Myotube Differentiation

Myotube differentiation is the developmental process in which proliferating muscle precursor cells, or myoblasts, become elongated, multinucleated cells that form the foundation of skeletal muscle fibers. It begins when myoblasts exit the cell cycle, align, and fuse, while myogenic regulatory factors such as MyoD and myogenin activate muscle-specific gene expression and drive structural maturation. In genetics, this process provides a tractable model for studying gene regulation during muscle development, identifying variants linked to muscle disorders, and testing how altered signaling affects cell fusion and muscle formation. Myotube cultures also support disease modeling, therapeutic research, and investigations of tissue regeneration.

Myotube Differentiation - Related Videos

Research

JoVE Journal - Biology

Glucose Uptake Measurement and Response to Insulin Stimulation in In Vitro Cultured Human Primary Myotubes

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Cited by 14 •

2017

In this method, human primary muscle cells are cultured in vitro to obtain differentiated myotubes and glucose uptake rates are measured. We provide a detailed protocol to quantify rates in basal and insulin-stimulated states using radiolabeled [3H] 2-deoxy-D-Glucose.

Research

JoVE Journal - Developmental Biology
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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.

Research

JoVE Journal - Genetics
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Exon Skipping in Directly Reprogrammed Myotubes Obtained from Human Urine-Derived Cells

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Cited by 6 •

2020

In this article, we describe a detailed protocol for efficient modelling of Duchenne muscular dystrophy muscle using MYOD1-converted urine-derived cells to evaluate the restoration of dystrophin mRNA and protein levels after exon skipping.

Measuring Trans-Plasma Membrane Electron Transport by C2C12 Myotubes

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Cited by 2 •

2018

The goal of this protocol is to spectrophotometrically monitor trans-plasma membrane electron transport utilizing extracellular electron acceptors and to analyze enzymatic interactions that may occur with these extracellular electron acceptors.

Isolation of Human Myoblasts, Assessment of Myogenic Differentiation, and Store-operated Calcium Entry Measurement

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Cited by 10 •

2017

Here, we describe a methodology to obtain a pure population of human myoblasts from adult muscle tissue. These cells are used to study in vitro skeletal muscle differentiation and, in particular, to study proteins involved in Ca2+ signaling.

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