Myofiber Satellite Association

Myofiber satellite association describes the physical and functional relationship between skeletal muscle fibers and satellite cells, which are resident muscle stem cells essential for tissue maintenance and repair. Satellite cells occupy a niche between the myofiber sarcolemma and surrounding basal lamina, where local signals maintain quiescence; injury or mechanical stress activates them to proliferate, differentiate into myoblasts, and fuse with existing or newly forming fibers. Understanding this association helps explain skeletal muscle regeneration, adaptation, and aging, while supporting research into muscular disorders, exercise responses, and regenerative therapies.

Myofiber Satellite Association - Related Videos

Research

JoVE Journal - Biology
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Isolation and Culture of Individual Myofibers and their Satellite Cells from Adult Skeletal Muscle

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Cited by 173 •

2013

Isolation and culture of myofibers is the gold standard in vitro system to study the transition of satellite cells through quiescence, activation and differentiation. Importantly, the single myofiber culture system preserves the myofiber/stem cell association, which is an essential component of the muscle stem cell niche.

Research

JoVE EoE - Rodent Models

Myofiber Isolation: A Technique to Obtain Single Myofibers from Harvested Mouse Extensor Digitorum Longus (EDL) Muscle

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2025

This video demonstrates the isolation of single myofibres from harvested murine Extensor Digitorum Longus (EDL) muscle. The isolated myofibres can be cultured to study myofiber-associated muscle stem cell activity.

In Vitro Differentiation of Mature Myofibers for Live Imaging

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Cited by 38 •

2017

Muscle cells are among the most complex eukaryotic cells. We present a protocol for the in vitro differentiation of highly mature myofibers that allows for genetic manipulation and clear imaging during all developmental stages.

DNA Electroporation, Isolation and Imaging of Myofibers

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Cited by 30 •

2015

This protocol utilizes electroporation to introduce and express fluorescently labeled proteins in mouse muscle fibers. Following recovery after electroporation, fibers are isolated. Individual fibers are then imaged using high resolution confocal microscopy to visualize muscle structure.

Analysis of Embryonic and Larval Zebrafish Skeletal Myofibers from Dissociated Preparations

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Cited by 21 •

2013

Zebrafish are an emerging system for modeling human disorders of the skeletal muscle. We describe a fast and efficient method to isolate skeletal muscle myofibers from embryonic and larval zebrafish. This method yields a high-density myofiber preparation suitable for study of single skeletal muscle fiber morphology, protein subcellular localization, and muscle physiology.

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