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Microbial tryptophan catabolites in health and disease

Accumulating evidence implicates metabolites produced by gut microbes as crucial mediators of diet-induced host-microbial cross-talk. Here, we review emerging data suggesting that microbial tryptophan catabolites resulting from proteolysis are influencing host health. These metabolites are suggested...

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Autores principales: Roager, Henrik M., Licht, Tine R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6098093/
https://www.ncbi.nlm.nih.gov/pubmed/30120222
http://dx.doi.org/10.1038/s41467-018-05470-4
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author Roager, Henrik M.
Licht, Tine R.
author_facet Roager, Henrik M.
Licht, Tine R.
author_sort Roager, Henrik M.
collection PubMed
description Accumulating evidence implicates metabolites produced by gut microbes as crucial mediators of diet-induced host-microbial cross-talk. Here, we review emerging data suggesting that microbial tryptophan catabolites resulting from proteolysis are influencing host health. These metabolites are suggested to activate the immune system through binding to the aryl hydrocarbon receptor (AHR), enhance the intestinal epithelial barrier, stimulate gastrointestinal motility, as well as secretion of gut hormones, exert anti-inflammatory, anti-oxidative or toxic effects in systemic circulation, and putatively modulate gut microbial composition. Tryptophan catabolites thus affect various physiological processes and may contribute to intestinal and systemic homeostasis in health and disease.
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spelling pubmed-60980932018-08-20 Microbial tryptophan catabolites in health and disease Roager, Henrik M. Licht, Tine R. Nat Commun Review Article Accumulating evidence implicates metabolites produced by gut microbes as crucial mediators of diet-induced host-microbial cross-talk. Here, we review emerging data suggesting that microbial tryptophan catabolites resulting from proteolysis are influencing host health. These metabolites are suggested to activate the immune system through binding to the aryl hydrocarbon receptor (AHR), enhance the intestinal epithelial barrier, stimulate gastrointestinal motility, as well as secretion of gut hormones, exert anti-inflammatory, anti-oxidative or toxic effects in systemic circulation, and putatively modulate gut microbial composition. Tryptophan catabolites thus affect various physiological processes and may contribute to intestinal and systemic homeostasis in health and disease. Nature Publishing Group UK 2018-08-17 /pmc/articles/PMC6098093/ /pubmed/30120222 http://dx.doi.org/10.1038/s41467-018-05470-4 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Review Article
Roager, Henrik M.
Licht, Tine R.
Microbial tryptophan catabolites in health and disease
title Microbial tryptophan catabolites in health and disease
title_full Microbial tryptophan catabolites in health and disease
title_fullStr Microbial tryptophan catabolites in health and disease
title_full_unstemmed Microbial tryptophan catabolites in health and disease
title_short Microbial tryptophan catabolites in health and disease
title_sort microbial tryptophan catabolites in health and disease
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6098093/
https://www.ncbi.nlm.nih.gov/pubmed/30120222
http://dx.doi.org/10.1038/s41467-018-05470-4
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