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二硫代氨基甲酸盐农药代森锌及其商品制剂阿祖罗的影响。五、对转化和未转化哺乳动物细胞系纺锤体装置诱导的异常情况。

Effect of the dithiocarbamate pesticide zineb and its commercial formulation, the azzurro. V. Abnormalities induced in the spindle apparatus of transformed and non-transformed mammalian cell lines.

作者信息

Soloneski Sonia, Reigosa Miguel A, Larramendy Marcelo L

机构信息

Laboratorio de Citogenética, Cátedra de Citología, Facultad de Ciencias Naturales y Museo, Universidad Nacional de La Plata, La Plata, Argentina.

出版信息

Mutat Res. 2003 Apr 20;536(1-2):121-9. doi: 10.1016/s1383-5718(03)00038-x.

DOI:10.1016/s1383-5718(03)00038-x
PMID:12694752
Abstract

Abnormalities induced in the mitotic spindle by zineb and azzurro (1.0-25.0 micro g/ml, 24h) were evaluated in Chinese hamster ovary (CHO) and HeLa cells, and in non-transformed human fibroblasts (NTHF). Spindles were stained with FITC-conjugated anti-beta tubulin. Treatment with 10.0 micro g/ml of zineb induced complete inhibition of cell viability in NTHF cells while 10.0 micro g/ml of azzurro decreased cell growth down to 62%. Higher doses of both compounds induced cell death. In HeLa and CHO cells, 15.0 micro g/ml of zineb and 10.0-15.0 micro g/ml of azzurro decreased viability, whereas 25.0 micro g/ml of both compounds was cytotoxic. A significantly decreased mitotic index (MI) was observed in NTHF treated with 5.0 micro g/ml zineb or azzurro, whereas 10.0 micro g/ml of both chemicals were necessary to induce the same phenomenon in HeLa and CHO cells. Treatment with 1.0-5.0 micro g/ml of zineb or azzurro induced a dose-dependent increase of degenerated spindles in NTHF and the number of degenerated or multipolar spindles in HeLa and CHO cells increased in a dose-dependent manner with 1.0-10.0 micro g/ml zineb and azzurro. Although zineb and azzurro were able to induce mitotic spindle abnormalities in all cell types, non-transformed cells were less resistant than immortalized cells.

摘要

在中华仓鼠卵巢(CHO)细胞、HeLa细胞和未转化的人成纤维细胞(NTHF)中,评估了代森锌和天蓝剂(浓度为1.0 - 25.0微克/毫升,处理24小时)对有丝分裂纺锤体的诱导异常情况。纺锤体用异硫氰酸荧光素(FITC)偶联的抗β微管蛋白进行染色。用10.0微克/毫升的代森锌处理可导致NTHF细胞的细胞活力完全受到抑制,而10.0微克/毫升的天蓝剂可使细胞生长降低至62%。两种化合物的更高剂量会诱导细胞死亡。在HeLa和CHO细胞中,15.0微克/毫升的代森锌和10.0 - 15.0微克/毫升的天蓝剂会降低细胞活力,而两种化合物浓度为25.0微克/毫升时具有细胞毒性。在用5.0微克/毫升代森锌或天蓝剂处理的NTHF细胞中观察到有丝分裂指数(MI)显著降低,而在HeLa和CHO细胞中则需要10.0微克/毫升的两种化学物质才能诱导相同现象。用1.0 - 5.0微克/毫升的代森锌或天蓝剂处理会导致NTHF细胞中退化纺锤体呈剂量依赖性增加,并且在HeLa和CHO细胞中,随着1.0 - 10.0微克/毫升代森锌和天蓝剂的处理,退化或多极纺锤体的数量呈剂量依赖性增加。尽管代森锌和天蓝剂能够在所有细胞类型中诱导有丝分裂纺锤体异常,但未转化细胞比永生化细胞的抗性更低。

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