Interaction of human osteoblast-like Saos-2 and MG-63 cells with thermally oxidized surfaces of a titanium-niobium alloy
Jazyk angličtina Země Spojené státy americké Médium electronic-ecollection
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
24977704
PubMed Central
PMC4076233
DOI
10.1371/journal.pone.0100475
PII: PONE-D-14-09805
Knihovny.cz E-zdroje
- MeSH
- biologické markery metabolismus MeSH
- buněčná adheze účinky léků MeSH
- buněčná diferenciace účinky léků MeSH
- buněčné linie MeSH
- kolagen typu I metabolismus MeSH
- lidé MeSH
- lipopolysacharidy farmakologie MeSH
- makrofágy cytologie účinky léků metabolismus MeSH
- myši MeSH
- osteoblasty cytologie účinky léků metabolismus MeSH
- osteokalcin metabolismus MeSH
- oxidace-redukce MeSH
- povrchové vlastnosti MeSH
- proliferace buněk účinky léků MeSH
- slitiny chemie farmakologie MeSH
- statická elektřina MeSH
- tkáňové podpůrné struktury * MeSH
- TNF-alfa farmakologie MeSH
- vysoká teplota MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- biologické markery MeSH
- kolagen typu I MeSH
- lipopolysacharidy MeSH
- osteokalcin MeSH
- slitiny MeSH
- titanium-niobium alloy MeSH Prohlížeč
- TNF-alfa MeSH
An investigation was made of the adhesion, growth and differentiation of osteoblast-like MG-63 and Saos-2 cells on titanium (Ti) and niobium (Nb) supports and on TiNb alloy with surfaces oxidized at 165°C under hydrothermal conditions and at 600°C in a stream of air. The oxidation mode and the chemical composition of the samples tuned the morphology, topography and distribution of the charge on their surfaces, which enabled us to evaluate the importance of these material characteristics in the interaction of the cells with the sample surface. Numbers of adhered MG-63 and Saos-2 cells correlated with the number of positively-charged (related with the Nb2O5 phase) and negatively-charged sites (related with the TiO2 phase) on the alloy surface. Proliferation of these cells is correlated with the presence of positively-charged (i.e. basic) sites of the Nb2O5 alloy phase, while cell differentiation is correlated with negatively-charged (acidic) sites of the TiO2 alloy phase. The number of charged sites and adhered cells was substantially higher on the alloy sample oxidized at 600°C than on the hydrothermally treated sample at 165°C. The expression values of osteoblast differentiation markers (collagen type I and osteocalcin) were higher for cells grown on the Ti samples than for those grown on the TiNb samples. This was more particularly apparent in the samples treated at 165°C. No considerable immune activation of murine macrophage-like RAW 264.7 cells on the tested samples was found. The secretion of TNF-α by these cells into the cell culture media was much lower than for either cells grown in the presence of bacterial lipopolysaccharide, or untreated control samples. Thus, oxidized Ti and TiNb are both promising materials for bone implantation; TiNb for applications where bone cell proliferation is desirable, and Ti for induction of osteogenic cell differentiation.
Faculty of Mechanical Engineering Czech Technical University Prague Prague Czech Republic
Faculty of Science J E Purkinje University Usti nad Labem Czech Republic
Institute of Physiology Academy of Sciences of the Czech Republic Prague Czech Republic
Zobrazit více v PubMed
Olivares-Navarrete R, Olaya JJ, Ramírez C, Rodil SE (2011) Biocompatibility of niobium coatings. Coatings 1: 72–87.
Velten D, Eisenbart E, Schanne N (2004) Biocompatible Nb2O5 thin films prepared by means of the sol-gel process. J Mater Sci-Mater Med 15: 457–461. PubMed
Liu X, Chu PK, Ding Ch (2004) Surface modification of titanium, titanium alloys and related materials for biomedical application. Materials Sci Engn R 47: 49–121.
Jirka I, Vandrovcova M, Frank O, Tolde Z, Plsek J, et al. (2013) On the role of Nb-related sites of an oxidized β-TiNb alloy surface in its interaction with osteoblast-like MG-63 cells Materials Sci Eng C. 33: 1636–1645. PubMed
Vandrovcova M, Hanus J, Drabik M, Kylian O, Biederman H, et al. (2012) Effect of different surface nano-roughness of titanium dioxide films on the growth of human osteoblast-like MG63 cells. J Biomed Mater Res A 100A: 1016–1032. PubMed
Steinemann SG (1998) Titanium – The material of choice? Periodontology 2000 17: 7–21. PubMed
Lee YJ, Cui DZ, Jeon HR, Chung HJ, Park YJ, et al. (2012) Surface characteristics of thermally treated titanium surfaces. J Periodontal Implant Sci 42: 81–87. PubMed PMC
Zorn G, Lesman A, Gotman I (2006) Oxide formation on low modulus Ti45Nb alloy by anodic versus thermal oxidation. Surface Coat Technol 201: 612–618.
