Abstract
The muscle satellite cell population is responsible for homeostatic maintenance of muscle fibers in response to muscle injury and normal wear and tear. This population is heterogeneous, and its capacity for self-renewal and differentiation can be altered either by mutation of genes that regulate these processes or with natural processes such as aging. The satellite cell colony assay is a facile way to extract information about the proliferation and differentiation potential of individual cells. Here, we provide a detailed protocol for the isolation, single cell plating, culture, and evaluation of colonies derived from single satellite cells. The variables of cell survival (cloning efficiency), proliferative potential (nuclei per colony), and differentiation propensity (ratio of nuclei within myosin heavy chain-positive cytoplasm to total nuclei) can thus be obtained.
Original language | English (US) |
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Title of host publication | Methods in Molecular Biology |
Publisher | Humana Press Inc. |
Pages | 45-55 |
Number of pages | 11 |
DOIs | |
State | Published - 2023 |
Publication series
Name | Methods in Molecular Biology |
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Volume | 2640 |
ISSN (Print) | 1064-3745 |
ISSN (Electronic) | 1940-6029 |
Bibliographical note
Publisher Copyright:© 2023, Springer Science+Business Media, LLC, part of Springer Nature.
Keywords
- Colony
- Differentiation
- Satellite cells
- Self-renewal
- Skeletal muscle
- Muscle Fibers, Skeletal
- Humans
- Cell Differentiation/physiology
- Cells, Cultured
- Muscular Diseases
- Muscle, Skeletal
- Satellite Cells, Skeletal Muscle
PubMed: MeSH publication types
- Journal Article