Panci Georgiana, E M Kneppers Anita, Mounier Rémi, Chazaud Bénédicte, Juban Gaëtan
Institut NeuroMyoGène, Unité Physiopathologie et Génétique du Neurone et du Muscle, CNRS, UMR5261, INSERM U1315, Université Claude Bernard Lyon 1, Lyon, France.
Methods Mol Biol. 2023;2640:57-71. doi: 10.1007/978-1-0716-3036-5_5.
Adult muscle stem cells rebuild myofibers after damage. Although they are highly powerful to implement the adult myogenic program, they need environmental cues provided by surrounding cells for efficient and complete regeneration. Muscle stem cell environment includes fibroadipogenic precursors, vascular cells, and macrophages. A way to decipher the complexity of the interactions muscle stem cells establish with their neighborhood is to co-culture cells freshly isolated from the muscle and assess the impact of one cell type on the behavior/fate of the other cell type. Here, we present a protocol allowing the isolation of primary muscle stem cells, macrophages, and fibroadipogenic precursors by Fluorescence Activated Cell Sorting (FACS) or Magnetic Cell Separation (MACS), together with co-culture methods using a specific setup for a short time window to keep as much as possible the in vivo properties of the isolated cells.
成年肌肉干细胞在损伤后可重建肌纤维。尽管它们它们它们在执行成年生肌程序方面具有强大能力,但需要周围细胞提供的环境信号才能实现高效且完全的再生。肌肉干细胞环境包括纤维脂肪生成前体细胞、血管细胞和巨噬细胞。解析肌肉干细胞与其周围细胞建立的复杂相互作用的一种方法是将刚从肌肉中分离出的细胞进行共培养,并评估一种细胞类型对另一种细胞类型行为/命运的影响。在此,我们展示了一种方案,该方案允许通过荧光激活细胞分选(FACS)或磁性细胞分离(MACS)分离原代肌肉干细胞、巨噬细胞和纤维脂肪生成前体细胞,以及使用特定设置在短时间窗口内进行共培养的方法,以尽可能保留分离细胞的体内特性。