Artificial membrane-binding proteins stimulate oxygenation of stem cells during engineering of large cartilage tissue
Author(s)
Type
Journal Article
Abstract
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.
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.
Date Issued
2015-06-17
Date Acceptance
2015-05-06
Citation
Nature Communications, 2015, 6
ISSN
2041-1723
Publisher
Nature Publishing Group
Journal / Book Title
Nature Communications
Volume
6
Copyright Statement
This work is licensed under a Creative Commons Attribution 4.0
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users will need to obtain permission from the license holder to reproduce the material.
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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/
License URL
Subjects
Science & Technology
Multidisciplinary Sciences
Science & Technology - Other Topics
MYOGLOBIN EXPRESSION
HYPOXIA
CONSTRUCTS
SCAFFOLDS
SURVIVAL
BONE
Escherichia coli
Glycolates
Humans
Hyaline Cartilage
Mesenchymal Stromal Cells
Myoglobin
Oxygen
Tissue Engineering
MD Multidisciplinary
Publication Status
Published
Article Number
7405