Inducible satellite cell depletion attenuates skeletal muscle regrowth following a scald-burn injury.
Celeste C FinnertyColleen F McKennaLauren A CambiasCamille R BrightwellAnesh PrasaiYe WangAmina El AyadiDavid N HerndonOscar E SumanChristopher S FryPublished in: The Journal of physiology (2017)
Severe burns result in profound skeletal muscle atrophy; persistent muscle atrophy and weakness are major complications that hamper recovery from burn injury. Many factors contribute to the erosion of muscle mass following burn trauma, and we have previously shown concurrent activation and apoptosis of muscle satellite cells following a burn injury in paediatric patients. To determine the necessity of satellite cells during muscle recovery following a burn injury, we utilized a genetically modified mouse model (Pax7CreER -DTA) that allows for the conditional depletion of satellite cells in skeletal muscle. Additionally, mice were provided 5-ethynyl-2'-deoxyuridine to determine satellite cell proliferation, activation and fusion. Juvenile satellite cell-wild-type (SC-WT) and satellite cell-depleted (SC-Dep) mice (8 weeks of age) were randomized to sham or burn injury consisting of a dorsal scald burn injury covering 30% of total body surface area. Both hindlimb and dorsal muscles were studied at 7, 14 and 21 days post-burn. SC-Dep mice had >93% depletion of satellite cells compared to SC-WT (P < 0.05). Burn injury induced robust atrophy in muscles located both proximal and distal to the injury site (∼30% decrease in fibre cross-sectional area, P < 0.05). Additionally, burn injury induced skeletal muscle regeneration, satellite cell proliferation and fusion. Depletion of satellite cells impaired post-burn recovery of both muscle fibre cross-sectional area and volume (P < 0.05). These findings support an integral role for satellite cells in the aetiology of lean tissue recovery following a severe burn injury.
Keyphrases
- skeletal muscle
- induced apoptosis
- cell cycle arrest
- wound healing
- cell proliferation
- cross sectional
- endoplasmic reticulum stress
- pi k akt
- emergency department
- squamous cell carcinoma
- wild type
- signaling pathway
- single cell
- clinical trial
- autism spectrum disorder
- intensive care unit
- open label
- spinal cord
- drug induced
- spinal cord injury
- bone marrow
- high glucose