Department of Orthopedics, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu, P.R.China.
Department of Orthopedics, The First People's Hospital of Yancheng, Yancheng, Jiangsu, P.R.China.
Bioengineered. 2021 Dec;12(1):1952-1963. doi: 10.1080/21655979.2021.1921553.
Osteoporosis poses a threat to human health worldwide. To date, there have been few studies regarding targeted treatment of osteoporosis. We aimed to identify the possible molecular mechanism of circular RNA (circ)_0062582 in osteogenic differentiation, and the interactions among circ_0062582, microRNA-145 (miR-145) and core-binding factor subunit β (CBFB). The proliferation of human bone marrow mesenchymal stem cells (hBMSCs) was tested with a cell counting kit-8 assay. Circ_0062582, miR-145 and CBFB were overexpressed by transient transfection. Dual-luciferase reporter assay system was used to analyze the combination among circ_0062582, miR-145 and CBFB. Additionally, the levels of circ_0062582, miR-145, CBFB, osterix (OSX), osteocalcin (OCN) and collagen type 1 (COL1) were detected by means of RT-qPCR or western blot analysis. Alkaline phosphatase and Alizarin red stainings were performed to analyze the degree of osteogenic differentiation under the control of circ_0062582, miR-145 and CBFB. The results demonstrated that circ_0062582 level was notably elvated during osteogenic differentiation of hBMSCs. Circ_0062582 overexpression significantly promoted osteogenic differentiation and upregulated the levels of osteogenic differentiation-related proteins, including OSX, OCN and COL1. In addition, miR-145, which was identified as the target gene of circ_0062582, could specifically target CBFB 3'-UTR regions. Next, these changes caused by the overexpression of circ_0062582 were reversed following the addition of miR-145 mimic. Following overexpression of CBFB, osteogenic differentiation was increased. In summary, these results demonstrated that the role of circ_0062582 in osteoporosis is mediated through regulating the expression level of CBFB via miR-145.
骨质疏松症对全球人类健康构成威胁。迄今为止,针对骨质疏松症的靶向治疗研究甚少。本研究旨在确定环状 RNA(circ)_0062582 在成骨分化过程中的可能分子机制,以及 circ_0062582、微小 RNA-145(miR-145)和核心结合因子亚基β(CBFB)之间的相互作用。采用细胞计数试剂盒-8 检测人骨髓间充质干细胞(hBMSCs)的增殖。通过瞬时转染过表达 circ_0062582、miR-145 和 CBFB。双荧光素酶报告基因检测系统分析 circ_0062582、miR-145 和 CBFB 之间的结合。此外,通过 RT-qPCR 或 Western blot 分析检测 circ_0062582、miR-145、CBFB、osterix(OSX)、骨钙素(OCN)和胶原 1 型(COL1)的水平。通过碱性磷酸酶和茜素红染色分析 circ_0062582、miR-145 和 CBFB 调控下成骨分化的程度。结果表明,hBMSCs 成骨分化过程中 circ_0062582 水平显著升高。circ_0062582 过表达显著促进成骨分化,并上调成骨分化相关蛋白的水平,包括 OSX、OCN 和 COL1。此外,鉴定为 circ_0062582 靶基因的 miR-145 可特异性靶向 CBFB 3'-UTR 区域。接下来,过表达 circ_0062582 引起的这些变化在添加 miR-145 模拟物后被逆转。过表达 CBFB 后,成骨分化增加。综上所述,这些结果表明 circ_0062582 在骨质疏松症中的作用是通过 miR-145 调节 CBFB 的表达水平来介导的。