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Antioxidant Functions of the Aryl Hydrocarbon Receptor

The aryl hydrocarbon receptor (AhR) is a transcription factor belonging to the basic helix-loop-helix/PER-ARNT-SIM family. It is activated by a variety of ligands, such as environmental contaminants like polycyclic aromatic hydrocarbons or dioxins, but also by naturally occurring compounds and endog...

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Detalles Bibliográficos
Autor principal: Dietrich, Cornelia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5088273/
https://www.ncbi.nlm.nih.gov/pubmed/27829840
http://dx.doi.org/10.1155/2016/7943495
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author Dietrich, Cornelia
author_facet Dietrich, Cornelia
author_sort Dietrich, Cornelia
collection PubMed
description The aryl hydrocarbon receptor (AhR) is a transcription factor belonging to the basic helix-loop-helix/PER-ARNT-SIM family. It is activated by a variety of ligands, such as environmental contaminants like polycyclic aromatic hydrocarbons or dioxins, but also by naturally occurring compounds and endogenous ligands. Binding of the ligand leads to dimerization of the AhR with aryl hydrocarbon receptor nuclear translocator (ARNT) and transcriptional activation of several xenobiotic phase I and phase II metabolizing enzymes. It is generally accepted that the toxic responses of polycyclic aromatic hydrocarbons, dioxins, and structurally related compounds are mediated by activation of the AhR. A multitude of studies indicate that the AhR operates beyond xenobiotic metabolism and exerts pleiotropic functions. Increasing evidence points to a protective role of the AhR against carcinogenesis and oxidative stress. Herein, I will highlight data demonstrating a causal role of the AhR in the antioxidant response and present novel findings on potential AhR-mediated antioxidative mechanisms.
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spelling pubmed-50882732016-11-09 Antioxidant Functions of the Aryl Hydrocarbon Receptor Dietrich, Cornelia Stem Cells Int Review Article The aryl hydrocarbon receptor (AhR) is a transcription factor belonging to the basic helix-loop-helix/PER-ARNT-SIM family. It is activated by a variety of ligands, such as environmental contaminants like polycyclic aromatic hydrocarbons or dioxins, but also by naturally occurring compounds and endogenous ligands. Binding of the ligand leads to dimerization of the AhR with aryl hydrocarbon receptor nuclear translocator (ARNT) and transcriptional activation of several xenobiotic phase I and phase II metabolizing enzymes. It is generally accepted that the toxic responses of polycyclic aromatic hydrocarbons, dioxins, and structurally related compounds are mediated by activation of the AhR. A multitude of studies indicate that the AhR operates beyond xenobiotic metabolism and exerts pleiotropic functions. Increasing evidence points to a protective role of the AhR against carcinogenesis and oxidative stress. Herein, I will highlight data demonstrating a causal role of the AhR in the antioxidant response and present novel findings on potential AhR-mediated antioxidative mechanisms. Hindawi Publishing Corporation 2016 2016-10-18 /pmc/articles/PMC5088273/ /pubmed/27829840 http://dx.doi.org/10.1155/2016/7943495 Text en Copyright © 2016 Cornelia Dietrich. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Dietrich, Cornelia
Antioxidant Functions of the Aryl Hydrocarbon Receptor
title Antioxidant Functions of the Aryl Hydrocarbon Receptor
title_full Antioxidant Functions of the Aryl Hydrocarbon Receptor
title_fullStr Antioxidant Functions of the Aryl Hydrocarbon Receptor
title_full_unstemmed Antioxidant Functions of the Aryl Hydrocarbon Receptor
title_short Antioxidant Functions of the Aryl Hydrocarbon Receptor
title_sort antioxidant functions of the aryl hydrocarbon receptor
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5088273/
https://www.ncbi.nlm.nih.gov/pubmed/27829840
http://dx.doi.org/10.1155/2016/7943495
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