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Strategies for the hypothermic preservation of cell sheets of human adipose stem cells

Cell Sheet (CS) Engineering is a regenerative medicine strategy proposed for the treatment of injured or diseased organs and tissues. In fact, several clinical trials are underway using CS-based methodologies. However, the clinical application of such cell-based methodologies poses several challenge...

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Autores principales: Freitas-Ribeiro, Sara, Carvalho, Andreia Filipa, Costa, Marina, Cerqueira, Mariana Teixeira, Marques, Alexandra Pinto, Reis, Rui Luís, Pirraco, Rogério Pedro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6793945/
https://www.ncbi.nlm.nih.gov/pubmed/31613935
http://dx.doi.org/10.1371/journal.pone.0222597
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author Freitas-Ribeiro, Sara
Carvalho, Andreia Filipa
Costa, Marina
Cerqueira, Mariana Teixeira
Marques, Alexandra Pinto
Reis, Rui Luís
Pirraco, Rogério Pedro
author_facet Freitas-Ribeiro, Sara
Carvalho, Andreia Filipa
Costa, Marina
Cerqueira, Mariana Teixeira
Marques, Alexandra Pinto
Reis, Rui Luís
Pirraco, Rogério Pedro
author_sort Freitas-Ribeiro, Sara
collection PubMed
description Cell Sheet (CS) Engineering is a regenerative medicine strategy proposed for the treatment of injured or diseased organs and tissues. In fact, several clinical trials are underway using CS-based methodologies. However, the clinical application of such cell-based methodologies poses several challenges related with the preservation of CS structure and function from the fabrication site to the bedside. Pausing cells at hypothermic temperatures has been suggested as a valuable method for short-term cell preservation. In this study, we tested the efficiency of two preservation strategies, one using culture medium supplementation with Rokepie and the other using the preservation solution Hypothermosol, in preserving human adipose stromal/stem cells (hASC) CS-like confluent cultures at 4°C, during 3 and 7 days. Both preservation strategies demonstrated excellent ability to preserve cell function during the first 3 days in hypothermia, as demonstrated by metabolic activity results and assessment of extracellular matrix integrity and differentiation potential. At the end of the 7(th) day of hypothermic incubation, the decrease in cell metabolic activity was more evident for all conditions. Nonetheless, hASC incubated with Rokepie and Hypothermosol retained a higher metabolic activity and extracellular matrix integrity in comparison with unsupplemented cells. Differentiation results for the later time point showed that supplementation with both Rokepie and Hypothermosol rescued adipogenic differentiation potential but only Rokepie was able to preserve hASC osteogenic potential.
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spelling pubmed-67939452019-10-25 Strategies for the hypothermic preservation of cell sheets of human adipose stem cells Freitas-Ribeiro, Sara Carvalho, Andreia Filipa Costa, Marina Cerqueira, Mariana Teixeira Marques, Alexandra Pinto Reis, Rui Luís Pirraco, Rogério Pedro PLoS One Research Article Cell Sheet (CS) Engineering is a regenerative medicine strategy proposed for the treatment of injured or diseased organs and tissues. In fact, several clinical trials are underway using CS-based methodologies. However, the clinical application of such cell-based methodologies poses several challenges related with the preservation of CS structure and function from the fabrication site to the bedside. Pausing cells at hypothermic temperatures has been suggested as a valuable method for short-term cell preservation. In this study, we tested the efficiency of two preservation strategies, one using culture medium supplementation with Rokepie and the other using the preservation solution Hypothermosol, in preserving human adipose stromal/stem cells (hASC) CS-like confluent cultures at 4°C, during 3 and 7 days. Both preservation strategies demonstrated excellent ability to preserve cell function during the first 3 days in hypothermia, as demonstrated by metabolic activity results and assessment of extracellular matrix integrity and differentiation potential. At the end of the 7(th) day of hypothermic incubation, the decrease in cell metabolic activity was more evident for all conditions. Nonetheless, hASC incubated with Rokepie and Hypothermosol retained a higher metabolic activity and extracellular matrix integrity in comparison with unsupplemented cells. Differentiation results for the later time point showed that supplementation with both Rokepie and Hypothermosol rescued adipogenic differentiation potential but only Rokepie was able to preserve hASC osteogenic potential. Public Library of Science 2019-10-15 /pmc/articles/PMC6793945/ /pubmed/31613935 http://dx.doi.org/10.1371/journal.pone.0222597 Text en © 2019 Freitas-Ribeiro et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Freitas-Ribeiro, Sara
Carvalho, Andreia Filipa
Costa, Marina
Cerqueira, Mariana Teixeira
Marques, Alexandra Pinto
Reis, Rui Luís
Pirraco, Rogério Pedro
Strategies for the hypothermic preservation of cell sheets of human adipose stem cells
title Strategies for the hypothermic preservation of cell sheets of human adipose stem cells
title_full Strategies for the hypothermic preservation of cell sheets of human adipose stem cells
title_fullStr Strategies for the hypothermic preservation of cell sheets of human adipose stem cells
title_full_unstemmed Strategies for the hypothermic preservation of cell sheets of human adipose stem cells
title_short Strategies for the hypothermic preservation of cell sheets of human adipose stem cells
title_sort strategies for the hypothermic preservation of cell sheets of human adipose stem cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6793945/
https://www.ncbi.nlm.nih.gov/pubmed/31613935
http://dx.doi.org/10.1371/journal.pone.0222597
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