2010 Volume No 20 – pages 178-196
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Title: Bioengineered titanium surfaces affect the gene-expression and phenotypic response of osteoprogenitor cells derived from mouse calvarial bones |
Author: J Isaac, A Galtayries, T Kizuki, T Kokubo, A Berdal, J-M Sautier |
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Address: Laboratoire de Physiopathologie Orale Moléculaire, Centre de Recherche des Cordeliers, INSERM, UMRS 872, Equipe 5, Esc. E – 2ème étage, 15-21 rue de l’Ecole de Médecine, F-75006 Paris, France |
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E-mail: isaacjuliane at yahoo.fr |
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Key Words: Biomaterials, biomimetics, surfaces, in vitro, cell/protein-material interactions, osteoblasts, differentiation.
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Publication date: September 28th 2010 |
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Abstract: This study investigated the in vitro effects of bioactive titanium surfaces on osteoblast differentiation. Three titanium substrates were tested: a commercially pure titanium (Cp Ti), an alkali- and heat-treated titanium (AH Ti), and an apatite-formed titanium (Ap Ti) generated by soaking AH Ti in a simulated body fluid. Chemical evaluation of the surface reactivity was analysed at nanometre scale by X-ray photoelectron spectroscopy (XPS), and at micrometre scale by energy dispersive X-ray microanalysis (EDX). It showed that the estimated proportion of the surface covered by adsorbed serum proteins differed between the three substrates and confirmed the bioactivity of AH Ti, illustrated by surface calcium and phosphate deposition when immersed in biological fluids. Mouse calvaria osteoblasts were cultured on the substrates for 15 days with no sign of cytotoxicity. Enzyme immunoassay and Real-Time RT-PCR were used to follow osteoblast differentiation through the production of osteocalcin (OC) and expression of several bone markers. At day 15, a significant up-regulation of Runx2, Osx, Dlx5, ALP, BSP, OC and DMP1 mRNA levels associated with an increase of OC production were observed on AH Ti and Ap Ti when compared to Cp Ti. These results suggest that bioengineered titanium has a great potential for dental applications in enhancing osseointegration. |
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Article download: Pages
178-196 (PDF file) |
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