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How Ah Receptor Ligand Specificity Became Important in Understanding Its Physiological Function

Increasingly, the aryl hydrocarbon receptor (AHR) is being recognized as a sensor for endogenous and pseudo-endogenous metabolites, and in particular microbiota and host generated tryptophan metabolites. One proposed explanation for this is the role of the AHR in innate immune signaling within barri...

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Autores principales: Murray, Iain A., Perdew, Gary H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7766308/
https://www.ncbi.nlm.nih.gov/pubmed/33348604
http://dx.doi.org/10.3390/ijms21249614
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author Murray, Iain A.
Perdew, Gary H.
author_facet Murray, Iain A.
Perdew, Gary H.
author_sort Murray, Iain A.
collection PubMed
description Increasingly, the aryl hydrocarbon receptor (AHR) is being recognized as a sensor for endogenous and pseudo-endogenous metabolites, and in particular microbiota and host generated tryptophan metabolites. One proposed explanation for this is the role of the AHR in innate immune signaling within barrier tissues in response to the presence of microorganisms. A number of cytokine/chemokine genes exhibit a combinatorial increase in transcription upon toll-like receptors and AHR activation, supporting this concept. The AHR also plays a role in the enhanced differentiation of intestinal and dermal epithelium leading to improved barrier function. Importantly, from an evolutionary perspective many of these tryptophan metabolites exhibit greater activation potential for the human AHR when compared to the rodent AHR. These observations underscore the importance of the AHR in barrier tissues and may lead to pharmacologic therapeutic intervention.
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spelling pubmed-77663082020-12-28 How Ah Receptor Ligand Specificity Became Important in Understanding Its Physiological Function Murray, Iain A. Perdew, Gary H. Int J Mol Sci Review Increasingly, the aryl hydrocarbon receptor (AHR) is being recognized as a sensor for endogenous and pseudo-endogenous metabolites, and in particular microbiota and host generated tryptophan metabolites. One proposed explanation for this is the role of the AHR in innate immune signaling within barrier tissues in response to the presence of microorganisms. A number of cytokine/chemokine genes exhibit a combinatorial increase in transcription upon toll-like receptors and AHR activation, supporting this concept. The AHR also plays a role in the enhanced differentiation of intestinal and dermal epithelium leading to improved barrier function. Importantly, from an evolutionary perspective many of these tryptophan metabolites exhibit greater activation potential for the human AHR when compared to the rodent AHR. These observations underscore the importance of the AHR in barrier tissues and may lead to pharmacologic therapeutic intervention. MDPI 2020-12-17 /pmc/articles/PMC7766308/ /pubmed/33348604 http://dx.doi.org/10.3390/ijms21249614 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Murray, Iain A.
Perdew, Gary H.
How Ah Receptor Ligand Specificity Became Important in Understanding Its Physiological Function
title How Ah Receptor Ligand Specificity Became Important in Understanding Its Physiological Function
title_full How Ah Receptor Ligand Specificity Became Important in Understanding Its Physiological Function
title_fullStr How Ah Receptor Ligand Specificity Became Important in Understanding Its Physiological Function
title_full_unstemmed How Ah Receptor Ligand Specificity Became Important in Understanding Its Physiological Function
title_short How Ah Receptor Ligand Specificity Became Important in Understanding Its Physiological Function
title_sort how ah receptor ligand specificity became important in understanding its physiological function
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7766308/
https://www.ncbi.nlm.nih.gov/pubmed/33348604
http://dx.doi.org/10.3390/ijms21249614
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