Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-8617
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dc.contributor.authorKarl, Martin-
dc.contributor.authorHasselwander, Solveig-
dc.contributor.authorZhou, Yawen-
dc.contributor.authorReifenberg, Gisela-
dc.contributor.authorKim, Yong Ook-
dc.contributor.authorPark, Kyoung-Sook-
dc.contributor.authorRidder, Dirk A.-
dc.contributor.authorWang, Xiaoyu-
dc.contributor.authorSeidel, Eric-
dc.contributor.authorHövelmeyer, Nadine-
dc.contributor.authorStraub, Beate K.-
dc.contributor.authorLi, Huige-
dc.contributor.authorSchuppan, Detlef-
dc.contributor.authorXia, Ning-
dc.date.accessioned2023-01-20T11:25:19Z-
dc.date.available2023-01-20T11:25:19Z-
dc.date.issued2022-
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/8633-
dc.description.abstractBackground and Aims Growing evidence suggests an important role of B cells in the development of NAFLD. However, a detailed functional analysis of B cell subsets in NAFLD pathogenesis is lacking. Approach and Results In wild-type mice, 21 weeks of high fat diet (HFD) feeding resulted in NAFLD with massive macrovesicular steatosis, modest hepatic and adipose tissue inflammation, insulin resistance, and incipient fibrosis. Remarkably, Bnull (JHT) mice were partially protected whereas B cell harboring but antibody-deficient IgMi mice were completely protected from the development of hepatic steatosis, inflammation, and fibrosis. The common feature of JHT and IgMi mice is that they do not secrete antibodies, whereas HFD feeding in wild-type mice led to increased levels of serum IgG2c. Whereas JHT mice have no B cells at all, regulatory B cells were found in the liver of both wild-type and IgMi mice. HFD reduced the number of regulatory B cells and IL-10 production in the liver of wild-type mice, whereas these increased in IgMi mice. Livers of patients with advanced liver fibrosis showed abundant deposition of IgG and stromal B cells and low numbers of IL-10 expressing cells, compatible with our experimental data. Conclusions B lymphocytes have both detrimental and protective effects in HFD-induced NAFLD. The lack of secreted pathogenic antibodies protects partially from NAFLD, whereas the presence of certain B cell subsets provides additional protection. IL-10–producing regulatory B cells may represent such a protective B cell subset.en_GB
dc.description.sponsorshipGefördert durch die Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 491381577de
dc.language.isoengde
dc.rightsCC BY-NC*
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/*
dc.subject.ddc610 Medizinde_DE
dc.subject.ddc610 Medical sciencesen_GB
dc.titleDual roles of B lymphocytes in mouse models of diet-induced nonalcoholic fatty liver diseaseen_GB
dc.typeZeitschriftenaufsatzde
dc.identifier.doihttp://doi.org/10.25358/openscience-8617-
jgu.type.dinitypearticleen_GB
jgu.type.versionPublished versionde
jgu.type.resourceTextde
jgu.organisation.departmentFB 04 Medizinde
jgu.organisation.number2700-
jgu.organisation.nameJohannes Gutenberg-Universität Mainz-
jgu.rights.accessrightsopenAccess-
jgu.journal.titleHepatologyde
jgu.journal.volume76de
jgu.journal.issue4de
jgu.pages.start1135de
jgu.pages.end1149de
jgu.publisher.year2022-
jgu.publisher.nameWiley Intersciencede
jgu.publisher.placeNew York, NY u.a.de
jgu.publisher.issn1527-3350de
jgu.organisation.placeMainz-
jgu.subject.ddccode610de
jgu.publisher.doi10.1002/hep.32428de
jgu.organisation.rorhttps://ror.org/023b0x485-
jgu.subject.dfgLebenswissenschaftende
Appears in collections:DFG-491381577-H

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