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Toll-Like Receptors: Regulators of the Immune Response in the Human Gut

Toll-like receptors (TLRs) are powerful molecular regulators by which the immune system may “sense” the environment and protect the host from pathogens or endogenous threats. In mammalian cells, several TLRs were identified with a tissue and cell type-specific distribution. Understanding the functio...

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Detalles Bibliográficos
Autores principales: Hug, Hubert, Mohajeri, M. Hasan, La Fata, Giorgio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852779/
https://www.ncbi.nlm.nih.gov/pubmed/29438282
http://dx.doi.org/10.3390/nu10020203
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author Hug, Hubert
Mohajeri, M. Hasan
La Fata, Giorgio
author_facet Hug, Hubert
Mohajeri, M. Hasan
La Fata, Giorgio
author_sort Hug, Hubert
collection PubMed
description Toll-like receptors (TLRs) are powerful molecular regulators by which the immune system may “sense” the environment and protect the host from pathogens or endogenous threats. In mammalian cells, several TLRs were identified with a tissue and cell type-specific distribution. Understanding the functions of specific TLRs is crucial for the development and discovery of compounds useful to maintaining or re-establishing homeostasis in the gastrointestinal tract (GIT). Due to their relevance in regulating the inflammatory response in the GIT, we will focus here on TLR2, TLR4, and TLR5. In particular, we describe (a) the molecular pathways activated by the stimulation of these receptors with their known bacterial ligands; (b) the non-bacterial ligands known to interact directly with TLR2 and TLR4 and their soluble forms. The scope of this minireview is to highlight the importance of bacterial and non-bacterial compounds in affecting the gut immune functions via the activation of the TLRs.
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spelling pubmed-58527792018-03-19 Toll-Like Receptors: Regulators of the Immune Response in the Human Gut Hug, Hubert Mohajeri, M. Hasan La Fata, Giorgio Nutrients Review Toll-like receptors (TLRs) are powerful molecular regulators by which the immune system may “sense” the environment and protect the host from pathogens or endogenous threats. In mammalian cells, several TLRs were identified with a tissue and cell type-specific distribution. Understanding the functions of specific TLRs is crucial for the development and discovery of compounds useful to maintaining or re-establishing homeostasis in the gastrointestinal tract (GIT). Due to their relevance in regulating the inflammatory response in the GIT, we will focus here on TLR2, TLR4, and TLR5. In particular, we describe (a) the molecular pathways activated by the stimulation of these receptors with their known bacterial ligands; (b) the non-bacterial ligands known to interact directly with TLR2 and TLR4 and their soluble forms. The scope of this minireview is to highlight the importance of bacterial and non-bacterial compounds in affecting the gut immune functions via the activation of the TLRs. MDPI 2018-02-13 /pmc/articles/PMC5852779/ /pubmed/29438282 http://dx.doi.org/10.3390/nu10020203 Text en © 2018 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
Hug, Hubert
Mohajeri, M. Hasan
La Fata, Giorgio
Toll-Like Receptors: Regulators of the Immune Response in the Human Gut
title Toll-Like Receptors: Regulators of the Immune Response in the Human Gut
title_full Toll-Like Receptors: Regulators of the Immune Response in the Human Gut
title_fullStr Toll-Like Receptors: Regulators of the Immune Response in the Human Gut
title_full_unstemmed Toll-Like Receptors: Regulators of the Immune Response in the Human Gut
title_short Toll-Like Receptors: Regulators of the Immune Response in the Human Gut
title_sort toll-like receptors: regulators of the immune response in the human gut
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852779/
https://www.ncbi.nlm.nih.gov/pubmed/29438282
http://dx.doi.org/10.3390/nu10020203
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