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Publicação:
Laser-Modified Ti Surface Improves Paracrine Osteogenesis by Modulating the Expression of DKK1 in Osteoblasts

dc.contributor.authorTeixeira, Jorge Felipe Lima [UNESP]
dc.contributor.authorde Souza, João Antônio Chaves
dc.contributor.authorMagalhães, Fernando Augusto Cintra
dc.contributor.authorde Oliveira, Guilherme José Pimentel Lopes
dc.contributor.authorde Santis, José Bernardo
dc.contributor.authorde Souza Costa, Carlos Alberto [UNESP]
dc.contributor.authorde Souza, Pedro Paulo Chaves
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionUniversidade Federal de Goiás (UFG)
dc.contributor.institutionFederal University of Maranhão
dc.contributor.institutionUniversidade Federal de Uberlândia (UFU)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2023-07-29T13:11:08Z
dc.date.available2023-07-29T13:11:08Z
dc.date.issued2023-04-01
dc.description.abstractTitanium surface modifications are widely used to modulate cellular behavior by recognition of topographical cues. However, how those modifications affect the expression of mediators that will influence neighboring cells is still elusive. This study aimed to evaluate the effects of conditioned media from osteoblasts cultured on laser-modified titanium surfaces on the differentiation of bone marrow cells in a paracrine manner and to analyze the expression of Wnt pathway inhibitors. Mice calvarial osteoblasts were seeded on polished (P) and Yb:YAG laser-irradiated (L) Ti surfaces. Osteoblast culture media were collected and filtered on alternate days to stimulate mice BMCs. Resazurin assay was performed every other day for 20 days to check BMC viability and proliferation. After 7 and 14 days of BMCs maintained with osteoblasts P and L-conditioned media, alkaline phosphatase activity, Alizarin Red staining, and RT-qPCR were performed. ELISA of conditioned media was conducted to investigate the expression of Wnt inhibitors Dickkopf-1 (DKK1) and Sclerostin (SOST). BMCs showed increased mineralized nodule formation and alkaline phosphatase activity. The L-conditioned media enhanced the BMC mRNA expression of bone-related markers Bglap, Alpl, and Sp7. L-conditioned media decreased the expression of DKK1 compared with P-conditioned media. The contact of osteoblasts with Yb:YAG laser-modified Ti surfaces induces the regulation of the expression of mediators that affect the osteoblastic differentiation of neighboring cells. DKK1 is among these regulated mediators.en
dc.description.affiliationDepartment of Physiology and Pathology School of Dentistry São Paulo State University
dc.description.affiliationSchool of Dentistry Federal University of Goiás
dc.description.affiliationNursing Department Federal University of Maranhão
dc.description.affiliationDepartment of Periodontology and Implant Dentistry School of Dentistry Federal University of Uberlândia
dc.description.affiliationDepartment of Basic and Oral Biology Bone Research Lab School of Dentistry of Ribeirão Preto University of São Paulo
dc.description.affiliationInnovation in Biomaterials Laboratory (iBioM) School of Dentistry Federal University of Goiás
dc.description.affiliationUnespDepartment of Physiology and Pathology School of Dentistry São Paulo State University
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipIdCNPq: 303599/2014-6
dc.identifierhttp://dx.doi.org/10.3390/jfb14040224
dc.identifier.citationJournal of Functional Biomaterials, v. 14, n. 4, 2023.
dc.identifier.doi10.3390/jfb14040224
dc.identifier.issn2079-4983
dc.identifier.scopus2-s2.0-85153972770
dc.identifier.urihttp://hdl.handle.net/11449/247261
dc.language.isoeng
dc.relation.ispartofJournal of Functional Biomaterials
dc.sourceScopus
dc.subjectlaser ablation
dc.subjectnanotopography
dc.subjectosseointegration
dc.subjectosteoblast
dc.subjectTi
dc.titleLaser-Modified Ti Surface Improves Paracrine Osteogenesis by Modulating the Expression of DKK1 in Osteoblastsen
dc.typeArtigo
dspace.entity.typePublication
unesp.author.orcid0000-0002-8244-622X[1]
unesp.author.orcid0000-0002-8053-2407[2]
unesp.author.orcid0000-0001-8778-0115[4]
unesp.author.orcid0000-0001-7985-6343[5]
unesp.author.orcid0000-0001-7266-6061[7]

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