首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Mutagenicity of the oral carcinogen 4-nitroquinoline-1-oxide in cultured BigBlue rat tongue epithelial cells and fibroblasts.
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Mutagenicity of the oral carcinogen 4-nitroquinoline-1-oxide in cultured BigBlue rat tongue epithelial cells and fibroblasts.

机译:口腔致癌物4-硝基喹啉-1-氧化物在BigBlue大鼠舌上皮细胞和成纤维细胞中的致突变性。

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摘要

Environmental carcinogen exposures contribute to the development of oral cancer and improved test systems for the analysis of such carcinogens are needed. We have previously isolated and characterized an epithelial cell line from the tongue of a BigBlue rat. Now, we have established an immortalized fibroblast cell line from the same organ. We exposed these cells to 4-nitroquinoline-1-oxide (NQO), a well-known experimental oral carcinogen in the rat and other species, and measured its cytotoxic and genotoxic (cII transgene mutagenesis) effects. Both cell lines were very sensitive to NQO toxicity and showed dose-dependent mutant frequency responses. At the highest NQO dose tested, 70ng/ml, the mutant frequency was elevated more than eight-fold above background for the epithelial cells and more than 25-fold for the fibroblast cells. We examined cellular parameters which could affect glutathione-dependent detoxication of mutagens. Glutathione (GSH) contents of the two cell lines were similar. Glutathione transferase (GST) activities were measured with several substrates and were generally higher in the epithelial cells. Although multiple biochemical and biological characteristics of individual cell lines are likely to determine responses to mutagens, the greater sensitivity of the fibroblast cells to NQO mutagenicity is in accord with the lower GST activity and the lower DNA content of these cells. These new cell lines are suitable for in vitro testing of chemicals as possible oral mutagens and for studies of their biochemical mechanisms of action.
机译:暴露于环境致癌物有助于口腔癌的发展,需要改进的测试系统来分析此类致癌物。我们以前已经从BigBlue大鼠的舌头分离并鉴定了上皮细胞系。现在,我们已经从同一器官建立了永生的成纤维细胞系。我们将这些细胞暴露于4-硝基喹啉-1-氧化物(NQO)(一种在大鼠和其他物种中众所周知的实验性口腔致癌物),并测量了其细胞毒性和遗传毒性(cII转基因诱变)作用。两种细胞系均对NQO毒性非常敏感,并显示出剂量依赖性突变体频率响应。在测试的最高NQO剂量为70ng / ml时,上皮细胞的突变频率比背景高出八倍以上,而成纤维细胞的突变频率高出二十五倍。我们检查了可能影响谷胱甘肽依赖性诱变的脱毒的细胞参数。两种细胞系的谷胱甘肽(GSH)含量相似。谷胱甘肽转移酶(GST)的活性用几种底物进行测量,通常在上皮细胞中更高。尽管单个细胞系的多种生化和生物学特性可能决定了对诱变剂的反应,但成纤维细胞对NQO致突变性的更高敏感性与这些细胞较低的GST活性和较低的DNA含量是一致的。这些新的细胞系适用于体外化学测试可能的口服诱变剂以及研究其生化作用机理。

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