Braathen Marte, Mortensen Anne Skjetne, Sandvik Morten, Skåre Janneche Utne, Arukwe Augustine
Norwegian School of Veterinary Science, Oslo, Norway.
Arch Environ Contam Toxicol. 2009 Jan;56(1):111-22. doi: 10.1007/s00244-008-9163-0. Epub 2008 Apr 15.
Many persistent organic pollutants are known to have endocrine-disrupting effects in several aquatic and terrestrial species. In this regard, hydroxylated metabolites of polychlorinated biphenyls (OH-PCBs) represent serious health and environmental concern because they are shown to act agonistic or antagonistic at hormone receptors (HRs) or to cause hormone-receptor-mediated responses. In the present study, salmon primary hepatocytes were used to study alterations in an estrogen signaling pathway resulting from exposure to four hydroxylated (4OH-CB 107, 4OH-CB146, 4OH-CB187, and 3OH-CB138) metabolites of PCB at different concentrations using quantitative real-time polymerase chain reaction. The effects of the PCB metabolites were compared to the mRNA expression in 17alpha-ethynylestradiol (EE2)-treated cells. Concentration-specific increase of vitellogenin (Vtg) mRNA transcription after exposure to OH-PCBs was observed. Decreased mRNA transcription was observed for zona radiata protein (Zr-protein) and cytochrome P450 side-chain cleavage (P450scc) enzyme. For estrogen receptor beta (ERbeta), the mRNA expression pattern was OH-PCB-metabolite congener-specific. A novel aspect of this study is that OH-PCBs produced effects on hepatic steroidogenic pathways by targeting the StAR protein and P450scc genes. Given that endocrine toxicology research mainly has focused on estrogenicity involving direct ER-mediated effects and that steroidogenic enzyme and proteins are highly tissue- and cell-type-specific and controlled by different promoters and second-messenger pathways, the present findings provide potential new targets for interaction with xenobiotics such as hydroxylated congeners of certain chemicals. The quantitative expression patterns of hepatic and extrahepatic steroidogenic genes and proteins after exposure to environmental contaminants are the subject of systematic investigations in our laboratory.
许多持久性有机污染物已知在多种水生和陆地物种中具有内分泌干扰作用。在这方面,多氯联苯的羟基化代谢物(OH-PCBs)引起了严重的健康和环境问题,因为它们在激素受体(HRs)上表现出激动或拮抗作用,或引发激素受体介导的反应。在本研究中,使用鲑鱼原代肝细胞,通过定量实时聚合酶链反应研究不同浓度的四种多氯联苯羟基化代谢物(4OH-CB 107、4OH-CB146、4OH-CB187和3OH-CB138)暴露导致的雌激素信号通路变化。将多氯联苯代谢物的作用与17α-乙炔雌二醇(EE2)处理细胞中的mRNA表达进行比较。观察到暴露于OH-PCBs后卵黄蛋白原(Vtg)mRNA转录呈浓度特异性增加。观察到放射带蛋白(Zr-蛋白)和细胞色素P450侧链裂解酶(P450scc)的mRNA转录减少。对于雌激素受体β(ERβ),mRNA表达模式具有OH-PCB代谢物同系物特异性。本研究的一个新方面是,OH-PCBs通过靶向类固醇生成急性调节蛋白(StAR)和P450scc基因对肝脏类固醇生成途径产生影响。鉴于内分泌毒理学研究主要集中在涉及直接雌激素受体介导作用的雌激素活性,且类固醇生成酶和蛋白质具有高度的组织和细胞类型特异性,并受不同启动子和第二信使途径控制,本研究结果为与某些化学物质的羟基化同系物等外源性物质相互作用提供了潜在的新靶点。暴露于环境污染物后肝脏和肝脏外类固醇生成基因及蛋白质的定量表达模式是我们实验室系统研究的主题。