期刊
INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH
卷 17, 期 13, 页码 -出版社
MDPI
DOI: 10.3390/ijerph17134874
关键词
PM2; 5; DNA damage; oxidative stress; DNA repair gene; human bronchial epithelial cells
资金
- National Natural Science Foundation of China [21677006]
- State Key Laboratory of Environmental Criteria and Risk Assessment, Chinese Research Academy of Environmental Sciences [SKLECRA2017OFP]
Epidemiological studies have corroborated that respiratory diseases, including lung cancer, are related to fine particulate matter (<2.5 mu m) (PM2.5) exposure. The toxic responses of PM(2.5)are greatly influenced by the source of PM2.5. However, the effects of PM(2.5)from Beijing on bronchial genotoxicity are scarce. In the present study, PM(2.5)from Beijing was sampled and applied in vitro to investigate its genotoxicity and the mechanisms behind it. Human bronchial epithelial cells 16HBE were used as a model for exposure. Low (67.5 mu g/mL), medium (116.9 mu g/mL), and high (202.5 mu g/mL) doses of PM(2.5)were used for cell exposure. After PM(2.5)exposure, cell viability, oxidative stress markers, DNA (deoxyribonucleic acid) strand breaks, 8-OH-dG levels, micronuclei formation, and DNA repair gene expression were measured. The results showed that PM(2.5)significantly induced cytotoxicity in 16HBE. Moreover, the levels of reactive oxygen species (ROS), malondialdehyde (MDA), and cellular heme oxygenase (HO-1) were increased, and the level of glutathione (GSH) was decreased, which represented the occurrence of severe oxidative stress in 16HBE. The micronucleus rate was elevated, and DNA damage occurred as indicators of the comet assay, gamma-H2AX and 8-OH-dG, were markedly enhanced by PM2.5, accompanied by the influence of 8-oxoguanine DNA glycosylase (OGG1), X-ray repair cross-complementing gene 1 (XRCC1), and poly (ADP-ribose) polymerase-1 (PARP1) expression. These results support the significant role of PM(2.5)genotoxicity in 16HBE cells, which may occur through the combined effect on oxidative stress and the influence of DNA repair genes.
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