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环境污染物诱导非整倍体的筛查试验的开发。

Development of screening tests for aneuploidy induction by environmental pollutants.

作者信息

Adler I D, Parry J M

机构信息

GSF-Institut für Säugetiergenetik, Neuherberg, Germany.

出版信息

Environ Health Perspect. 1993 Oct;101 Suppl 3(Suppl 3):5-9. doi: 10.1289/ehp.93101s35.

Abstract

When legally required mutagenicity testing of chemicals is undertaken, the important genetic end point of aneuploidy is not included because validated test methods are lacking. Therefore, the Commission of the European Communities (CEC) has funded a research program to develop and validate tests for aneuploidy induction. Ten chemicals, selected on the basis of their ability to interact with cell organelles relevant for aneuploidy induction, were tested in 11 laboratories. The assays ranged from in vitro tubulin assembly studies to in vivo germ-cell tests. The results allow several conclusions: a) Fungal aneuploidy tests are not capable of detecting inhibitors of mammalian tubulin polymerization such as colchicine and vinblastine. Therefore, they will not play a role in screening for aneuploidy but are of value for studying the relationship between induced aneuploidy and recombination. b) Chemicals that induce aneuploidy in mammalian germ cells are readily detected in the in vitro mammalian cell systems. Some chemicals such as thiabendazole and thimerosal induce aneuploidy in vitro but do not appear to be very effective in vivo. c) Cell division aberrations induced in mammalian cells in vitro seem to be predictive for aneuploidy induction in the same cell type. Likewise, c-mitotic effects and cell cycle delay in vivo in mitotic and meiotic cells correlate with aneuploidy induction in the respective tissue. A second CEC Aneuploidy Program has started recently to refine the most promising test protocols, to provide understanding of variety of mechanisms by which chemicals induce aneuploidy, and to establish a data base for aneugens among environmental pollutants.

摘要

当依法对化学品进行致突变性测试时,由于缺乏经过验证的测试方法,非整倍体这一重要的遗传终点未被纳入测试范围。因此,欧洲共同体委员会(CEC)资助了一项研究计划,以开发和验证非整倍体诱导测试方法。基于与非整倍体诱导相关的细胞器相互作用能力挑选出的10种化学品,在11个实验室进行了测试。这些检测方法从体外微管蛋白组装研究到体内生殖细胞测试不等。结果得出了几个结论:a)真菌非整倍体测试无法检测出诸如秋水仙碱和长春花碱等哺乳动物微管蛋白聚合抑制剂。因此,它们在非整倍体筛查中不会发挥作用,但对于研究诱导的非整倍体与重组之间的关系具有价值。b)在体外哺乳动物细胞系统中能够轻易检测出在哺乳动物生殖细胞中诱导非整倍体的化学品。一些化学品,如噻苯达唑和硫柳汞,在体外可诱导非整倍体,但在体内似乎效果不佳。c)体外哺乳动物细胞中诱导的细胞分裂异常似乎可预测同一细胞类型中的非整倍体诱导情况。同样,有丝分裂和减数分裂细胞体内的c - 有丝分裂效应和细胞周期延迟与各自组织中的非整倍体诱导相关。欧洲共同体委员会的第二个非整倍体计划最近已经启动,旨在完善最有前景的测试方案,深入了解化学品诱导非整倍体的各种机制,并建立环境污染物中致非整倍体物质的数据库。

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本文引用的文献

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Immunofluorescent staining of kinetochores in micronuclei: a new assay for the detection of aneuploidy.
Mutat Res. 1988 Oct;203(5):339-45. doi: 10.1016/0165-1161(88)90030-1.

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