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The osteogenic response of mesenchymal stromal cells to strontium‐substituted bioactive glasses
Bioactive glasses are known to stimulate bone healing, and the incorporation of strontium has the potential to increase their potency. In this study, calcium oxide in the 45S5 bioactive glass composition was partially (50%, Sr50) or fully (100%, Sr100) substituted with strontium oxide on a molar bas...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5053305/ https://www.ncbi.nlm.nih.gov/pubmed/25757935 http://dx.doi.org/10.1002/term.2003 |
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author | Santocildes‐Romero, Martin E. Crawford, Aileen Hatton, Paul V. Goodchild, Rebecca L. Reaney, Ian M. Miller, Cheryl A. |
author_facet | Santocildes‐Romero, Martin E. Crawford, Aileen Hatton, Paul V. Goodchild, Rebecca L. Reaney, Ian M. Miller, Cheryl A. |
author_sort | Santocildes‐Romero, Martin E. |
collection | PubMed |
description | Bioactive glasses are known to stimulate bone healing, and the incorporation of strontium has the potential to increase their potency. In this study, calcium oxide in the 45S5 bioactive glass composition was partially (50%, Sr50) or fully (100%, Sr100) substituted with strontium oxide on a molar basis. The effects of the substitution on bioactive glass properties were studied, including density, solubility, and in vitro cytotoxicity. Stimulation of osteogenic differentiation was investigated using mesenchymal stromal cells obtained from rat bone marrow. Strontium substitution resulted in altered physical properties including increased solubility. Statistically significant reductions in cell viability were observed with the addition of bioactive glass powders to culture medium. Specifically, addition of ≥ 13.3 mg/ml of 45S5 bioactive glass or Sr50, or ≥ 6.7 mg/ml of Sr100, resulted in significant inhibition. Real‐time PCR analyses detected the upregulation of genes associated with osteoblastic differentiation in the presence of all bioactive glass compositions. Some genes, including Alpl and Bglap, were further stimulated in the presence of Sr50 and Sr100. It was concluded that strontium‐substituted bioactive glasses promoted osteogenesis in a differentiating bone cell culture model and, therefore, have considerable potential for use as improved bioactive glasses for bone tissue regeneration. © 2015 The Authors. Journal of Tissue Engineering and Regenerative Medicine Published by John Wiley & Sons Ltd. |
format | Online Article Text |
id | pubmed-5053305 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50533052016-10-19 The osteogenic response of mesenchymal stromal cells to strontium‐substituted bioactive glasses Santocildes‐Romero, Martin E. Crawford, Aileen Hatton, Paul V. Goodchild, Rebecca L. Reaney, Ian M. Miller, Cheryl A. J Tissue Eng Regen Med Research Articles Bioactive glasses are known to stimulate bone healing, and the incorporation of strontium has the potential to increase their potency. In this study, calcium oxide in the 45S5 bioactive glass composition was partially (50%, Sr50) or fully (100%, Sr100) substituted with strontium oxide on a molar basis. The effects of the substitution on bioactive glass properties were studied, including density, solubility, and in vitro cytotoxicity. Stimulation of osteogenic differentiation was investigated using mesenchymal stromal cells obtained from rat bone marrow. Strontium substitution resulted in altered physical properties including increased solubility. Statistically significant reductions in cell viability were observed with the addition of bioactive glass powders to culture medium. Specifically, addition of ≥ 13.3 mg/ml of 45S5 bioactive glass or Sr50, or ≥ 6.7 mg/ml of Sr100, resulted in significant inhibition. Real‐time PCR analyses detected the upregulation of genes associated with osteoblastic differentiation in the presence of all bioactive glass compositions. Some genes, including Alpl and Bglap, were further stimulated in the presence of Sr50 and Sr100. It was concluded that strontium‐substituted bioactive glasses promoted osteogenesis in a differentiating bone cell culture model and, therefore, have considerable potential for use as improved bioactive glasses for bone tissue regeneration. © 2015 The Authors. Journal of Tissue Engineering and Regenerative Medicine Published by John Wiley & Sons Ltd. John Wiley and Sons Inc. 2015-03-11 2015-05 /pmc/articles/PMC5053305/ /pubmed/25757935 http://dx.doi.org/10.1002/term.2003 Text en © 2015 The Authors. Journal of Tissue Engineering and Regenerative Medicine Published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Santocildes‐Romero, Martin E. Crawford, Aileen Hatton, Paul V. Goodchild, Rebecca L. Reaney, Ian M. Miller, Cheryl A. The osteogenic response of mesenchymal stromal cells to strontium‐substituted bioactive glasses |
title | The osteogenic response of mesenchymal stromal cells to strontium‐substituted bioactive glasses |
title_full | The osteogenic response of mesenchymal stromal cells to strontium‐substituted bioactive glasses |
title_fullStr | The osteogenic response of mesenchymal stromal cells to strontium‐substituted bioactive glasses |
title_full_unstemmed | The osteogenic response of mesenchymal stromal cells to strontium‐substituted bioactive glasses |
title_short | The osteogenic response of mesenchymal stromal cells to strontium‐substituted bioactive glasses |
title_sort | osteogenic response of mesenchymal stromal cells to strontium‐substituted bioactive glasses |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5053305/ https://www.ncbi.nlm.nih.gov/pubmed/25757935 http://dx.doi.org/10.1002/term.2003 |
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