The Ah Receptor: Adaptive Metabolism, Ligand Diversity, and the Xenokine Model

被引:92
作者
Avilla, Mele N. [1 ]
Malecki, Kristen M. C. [1 ,3 ]
Hahn, Mark E. [4 ]
Wilson, Rachel H. [1 ]
Bradfield, Christopher A. [1 ,2 ]
机构
[1] Univ Wisconsin, Sch Med & Publ Hlth, Mol & Environm Toxicol Ctr, Madison, WI 53726 USA
[2] Univ Wisconsin, Sch Med & Publ Hlth, McArdle Lab Canc Res, Madison, WI 53726 USA
[3] Univ Wisconsin, Sch Med & Publ Hlth, Dept Populat Hlth Sci, Madison, WI 53726 USA
[4] Woods Hole Oceanog Inst, Biol Dept, Woods Hole, MA 02543 USA
基金
美国国家卫生研究院;
关键词
ARYL-HYDROCARBON RECEPTOR; HELIX-LOOP-HELIX; REGULATES INTRACELLULAR-LOCALIZATION; EQUIVALENCY FACTOR APPROACH; DIOXIN-LIKE COMPOUNDS; DIBENZO-P-DIOXINS; NUCLEAR TRANSLOCATOR; DNA-BINDING; TRANSCRIPTIONAL ACTIVATION; RISK-ASSESSMENT;
D O I
10.1021/acs.chemrestox.9b00476
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The Ah receptor (AHR) has been studied for almost five decades. Yet, we still have many important questions about its role in normal physiology and development. Moreover, we still do not fully understand how this protein mediates the adverse effects of a variety of environmental pollutants, such as the polycyclic aromatic hydrocarbons (PAHs), the chlorinated dibenzo-p-dioxins ("dioxins"), and many polyhalogenated biphenyls. To provide a platform for future research, we provide the historical underpinnings of our current state of knowledge about AHR signal transduction, identify a few areas of needed research, and then develop concepts such as adaptive metabolism, ligand structural diversity, and the importance of proligands in receptor activation. We finish with a discussion of the cognate physiological role of the AHR, our perspective on why this receptor is so highly conserved, and how we might think about its cognate ligands in the future.
引用
收藏
页码:860 / 879
页数:20
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