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Artificial membrane-binding proteins stimulate oxygenation of stem cells during engineering of large cartilage tissue
Restricted oxygen diffusion can result in central cell necrosis in engineered tissue, a problem that is exacerbated when engineering large tissue constructs for clinical application. Here we show that pre-treating human mesenchymal stem cells (hMSCs) with synthetic membrane-active myoglobin-polymer–...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4557285/ https://www.ncbi.nlm.nih.gov/pubmed/26080734 http://dx.doi.org/10.1038/ncomms8405 |
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author | Armstrong, James P. K. Shakur, Rameen Horne, Joseph P. Dickinson, Sally C. Armstrong, Craig T. Lau, Katherine Kadiwala, Juned Lowe, Robert Seddon, Annela Mann, Stephen Anderson, J. L. Ross Perriman, Adam W. Hollander, Anthony P. |
author_facet | Armstrong, James P. K. Shakur, Rameen Horne, Joseph P. Dickinson, Sally C. Armstrong, Craig T. Lau, Katherine Kadiwala, Juned Lowe, Robert Seddon, Annela Mann, Stephen Anderson, J. L. Ross Perriman, Adam W. Hollander, Anthony P. |
author_sort | Armstrong, James P. K. |
collection | PubMed |
description | Restricted oxygen diffusion can result in central cell necrosis in engineered tissue, a problem that is exacerbated when engineering large tissue constructs for clinical application. Here we show that pre-treating human mesenchymal stem cells (hMSCs) with synthetic membrane-active myoglobin-polymer–surfactant complexes can provide a reservoir of oxygen capable of alleviating necrosis at the centre of hyaline cartilage. This is achieved through the development of a new cell functionalization methodology based on polymer–surfactant conjugation, which allows the delivery of functional proteins to the hMSC membrane. This new approach circumvents the need for cell surface engineering using protein chimerization or genetic transfection, and we demonstrate that the surface-modified hMSCs retain their ability to proliferate and to undergo multilineage differentiation. The functionalization technology is facile, versatile and non-disruptive, and in addition to tissue oxygenation, it should have far-reaching application in a host of tissue engineering and cell-based therapies. |
format | Online Article Text |
id | pubmed-4557285 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-45572852015-09-11 Artificial membrane-binding proteins stimulate oxygenation of stem cells during engineering of large cartilage tissue Armstrong, James P. K. Shakur, Rameen Horne, Joseph P. Dickinson, Sally C. Armstrong, Craig T. Lau, Katherine Kadiwala, Juned Lowe, Robert Seddon, Annela Mann, Stephen Anderson, J. L. Ross Perriman, Adam W. Hollander, Anthony P. Nat Commun Article Restricted oxygen diffusion can result in central cell necrosis in engineered tissue, a problem that is exacerbated when engineering large tissue constructs for clinical application. Here we show that pre-treating human mesenchymal stem cells (hMSCs) with synthetic membrane-active myoglobin-polymer–surfactant complexes can provide a reservoir of oxygen capable of alleviating necrosis at the centre of hyaline cartilage. This is achieved through the development of a new cell functionalization methodology based on polymer–surfactant conjugation, which allows the delivery of functional proteins to the hMSC membrane. This new approach circumvents the need for cell surface engineering using protein chimerization or genetic transfection, and we demonstrate that the surface-modified hMSCs retain their ability to proliferate and to undergo multilineage differentiation. The functionalization technology is facile, versatile and non-disruptive, and in addition to tissue oxygenation, it should have far-reaching application in a host of tissue engineering and cell-based therapies. Nature Pub. Group 2015-06-17 /pmc/articles/PMC4557285/ /pubmed/26080734 http://dx.doi.org/10.1038/ncomms8405 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Armstrong, James P. K. Shakur, Rameen Horne, Joseph P. Dickinson, Sally C. Armstrong, Craig T. Lau, Katherine Kadiwala, Juned Lowe, Robert Seddon, Annela Mann, Stephen Anderson, J. L. Ross Perriman, Adam W. Hollander, Anthony P. Artificial membrane-binding proteins stimulate oxygenation of stem cells during engineering of large cartilage tissue |
title | Artificial membrane-binding proteins stimulate oxygenation of stem cells during engineering of large cartilage tissue |
title_full | Artificial membrane-binding proteins stimulate oxygenation of stem cells during engineering of large cartilage tissue |
title_fullStr | Artificial membrane-binding proteins stimulate oxygenation of stem cells during engineering of large cartilage tissue |
title_full_unstemmed | Artificial membrane-binding proteins stimulate oxygenation of stem cells during engineering of large cartilage tissue |
title_short | Artificial membrane-binding proteins stimulate oxygenation of stem cells during engineering of large cartilage tissue |
title_sort | artificial membrane-binding proteins stimulate oxygenation of stem cells during engineering of large cartilage tissue |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4557285/ https://www.ncbi.nlm.nih.gov/pubmed/26080734 http://dx.doi.org/10.1038/ncomms8405 |
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