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Antimicrobial proteins: intestinal guards to protect against liver disease

Alterations of gut microbes play a role in the pathogenesis and progression of many disorders including liver and gastrointestinal diseases. Both qualitative and quantitative changes in gut microbiota have been associated with liver disease. Intestinal dysbiosis can disrupt the integrity of the inte...

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Autores principales: Hendrikx, Tim, Schnabl, Bernd
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Japan 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391196/
https://www.ncbi.nlm.nih.gov/pubmed/30392013
http://dx.doi.org/10.1007/s00535-018-1521-8
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author Hendrikx, Tim
Schnabl, Bernd
author_facet Hendrikx, Tim
Schnabl, Bernd
author_sort Hendrikx, Tim
collection PubMed
description Alterations of gut microbes play a role in the pathogenesis and progression of many disorders including liver and gastrointestinal diseases. Both qualitative and quantitative changes in gut microbiota have been associated with liver disease. Intestinal dysbiosis can disrupt the integrity of the intestinal barrier leading to pathological bacterial translocation and the initiation of an inflammatory response in the liver. In order to sustain symbiosis and protect from pathological bacterial translocation, antimicrobial proteins (AMPs) such as a-defensins and C-type lectins are expressed in the gastrointestinal tract. In this review, we provide an overview of the role of AMPs in different chronic liver disease such as alcoholic steatohepatitis, non-alcoholic fatty liver disease, and cirrhosis. In addition, potential approaches to modulate the function of AMPs and prevent bacterial translocation are discussed.
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spelling pubmed-63911962019-03-15 Antimicrobial proteins: intestinal guards to protect against liver disease Hendrikx, Tim Schnabl, Bernd J Gastroenterol Review Alterations of gut microbes play a role in the pathogenesis and progression of many disorders including liver and gastrointestinal diseases. Both qualitative and quantitative changes in gut microbiota have been associated with liver disease. Intestinal dysbiosis can disrupt the integrity of the intestinal barrier leading to pathological bacterial translocation and the initiation of an inflammatory response in the liver. In order to sustain symbiosis and protect from pathological bacterial translocation, antimicrobial proteins (AMPs) such as a-defensins and C-type lectins are expressed in the gastrointestinal tract. In this review, we provide an overview of the role of AMPs in different chronic liver disease such as alcoholic steatohepatitis, non-alcoholic fatty liver disease, and cirrhosis. In addition, potential approaches to modulate the function of AMPs and prevent bacterial translocation are discussed. Springer Japan 2018-11-03 2019 /pmc/articles/PMC6391196/ /pubmed/30392013 http://dx.doi.org/10.1007/s00535-018-1521-8 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Review
Hendrikx, Tim
Schnabl, Bernd
Antimicrobial proteins: intestinal guards to protect against liver disease
title Antimicrobial proteins: intestinal guards to protect against liver disease
title_full Antimicrobial proteins: intestinal guards to protect against liver disease
title_fullStr Antimicrobial proteins: intestinal guards to protect against liver disease
title_full_unstemmed Antimicrobial proteins: intestinal guards to protect against liver disease
title_short Antimicrobial proteins: intestinal guards to protect against liver disease
title_sort antimicrobial proteins: intestinal guards to protect against liver disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391196/
https://www.ncbi.nlm.nih.gov/pubmed/30392013
http://dx.doi.org/10.1007/s00535-018-1521-8
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