Effect of chemically modified titanium surfaces on protein adsorption and osteoblast precursor cell Behavior

被引:1
|
作者
Protivinsky, Jiri
Appleford, Mark
Strnad, Jakob
Helebrant, Alse
Ong, Joo L.
机构
[1] Univ Texas, Dept Biomed Engn, San Antonio, TX 78249 USA
[2] Inst Chem Technol, Dept Glass & Ceram, CR-16628 Prague, Czech Republic
关键词
cell attachment; cell proliferation; differentiation and mineralization; fibronectin; osteoblast precursor cells; protein adsorption;
D O I
暂无
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Purpose: To investigate the effects of different chemically modified titanium surfaces on protein adsorption and the osteoblastic differentiation of human embryonic palatal mesenchymal (HEPM) cells. Materials and Methods: Three different surfaces were evaluated. The first, a machined surface (Ti-M), was considered a control. The second surface was acid etched (Ti-AE). The third surface was prepared by exposing the Ti-AE samples to sodium hydroxide (NaOH) solution (Ti-AAE). The surface characteristics of chemically modified titanium were investigated by means of scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), and profilometry. To evaluate the production of biomarkers, commercial kits were utilized. Results: Surface composition and morphology affected the kinetics of protein adsorption. Ti-AE surfaces manifested a greater affinity for fibronectin adsorption compared to Ti-M or Ti-AAE surfaces. It was observed that Ti-AE and Ti-AAE surfaces promoted significantly greater cell attachment compared to Ti-M surfaces. Statistically significant differences were also observed in the expression of alkaline phosphatase (ALP) activity, osteocalcin, and osteopontin on all 3 titanium surfaces. ALP activity and osteocalcin production up to day 12 suggested that differentiation of the cells into osteoblasts had occurred and that cells were expressing a bone-forming phenotype. Conclusions: It was thus concluded from this study that surface morphology and composition play a critical role in enhancing HEPM cell proliferation and differentiation into osteoblast cells.
引用
收藏
页码:542 / 550
页数:9
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