Surface Functionalization of Orthopedic Titanium Implants with Bone Sialoprotein.

Orthopedic implant failure due to aseptic loosening and mechanical instability remains a major problem in total joint replacement. Improving osseointegration at the bone-implant interface may reduce micromotion and loosening. Bone sialoprotein (BSP) has been shown to enhance bone formation when coat...

Full description

Bibliographic Details
Main Authors: Andreas Baranowski, Anja Klein, Ulrike Ritz, Angelika Ackermann, Joris Anthonissen, Kerstin B Kaufmann, Christian Brendel, Hermann Götz, Pol M Rommens, Alexander Hofmann
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4844107?pdf=render
id doaj-00bb91436091411faa56b5ec88710c2b
record_format Article
spelling doaj-00bb91436091411faa56b5ec88710c2b2020-11-25T00:44:18ZengPublic Library of Science (PLoS)PLoS ONE1932-62032016-01-01114e015397810.1371/journal.pone.0153978Surface Functionalization of Orthopedic Titanium Implants with Bone Sialoprotein.Andreas BaranowskiAnja KleinUlrike RitzAngelika AckermannJoris AnthonissenKerstin B KaufmannChristian BrendelHermann GötzPol M RommensAlexander HofmannOrthopedic implant failure due to aseptic loosening and mechanical instability remains a major problem in total joint replacement. Improving osseointegration at the bone-implant interface may reduce micromotion and loosening. Bone sialoprotein (BSP) has been shown to enhance bone formation when coated onto titanium femoral implants and in rat calvarial defect models. However, the most appropriate method of BSP coating, the necessary level of BSP coating, and the effect of BSP coating on cell behavior remain largely unknown. In this study, BSP was covalently coupled to titanium surfaces via an aminosilane linker (APTES), and its properties were compared to BSP applied to titanium via physisorption and untreated titanium. Cell functions were examined using primary human osteoblasts (hOBs) and L929 mouse fibroblasts. Gene expression of specific bone turnover markers at the RNA level was detected at different intervals. Cell adhesion to titanium surfaces treated with BSP via physisorption was not significantly different from that of untreated titanium at any time point, whereas BSP application via covalent coupling caused reduced cell adhesion during the first few hours in culture. Cell migration was increased on titanium disks that were treated with higher concentrations of BSP solution, independent of the coating method. During the early phases of hOB proliferation, a suppressive effect of BSP was observed independent of its concentration, particularly when BSP was applied to the titanium surface via physisorption. Although alkaline phosphatase activity was reduced in the BSP-coated titanium groups after 4 days in culture, increased calcium deposition was observed after 21 days. In particular, the gene expression level of RUNX2 was upregulated by BSP. The increase in calcium deposition and the stimulation of cell differentiation induced by BSP highlight its potential as a surface modifier that could enhance the osseointegration of orthopedic implants. Both physisorption and covalent coupling of BSP are similarly effective, feasible methods, although a higher BSP concentration is recommended.http://europepmc.org/articles/PMC4844107?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Andreas Baranowski
Anja Klein
Ulrike Ritz
Angelika Ackermann
Joris Anthonissen
Kerstin B Kaufmann
Christian Brendel
Hermann Götz
Pol M Rommens
Alexander Hofmann
spellingShingle Andreas Baranowski
Anja Klein
Ulrike Ritz
Angelika Ackermann
Joris Anthonissen
Kerstin B Kaufmann
Christian Brendel
Hermann Götz
Pol M Rommens
Alexander Hofmann
Surface Functionalization of Orthopedic Titanium Implants with Bone Sialoprotein.
PLoS ONE
author_facet Andreas Baranowski
Anja Klein
Ulrike Ritz
Angelika Ackermann
Joris Anthonissen
Kerstin B Kaufmann
Christian Brendel
Hermann Götz
Pol M Rommens
Alexander Hofmann
author_sort Andreas Baranowski
title Surface Functionalization of Orthopedic Titanium Implants with Bone Sialoprotein.
title_short Surface Functionalization of Orthopedic Titanium Implants with Bone Sialoprotein.
title_full Surface Functionalization of Orthopedic Titanium Implants with Bone Sialoprotein.
title_fullStr Surface Functionalization of Orthopedic Titanium Implants with Bone Sialoprotein.
title_full_unstemmed Surface Functionalization of Orthopedic Titanium Implants with Bone Sialoprotein.
title_sort surface functionalization of orthopedic titanium implants with bone sialoprotein.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2016-01-01
description Orthopedic implant failure due to aseptic loosening and mechanical instability remains a major problem in total joint replacement. Improving osseointegration at the bone-implant interface may reduce micromotion and loosening. Bone sialoprotein (BSP) has been shown to enhance bone formation when coated onto titanium femoral implants and in rat calvarial defect models. However, the most appropriate method of BSP coating, the necessary level of BSP coating, and the effect of BSP coating on cell behavior remain largely unknown. In this study, BSP was covalently coupled to titanium surfaces via an aminosilane linker (APTES), and its properties were compared to BSP applied to titanium via physisorption and untreated titanium. Cell functions were examined using primary human osteoblasts (hOBs) and L929 mouse fibroblasts. Gene expression of specific bone turnover markers at the RNA level was detected at different intervals. Cell adhesion to titanium surfaces treated with BSP via physisorption was not significantly different from that of untreated titanium at any time point, whereas BSP application via covalent coupling caused reduced cell adhesion during the first few hours in culture. Cell migration was increased on titanium disks that were treated with higher concentrations of BSP solution, independent of the coating method. During the early phases of hOB proliferation, a suppressive effect of BSP was observed independent of its concentration, particularly when BSP was applied to the titanium surface via physisorption. Although alkaline phosphatase activity was reduced in the BSP-coated titanium groups after 4 days in culture, increased calcium deposition was observed after 21 days. In particular, the gene expression level of RUNX2 was upregulated by BSP. The increase in calcium deposition and the stimulation of cell differentiation induced by BSP highlight its potential as a surface modifier that could enhance the osseointegration of orthopedic implants. Both physisorption and covalent coupling of BSP are similarly effective, feasible methods, although a higher BSP concentration is recommended.
url http://europepmc.org/articles/PMC4844107?pdf=render
work_keys_str_mv AT andreasbaranowski surfacefunctionalizationoforthopedictitaniumimplantswithbonesialoprotein
AT anjaklein surfacefunctionalizationoforthopedictitaniumimplantswithbonesialoprotein
AT ulrikeritz surfacefunctionalizationoforthopedictitaniumimplantswithbonesialoprotein
AT angelikaackermann surfacefunctionalizationoforthopedictitaniumimplantswithbonesialoprotein
AT jorisanthonissen surfacefunctionalizationoforthopedictitaniumimplantswithbonesialoprotein
AT kerstinbkaufmann surfacefunctionalizationoforthopedictitaniumimplantswithbonesialoprotein
AT christianbrendel surfacefunctionalizationoforthopedictitaniumimplantswithbonesialoprotein
AT hermanngotz surfacefunctionalizationoforthopedictitaniumimplantswithbonesialoprotein
AT polmrommens surfacefunctionalizationoforthopedictitaniumimplantswithbonesialoprotein
AT alexanderhofmann surfacefunctionalizationoforthopedictitaniumimplantswithbonesialoprotein
_version_ 1725275156948975616