Ochi Takafumi, Suzuki Toshihide, Barrett J Carl, Tsutsui Takeki
Laboratory of Toxicology, Faculty of Pharmaceutical Sciences, Teikyo University, Sagamiko, Kanagawa 199-0195, Japan.
Toxicology. 2004 Oct 15;203(1-3):155-63. doi: 10.1016/j.tox.2004.06.006.
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.
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碘化二甲基胂(DMI)诱导细胞转化、非整倍体、中心体异常和多极纺锤体形成的能力。浓度超过0.1微摩尔时,用DMI处理会以浓度依赖的方式降低细胞生长。浓度为0.1至1.0微摩尔的DMI处理可诱导SHE细胞发生形态转化。由形态转化菌落频率确定的DMI转化活性比相同浓度亚砷酸钠处理诱导的活性高约30倍。流式细胞术表明DMI导致非整倍体群体增加,表现为亚2N、亚4N和亚8N的出现。DMI还导致γ-微管蛋白染色异常,表明中心体完整性丧失,从而在有丝分裂细胞中诱导多极纺锤体形成。检测到中心体部分在细胞周边而非细胞中心融合的有丝分裂细胞是导致多极纺锤体的早期变化。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诱导非整倍体的因果变化的重要性。