Research Article

Role of Human NADPH Quinone Oxidoreductase (NQO1) in Oxygen-Mediated Cellular Injury and Oxidative DNA Damage in Human Pulmonary Cells

Figure 3

NQO1 overexpression protected cells from hyperoxic toxicity. BEAS-2B cells stably transfected with pcDNA3.1 (Ctr), pCMV-NQO1 (CMV-NQO1), pWT-NQONQO1 (NQO1-NQO1), and pSNP-NQONQO1 (SNP) were incubated under room air (RA) or 80% O2 (O2) condition for 48 h and the MTT cell viability assay (a), the live cell protease activity assay (b), the dead cell protease activity assay (c), and the caspase 3/7 activity assay (d) were determined using the Promega ApoTox-Glo Triplex Assay. Statistically significant differences between the RA and O2 groups. Statistically significant difference with Ctr. Statistically significant difference between the WT- and SNP-NQO1 promoter (; ). Hyperoxia decreased cell viability, which was attenuated by overexpression of NQO1 (a and b).
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