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Silk fibroin scaffolds with inverse opal structure for bone tissue engineering
How scaffold porosity, pore diameter and geometry influence cellular behavior is‐although heavily researched ‐ merely understood, especially in 3D. This is mainly caused by a lack of suitable, reproducible scaffold fabrication methods, with processes such as gas foaming, lyophilization or particulat...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5599946/ https://www.ncbi.nlm.nih.gov/pubmed/27407014 http://dx.doi.org/10.1002/jbm.b.33737 |
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author | Sommer, Marianne R. Vetsch, Jolanda R. Leemann, Jessica Müller, Ralph Studart, André R. Hofmann, Sandra |
author_facet | Sommer, Marianne R. Vetsch, Jolanda R. Leemann, Jessica Müller, Ralph Studart, André R. Hofmann, Sandra |
author_sort | Sommer, Marianne R. |
collection | PubMed |
description | How scaffold porosity, pore diameter and geometry influence cellular behavior is‐although heavily researched ‐ merely understood, especially in 3D. This is mainly caused by a lack of suitable, reproducible scaffold fabrication methods, with processes such as gas foaming, lyophilization or particulate leaching still being the standard. Here we propose a method to generate highly porous silk fibroin scaffolds with monodisperse spherical pores, namely inverse opals, and study their effect on cell behavior. These silk fibroin inverse opal scaffolds were compared to salt‐leached silk fibroin scaffolds in terms of human mesenchymal stem cell response upon osteogenic differentiation signals. While cell number remained similar on both scaffold types, extracellular matrix mineralization nearly doubled on the newly developed scaffolds, suggesting a positive effect on cell differentiation. By using the very same material with comparable average pore diameters, this increase in mineral content can be attributed to either the differences in pore diameter distribution or the pore geometry. Although the exact mechanisms leading to enhanced mineralization in inverse opals are not yet fully understood, our results indicate that control over pore geometry alone can have a major impact on the bioactivity of a scaffold toward stem cell differentiation into bone tissue. © 2016 The Authors Journal of Biomedical Materials Research Part B: Applied Biomaterials Published by Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 105B: 2074–2084, 2017. |
format | Online Article Text |
id | pubmed-5599946 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-55999462017-10-02 Silk fibroin scaffolds with inverse opal structure for bone tissue engineering Sommer, Marianne R. Vetsch, Jolanda R. Leemann, Jessica Müller, Ralph Studart, André R. Hofmann, Sandra J Biomed Mater Res B Appl Biomater Original Research Reports How scaffold porosity, pore diameter and geometry influence cellular behavior is‐although heavily researched ‐ merely understood, especially in 3D. This is mainly caused by a lack of suitable, reproducible scaffold fabrication methods, with processes such as gas foaming, lyophilization or particulate leaching still being the standard. Here we propose a method to generate highly porous silk fibroin scaffolds with monodisperse spherical pores, namely inverse opals, and study their effect on cell behavior. These silk fibroin inverse opal scaffolds were compared to salt‐leached silk fibroin scaffolds in terms of human mesenchymal stem cell response upon osteogenic differentiation signals. While cell number remained similar on both scaffold types, extracellular matrix mineralization nearly doubled on the newly developed scaffolds, suggesting a positive effect on cell differentiation. By using the very same material with comparable average pore diameters, this increase in mineral content can be attributed to either the differences in pore diameter distribution or the pore geometry. Although the exact mechanisms leading to enhanced mineralization in inverse opals are not yet fully understood, our results indicate that control over pore geometry alone can have a major impact on the bioactivity of a scaffold toward stem cell differentiation into bone tissue. © 2016 The Authors Journal of Biomedical Materials Research Part B: Applied Biomaterials Published by Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 105B: 2074–2084, 2017. John Wiley and Sons Inc. 2016-07-13 2017-10 /pmc/articles/PMC5599946/ /pubmed/27407014 http://dx.doi.org/10.1002/jbm.b.33737 Text en © 2016 The Authors Journal of Biomedical Materials Research Part B: Applied Biomaterials Published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Research Reports Sommer, Marianne R. Vetsch, Jolanda R. Leemann, Jessica Müller, Ralph Studart, André R. Hofmann, Sandra Silk fibroin scaffolds with inverse opal structure for bone tissue engineering |
title | Silk fibroin scaffolds with inverse opal structure for bone tissue engineering |
title_full | Silk fibroin scaffolds with inverse opal structure for bone tissue engineering |
title_fullStr | Silk fibroin scaffolds with inverse opal structure for bone tissue engineering |
title_full_unstemmed | Silk fibroin scaffolds with inverse opal structure for bone tissue engineering |
title_short | Silk fibroin scaffolds with inverse opal structure for bone tissue engineering |
title_sort | silk fibroin scaffolds with inverse opal structure for bone tissue engineering |
topic | Original Research Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5599946/ https://www.ncbi.nlm.nih.gov/pubmed/27407014 http://dx.doi.org/10.1002/jbm.b.33737 |
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