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Toxicological study at inflammatory factors and DNA damages effects of Beijing atmospheric PM2.5 and its different fractions to pulmonary epithelial cells A549 of human |
JIAO Zhou-guang1, FU Xu-lei2, WEN Zhan-bo1, LI Jin-song1, LI Na1, ZHANG Ke1, WANG Jie1, HU Ling-fei1 |
1. State Key Laboratory of Pathogen and Biosecurity, Institute of Microbiology and Epidemiology, Academy of Military Medical Sciences, Beijing 100071, China;
2. College of Food Science and Technology, Bohai University, Jinzhou 121013, China |
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Abstract In order to investigate the toxicity effect of atmospheric PM2.5 and its different fractions to human pulmonary epithelial cells A549 with respect to the relationship between PM2.5 dosage and cell response, the water-soluble, fat-soluble, pure particle fractions of PM2.5 (designated WSP2.5, FSP2.5 and PPP2.5, respectively) prepared from original PM2.5 samples (designated OP2.5) and OP2.5 were to treat A549 cells at different PM concentrations (10, 50, 100, 200, 400μg/mL, respectively). The MTS method was used to test the cell viability at 6h, 10h, 24h, 48h and 72h post-treatment, while ELISA and RT-QPCR were employed to detect the production of inflammatory cytokines IL-6 and TNF-α and the AP-sites counting was conducted to determine the level of intracellular DNA damage at 24h post-treatment. WSP2.5 had very limited effect to inhibit cell growth and induce inflammatory damages and DNA base deletion. FSP2.5, PPP2.5 and OP2.5 at high concentrations showed the inhibitory effect to cell growth across treatment; when cells were treated with low concentrations of FSP2.5, PPP2.5 or OP2.5, the inhibition of cell growth occurred within a short period and then disappeared over time. FSP2.5, PPP2.5 and OP2.5 treatment significantly induced the production of IL-6at both mRNA and protein levels, while WSP2.5, PPP2.5 and OP2.5 treatment significantly induced the mRNA expression of TNF-α. FSP2.5, PPP2.5 and OP2.5 treatment also induced the considerable DNA base deletion. In a word, not only the complex components adsorbed on the solid core granules of PM2.5, but also the solid core granules themselves contributed to the cytotoxicity effects.
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Received: 18 October 2015
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