Yoshioka Kiyoshi, Kitajima Yasuo, Okazaki Narihiro, Chiba Ko, Yonekura Akihiko, Ono Yusuke
Department of Muscle Development and Regeneration, Institute of Molecular Embryology and Genetics, Kumamoto University, Kumamoto, Japan.
Department of Orthopaedic Surgery, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Front Cell Dev Biol. 2020 Aug 13;8:793. doi: 10.3389/fcell.2020.00793. eCollection 2020.
Primary culture of skeletal muscle stem cells (MuSCs) is indispensable to study the dynamics of muscle regeneration and homeostasis. Here we describe the modified pre-plating method for isolating MuSCs in culture with greatly improved purity, yield, and procedure time. The protocol is based on the distinct adhesion characteristics of MuSCs. We reduced the procedure time to 2.5 days to obtain highly purified MuSCs through a newly employed re-plating step, which repeats incubation and cell-suspension. The re-plating step efficiently traps remaining fibroblastic cells, but not MuSCs, on a collagen-coated dish. Additionally, we confirmed that MuSCs can be isolated from small amounts of human/mouse muscle tissues, enabling us to perform experiments with amount-limited specimens. Thus, our method can be performed with basic laboratory equipment suitable for most facilities and without sophisticated MuSC handling techniques.
骨骼肌干细胞(MuSCs)的原代培养对于研究肌肉再生和内环境稳定的动态过程不可或缺。在此,我们描述了一种改良的预铺板方法,用于在培养中分离MuSCs,该方法在纯度、产量和操作时间方面都有显著提高。该方案基于MuSCs独特的黏附特性。我们通过新采用的再铺板步骤将操作时间缩短至2.5天,以获得高度纯化的MuSCs,该步骤重复孵育和细胞悬浮过程。再铺板步骤有效地将残留的成纤维细胞而非MuSCs捕获在胶原包被的培养皿上。此外,我们证实可以从小鼠/人类少量肌肉组织中分离出MuSCs,这使我们能够对数量有限的样本进行实验。因此,我们的方法可以使用大多数实验室都具备的基本设备来完成,无需复杂的MuSCs处理技术。