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苯并[a]芘对肺上皮 BEAS-2B 细胞纺锤体取向和染色体分离保真度的影响。

Effect of Benzo[a]Pyrene on Spindle Misorientation and Fidelity of Chromosome Segregation in Lung Epithelial BEAS-2B Cells.

机构信息

Department of Radiology, Houston Methodist Research Institute, Houston, Texas.

出版信息

Toxicol Sci. 2018 Mar 1;162(1):167-176. doi: 10.1093/toxsci/kfx229.

Abstract

Benzo[a]pyrene (B[a]P) is an environmental carcinogen found in tobacco smoke. It leads to high levels of DNA adducts in the lungs of cigarette smokers contributing to genomic instability. Alterations in the mitotic spindle apparatus play a major role in the generation of genomic instability through promoting chromosome mis-segregation and aneuploidy. To date, the effect of B[a]P exposure on altering the mitotic apparatus in normal lung epithelial cells remains unknown. In our study, BEAS-2B human bronchial epithelial cells were exposed to B[a]P and spindle dynamics were evaluated. Confocal imaging showed that B[a]P exposure significantly alters spindles misorientation, leading to chromosome mis-segregations in the form of chromosome lags and bridges. In addition, centrosome duplication and premature centriole disengagement were induced leading to misaligned and multipolar spindle formation. Comparative genomic analysis of mitotic spindle associated genes, revealed downregulation of AurA-Plk1-AurB signaling cascade by B[a]P. In addition, we analyzed the status of p53 and its downstream p21 in B[a]P-treated cells and showed a suppression of p53-p21 axis. When the extent of DNA damage associated with induced mitotic abnormalities was investigated using γ-H2AX, a significant increase and persistence in DNA damage was observed. Overall, our findings show that B[a]P potently induces mitotic abnormalities, DNA damage, and genetic instability.

摘要

苯并[a]芘(B[a]P)是一种存在于烟草烟雾中的环境致癌物。它会导致吸烟人群肺部的 DNA 加合物水平升高,从而导致基因组不稳定。有丝分裂纺锤体装置的改变通过促进染色体错误分离和非整倍体在产生基因组不稳定性方面起着重要作用。迄今为止,B[a]P 暴露对改变正常肺上皮细胞有丝分裂装置的影响尚不清楚。在我们的研究中,用 B[a]P 暴露 BEAS-2B 人支气管上皮细胞,并评估纺锤体动力学。共聚焦成像显示,B[a]P 暴露显著改变纺锤体取向,导致染色体滞后和桥接等染色体错误分离。此外,还诱导了中心体复制和过早的中心粒脱离,导致纺锤体排列不齐和多极化。对有丝分裂纺锤体相关基因的比较基因组分析表明,B[a]P 下调了 AurA-Plk1-AurB 信号级联。此外,我们分析了 B[a]P 处理细胞中 p53 及其下游 p21 的状态,并显示 p53-p21 轴受到抑制。当使用 γ-H2AX 研究与诱导的有丝分裂异常相关的 DNA 损伤程度时,观察到 DNA 损伤显著增加和持续存在。总的来说,我们的研究结果表明,B[a]P 强烈诱导有丝分裂异常、DNA 损伤和遗传不稳定性。

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