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The cell cycle distribution should be given more consideration in cell-based in vitro toxicological studies

机译:在基于细胞的体外毒理学研究中应更多考虑细胞周期分布

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In this study, to discuss the importance of the cell cycle distribution in cell-based in vitro toxicity mechanism studies, diethyl sulfate (DES) was selected as a model chemical that induced the alteration of the cell cycle distribution in human bronchial epithelial cell line 16HBE 14o- (HBE) cells. Cells were treated with various concentrations of DES, cell proliferation and apoptosis were then determined. The results showed that DES concentration- dependently inhibited HBE cells proliferation and induced apoptosis. When cells were treated with 2.0 mM of DES for 20 or 28 h, significant S and G2/M phase accumulation was observed. Then, the relative cellular levels of Cdk4, p-Cdk2 (Thr160), Cyclins A and B1 in DES-treated HBE cells at 20 and 28 h were determined by two ways. The differences of the cell cycle distribution between DES and control groups were ignored in one way and eliminated by using flow cytometric cell sorting in the other. The results obtained by the two ways were quite different, which indicated that the cell cycle distribution might result in confounding if it was significantly different between the treated and control groups. Therefore, we propose that the cell cycle distribution should be given more consideration in cell-based in vitro toxicological studies.
机译:在这项研究中,为了讨论细胞周期分布在基于细胞的体外毒性机制研究中的重要性,选择了硫酸二乙酯(DES)作为模型化学物质,其诱导人支气管上皮细胞系16HBE细胞周期分布的改变14o-(HBE)细胞。用各种浓度的DES处理细胞,然后测定细胞增殖和凋亡。结果表明,DES浓度依赖性抑制HBE细胞增殖并诱导凋亡。当细胞用2.0 mM DES处理20或28 h时,观察到明显的S和G2 / M相积累。然后,通过两种方法确定在DES处理的HBE细胞中Cdk4,p-Cdk2(Thr160),Cyclins A和B1在20和28 h时的相对细胞水平。 DES和对照组之间的细胞周期分布差异以一种方式被忽略,而通过另一种方式通过流式细胞仪分选得以消除。两种方法获得的结果完全不同,这表明如果治疗组和对照组之间的细胞周期分布明显不同,则可能导致混淆。因此,我们建议在基于细胞的体外毒理学研究中应更多考虑细胞周期的分布。

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