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In vitro evaluation of a bone morphogenetic protein-2 nanometer hydroxyapatite collagen scaffold for bone regeneration
Scaffold fabrication and biocompatibility are crucial for successful bone tissue engineering. Nanometer hydroxyapatite (nHAP) combined with collagen (COL) is frequently utilized as a suitable osseous scaffold material. Furthermore, growth factors, including bone morphogenetic protein-2 (BMP-2), are...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5866027/ https://www.ncbi.nlm.nih.gov/pubmed/29436646 http://dx.doi.org/10.3892/mmr.2018.8579 |
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author | Cai, Yue Tong, Shuang Zhang, Ran Zhu, Tong Wang, Xukai |
author_facet | Cai, Yue Tong, Shuang Zhang, Ran Zhu, Tong Wang, Xukai |
author_sort | Cai, Yue |
collection | PubMed |
description | Scaffold fabrication and biocompatibility are crucial for successful bone tissue engineering. Nanometer hydroxyapatite (nHAP) combined with collagen (COL) is frequently utilized as a suitable osseous scaffold material. Furthermore, growth factors, including bone morphogenetic protein-2 (BMP-2), are used to enhance the scaffold properties. The present study used blending and freeze-drying methods to develop a BMP-2-nHAP-COL scaffold. An ELISA was performed to determine the BMP-2 release rate from the scaffold. Flow cytometry was used to identify rat bone marrow-derived mesenchymal stem cells (BMSCs) prior to their combination with the scaffold. Scanning electron microscopy was used to observe the scaffold structure and BMSC morphology following seeding onto the scaffold. BMSCs were also used to assess the biological compatibility of the scaffold in vitro. BMP-2-nHAP-COL and nHAP-COL scaffolds were assessed alongside the appropriate control groups. Cells were counted to determine early cell adhesion. Cell Counting kit-8 and alkaline phosphatase assays were used to detect cell proliferation and differentiation, respectively. Gross morphology confirmed that the BMP-2-nHAP-COL scaffold microstructure conformed to the optimal characteristics of a bone tissue engineering scaffold. Furthermore, the BMP-2-nHAP-COL scaffold exhibited no biological toxicity and was demonstrated to promote BMSC adhesion, proliferation and differentiation. The BMP-2-nHAP-COL scaffold had good biocompatibility in vitro, and may therefore be modified further to construct an optimized scaffold for future bone tissue engineering. |
format | Online Article Text |
id | pubmed-5866027 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-58660272018-03-28 In vitro evaluation of a bone morphogenetic protein-2 nanometer hydroxyapatite collagen scaffold for bone regeneration Cai, Yue Tong, Shuang Zhang, Ran Zhu, Tong Wang, Xukai Mol Med Rep Articles Scaffold fabrication and biocompatibility are crucial for successful bone tissue engineering. Nanometer hydroxyapatite (nHAP) combined with collagen (COL) is frequently utilized as a suitable osseous scaffold material. Furthermore, growth factors, including bone morphogenetic protein-2 (BMP-2), are used to enhance the scaffold properties. The present study used blending and freeze-drying methods to develop a BMP-2-nHAP-COL scaffold. An ELISA was performed to determine the BMP-2 release rate from the scaffold. Flow cytometry was used to identify rat bone marrow-derived mesenchymal stem cells (BMSCs) prior to their combination with the scaffold. Scanning electron microscopy was used to observe the scaffold structure and BMSC morphology following seeding onto the scaffold. BMSCs were also used to assess the biological compatibility of the scaffold in vitro. BMP-2-nHAP-COL and nHAP-COL scaffolds were assessed alongside the appropriate control groups. Cells were counted to determine early cell adhesion. Cell Counting kit-8 and alkaline phosphatase assays were used to detect cell proliferation and differentiation, respectively. Gross morphology confirmed that the BMP-2-nHAP-COL scaffold microstructure conformed to the optimal characteristics of a bone tissue engineering scaffold. Furthermore, the BMP-2-nHAP-COL scaffold exhibited no biological toxicity and was demonstrated to promote BMSC adhesion, proliferation and differentiation. The BMP-2-nHAP-COL scaffold had good biocompatibility in vitro, and may therefore be modified further to construct an optimized scaffold for future bone tissue engineering. D.A. Spandidos 2018-04 2018-02-08 /pmc/articles/PMC5866027/ /pubmed/29436646 http://dx.doi.org/10.3892/mmr.2018.8579 Text en Copyright: © Cai et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Cai, Yue Tong, Shuang Zhang, Ran Zhu, Tong Wang, Xukai In vitro evaluation of a bone morphogenetic protein-2 nanometer hydroxyapatite collagen scaffold for bone regeneration |
title | In vitro evaluation of a bone morphogenetic protein-2 nanometer hydroxyapatite collagen scaffold for bone regeneration |
title_full | In vitro evaluation of a bone morphogenetic protein-2 nanometer hydroxyapatite collagen scaffold for bone regeneration |
title_fullStr | In vitro evaluation of a bone morphogenetic protein-2 nanometer hydroxyapatite collagen scaffold for bone regeneration |
title_full_unstemmed | In vitro evaluation of a bone morphogenetic protein-2 nanometer hydroxyapatite collagen scaffold for bone regeneration |
title_short | In vitro evaluation of a bone morphogenetic protein-2 nanometer hydroxyapatite collagen scaffold for bone regeneration |
title_sort | in vitro evaluation of a bone morphogenetic protein-2 nanometer hydroxyapatite collagen scaffold for bone regeneration |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5866027/ https://www.ncbi.nlm.nih.gov/pubmed/29436646 http://dx.doi.org/10.3892/mmr.2018.8579 |
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