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Development of a 3D Collagen Model for the In Vitro Evaluation of Magnetic-assisted Osteogenesis

Magnetic stimulation has been applied to bone regeneration, however, the cellular and molecular mechanisms of repair still require a better understanding. A three-dimensional (3D) collagen model was developed using plastic compression, which produces dense, cellular, mechanically strong native colla...

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Autores principales: Yuan, Zhiyu, Memarzadeh, Kaveh, Stephen, Abish S., Allaker, Robert P., Brown, Robert A., Huang, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6214996/
https://www.ncbi.nlm.nih.gov/pubmed/30389949
http://dx.doi.org/10.1038/s41598-018-33455-2
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author Yuan, Zhiyu
Memarzadeh, Kaveh
Stephen, Abish S.
Allaker, Robert P.
Brown, Robert A.
Huang, Jie
author_facet Yuan, Zhiyu
Memarzadeh, Kaveh
Stephen, Abish S.
Allaker, Robert P.
Brown, Robert A.
Huang, Jie
author_sort Yuan, Zhiyu
collection PubMed
description Magnetic stimulation has been applied to bone regeneration, however, the cellular and molecular mechanisms of repair still require a better understanding. A three-dimensional (3D) collagen model was developed using plastic compression, which produces dense, cellular, mechanically strong native collagen structures. Osteoblast cells (MG-63) and magnetic iron oxide nanoparticles (IONPs) were incorporated into collagen gels to produce a range of cell-laden models. A magnetic bio-reactor to support cell growth under static magnetic fields (SMFs) was designed and fabricated by 3D printing. The influences of SMFs on cell proliferation, differentiation, extracellular matrix production, mineralisation and gene expression were evaluated. Polymerase chain reaction (PCR) further determined the effects of SMFs on the expression of runt-related transcription factor 2 (Runx2), osteonectin (ON), and bone morphogenic proteins 2 and 4 (BMP-2 and BMP-4). Results demonstrate that SMFs, IONPs and the collagen matrix can stimulate the proliferation, alkaline phosphatase production and mineralisation of MG-63 cells, by influencing matrix/cell interactions and encouraging the expression of Runx2, ON, BMP-2 and BMP-4. Therefore, the collagen model developed here not only offers a novel 3D bone model to better understand the effect of magnetic stimulation on osteogenesis, but also paves the way for further applications in tissue engineering and regenerative medicine.
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spelling pubmed-62149962018-11-06 Development of a 3D Collagen Model for the In Vitro Evaluation of Magnetic-assisted Osteogenesis Yuan, Zhiyu Memarzadeh, Kaveh Stephen, Abish S. Allaker, Robert P. Brown, Robert A. Huang, Jie Sci Rep Article Magnetic stimulation has been applied to bone regeneration, however, the cellular and molecular mechanisms of repair still require a better understanding. A three-dimensional (3D) collagen model was developed using plastic compression, which produces dense, cellular, mechanically strong native collagen structures. Osteoblast cells (MG-63) and magnetic iron oxide nanoparticles (IONPs) were incorporated into collagen gels to produce a range of cell-laden models. A magnetic bio-reactor to support cell growth under static magnetic fields (SMFs) was designed and fabricated by 3D printing. The influences of SMFs on cell proliferation, differentiation, extracellular matrix production, mineralisation and gene expression were evaluated. Polymerase chain reaction (PCR) further determined the effects of SMFs on the expression of runt-related transcription factor 2 (Runx2), osteonectin (ON), and bone morphogenic proteins 2 and 4 (BMP-2 and BMP-4). Results demonstrate that SMFs, IONPs and the collagen matrix can stimulate the proliferation, alkaline phosphatase production and mineralisation of MG-63 cells, by influencing matrix/cell interactions and encouraging the expression of Runx2, ON, BMP-2 and BMP-4. Therefore, the collagen model developed here not only offers a novel 3D bone model to better understand the effect of magnetic stimulation on osteogenesis, but also paves the way for further applications in tissue engineering and regenerative medicine. Nature Publishing Group UK 2018-11-02 /pmc/articles/PMC6214996/ /pubmed/30389949 http://dx.doi.org/10.1038/s41598-018-33455-2 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Yuan, Zhiyu
Memarzadeh, Kaveh
Stephen, Abish S.
Allaker, Robert P.
Brown, Robert A.
Huang, Jie
Development of a 3D Collagen Model for the In Vitro Evaluation of Magnetic-assisted Osteogenesis
title Development of a 3D Collagen Model for the In Vitro Evaluation of Magnetic-assisted Osteogenesis
title_full Development of a 3D Collagen Model for the In Vitro Evaluation of Magnetic-assisted Osteogenesis
title_fullStr Development of a 3D Collagen Model for the In Vitro Evaluation of Magnetic-assisted Osteogenesis
title_full_unstemmed Development of a 3D Collagen Model for the In Vitro Evaluation of Magnetic-assisted Osteogenesis
title_short Development of a 3D Collagen Model for the In Vitro Evaluation of Magnetic-assisted Osteogenesis
title_sort development of a 3d collagen model for the in vitro evaluation of magnetic-assisted osteogenesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6214996/
https://www.ncbi.nlm.nih.gov/pubmed/30389949
http://dx.doi.org/10.1038/s41598-018-33455-2
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