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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Main Authors: Gerard Rubí-Sans, Irene Cano-Torres, Soledad Pérez-Amodio, Barbara Blanco-Fernandez, Miguel A. Mateos-Timoneda, Elisabeth Engel
Format: Article
Language:English
Published: MDPI AG 2021-02-01
Series:Biomedicines
Subjects:
Online Access:https://www.mdpi.com/2227-9059/9/3/232
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author Gerard Rubí-Sans
Irene Cano-Torres
Soledad Pérez-Amodio
Barbara Blanco-Fernandez
Miguel A. Mateos-Timoneda
Elisabeth Engel
author_facet Gerard Rubí-Sans
Irene Cano-Torres
Soledad Pérez-Amodio
Barbara Blanco-Fernandez
Miguel A. Mateos-Timoneda
Elisabeth Engel
author_sort Gerard Rubí-Sans
collection DOAJ
description 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<sup>®</sup> 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.
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spelling doaj.art-cb51f069809b441283872f180cb895082023-12-11T18:28:36ZengMDPI AGBiomedicines2227-90592021-02-019323210.3390/biomedicines9030232Development and Angiogenic Potential of Cell-Derived Microtissues Using Microcarrier-TemplateGerard Rubí-Sans0Irene Cano-Torres1Soledad Pérez-Amodio2Barbara Blanco-Fernandez3Miguel A. Mateos-Timoneda4Elisabeth Engel5Biomaterials for Regenerative Therapies Group, Institute for Bioengineering of Catalonia (IBEC), The Barcelona Institute of Science and Technology (BIST), 08028 Barcelona, SpainBiomaterials for Regenerative Therapies Group, Institute for Bioengineering of Catalonia (IBEC), The Barcelona Institute of Science and Technology (BIST), 08028 Barcelona, SpainBiomaterials for Regenerative Therapies Group, Institute for Bioengineering of Catalonia (IBEC), The Barcelona Institute of Science and Technology (BIST), 08028 Barcelona, SpainBiomaterials for Regenerative Therapies Group, Institute for Bioengineering of Catalonia (IBEC), The Barcelona Institute of Science and Technology (BIST), 08028 Barcelona, SpainBiomaterials for Regenerative Therapies Group, Institute for Bioengineering of Catalonia (IBEC), The Barcelona Institute of Science and Technology (BIST), 08028 Barcelona, SpainBiomaterials for Regenerative Therapies Group, Institute for Bioengineering of Catalonia (IBEC), The Barcelona Institute of Science and Technology (BIST), 08028 Barcelona, SpainTissue 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<sup>®</sup> 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.https://www.mdpi.com/2227-9059/9/3/232poly-lactic acid microcarriersCultispher<sup>®</sup> Srat bone marrow mesenchymal stem cellsmicrotissuecell-derived matrixangiogenesis
spellingShingle Gerard Rubí-Sans
Irene Cano-Torres
Soledad Pérez-Amodio
Barbara Blanco-Fernandez
Miguel A. Mateos-Timoneda
Elisabeth Engel
Development and Angiogenic Potential of Cell-Derived Microtissues Using Microcarrier-Template
Biomedicines
poly-lactic acid microcarriers
Cultispher<sup>®</sup> S
rat bone marrow mesenchymal stem cells
microtissue
cell-derived matrix
angiogenesis
title Development and Angiogenic Potential of Cell-Derived Microtissues Using Microcarrier-Template
title_full Development and Angiogenic Potential of Cell-Derived Microtissues Using Microcarrier-Template
title_fullStr Development and Angiogenic Potential of Cell-Derived Microtissues Using Microcarrier-Template
title_full_unstemmed Development and Angiogenic Potential of Cell-Derived Microtissues Using Microcarrier-Template
title_short Development and Angiogenic Potential of Cell-Derived Microtissues Using Microcarrier-Template
title_sort development and angiogenic potential of cell derived microtissues using microcarrier template
topic poly-lactic acid microcarriers
Cultispher<sup>®</sup> S
rat bone marrow mesenchymal stem cells
microtissue
cell-derived matrix
angiogenesis
url https://www.mdpi.com/2227-9059/9/3/232
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