Activation of HSPA1A promoter by environmental pollutants: An early and rapid response to cellular damage

被引:1
作者
Xin, Lili [1 ]
Wang, Jianshu [2 ]
Fan, Guoqiang [3 ]
Wu, Yanhu [1 ]
Guo, Sifan [1 ]
机构
[1] Soochow Univ, Coll Med, Sch Publ Hlth, Suzhou 215123, Jiangsu, Peoples R China
[2] Suzhou Ctr Dis Prevent & Control, Suzhou, Jiangsu, Peoples R China
[3] Suzhou Ind Pk Ctr Dis Control & Prevent, Suzhou, Jiangsu, Peoples R China
基金
中国博士后科学基金;
关键词
Transcriptional activation; Environmental pollutants; Oxidative stress; Genotoxic damage; Toxicity screening; INDUCED OXIDATIVE STRESS; DNA-DAMAGE; HEAT-SHOCK; INDIVIDUAL CELLS; SULFUR-DIOXIDE; FORMALDEHYDE; EXPRESSION; INDUCTION; HSP70; PROTEINS;
D O I
10.1016/j.etap.2015.03.011
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
We established the HepG2-luciferase cells containing a luciferase reporter gene regulated by human HSPA1A promoter. The screening of heat shock and three typical environmental toxicants revealed differences in their capacities to activate HSPA1A promoter in HepG2-luciferase cells. After heat shock, a progressive time-dependent increase in relative luciferase activity was detected peaking at 8 h of recovery. Benzo[a]pyrene, formaldehyde and sodium bisulfite induced significant time-dependent elevation of relative luciferase activity, which were positively correlated with MDA concentration, Olive tail moment and micronuclei frequency. The significant increase in relative luciferase activity was already evident after 4h of benzo[a]pyrene, 1 h of formaldehyde and sodium bisulfite exposure, when no increases in cellular damage were detected by other toxicity tests. Therefore, the HepG2-luciferase cells are useful model for examining the overall cellular responses to oxidative stress and genotoxic damage, and provide a reporter system for rapid and sensitive screening of environmental pollutants. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:1027 / 1033
页数:7
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