首页> 外文期刊>Toxicology and Applied Pharmacology >Transactivation activity of human, zebrafish, and rainbow trout aryl hydrocarbon receptors expressed in COS-7 cells: greater insight into species differences in toxic potency of polychlorinated dibenzo-p-dioxin, dibenzofuran, and biphenyl congeners.
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Transactivation activity of human, zebrafish, and rainbow trout aryl hydrocarbon receptors expressed in COS-7 cells: greater insight into species differences in toxic potency of polychlorinated dibenzo-p-dioxin, dibenzofuran, and biphenyl congeners.

机译:在COS-7细胞中表达的人类,斑马鱼和虹鳟芳烃受体的反式激活活性:更深入地了解多氯联苯对二恶英,二苯并呋喃和联苯同源物的毒性之间的物种差异。

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摘要

Transactivation assays were used to compare the potency and efficacy of polychlorinated dibenzo-p-dioxin (PCDD), dibenzofuran (PCDF), and biphenyl (PCB) congeners in activating aryl hydrocarbon receptors (AhRs) from rainbow trout (rtAhR2alpha and rtAhR2beta), zebrafish (zfAhR2), and human (huAhR), respectively. All AhRs were expressed with their species-specific AhR nuclear translocator (ARNT) in COS-7 cells. Transactivation activity was determined for two PCDD, two PCDF, and seven PCB congeners with each of the four AhR/ARNT pairs using prt1Aluc, a luciferase reporter driven by two dioxin-responsive enhancer elements (DREs) from the rainbow trout cyp1A gene. Maximal-fold induction, EC50, and relative potency values were calculated for congeners that exhibited dose-related activity in the assay. Of the four AhR/ARNT pairs tested with PCDD, PCDF, and non-ortho PCB congeners, three exhibited high activity (rainbow trout AhR2alpha, zebrafish AhR2, and human AhR), while rainbow trout AhR2beta had very weak or no activity. Comparisons between these AhRs showed that while mono-ortho PCBs were able to activate the human AhR, they were generally ineffective in activating rainbow trout and zebrafish AhR2s. This supports the hypothesis that structural differences between mammalian and fish AhRs may account for differences in relative potencies of the mono-ortho PCBs between mammals and fish. Another important finding was a significant difference in transactivation activity between the two rainbow trout AhR2 isoforms despite the fact that they are 95% identical at the amino acid level. For all PCDD, PCDF, and PCB agonists tested, rainbow trout AhR2alpha was significantly more active than AhR2beta. However, rainbow trout AhR2beta is active as a 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)-activated transcription factor, with enhancer elements from the mouse cyp1A gene. This suggests that AhR2beta may have evolved to serve a different physiological function than AhR2alpha in salmonid fish species. Copyright 1999 Academic Press.
机译:使用反转录激活试验来比较多氯联苯对二恶英(PCDD),二苯并呋喃(PCDF)和联苯(PCB)同系物在激活虹鳟鱼(rtAhR2alpha和rtAhR2beta),斑马鱼中的芳烃受体(AhRs)方面的效力和功效(zfAhR2)和人类(huAhR)。所有AhRs均以其物种特异性AhR核转运子(ARNT)在COS-7细胞中表达。使用prt1Aluc确定了两个PCDD,两个PCDF和七个PCB同源物与四个AhR / ARNT对的反式激活活性,prt1Aluc是由来自虹鳟鱼cyp1A基因的两个二恶英响应增强子(DRE)驱动的荧光素酶报告基因。计算在分析中显示剂量相关活性的同类物的最大倍数诱导,EC50和相对效价。在用PCDD,PCDF和非邻位PCB同系物测试的四对AhR / ARNT中,三对显示出高活性(虹鳟鱼AhR2alpha,斑马鱼AhR2和人类AhR),而虹鳟鱼AhR2beta则非常弱或没有活性。这些AhR之间的比较表明,虽然单原位PCB能够激活人类AhR,但它们通常不能激活虹鳟鱼和斑马鱼AhR2。这支持了以下假设:哺乳动物和鱼类的AhRs之间的结构差异可能解释了哺乳动物和鱼类之间的单邻位多氯联苯的相对效能差异。另一个重要发现是,尽管两个虹鳟鱼AhR2亚型​​在氨基酸水平上具有95%的同一性,但它们的反式激活活性却存在显着差异。对于所有经过测试的PCDD,PCDF和PCB激动剂,虹鳟鱼AhR2alpha的活性明显高于AhR2beta。但是,虹鳟鱼AhR2beta作为2,3,7,8-四氯二苯并-p-二恶英(TCDD)激活的转录因子具有活性,具有来自小鼠cyp1A基因的增强子。这表明在鲑鱼鱼类中,AhR2beta可能已进化出与AhR2alpha不同的生理功能。版权所有1999,学术出版社。

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