Anodic oxidation and hydrothermal treatment of commercially pure titanium surfaces increases expression of bone morphogenetic protein-2 in the adherent macrophage cell line J774A.1

被引:43
作者
Takebe, J.
Ito, S.
Champagne, C. M.
Cooper, L. F.
Ishibashi, K.
机构
[1] Iwate Med Univ, Sch Dent, Dept Fixed Prosthodont, Morioka, Iwate 0208505, Japan
[2] Univ N Carolina, Sch Dent, Dent Res Ctr, Chapel Hill, NC 27599 USA
关键词
anodic oxidation and hydrothermal treatment; endosseous implants; osseointegration; macrophage phenotype; bone morphogenetic protein;
D O I
10.1002/jbm.a.30988
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The surface property of commercially pure titanium (cpTi) was improved by forming a thin hydroxyapatite (HA) layer by anodic oxidation and hydrothermal treatment (HA/cpTi). We hypothesize that the adhesion of macrophages to HA/cpTi surfaces is important to the process of osseointegration. This study investigates the effect of adhesion of macrophages to HA/cpTi surfaces on the expression of bone morphogenetic protein-2 (BMP-2). The murine macrophage cell line J774A.1 was cultured on HA/cpTi and polished cpTi (S/cpTi). Macrophage cell adhesion was examined by SEM, 0-72 h following plating onto HA/cpTi and S/cpTi. BMP-2 gene expression was examined by RT-PCR analysis. The level of BMP-2 secreted into the supernatant was measured using an ELISA assay. The extent of macrophage adhesion increased with time on both the HA/cpTi and S/cpTi surfaces, with a higher degree of spreading observed on HA/cpTi than on S/cpTi surfaces after 24 or 72 h. The ratio of BMP-2 mRNA was higher on HA/cpTi than on S/cpTi after 24 h (0.348 vs. 0, p < 0.05) and 72 h (0.584 vs. 0.189, p < 0.05). After 24 h, secretion of BMP-2 was detected in culture,; grown on HA/cpTi, but not on S/cpTi. After 72 h, secretion of BMP-2 was detected in cultures grown on S/cpTi, but the levels were higher in cultures grown on HA/cpTi. These findings show that macrophages have the capacity to adhere o HA/cpTi endosseous implants and provide a source of osteoinductive cytokines that may play a key role in the process of osseointegration. (c) 2006 Wiley Periodicals, Inc.
引用
收藏
页码:711 / 718
页数:8
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