Tucciarone Luca, Etxaniz Usue, Sandoná Martina, Consalvi Silvia, Puri Pier Lorenzo, Saccone Valentina
Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Fondazione Santa Lucia, Fosso di Fiorano 64, 00143, Rome, Italy.
DAHFMO, Unit of Histology and Medical Embryology, Sapienza University of Rome, Via A. Scarpa 14, 00161, Rome, Italy.
Methods Mol Biol. 2018;1687:231-256. doi: 10.1007/978-1-4939-7374-3_17.
Functional interactions between muscle (satellite) stem cells-MuSCs-and other cellular components of their niche (the fibro-adipogenic progenitors-FAPs) coordinate regeneration of injured as well as diseased skeletal muscles. These interactions are largely mediated by secretory networks, whose integrity is critical to determine whether repair occurs by compensatory regeneration leading to formation of new contractile fibers, or by maladaptive formation of fibrotic scars and fat infiltration. Here we provide the description of methods for isolation of FAPs and MuSCs from muscles of wild type and dystrophic mice, and protocols of cocultures as well as MuSC's exposure to FAP- derived exosomes. These methods and protocols can be exploited in murine models of acute muscle injury to investigate salient features of physiological repair, and in models of muscular diseases to identify dysregulated networks that compromise functional interactions between cellular components of the regeneration environment during disease progression. We predict that exporting these procedures to patient-derived muscle samples will contribute to advance our understanding of human skeletal myogenesis and related disorders.
肌肉(卫星)干细胞(MuSCs)与其微环境中的其他细胞成分(成纤维脂肪生成祖细胞,FAPs)之间的功能相互作用协调受损和患病骨骼肌的再生。这些相互作用很大程度上由分泌网络介导,其完整性对于确定修复是通过代偿性再生形成新的收缩纤维,还是通过纤维化瘢痕的适应性不良形成和脂肪浸润至关重要。在这里,我们描述了从野生型和营养不良小鼠的肌肉中分离FAPs和MuSCs的方法,以及共培养方案和MuSCs暴露于FAP衍生外泌体的方案。这些方法和方案可用于急性肌肉损伤的小鼠模型,以研究生理修复的显著特征,并用于肌肉疾病模型,以识别在疾病进展过程中破坏再生环境细胞成分之间功能相互作用的失调网络。我们预测,将这些程序应用于患者来源的肌肉样本将有助于推进我们对人类骨骼肌生成及相关疾病的理解。