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基因毒素可诱导L5178Y和TK6细胞出现双核化。

Genotoxins induce binucleation in L5178Y and TK6 cells.

作者信息

Doherty Ann T, Wilson Amy, Chocian Karolina, Molloy Jennifer, Clatworthy Margaret, Doak Shareen, Jenkins Gareth, O'Donovan Mike

机构信息

Genetic Toxicology, Drug Safety and Metabolism, AstraZeneca R&D, Alderley Park, Macclesfield, Cheshire SK10 4TG, United Kingdom.

Genetic Toxicology, Drug Safety and Metabolism, AstraZeneca R&D, Alderley Park, Macclesfield, Cheshire SK10 4TG, United Kingdom.

出版信息

Mutat Res Genet Toxicol Environ Mutagen. 2014 Aug;770:29-34. doi: 10.1016/j.mrgentox.2014.05.005. Epub 2014 May 28.

Abstract

Following the initial observation that methyl methanesulphonate induced binucleated cells in the AHH-1 line and a significant number of them contained micronuclei, human lymphoblastoid TK6 and mouse lymphoma L5178Y cells were treated with methyl methanesulphonate, methylnitrosourea, mitomycin C, cytosine arabinoside, colchicine and triton X. All except triton X induced binucleated cells in both lines but an increased micronucleus incidence in them was seen only in TK6. The two lines also differed in the numbers of binucleates in the control cultures with 2.0% and 0.5% in TK6 and L5178Y, respectively, and a much higher proportion of those in TK6 contained micronuclei. The differences in behaviour between the two cell lines could not clearly be ascribed to their P53 status. Colchicine induced binucleates in both cell lines but they did not contain increased numbers of micronuclei. The effect on binucleate incidence was not a non-specific cytotoxic response because no increase was seen with triton X even at highly cytotoxic concentrations. The initial concern that not scoring micronuclei in binucleated cells might lead to erroneous results in in vitro micronucleus tests not using a cytokinesis block, was not proven because all the genotoxins tested here induced significant increases in micronucleus frequency in mononuclear cells. When testing less potently active agents in in vitro micronucleus tests not employing a cytokinesis block, care should be taken to understand better this phenomenon and not to include these damaged cells until we do.

摘要

在最初观察到甲磺酸甲酯在AHH - 1细胞系中诱导产生双核细胞,且其中大量细胞含有微核之后,人类淋巴母细胞TK6和小鼠淋巴瘤L5178Y细胞用甲磺酸甲酯、甲基亚硝基脲、丝裂霉素C、阿糖胞苷、秋水仙碱和曲拉通X进行处理。除曲拉通X外,所有试剂在这两种细胞系中均诱导产生了双核细胞,但仅在TK6细胞中观察到微核发生率增加。这两种细胞系在对照培养物中的双核细胞数量也存在差异,TK6和L5178Y分别为2.0%和0.5%,且TK6中双核细胞含有微核的比例更高。这两种细胞系行为上的差异不能明确归因于它们的P53状态。秋水仙碱在两种细胞系中均诱导产生双核细胞,但它们不含数量增加的微核。对双核细胞发生率的影响不是非特异性细胞毒性反应,因为即使在高细胞毒性浓度下,曲拉通X也未导致增加。最初担心在不使用胞质分裂阻断剂的体外微核试验中不对双核细胞中的微核进行计数可能会导致错误结果,这一点未得到证实,因为此处测试的所有基因毒素均在单核细胞中诱导微核频率显著增加。在不采用胞质分裂阻断剂的体外微核试验中检测活性较低的试剂时,应更加注意了解这一现象,并且在我们了解清楚之前不要将这些受损细胞纳入计数。

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