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Immunological Relevance of the Coevolution of IDO1 and AHR

The aryl hydrocarbon receptor (AHR) is a ligand-activated transcription factor initially identified because of its role in controlling the cellular response to environmental molecules. More recently, AHR has been shown to play a crucial role in controlling innate and adaptive immune responses throug...

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Autores principales: Jaronen, Merja, Quintana, Francisco J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4202789/
https://www.ncbi.nlm.nih.gov/pubmed/25368620
http://dx.doi.org/10.3389/fimmu.2014.00521
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author Jaronen, Merja
Quintana, Francisco J.
author_facet Jaronen, Merja
Quintana, Francisco J.
author_sort Jaronen, Merja
collection PubMed
description The aryl hydrocarbon receptor (AHR) is a ligand-activated transcription factor initially identified because of its role in controlling the cellular response to environmental molecules. More recently, AHR has been shown to play a crucial role in controlling innate and adaptive immune responses through several mechanisms, one of which is the regulation of tryptophan metabolism. Indoleamine-2,3-dioxygenase (IDO) and tryptophan-2,3-dioxygenase (TDO) are considered rate-limiting enzymes in the tryptophan catabolism and play important roles in the regulation of the immunity. Moreover, AHR and IDO/TDO are closely interconnected: AHR regulates IDO and TDO expression, and kynurenine produced by IDO/TDO is an AHR agonist. In this review, we propose to examine the relationship between AHR and IDO/TDO and its relevance for the regulation of the immune response in health and disease.
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spelling pubmed-42027892014-11-03 Immunological Relevance of the Coevolution of IDO1 and AHR Jaronen, Merja Quintana, Francisco J. Front Immunol Immunology The aryl hydrocarbon receptor (AHR) is a ligand-activated transcription factor initially identified because of its role in controlling the cellular response to environmental molecules. More recently, AHR has been shown to play a crucial role in controlling innate and adaptive immune responses through several mechanisms, one of which is the regulation of tryptophan metabolism. Indoleamine-2,3-dioxygenase (IDO) and tryptophan-2,3-dioxygenase (TDO) are considered rate-limiting enzymes in the tryptophan catabolism and play important roles in the regulation of the immunity. Moreover, AHR and IDO/TDO are closely interconnected: AHR regulates IDO and TDO expression, and kynurenine produced by IDO/TDO is an AHR agonist. In this review, we propose to examine the relationship between AHR and IDO/TDO and its relevance for the regulation of the immune response in health and disease. Frontiers Media S.A. 2014-10-20 /pmc/articles/PMC4202789/ /pubmed/25368620 http://dx.doi.org/10.3389/fimmu.2014.00521 Text en Copyright © 2014 Jaronen and Quintana. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Jaronen, Merja
Quintana, Francisco J.
Immunological Relevance of the Coevolution of IDO1 and AHR
title Immunological Relevance of the Coevolution of IDO1 and AHR
title_full Immunological Relevance of the Coevolution of IDO1 and AHR
title_fullStr Immunological Relevance of the Coevolution of IDO1 and AHR
title_full_unstemmed Immunological Relevance of the Coevolution of IDO1 and AHR
title_short Immunological Relevance of the Coevolution of IDO1 and AHR
title_sort immunological relevance of the coevolution of ido1 and ahr
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4202789/
https://www.ncbi.nlm.nih.gov/pubmed/25368620
http://dx.doi.org/10.3389/fimmu.2014.00521
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