Park YJ, Song HJ, Kim I, Yang HS (2007) Surface characteristics and bioactivity of oxide film on titanium metal formed by thermal oxidation. J Mater Sci Mater Med 18: 565–575. PubMed
Bello SA, de Jesús-Maldonado I, Rosim-Fachini E, Sundaram PA, Diffoot-Carlo N (2010) In vitro evaluation of human osteoblast adhesion to a thermally oxidized gamma-TiAl intermetallic alloy of composition Ti-48Al-2Cr-2Nb (at.%). J Mater Sci Mater Med 21: 1739–1750. PubMed PMC
Chrzanowski W, Abou Neel EA, Armitage DA, Knowles JC (2008) Surface preparation of bioactive Ni-Ti alloy using alkali, thermal treatments and spark oxidation. J Mater Sci Mater Med 19: 1553–1557. PubMed
Saldaña L, Vilaboa N, Vallés G, González-Cabrero J, Munuera L (2005) Osteoblast response to thermally oxidized Ti6Al4V alloy. J Biomed Mater Res A 73: 97–107. PubMed
Saldaña L, Barranco V, García-Alonso MC, Vallés G, Escudero ML, et al. (2006) Concentration-dependent effects of titanium and aluminium ions released from thermally oxidized Ti6Al4V alloy on human osteoblasts. J Biomed Mater Res A 77: 220–229. PubMed
Saldana L, Bensiamar F, Bore A, Vilaboa N (2011) In search of representative models of human bone-forming cells for cytocompatibility studies. Acta Biomater 7: 4210–4221. PubMed
Clover J, Gowen M (1995) Are MG-63 and HOS TE85 human osteosarcoma cell lines representative models of the osteoblastic phenotype? Bone 15: 585–591. PubMed
Czekanska EM, Stoddart MJ, Richards RG, Hayes JS (2012) In search of an osteoblast cell model for in vitro research. Eur Cells Mater 24: 1473–2262. PubMed
Briggs D, Seah MP (1990) Practical surface analysis. Wiley, Chichester.
Luxbacher T (2006) Electrokinetic characterization of flat sheet membranes by streaming current measurement. Desalination 199: 376–377.
Parizek M, Douglas TEL, Novotna K, Kromka A, Brady MA, et al. (2012) Nanofibrous poly(lactide-co-glycolide) membranes loaded with diamond nanoparticles as promising substrates for bone tissue engineering. Int J Nanomed 7: 1931–1951. PubMed PMC
Bacakova L, Stary V, Kofronova O, Lisa V (2001) Polishing and coating carbon fibre-reinforced carbon composites with a carbon-titanium layer enhances adhesion and growth of osteoblast-like MG63 cells and vascular smooth muscle cells in vitro. J Biomed Mater Res 54: 567–578. PubMed
Zhao X, Wang G, Zheng H, Lu Z, Zhong X, et al. (2013) Delicate refinement of surface nanotopography by adjusting TiO2 coating chemical composition for enhanced interfacial biocompatibility, ACS Appl Mater Inter. 5: 8203–8209. PubMed
Helth A, Gostin PF, Oswald S, Wendrock H, Wolff U, et al. (2014) Chemical nanoroughening of Ti40Nb surfaces and its effect on human mesenchymal stromal cell response. J Biomed Mater Res B Appl Biomater 102: 31–41. PubMed
Lim JY, Dreiss AD, Zhou Z, Hansen JC, Siedlecki CA (2007) The regulation of integrin-mediated osteoblast focal adhesion and focal adhesion kinase expression by nanoscale topography. Biomaterials 28: 1787–1797. PubMed
Hovgaard MB, Rechendorff K, Chevallier J, Foss M, Besenbacher F (2008) Fibronectin adsorption on tantalum: the influence of nanoroughness. J Phys Chem B 112: 8241–8249. PubMed
Dee KC, Andersen TT, Bizios R (1998) Design and function of novel osteoblast-adhesive peptides for chemical modification of biomaterials. J Biomed Mater Res 40: 371–377. PubMed
Bacakova L, Filova E, Parizek M, Ruml T, Svorcik V (2011) Modulation of cell adhesion, proliferation and differentiation on materials designed for body implants. Biotechnol Adv 29: 739–767. PubMed
Horton MA (1997) The alpha v beta 3 integrin “vitronectin receptor”. Int J Biochem Cell Biol 29: 721–725. PubMed
