Towards in vitro vascularisation of collagen-GAG scaffolds

Collagen-glycosaminoglycan scaffolds that have been used clinically for skin regeneration have also shown significant promise for other applications in tissue engineering. However, regeneration of thicker tissues with the aid of implanted biomaterials is likely to depend on, or be accelerated by, th...

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Main Authors: GP Duffy, TM McFadden, EM Byrne, S-L Gill, E Farrell, FJ O’Brien
Format: Article
Language:English
Published: AO Research Institute Davos 2011-01-01
Series:European Cells & Materials
Subjects:
Online Access:http://www.ecmjournal.org/journal/papers/vol021/pdf/v021a02.pdf
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spelling doaj-93bd1909cb3e4f2b976d8593414df1c12020-11-24T21:07:48Zeng AO Research Institute DavosEuropean Cells & Materials1473-22622011-01-01211530Towards in vitro vascularisation of collagen-GAG scaffoldsGP DuffyTM McFaddenEM ByrneS-L GillE FarrellFJ O’BrienCollagen-glycosaminoglycan scaffolds that have been used clinically for skin regeneration have also shown significant promise for other applications in tissue engineering. However, regeneration of thicker tissues with the aid of implanted biomaterials is likely to depend on, or be accelerated by, the ability to establish rapid vascularisation of the implant. The present study aims to establish a nascent vascular network in vitro within a CG scaffold as a first step towards that goal. Mesenchymal stem cells (MSCs) were chosen as primary vasculogenic candidate cells and a culture medium that promoted maximal network formation on Matrigel by these cells was selected. MSCs seeded in the CG scaffold formed networks of cord-like structures after one to two weeks in the presence of the vasculogenic medium; similar structures were formed by aortic endothelial cells (ECs) cultured for comparison. Gene expression analysis suggested that the MSCs began to adopt an endothelial phenotype, with RNA for PECAM and VCAM rising while that for alpha-smooth muscle actin fell. However there was no increase in Tie-2 and vWF expression. Addition of smooth muscle cells (SMCs) as a potential perivascular stabilising component did not have a noticeable effect on MSC-derived networks, although it enhanced EC-derived structures.http://www.ecmjournal.org/journal/papers/vol021/pdf/v021a02.pdfTissue engineeringcollagen-GAG scaffoldpre-vascularisationmesenchymal stem cellsendothelial cellssmooth muscle cellsco-culture
collection DOAJ
language English
format Article
sources DOAJ
author GP Duffy
TM McFadden
EM Byrne
S-L Gill
E Farrell
FJ O’Brien
spellingShingle GP Duffy
TM McFadden
EM Byrne
S-L Gill
E Farrell
FJ O’Brien
Towards in vitro vascularisation of collagen-GAG scaffolds
European Cells & Materials
Tissue engineering
collagen-GAG scaffold
pre-vascularisation
mesenchymal stem cells
endothelial cells
smooth muscle cells
co-culture
author_facet GP Duffy
TM McFadden
EM Byrne
S-L Gill
E Farrell
FJ O’Brien
author_sort GP Duffy
title Towards in vitro vascularisation of collagen-GAG scaffolds
title_short Towards in vitro vascularisation of collagen-GAG scaffolds
title_full Towards in vitro vascularisation of collagen-GAG scaffolds
title_fullStr Towards in vitro vascularisation of collagen-GAG scaffolds
title_full_unstemmed Towards in vitro vascularisation of collagen-GAG scaffolds
title_sort towards in vitro vascularisation of collagen-gag scaffolds
publisher AO Research Institute Davos
series European Cells & Materials
issn 1473-2262
publishDate 2011-01-01
description Collagen-glycosaminoglycan scaffolds that have been used clinically for skin regeneration have also shown significant promise for other applications in tissue engineering. However, regeneration of thicker tissues with the aid of implanted biomaterials is likely to depend on, or be accelerated by, the ability to establish rapid vascularisation of the implant. The present study aims to establish a nascent vascular network in vitro within a CG scaffold as a first step towards that goal. Mesenchymal stem cells (MSCs) were chosen as primary vasculogenic candidate cells and a culture medium that promoted maximal network formation on Matrigel by these cells was selected. MSCs seeded in the CG scaffold formed networks of cord-like structures after one to two weeks in the presence of the vasculogenic medium; similar structures were formed by aortic endothelial cells (ECs) cultured for comparison. Gene expression analysis suggested that the MSCs began to adopt an endothelial phenotype, with RNA for PECAM and VCAM rising while that for alpha-smooth muscle actin fell. However there was no increase in Tie-2 and vWF expression. Addition of smooth muscle cells (SMCs) as a potential perivascular stabilising component did not have a noticeable effect on MSC-derived networks, although it enhanced EC-derived structures.
topic Tissue engineering
collagen-GAG scaffold
pre-vascularisation
mesenchymal stem cells
endothelial cells
smooth muscle cells
co-culture
url http://www.ecmjournal.org/journal/papers/vol021/pdf/v021a02.pdf
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