Yin Chong, Tian Ye, Yu Yang, Yang Chaofei, Su Peihong, Zhao Yipu, Wang Xue, Zhang Kewen, Pei Jiawei, Li Dijie, Chen Zhihao, Zhang Yan, Miao Zhiping, Qian Airong
Lab for Bone Metabolism, Xi'an Key Laboratory of Special Medicine and Health Engineering, Key Lab for Space Biosciences and Biotechnology, Research Center for Special Medicine and Health Systems Engineering, NPU-UAB Joint Laboratory for Bone Metabolism, School of Life Sciences, Northwestern Polytechnical University, Xi'an, China.
Tianjin Key Laboratory on Technologies Enabling Development Clinical Therapeutics and Diagnostics (Theranostics), School of pharmacy, Tianjin Medical University, Tianjin, China.
Front Cell Dev Biol. 2020 Nov 6;8:600641. doi: 10.3389/fcell.2020.600641. eCollection 2020.
Osteoporosis is a frequently occurring bone disease in middle-aged and aged men and women. However, current therapies on this disease are still not ideal. MicroRNAs (miRNAs) are a class of endogenous non-protein-coding RNA with a length of 18-25 nucleotides. miRNAs have been identified as important regulators for development, metabolism, carcinogenesis, and bone formation. miR-129-5p has been reported as a regulator of cancer and neuroscience, whereas studies about its function on bone formation is still limited. In this study, we investigated the function and mechanism of miR-129-5p on osteoblast differentiation and bone formation. We have assessed the expression of miRNAs in bone mesenchymal stem cells from aging and menopause osteoporosis C57BL6 mice. The expression of miR-129-5p was altered in all osteoporosis models. Besides, the expression of miR-129-5p was negatively correlated with osteoblastic differentiation markers in the femur tissues of C57BL/6 mice of different ages. We further demonstrated that overexpression of miR-129-5p inhibited osteoblast differentiation in MC3T3-E1 cell line, as well as bone formation of C57BL/6 mice. On the other hand, down-regulation of miR-129-5p enhanced osteoblast differentiation and bone formation. We also found that miR-129-5p inhibited Wnt/β-catenin pathway in osteoblast. The target gene of miR-129-5p has been forecasted and proved as . We further found that plasmid containing 3' UTR sequence enhanced osteoblast differentiation, as well as Wnt/β-catenin pathway in MC3T3-E1 cells. To further investigate the rescue effect of miR-129-5p inhibitor, we manufactured bioengineered novel recombinant miR-129-5p inhibitor through system and then tested its function. The results showed that the novel recombinant miR-129-5p inhibitor promoted osteoblast differentiation and greatly ameliorated menopause osteoporosis in C57BL6 mice. In conclusion, we have discovered miR-129-5p as an inhibitor of bone formation. miR-129-5p inhibited downstream transcription factors of Wnt/β-catenin pathway through targeting . Moreover, novel recombinant miR-129-5p inhibitor showed rescue effect on osteoporosis. This study has revealed a new mechanism of osteogenic differentiation and provided novel therapeutic strategies for treatment of skeletal disorders.
骨质疏松症是一种在中老年男性和女性中频繁发生的骨病。然而,目前针对这种疾病的治疗方法仍不理想。微小RNA(miRNA)是一类长度为18 - 25个核苷酸的内源性非蛋白质编码RNA。miRNA已被确定为发育、代谢、致癌作用和骨形成的重要调节因子。miR - 129 - 5p已被报道为癌症和神经科学的调节因子,而关于其在骨形成方面功能的研究仍然有限。在本研究中,我们调查了miR - 129 - 5p在成骨细胞分化和骨形成中的功能及机制。我们评估了衰老和绝经后骨质疏松症C57BL6小鼠的骨髓间充质干细胞中miRNA的表达。在所有骨质疏松模型中,miR - 129 - 5p的表达均发生了改变。此外,在不同年龄的C57BL / 6小鼠股骨组织中,miR - 129 - 5p的表达与成骨细胞分化标志物呈负相关。我们进一步证明,miR - 129 - 5p的过表达抑制了MC3T3 - E1细胞系中的成骨细胞分化以及C57BL / 6小鼠的骨形成。另一方面,miR - 129 - 5p的下调增强了成骨细胞分化和骨形成。我们还发现miR - 129 - 5p抑制了成骨细胞中的Wnt/β - 连环蛋白通路。miR - 129 - 5p的靶基因已被预测并证实为 。我们进一步发现,含有3'UTR序列的质粒增强了MC3T3 - E1细胞中的成骨细胞分化以及Wnt/β - 连环蛋白通路。为了进一步研究miR - 129 - 5p抑制剂的挽救作用,我们通过 系统制备了生物工程新型重组miR - 129 - 5p抑制剂,然后测试了其功能。结果表明,新型重组miR - 129 - 5p抑制剂促进了成骨细胞分化,并极大地改善了C57BL6小鼠的绝经后骨质疏松症。总之,我们发现miR - 129 - 5p是骨形成的抑制剂。miR - 129 - 5p通过靶向 抑制Wnt/β - 连环蛋白通路的下游转录因子。此外,新型重组miR - 129 - 5p抑制剂对骨质疏松症显示出挽救作用。本研究揭示了成骨分化的新机制,并为骨骼疾病的治疗提供了新 的治疗策略。