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dc.contributor.authorMeen, A.J.*
dc.contributor.authorDoncheva, A.I.*
dc.contributor.authorBöttcher, Y.*
dc.contributor.authorDankel, S.N.*
dc.contributor.authorHoffmann, A.*
dc.contributor.authorBlüher, M.*
dc.contributor.authorFerno, Johan*
dc.contributor.authorMellgren, G.*
dc.contributor.authorGhosh, A.*
dc.contributor.authorSun, W.*
dc.contributor.authorDong, H.*
dc.contributor.authorNoé, F.*
dc.contributor.authorWolfrum, C.*
dc.contributor.authorPejler, G.*
dc.contributor.authorDalen, K.T.*
dc.contributor.authorKolset, S.O.*
dc.date.accessioned2025-09-12T11:46:58Z
dc.date.available2025-09-12T11:46:58Z
dc.date.issued2023
dc.identifier.citationMeen AJ, Doncheva AI, Böttcher Y, Dankel SN, Hoffmann A, Blüher M, et al. Obesity Is Associated with Distorted Proteoglycan Expression in Adipose Tissue. International Journal of Molecular Sciences. 2023;24(8).
dc.identifier.issn1422-0067
dc.identifier.otherhttps://portalcientifico.sergas.gal//documentos/64609f17c6d6be6c90fc609d
dc.identifier.urihttp://hdl.handle.net/20.500.11940/21797
dc.description.abstractProteoglycans are central components of the extracellular matrix (ECM) and binding partners for inflammatory chemokines. Morphological differences in the ECM and increased inflammation are prominent features of the white adipose tissues in patients with obesity. The impact of obesity and weight loss on the expression of specific proteoglycans in adipose tissue is not well known. This study aimed to investigate the relationship between adiposity and proteoglycan expression. We analyzed transcriptomic data from two human bariatric surgery cohorts. In addition, RT-qPCR was performed on adipose tissues from female and male mice fed a high-fat diet. Both visceral and subcutaneous adipose tissue depots were analyzed. Adipose mRNA expression of specific proteoglycans, proteoglycan biosynthetic enzymes, proteoglycan partner molecules, and other ECM-related proteins were altered in both human cohorts. We consistently observed more profound alterations in gene expression of ECM targets in the visceral adipose tissues after surgery (among others VCAN (p = 0.000309), OGN (p = 0.000976), GPC4 (p = 0.00525), COL1A1 (p = 0.00221)). Further, gene analyses in mice revealed sex differences in these two tissue compartments in obese mice. We suggest that adipose tissue repair is still in progress long after surgery, which may reflect challenges in remodeling increased adipose tissues. This study can provide the basis for more mechanistic studies on the role of proteoglycans in adipose tissues in obesity.
dc.description.sponsorshipThis work was supported by grants from the Institute of Basic Medical Sciences, University of Oslo (A.I.D. and K.T.D.), The Throne Holst Foundation (K.T.D. and S.O.K.), Western Norway Regional Health Authority (Helse Vest RHF) (J.F., G.M., and S.N.D.), the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation)-Projektnummer 209933838-SFB 1052 (project B01) to M.B., and by Deutsches Zentrum fuer Diabetesforschung (DZD, Grant: 82DZD00601 to M.B.) and Trond Mohn Stiftelse (J.F., G.M., and S.N.D.).
dc.languageeng
dc.rightsAttribution 4.0 International (CC BY 4.0)*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.meshFemale *
dc.subject.meshHumans *
dc.subject.meshMale *
dc.subject.meshAnimals *
dc.subject.meshMice *
dc.subject.meshProteoglycans *
dc.subject.meshAdipose Tissue *
dc.subject.meshObesity *
dc.subject.meshSubcutaneous Fat *
dc.subject.meshAdiposity *
dc.subject.meshExtracellular Matrix Proteins *
dc.subject.meshDiet, High-Fat *
dc.titleObesity Is Associated with Distorted Proteoglycan Expression in Adipose Tissue
dc.typeArtigo
dc.authorsophosMeen, A.J.; Doncheva, A.I.; Böttcher, Y.; Dankel, S.N.; Hoffmann, A.; Blüher, M.; Fernø, J.; Mellgren, G.; Ghosh, A.; Sun, W.; Dong, H.; Noé, F.; Wolfrum, C.; Pejler, G.; Dalen, K.T.; Kolset, S.O.
dc.identifier.doi10.3390/ijms24086884
dc.identifier.sophos64609f17c6d6be6c90fc609d
dc.issue.number8
dc.journal.titleInternational Journal of Molecular Sciences*
dc.organizationServizo Galego de Saúde::Áreas Sanitarias (A.S.) - Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS)
dc.relation.projectIDInstitute of Basic Medical Sciences, University of Oslo
dc.relation.projectIDThrone Holst Foundation
dc.relation.projectIDWestern Norway Regional Health Authority (Helse Vest RHF)
dc.relation.projectIDDeutsche Forschungsgemeinschaft (DFG, German Research Foundation) [B01]
dc.relation.projectIDDeutsches Zentrum fur Diabetesforschung [209933838-SFB 1052]
dc.relation.projectIDTrond Mohn Stiftelse
dc.relation.projectID[82DZD00601]
dc.relation.publisherversionhttps://doi.org/10.3390/ijms24086884
dc.rights.accessRightsopenAccess*
dc.subject.keywordAS Santiago
dc.subject.keywordIDIS
dc.typefidesArtículo Científico (incluye Original, Original breve, Revisión Sistemática y Meta-análisis)
dc.typesophosArtículo Original
dc.volume.number24


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Attribution 4.0 International (CC BY 4.0)
Excepto si se señala otra cosa, la licencia del ítem se describe como Attribution 4.0 International (CC BY 4.0)