| Literature DB >> 26002045 |
Diqiu Li1, Qingchun Huang2, Miaoqing Lu1, Lei Zhang1, Zhichuan Yang1, Mimi Zong1, Liming Tao3.
Abstract
The organophosphate insecticide chlorpyrifos (CPF) is known to induce neurological effects, malformation and micronucleus formation, persistent developmental disorders, and maternal toxicity in rats and mice. The binding of chlorpyrifos with DNA to produce DNA adducts leads to an increasing social concern about the genotoxic risk of CPF in human, but CPF-induced cytotoxicity through DNA damage and cell apoptosis is not well understood. Here, we quantified the cytotoxicity and potential genotoxicity of CPF using the alkaline comet assay, γH2AX foci formation, and the DNA laddering assay in order to detect DNA damage and apoptosis in human HeLa and HEK293 cells in vitro. Drosophila S2 cells were used as a positive control. The alkaline comet assay showed that sublethal concentrations of CPF induced significant concentration-dependent increases in single-strand DNA breaks in the treated cells compared with the control. The percentage of γH2AX-positive HeLa cells revealed that CPF also causes DNA double-strand breaks in a time-dependent manner. Moreover, DNA fragmentation analysis demonstrated that exposure to CPF induced a significant concentration- and time-dependent increase in cell apoptosis. We conclude that CPF is a strongly genotoxic agent that induces DNA damage and cell apoptosis.Entities:
Keywords: Cell apoptosis; Chlorpyrifos; DNA damage; Genotoxicity; H2AX foci
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Year: 2015 PMID: 26002045 DOI: 10.1016/j.chemosphere.2015.05.024
Source DB: PubMed Journal: Chemosphere ISSN: 0045-6535 Impact factor: 7.086