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Mesenchymal stem cell interaction with Ti(6)Al(4)V alloy pre-exposed to simulated body fluid

Titanium and its alloys are widely used for substitution of hard tissues, especially in orthopaedic and dental surgery. Despite the benefit of the use of titanium for such applications, there are still questions which must be sorted out. Surface properties are crucial for cell adhesion, proliferatio...

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Autores principales: Jarolimova, Petra, Voltrova, Barbora, Blahnova, Veronika, Sovkova, Vera, Pruchova, Eva, Hybasek, Vojtech, Fojt, Jaroslav, Filova, Eva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9049760/
https://www.ncbi.nlm.nih.gov/pubmed/35493900
http://dx.doi.org/10.1039/c9ra08912h
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author Jarolimova, Petra
Voltrova, Barbora
Blahnova, Veronika
Sovkova, Vera
Pruchova, Eva
Hybasek, Vojtech
Fojt, Jaroslav
Filova, Eva
author_facet Jarolimova, Petra
Voltrova, Barbora
Blahnova, Veronika
Sovkova, Vera
Pruchova, Eva
Hybasek, Vojtech
Fojt, Jaroslav
Filova, Eva
author_sort Jarolimova, Petra
collection PubMed
description Titanium and its alloys are widely used for substitution of hard tissues, especially in orthopaedic and dental surgery. Despite the benefit of the use of titanium for such applications, there are still questions which must be sorted out. Surface properties are crucial for cell adhesion, proliferation and differentiation. Mainly, micro/nanostructured surfaces positively influence osteogenic differentiation of human mesenchymal stem cells. Ti(6)Al(4)V is a biocompatible α + β alloy which is widely used in orthopaedics. The aim of this study was to investigate the interaction of the nanostructured and ground Ti(6)Al(4)V titanium alloys with simulated body fluid complemented by the defined precipitation of hydroxyapatite-like coating and to study the cytotoxicity and differentiation capacity of cells with such a modified titanium alloy. Nanostructures were fabricated using electrochemical oxidation. Human mesenchymal stem cells (hMSC) were used to evaluate cell adhesion, metabolic activity and proliferation on the specimens. The differentiation potential of the samples was investigated using PCR and specific staining of osteogenic markers collagen type I and osteocalcin. Our results demonstrate that both pure Ti(6)Al(4)V, nanostructured samples, and hydroxyapatite-like coating supported hMSC growth and metabolic activity. Nanostructured samples improved collagen type I synthesis after 14 days, while both nanostructured and hydroxyapatite-like coated samples enhanced collagen synthesis on day 21. Osteocalcin synthesis was the most enhanced by hydroxyapatite-like coating on the nanostructured surfaces. Our results indicate that hydroxyapatite-like coating is a useful tool guiding hMSC osteogenic differentiation.
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spelling pubmed-90497602022-04-29 Mesenchymal stem cell interaction with Ti(6)Al(4)V alloy pre-exposed to simulated body fluid Jarolimova, Petra Voltrova, Barbora Blahnova, Veronika Sovkova, Vera Pruchova, Eva Hybasek, Vojtech Fojt, Jaroslav Filova, Eva RSC Adv Chemistry Titanium and its alloys are widely used for substitution of hard tissues, especially in orthopaedic and dental surgery. Despite the benefit of the use of titanium for such applications, there are still questions which must be sorted out. Surface properties are crucial for cell adhesion, proliferation and differentiation. Mainly, micro/nanostructured surfaces positively influence osteogenic differentiation of human mesenchymal stem cells. Ti(6)Al(4)V is a biocompatible α + β alloy which is widely used in orthopaedics. The aim of this study was to investigate the interaction of the nanostructured and ground Ti(6)Al(4)V titanium alloys with simulated body fluid complemented by the defined precipitation of hydroxyapatite-like coating and to study the cytotoxicity and differentiation capacity of cells with such a modified titanium alloy. Nanostructures were fabricated using electrochemical oxidation. Human mesenchymal stem cells (hMSC) were used to evaluate cell adhesion, metabolic activity and proliferation on the specimens. The differentiation potential of the samples was investigated using PCR and specific staining of osteogenic markers collagen type I and osteocalcin. Our results demonstrate that both pure Ti(6)Al(4)V, nanostructured samples, and hydroxyapatite-like coating supported hMSC growth and metabolic activity. Nanostructured samples improved collagen type I synthesis after 14 days, while both nanostructured and hydroxyapatite-like coated samples enhanced collagen synthesis on day 21. Osteocalcin synthesis was the most enhanced by hydroxyapatite-like coating on the nanostructured surfaces. Our results indicate that hydroxyapatite-like coating is a useful tool guiding hMSC osteogenic differentiation. The Royal Society of Chemistry 2020-02-13 /pmc/articles/PMC9049760/ /pubmed/35493900 http://dx.doi.org/10.1039/c9ra08912h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Jarolimova, Petra
Voltrova, Barbora
Blahnova, Veronika
Sovkova, Vera
Pruchova, Eva
Hybasek, Vojtech
Fojt, Jaroslav
Filova, Eva
Mesenchymal stem cell interaction with Ti(6)Al(4)V alloy pre-exposed to simulated body fluid
title Mesenchymal stem cell interaction with Ti(6)Al(4)V alloy pre-exposed to simulated body fluid
title_full Mesenchymal stem cell interaction with Ti(6)Al(4)V alloy pre-exposed to simulated body fluid
title_fullStr Mesenchymal stem cell interaction with Ti(6)Al(4)V alloy pre-exposed to simulated body fluid
title_full_unstemmed Mesenchymal stem cell interaction with Ti(6)Al(4)V alloy pre-exposed to simulated body fluid
title_short Mesenchymal stem cell interaction with Ti(6)Al(4)V alloy pre-exposed to simulated body fluid
title_sort mesenchymal stem cell interaction with ti(6)al(4)v alloy pre-exposed to simulated body fluid
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9049760/
https://www.ncbi.nlm.nih.gov/pubmed/35493900
http://dx.doi.org/10.1039/c9ra08912h
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