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De novo myogenesis, or the formation of muscle fibers, begins during the early embryonic stages. The skeletal muscle is formed from somites– blocks of embryonic cell layers. The somites are further divided into dermatomes, myotomes, sclerotomes, and syndetomes. Among these, the myotomes give rise to muscle fibers.
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Mitochondrial precursors are translocated to the internal subcompartments via independent mechanisms involving distinct protein machineries called translocases.
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The inner mitochondrial membrane is the primary site of ATP synthesis. The inner membrane domain that forms a smooth layer adjacent to the outer membrane is called the inner boundary membrane. This domain contains membrane transporters that drive metabolites in and out of the mitochondria.  In contrast, the inner membrane network that invaginates into the matrix space is called the cristae membrane. This domain accounts for principle mitochondrial function as it accommodates the protein...
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Mitochondria01:37

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Mitochondria are eukaryotic cellular organelles that are known to produce energy through a process called oxidative phosphorylation. Besides their primary function, mitochondria are involved in various cellular processes, including cell growth, differentiation, signaling, metabolism, and senescence. Age-related changes cause a decline in mitochondrial quality and integrity due to increased mitochondrial mutations and oxidative damage. Thus, aging can severely impact mitochondrial functions,...
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Updated: Sep 9, 2025

Author Spotlight: Mitochondrial Remodeling in Skeletal Muscle
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Mitochondrial Biogenesis in Skeletal Muscle.

David A Hood1, Jonathan M Memme2, Ashley N Oliveira2

  • 1Muscle Health Research Centre, School of Kinesiology and Health Science, York University, Toronto, ON, Canada. dhood@yorku.ca.

Advances in Experimental Medicine and Biology
|August 29, 2025
PubMed
Summary

Mitochondrial biogenesis in skeletal muscle involves synthesizing proteins and phospholipids to expand the mitochondrial network. This process is crucial for adapting to exercise, cold, and starvation, with age impacting its signaling.

Keywords:
AgingCalciumExercise signalingExercise trainingGene expressionMitochondriaMitochondrial dynamicsMuscle disuseProtein importROS

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Area of Science:

  • Physiology
  • Cell Biology
  • Skeletal Muscle Biology

Background:

  • Mitochondria form a reticulum in skeletal muscle, optimizing substrate diffusion and metabolic function.
  • Mitochondria are key responders to metabolic homeostasis disruptions from stimuli like exercise, cold, and starvation.
  • Skeletal muscle mitochondrial adaptability is central to tissue function and response to external demands.

Purpose of the Study:

  • To introduce the subcellular events driving mitochondrial biogenesis in skeletal muscle.
  • To explore mitochondrial content, subpopulations, signaling cascades, and regulatory elements involved.
  • To review age-related changes in signaling pathways that regulate mitochondrial biogenesis.

Main Methods:

  • Utilizing models of exercise and muscle disuse to characterize mitochondrial biogenesis.
  • Incorporating genetic modifications of key regulatory elements in study models.
  • Reviewing existing literature on mitochondrial biogenesis and its regulation.

Main Results:

  • Mitochondrial biogenesis is essential for skeletal muscle adaptation to various physiological stressors.
  • Signaling pathways and regulatory elements significantly influence mitochondrial content and function.
  • Age-related alterations in signaling impact the capacity for mitochondrial biogenesis.

Conclusions:

  • Mitochondrial biogenesis is a dynamic process critical for skeletal muscle's metabolic flexibility.
  • Understanding the regulation of mitochondrial biogenesis provides insights into muscle health and aging.
  • Targeting mitochondrial biogenesis pathways holds potential for therapeutic interventions in muscle disorders.