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The effect of short-chain fatty acids on human monocyte-derived dendritic cells

The gut microbiota is essential for human health and plays an important role in the pathogenesis of several diseases. Short-chain fatty acids (SCFA), such as acetate, butyrate and propionate, are end-products of microbial fermentation of macronutrients that distribute systemically via the blood. The...

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Autores principales: Nastasi, Claudia, Candela, Marco, Bonefeld, Charlotte Menné, Geisler, Carsten, Hansen, Morten, Krejsgaard, Thorbjørn, Biagi, Elena, Andersen, Mads Hald, Brigidi, Patrizia, Ødum, Niels, Litman, Thomas, Woetmann, Anders
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4635422/
https://www.ncbi.nlm.nih.gov/pubmed/26541096
http://dx.doi.org/10.1038/srep16148
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author Nastasi, Claudia
Candela, Marco
Bonefeld, Charlotte Menné
Geisler, Carsten
Hansen, Morten
Krejsgaard, Thorbjørn
Biagi, Elena
Andersen, Mads Hald
Brigidi, Patrizia
Ødum, Niels
Litman, Thomas
Woetmann, Anders
author_facet Nastasi, Claudia
Candela, Marco
Bonefeld, Charlotte Menné
Geisler, Carsten
Hansen, Morten
Krejsgaard, Thorbjørn
Biagi, Elena
Andersen, Mads Hald
Brigidi, Patrizia
Ødum, Niels
Litman, Thomas
Woetmann, Anders
author_sort Nastasi, Claudia
collection PubMed
description The gut microbiota is essential for human health and plays an important role in the pathogenesis of several diseases. Short-chain fatty acids (SCFA), such as acetate, butyrate and propionate, are end-products of microbial fermentation of macronutrients that distribute systemically via the blood. The aim of this study was to investigate the transcriptional response of immature and LPS-matured human monocyte-derived DC to SCFA. Our data revealed distinct effects exerted by each individual SCFA on gene expression in human monocyte-derived DC, especially in the mature ones. Acetate only exerted negligible effects, while both butyrate and propionate strongly modulated gene expression in both immature and mature human monocyte-derived DC. An Ingenuity pathway analysis based on the differentially expressed genes suggested that propionate and butyrate modulate leukocyte trafficking, as SCFA strongly reduced the release of several pro-inflammatory chemokines including CCL3, CCL4, CCL5, CXCL9, CXCL10, and CXCL11. Additionally, butyrate and propionate inhibited the expression of lipopolysaccharide (LPS)-induced cytokines such as IL-6 and IL-12p40 showing a strong anti-inflammatory effect. This work illustrates that bacterial metabolites far from the site of their production can differentially modulate the inflammatory response and generally provides new insights into host-microbiome interactions.
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spelling pubmed-46354222015-11-25 The effect of short-chain fatty acids on human monocyte-derived dendritic cells Nastasi, Claudia Candela, Marco Bonefeld, Charlotte Menné Geisler, Carsten Hansen, Morten Krejsgaard, Thorbjørn Biagi, Elena Andersen, Mads Hald Brigidi, Patrizia Ødum, Niels Litman, Thomas Woetmann, Anders Sci Rep Article The gut microbiota is essential for human health and plays an important role in the pathogenesis of several diseases. Short-chain fatty acids (SCFA), such as acetate, butyrate and propionate, are end-products of microbial fermentation of macronutrients that distribute systemically via the blood. The aim of this study was to investigate the transcriptional response of immature and LPS-matured human monocyte-derived DC to SCFA. Our data revealed distinct effects exerted by each individual SCFA on gene expression in human monocyte-derived DC, especially in the mature ones. Acetate only exerted negligible effects, while both butyrate and propionate strongly modulated gene expression in both immature and mature human monocyte-derived DC. An Ingenuity pathway analysis based on the differentially expressed genes suggested that propionate and butyrate modulate leukocyte trafficking, as SCFA strongly reduced the release of several pro-inflammatory chemokines including CCL3, CCL4, CCL5, CXCL9, CXCL10, and CXCL11. Additionally, butyrate and propionate inhibited the expression of lipopolysaccharide (LPS)-induced cytokines such as IL-6 and IL-12p40 showing a strong anti-inflammatory effect. This work illustrates that bacterial metabolites far from the site of their production can differentially modulate the inflammatory response and generally provides new insights into host-microbiome interactions. Nature Publishing Group 2015-11-06 /pmc/articles/PMC4635422/ /pubmed/26541096 http://dx.doi.org/10.1038/srep16148 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Nastasi, Claudia
Candela, Marco
Bonefeld, Charlotte Menné
Geisler, Carsten
Hansen, Morten
Krejsgaard, Thorbjørn
Biagi, Elena
Andersen, Mads Hald
Brigidi, Patrizia
Ødum, Niels
Litman, Thomas
Woetmann, Anders
The effect of short-chain fatty acids on human monocyte-derived dendritic cells
title The effect of short-chain fatty acids on human monocyte-derived dendritic cells
title_full The effect of short-chain fatty acids on human monocyte-derived dendritic cells
title_fullStr The effect of short-chain fatty acids on human monocyte-derived dendritic cells
title_full_unstemmed The effect of short-chain fatty acids on human monocyte-derived dendritic cells
title_short The effect of short-chain fatty acids on human monocyte-derived dendritic cells
title_sort effect of short-chain fatty acids on human monocyte-derived dendritic cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4635422/
https://www.ncbi.nlm.nih.gov/pubmed/26541096
http://dx.doi.org/10.1038/srep16148
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