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A comparative study of cytotoxic effects of N-ethyl-N-nitrosourea, adriamycin, and mono-(2-ethylhexyl)phthalate on mouse primordial germ cells

机译:N-乙基-N-亚硝基脲,阿霉素和邻苯二甲酸单-(2-乙基己基)酯对小鼠原始生殖细胞的细胞毒性作用的比较研究

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摘要

Several strategies for the assessment of reproductive toxicity of chemical compounds has have been proposed. In the present work, we devised experimental in vitro assays to test the effect of potential toxicants on proliferating primordial germ cells (PGCs) in vitro using recently developed methods for isolation and culture of mouse PGCs. Primordial germ cells are the embryonic precursors of gametes of the adult that carry the genome from generation to generation. Any damage or mutations caused to these cells by potential toxicants might impair normal reproduction and be transmitted to next generation. Three representative compounds, N-ethyl-N-nitrosourea (ENU), adriamycin (ADR), and mono-(2-ethylhexyl)phthalate (MEHP), toxic to different targets and known to affect germ cell development and impair fertility, were tested on PGCs in culture using three different experimental protocols. Survival and growth of PGCs and their ability to adhere to cell monolayers, were taken as endpoints for drug effects. For each compound, sublethal and acute toxicity doses were determined. In addition, information about the mechanisms of action of these compounds on PGCs was obtained. Whereas the effects of ENU and ADR on PGCs were attributable to growth inhibition and apoptosis induction, MEHP affected PGC adhesion to somatic cells without significantly altering their growth and survival. The results of our in vitro tests were not always exactly predictive of the effects of the tested compounds on PGCs in vivo, determined in parallel experiments in which pregnant mice were exposed to the same compounds. Nevertheless, they can provide information on the sensitivity of PGCs to the direct action of drugs or the mechanisms of action of such agents.
机译:已经提出了几种评估化合物的生殖毒性的策略。在本工作中,我们设计了实验性体外试验,以使用最近开发的分离和培养小鼠PGC的方法在体外测试潜在毒物对增殖的原始生殖细胞(PGC)的影响。原始生殖细胞是成年配子的胚胎前体,携带着一代又一代的基因组。潜在有毒物质对这些细胞造成的任何损害或突变都可能损害正常繁殖,并传播给下一代。测试了三种代表性化合物N-乙基-N-亚硝基脲(ENU),阿霉素(ADR)和邻苯二甲酸单-(2-乙基己基)酯(MEHP),它们对不同的靶标有毒并已知会影响生殖细胞发育并损害生育能力使用三种不同的实验方案对培养中的PGC进行分析。 PGC的存活和生长及其粘附细胞单层的能力被视为药物作用的终点。对于每种化合物,确定了亚致死剂量和急性毒性剂量。此外,获得了有关这些化合物对PGC作用机理的信息。 ENU和ADR对PGC的作用可归因于生长抑制和凋亡诱导,而MEHP影响PGC与体细胞的粘附,而不会显着改变其生长和存活率。我们的体外测试结果并不总是能准确预测被测化合物对体内PGC的影响,这是在平行实验中确定的,在该实验中,怀孕的小鼠暴露于相同的化合物。但是,它们可以提供有关PGC对药物直接作用的敏感性或此类药物作用机制的信息。

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