Mechanical loading of tissue engineered skeletal muscle prevents dexamethasone induced myotube atrophy

• Published in: Journal of muscle research and cell motility Vol. 42; no. 2; pp. 149 - 159
• Main Authors: Aguilar-Agon, Kathryn W., Capel, Andrew J., Fleming, Jacob W., Player, Darren J., Martin, Neil R. W., Lewis, Mark P.
• Format: Journal Article
• Language: English
• Published: Cham Springer International Publishing 01-06-2021; Springer Nature B.V
• Subjects: Aging; Animal Anatomy; Animals; Atrophy; Biomedical and Life Sciences; Biomedicine; Cell Biology; Cell Line; Chronic illnesses; Degeneration; Dexamethasone; Dexamethasone - adverse effects; Gene expression; Histology; Hypertrophy; Immobilization; Life Sciences; Mechanical loading; Mechanical properties; Mice; Morphology; Muscle Fibers, Skeletal - pathology; Muscle, Skeletal - pathology; Muscular Atrophy - chemically induced; Muscular Atrophy - pathology; Musculoskeletal system; Myotubes; Original Paper; Proteomics; Skeletal muscle; Steroids; Tissue engineering; C2C12; Dexamethasone; Myotubes; Ubiquitin–proteasome; Skeletal muscle; Hypertrophy
• ISSN: 0142-4319; 1573-2657
• DOI: 10.1007/s10974-020-09589-0

Skeletal muscle atrophy as a consequence of acute and chronic illness, immobilisation, muscular dystrophies and aging, leads to severe muscle weakness, inactivity and increased mortality. Mechanical loading is thought to be the primary driver for skeletal muscle hypertrophy, however the extent to which mechanical loading can offset muscle catabolism has not been thoroughly explored. In vitro 3D-models of skeletal muscle provide a controllable, high throughput environment and mitigating many of the ethical and methodological constraints present during in vivo experimentation. This work aimed to determine if mechanical loading would offset dexamethasone (DEX) induced skeletal muscle atrophy, in muscle engineered using the C2C12 murine cell line. Mechanical loading successfully offset myotube atrophy and functional degeneration associated with DEX regardless of whether the loading occurred before or after 24 h of DEX treatment. Furthermore, mechanical load prevented increases in MuRF-1 and MAFbx mRNA expression, critical regulators of muscle atrophy. Overall, we demonstrate the application of tissue engineered muscle to study skeletal muscle health and disease, offering great potential for future use to better understand treatment modalities for skeletal muscle atrophy.