Chen Qiaojie, Shen Pingping, Zhang Bo, Chen Yang, Zheng Chunli
Department of Orthopedics, Ningbo No.2 Hospital, Ningbo, China.
Department of Gastroenterology, Ningbo Yinzhou No. 2 Hospital, Ningbo, China.
Cells Tissues Organs. 2025;214(1):14-25. doi: 10.1159/000525703. Epub 2022 Jun 28.
Circular RNAs (circRNAs) play crucial roles in many human diseases. However, the functions of circRNAs in osteoporosis (OP) are barely reported. In this study, we aimed to explore the function of circ_0062582 in osteogenic differentiation of human bone marrow mesenchymal stem cells (hBMSCs) in vitro. circ_0062582 and SMAD5 were downregulated and miR-197-3p was upregulated in OP patients and increased in osteoblast medium (OM)-induced hBMSCs in vitro. circ_0062582 knockdown inhibited the viability and osteogenic differentiation of hBMSCs. circ_0062582 directly targeted miR-197-3p, and miR-197-3p inhibition reversed the effects of circ_0062582 on hBMSC viability and osteogenic differentiation. SMAD5 was the target gene of miR-197-3p. SMAD5 overexpression promoted the viability and osteogenic differentiation of hBMSCs and attenuated miR-197-3p-mediated suppressive roles in hBMSC viability and osteogenic differentiation. In conclusion, circ_0062582 sponged miR-197-3p to elevate SMAD5 expression, thereby inducing hBMSC proliferation and osteogenic differentiation in vitro.
环状RNA(circRNAs)在许多人类疾病中发挥着关键作用。然而,circRNAs在骨质疏松症(OP)中的功能鲜有报道。在本研究中,我们旨在探讨circ_0062582在体外人骨髓间充质干细胞(hBMSCs)成骨分化中的作用。在OP患者中,circ_0062582和SMAD5表达下调,miR-197-3p表达上调,且在体外成骨细胞培养基(OM)诱导的hBMSCs中也升高。敲低circ_0062582可抑制hBMSCs的活力和成骨分化。circ_0062582直接靶向miR-197-3p,抑制miR-197-3p可逆转circ_0062582对hBMSC活力和成骨分化的影响。SMAD5是miR-197-3p的靶基因。过表达SMAD5可促进hBMSCs的活力和成骨分化,并减弱miR-197-3p介导的对hBMSC活力和成骨分化的抑制作用。总之,circ_0062582通过吸附miR-197-3p来提高SMAD5表达,从而在体外诱导hBMSC增殖和成骨分化。