A thermosensitive low molecular weight hydrogel as scaffold for tissue engineering
Hydrogels that are non-toxic, easy to use, cytocompatible, injectable and degradable are valuable biomaterials for tissue engineering and tissue repair. However, few compounds currently fulfil these requirements. In this study, we describe the biological properties of a new type of thermosensitive h...
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AO Research Institute Davos
2012-02-01
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Online Access: | http://www.ecmjournal.org/journal/papers/vol023/pdf/v023a11.pdf |
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doaj-f3fd88e7a7ed4a8285a019b7705b283d2020-11-24T21:07:48Zeng AO Research Institute DavosEuropean Cells & Materials1473-22622012-02-0123147160A thermosensitive low molecular weight hydrogel as scaffold for tissue engineeringS ZianeS SchlaubitzS MirauxA PatwaC LalandeI BilemS LepreuxB RousseauJ-F Le MeinsL LatxagueP BarthélémyO ChassandeHydrogels that are non-toxic, easy to use, cytocompatible, injectable and degradable are valuable biomaterials for tissue engineering and tissue repair. However, few compounds currently fulfil these requirements. In this study, we describe the biological properties of a new type of thermosensitive hydrogel based on low-molecular weight glycosyl-nucleosyl-fluorinated (GNF) compound. This gel forms within 25 min by self-assembly of monomers as temperature decreases. It degrades slowly in vitro and in vivo. It induces moderate chronic inflammation and is progressively invaded by host cells and vessels, suggesting good integration to the host environment. Although human adult mesenchymal stem cells derived from adipose tissue (ASC) cannot adhere on the gel surface or within a 3D gel scaffold, cell aggregates grow and differentiate normally when entrapped in the GNF-based gel. Moreover, this hydrogel stimulates osteoblast differentiation of ASC in the absence of osteogenic factors. When implanted in mice, gel-entrapped cell aggregates survive for several weeks in contrast with gel-free spheroids. They are maintained in their original site of implantation where they interact with the host tissue and adhere on the extracellular matrix. They can differentiate in situ into alkaline phosphatase positive osteoblasts, which deposit a calcium phosphate-rich matrix. When injected into subcutaneous sites, gel-encapsulated cells show similar biological properties as implanted gel-cells complexes. These data point GNF-based gels as a novel class of hydrogels with original properties, in particular osteogenic potential, susceptible of providing new therapeutic solutions especially for bone tissue engineering applications.http://www.ecmjournal.org/journal/papers/vol023/pdf/v023a11.pdfLow molecular weight gelsupramolecular assembliesnucleoside amphiphilesadipose tissue derived stem cellsbiocompatibility |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
S Ziane S Schlaubitz S Miraux A Patwa C Lalande I Bilem S Lepreux B Rousseau J-F Le Meins L Latxague P Barthélémy O Chassande |
spellingShingle |
S Ziane S Schlaubitz S Miraux A Patwa C Lalande I Bilem S Lepreux B Rousseau J-F Le Meins L Latxague P Barthélémy O Chassande A thermosensitive low molecular weight hydrogel as scaffold for tissue engineering European Cells & Materials Low molecular weight gel supramolecular assemblies nucleoside amphiphiles adipose tissue derived stem cells biocompatibility |
author_facet |
S Ziane S Schlaubitz S Miraux A Patwa C Lalande I Bilem S Lepreux B Rousseau J-F Le Meins L Latxague P Barthélémy O Chassande |
author_sort |
S Ziane |
title |
A thermosensitive low molecular weight hydrogel as scaffold for tissue engineering |
title_short |
A thermosensitive low molecular weight hydrogel as scaffold for tissue engineering |
title_full |
A thermosensitive low molecular weight hydrogel as scaffold for tissue engineering |
title_fullStr |
A thermosensitive low molecular weight hydrogel as scaffold for tissue engineering |
title_full_unstemmed |
A thermosensitive low molecular weight hydrogel as scaffold for tissue engineering |
title_sort |
thermosensitive low molecular weight hydrogel as scaffold for tissue engineering |
publisher |
AO Research Institute Davos |
series |
European Cells & Materials |
issn |
1473-2262 |
publishDate |
2012-02-01 |
description |
Hydrogels that are non-toxic, easy to use, cytocompatible, injectable and degradable are valuable biomaterials for tissue engineering and tissue repair. However, few compounds currently fulfil these requirements. In this study, we describe the biological properties of a new type of thermosensitive hydrogel based on low-molecular weight glycosyl-nucleosyl-fluorinated (GNF) compound. This gel forms within 25 min by self-assembly of monomers as temperature decreases. It degrades slowly in vitro and in vivo. It induces moderate chronic inflammation and is progressively invaded by host cells and vessels, suggesting good integration to the host environment. Although human adult mesenchymal stem cells derived from adipose tissue (ASC) cannot adhere on the gel surface or within a 3D gel scaffold, cell aggregates grow and differentiate normally when entrapped in the GNF-based gel. Moreover, this hydrogel stimulates osteoblast differentiation of ASC in the absence of osteogenic factors. When implanted in mice, gel-entrapped cell aggregates survive for several weeks in contrast with gel-free spheroids. They are maintained in their original site of implantation where they interact with the host tissue and adhere on the extracellular matrix. They can differentiate in situ into alkaline phosphatase positive osteoblasts, which deposit a calcium phosphate-rich matrix. When injected into subcutaneous sites, gel-encapsulated cells show similar biological properties as implanted gel-cells complexes. These data point GNF-based gels as a novel class of hydrogels with original properties, in particular osteogenic potential, susceptible of providing new therapeutic solutions especially for bone tissue engineering applications. |
topic |
Low molecular weight gel supramolecular assemblies nucleoside amphiphiles adipose tissue derived stem cells biocompatibility |
url |
http://www.ecmjournal.org/journal/papers/vol023/pdf/v023a11.pdf |
work_keys_str_mv |
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