Cargando…

Templated Assembly of Collagen Fibers Directs Cell Growth in 2D and 3D

Collagen is widely used in tissue engineering and regenerative medicine, with many examples of collagen-based biomaterials emerging in recent years. While there are numerous methods available for forming collagen scaffolds from isolated collagen, existing biomaterial processing techniques are unable...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, G. Y., Agarwal, R., Ko, K. R, Ruthven, M., Sarhan, H. T., Frampton, J. P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5575125/
https://www.ncbi.nlm.nih.gov/pubmed/28852121
http://dx.doi.org/10.1038/s41598-017-10182-8
_version_ 1783259978528718848
author Liu, G. Y.
Agarwal, R.
Ko, K. R
Ruthven, M.
Sarhan, H. T.
Frampton, J. P.
author_facet Liu, G. Y.
Agarwal, R.
Ko, K. R
Ruthven, M.
Sarhan, H. T.
Frampton, J. P.
author_sort Liu, G. Y.
collection PubMed
description Collagen is widely used in tissue engineering and regenerative medicine, with many examples of collagen-based biomaterials emerging in recent years. While there are numerous methods available for forming collagen scaffolds from isolated collagen, existing biomaterial processing techniques are unable to efficiently align collagen at the microstructural level, which is important for providing appropriate cell recognition and mechanical properties. Although some attention has shifted to development of fiber-based collagen biomaterials, existing techniques for producing and aligning collagen fibers are not appropriate for large-scale fiber manufacturing. Here, we report a novel biomaterial fabrication approach capable of efficiently generating collagen fibers of appropriate sizes using a viscous solution of dextran as a dissolvable template. We demonstrate that myoblasts readily attach and align along 2D collagen fiber networks created by this process. Furthermore, encapsulation of collagen fibers with myoblasts into non-cell-adherent hydrogels promotes aligned growth of cells and supports their differentiation. The ease-of-production and versatility of this technique will support future development of advanced in vitro tissue models and materials for regenerative medicine.
format Online
Article
Text
id pubmed-5575125
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-55751252017-09-01 Templated Assembly of Collagen Fibers Directs Cell Growth in 2D and 3D Liu, G. Y. Agarwal, R. Ko, K. R Ruthven, M. Sarhan, H. T. Frampton, J. P. Sci Rep Article Collagen is widely used in tissue engineering and regenerative medicine, with many examples of collagen-based biomaterials emerging in recent years. While there are numerous methods available for forming collagen scaffolds from isolated collagen, existing biomaterial processing techniques are unable to efficiently align collagen at the microstructural level, which is important for providing appropriate cell recognition and mechanical properties. Although some attention has shifted to development of fiber-based collagen biomaterials, existing techniques for producing and aligning collagen fibers are not appropriate for large-scale fiber manufacturing. Here, we report a novel biomaterial fabrication approach capable of efficiently generating collagen fibers of appropriate sizes using a viscous solution of dextran as a dissolvable template. We demonstrate that myoblasts readily attach and align along 2D collagen fiber networks created by this process. Furthermore, encapsulation of collagen fibers with myoblasts into non-cell-adherent hydrogels promotes aligned growth of cells and supports their differentiation. The ease-of-production and versatility of this technique will support future development of advanced in vitro tissue models and materials for regenerative medicine. Nature Publishing Group UK 2017-08-29 /pmc/articles/PMC5575125/ /pubmed/28852121 http://dx.doi.org/10.1038/s41598-017-10182-8 Text en © The Author(s) 2017 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
Liu, G. Y.
Agarwal, R.
Ko, K. R
Ruthven, M.
Sarhan, H. T.
Frampton, J. P.
Templated Assembly of Collagen Fibers Directs Cell Growth in 2D and 3D
title Templated Assembly of Collagen Fibers Directs Cell Growth in 2D and 3D
title_full Templated Assembly of Collagen Fibers Directs Cell Growth in 2D and 3D
title_fullStr Templated Assembly of Collagen Fibers Directs Cell Growth in 2D and 3D
title_full_unstemmed Templated Assembly of Collagen Fibers Directs Cell Growth in 2D and 3D
title_short Templated Assembly of Collagen Fibers Directs Cell Growth in 2D and 3D
title_sort templated assembly of collagen fibers directs cell growth in 2d and 3d
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5575125/
https://www.ncbi.nlm.nih.gov/pubmed/28852121
http://dx.doi.org/10.1038/s41598-017-10182-8
work_keys_str_mv AT liugy templatedassemblyofcollagenfibersdirectscellgrowthin2dand3d
AT agarwalr templatedassemblyofcollagenfibersdirectscellgrowthin2dand3d
AT kokr templatedassemblyofcollagenfibersdirectscellgrowthin2dand3d
AT ruthvenm templatedassemblyofcollagenfibersdirectscellgrowthin2dand3d
AT sarhanht templatedassemblyofcollagenfibersdirectscellgrowthin2dand3d
AT framptonjp templatedassemblyofcollagenfibersdirectscellgrowthin2dand3d