Horsley Valerie, Jansen Katie M, Mills Stephen T, Pavlath Grace K
Graduate Program in Biochemistry, Cell, and Developmental Biology, Emory University, Atlanta, GA 30322, USA.
Cell. 2003 May 16;113(4):483-94. doi: 10.1016/s0092-8674(03)00319-2.
Skeletal muscle formation and growth require the fusion of myoblasts to form multinucleated myofibers or myotubes, but few molecules are known to regulate myoblast fusion in mammals. The transcription factor NFATc2 controls myoblast fusion at a specific stage of myogenesis after the initial formation of a myotube and is necessary for further cell growth. By examining genes regulated by NFATc2 in muscle, this study identifies the cytokine IL-4 as a molecular signal that controls myoblast fusion with myotubes. Muscle cells lacking IL-4 or the IL-4alpha receptor subunit form normally but are reduced in size and myonuclear number. IL-4 is expressed by a subset of muscle cells in fusing muscle cultures and requires the IL-4alpha receptor subunit on myoblasts to promote fusion and growth. These data demonstrate that following myotube formation, myotubes recruit myoblast fusion by secretion of IL-4, leading to muscle growth.
骨骼肌的形成和生长需要成肌细胞融合形成多核肌纤维或肌管,但在哺乳动物中,已知很少有分子能调节成肌细胞融合。转录因子NFATc2在肌管初始形成后的特定肌生成阶段控制成肌细胞融合,是进一步细胞生长所必需的。通过研究NFATc2在肌肉中调控的基因,本研究确定细胞因子IL-4是控制成肌细胞与肌管融合的分子信号。缺乏IL-4或IL-4α受体亚基的肌肉细胞正常形成,但大小和肌核数量减少。IL-4在融合的肌肉培养物中的一部分肌肉细胞中表达,并且需要成肌细胞上的IL-4α受体亚基来促进融合和生长。这些数据表明,在肌管形成后,肌管通过分泌IL-4招募成肌细胞融合,从而导致肌肉生长。