Publicação:
Role of 1α,25-Dihydroxyvitamin D3 in Adipogenesis of SGBS Cells: New Insights into Human Preadipocyte Proliferation

dc.contributor.authorFelicidade, Ingrid [UNESP]
dc.contributor.authorSartori, Daniele
dc.contributor.authorCoort, Susan L.M.
dc.contributor.authorSemprebon, Simone Cristine
dc.contributor.authorNiwa, Andressa Megumi
dc.contributor.authorD'Epiro, Gláucia Fernanda Rocha
dc.contributor.authorBiazi, Bruna Isabela
dc.contributor.authorMarques, Lilian Areal
dc.contributor.authorEvelo, Chris T.
dc.contributor.authorMantovani, Mário Sérgio
dc.contributor.authorRibeiro, Lúcia Regina [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionNUTRIM School for Nutrition and Translational Research in Metabolism
dc.contributor.institutionUniversidade Estadual de Londrina (UEL)
dc.contributor.institutionMaastricht Centre for Systems Biology (MaCSBio)
dc.contributor.institutionUniv. Estadual de Londrina Rodovia Celso Garcia Cid
dc.date.accessioned2018-12-11T17:22:02Z
dc.date.available2018-12-11T17:22:02Z
dc.date.issued2018-08-01
dc.description.abstractBackground/Aims: Compared with non-obese individuals, obese individuals commonly store more vitamin D in adipose tissue. VDR expression in adipose tissue can influence adipogenesis and is therefore a target pathway deserving further study. This study aims to assess the role of 1,25(OH)2D3 in human preadipocyte proliferation and differentiation. Methods: RTCA, MTT, and trypan blue assays were used to assess the effects of 1,25(OH)2D3 on the viability, proliferation, and adipogenic differentiation of SGBS cells. Cell cycle and apoptosis analyses were performed with flow cytometry, triglycerides were quantified, and RT-qPCR was used to assess gene expression. Results: We confirmed that the SGBS cell model is suitable for studying adipogenesis and demonstrated that the differentiation protocol induces cell maturation, thereby increasing the lipid content of cells independently of treatment. 1,25(OH)2D3 treatment had different effects according to the cell stage, indicating different modes of action driving proliferation and differentiation. In preadipocytes, 1,25(OH)2D3 induced G1 growth arrest at both tested concentrations without altering CDKN1A gene expression. Treatment with 100 nM 1,25(OH)2D3 also decreased MTT absorbance and the lipid concentration. Moreover, increased normalized cell index values and decreased metabolic activity were not induced by proliferation or apoptosis. Exposure to 100 nM 1,25(OH)2D3 induced VDR, CEBPA, and CEBPB expression, even in the preadipocyte stage. During adipogenesis, 1,25(OH)2D3 had limited effects on processes such as VDR and PPARG gene expression, but it upregulated CEBPA expression. Conclusions: We demonstrated for the first time that 1,25(OH)2D3 induces changes in preadipocytes, including VDR expression and growth arrest, and increases the lipid content in adipocytes treated for 16 days. Preadipocytes are important cells in adipose tissue homeostasis, and understanding the role of 1,25(OH)2D3 in adipogenesis is a crucial step in ensuring adequate vitamin D supplementation, especially for obese individuals.en
dc.description.affiliationSão Paulo State University (UNESP) School of Medicine Department of Pathology
dc.description.affiliationMaastricht University Department of Bioinformatics - BiGCaT NUTRIM School for Nutrition and Translational Research in Metabolism
dc.description.affiliationState University of Londrina (UEL) Department of Biochemistry and Biotechnology
dc.description.affiliationState University of Londrina (UEL) Department of General Biology
dc.description.affiliationMaastricht University Maastricht Centre for Systems Biology (MaCSBio)
dc.description.affiliationCentro de Ciências Bio. Dept. de Bio. Geral Lab. de Genética Toxicológica Univ. Estadual de Londrina Rodovia Celso Garcia Cid, PR 445 Km 380, Campus Universitário
dc.description.affiliationUnespSão Paulo State University (UNESP) School of Medicine Department of Pathology
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipFinanciadora de Estudos e Projetos
dc.description.sponsorshipIdCNPq: 150067/2017-8
dc.description.sponsorshipIdCAPES: 9933/2014-00
dc.format.extent407-418
dc.identifierhttp://dx.doi.org/10.1159/000491770
dc.identifier.citationCellular Physiology and Biochemistry, v. 48, n. 1, p. 407-418, 2018.
dc.identifier.doi10.1159/000491770
dc.identifier.file2-s2.0-85051069274.pdf
dc.identifier.issn1421-9778
dc.identifier.issn1015-8987
dc.identifier.scopus2-s2.0-85051069274
dc.identifier.urihttp://hdl.handle.net/11449/176678
dc.language.isoeng
dc.relation.ispartofCellular Physiology and Biochemistry
dc.relation.ispartofsjr1,561
dc.relation.ispartofsjr1,561
dc.rights.accessRightsAcesso aberto
dc.sourceScopus
dc.subjectAdipogenesis
dc.subjectPreadipocyte
dc.subjectSGBS
dc.subjectVitamin D
dc.titleRole of 1α,25-Dihydroxyvitamin D3 in Adipogenesis of SGBS Cells: New Insights into Human Preadipocyte Proliferationen
dc.typeArtigo
dspace.entity.typePublication
unesp.campusUniversidade Estadual Paulista (Unesp), Faculdade de Medicina, Botucatupt
unesp.departmentPatologia - FMBpt

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