Cai Haijun, Guo Hui, Deng Yixuan, Jiang Jinhai, Liu Siyuan, He Wenge, Jian Huagang
Department of Emergency, The Second Affiliated Hospital, Chongqing Medical University, Yuzhong, Chongqing 400010, P.R. China.
Department of Pharmacology, School of Pharmacy, Chongqing Medical University, Yuzhong, Chongqing 400016, P.R. China.
Exp Ther Med. 2022 Jul 29;24(4):605. doi: 10.3892/etm.2022.11542. eCollection 2022 Oct.
Osteoporosis is a widespread bone metabolic disease characterized by reduced bone mass and bone microstructure deterioration. Ribonucleotide reductase M2 (RRM2) is a key enzyme in DNA synthesis and repair. The present study investigated the effect of RRM2 on osteogenesis of mouse embryo fibroblasts (MEFs) and its molecular mechanism. Bioinformatics analysis revealed that RRM2 expression was increased during osteogenesis of MEFs triggered by bone morphogenetic protein 9. Subsequently, MEFs were used as a mesenchymal stem cell model and osteogenic inducing medium was used to induce osteogenic differentiation. RRM2 protein expression was measured by western blotting during osteogenic differentiation induction of MEFs. RRM2 levels in MEFs were upregulated and downregulated by RRM2-overexpressing recombinant adenovirus and small interfering RNA-RRM2, respectively. Bone formation markers (RUNX family transcription factor 2, osterix, distal-less homeobox 5, collagen type I α1 chain, osteopontin and osteocalcin) were detected by reverse transcription-quantitative (RT-q) PCR and alkaline phosphatase (ALP) and Alizarin Red S staining were examined. The protein expression levels of β-catenin and the ratio of phosphorylated (p-)GSK-3β to GSK-3β were detected by western blotting and the RNA expression of downstream related target genes (β-catenin, axis inhibition protein 2 (AXIN2), transcription factor 7 like 2, lymphoid enhancer binding factor 1, c-MYC and Cyclin D1) in the Wnt/β-catenin signaling pathway was measured by RT-qPCR. RRM2 protein expression increased as the osteogenic differentiation induction period was extended. RRM2 overexpression increased osteogenic marker RNA expression, ALP activity, bone mineralization, the protein expression levels of β-catenin, the ratio of p-GSK-3β to GSK-3β and the RNA expression of downstream related target genes in the Wnt/β-catenin signaling pathway, whereas RRM2 knockdown had the opposite effect. The findings of the present study revealed that RRM2 overexpression enhanced osteogenic differentiation, while RRM2 knockdown reduced osteogenic differentiation. RRM2 may regulate osteogenic differentiation of MEFs via the canonical Wnt/β-catenin signaling pathway, providing a possible therapeutic target for osteoporosis.
骨质疏松症是一种广泛存在的骨代谢疾病,其特征为骨量减少和骨微结构恶化。核糖核苷酸还原酶M2(RRM2)是DNA合成与修复中的关键酶。本研究调查了RRM2对小鼠胚胎成纤维细胞(MEFs)成骨作用的影响及其分子机制。生物信息学分析显示,在由骨形态发生蛋白9触发的MEFs成骨过程中,RRM2表达增加。随后,将MEFs用作间充质干细胞模型,并使用成骨诱导培养基诱导成骨分化。在MEFs成骨分化诱导过程中,通过蛋白质免疫印迹法检测RRM2蛋白表达。分别用RRM2过表达重组腺病毒和小干扰RNA-RRM2上调和下调MEFs中的RRM2水平。通过逆转录定量(RT-q)PCR检测骨形成标志物(RUNX家族转录因子2、osterix、远端缺失同源盒5、I型胶原α1链、骨桥蛋白和骨钙素),并检测碱性磷酸酶(ALP)和茜素红S染色。通过蛋白质免疫印迹法检测β-连环蛋白的蛋白表达水平以及磷酸化(p-)GSK-3β与GSK-3β的比值,并通过RT-qPCR检测Wnt/β-连环蛋白信号通路中下游相关靶基因(β-连环蛋白、轴抑制蛋白2(AXIN2)、转录因子7样2、淋巴增强子结合因子1、c-MYC和细胞周期蛋白D1)的RNA表达。随着成骨分化诱导期延长,RRM2蛋白表达增加。RRM2过表达增加了成骨标志物RNA表达、ALP活性、骨矿化、β-连环蛋白的蛋白表达水平、p-GSK-3β与GSK-3β的比值以及Wnt/β-连环蛋白信号通路中下游相关靶基因的RNA表达,而RRM2基因敲低则产生相反的效果。本研究结果显示,RRM2过表达增强了成骨分化,而RRM2基因敲低则降低了成骨分化。RRM2可能通过经典Wnt/β-连环蛋白信号通路调节MEFs的成骨分化,为骨质疏松症提供了一个可能的治疗靶点。