College of Animal Science and Technology, Sichuan Agricultural University, Chengdu, Sichuan 611130, China.
Farm Animal Genetic Resources Exploration and Innovation Key Laboratory of Sichuan Province, Sichuan Agricultural University, Chengdu, Sichuan 611130, China.
Biomed Res Int. 2020 Nov 17;2020:3183296. doi: 10.1155/2020/3183296. eCollection 2020.
Skeletal muscle is the most abundant and a highly plastic tissue of the mammals, especially when it comes to regenerate after trauma, but there is limited information about the mechanism of muscle repair and its regeneration. In the present study, we found that miR-204 is downregulated after skeletal muscle injury. In vitro experiments showed that over-expression of miR-204 by transfecting with miR-204 mimics suppressed C2C12 cell proliferation, migration, and blocked subsequent differentiation, whereas inhibition of miR-204 by transfecting with miR-204 inhibitor showed the converse effects. Furthermore, through the dual luciferase reporter system, we demonstrated that miR-204 can target the 3'UTR regions of , , and and inhibit their expression. Taken together, our results suggest that , , and are the target genes of miR-204 in the process of myoblasts proliferation, cell migration, and differentiation, respectively, and may contribute to mouse skeletal muscle regeneration. Our results may provide new ideas and references for the skeletal muscle study and may also provide therapeutic strategies of skeletal muscle injury.
骨骼肌是哺乳动物中最丰富和高度可塑的组织,尤其是在创伤后进行再生时,但关于肌肉修复和再生的机制知之甚少。在本研究中,我们发现 miR-204 在骨骼肌损伤后下调。体外实验表明,通过转染 miR-204 模拟物过表达 miR-204 抑制 C2C12 细胞增殖、迁移,并阻止随后的分化,而通过转染 miR-204 抑制剂抑制 miR-204 则显示出相反的效果。此外,通过双荧光素酶报告基因系统,我们证明 miR-204 可以靶向 、 、 和的 3'UTR 区域并抑制它们的表达。总之,我们的结果表明,在成肌细胞增殖、细胞迁移和分化过程中, 、 、 和分别是 miR-204 的靶基因,可能有助于小鼠骨骼肌再生。我们的研究结果可能为骨骼肌研究提供新的思路和参考,也可能为骨骼肌损伤的治疗策略提供依据。