Buttiglieri S, Pasqui D, Migliori M, Johnstone H, Affrossman S (2003) Endothelization and adherence of leucocytes to nanostructured surfaces. Biomaterials 24: 2731–2738. PubMed
Tsou HK, Hsieh PY, Chi MH, Chung CJ, He JL (2012) Improved osteoblast compatibility of medical-grade polyetherketone using arc ionplated rutile/anatase titanium dioxide films for spinal implants. J Biomed Mater Res A 100: 2787–2792. PubMed
Kosmulski M (2001) Chemical properties of material surfaces. Marcel Dekker, Amsterdam
Hamdan M, Blanco L, Khraisat A, Tresguerres IF (2006) Influence of titanium surface charge on fibroblast adhesion. Clin Implant Dent Relat Res 8: 32–38. PubMed
Kokubo T, Pattanayak DK, Yamaguchi S, Takadama H, Matsushita T, et al. (2010) Positively charged bioactive Ti metal prepared by simple chemical and heat treatments. J R Soc Interface 7: S503–S513. PubMed PMC
Schneider GB, English A, Abraham M, Zaharias R, Stanford C, et al. (2004) The effect of hydrogel charge density on cell attachment. Biomaterials 25: 3023–3028. PubMed
Dadsetan M, Pumberger M, Casper ME, Shogren K, Giuliani M, et al. (2011) The effects of fixed electrical charge on chondrocyte behavior. Acta Biomater 7: 2080–2090. PubMed PMC
Dubiel EA, Martin Y, Vermette P (2011) Bridging the gap between physicochemistry and interpretation prevalent in cell-surface intreractions. Chem Rev 111: 2900–2936. PubMed
Lesny P, Pradny M, Jendelova P, Michalek J, Vacik J (2006) Macroporous hydrogels based on 2-hydroxyethyl methacrylate. Part 4: growth of rat bone marrow stromal cells in three-dimensional hydrogels with positive and negative surface charges and in polyelectrolyte complexes. J Mater Sci Mater Med 17: 829–33. PubMed
Born A-K, Rottmar M, Lischer S, Pleckova M, Bruinink A, et al. (2009) Correlationg cell architecture with osteogenesis: First steps towards live single cell monitoring. Eur Cells Mater 18: 49–62. PubMed
Sista S, Wen C, Hodgson PD, Pande G (2011) The influence of surface energy of titanium-zirconium alloy on osteoblast cell functions in vitro. J Biomed Mater Res A 97A: 27–36. PubMed
Stein GS, Lian JB, Owen TA (1990) Relationship of cell growth to the regulation of tissue-specific gene expression during osteoblast differentiation. The FASEB J 4: 3111–3123. PubMed
Lai M, Cai K, Hu Y, Zhang Y, Li L (2013) Construction of microenvironment onto titanium substrates to regulate the osteoblastic differentiation of bone marrow stromal cells in vitro and osteogenesis in vivo. J Biomed Mater Res A 101: 653–666. PubMed
Qiu Q, Sayer M, Kawaja M, Shen X, Davies JE (1998) Attachment, morphology, and protein expression of rat marrow stromal cells cultured on charged substrate surfaces. J Biomed Mater Res 42: 117–127. PubMed
Zaveri TD, Dolgova NV, Chu BH, Lee J, Wong J (2010) Contributions of surface topography and cytotoxicity to the macrophage response to zinc oxide nanorods. Biomaterials 31: 2999–3007. PubMed
Refai AK, Textor M, Brunette DM, Waterfield J (2004) Effect of titanium surface topography on macrophage activation and secretion of proinflammatory cytokines and chemokines. J Biomed Mater Res Part A 70A: 194–205. PubMed
Treves C, Martinesi M, Stio M, Gutiérrez A, Jiménez JA, et al. (2010) In vitro biocompatibility evaluation of surface-modified titanium alloys. J Biomed Mater Res A 92: 1623–1634. PubMed
Lee S, Choi J, Shin S, Im YM, Song J, et al. (2011) Analysis on migration and activation of live macrophages on transparent flat and nanostructured titanium. Acta Biomater 7: 2337–2344. PubMed
The Photodynamic Properties and the Genotoxicity of Heat-Treated Silicalite-1 Films
Growth and potential damage of human bone-derived cells cultured on fresh and aged C60/Ti films