Department of Comparative Biosciences, University of Wisconsin - Madison, Madison, WI, USA.
School of Veterinary Medicine, University of Wisconsin - Madison, Madison, WI, USA.
EMBO Rep. 2024 Sep;25(9):3812-3841. doi: 10.1038/s44319-024-00227-1. Epub 2024 Aug 14.
Satellite cells are skeletal muscle stem cells that contribute to postnatal muscle growth, and they endow skeletal muscle with the ability to regenerate after a severe injury. Here we discover that this myogenic potential of satellite cells requires a protein called tripartite motif-containing 28 (TRIM28). Interestingly, different from the role reported in a previous study based on C2C12 myoblasts, multiple lines of both in vitro and in vivo evidence reveal that the myogenic function of TRIM28 is not dependent on changes in the phosphorylation of its serine 473 residue. Moreover, the functions of TRIM28 are not mediated through the regulation of satellite cell proliferation or differentiation. Instead, our findings indicate that TRIM28 regulates the ability of satellite cells to progress through the process of fusion. Specifically, we discover that TRIM28 controls the expression of a fusogenic protein called myomixer and concomitant fusion pore formation. Collectively, the outcomes of this study expose the framework of a novel regulatory pathway that is essential for myogenesis.
卫星细胞是骨骼肌干细胞,它们有助于出生后的肌肉生长,并且使骨骼肌在遭受严重损伤后具有再生的能力。在这里,我们发现卫星细胞的这种成肌潜能需要一种叫做三基序蛋白 28(TRIM28)的蛋白质。有趣的是,与之前基于 C2C12 成肌细胞的研究报告中的作用不同,体外和体内的多种证据表明,TRIM28 的成肌功能不依赖于其丝氨酸 473 残基磷酸化的变化。此外,TRIM28 的功能不是通过调节卫星细胞的增殖或分化来介导的。相反,我们的发现表明,TRIM28 调节卫星细胞通过融合过程的能力。具体来说,我们发现 TRIM28 控制一种叫做肌融合器的融合蛋白的表达和伴随的融合孔形成。总的来说,这项研究的结果揭示了一个新的调控途径的框架,该途径对于肌发生是必不可少的。