Department of Environmental and Molecular Toxicology, The Sinnhuber Aquatic Research Laboratory, Oregon State University, Corvallis, Oregon 97331.
Biology Department, Woods Hole Oceanographic Institution, Woods Hole, Massachusetts 02543.
Toxicol Sci. 2020 Dec 1;178(2):215-238. doi: 10.1093/toxsci/kfaa143.
Over the last 2 decades, the zebrafish (Danio rerio) has emerged as a stellar model for unraveling molecular signaling events mediated by the aryl hydrocarbon receptor (AHR), an important ligand-activated receptor found in all eumetazoan animals. Zebrafish have 3 AHRs-AHR1a, AHR1b, and AHR2, and studies have demonstrated the diversity of both the endogenous and toxicological functions of the zebrafish AHRs. In this contemporary review, we first highlight the evolution of the zebrafish ahr genes, and the characteristics of the receptors including developmental and adult expression, their endogenous and inducible roles, and the predicted ligands from homology modeling studies. We then review the toxicity of a broad spectrum of AHR ligands across multiple life stages (early stage, and adult), discuss their transcriptomic and epigenetic mechanisms of action, and report on any known interactions between the AHRs and other signaling pathways. Through this article, we summarize the promising research that furthers our understanding of the complex AHR pathway through the extensive use of zebrafish as a model, coupled with a large array of molecular techniques. As much of the research has focused on the functions of AHR2 during development and the mechanism of TCDD (2,3,7,8-tetrachlorodibenzo-p-dioxin) toxicity, we illustrate the need to address the considerable knowledge gap in our understanding of both the mechanistic roles of AHR1a and AHR1b, and the diverse modes of toxicity of the various AHR ligands.
在过去的 20 年中,斑马鱼(Danio rerio)已成为阐明芳烃受体(AHR)介导的分子信号事件的杰出模型,AHR 是所有后生动物中存在的一种重要的配体激活受体。斑马鱼有 3 种 AHRs-AHR1a、AHR1b 和 AHR2,研究表明斑马鱼 AHRs 的内源性和毒理学功能具有多样性。在这篇当代综述中,我们首先强调了斑马鱼 ahr 基因的进化,以及受体的特征,包括发育和成年表达、它们的内源性和诱导作用,以及同源建模研究预测的配体。然后,我们综述了多种生命阶段(早期和成年)中广泛 AHR 配体的毒性,讨论了它们的转录组和表观遗传作用机制,并报告了 AHR 与其他信号通路之间的任何已知相互作用。通过本文,我们总结了有前途的研究,这些研究通过广泛使用斑马鱼作为模型,结合大量分子技术,进一步加深了我们对复杂 AHR 途径的理解。由于大部分研究都集中在 AHR2 在发育过程中的功能和 TCDD(2,3,7,8-四氯二苯并对二恶英)毒性的机制上,我们说明了需要解决我们对 AHR1a 和 AHR1b 的机制作用以及各种 AHR 配体的不同毒性模式的理解方面存在的相当大的知识差距。