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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/116592
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dc.contributor.authorTurrioni, Ana Paula S.-
dc.contributor.authorBasso, Fernanda G.-
dc.contributor.authorMontoro, Liege A.-
dc.contributor.authorAlmeida, Leopoldina de Fatima D. de-
dc.contributor.authorSouza Costa, Carlos A. de-
dc.contributor.authorHebling, Josimeri-
dc.date.accessioned2015-03-18T15:53:33Z-
dc.date.accessioned2016-10-25T20:25:10Z-
dc.date.available2015-03-18T15:53:33Z-
dc.date.available2016-10-25T20:25:10Z-
dc.date.issued2014-10-01-
dc.identifierhttp://dx.doi.org/10.1016/j.jdent.2014.07.014-
dc.identifier.citationJournal Of Dentistry. Oxford: Elsevier Sci Ltd, v. 42, n. 10, p. 1292-1299, 2014.-
dc.identifier.issn0300-5712-
dc.identifier.urihttp://hdl.handle.net/11449/116592-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/116592-
dc.description.abstractObjectives: The aim of this study was to evaluate the effects of infrared LED (850 nm) irradiation on dentin matrix proteins expression and synthesis by cultured stem cells from human exfoliated deciduous teeth (SHED).Methods: Near-exfoliation primary teeth were extracted (n = 3), and SHED cultures were characterized by immunofluorescence using STRO-1, CD44, CD146, Nanog and OCT3/4 antibodies, before experimental protocol. The SHEDs were seeded (3 x 10(4) cells/cm(2)) with DMEM containing 10% FBS. After 24-h incubation, the culture medium was replaced by osteogenic differentiation medium, and the cells were irradiated with LED light at energy densities (EDs) of 0 (control), 2, or 4 J/cm(2) (n = 8). The irradiated SHEDs were then evaluated for alkaline phosphatase (ALP) activity, total protein (TP) production, and collagen synthesis (SIRCOL (TM) Assay), as well as ALP, collagen type I (Col I), dentin sialophosphoprotein (DSPP), and dentin matrix acidic phosphoprotein (DMP-1) gene expression (qPCR). Data were analyzed by Kruskal-Wallis and Mann-Whitney tests (alpha = 0.05).Results: Increased ALP activity and collagen synthesis, as well as gene expression of DSPP and ALP, were observed for both EDs compared with non-irradiated cells. The ED of 4 J/cm(2) also increased gene expression of COL I and DMP-1.Conclusions: In conclusion, infrared LED irradiation was capable of biostimulating SHEDs by increasing the expression and synthesis of proteins related with mineralized tissue formation, with overall better results for the energy dose of 4 J/cm(2).Clinical significance: Phototherapy is an additional approach for the clinical application of LED in Restorative Dentistry. Infrared LED irradiation of the cavity's floor could biostimulate subjacent pulp cells, improving local tissue healing. (C) 2014 Elsevier Ltd. All rights reserved.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)-
dc.format.extent1292-1299-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.sourceWeb of Science-
dc.subjectDentinen
dc.subjectOdontoblastsen
dc.subjectPhototherapyen
dc.subjectProtein expressionen
dc.subjectPulp biologyen
dc.subjectStem cellsen
dc.titlePhototherapy up-regulates dentin matrix proteins expression and synthesis by stem cells from human-exfoliated deciduous teethen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationUniv Estadual Paulista, UNESP, Sch Dent, Dept Pediat Dent & Orthodont, BR-14801903 Araraquara, SP, Brazil-
dc.description.affiliationUniv Estadual Paulista, UNESP, Sch Dent, Dept Physiol & Pathol, BR-14801903 Araraquara, SP, Brazil-
dc.description.affiliationUniv Estadual Paulista, UNESP, Sch Dent, Dept Restorat Dent, BR-14801903 Araraquara, SP, Brazil-
dc.description.affiliationUnespUniv Estadual Paulista, UNESP, Sch Dent, Dept Pediat Dent & Orthodont, BR-14801903 Araraquara, SP, Brazil-
dc.description.affiliationUnespUniv Estadual Paulista, UNESP, Sch Dent, Dept Physiol & Pathol, BR-14801903 Araraquara, SP, Brazil-
dc.description.affiliationUnespUniv Estadual Paulista, UNESP, Sch Dent, Dept Restorat Dent, BR-14801903 Araraquara, SP, Brazil-
dc.description.sponsorshipIdFAPESP: 11/13895-0-
dc.description.sponsorshipIdFAPESP: 13/17758-3-
dc.description.sponsorshipIdCNPq: 301291/2010-1-
dc.identifier.doi10.1016/j.jdent.2014.07.014-
dc.identifier.wosWOS:000342361400010-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal Of Dentistry-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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