Department of Orthopedics, The First Affiliated Hospital of Zhengzhou University, No. 1 Jianshe East Road, Zhengzhou City, Henan Province, China.
Department of Orthopedics, The First Affiliated Hospital of Zhengzhou University, No. 1 Jianshe East Road, Zhengzhou City, Henan Province, China
Biosci Rep. 2019 Jan 30;39(1). doi: 10.1042/BSR20180921. Print 2019 Jan 31.
Various miRNAs have been reported to regulate the chondrogenic differentiation of bone marrow mesenchymal stem cells (BMSCs); however, whether miR-134 plays a role in this biological process remains undetermined. In the present study, we first evaluated the chondrogenic differentiation of BMSCs by Alcian blue staining, and examined the miR-134 expression by quantitative real-time PCR (qRT-PCR) during this process. And miR-134 inhibitor was used to investigate the functions of miR-134 in chondrogenic differentiation of BMSCs by Alcian blue staining, qRT-PCR, and Western blot. Subsequently, the correlation between miR-134 and SMAD6 was assessed via bioinformatics analysis and dual-luciferase reporter assay. Finally, the role of SMAD6 in chondrogenic differentiation of BMSCs was also determined through Alcian blue staining, qRT-PCR, and Western blot. As results showed that miR-134 expression was significantly down-regulated during chondrogenic differentiation, and inhibition of miR-134 obviously promoted chondrogenic differentiation. Dual-luciferase reporter assay indicated that miR-134 could directly target the 3'-UTRs of SMAD6, inhibit miR-134 expression in BMSCs, and up-regulate SMAD6 expression. Moreover, we found that overexpression of SMAD6 significantly promoted chondrogenic differentiation, and that SMAD6-induced promotion of chondrogenic differentiation could be reversed by miR-134 mimics. In conclusion, our findings suggest that miR-134 may act as a negative regulator during chondrogenic differentiation of BMSCs by interacting with SMAD6.
多种 miRNA 已被报道可调节骨髓间充质干细胞(BMSCs)的软骨分化;然而,miR-134 是否在这一生物学过程中发挥作用仍未确定。在本研究中,我们首先通过阿尔新蓝染色评估 BMSCs 的软骨分化,并通过实时定量 PCR(qRT-PCR)检测这一过程中 miR-134 的表达。然后,通过阿尔新蓝染色、qRT-PCR 和 Western blot 检测 miR-134 抑制剂在 BMSCs 软骨分化中的作用。接着,通过生物信息学分析和双荧光素酶报告基因检测评估 miR-134 与 SMAD6 之间的相关性。最后,通过阿尔新蓝染色、qRT-PCR 和 Western blot 检测 SMAD6 在 BMSCs 软骨分化中的作用。结果表明,miR-134 的表达在软骨分化过程中明显下调,抑制 miR-134 明显促进软骨分化。双荧光素酶报告基因检测表明,miR-134 可直接靶向 SMAD6 的 3'-UTR,抑制 BMSCs 中的 miR-134 表达,并上调 SMAD6 表达。此外,我们发现 SMAD6 的过表达显著促进软骨分化,而 miR-134 模拟物可逆转 SMAD6 诱导的软骨分化促进作用。综上所述,我们的研究结果表明,miR-134 可能通过与 SMAD6 相互作用在 BMSCs 的软骨分化过程中发挥负调控作用。