Role of heat shock protein 70 expression in DNA damage induced by benzo(a)pyrene.
- Author:
Qian XU
1
;
Jin-bo YANG
;
Chang-zheng JIANG
;
Miao YANG
;
Lei KE
;
Mei-an HE
;
Feng WANG
;
Tang-chun WU
Author Information
- Publication Type:Journal Article
- MeSH: Benzo(a)pyrene; toxicity; Blotting, Western; Cell Line, Tumor; Comet Assay; DNA; drug effects; genetics; DNA Damage; Dose-Response Relationship, Drug; HSP70 Heat-Shock Proteins; analysis; Humans; Time Factors
- From: Chinese Journal of Industrial Hygiene and Occupational Diseases 2004;22(2):96-99
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo explore heat shock protein 70 (HSP70) expression of A549 cells and its role in DNA damage caused by benzo(a)pyrene (BaP).
METHODSHuman adenocarcinoma A549 cells were cultured in vitro, exposed by different concentrations of BaP (0, 1.25, 2.50, 5.00, 10.00 micro mol/L) for 6 hours, or 10 micro mol/L of BaP for different time (0, 4, 8, 12, 16, 24 and 48 h). Then HSP70 expression and DNA damage were detected using Western-blot and single cell gel electrophoresis (SCGE) assay respectively, and the relationship between HSP70 expression and DNA damage was further analyzed.
RESULTSThe integral optical densities of HSP70 in A549 cells treated with 1.25, 2.50, 5.00 and 10.00 micro mol/L BaP for 6 h (49.63 +/- 1.30, 45.72 +/- 1.03, 40.53 +/- 0.95, 37.50 +/- 1.20 respectively) were lower than that of the control cells (59.43 +/- 1.17) (P < 0.05). When A549 cells were exposed to 10 micro mol/L BaP for 4, 8, 12, 16 h, the integral optical densities of HSP70 were 33.33 +/- 0.80, 29.23 +/- 0.91, 12.51 +/- 0.96, 9.50 +/- 1.25 respectively, and there was an increasing tendency of the expression of HSP70 for 24 - 48 h (20.06 +/- 1.38, 24.51 +/- 1.39), however, all were different from that in control group (56.59 +/- 0.85) (P < 0.05). DNA damage scores in 10(6) A549 cells treated with 2.50, 5.00 and 10.00 micro mol/L BaP for 6 h (23,718 +/- 2,938, 30,128 +/- 2,937, 44,231 +/- 3,846) were significantly higher than that of the control cell (9,615 +/- 1,923) (P < 0.05). When A549 cells were exposed to 10 micro mol/L BaP for 4, 8, 12, 16, 24, 48 h, DNA damage scores (16,667 +/- 4,003, 38,461 +/- 1,924, 5,615 +/- 3,847, 76,282 +/- 2,937, 7,513 +/- 1,110 and 58,975 +/- 9,487) were also higher than that of control group (P < 0.05). There was a negative correlation between DNA damage and the expression of HSP70 when A549 cells were exposed to different concentrations of BaP.
CONCLUSIONHSP70 might enhance intracellular defenses against DNA damage induced by BaP.
