Association between hepatocyte TM4SF5 expression and gut microbiome dysbiosis during non-alcoholic fatty liver disease development

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dc.contributor.authorY D Pinanga-
dc.contributor.authorK H Pyo-
dc.contributor.authorE A Shin-
dc.contributor.authorH Lee-
dc.contributor.authorE H Lee-
dc.contributor.authorW Kim-
dc.contributor.authorS Kim-
dc.contributor.authorJ E Kim-
dc.contributor.authorSemi Kim-
dc.contributor.authorJ W Lee-
dc.date.accessioned2024-10-28T16:32:52Z-
dc.date.available2024-10-28T16:32:52Z-
dc.date.issued2024-
dc.identifier.issn0024-3205-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/36231-
dc.description.abstractGut microbiome dysbiosis is involved in non-alcoholic fatty liver disease (NAFLD) development. Hepatic transmembrane 4 L six family member 5 (TM4SF5) overexpression promotes NAFLD. However, how gut microbiota are associated with TM4SF5-mediated NAFLD remains unexplored. We analyzed the gut microbiome using feces from hepatocyte-specific TM4SF5-overexpressing transgenic (Alb-TGTm4sf5-Flag, TG) or Tm4sf5-/- knock-out (KO) mice fed a normal chow diet (NCD), high-fat diet (HFD) for 2 weeks (HFD2W), or methionine-choline-deficient diet (MCD) for 4 weeks to investigate associations among Tm4sf5 expression, diet, and the gut microbiome. TG-NCD mice showed a higher Firmicutes-to-Bacteroidetes (F/B) ratio, with less enrichment of Akkermansia muciniphila and Lactobacillus reuteri. NASH-related microbiomes in feces were more abundant in TG-HFD2w mice than in KO-HFD2w mice. Further, TG-MCD showed a higher F/B ratio than TG-NCD or KO mice, with decreases or increases in microbiomes beneficial or detrimental to the liver, respectively. Such effects in TG-MCD animals were correlated with functional pathways producing short-chain fatty acids (SCFAs). Furthermore, potential functional pathways of the gut microbiome were metabolically parallel to NAFLD features in TG-MCD mice. These results suggest that hepatocyte Tm4sf5 supports gut microbiome dysbiosis and metabolic activity, leading to SCFA production and hepatic inflammation during NAFLD development.-
dc.publisherElsevier-
dc.titleAssociation between hepatocyte TM4SF5 expression and gut microbiome dysbiosis during non-alcoholic fatty liver disease development-
dc.title.alternativeAssociation between hepatocyte TM4SF5 expression and gut microbiome dysbiosis during non-alcoholic fatty liver disease development-
dc.typeArticle-
dc.citation.titleLife Sciences-
dc.citation.number0-
dc.citation.endPage123164-
dc.citation.startPage123164-
dc.citation.volume358-
dc.contributor.affiliatedAuthorSemi Kim-
dc.contributor.alternativeNamePinanga-
dc.contributor.alternativeName표경희-
dc.contributor.alternativeName신은애-
dc.contributor.alternativeName이해송-
dc.contributor.alternativeName이은해-
dc.contributor.alternativeName김원식-
dc.contributor.alternativeName김소연-
dc.contributor.alternativeName김지언-
dc.contributor.alternativeName김세미-
dc.contributor.alternativeName이정원-
dc.identifier.bibliographicCitationLife Sciences, vol. 358, pp. 123164-123164-
dc.identifier.doi10.1016/j.lfs.2024.123164-
dc.subject.keywordFunctional metabolic pathway-
dc.subject.keywordGut microbiome dysbiosis-
dc.subject.keywordLiver inflammation-
dc.subject.keywordNAFLD-
dc.subject.keywordShort chain fatty acids-
dc.subject.keywordTetraspanin-
dc.subject.localNAFLD-
dc.description.journalClassY-
Appears in Collections:
Division of A.I. & Biomedical Research > Microbiome Convergence Research Center > 1. Journal Articles
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