Mitochondrial DNA-depleted A549 cells are resistant to bleomycin

作者：Brar Sukhdev S; Meyer Joel N; Bortner Carl D; Van Houten Bennett; Martin William J II^*

来源：American Journal of Physiology - Lung Cellular and Molecular Physiology, 2012, 303(5): L413-L424.

DOI：10.1152/ajplung.00343.2011

• mitochondrial DNA damage
• protein kinase D1
• apoptosis
• reactive oxygen species
• fibrosis

Brar SS, Meyer JN, Bortner CD, Van Houten B, Martin WJ II. Mitochondrial DNA-depleted A549 cells are resistant to bleomycin. Am J Physiol Lung Cell Mol Physiol 303: L413-L424, 2012. First published July 6, 2012; doi:10.1152/ajplung.00343.2011.-Alveolar epithelial cells are considered to be the primary target of bleomycin-induced lung injury, leading to interstitial fibrosis. The molecular mechanisms by which bleomycin causes this damage are poorly understood but are suspected to involve generation of reactive oxygen species and DNA damage. We studied the effect of bleomycin on mitochondrial DNA (mtDNA) and nuclear DNA (nDNA) in human alveolar epithelial A549 cells. Bleomycin caused an increase in reactive oxygen species production, DNA damage, and apoptosis in A549 cells; however, bleomycin induced more mtDNA than nDNA damage. DNA damage was associated with activation of caspase-3, cleavage of poly(ADPribose) polymerase, and cleavage and activation of protein kinase D1 (PKD1), a newly identified mitochondrial oxidative stress sensor. These effects appear to be mtDNA-dependent, because no caspase-3 or PKD1 activation was observed in mtDNA-depleted (rho(0)) A549 cells. Survival rate after bleomycin treatment was higher for A549 rho(0) than A549 cells. These results suggest that A549 rho(0) cells are more resistant to bleomycin toxicity than are parent A549 cells, likely in part due to the depletion of mtDNA and impairment of mitochondria-dependent apoptotic pathways.

• 出版日期2012-9