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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/