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The relative effects of Ca and Mg ions on MSC osteogenesis in the surface modification of microrough Ti implants
PURPOSE: Calcium (Ca) and magnesium (Mg) ions have been used as promising bioactive ions in the surface chemistry modification of titanium (Ti) bone implants to increase bone regeneration capacity. However, it is not clear which (Ca or Mg) plays the more important role in the early osteogenic differ...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6662177/ https://www.ncbi.nlm.nih.gov/pubmed/31413570 http://dx.doi.org/10.2147/IJN.S214363 |
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author | Park, Jin-Woo Hanawa, Takao Chung, Jong-Hyuk |
author_facet | Park, Jin-Woo Hanawa, Takao Chung, Jong-Hyuk |
author_sort | Park, Jin-Woo |
collection | PubMed |
description | PURPOSE: Calcium (Ca) and magnesium (Mg) ions have been used as promising bioactive ions in the surface chemistry modification of titanium (Ti) bone implants to increase bone regeneration capacity. However, it is not clear which (Ca or Mg) plays the more important role in the early osteogenic differentiation of mesenchymal stem cells (MSCs) when applied to the surface of commercially available microstructured Ti implants. This study investigated the relative effect of these two ions on the early osteogenic functionality of primary mouse bone marrow MSCs in order to obtain insights into the surface design of Ti implants with enhanced early osteogenic capacity. METHODS AND RESULTS: Wet chemical treatment was performed to modify a microrough Ti implant surface using Ca or Mg ions. Both the Ca and Mg-incorporated surfaces accelerated early cellular events and the subsequent osteogenic differentiation of MSCs compared with an unmodified microrough Ti surface. Surface Mg modification exhibited a more potent osteoblast differentiation-promoting effect than the Ca modification. Surface Mg incorporation markedly inhibited the phosphorylation of β-catenin. CONCLUSION: These results indicate that alteration of the surface chemistry of microstructured Ti implants by wet chemical treatment with Mg ions exerts a more effect on promoting the early osteogenic differentiation of MSCs than Ca ions by enhancing early cellular functions, including focal adhesion development and stabilization of intracellular β-catenin. |
format | Online Article Text |
id | pubmed-6662177 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-66621772019-08-14 The relative effects of Ca and Mg ions on MSC osteogenesis in the surface modification of microrough Ti implants Park, Jin-Woo Hanawa, Takao Chung, Jong-Hyuk Int J Nanomedicine Original Research PURPOSE: Calcium (Ca) and magnesium (Mg) ions have been used as promising bioactive ions in the surface chemistry modification of titanium (Ti) bone implants to increase bone regeneration capacity. However, it is not clear which (Ca or Mg) plays the more important role in the early osteogenic differentiation of mesenchymal stem cells (MSCs) when applied to the surface of commercially available microstructured Ti implants. This study investigated the relative effect of these two ions on the early osteogenic functionality of primary mouse bone marrow MSCs in order to obtain insights into the surface design of Ti implants with enhanced early osteogenic capacity. METHODS AND RESULTS: Wet chemical treatment was performed to modify a microrough Ti implant surface using Ca or Mg ions. Both the Ca and Mg-incorporated surfaces accelerated early cellular events and the subsequent osteogenic differentiation of MSCs compared with an unmodified microrough Ti surface. Surface Mg modification exhibited a more potent osteoblast differentiation-promoting effect than the Ca modification. Surface Mg incorporation markedly inhibited the phosphorylation of β-catenin. CONCLUSION: These results indicate that alteration of the surface chemistry of microstructured Ti implants by wet chemical treatment with Mg ions exerts a more effect on promoting the early osteogenic differentiation of MSCs than Ca ions by enhancing early cellular functions, including focal adhesion development and stabilization of intracellular β-catenin. Dove 2019-07-23 /pmc/articles/PMC6662177/ /pubmed/31413570 http://dx.doi.org/10.2147/IJN.S214363 Text en © 2019 Park et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Park, Jin-Woo Hanawa, Takao Chung, Jong-Hyuk The relative effects of Ca and Mg ions on MSC osteogenesis in the surface modification of microrough Ti implants |
title | The relative effects of Ca and Mg ions on MSC osteogenesis in the surface modification of microrough Ti implants |
title_full | The relative effects of Ca and Mg ions on MSC osteogenesis in the surface modification of microrough Ti implants |
title_fullStr | The relative effects of Ca and Mg ions on MSC osteogenesis in the surface modification of microrough Ti implants |
title_full_unstemmed | The relative effects of Ca and Mg ions on MSC osteogenesis in the surface modification of microrough Ti implants |
title_short | The relative effects of Ca and Mg ions on MSC osteogenesis in the surface modification of microrough Ti implants |
title_sort | relative effects of ca and mg ions on msc osteogenesis in the surface modification of microrough ti implants |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6662177/ https://www.ncbi.nlm.nih.gov/pubmed/31413570 http://dx.doi.org/10.2147/IJN.S214363 |
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