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首页> 外文期刊>Environmental and molecular mutagenesis. >Development of a High-Throughput Genotoxicity Assay Using Umu Test Strains Expressing Human Cytochrome P450s and NADPH-P450 Reductase and Bacterial O-Acetyltransferase
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Development of a High-Throughput Genotoxicity Assay Using Umu Test Strains Expressing Human Cytochrome P450s and NADPH-P450 Reductase and Bacterial O-Acetyltransferase

机译:使用UMU试验菌株表达人细胞色素P450S和NADPH-P450还原酶和细菌O-乙酰转移酶的高通量基因毒性测定

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Umu test is one of the in vitro genotoxicity test that has been used widely. It was developed as a high-throughput test system using the 96-well microplate. We have previously constructed new umu test strains for the evaluation of genotoxicity of procarcinogenic metabolic products formed by cytochrome P450 (CYP) enzymes. In this study, a highly sensitive high-throughput genotoxicity test was developed using four umu test strains (OY1002/1A1, OY1002/1B1, OY1002/1A2, and OY1002/3A4) that express human CYPs and NADPH-P450 reductase. We found that the modified umu-microplate method was more sensitive than the conventional microplate method using strain OY1002/1A2. In addition, the new microplate method was better able to detect genotoxicity than the test tube method when the strain OY1002/1A2 was used and had similar sensitivity for the remaining three strains. When the microplate method was used, OY1002/1A2 showed stronger umuC gene expression in the presence of 2amino-6-methyldipyrido[1,2-a: 3', 2'-d] imidazole, 2-amino-3-methylimidazo[4,5-f] quinoline, 2-amino3,4-dimethylimidazo[4,5-f] quinoline, 2-amino-3,8dimethylimidazo[4,5-f] quinoxaline, 2-aminofluorene, and 2-aminoanthracene compared to other strains. We also confirmed CYP1A2 expression in OY1002/1A2 in this condition. These results indicate that the microplate version of this test system can detect the genotoxicity of heterocyclic and aromatic amines with high sensitivity and can be used for highthroughput screening of potentially genotoxic compounds. (C) 2017Wiley Periodicals, Inc.
机译:UMU试验是广泛使用的体外遗传毒性试验之一。它是使用96孔微孔板开发的高通量测试系统。我们以前构建了新的UMU测试株,用于评估通过细胞色素P450(CYP)酶形成的促进植物学代谢产物的遗传毒性。在该研究中,使用四个UMU试验株(OY1002 / 1A1,OY1002 / 1B1,OY1002 / 1A2和OY1002 / 3A4)开发出高度敏感的高通量毒性试验,其表达人CYPS和NADPH-P450还原酶。我们发现,改性的Umu-Microplate方法比使用应变OY1002 / 1A2的常规微孔板方法更敏感。另外,当使用菌株OY1002 / 1A2时,新的微孔板方法更好地检测遗传毒性而不是试管方法,并且对于剩余的三种菌株具有相似的灵敏度。当使用微孔板方法时,OY1002 / 1A2在2个氨基-6-甲基二吡啶[1,2-A:3',2'-D]咪唑,2-氨基-3-甲基咪唑(2-氨基-3-甲基咪唑)中显示出更强的UMUC基因表达[4 ,5-F]喹啉,2-氨基3,4-二甲基咪唑[4,5-F]喹啉,2-氨基-3,8dimethylimaIdazo [4,5-F]喹喔啉,2-氨基氟烯和2-氨基蒽与其他相比菌株。我们还在这种情况下确认了OY1002 / 1A2中的CYP1A2表达。这些结果表明,该测试系统的微孔板版本可以检测具有高灵敏度的杂环和芳族胺的遗传毒性,并且可用于潜在的遗传毒性化合物的筛选筛选。 (c)2017Wiley期刊,Inc。

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