Effects of Titanium Surfaces on the Developmental Profile of Monocytes/Macrophages

Detalhes bibliográficos
Autor(a) principal: Moura,Camilla Christian Gomes
Data de Publicação: 2014
Outros Autores: Zanetta-Barbosa,Darceny, Dechichi,Paula, Carvalho,Valessa Florindo, Soares,Priscilla Barbosa Ferreira
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Dental Journal
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-64402014000200096
Resumo: Due to the critical role of monocytes/macrophages (Mϕ) in bone healing, this study evaluated the effects of bio-anodized, acid-etched, and machined titanium surfaces (Ti) on Mϕ behavior. Cells were separated from whole human blood from 10 patients, plated on Ti or polystyrene (control) surfaces, and cultured for 72 h. At 24, 48 and 72 h, cell viability, levels of IL1β, IL10, TNFα, TGFβ1 inflammatory mediators, and nitric oxide (NO) release were analyzed by mitochondrial colorimetric assay (MTT assay) and immunoenzymatic assays, respectively. Real-time PCR was used to verify the expression of TNFα and IL10 at 72 h. The data were subjected to a Kruskal-Wallis analysis. IL1β, TNFα and TGFβ1 release were not significantly different between the Ti surfaces (p>0.05). The presence of NO and IL10 was not detected in the samples. Cell viability did not differ between the samples cultivated on Ti and those cultivated on control surfaces, except at 24 h (p=0.0033). With respect to the mediators evaluated, the surface characteristics did not induce a typical Th1 or Th2 cytokine profile, although the cell morphology and topography were influenced by the Ti surface during the initial period.
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spelling Effects of Titanium Surfaces on the Developmental Profile of Monocytes/Macrophagesmacrophagecytokinesinflammationtitanium surfaceDue to the critical role of monocytes/macrophages (Mϕ) in bone healing, this study evaluated the effects of bio-anodized, acid-etched, and machined titanium surfaces (Ti) on Mϕ behavior. Cells were separated from whole human blood from 10 patients, plated on Ti or polystyrene (control) surfaces, and cultured for 72 h. At 24, 48 and 72 h, cell viability, levels of IL1β, IL10, TNFα, TGFβ1 inflammatory mediators, and nitric oxide (NO) release were analyzed by mitochondrial colorimetric assay (MTT assay) and immunoenzymatic assays, respectively. Real-time PCR was used to verify the expression of TNFα and IL10 at 72 h. The data were subjected to a Kruskal-Wallis analysis. IL1β, TNFα and TGFβ1 release were not significantly different between the Ti surfaces (p>0.05). The presence of NO and IL10 was not detected in the samples. Cell viability did not differ between the samples cultivated on Ti and those cultivated on control surfaces, except at 24 h (p=0.0033). With respect to the mediators evaluated, the surface characteristics did not induce a typical Th1 or Th2 cytokine profile, although the cell morphology and topography were influenced by the Ti surface during the initial period.Fundação Odontológica de Ribeirão Preto2014-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-64402014000200096Brazilian Dental Journal v.25 n.2 2014reponame:Brazilian Dental Journalinstname:Fundação Odontológica de Ribeirão Preto (FUNORP)instacron:FUNORP10.1590/0103-6440201302260info:eu-repo/semantics/openAccessMoura,Camilla Christian GomesZanetta-Barbosa,DarcenyDechichi,PaulaCarvalho,Valessa FlorindoSoares,Priscilla Barbosa Ferreiraeng2014-08-15T00:00:00Zoai:scielo:S0103-64402014000200096Revistahttps://www.scielo.br/j/bdj/https://old.scielo.br/oai/scielo-oai.phpbdj@forp.usp.br||sergio@fosjc.unesp.br1806-47600103-6440opendoar:2014-08-15T00:00Brazilian Dental Journal - Fundação Odontológica de Ribeirão Preto (FUNORP)false
dc.title.none.fl_str_mv Effects of Titanium Surfaces on the Developmental Profile of Monocytes/Macrophages
title Effects of Titanium Surfaces on the Developmental Profile of Monocytes/Macrophages
spellingShingle Effects of Titanium Surfaces on the Developmental Profile of Monocytes/Macrophages
Moura,Camilla Christian Gomes
macrophage
cytokines
inflammation
titanium surface
title_short Effects of Titanium Surfaces on the Developmental Profile of Monocytes/Macrophages
title_full Effects of Titanium Surfaces on the Developmental Profile of Monocytes/Macrophages
title_fullStr Effects of Titanium Surfaces on the Developmental Profile of Monocytes/Macrophages
title_full_unstemmed Effects of Titanium Surfaces on the Developmental Profile of Monocytes/Macrophages
title_sort Effects of Titanium Surfaces on the Developmental Profile of Monocytes/Macrophages
author Moura,Camilla Christian Gomes
author_facet Moura,Camilla Christian Gomes
Zanetta-Barbosa,Darceny
Dechichi,Paula
Carvalho,Valessa Florindo
Soares,Priscilla Barbosa Ferreira
author_role author
author2 Zanetta-Barbosa,Darceny
Dechichi,Paula
Carvalho,Valessa Florindo
Soares,Priscilla Barbosa Ferreira
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Moura,Camilla Christian Gomes
Zanetta-Barbosa,Darceny
Dechichi,Paula
Carvalho,Valessa Florindo
Soares,Priscilla Barbosa Ferreira
dc.subject.por.fl_str_mv macrophage
cytokines
inflammation
titanium surface
topic macrophage
cytokines
inflammation
titanium surface
description Due to the critical role of monocytes/macrophages (Mϕ) in bone healing, this study evaluated the effects of bio-anodized, acid-etched, and machined titanium surfaces (Ti) on Mϕ behavior. Cells were separated from whole human blood from 10 patients, plated on Ti or polystyrene (control) surfaces, and cultured for 72 h. At 24, 48 and 72 h, cell viability, levels of IL1β, IL10, TNFα, TGFβ1 inflammatory mediators, and nitric oxide (NO) release were analyzed by mitochondrial colorimetric assay (MTT assay) and immunoenzymatic assays, respectively. Real-time PCR was used to verify the expression of TNFα and IL10 at 72 h. The data were subjected to a Kruskal-Wallis analysis. IL1β, TNFα and TGFβ1 release were not significantly different between the Ti surfaces (p>0.05). The presence of NO and IL10 was not detected in the samples. Cell viability did not differ between the samples cultivated on Ti and those cultivated on control surfaces, except at 24 h (p=0.0033). With respect to the mediators evaluated, the surface characteristics did not induce a typical Th1 or Th2 cytokine profile, although the cell morphology and topography were influenced by the Ti surface during the initial period.
publishDate 2014
dc.date.none.fl_str_mv 2014-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-64402014000200096
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-64402014000200096
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/0103-6440201302260
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Fundação Odontológica de Ribeirão Preto
publisher.none.fl_str_mv Fundação Odontológica de Ribeirão Preto
dc.source.none.fl_str_mv Brazilian Dental Journal v.25 n.2 2014
reponame:Brazilian Dental Journal
instname:Fundação Odontológica de Ribeirão Preto (FUNORP)
instacron:FUNORP
instname_str Fundação Odontológica de Ribeirão Preto (FUNORP)
instacron_str FUNORP
institution FUNORP
reponame_str Brazilian Dental Journal
collection Brazilian Dental Journal
repository.name.fl_str_mv Brazilian Dental Journal - Fundação Odontológica de Ribeirão Preto (FUNORP)
repository.mail.fl_str_mv bdj@forp.usp.br||sergio@fosjc.unesp.br
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