Impact of Different Methods of Induction of Cellular Hypoxia: Focus on Protein Homeostasis Signaling Pathways and Morphology of C2C12 Skeletal Muscle Cells Differentiated into Myotubes
Abstract
Hypoxia, occurring in several pathologies, has deleterious effects on skeletal muscle, in particular on protein homeostasis. Different induction methods of hypoxia are commonly used in cellular models to investigate the alterations of muscular function consecutive to hypoxic stress. However, a consensus is not clearly established concerning hypoxia induction methodology. Our aim was to compare oxygen deprivation with chemically induced hypoxia using cobalt chloride (CoCl 2 ) or desferrioxamine (DFO) on C2C12 myotubes which were either cultured in hypoxia chamber at an oxygen level of 4% or treated with CoCl 2 or DFO. For each method of hypoxia induction, we determined their impact on muscle cell morphology and on expression or activation status of key signaling proteins of synthesis and degradation pathways. The expression of HIF-1α increased whatever the method of hypoxia induction. Myotube diameter and protein content decreased exclusively for C2C12 myotubes submitted to physiological hypoxia (4% O 2 ) or treated with CoCl 2 . Results were correlated with a hypophosphorylation of key proteins regulated synthesis pathway (Akt, GSK3-β and P70S6K). Similarly, the phosphorylation of FoxO1 decreased and the autophagy-related LC3-II was overexpressed with 4% O 2 and CoCl 2 conditions. Our results demonstrated that in vitro oxygen deprivation and the use of mimetic agent such as CoCl 2 , unlike DFO, induced similar responses on myotube morphology and atrophy/hypertrophy markers. T…
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A recent study showed an inhibition of the AKT/GSK3-β/P70S6K protein synthesis pathway associated with an increased autophagy-related LC3BII/LC3BI ratio in C2C12 myotubes cultured in hypoxic conditions.
“A recent study showed an inhibition of the AKT/GSK3-β/P70S6K protein synthesis pathway associated with an increased autophagy-related LC3BII/LC3BI ratio in C2C12 myotubes cultured in hypoxic conditions [70].”
From Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting (2023) · cites this paper as [70]
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Protein breakdown in muscle wasting: Role of autophagy-lysosome and ubiquitin-proteasome
Sandri, M. (2013) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2013.04.023 · Cited by 689 · see citing works
Chaillou1, T., & Lanner, J. T. (2016) · The FASEB Journal · doi:10.1096/fj.201600757r · Cited by 84 · see citing works
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Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting
Henrot, P., Dupin, I., Schilfarth, P., Esteves, P., Blervaque, L., Zysman, M., Gouzi, F., Hayot, M., Pomiès, P., & Berger, P. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24076454 · Cited by 85 · see citing works
“HIF1-α expression increases in C2C12 myotubes submitted to hypoxia [70].”
Background
- Authors
- Bensaid, S., Fabre, C., Fourneau, J., & Cieniewski-Bernard, C.
- Affiliations
- Université de Lille (FR)
- Venue
- Journal of Physiology and Biochemistry
- Published
- 2019-07-02
- Volume
- 75
- Issue
- 3
- Pages
- 367-377
- ISSN
- 1138-7548 (ISSN-L)
- 1877-8755
- OpenAlex
- W2954213593
- Cited by
- 16
- References
- 2
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 1 · 2023: 1 · 2022: 2 · 2021: 3 · 2020: 5
- FWCI
- 0.83
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Physiology and Biochemistry (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Muscle metabolism and nutrition
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer, Hypoxia, and Metabolism
- Keywords
- cellular hypoxia, cobalt chloride, deferoxamine, C2C12 myotubes, skeletal muscle atrophy, proteostasis, HIF-1α, Akt signaling, GSK3β, p70S6K, FOXO1, autophagy, LC3-II, hypoxic stress
- MeSH terms
- Animals, Hypoxia, Cell Differentiation, Cell Line, Cell Survival, Cobalt, Deferoxamine, Homeostasis, Oxygen, Signal Transduction, Cell Hypoxia, Muscle Fibers, Skeletal, Myoblasts, Hypoxia-Inducible Factor 1, alpha Subunit
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