Satellite cell activation and apoptosis in skeletal muscle from severely burned children

Abstract

Severe burns result in profound skeletal muscle atrophy; persistent muscle loss 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 propose that an impaired muscle satellite cell response is key in the etiology of burn-induced cachexia. Muscle biopsies from the m. vastus lateralis were obtained from 12 male pediatric burn patients (>30% total body surface area burn) and 12 young, healthy male subjects. Satellite cell content, activation and apoptosis were determined via immunohistochemistry, as were muscle fibre regeneration and myonuclear apoptosis. Embryonic myosin heavy chain expression and central nucleation, indices of skeletal muscle regeneration, were elevated in burn patients (P<0.05). Myonuclear apoptosis, quantified by TUNEL positive myonuclei and cleaved caspase 3 positive myonuclei, was also elevated in burn patients (P<0.05). Satellite cell content was reduced in burn patients, with approximately 20% of satellite cells positive for TUNEL staining, indicating DNA damage associated with apoptosis (P<0.05). Additionally, a significant percentage of satellite cells in burn patients expressed Ki67, a marker for cellular proliferation (P<0.05). Satellite cell activation was also observed in burn patients with increased expression of MyoD compared to healthy controls (P<0.05). Robust skeletal muscle atrophy occurs after burn injury, even in muscles located distally to the site of injury. The activation and apoptosis of satellite cells likely impacts the recovery of lean tissue following a severe burn, contributing to prolonged frailty in burn survivors.

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