Modified Titanium Surface-Mediated Effects on Human Bone Marrow Stromal Cell Response

Surface modification of titanium implants is used to enhance osseointegration. The study objective was to evaluate five modified titanium surfaces in terms of cytocompatibility and pro-osteogenic/pro-angiogenic properties for human mesenchymal stromal cells: amorphous microporous silica (AMS), bone...

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Main Authors: Amol Chaudhari, Joke Duyck, Annabel Braem, Jozef Vleugels, Hervé Petite, Delphine Logeart-Avramoglou, Ignace Naert, Johan A. Martens, Katleen Vandamme
Format: Article
Language:English
Published: MDPI AG 2013-11-01
Series:Materials
Subjects:
Online Access:http://www.mdpi.com/1996-1944/6/12/5533
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spelling doaj-670d6cd61e1540309d879d536570ceac2020-11-24T22:28:57ZengMDPI AGMaterials1996-19442013-11-016125533554810.3390/ma6125533ma6125533Modified Titanium Surface-Mediated Effects on Human Bone Marrow Stromal Cell ResponseAmol Chaudhari0Joke Duyck1Annabel Braem2Jozef Vleugels3Hervé Petite4Delphine Logeart-Avramoglou5Ignace Naert6Johan A. Martens7Katleen Vandamme8BIOMAT Research Cluster, Department of Oral Health Sciences and Prosthetic Dentistry, KU Leuven and University Hospitals Leuven, Kapucijnenvoer 7 box 7001, Leuven 3000, BelgiumBIOMAT Research Cluster, Department of Oral Health Sciences and Prosthetic Dentistry, KU Leuven and University Hospitals Leuven, Kapucijnenvoer 7 box 7001, Leuven 3000, BelgiumDepartment of Metallurgy and Materials Engineering (MTM), KU Leuven, Kasteelpark Arenberg 44 box 2450, Heverlee 3001, BelgiumDepartment of Metallurgy and Materials Engineering (MTM), KU Leuven, Kasteelpark Arenberg 44 box 2450, Heverlee 3001, BelgiumLaboratory of Bioengineering and Biomechanics for Bone Articulation, Faculty of Medicine, University Paris Diderot, 10 Avenue de Verdun, Paris 75010, FranceLaboratory of Bioengineering and Biomechanics for Bone Articulation, Faculty of Medicine, University Paris Diderot, 10 Avenue de Verdun, Paris 75010, FranceBIOMAT Research Cluster, Department of Oral Health Sciences and Prosthetic Dentistry, KU Leuven and University Hospitals Leuven, Kapucijnenvoer 7 box 7001, Leuven 3000, BelgiumCenter of Surface Chemistry and Catalysis, KU Leuven, Kasteelpark Arenberg 23 box 2461, Heverlee 3001, BelgiumBIOMAT Research Cluster, Department of Oral Health Sciences and Prosthetic Dentistry, KU Leuven and University Hospitals Leuven, Kapucijnenvoer 7 box 7001, Leuven 3000, BelgiumSurface modification of titanium implants is used to enhance osseointegration. The study objective was to evaluate five modified titanium surfaces in terms of cytocompatibility and pro-osteogenic/pro-angiogenic properties for human mesenchymal stromal cells: amorphous microporous silica (AMS), bone morphogenetic protein-2 immobilized on AMS (AMS + BMP), bio-active glass (BAG) and two titanium coatings with different porosity (T1; T2). Four surfaces served as controls: uncoated Ti (Ti), Ti functionalized with BMP-2 (Ti + BMP), Ti surface with a thickened titanium oxide layer (TiO2) and a tissue culture polystyrene surface (TCPS). The proliferation of eGFP-fLuc (enhanced green fluorescence protein-firefly luciferase) transfected cells was tracked non-invasively by fluorescence microscopy and bio-luminescence imaging. The implant surface-mediated effects on cell differentiation potential was tracked by determination of osteogenic and angiogenic parameters [alkaline phosphatase (ALP); osteocalcin (OC); osteoprotegerin (OPG); vascular endothelial growth factor-A (VEGF-A)]. Unrestrained cell proliferation was observed on (un)functionalized Ti and AMS surfaces, whereas BAG and porous titanium coatings T1 and T2 did not support cell proliferation. An important pro-osteogenic and pro-angiogenic potential of the AMS + BMP surface was observed. In contrast, coating the Ti surface with BMP did not affect the osteogenic differentiation of the progenitor cells. A significantly slower BMP-2 release from AMS compared to Ti supports these findings. In the unfunctionalized state, Ti was found to be superior to AMS in terms of OPG and VEGF-A production. AMS is suggested to be a promising implant coating material for bioactive agents delivery.http://www.mdpi.com/1996-1944/6/12/5533titaniumsurface coatinghuman bone marrow stromal cellsin vitro cytocompatibilityosteogenic differentiationosseointegration
