Kanno S, Suzuki J S, Aoki Y, Suzuki K T
National Institute for Environmental Studies, Tsukuba, Japan.
Res Commun Chem Pathol Pharmacol. 1994 May;84(2):153-62.
Mechanisms for the abnormal copper (Cu) accumulation in the liver of LEC rats were examined using primary cultured liver parenchymal cells prepared from mutant LEC rats and those from control LEA rats (original strain). The Cu and metallothionein (MT) mRNA levels in the liver of LEC rats were caused to decrease to the same levels as those of LEA rats by removing Cu in vivo selectively with tetrathiomolybdate. Cu was taken up by LEC rat cells to the same extent as LEA rat cells by exposure to low medium Cu and to a higher extent by exposure to high medium Cu, while the MT mRNA level in LEC rat cells increased dose-dependently at a much higher rate than that in LEA rats. MT mRNA levels in both cells were comparable by exposure to cadmium, zinc and dexamethasone. The results indicate that expression of MT mRNA is selectively enhanced by Cu in LEC cells despite the fact that uptake of Cu is comparable with normal cells.
利用从突变型LEC大鼠和对照LEA大鼠(原种系)制备的原代培养肝实质细胞,研究了LEC大鼠肝脏中铜(Cu)异常蓄积的机制。通过用四硫代钼酸盐在体内选择性去除铜,使LEC大鼠肝脏中的铜和金属硫蛋白(MT)mRNA水平降低到与LEA大鼠相同的水平。通过暴露于低培养基铜环境,LEC大鼠细胞摄取铜的程度与LEA大鼠细胞相同;而通过暴露于高培养基铜环境,LEC大鼠细胞摄取铜的程度更高,同时LEC大鼠细胞中的MT mRNA水平以比LEA大鼠高得多的速率呈剂量依赖性增加。通过暴露于镉、锌和地塞米松,两种细胞中的MT mRNA水平相当。结果表明,尽管LEC细胞对铜的摄取与正常细胞相当,但铜可选择性增强LEC细胞中MT mRNA的表达。