心肌细胞
骨骼肌
单元格排序
人口
细胞生物学
肌发生
细胞
肌肉疾病
生物
细胞培养
干细胞
原电池
分离(微生物学)
免疫学
抗体
C2C12型
肌肉组织
病理
再生(生物学)
组织培养
分子生物学
人体肌肉
解剖
作者
Felipe de Souza Leite,Emanuela Gussoni
出处
期刊:PubMed
日期:2026-01-01
卷期号:2975: 151-163
标识
DOI:10.1007/978-1-0716-4811-7_10
摘要
Primary myoblasts are generated from committed stem cells, responsible for repairing skeletal muscle fibers upon injury. They are a valuable resource for scientific research in muscle disease and drug screening and hold promise for cell-based therapies. However, skeletal muscle biopsies contain a plethora of non-myogenic cells, exacerbated in diseased muscle tissues. Thus, purification methods of the myogenic cell population are necessary. This protocol describes techniques for dissociating cells from human and mouse skeletal muscle biopsies and enrichment for a highly myogenic population using magnetic isolation for mouse muscles and by fluorescence-activated cell sorting (FACS) using cell surface antibodies for humans. We also describe methods to expand myoblasts in culture and assess myogenicity.
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