel-miR-81 promotes the chondrocytes differentiation of BMSCs by inhibiting the expression of target gene Rac2, which provides potential targets for BMSCs transplantation to repair cartilage defects.
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