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dc.contributor.author
Baumann, Anja
dc.contributor.author
Nier, Anika
dc.contributor.author
Hernández Arriaga, Angélica
dc.contributor.author
Brandt, Annette
dc.contributor.author
Lorenzo Pisarello, Maria Jose
dc.contributor.author
Jin, Cheng J.
dc.contributor.author
Pilar, Esther
dc.contributor.author
Camarinha-Silva, Amélia
dc.contributor.author
Schattenberg, Jörn M.
dc.contributor.author
Bergheim, Ina
dc.date.available
2022-03-18T12:12:33Z
dc.date.issued
2021-09
dc.identifier.citation
Baumann, Anja; Nier, Anika; Hernández Arriaga, Angélica; Brandt, Annette; Lorenzo Pisarello, Maria Jose; et al.; Toll-like receptor 1 as a possible target in non-alcoholic fatty liver disease; Nature Publishing Group; Scientific Reports; 11; 1; 9-2021; 1-15;17815
dc.identifier.issn
2045-2322
dc.identifier.uri
http://hdl.handle.net/11336/153582
dc.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.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Nature Publishing Group
dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by/2.5/ar/
dc.subject
TOLL-LIKE RECEPTORS
dc.subject
INTESTINAL MICROBIOTA
dc.subject
ENDOTOXIN
dc.subject
NASH
dc.subject.classification
Otras Ciencias de la Salud
dc.subject.classification
Ciencias de la Salud
dc.subject.classification
CIENCIAS MÉDICAS Y DE LA SALUD
dc.title
Toll-like receptor 1 as a possible target in non-alcoholic fatty liver disease
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2021-12-13T19:17:26Z
dc.journal.volume
11
dc.journal.number
1
dc.journal.pagination
1-15;17815
dc.journal.pais
Reino Unido
dc.journal.ciudad
Londres
dc.description.fil
Fil: Baumann, Anja. Universidad de Viena; Austria
dc.description.fil
Fil: Nier, Anika. Universidad de Viena; Austria
dc.description.fil
Fil: Hernández Arriaga, Angélica. Universidad de Hohenheim; Alemania
dc.description.fil
Fil: Brandt, Annette. Universidad de Viena; Austria
dc.description.fil
Fil: Lorenzo Pisarello, Maria Jose. Universidad de Viena; Austria. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Centro de Referencia para Lactobacilos; Argentina
dc.description.fil
Fil: Jin, Cheng J.. Universitat Jena; Alemania
dc.description.fil
Fil: Pilar, Esther. Universidad de Viena; Austria
dc.description.fil
Fil: Camarinha-Silva, Amélia. Universidad de Hohenheim; Alemania
dc.description.fil
Fil: Schattenberg, Jörn M.. University Medical Center of the Johannes Gutenberg; Alemania
dc.description.fil
Fil: Bergheim, Ina. Universidad de Viena; Austria
dc.journal.title
Scientific Reports
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1038/s41598-021-97346-9
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.nature.com/articles/s41598-021-97346-9
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8426394/
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