Protocol for accelerated skeletal muscle regeneration and hypertrophic muscle formation in mice

The skeletal muscle system is the major organ associated with movement of the body. Myogenesis and regeneration induced post-injury contribute to muscle formation and maintenance. Here, we provide detailed protocol for the accelerated repair of injured skeletal muscles and generation of hypertrophic...

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Veröffentlicht in:STAR protocols 2022-03, Vol.3 (1), p.101111-101111, Article 101111
Hauptverfasser: Ray, Rashmi, Rai, Vivek
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Sprache:eng
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Zusammenfassung:The skeletal muscle system is the major organ associated with movement of the body. Myogenesis and regeneration induced post-injury contribute to muscle formation and maintenance. Here, we provide detailed protocol for the accelerated repair of injured skeletal muscles and generation of hypertrophic muscle fibers. This protocol includes cardiotoxin induced muscle injury and also describes isolation of satellite cells from skeletal muscle tissues of mice. This protocol can be used to study the mechanisms associated with accelerated muscle repair and hypertrophy. For complete details on the use and execution of this protocol, please refer to Ray et al. (2021). [Display omitted] •Satellite cell isolation from mouse skeletal muscle tissue and induction of hypertrophy•An optimized protocol for accelerated muscle regeneration in mice•Protocol for generation of hypertrophic muscles in mice Skeletal muscle system is the major organ associated with movement of the body. Myogenesis and regeneration induced post-injury contribute to muscle formation and maintenance. Here, we provide detailed protocol for the accelerated repair of injured skeletal muscles and generation of hypertrophic muscle fibers. This protocol includes cardiotoxin induced muscle injury and also describes isolation of satellite cells from skeletal muscle tissues of mice. This protocol can be used to study the mechanisms associated with accelerated muscle repair and hypertrophy.
ISSN:2666-1667
2666-1667
DOI:10.1016/j.xpro.2021.101111