Jennings G S, Oesch F, Steinberg P
Institute for Toxicology, University of Mainz, Germany.
Carcinogenesis. 1992 May;13(5):831-5. doi: 10.1093/carcin/13.5.831.
The induction of hepatocellular carcinoma from liver parenchymal cells in laboratory animals by aflatoxin B1 (AFB1) is well documented. In contrast no tumours arising from the sinusoidal cell population have been reported after exposure to AFB1. The apparent resistance of the latter cell type was investigated at the level of DNA adduct formation in vivo in male Sprague-Dawley rats. Liver parenchymal and non-parenchymal cell populations were isolated from rats at 20 min and 1, 24 and 72 h after administration of 240 microCi (0.6 mg) [G-3H]AFB1/kg. AFB1-DNA binding was observed in both liver cell subpopulations and was 3- to 5-fold higher in parenchymal cells than in non-parenchymal cells. The major DNA adduct found in parenchymal cells at 1 h after AFB1 administration was 8,9-dihydro-8-(N7-guanyl)-9-hydroxyaflatoxin B1 (AFB1-gua), whereas at later time points the persistent secondary adduct, AFB1-formamidopyrimidine, predominated. In contrast, AFB1-gua was not observed at any time in DNA from non-parenchymal cells and the secondary adducts predominated throughout. These observations are discussed with reference to the susceptibility of different liver cell types to AFB1-carcinogenesis and the possible roles of the major AFB1-DNA adduct species.
黄曲霉毒素B1(AFB1)在实验动物中诱导肝实质细胞发生肝细胞癌已有充分记录。相比之下,尚未有暴露于AFB1后窦状细胞群体产生肿瘤的报道。在雄性斯普拉格-道利大鼠体内,从DNA加合物形成水平研究了后一种细胞类型的明显抗性。在给予240微居里(0.6毫克)[G-3H]AFB1/千克后20分钟、1小时、24小时和72小时,从大鼠中分离出肝实质细胞和非实质细胞群体。在两种肝细胞亚群中均观察到AFB1与DNA的结合,且实质细胞中的结合量比非实质细胞高3至5倍。AFB1给药后1小时在实质细胞中发现的主要DNA加合物是8,9-二氢-8-(N7-鸟嘌呤基)-9-羟基黄曲霉毒素B1(AFB1-鸟嘌呤),而在随后的时间点,持久性二级加合物AFB1-甲酰胺嘧啶占主导。相比之下,在非实质细胞的DNA中任何时候都未观察到AFB1-鸟嘌呤,且二级加合物始终占主导。结合不同肝细胞类型对AFB1致癌作用的敏感性以及主要AFB1-DNA加合物种类的可能作用对这些观察结果进行了讨论。