Cited by 118Mitochondrial Function and PathologyAdipose Tissue and MetabolismMuscle Physiology and Disorders

Interactions between bioenergetics and mitochondrial biogenesis

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Leary, Scot C., Battersby, Brendan J., Hansford, Richard G., Moyes, Christopher D.·1998·Biochimica et Biophysica Acta (BBA) - Bioenergetics

Abstract

We studied the interaction between energy metabolism and mitochondrial biogenesis during myogenesis in C2C12 myoblasts. Metabolic rate was nearly constant throughout differentiation, although there was a shift in the relative importance of glycolytic and oxidative metabolism, accompanied by increases in pyruvate dehydrogenase activation state and total activity. These changes in mitochondrial bioenergetic parameters observed during differentiation occurred in the absence of a hypermetabolic stress. A chronic (3 day) energetic stress was imposed on differentiated myotubes using sodium azide to inhibit oxidative metabolism. When used at low concentrations, azide inhibited more than 70% of cytochrome oxidase (COX) activity without changes in bioenergetics (either lactate production or creatine phosphorylation) or mRNA for mitochondrial enzymes. Higher azide concentrations resulted in changes in bioenergetic parameters and increases in steady state COX II mRNA levels. Azide did not affect mtDNA copy number or mRNA levels for other mitochondrial transcripts, suggesting azide affects stability, rather than synthesis, of COX II mRNA. These results indicate that changes in bioenergetics can alter mitochondrial genetic regulation, but that mitochondrial biogenesis accompanying differentiation occurs in the absence of hypermetabolic challenge.

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Crossref · 10.1016/s0005-2728(98)00105-4

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  • Myogenic differentiation is coupled with increased pyruvate oxidation and OXPHOS, and this metabolic shift is likely driven, in part, by the significant energy demands of skeletal muscle.

    “Myogenic differentiation is also coupled with increased pyruvate oxidation and OXPHOS, and this metabolic shift is likely driven, in part, by the significant energy demands of skeletal muscle (121, 204, 209).”

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References 36 · Cited by 118

Authors
Leary, S. C., Battersby, B. J., Hansford, R. G., & Moyes, C. D.
Affiliations
  • Queen's University (CA)
  • National Institutes of Health (US)
Corresponding author
Moyes, Christopher D.
Venue
Biochimica et Biophysica Acta (BBA) - Bioenergetics
Publisher
Elsevier BV
Published
1998-07
Volume
1365
Issue
3
Pages
522-530
ISSN
0005-2728 (ISSN-L)
OpenAlex
W1986451029
Cited by
118
References
36
Citations by year
2026: 4 · 2025: 1 · 2024: 6 · 2023: 7 · 2022: 5 · 2021: 1 · 2020: 13 · 2019: 8 · 2018: 6 · 2017: 5 · 2016: 7 · 2015: 7 · 2013: 6 · 2012: 2
FWCI
0.93
Type
journal article
Language
en
Open access
Locations
  • Biochimica et Biophysica Acta (BBA) - Bioenergetics (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
  • Health Sciences › Medicine › Physiology › Adipose Tissue and Metabolism
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
Keywords
mitochondrial biogenesis, myogenesis, C2C12 myoblasts, energy metabolism, glycolysis, oxidative metabolism, pyruvate dehydrogenase, sodium azide, cytochrome c oxidase, mitochondrial DNA copy number, lactic acid production
MeSH terms
RNA, Mitochondrial, Adenosine Triphosphate, Animals, Cell Differentiation, Cell Line, Electron Transport Complex IV, DNA, Mitochondrial, Energy Metabolism, Mitochondria, Oxygen Consumption, Pyruvate Dehydrogenase Complex, RNA, RNA, Messenger, Muscle, Skeletal, Gene Expression Regulation, Developmental, Sodium Azide, Mice

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