Upadhyay Daya, Panduri Vijayalakshmi, Ghio Andrew, Kamp David W
Division of Pulmonary and Critical Care Medicine, Northwestern University Feinberg School of Medicine, and Department of Medicine, Veterans Administration Chicago Healthcare System, Lakeside Division, Chicago, IL 60611, USA.
Am J Respir Cell Mol Biol. 2003 Aug;29(2):180-7. doi: 10.1165/rcmb.2002-0269OC. Epub 2003 Feb 21.
Airborne particulate matter (PM) increases morbidity and mortality resulting from cardiopulmonary diseases including cancer. We hypothesized that PM is genotoxic to alveolar epithelial cells (AEC) by causing DNA damage and apoptosis. PM caused dose-dependent AEC DNA strand break formation, reductions in mitochondrial membrane potential (Delta psi m), caspase 9 activation, and apoptosis. An iron chelator and a free radical scavenger prevented these effects. Finally, overexpression of Bcl-xl, a mitochondrial anti-apoptotic protein, blocked PM-induced Delta psi m and DNA fragmentation. We conclude that PM causes AEC DNA damage and apoptosis by mechanisms that involve the mitochondria-regulated death pathway and the generation of iron-derived free radicals.
空气传播的颗粒物(PM)会增加包括癌症在内的心肺疾病导致的发病率和死亡率。我们推测,PM通过引起DNA损伤和凋亡对肺泡上皮细胞(AEC)具有遗传毒性。PM导致AEC形成剂量依赖性的DNA链断裂、线粒体膜电位(Δψm)降低、半胱天冬酶9激活及凋亡。一种铁螯合剂和一种自由基清除剂可预防这些效应。最后,线粒体抗凋亡蛋白Bcl-xl的过表达可阻断PM诱导的Δψm和DNA片段化。我们得出结论,PM通过涉及线粒体调节的死亡途径和铁衍生自由基生成的机制导致AEC DNA损伤和凋亡。