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Osteogenesis induced in goat bone marrow progenitor cells by recombinant adenovirus coexpressing bone morphogenetic protein 2 and basic fibroblast growth factor
Bone morphogenetic protein 2 (BMP2) and basic fibroblast growth factor (bFGF) have been shown to exhibit a synergistic effect to promote bone repair and healing. In this study, we constructed a novel adenovirus with high coexpression of BMP2 and bFGF and evaluated its effect on osteogenic differenti...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Associação Brasileira de Divulgação Científica
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3854432/ https://www.ncbi.nlm.nih.gov/pubmed/24068195 http://dx.doi.org/10.1590/1414-431X20132929 |
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author | Xu, H.H. Liu, S.H. Guo, Q.F. Liu, Q.H. Li, X.Y. |
author_facet | Xu, H.H. Liu, S.H. Guo, Q.F. Liu, Q.H. Li, X.Y. |
author_sort | Xu, H.H. |
collection | PubMed |
description | Bone morphogenetic protein 2 (BMP2) and basic fibroblast growth factor (bFGF) have been shown to exhibit a synergistic effect to promote bone repair and healing. In this study, we constructed a novel adenovirus with high coexpression of BMP2 and bFGF and evaluated its effect on osteogenic differentiation of goat bone marrow progenitor cells (BMPCs). Recombinant adenovirus Ad-BMP2-bFGF was constructed by using the T2A sequence. BMPCs were isolated from goats by density gradient centrifugation and adherent cell culture, and were then infected with Ad-BMP2-bFGF or Ad-BMP2. Expression of BMP2 and bFGF was detected by ELISA, and alkaline phosphatase (ALP) activity was detected by an ALP assay kit. In addition, von Kossa staining and immunocytochemical staining of collagen II were performed on BMPCs 21 days after infection. There was a high coexpression of BMP2 and bFGF in BMPCs infected with Ad-BMP2-bFGF. Twenty-one days after infection, ALP activity was significantly higher in BMPCs infected with Ad-BMP2-bFGF than in those infected with Ad-BMP2. Larger and more mineralized calcium nodules, as well as stronger collagen II staining, were observed in BMPCs infected with Ad-BMP2-bFGF than in those infected with Ad-BMP2. In summary, we developed a novel adenovirus vector Ad-BMP2-bFGF for simultaneous high coexpression of BMP2 and bFGF, which could induce BMPCs to differentiate efficiently into osteoblasts. |
format | Online Article Text |
id | pubmed-3854432 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Associação Brasileira de Divulgação Científica |
record_format | MEDLINE/PubMed |
spelling | pubmed-38544322013-12-16 Osteogenesis induced in goat bone marrow progenitor cells by recombinant adenovirus coexpressing bone morphogenetic protein 2 and basic fibroblast growth factor Xu, H.H. Liu, S.H. Guo, Q.F. Liu, Q.H. Li, X.Y. Braz J Med Biol Res Clinical Investigation Bone morphogenetic protein 2 (BMP2) and basic fibroblast growth factor (bFGF) have been shown to exhibit a synergistic effect to promote bone repair and healing. In this study, we constructed a novel adenovirus with high coexpression of BMP2 and bFGF and evaluated its effect on osteogenic differentiation of goat bone marrow progenitor cells (BMPCs). Recombinant adenovirus Ad-BMP2-bFGF was constructed by using the T2A sequence. BMPCs were isolated from goats by density gradient centrifugation and adherent cell culture, and were then infected with Ad-BMP2-bFGF or Ad-BMP2. Expression of BMP2 and bFGF was detected by ELISA, and alkaline phosphatase (ALP) activity was detected by an ALP assay kit. In addition, von Kossa staining and immunocytochemical staining of collagen II were performed on BMPCs 21 days after infection. There was a high coexpression of BMP2 and bFGF in BMPCs infected with Ad-BMP2-bFGF. Twenty-one days after infection, ALP activity was significantly higher in BMPCs infected with Ad-BMP2-bFGF than in those infected with Ad-BMP2. Larger and more mineralized calcium nodules, as well as stronger collagen II staining, were observed in BMPCs infected with Ad-BMP2-bFGF than in those infected with Ad-BMP2. In summary, we developed a novel adenovirus vector Ad-BMP2-bFGF for simultaneous high coexpression of BMP2 and bFGF, which could induce BMPCs to differentiate efficiently into osteoblasts. Associação Brasileira de Divulgação Científica 2013-09-06 /pmc/articles/PMC3854432/ /pubmed/24068195 http://dx.doi.org/10.1590/1414-431X20132929 Text en http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Investigation Xu, H.H. Liu, S.H. Guo, Q.F. Liu, Q.H. Li, X.Y. Osteogenesis induced in goat bone marrow progenitor cells by recombinant adenovirus coexpressing bone morphogenetic protein 2 and basic fibroblast growth factor |
title | Osteogenesis induced in goat bone marrow progenitor
cells by recombinant adenovirus coexpressing bone morphogenetic protein 2 and
basic fibroblast growth factor |
title_full | Osteogenesis induced in goat bone marrow progenitor
cells by recombinant adenovirus coexpressing bone morphogenetic protein 2 and
basic fibroblast growth factor |
title_fullStr | Osteogenesis induced in goat bone marrow progenitor
cells by recombinant adenovirus coexpressing bone morphogenetic protein 2 and
basic fibroblast growth factor |
title_full_unstemmed | Osteogenesis induced in goat bone marrow progenitor
cells by recombinant adenovirus coexpressing bone morphogenetic protein 2 and
basic fibroblast growth factor |
title_short | Osteogenesis induced in goat bone marrow progenitor
cells by recombinant adenovirus coexpressing bone morphogenetic protein 2 and
basic fibroblast growth factor |
title_sort | osteogenesis induced in goat bone marrow progenitor
cells by recombinant adenovirus coexpressing bone morphogenetic protein 2 and
basic fibroblast growth factor |
topic | Clinical Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3854432/ https://www.ncbi.nlm.nih.gov/pubmed/24068195 http://dx.doi.org/10.1590/1414-431X20132929 |
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