Langenbach R, Freed H J, Huberman E
Proc Natl Acad Sci U S A. 1978 Jun;75(6):2864-7. doi: 10.1073/pnas.75.6.2864.
A cell-mediated mutagenesis assay using primary cultures of rat liver cells and V79 Chinese hamster cells has been developed. Liver carcinogens and their structural analogues were studied. Mutations in the V79 cells were characterized by resistance to ouabain. Cocultivation of the liver cells and V79 cells in the presence of the carcinogens N-nitrosodimethylamine, N-nitrosodiethylamine, and aflatoxin B1 caused the induction of ouabain-resistant mutants of V79 cells. In the absence of liver cells, the carcinogens did not induce ouabain resistance. The analogues N-nitrosomethyl-tert-butylamine and aflatoxin G2 were not mutagenic. The carcinogens exhibited a dose-dependent enhancement of mutation frequency. The mutation frequency also increased with increasing numbers of liver cells seeded. It is suggested that such an experimental system may be useful for screening for chemical carcinogens.
已开发出一种使用大鼠肝细胞原代培养物和V79中国仓鼠细胞的细胞介导诱变试验。对肝脏致癌物及其结构类似物进行了研究。V79细胞中的突变以对哇巴因的抗性为特征。在致癌物N-亚硝基二甲胺、N-亚硝基二乙胺和黄曲霉毒素B1存在的情况下,肝细胞与V79细胞共培养导致V79细胞产生对哇巴因抗性的突变体。在没有肝细胞的情况下,致癌物不会诱导对哇巴因的抗性。类似物N-亚硝基甲基叔丁胺和黄曲霉毒素G2没有致突变性。致癌物表现出剂量依赖性的突变频率增加。随着接种肝细胞数量的增加,突变频率也增加。有人认为,这样的实验系统可能有助于筛选化学致癌物。