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Enhanced human bone marrow mesenchymal stem cell functions on cathodic arc plasma-treated titanium

Surface modification of titanium for use in orthopedics has been explored for years; however, an ideal method of integrating titanium with native bone is still required to this day. Since human bone cells directly interact with nanostructured extracellular matrices, one of the most promising methods...

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Autores principales: Zhu, Wei, Teel, George, O’Brien, Christopher M, Zhuang, Taisen, Keidar, Michael, Zhang, Lijie Grace
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4677661/
https://www.ncbi.nlm.nih.gov/pubmed/26677327
http://dx.doi.org/10.2147/IJN.S92733
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author Zhu, Wei
Teel, George
O’Brien, Christopher M
Zhuang, Taisen
Keidar, Michael
Zhang, Lijie Grace
author_facet Zhu, Wei
Teel, George
O’Brien, Christopher M
Zhuang, Taisen
Keidar, Michael
Zhang, Lijie Grace
author_sort Zhu, Wei
collection PubMed
description Surface modification of titanium for use in orthopedics has been explored for years; however, an ideal method of integrating titanium with native bone is still required to this day. Since human bone cells directly interact with nanostructured extracellular matrices, one of the most promising methods of improving titanium’s osseointegration involves inducing bio-mimetic nanotopography to enhance cell–implant interaction. In this regard, we explored an approach to functionalize the surface of titanium by depositing a thin film of textured titanium nanoparticles via a cathodic arc discharge plasma. The aim is to improve human bone marrow mesenchymal stem cell (MSC) attachment and differentiation and to reduce deleterious effects of more complex surface modification methods. Surface functionalization was analyzed by scanning electron microscopy, atomic force microscopy, contact angle testing, and specific protein adsorption. Scanning electron microscopy and atomic force microscopy examination demonstrate the deposition of titanium nanoparticles and the surface roughness change after coating. The specific fibronectin adsorption was enhanced on the modified titanium surface that associates with the improved hydrophilicity. MSC adhesion and proliferation were significantly promoted on the nanocoated surface. More importantly, compared to bare titanium, greater production of total protein, deposition of calcium mineral, and synthesis of alkaline phosphatase were observed from MSCs on nanocoated titanium after 21 days. The method described herein presents a promising alternative method for inducing more cell favorable nanosurface for improved orthopedic applications.
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spelling pubmed-46776612015-12-16 Enhanced human bone marrow mesenchymal stem cell functions on cathodic arc plasma-treated titanium Zhu, Wei Teel, George O’Brien, Christopher M Zhuang, Taisen Keidar, Michael Zhang, Lijie Grace Int J Nanomedicine Original Research Surface modification of titanium for use in orthopedics has been explored for years; however, an ideal method of integrating titanium with native bone is still required to this day. Since human bone cells directly interact with nanostructured extracellular matrices, one of the most promising methods of improving titanium’s osseointegration involves inducing bio-mimetic nanotopography to enhance cell–implant interaction. In this regard, we explored an approach to functionalize the surface of titanium by depositing a thin film of textured titanium nanoparticles via a cathodic arc discharge plasma. The aim is to improve human bone marrow mesenchymal stem cell (MSC) attachment and differentiation and to reduce deleterious effects of more complex surface modification methods. Surface functionalization was analyzed by scanning electron microscopy, atomic force microscopy, contact angle testing, and specific protein adsorption. Scanning electron microscopy and atomic force microscopy examination demonstrate the deposition of titanium nanoparticles and the surface roughness change after coating. The specific fibronectin adsorption was enhanced on the modified titanium surface that associates with the improved hydrophilicity. MSC adhesion and proliferation were significantly promoted on the nanocoated surface. More importantly, compared to bare titanium, greater production of total protein, deposition of calcium mineral, and synthesis of alkaline phosphatase were observed from MSCs on nanocoated titanium after 21 days. The method described herein presents a promising alternative method for inducing more cell favorable nanosurface for improved orthopedic applications. Dove Medical Press 2015-12-10 /pmc/articles/PMC4677661/ /pubmed/26677327 http://dx.doi.org/10.2147/IJN.S92733 Text en © 2015 Zhu et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Zhu, Wei
Teel, George
O’Brien, Christopher M
Zhuang, Taisen
Keidar, Michael
Zhang, Lijie Grace
Enhanced human bone marrow mesenchymal stem cell functions on cathodic arc plasma-treated titanium
title Enhanced human bone marrow mesenchymal stem cell functions on cathodic arc plasma-treated titanium
title_full Enhanced human bone marrow mesenchymal stem cell functions on cathodic arc plasma-treated titanium
title_fullStr Enhanced human bone marrow mesenchymal stem cell functions on cathodic arc plasma-treated titanium
title_full_unstemmed Enhanced human bone marrow mesenchymal stem cell functions on cathodic arc plasma-treated titanium
title_short Enhanced human bone marrow mesenchymal stem cell functions on cathodic arc plasma-treated titanium
title_sort enhanced human bone marrow mesenchymal stem cell functions on cathodic arc plasma-treated titanium
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4677661/
https://www.ncbi.nlm.nih.gov/pubmed/26677327
http://dx.doi.org/10.2147/IJN.S92733
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