Department of Medicine, University of Louisville, Louisville, KY 40202, USA.
FEBS Lett. 2010 Jul 2;584(13):2947-52. doi: 10.1016/j.febslet.2010.05.025. Epub 2010 May 21.
The major pulmonary antioxidant enzyme involved in the protection of the lung interstitium from oxidative stress is extracellular superoxide dismutase (EC-SOD). It has been previously shown that EC-SOD knock-out mice are more susceptible to bleomycin-induced lung injury, however, the molecular mechanism(s) remains unclear. We report here that bleomycin-induced lung damage, in EC-SOD KO mice, is associated with increased hyaluronan release into alveolar fluid. Analysis of hyaluronan synthase gene expression and hyaluronan molecular weight distribution suggested that elevated levels of hyaluronan in the alveolar fluid are mostly due to its release from the interstitium. Our results indicate that EC-SOD attenuates bleomycin-induced pulmonary injury, at least in part, by preventing superoxide-mediated release of hyaluronan into alveolar space.
参与保护肺间质免受氧化应激的主要肺抗氧化酶是细胞外超氧化物歧化酶 (EC-SOD)。先前的研究表明,EC-SOD 敲除小鼠对博来霉素诱导的肺损伤更为敏感,但是,其分子机制尚不清楚。我们在这里报告,在 EC-SOD KO 小鼠中,博来霉素诱导的肺损伤与透明质酸释放到肺泡液中增加有关。对透明质酸合酶基因表达和透明质酸分子量分布的分析表明,肺泡液中透明质酸水平升高主要是由于其从间质释放。我们的结果表明,EC-SOD 通过防止超氧化物介导的透明质酸释放到肺泡空间,至少部分减轻了博来霉素诱导的肺损伤。