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首页> 外文期刊>Toxicology: An International Journal Concerned with the Effects of Chemicals on Living Systems >A trivalent dimethylarsenic compound, dimethylarsine iodide, induces cellular transformation, aneuploidy, centrosome abnormality and multipolar spindle formation in Syrian hamster embryo cells.
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A trivalent dimethylarsenic compound, dimethylarsine iodide, induces cellular transformation, aneuploidy, centrosome abnormality and multipolar spindle formation in Syrian hamster embryo cells.

机译:三价二甲基砷化合物碘二甲基ar可诱导叙利亚仓鼠胚胎细胞发生细胞转化,非整倍性,中心体异常和多极纺锤体形成。

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摘要

The abilities of dimethylarsine iodide (DMI), a model compound of trivalent dimethylarsenicals, to induce cellular transformation, aneuploidy, centrosome abnormality, and multipolar spindle formations were investigated using the Syrian hamster embryo (SHE) cell model. Cellular growth was decreased in a concentration-dependent manner by treatment with DMI at concentrations over 0.1 microM. Treatment with DMI at concentrations from 0.1 to 1.0 microM induced morphological transformation in SHE cells. The transforming activity of DMI, determined by the frequency of morphologically transformed colonies, was approximately 30 times higher than that induced by treatment with the same concentration of sodium arsenite. Flow cytometry suggested an increase in the aneuploid population caused by DMI, as shown by the appearance of hypo-2N, hypo-4N and hypo-8N. DMI also caused abnormal staining of gamma-tubulin, indicating loss of centrosome integrity and a resultant induction of multipolar spindles in mitotic cells.Mitotic cells with centrosomes that coalesced partly at the cell periphery, not the cell center, were detected as early changes that resulted in multipolar spindles. These findings indicate that DMI has transforming activity in SHE cells. Moreover, the results suggest the importance of centrosome abnormalities as a causal change of DMI-induced aneuploidy.
机译:使用叙利亚仓鼠胚胎(SHE)细胞模型研究了三价二甲基砷化合物的模型化合物二甲基ar碘化物(DMI)诱导细胞转化,非整倍性,中心体异常和多极纺锤体形成的能力。通过用浓度超过0.1 microM的DMI处理,细胞生长以浓度依赖性的方式降低。在0.1至1.0 microM的浓度下用DMI处理可诱导SHE细胞发生形态转化。由形态转化菌落的频率确定的DMI转化活性,比相同浓度的亚砷酸钠处理诱导的转化活性高约30倍。流式细胞仪表明由DMI引起的非整倍体数量增加,如hypo-2N,hypo-4N和hypo-8N的出现所示。 DMI还引起γ-微管蛋白异常染色,表明有丝分裂细胞中中心体完整性丧失并诱导多极纺锤体。在多极主轴中。这些发现表明DMI在SHE细胞中具有转化活性。此外,结果表明中心体异常作为DMI诱导的非整倍性的因果变化的重要性。

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