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Combined effect of alpha particles and cigarette smoke on human lung epithelial cells in vitro

机译:α粒子和香烟烟雾对体外人肺上皮细胞的综合作用

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摘要

Purpose: The combined toxicity of alpha particles and cigarette smoke to the critical cells in the lungs was investigated to assess the risk of smoking workers who handle naturally occurring radioactive materials. Materials and methods: The toxicity of alpha particles and cigarette smoke extract (CSE) was evaluated in terms of DNA double-strand break (DSB) induction and clonogenic cell death of human lung epithelial cells in vitro. The cells were exposed to alpha particles at doses of up to 0.25 Gy for gamma-H2AX assay and from 1.25 Gy to 5 Gy for clonogenic assay. CSE exposure of the cells was facilitated in the culture medium at CSE concentrations ranging from 1% to 12%. Additional experiments were performed using mouse endothelial cells for comparison. Results: The increases in the levels of DNA DSBs were linearly dependent on radiation dose and CSE concentration. The CSE-treated cells also responded with a linearly increasing number of DNA DSBs to the radiation dose. Both human lung epithelial cells and mouse endothelial cells showed exponential decreases in clonogenic surviving fraction as the dose from alpha particle exposure increased. Both cells responded with the clonogenic surviving fractions decreasing in a linear proportion to the CSE concentration in the culture medium. Conclusion: In our experimental in vitro setup, CSE treatment and alpha particle exposure affected the cells in an additive manner either for DNA DSB production or for clonogenic cell death induction.
机译:目的:研究了α颗粒和香烟烟雾对肺部临界细胞的组合毒性,评估了处理自然发生的放射性物质的吸烟工人的风险。材料和方法:在体外DNA双链断裂(DSB)诱导和克隆灭菌细胞死亡方面评价α颗粒和香烟烟雾提取物(CSE)的毒性。将细胞以高达0.25Gy的剂量暴露于γ-H2AX测定的α颗粒,并且1.25Gy至5Gy用于克隆灭菌。 CSE在CSE浓度的培养基中促进细胞的CSE暴露,其范围为1%至12%。使用小鼠内皮细胞进行另外的实验进行比较。结果:DNA DSB水平的增加是线性的,依赖于辐射剂量和CSE浓度。 CSE处理的细胞也用线性越来越多的DNA DNA DSB响应于辐射剂量。当来自α颗粒暴露的剂量增加时,人肺上皮细胞和小鼠内皮细胞和小鼠内皮细胞都显示出克隆源存活率的指数降低。两种细胞随着克隆源存活的级分响应与培养基中的CSE浓度的线性比例下降。结论:在我们的实验体外设置,CSE治疗和α粒子暴露以添加剂的方式影响细胞,用于DNA DNA DNSB生产或用于克隆核酸细胞死亡诱导。

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