Kim Kun Ho, Qiu Jiamin, Kuang Shihuan
Department of Animal Sciences, Purdue University, West Lafayette, United States.
Bio Protoc. 2020 Jul 20;10(14):e3686. doi: 10.21769/BioProtoc.3686.
The skeletal muscle is key for body mobility and motor performance, but aging and diseases often lead to progressive loss of muscle mass due to wasting or degeneration of muscle cells. Muscle satellite cells (MuSCs) represent a population of tissue stem cells residing in the skeletal muscles and are responsible for homeostatic maintenance and regeneration of skeletal muscles. Growth, injury, and degenerative signals activate MuSCs, which then proliferate (proliferating MuSCs are called myoblasts), differentiate and fuse with existing multinuclear muscle cells (myofibers) to mediate muscle growth and repair. Here, we describe a protocol for isolating MuSCs from skeletal muscles of mice for analysis. In addition, we provide a detailed protocol on how to culture and differentiate primary myoblasts into myotubes and an immunofluorescent staining procedure to characterize the cells. These methods are essential for modeling regenerative myogenesis to understand the dynamics, function and molecular regulation of MuSCs.
骨骼肌对于身体的活动能力和运动表现至关重要,但衰老和疾病常常因肌肉细胞的萎缩或退化而导致肌肉质量逐渐丧失。肌肉卫星细胞(MuSCs)是存在于骨骼肌中的一群组织干细胞,负责骨骼肌的稳态维持和再生。生长、损伤和退化信号激活MuSCs,随后MuSCs增殖(增殖的MuSCs称为成肌细胞),分化并与现有的多核肌肉细胞(肌纤维)融合,以介导肌肉生长和修复。在这里,我们描述了一种从小鼠骨骼肌中分离MuSCs用于分析的方案。此外,我们还提供了一份关于如何将原代成肌细胞培养和分化为肌管的详细方案以及用于细胞鉴定的免疫荧光染色程序。这些方法对于模拟再生性肌生成以了解MuSCs的动态、功能和分子调控至关重要。