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Bone and cartilage differentiation of a single stem cell population driven by material interface

Adult stem cells, such as mesenchymal stem cells, are a multipotent cell source able to differentiate towards multiple cell types. While used widely in tissue engineering and biomaterials research, they present inherent donor variability and functionalities. In addition, their potential to form mult...

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Autores principales: Donnelly, Hannah, Smith, Carol-Anne, Sweeten, Paula E, Gadegaard, Nikolaj, Meek, RM Dominic, D’Este, Matteo, Mata, Alvaro, Eglin, David, Dalby, Matthew J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5438107/
https://www.ncbi.nlm.nih.gov/pubmed/28567273
http://dx.doi.org/10.1177/2041731417705615
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author Donnelly, Hannah
Smith, Carol-Anne
Sweeten, Paula E
Gadegaard, Nikolaj
Meek, RM Dominic
D’Este, Matteo
Mata, Alvaro
Eglin, David
Dalby, Matthew J
author_facet Donnelly, Hannah
Smith, Carol-Anne
Sweeten, Paula E
Gadegaard, Nikolaj
Meek, RM Dominic
D’Este, Matteo
Mata, Alvaro
Eglin, David
Dalby, Matthew J
author_sort Donnelly, Hannah
collection PubMed
description Adult stem cells, such as mesenchymal stem cells, are a multipotent cell source able to differentiate towards multiple cell types. While used widely in tissue engineering and biomaterials research, they present inherent donor variability and functionalities. In addition, their potential to form multiple tissues is rarely exploited. Here, we combine an osteogenic nanotopography and a chondrogenic hyaluronan hydrogel with the hypothesis that we can make a complex tissue from a single multipotent cell source with the exemplar of creating a three-dimensional bone–cartilage boundary environment. Marrow stromal cells were seeded onto the topographical surface and the temperature gelling hydrogel laid on top. Cells that remained on the nanotopography spread and formed osteoblast-like cells, while those that were seeded into or migrated into the gel remained rounded and expressed chondrogenic markers. This novel, simple interfacial environment provides a platform for anisotropic differentiation of cells from a single source, which could ultimately be exploited to sort osteogenic and chondrogenic progenitor cells from a marrow stromal cell population and to develop a tissue engineered interface.
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spelling pubmed-54381072017-05-31 Bone and cartilage differentiation of a single stem cell population driven by material interface Donnelly, Hannah Smith, Carol-Anne Sweeten, Paula E Gadegaard, Nikolaj Meek, RM Dominic D’Este, Matteo Mata, Alvaro Eglin, David Dalby, Matthew J J Tissue Eng Tissue Engineering Biomimetic Micro-environments to Direct Cell Function Adult stem cells, such as mesenchymal stem cells, are a multipotent cell source able to differentiate towards multiple cell types. While used widely in tissue engineering and biomaterials research, they present inherent donor variability and functionalities. In addition, their potential to form multiple tissues is rarely exploited. Here, we combine an osteogenic nanotopography and a chondrogenic hyaluronan hydrogel with the hypothesis that we can make a complex tissue from a single multipotent cell source with the exemplar of creating a three-dimensional bone–cartilage boundary environment. Marrow stromal cells were seeded onto the topographical surface and the temperature gelling hydrogel laid on top. Cells that remained on the nanotopography spread and formed osteoblast-like cells, while those that were seeded into or migrated into the gel remained rounded and expressed chondrogenic markers. This novel, simple interfacial environment provides a platform for anisotropic differentiation of cells from a single source, which could ultimately be exploited to sort osteogenic and chondrogenic progenitor cells from a marrow stromal cell population and to develop a tissue engineered interface. SAGE Publications 2017-05-15 /pmc/articles/PMC5438107/ /pubmed/28567273 http://dx.doi.org/10.1177/2041731417705615 Text en © The Author(s) 2017 http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution 4.0 License (http://www.creativecommons.org/licenses/by/4.0/) which permits any 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 Tissue Engineering Biomimetic Micro-environments to Direct Cell Function
Donnelly, Hannah
Smith, Carol-Anne
Sweeten, Paula E
Gadegaard, Nikolaj
Meek, RM Dominic
D’Este, Matteo
Mata, Alvaro
Eglin, David
Dalby, Matthew J
Bone and cartilage differentiation of a single stem cell population driven by material interface
title Bone and cartilage differentiation of a single stem cell population driven by material interface
title_full Bone and cartilage differentiation of a single stem cell population driven by material interface
title_fullStr Bone and cartilage differentiation of a single stem cell population driven by material interface
title_full_unstemmed Bone and cartilage differentiation of a single stem cell population driven by material interface
title_short Bone and cartilage differentiation of a single stem cell population driven by material interface
title_sort bone and cartilage differentiation of a single stem cell population driven by material interface
topic Tissue Engineering Biomimetic Micro-environments to Direct Cell Function
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5438107/
https://www.ncbi.nlm.nih.gov/pubmed/28567273
http://dx.doi.org/10.1177/2041731417705615
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