Cigarette smoke and asbestos activate poly-ADP-ribose polymerase in alveolar epithelial cells

被引:19
|
作者
Kamp, DW
Srinivasan, M
Weitzman, SA
机构
[1] Northwestern Univ, Sch Med, Dept Med, Div Pulm & Crit Care Med, Chicago, IL 60611 USA
[2] Vet Affairs Chicago Hlth Care Syst Lakeside Div, Dept Med, Div Pulm & Crit Care Med, Chicago, IL USA
[3] Vet Affairs Chicago Hlth Care Syst Lakeside Div, Dept Med, Div Hematol Oncol, Chicago, IL USA
关键词
asbestos; cigarette smoke; alveolar epithelial cells; DNA damage; reactive oxygen species; lung injury; DNA repair;
D O I
10.2310/6650.2001.34092
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Cigarette smoke augments asbestos-induced bronchogenic carcinoma in a synergistic manner by mechanisms that are not established. One important mechanism may involve alveolar epithelial cell (AEC) injury resulting from oxidant-induced DNA damage that subsequently activates poly (ADP-ribose) polymerase (PARP), an enzyme involved in DNA repair that can deplete cellular energy stores. We previously showed that whole aqueous cigarette smoke extracts (CSE) augment amosite asbestos-induced DNA damage and cytotoxicity to cultured AEC in part by generating iron-induced free radicals. We hypothesized that CSE increase asbestos-induced AEC injury by triggering PARP activation resulting from DNA damage caused by iron-induced free radicals. Methods: Aqueous CSE were prepared fresh on the day of each experiment. PARP activity in WI-26 (a type I-like cell line) and A549 (a type II-like cell line) cells was assessed by the uptake of labeled NAD over 4 hours and confirmed on the basis of the reduction of PARP levels in the presence of a PARP inhibitor, 3-aminobenzamide (3-ABA). Cell survival was assessed by trypan blue dye exclusion. Results: Hydrogen peroxide (H2O2; 1-250 muM), CSE (0.4-10 vol%), and amosite asbestos (5-250 mug/cm(2)) each caused PARP activation in WI-26 and A549 cells. The combination of asbestos (5 mug/cm(2)) and CSE (0.04-10 %) induced WI-26 and A549 cell PARP activation without evidence of synergism. 3-ABA significantlyattenuatedWI-26 and A549 cell PARP activity and cell death after exposure to H2O2, CSE, and asbestos, Phytic acid, an iron chelator, catalase, and superoxide dismutase each decreased WI-26 cell PARP activation caused by asbestos and CSE. Conclusions: CSE and asbestos induce PARP activation in cultured AEC in a nonsynergistic manner, These data provide further support that asbestos and cigarette smoke are genotoxic to relevant lung target cells and that iron-induced free radicals in part cause these effects.
引用
收藏
页码:68 / 76
页数:9
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