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Osteogenic differentiation of human mesenchymal stem cells promotes mineralization within a biodegradable peptide hydrogel
An attractive strategy for the regeneration of tissues has been the use of extracellular matrix analogous biomaterials. Peptide-based fibrillar hydrogels have been shown to mimic the structure of extracellular matrix offering cells a niche to undertake their physiological functions. In this study, t...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4959308/ https://www.ncbi.nlm.nih.gov/pubmed/27493714 http://dx.doi.org/10.1177/2041731416649789 |
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author | Castillo Diaz, Luis A Elsawy, Mohamed Saiani, Alberto Gough, Julie E Miller, Aline F |
author_facet | Castillo Diaz, Luis A Elsawy, Mohamed Saiani, Alberto Gough, Julie E Miller, Aline F |
author_sort | Castillo Diaz, Luis A |
collection | PubMed |
description | An attractive strategy for the regeneration of tissues has been the use of extracellular matrix analogous biomaterials. Peptide-based fibrillar hydrogels have been shown to mimic the structure of extracellular matrix offering cells a niche to undertake their physiological functions. In this study, the capability of an ionic-complementary peptide FEFEFKFK (F, E, and K are phenylalanine, glutamic acid, and lysine, respectively) hydrogel to host human mesenchymal stem cells in three dimensions and induce their osteogenic differentiation is demonstrated. Assays showed sustained cell viability and proliferation throughout the hydrogel over 12 days of culture and these human mesenchymal stem cells differentiated into osteoblasts simply upon addition of osteogenic stimulation. Differentiated osteoblasts synthesized key bone proteins, including collagen-1 (Col-1), osteocalcin, and alkaline phosphatase. Moreover, mineralization occurred within the hydrogel. The peptide hydrogel is a naturally biodegradable material as shown by oscillatory rheology and reversed-phase high-performance liquid chromatography, where both viscoelastic properties and the degradation of the hydrogel were monitored over time, respectively. These findings demonstrate that a biodegradable octapeptide hydrogel can host and induce the differentiation of stem cells and has the potential for the regeneration of hard tissues such as alveolar bone. |
format | Online Article Text |
id | pubmed-4959308 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-49593082016-08-04 Osteogenic differentiation of human mesenchymal stem cells promotes mineralization within a biodegradable peptide hydrogel Castillo Diaz, Luis A Elsawy, Mohamed Saiani, Alberto Gough, Julie E Miller, Aline F J Tissue Eng Original Article An attractive strategy for the regeneration of tissues has been the use of extracellular matrix analogous biomaterials. Peptide-based fibrillar hydrogels have been shown to mimic the structure of extracellular matrix offering cells a niche to undertake their physiological functions. In this study, the capability of an ionic-complementary peptide FEFEFKFK (F, E, and K are phenylalanine, glutamic acid, and lysine, respectively) hydrogel to host human mesenchymal stem cells in three dimensions and induce their osteogenic differentiation is demonstrated. Assays showed sustained cell viability and proliferation throughout the hydrogel over 12 days of culture and these human mesenchymal stem cells differentiated into osteoblasts simply upon addition of osteogenic stimulation. Differentiated osteoblasts synthesized key bone proteins, including collagen-1 (Col-1), osteocalcin, and alkaline phosphatase. Moreover, mineralization occurred within the hydrogel. The peptide hydrogel is a naturally biodegradable material as shown by oscillatory rheology and reversed-phase high-performance liquid chromatography, where both viscoelastic properties and the degradation of the hydrogel were monitored over time, respectively. These findings demonstrate that a biodegradable octapeptide hydrogel can host and induce the differentiation of stem cells and has the potential for the regeneration of hard tissues such as alveolar bone. SAGE Publications 2016-07-12 /pmc/articles/PMC4959308/ /pubmed/27493714 http://dx.doi.org/10.1177/2041731416649789 Text en © The Author(s) 2016 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page(https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Castillo Diaz, Luis A Elsawy, Mohamed Saiani, Alberto Gough, Julie E Miller, Aline F Osteogenic differentiation of human mesenchymal stem cells promotes mineralization within a biodegradable peptide hydrogel |
title | Osteogenic differentiation of human mesenchymal stem cells promotes mineralization within a biodegradable peptide hydrogel |
title_full | Osteogenic differentiation of human mesenchymal stem cells promotes mineralization within a biodegradable peptide hydrogel |
title_fullStr | Osteogenic differentiation of human mesenchymal stem cells promotes mineralization within a biodegradable peptide hydrogel |
title_full_unstemmed | Osteogenic differentiation of human mesenchymal stem cells promotes mineralization within a biodegradable peptide hydrogel |
title_short | Osteogenic differentiation of human mesenchymal stem cells promotes mineralization within a biodegradable peptide hydrogel |
title_sort | osteogenic differentiation of human mesenchymal stem cells promotes mineralization within a biodegradable peptide hydrogel |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4959308/ https://www.ncbi.nlm.nih.gov/pubmed/27493714 http://dx.doi.org/10.1177/2041731416649789 |
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