Toll-like receptor 1 as a possible target in non-alcoholic fatty liver disease

Abstract Toll-like receptors (TLRs) in the liver compartment have repeatedly been attributed to the development of non-alcoholic fatty liver disease (NAFLD). Knowledge on TLR expression in blood cells and their relation to intestinal microbiota and NAFLD development is limited. Here, we determined T...

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Main Authors: Anja Baumann, Anika Nier, Angélica Hernández-Arriaga, Annette Brandt, Maria J. Lorenzo Pisarello, Cheng J. Jin, Esther Pilar, Amélia Camarinha-Silva, Jörn M. Schattenberg, Ina Bergheim
Format: Article
Language:English
Published: Nature Publishing Group 2021-09-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-97346-9
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spelling doaj-4bf6f872572040e897d0b276027d7f172021-09-12T11:21:51ZengNature Publishing GroupScientific Reports2045-23222021-09-0111111510.1038/s41598-021-97346-9Toll-like receptor 1 as a possible target in non-alcoholic fatty liver diseaseAnja Baumann0Anika Nier1Angélica Hernández-Arriaga2Annette Brandt3Maria J. Lorenzo Pisarello4Cheng J. Jin5Esther Pilar6Amélia Camarinha-Silva7Jörn M. Schattenberg8Ina Bergheim9Department of Nutritional Sciences, Molecular Nutritional Science, University of ViennaDepartment of Nutritional Sciences, Molecular Nutritional Science, University of ViennaInstitute of Animal Science, University of HohenheimDepartment of Nutritional Sciences, Molecular Nutritional Science, University of ViennaDepartment of Nutritional Sciences, Molecular Nutritional Science, University of ViennaInstitute of Nutrition, SD Model Systems of Molecular Nutrition, Friedrich-Schiller-University JenaDepartment of Nutritional Sciences, Molecular Nutritional Science, University of ViennaInstitute of Animal Science, University of HohenheimMetabolic Liver Research Program, Department of Internal Medicine I, University Medical Center of the Johannes Gutenberg-UniversityDepartment of Nutritional Sciences, Molecular Nutritional Science, University of ViennaAbstract Toll-like receptors (TLRs) in the liver compartment have repeatedly been attributed to the development of non-alcoholic fatty liver disease (NAFLD). Knowledge on TLR expression in blood cells and their relation to intestinal microbiota and NAFLD development is limited. Here, we determined TLR expression patterns in peripheral blood mononuclear cells (PBMCs) of NAFLD patients and controls, their relation to intestinal microbiota and the impact of TLRs found altered in NAFLD development. Markers of intestinal permeability in blood and TLR mRNA expression in PBMCs were determined in 37 NAFLD patients and 15 age-matched healthy controls. Fecal microbiota composition was evaluated in 21 NAFLD patients and 9 controls using 16S rRNA gene amplicon sequencing. Furthermore, TLR1 −/− and C57BL/6 mice (n = 5–6/group) were pair-fed a liquid control or a fat-, fructose- and cholesterol-rich diet. Intestinal microbiota composition and markers of intestinal permeability like zonulin and bacterial endotoxin differed significantly between groups with the latter markers being significantly higher in NAFLD patients. Expression of TLR1-8 and 10 mRNA was detectable in PBMCs; however, only TLR1 expression, being higher in NAFLD patients, were significantly positively correlated with the prevalence of Holdemanella genus while negative correlations were found with Gemmiger and Ruminococcus genera. TLR1 −/− mice were significantly protected from the development of diet-induced NAFLD when compared to wild-type mice. While intestinal microbiota composition and permeability differed significantly between NAFLD patients and healthy subjects, in PBMCs, only TLR1 expression differed between groups. Still, targeting these alterations might be a beneficial approach in the treatment of NAFLD in some patients.https://doi.org/10.1038/s41598-021-97346-9
collection DOAJ
language English
format Article
sources DOAJ
author Anja Baumann
Anika Nier
Angélica Hernández-Arriaga
Annette Brandt
Maria J. Lorenzo Pisarello
Cheng J. Jin
Esther Pilar
Amélia Camarinha-Silva
Jörn M. Schattenberg
Ina Bergheim
spellingShingle Anja Baumann
Anika Nier
Angélica Hernández-Arriaga
Annette Brandt
Maria J. Lorenzo Pisarello
Cheng J. Jin
Esther Pilar
Amélia Camarinha-Silva
Jörn M. Schattenberg
Ina Bergheim
Toll-like receptor 1 as a possible target in non-alcoholic fatty liver disease
Scientific Reports
author_facet Anja Baumann
Anika Nier
Angélica Hernández-Arriaga
Annette Brandt
Maria J. Lorenzo Pisarello
Cheng J. Jin
Esther Pilar
Amélia Camarinha-Silva
Jörn M. Schattenberg
Ina Bergheim
author_sort Anja Baumann
title Toll-like receptor 1 as a possible target in non-alcoholic fatty liver disease
title_short Toll-like receptor 1 as a possible target in non-alcoholic fatty liver disease
title_full Toll-like receptor 1 as a possible target in non-alcoholic fatty liver disease
title_fullStr Toll-like receptor 1 as a possible target in non-alcoholic fatty liver disease
title_full_unstemmed Toll-like receptor 1 as a possible target in non-alcoholic fatty liver disease
title_sort toll-like receptor 1 as a possible target in non-alcoholic fatty liver disease
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2021-09-01
description Abstract Toll-like receptors (TLRs) in the liver compartment have repeatedly been attributed to the development of non-alcoholic fatty liver disease (NAFLD). Knowledge on TLR expression in blood cells and their relation to intestinal microbiota and NAFLD development is limited. Here, we determined TLR expression patterns in peripheral blood mononuclear cells (PBMCs) of NAFLD patients and controls, their relation to intestinal microbiota and the impact of TLRs found altered in NAFLD development. Markers of intestinal permeability in blood and TLR mRNA expression in PBMCs were determined in 37 NAFLD patients and 15 age-matched healthy controls. Fecal microbiota composition was evaluated in 21 NAFLD patients and 9 controls using 16S rRNA gene amplicon sequencing. Furthermore, TLR1 −/− and C57BL/6 mice (n = 5–6/group) were pair-fed a liquid control or a fat-, fructose- and cholesterol-rich diet. Intestinal microbiota composition and markers of intestinal permeability like zonulin and bacterial endotoxin differed significantly between groups with the latter markers being significantly higher in NAFLD patients. Expression of TLR1-8 and 10 mRNA was detectable in PBMCs; however, only TLR1 expression, being higher in NAFLD patients, were significantly positively correlated with the prevalence of Holdemanella genus while negative correlations were found with Gemmiger and Ruminococcus genera. TLR1 −/− mice were significantly protected from the development of diet-induced NAFLD when compared to wild-type mice. While intestinal microbiota composition and permeability differed significantly between NAFLD patients and healthy subjects, in PBMCs, only TLR1 expression differed between groups. Still, targeting these alterations might be a beneficial approach in the treatment of NAFLD in some patients.
url https://doi.org/10.1038/s41598-021-97346-9
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