collection DOAJ
language English
format Article
sources DOAJ
author Amol Chaudhari
Joke Duyck
Annabel Braem
Jozef Vleugels
Hervé Petite
Delphine Logeart-Avramoglou
Ignace Naert
Johan A. Martens
Katleen Vandamme
spellingShingle Amol Chaudhari
Joke Duyck
Annabel Braem
Jozef Vleugels
Hervé Petite
Delphine Logeart-Avramoglou
Ignace Naert
Johan A. Martens
Katleen Vandamme
Modified Titanium Surface-Mediated Effects on Human Bone Marrow Stromal Cell Response
Materials
titanium
surface coating
human bone marrow stromal cells
in vitro cytocompatibility
osteogenic differentiation
osseointegration
author_facet Amol Chaudhari
Joke Duyck
Annabel Braem
Jozef Vleugels
Hervé Petite
Delphine Logeart-Avramoglou
Ignace Naert
Johan A. Martens
Katleen Vandamme
author_sort Amol Chaudhari
title Modified Titanium Surface-Mediated Effects on Human Bone Marrow Stromal Cell Response
title_short Modified Titanium Surface-Mediated Effects on Human Bone Marrow Stromal Cell Response
title_full Modified Titanium Surface-Mediated Effects on Human Bone Marrow Stromal Cell Response
title_fullStr Modified Titanium Surface-Mediated Effects on Human Bone Marrow Stromal Cell Response
title_full_unstemmed Modified Titanium Surface-Mediated Effects on Human Bone Marrow Stromal Cell Response
title_sort modified titanium surface-mediated effects on human bone marrow stromal cell response
publisher MDPI AG
series Materials
issn 1996-1944
publishDate 2013-11-01
description Surface modification of titanium implants is used to enhance osseointegration. The study objective was to evaluate five modified titanium surfaces in terms of cytocompatibility and pro-osteogenic/pro-angiogenic properties for human mesenchymal stromal cells: amorphous microporous silica (AMS), bone morphogenetic protein-2 immobilized on AMS (AMS + BMP), bio-active glass (BAG) and two titanium coatings with different porosity (T1; T2). Four surfaces served as controls: uncoated Ti (Ti), Ti functionalized with BMP-2 (Ti + BMP), Ti surface with a thickened titanium oxide layer (TiO2) and a tissue culture polystyrene surface (TCPS). The proliferation of eGFP-fLuc (enhanced green fluorescence protein-firefly luciferase) transfected cells was tracked non-invasively by fluorescence microscopy and bio-luminescence imaging. The implant surface-mediated effects on cell differentiation potential was tracked by determination of osteogenic and angiogenic parameters [alkaline phosphatase (ALP); osteocalcin (OC); osteoprotegerin (OPG); vascular endothelial growth factor-A (VEGF-A)]. Unrestrained cell proliferation was observed on (un)functionalized Ti and AMS surfaces, whereas BAG and porous titanium coatings T1 and T2 did not support cell proliferation. An important pro-osteogenic and pro-angiogenic potential of the AMS + BMP surface was observed. In contrast, coating the Ti surface with BMP did not affect the osteogenic differentiation of the progenitor cells. A significantly slower BMP-2 release from AMS compared to Ti supports these findings. In the unfunctionalized state, Ti was found to be superior to AMS in terms of OPG and VEGF-A production. AMS is suggested to be a promising implant coating material for bioactive agents delivery.
topic titanium
surface coating
human bone marrow stromal cells
in vitro cytocompatibility
osteogenic differentiation
osseointegration
url http://www.mdpi.com/1996-1944/6/12/5533
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