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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8025087/ https://www.ncbi.nlm.nih.gov/pubmed/33669131 http://dx.doi.org/10.3390/biomedicines9030232 |
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author | Rubí-Sans, Gerard Cano-Torres, Irene Pérez-Amodio, Soledad Blanco-Fernandez, Barbara Mateos-Timoneda, Miguel A. Engel, Elisabeth |
author_facet | Rubí-Sans, Gerard Cano-Torres, Irene Pérez-Amodio, Soledad Blanco-Fernandez, Barbara Mateos-Timoneda, Miguel A. Engel, Elisabeth |
author_sort | Rubí-Sans, Gerard |
collection | PubMed |
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(®) 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. |
format | Online Article Text |
id | pubmed-8025087 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-80250872021-04-08 Development and Angiogenic Potential of Cell-Derived Microtissues Using Microcarrier-Template Rubí-Sans, Gerard Cano-Torres, Irene Pérez-Amodio, Soledad Blanco-Fernandez, Barbara Mateos-Timoneda, Miguel A. Engel, Elisabeth Biomedicines Article 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. MDPI 2021-02-25 /pmc/articles/PMC8025087/ /pubmed/33669131 http://dx.doi.org/10.3390/biomedicines9030232 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) ). |
spellingShingle | Article Rubí-Sans, Gerard Cano-Torres, Irene Pérez-Amodio, Soledad Blanco-Fernandez, Barbara Mateos-Timoneda, Miguel A. Engel, Elisabeth Development and Angiogenic Potential of Cell-Derived Microtissues Using Microcarrier-Template |
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 | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8025087/ https://www.ncbi.nlm.nih.gov/pubmed/33669131 http://dx.doi.org/10.3390/biomedicines9030232 |
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