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环状 RNA_0062582 通过调控 microRNA-145/CBFB 轴促进人骨髓间充质干细胞成骨分化。

Circular RNA_0062582 promotes osteogenic differentiation of human bone marrow mesenchymal stem cells via regulation of microRNA-145/CBFB axis.

机构信息

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.

出版信息

Bioengineered. 2021 Dec;12(1):1952-1963. doi: 10.1080/21655979.2021.1921553.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9848/8806255/806fc12c5de4/KBIE_A_1921553_UF0001_OC.jpg

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