Indole and Tryptophan Metabolism: Endogenous and Dietary Routes to Ah Receptor Activation

被引:471
作者
Hubbard, Troy D. [1 ,2 ,3 ]
Murray, Iain A. [2 ,3 ]
Perdew, Gary H. [2 ,3 ]
机构
[1] Penn State Univ, Grad Program Biochem Microbiol & Mol Biol, University Pk, PA 16802 USA
[2] Penn State Univ, Ctr Mol Toxicol & Carcinogenesis, University Pk, PA 16802 USA
[3] Penn State Univ, Dept Vet & Biomed Sci, University Pk, PA 16802 USA
基金
美国国家卫生研究院;
关键词
ARYL-HYDROCARBON RECEPTOR; REGULATORY T-CELLS; PROTEIN-DNA INTERACTIONS; CHRONIC KIDNEY-DISEASE; PROSTATE-CANCER CELLS; ESCHERICHIA-COLI; DIOXIN RECEPTOR; INDOXYL SULFATE; HIGH-AFFINITY; TRANSCRIPTIONAL ENHANCER;
D O I
10.1124/dmd.115.064246
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aryl hydrocarbon receptor (AHR) is a ligand-activated transcription factor recognized for its role in xenobiotic metabolism. The physiologic function of AHR has expanded to include roles in immune regulation, organogenesis, mucosal barrier function, and the cell cycle. These functions are likely dependent upon ligand-mediated activation of the receptor. High-affinity ligands of AHR have been classically defined as xenobiotics, such as polychlorinated biphenyls and dioxins. Identification of endogenous AHR ligands is key to understanding the physiologic functions of this enigmatic receptor. Metabolic pathways targeting the amino acid tryptophan and indole can lead to a myriad of metabolites, some of which are AHR ligands. Many of these ligands exhibit species selective preferential binding to AHR. The discovery of specific tryptophan metabolites as AHR ligands may provide insight concerning where AHR is activated in an organism, such as at the site of inflammation and within the intestinal tract.
引用
收藏
页码:1522 / 1535
页数:14
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