Zheng H, Liu J, Choo K H, Michalska A E, Klaassen C D
Department of Pharmacology, Toxicology, and Therapeutics, University of Kansas Medical Center, Kansas City 66160-7417, USA.
Toxicol Appl Pharmacol. 1996 Feb;136(2):229-35. doi: 10.1006/taap.1996.0029.
Zinc pretreatment has been shown in vitro (rat myoblasts) to induce metallothionein (MT) and inhibit cadmium (Cd)-induced protooncogenes c-myc and c-jun mRNA levels. therefore, the purpose of this study was to determine whether the mRNA expression of the protooncogene c-jun as well as the tumor suppressor gene p53 is increased by Cd in the intact animal and, more specifically, in the target organ for Cd toxicity, the liver. Additionally, modulation of the expression of these genes was investigated in the absence of MT. The effect of CdCl2 on the mRNA levels of c-jun and p53 was studied in livers of C57BL/6J (control) and MT-null mice by Northern- and slot-blot analyses. The mRNA for c-jun and p53 were increased by Cd in a dose-dependent fashion. In the control mice, Cd induced c-jun mRNA (5-fold) at 3 and 12 hr and p53 mRNA (1.8- to 2-fold) at 6 and 12 hr. Compared to controls, the MT-null mice were more sensitive to the Cd-induced gene expression. The magnitude of the inductions was more pronounced and the elevated mRNA levels of c-jun and p53 were seen at lower doses of Cd (10mumol/kg in MT-null mice vs 40 mmol/kg in control mice). In conclusion, these data demonstrate that Cd induces mRNA expression of the protooncogene c-jun and tumor suppressor gene p53 in liver, and that MT modulates this effect.
体外实验(大鼠成肌细胞)表明,锌预处理可诱导金属硫蛋白(MT)生成,并抑制镉(Cd)诱导的原癌基因c-myc和c-jun的mRNA水平。因此,本研究旨在确定在完整动物体内,尤其是在Cd毒性的靶器官肝脏中,原癌基因c-jun以及肿瘤抑制基因p53的mRNA表达是否会因Cd而增加。此外,还研究了在缺乏MT的情况下这些基因表达的调节情况。通过Northern印迹和狭缝印迹分析,研究了CdCl2对C57BL/6J(对照)小鼠和MT基因敲除小鼠肝脏中c-jun和p53 mRNA水平的影响。Cd以剂量依赖的方式增加c-jun和p53的mRNA水平。在对照小鼠中,Cd在3小时和12小时诱导c-jun mRNA(增加5倍),在6小时和12小时诱导p53 mRNA(增加1.8至2倍)。与对照相比,MT基因敲除小鼠对Cd诱导的基因表达更敏感。诱导程度更明显,在较低剂量的Cd(MT基因敲除小鼠为10μmol/kg,对照小鼠为40μmol/kg)下即可观察到c-jun和p53的mRNA水平升高。总之,这些数据表明,Cd可诱导肝脏中原癌基因c-jun和肿瘤抑制基因p53的mRNA表达,且MT可调节这种作用。