Schmidt J V, Bradfield C A
Department of Molecular Pharmacology and Biological Chemistry, Northwestern University Medical School, Chicago, Illinois 60611, USA.
Annu Rev Cell Dev Biol. 1996;12:55-89. doi: 10.1146/annurev.cellbio.12.1.55.
The aryl hydrocarbon (Ah) receptor has occupied the attention of toxicologists for over two decades. Interest arose from the early observation that this soluble protein played key roles in the adaptive metabolic response to polycyclic aromatic hydrocarbons and in the toxic mechanism of halogenated dioxins and dibenzofurans. More recent investigations have provided a fairly clear picture of the primary adaptive signaling pathway, from agonist binding to the transcriptional activation of genes involved in the metabolism of xenobiotics. Structure-activity studies have provided an understanding of the pharmacology of this receptor; recombinant DNA approaches have identified the enhancer sequences through which this factor regulates gene expression; and functional analysis of cloned cDNAs has allowed the characterization of the major signaling components in this pathway. Our objective is to review the Ah receptor's role in regulation of xenobiotic metabolism and use this model as a framework for understanding the less well-characterized mechanism of dioxin toxicity. In addition, it is hoped that this information can serve as a model for future efforts to understand an emerging superfamily of related signaling pathways that control biological responses to an array of environmental stimuli.
二十多年来,芳基烃(Ah)受体一直吸引着毒理学家的关注。这种兴趣源于早期的观察结果,即这种可溶性蛋白在对多环芳烃的适应性代谢反应以及卤代二恶英和二苯并呋喃的毒性机制中发挥着关键作用。最近的研究已经对主要的适应性信号通路有了相当清晰的认识,从激动剂结合到参与外源性物质代谢的基因的转录激活。构效关系研究已经让人们对这种受体的药理学有了一定的了解;重组DNA方法已经确定了该因子调节基因表达所通过的增强子序列;对克隆的cDNA的功能分析已经能够对该通路中的主要信号成分进行表征。我们的目标是回顾Ah受体在调节外源性物质代谢中的作用,并将这个模型作为一个框架,用于理解二恶英毒性中特征较少的机制。此外,希望这些信息能够作为一个模型,为未来理解一个新兴的相关信号通路超家族的努力提供参考,该超家族控制着对一系列环境刺激的生物反应。