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首页> 外文期刊>Particle Fibre Toxicology >Cell cycle alterations induced by urban PM2.5 in bronchial epithelial cells: characterization of the process and possible mechanisms involved
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Cell cycle alterations induced by urban PM2.5 in bronchial epithelial cells: characterization of the process and possible mechanisms involved

机译:市区PM2.5在支气管上皮细胞中诱导的细胞周期改变:该过程的表征及其可能的机制

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Background This study explores and characterizes cell cycle alterations induced by urban PM2.5 in the human epithelial cell line BEAS-2B, and elucidates possible mechanisms involved. Methods The cells were exposed to a low dose (7.5?μg/cm2) of Milan winter PM2.5 for different time points, and the cell cycle progression was analyzed by fluorescent microscopy and flow cytometry. Activation of proteins involved in cell cycle control was investigated by Western blotting and DNA damage by 32P-postlabelling, immunostaining and comet assay. The formation of reactive oxygen species (ROS) was quantified by flow cytometry. The role of PM organic fraction versus washed PM on the cell cycle alterations was also examined. Finally, the molecular pathways activated were further examined using specific inhibitors. Results Winter PM2.5 induced marked cell cycle alteration already after 3?h of exposure, represented by an increased number of cells (transient arrest) in G2. This effect was associated with an increased phosphorylation of Chk2, while no changes in p53 phosphorylation were observed at this time point. The increase in G2 was followed by a transient arrest in the metaphase/anaphase transition point (10?h), which was associated with the presence of severe mitotic spindle aberrations. The metaphase/anaphase delay was apparently followed by mitotic slippage at 24?h, resulting in an increased number of tetraploid G1 cells and cells with micronuclei (MN), and by apoptosis at 40?h. Winter PM2.5 increased the level of ROS at 2?h and DNA damage (8-oxodG, single- and double stand breaks) was detected after 3?h of exposure. The PM organic fraction caused a similar G2/M arrest and augmented ROS formation, while washed PM had no such effects. DNA adducts were detected after 24?h. Both PM-induced DNA damage and G2 arrest were inhibited by the addition of antioxidants and α-naphthoflavone, suggesting the involvement of ROS and reactive electrophilic metabolites formed via a P450-dependent reaction. Conclusions Milan winter PM2.5 rapidly induces severe cell cycle alterations, resulting in increased frequency of cells with double nuclei and MN. This effect is related to the metabolic activation of PM2.5 organic chemicals, which cause damages to DNA and spindle apparatus.
机译:背景技术这项研究探索并表征了城市PM2.5在人上皮细胞系BEAS-2B中诱导的细胞周期改变,并阐明了可能的机制。方法将细胞暴露于低剂量(7.5?μg/ cm 2 )的米兰冬季PM2.5的不同时间点,并通过荧光显微镜和流式细胞术分析细胞周期进程。通过蛋白质印迹和 32 P-后标记,免疫染色和彗星试验检测DNA损伤,研究参与细胞周期控制的蛋白质的活化。通过流式细胞术定量反应性氧(ROS)的形成。还检查了PM有机组分与洗涤过的PM在细胞周期变化中的作用。最后,使用特异性抑制剂进一步检查了激活的分子途径。结果冬季PM2.5在暴露3小时后已经诱导了明显的细胞周期改变,其表现为G2中细胞数量增加(瞬时停滞)。这种作用与Chk2的磷酸化增加有关,而在此时间点未观察到p53磷酸化的变化。 G2的增加是在中期/后期过渡点(10?h)的短暂停顿,这与严重的有丝分裂纺锤体畸变有关。中期/后期延迟显然是在24?h后有丝分裂滑移,导致四倍体G1细胞和具有微核(MN)的细胞数量增加,并在40?h细胞凋亡。冬季PM2.5在2?h时会增加ROS的水平,在暴露3?h后会检测到DNA损伤(8-oxodG,单和双断裂)。 PM有机组分引起类似的G2 / M阻滞并增加ROS形成,而洗涤后的PM没有这种作用。 24小时后检测到DNA加合物。 PM诱导的DNA损伤和G2阻滞都通过添加抗氧化剂和α-萘黄酮来抑制,这表明ROS和通过P450依赖性反应形成的反应性亲电子代谢物的参与。结论米兰冬季PM2.5快速诱导严重的细胞周期改变,导致双核和MN的细胞频率增加。此作用与PM2.5有机化学物质的代谢活化有关,后者会破坏DNA和纺锤体。

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