An introduction to the molecular basics of aryl hydrocarbon receptor biology

被引:234
作者
Abel, Josef [1 ]
Haarmann-Stemmann, Thomas [1 ]
机构
[1] Heinrich Heine Univ Dusseldorf gGmbH, IUF, D-40225 Dusseldorf, Germany
关键词
aryl hydrocarbon receptor; cytochrome P450; dioxin; transcription factor; xenobiotic metabolism; TRANSFORMING GROWTH FACTOR-BETA(1); NUCLEAR TRANSLOCATOR PROTEIN; HEAT-SHOCK-PROTEIN; AH DIOXIN RECEPTOR; POLYMERASE-CHAIN-REACTION; MESSENGER-RNA EXPRESSION; HYPOXIA-INDUCIBLE FACTOR; PROSTATE-CANCER CELLS; HUMAN HEPATOMA HEPG2; FACTOR-KAPPA-B;
D O I
10.1515/BC.2010.128
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Depending on their chemical structure and properties, environmental chemicals and other xenobiotics that enter the cell can affect cellular function by either nonselective binding to cellular macromolecules or by interference with cellular receptors, which would initiate a more defined cell biological response. One of these intracellular chemosensor molecules is the aryl hydrocarbon receptor (AhR), a transcription factor of the bHLH/PAS family that is known to mediate the biochemical and toxic effects of dioxins, polyaromatic hydrocarbons and related compounds. Numerous investigations have revealed that the AhR is not only a master regulator of drug metabolism activated by anthropogenic chemicals, but is also triggered by natural and endogenous ligands and can influence cell biological endpoints such as growth and differentiation. Cutting-edge research has identified new intriguing functions of the AhR, such as during proteasomal degradation of steroid hormone receptors, the cellular UVB stress response and the differentiation of certain T-cell subsets. In this review we provide both a survey of the fundamental basics of AhR biology and an insight into new functional aspects of AhR signaling to further stimulate research on this intriguing transcription factor at the interface between toxicology, cell biology and immunology.
引用
收藏
页码:1235 / 1248
页数:14
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