Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
Nature. 2013 Jul 18;499(7458):301-5. doi: 10.1038/nature12343.
Fusion of myoblasts is essential for the formation of multi-nucleated muscle fibres. However, the identity of muscle-specific proteins that directly govern this fusion process in mammals has remained elusive. Here we identify a muscle-specific membrane protein, named myomaker, that controls myoblast fusion. Myomaker is expressed on the cell surface of myoblasts during fusion and is downregulated thereafter. Overexpression of myomaker in myoblasts markedly enhances fusion, and genetic disruption of myomaker in mice causes perinatal death due to an absence of multi-nucleated muscle fibres. Remarkably, forced expression of myomaker in fibroblasts promotes fusion with myoblasts, demonstrating the direct participation of this protein in the fusion process. Pharmacological perturbation of the actin cytoskeleton abolishes the activity of myomaker, consistent with previous studies implicating actin dynamics in myoblast fusion. These findings reveal a long-sought myogenic fusion protein that controls mammalian myoblast fusion and provide new insights into the molecular underpinnings of muscle formation.
成肌细胞的融合对于形成多核肌纤维是必不可少的。然而,直接调控哺乳动物这一融合过程的肌肉特异性蛋白的身份仍然难以捉摸。在这里,我们鉴定出一种肌肉特异性膜蛋白,命名为肌生成蛋白,它控制着成肌细胞的融合。肌生成蛋白在融合过程中成肌细胞的细胞表面表达,随后下调。成肌细胞中肌生成蛋白的过表达显著增强融合,而肌生成蛋白在小鼠中的基因缺失会导致围产期死亡,因为缺乏多核肌纤维。值得注意的是,肌生成蛋白在成纤维细胞中的强制表达促进了与成肌细胞的融合,表明该蛋白直接参与了融合过程。肌动蛋白细胞骨架的药理学扰动消除了肌生成蛋白的活性,这与先前的研究表明肌动蛋白动力学参与成肌细胞融合一致。这些发现揭示了一种长期以来被寻找的肌源性融合蛋白,它控制着哺乳动物成肌细胞的融合,并为肌肉形成的分子基础提供了新的见解。