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Opposite effects of bFGF and TGF-beta on collagen metabolism by human periodontal ligament fibroblasts

dc.contributor.authorGonzales Silverio-Ruiz, Karina
dc.contributor.authorTraverso Martinez, Aurora Esmeralda
dc.contributor.authorPompermaier Garlet, Gustavo
dc.contributor.authorFregonesi Barbosa, Carolina
dc.contributor.authorSantana Silva, Joao
dc.contributor.authorBarreto Cicarelli, Regina Maria
dc.contributor.authorValentini, Sandro Roberto [UNESP]
dc.contributor.authorGeorges Abi-Rached, Ricardo Sarnih
dc.contributor.authorRossa, Carlos Junior
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2014-05-20T15:19:51Z
dc.date.available2014-05-20T15:19:51Z
dc.date.issued2007-08-01
dc.description.abstractThis study evaluated the effects of bFGF and TGF-beta, individually and combined, on cell proliferation and collagen metabolism. Primary human periodontal ligament cells were stimulated with two concentrations (I and 10 ng/ml) of each growth factor, both individually and combined. Proliferation was determined by a commercial biochemical assay. Real time RT-PCR determined gene expression of NMP-1 and -2, collagen types I and III, TIMP-1, -2 and -3. Autocrine effects on synthesis of bFGF and TGF-beta were evaluated by ELISA. Only TGF-beta, either isolated or associated with bFGF, significantly increased cell proliferation. TGF-beta had anabolic effects, increasing expression of type I and III collagen as well as of TIMPs, whereas bFGF had opposite effects. When bFGF and TGF-beta were associated, the anabolic effects prevailed. Synthesis of TGF-beta was induced only by the association of lower concentrations of the growth factors, whereas there was a dose-dependent production of bFGF. It is concluded that bFGF had a predominantly catabolic effect, and TGF-beta exerted an anabolic effect on hPDL cells. (c) 2007 Elsevier Ltd. All rights reserved.en
dc.description.affiliationSão Paulo State Univ, Sch Dent, Dept Diagnost & Imaging, BR-14801903 São Paulo, Brazil
dc.description.affiliationSão Paulo State Univ, Sch Dent, Dept Biol Sci, BR-17012901 São Paulo, Brazil
dc.description.affiliationUniv São Paulo, Sch Med Ribeirao Preto, Dept Biochem & Immunol, BR-14049900 São Paulo, Brazil
dc.description.affiliationSão Paulo State Univ, Sch Pharmaceut Sci, Dept Biol Sci, BR-14801902 Araraquara, SP, Brazil
dc.description.affiliationUnespSão Paulo State Univ, Sch Dent, Dept Diagnost & Imaging, BR-14801903 São Paulo, Brazil
dc.description.affiliationUnespSão Paulo State Univ, Sch Dent, Dept Biol Sci, BR-17012901 São Paulo, Brazil
dc.description.affiliationUnespSão Paulo State Univ, Sch Pharmaceut Sci, Dept Biol Sci, BR-14801902 Araraquara, SP, Brazil
dc.format.extent130-137
dc.identifierhttp://dx.doi.org/10.1016/j.cyto.2007.06.009
dc.identifier.citationCytokine. London: Academic Press Ltd Elsevier B.V. Ltd, v. 39, n. 2, p. 130-137, 2007.
dc.identifier.doi10.1016/j.cyto.2007.06.009
dc.identifier.issn1043-4666
dc.identifier.lattes5333250355049814
dc.identifier.urihttp://hdl.handle.net/11449/31237
dc.identifier.wosWOS:000250913700006
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofCytokine
dc.relation.ispartofjcr3.514
dc.relation.ispartofsjr1,433
dc.rights.accessRightsAcesso restritopt
dc.sourceWeb of Science
dc.subjecthuman periodontal ligament cellspt
dc.subjecttransforming growth factor betapt
dc.subjectbasic fibroblast growth factorpt
dc.subjectcollagenpt
dc.subjectmatrix metalloproteasespt
dc.subjecttissue inhibitor of matrix metalloproteasespt
dc.subjectperiodontal regenerationpt
dc.titleOpposite effects of bFGF and TGF-beta on collagen metabolism by human periodontal ligament fibroblastsen
dc.typeArtigopt
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
relation.isDepartmentOfPublication5004bcab-94af-4939-b980-091ae9d0a19e
relation.isDepartmentOfPublication.latestForDiscovery5004bcab-94af-4939-b980-091ae9d0a19e
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.author.lattes5333250355049814
unesp.author.lattes7634063102292261[9]
unesp.author.orcid0000-0003-1705-5481[9]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt
unesp.departmentCiências Biológicas - FCFpt

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