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Biological responses in osteoblast‐like cell line according to thin layer hydroxyapatite coatings on anodized titanium
Author(s) -
SOHN SH.,
JUN HK.,
KIM CS.,
KIM KN.,
CHUNG SM.,
SHIN SW.,
RYU JJ.,
KIM MK.
Publication year - 2006
Publication title -
journal of oral rehabilitation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.991
H-Index - 93
eISSN - 1365-2842
pISSN - 0305-182X
DOI - 10.1111/j.1365-2842.2006.01643.x
Subject(s) - anodizing , materials science , osseointegration , titanium , osteoblast , scanning electron microscope , chemistry , implant , in vitro , biochemistry , metallurgy , composite material , aluminium , medicine , surgery
summary Several features of the implant surface, such as roughness, topography and composition play a relevant role in implant integration with bone. This study was conducted in order to determine the effects of various thin layer hydroxyapatite (HA) coatings on anodized Ti surfaces on the biological responses of a human osteoblast‐like cell line (MG63). MG63 cells were cultured on 100 nm HA (100 nm HA coating on anodized surface), 500–700 nm HA (500–700 nm HA coating on anodized surface), 1 μ m HA (1 μ m HA coating on anodized surface) and anodize (non‐HA coating on anodized surface) Ti. The morphology of these cells was assessed by scanning electron microscopy (SEM). The cDNAs prepared from the total RNAs of the MG63 were hybridized into a human cDNA microarray (1152 elements). The appearances of the surfaces observed by SEM were different on each of the four dental substrate types. MG63 cells cultured on 100 nm HA, 1 μ m HA and anodize exhibited cell–matrix interactions. It was 500–700 nm HA surface showing cell–cell interaction. In the expression of genes involved in osseointegration, several genes, including bone morphogenetic protein 2, latent transforming growth factor beta binding protein 1, catenin (cadherin‐associated protein), integrin, PDGFRB and GDF‐1 growth differentiation factor 1 were up‐regulated on the different surfaces. Several genes, including fibroblast growth factor receptor 3, fibroblast growth factor 12 and CD4 were down‐regulated on the different surfaces. The attachment and expression of key osteogenic regulatory genes were enhanced by the surface morphology of the dental materials used.