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Effect of chemically modified titanium surfaces on protein adsorption and osteoblast precursor cell behavior
J Protivinsky, M Appleford, J Strnad, A Helebrant, JL Ong
Jazyk angličtina Země Spojené státy americké
Typ dokumentu srovnávací studie
- MeSH
- adsorpce MeSH
- alkalická fosfatasa chemie MeSH
- biologické markery analýza MeSH
- buněčná adheze fyziologie MeSH
- buněčná diferenciace fyziologie MeSH
- embryonální kmenové buňky fyziologie MeSH
- fenotyp MeSH
- fibronektiny chemie MeSH
- financování organizované MeSH
- hydroxid sodný chemie MeSH
- kyselina chlorovodíková chemie MeSH
- leptání zubů kyselinou MeSH
- leptání zubů metody MeSH
- lidé MeSH
- mezenchymální kmenové buňky fyziologie MeSH
- osteoblasty fyziologie MeSH
- osteokalcin chemie MeSH
- osteopontin chemie MeSH
- oxid hlinitý chemie MeSH
- patro embryologie MeSH
- povrchové vlastnosti MeSH
- proteiny chemie MeSH
- testování materiálů MeSH
- titan chemie MeSH
- zubní materiály chemie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- srovnávací studie MeSH
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.
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- $a Department of Glass and Ceramics, Institute of Chemical Technology, Prague, Czech Republic
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- $a 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.
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