Influence of scaffold morphology on co-cultures of human endothelial and adipose tissue-derived stem cells

[EN] The interior of tissue engineering scaffolds must be vascularizable and allow adequate nutrients perfusion in order to ensure the viability of the cells colonizing them. The promotion of rapid vascularization of scaffolds is critical for thick artificial constructs. In the present study co-cult...

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Detalles Bibliográficos
Autores: Arnal Pastor, María Pilar, Martínez-Ramos, Cristina|||0000-0002-6540-4714, Vallés Lluch, Ana|||0000-0002-7896-8666, Monleón Pradas, Manuel|||0000-0001-6457-0414
Tipo de recurso: artículo
Fecha de publicación:2016
País:España
Institución:Universitat Politècnica de València (UPV)
Repositorio:RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
Idioma:inglés
OAI Identifier:oai:riunet.upv.es:10251/106289
Acceso en línea:https://riunet.upv.es/handle/10251/106289
Access Level:acceso abierto
Palabra clave:Scaffolds
Self-assembling peptide
HUVECs
hADSCs
Endothelial markers
MAQUINAS Y MOTORES TERMICOS
TERMODINAMICA APLICADA (UPV)
Descripción
Sumario:[EN] The interior of tissue engineering scaffolds must be vascularizable and allow adequate nutrients perfusion in order to ensure the viability of the cells colonizing them. The promotion of rapid vascularization of scaffolds is critical for thick artificial constructs. In the present study co-cultures of human endothelial and adipose tissue-derived stem cells have been performed in poly(ethyl acrylate) scaffolds with two different pore structures: grid-like (PEA-o) or sponge-like (PEA-s), in combination with a self-assembling peptide gel filling the pores, which aims to mimic the physiological niche. After 2 and 7 culture days, cell adhesion, proliferation and migration, the expression of cell surface markers like CD31 and CD90 and the release of VEGF were assessed by means of immunocytochemistry, scanning electronic microscopy, flow cytometry and ELISA analyses. The study demonstrated that PEA-s scaffolds promoted greater cell organization into tubular-like structures than PEA-o scaffolds, and this was enhanced by the presence of the peptide gel. Paracrine signaling from adipose cells significantly improved endothelial cell viability, proving the advantageous combination of this system for obtaining easily vascularizable tissue engineered grafts.