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Characterization of Tissue Engineered Endothelial Cell Networks in Composite Collagen-Agarose Hydrogels

Scaffolds constitute an important element in vascularized tissues and are therefore investigated for providing the desired mechanical stability and enabling vasculogenesis and angiogenesis. In this study, supplementation of hydrogels containing either Matrigel(TM) and rat tail collagen I (Matrigel(T...

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Autores principales: Ichanti, Houda, Sladic, Sanja, Kalies, Stefan, Haverich, Axel, Andrée, Birgit, Hilfiker, Andres
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7559300/
https://www.ncbi.nlm.nih.gov/pubmed/32899293
http://dx.doi.org/10.3390/gels6030027
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author Ichanti, Houda
Sladic, Sanja
Kalies, Stefan
Haverich, Axel
Andrée, Birgit
Hilfiker, Andres
author_facet Ichanti, Houda
Sladic, Sanja
Kalies, Stefan
Haverich, Axel
Andrée, Birgit
Hilfiker, Andres
author_sort Ichanti, Houda
collection PubMed
description Scaffolds constitute an important element in vascularized tissues and are therefore investigated for providing the desired mechanical stability and enabling vasculogenesis and angiogenesis. In this study, supplementation of hydrogels containing either Matrigel(TM) and rat tail collagen I (Matrigel(TM)/rCOL) or human collagen (hCOL) with SeaPlaque(TM) agarose were analyzed with regard to construct thickness and formation and characteristics of endothelial cell (EC) networks compared to constructs without agarose. Additionally, the effect of increased rCOL content in Matrigel(TM)/rCOL constructs was studied. An increase of rCOL content from 1 mg/mL to 3 mg/mL resulted in an increase of construct thickness by approximately 160%. The high rCOL content, however, impaired the formation of an EC network. The supplementation of Matrigel(TM)/rCOL with agarose increased the thickness of the hydrogel construct by approximately 100% while supporting the formation of a stable EC network. The use of hCOL/agarose composite hydrogels led to a slight increase in the thickness of the 3D hydrogel construct and supported the formation of a multi-layered EC network compared to control constructs. Our findings suggest that agarose/collagen-based composite hydrogels are promising candidates for tissue engineering of vascularized constructs as cell viability is maintained and the formation of a stable and multi-layered EC network is supported.
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spelling pubmed-75593002020-10-29 Characterization of Tissue Engineered Endothelial Cell Networks in Composite Collagen-Agarose Hydrogels Ichanti, Houda Sladic, Sanja Kalies, Stefan Haverich, Axel Andrée, Birgit Hilfiker, Andres Gels Article Scaffolds constitute an important element in vascularized tissues and are therefore investigated for providing the desired mechanical stability and enabling vasculogenesis and angiogenesis. In this study, supplementation of hydrogels containing either Matrigel(TM) and rat tail collagen I (Matrigel(TM)/rCOL) or human collagen (hCOL) with SeaPlaque(TM) agarose were analyzed with regard to construct thickness and formation and characteristics of endothelial cell (EC) networks compared to constructs without agarose. Additionally, the effect of increased rCOL content in Matrigel(TM)/rCOL constructs was studied. An increase of rCOL content from 1 mg/mL to 3 mg/mL resulted in an increase of construct thickness by approximately 160%. The high rCOL content, however, impaired the formation of an EC network. The supplementation of Matrigel(TM)/rCOL with agarose increased the thickness of the hydrogel construct by approximately 100% while supporting the formation of a stable EC network. The use of hCOL/agarose composite hydrogels led to a slight increase in the thickness of the 3D hydrogel construct and supported the formation of a multi-layered EC network compared to control constructs. Our findings suggest that agarose/collagen-based composite hydrogels are promising candidates for tissue engineering of vascularized constructs as cell viability is maintained and the formation of a stable and multi-layered EC network is supported. MDPI 2020-09-03 /pmc/articles/PMC7559300/ /pubmed/32899293 http://dx.doi.org/10.3390/gels6030027 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ichanti, Houda
Sladic, Sanja
Kalies, Stefan
Haverich, Axel
Andrée, Birgit
Hilfiker, Andres
Characterization of Tissue Engineered Endothelial Cell Networks in Composite Collagen-Agarose Hydrogels
title Characterization of Tissue Engineered Endothelial Cell Networks in Composite Collagen-Agarose Hydrogels
title_full Characterization of Tissue Engineered Endothelial Cell Networks in Composite Collagen-Agarose Hydrogels
title_fullStr Characterization of Tissue Engineered Endothelial Cell Networks in Composite Collagen-Agarose Hydrogels
title_full_unstemmed Characterization of Tissue Engineered Endothelial Cell Networks in Composite Collagen-Agarose Hydrogels
title_short Characterization of Tissue Engineered Endothelial Cell Networks in Composite Collagen-Agarose Hydrogels
title_sort characterization of tissue engineered endothelial cell networks in composite collagen-agarose hydrogels
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7559300/
https://www.ncbi.nlm.nih.gov/pubmed/32899293
http://dx.doi.org/10.3390/gels6030027
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