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AhR signaling pathways and regulatory functions

Animals and humans are exposed each day to a multitude of chemicals in the air, water and food. They have developed a battery of enzymes and transporters that facilitate the biotransformation and elimination of these compounds. Moreover, a majority of these enzymes and transporters are inducible due...

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Autores principales: Larigot, Lucie, Juricek, Ludmila, Dairou, Julien, Coumoul, Xavier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6039966/
https://www.ncbi.nlm.nih.gov/pubmed/30003042
http://dx.doi.org/10.1016/j.biopen.2018.05.001
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author Larigot, Lucie
Juricek, Ludmila
Dairou, Julien
Coumoul, Xavier
author_facet Larigot, Lucie
Juricek, Ludmila
Dairou, Julien
Coumoul, Xavier
author_sort Larigot, Lucie
collection PubMed
description Animals and humans are exposed each day to a multitude of chemicals in the air, water and food. They have developed a battery of enzymes and transporters that facilitate the biotransformation and elimination of these compounds. Moreover, a majority of these enzymes and transporters are inducible due to the activation of xenobiotic receptors which act as transcription factors for the regulation of their target genes (such as xenobiotic metabolizing enzymes, see below §4 for the AhR). These receptors include several members of the nuclear/steroid receptor family (CAR for Constitutive Androstane Receptor, PXR for Pregnane X Receptor) but also the Aryl hydrocarbon Receptor or AhR, a member of the bHLH-PAS family (basic Helix-Loop-Helix - Period/ARNT/Single minded). In addition to the regulation of xenobiotic metabolism, numerous alternative functions have been characterized for the AhR since its discovery. These alternative functions will be described in this review along with its endogenous functions as revealed by experiments performed on knock-out animals.
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spelling pubmed-60399662018-07-12 AhR signaling pathways and regulatory functions Larigot, Lucie Juricek, Ludmila Dairou, Julien Coumoul, Xavier Biochim Open Review Animals and humans are exposed each day to a multitude of chemicals in the air, water and food. They have developed a battery of enzymes and transporters that facilitate the biotransformation and elimination of these compounds. Moreover, a majority of these enzymes and transporters are inducible due to the activation of xenobiotic receptors which act as transcription factors for the regulation of their target genes (such as xenobiotic metabolizing enzymes, see below §4 for the AhR). These receptors include several members of the nuclear/steroid receptor family (CAR for Constitutive Androstane Receptor, PXR for Pregnane X Receptor) but also the Aryl hydrocarbon Receptor or AhR, a member of the bHLH-PAS family (basic Helix-Loop-Helix - Period/ARNT/Single minded). In addition to the regulation of xenobiotic metabolism, numerous alternative functions have been characterized for the AhR since its discovery. These alternative functions will be described in this review along with its endogenous functions as revealed by experiments performed on knock-out animals. Elsevier 2018-06-11 /pmc/articles/PMC6039966/ /pubmed/30003042 http://dx.doi.org/10.1016/j.biopen.2018.05.001 Text en © 2018 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review
Larigot, Lucie
Juricek, Ludmila
Dairou, Julien
Coumoul, Xavier
AhR signaling pathways and regulatory functions
title AhR signaling pathways and regulatory functions
title_full AhR signaling pathways and regulatory functions
title_fullStr AhR signaling pathways and regulatory functions
title_full_unstemmed AhR signaling pathways and regulatory functions
title_short AhR signaling pathways and regulatory functions
title_sort ahr signaling pathways and regulatory functions
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6039966/
https://www.ncbi.nlm.nih.gov/pubmed/30003042
http://dx.doi.org/10.1016/j.biopen.2018.05.001
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