Development and angiogenic potential of cell-derived microtissues using microcarrier-template

Tissue engineering and regenerative medicine approaches use biomaterials in combination with cells to regenerate lost functions of tissues and organs to prevent organ transplantation. However, most of the current strategies fail in mimicking the tissue’s extracellular matrix properties. In order to...

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Detalles Bibliográficos
Autores: Rubí Sans, Gerard|||0000-0003-2782-8716, Cano Garcia, Irene, Pérez Amodio, Soledad Graciela|||0000-0001-6825-0194, Blanco, Bárbara, Mateos Timoneda, Miguel Ángel|||0000-0001-7657-1414, Engel López, Elisabeth|||0000-0003-4855-8874
Tipo de recurso: artículo
Fecha de publicación:2021
País:España
Institución:Universitat Politècnica de Catalunya (UPC)
Repositorio:UPCommons. Portal del coneixement obert de la UPC
Idioma:inglés
OAI Identifier:oai:upcommons.upc.edu:2117/351411
Acceso en línea:https://hdl.handle.net/2117/351411
https://dx.doi.org/10.3390/biomedicines9030232
Access Level:acceso abierto
Palabra clave:Tissue engineering
Regenerative medicine
Biomedical materials
Poly-lactic acid microcarriers
Cultispher® S
Rat bone marrow mesenchymal stem cells
Microtissue
Cell-derived matrix
Angiogenesis
Enginyeria de teixits
Medicina regenerativa
Materials biomèdics
Àrees temàtiques de la UPC::Enginyeria dels materials
Descripción
Sumario:Tissue engineering and regenerative medicine approaches use biomaterials in combination with cells to regenerate lost functions of tissues and organs to prevent organ transplantation. However, most of the current strategies fail in mimicking the tissue’s extracellular matrix properties. In order to mimic native tissue conditions, we developed cell-derived matrix (CDM) microtissues (MT). Our methodology uses poly-lactic acid (PLA) and Cultispher® S microcarriers’ (MCs’) as scaffold templates, which are seeded with rat bone marrow mesenchymal stem cells (rBM-MSCs). The scaffold template allows cells to generate an extracellular matrix, which is then extracted for downstream use. The newly formed CDM provides cells with a complex physical (MT architecture) and biochemical (deposited ECM proteins) environment, also showing spontaneous angiogenic potential. Our results suggest that MTs generated from the combination of these two MCs (mixed MTs) are excellent candidates for tissue vascularization. Overall, this study provides a methodology for in-house fabrication of microtissues with angiogenic potential for downstream use in various tissue regenerative strategies.