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Biomimetic Polymers for Cardiac Tissue Engineering
[Image: see text] Heart failure is a morbid disorder characterized by progressive cardiomyocyte (CM) dysfunction and death. Interest in cell-based therapies is growing, but sustainability of injected CMs remains a challenge. To mitigate this, we developed an injectable biomimetic Reverse Thermal Gel...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4863197/ https://www.ncbi.nlm.nih.gov/pubmed/27073119 http://dx.doi.org/10.1021/acs.biomac.5b01734 |
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author | Peña, Brisa Martinelli, Valentina Jeong, Mark Bosi, Susanna Lapasin, Romano Taylor, Matthew R. G. Long, Carlin S. Shandas, Robin Park, Daewon Mestroni, Luisa |
author_facet | Peña, Brisa Martinelli, Valentina Jeong, Mark Bosi, Susanna Lapasin, Romano Taylor, Matthew R. G. Long, Carlin S. Shandas, Robin Park, Daewon Mestroni, Luisa |
author_sort | Peña, Brisa |
collection | PubMed |
description | [Image: see text] Heart failure is a morbid disorder characterized by progressive cardiomyocyte (CM) dysfunction and death. Interest in cell-based therapies is growing, but sustainability of injected CMs remains a challenge. To mitigate this, we developed an injectable biomimetic Reverse Thermal Gel (RTG) specifically engineered to support long-term CM survival. This RTG biopolymer provided a solution-based delivery vehicle of CMs, which transitioned to a gel-based matrix shortly after reaching body temperature. In this study we tested the suitability of this biopolymer to sustain CM viability. The RTG was biomolecule-functionalized with poly-l-lysine or laminin. Neonatal rat ventricular myocytes (NRVM) and adult rat ventricular myocytes (ARVM) were cultured in plain-RTG and biomolecule-functionalized-RTG both under 3-dimensional (3D) conditions. Traditional 2D biomolecule-coated dishes were used as controls. We found that the RTG-lysine stimulated NRVM to spread and form heart-like functional syncytia. Regarding cell contraction, in both RTG and RTG-lysine, beating cells were recorded after 21 days. Additionally, more than 50% (p value < 0.05; n = 5) viable ARVMs, characterized by a well-defined cardiac phenotype represented by sarcomeric cross-striations, were found in the RTG-laminin after 8 days. These results exhibit the tremendous potential of a minimally invasive CM transplantation through our designed RTG-cell therapy platform. |
format | Online Article Text |
id | pubmed-4863197 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-48631972016-05-12 Biomimetic Polymers for Cardiac Tissue Engineering Peña, Brisa Martinelli, Valentina Jeong, Mark Bosi, Susanna Lapasin, Romano Taylor, Matthew R. G. Long, Carlin S. Shandas, Robin Park, Daewon Mestroni, Luisa Biomacromolecules [Image: see text] Heart failure is a morbid disorder characterized by progressive cardiomyocyte (CM) dysfunction and death. Interest in cell-based therapies is growing, but sustainability of injected CMs remains a challenge. To mitigate this, we developed an injectable biomimetic Reverse Thermal Gel (RTG) specifically engineered to support long-term CM survival. This RTG biopolymer provided a solution-based delivery vehicle of CMs, which transitioned to a gel-based matrix shortly after reaching body temperature. In this study we tested the suitability of this biopolymer to sustain CM viability. The RTG was biomolecule-functionalized with poly-l-lysine or laminin. Neonatal rat ventricular myocytes (NRVM) and adult rat ventricular myocytes (ARVM) were cultured in plain-RTG and biomolecule-functionalized-RTG both under 3-dimensional (3D) conditions. Traditional 2D biomolecule-coated dishes were used as controls. We found that the RTG-lysine stimulated NRVM to spread and form heart-like functional syncytia. Regarding cell contraction, in both RTG and RTG-lysine, beating cells were recorded after 21 days. Additionally, more than 50% (p value < 0.05; n = 5) viable ARVMs, characterized by a well-defined cardiac phenotype represented by sarcomeric cross-striations, were found in the RTG-laminin after 8 days. These results exhibit the tremendous potential of a minimally invasive CM transplantation through our designed RTG-cell therapy platform. American Chemical Society 2016-04-13 2016-05-09 /pmc/articles/PMC4863197/ /pubmed/27073119 http://dx.doi.org/10.1021/acs.biomac.5b01734 Text en Copyright © 2016 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Peña, Brisa Martinelli, Valentina Jeong, Mark Bosi, Susanna Lapasin, Romano Taylor, Matthew R. G. Long, Carlin S. Shandas, Robin Park, Daewon Mestroni, Luisa Biomimetic Polymers for Cardiac Tissue Engineering |
title | Biomimetic Polymers for Cardiac Tissue Engineering |
title_full | Biomimetic Polymers for Cardiac Tissue Engineering |
title_fullStr | Biomimetic Polymers for Cardiac Tissue Engineering |
title_full_unstemmed | Biomimetic Polymers for Cardiac Tissue Engineering |
title_short | Biomimetic Polymers for Cardiac Tissue Engineering |
title_sort | biomimetic polymers for cardiac tissue engineering |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4863197/ https://www.ncbi.nlm.nih.gov/pubmed/27073119 http://dx.doi.org/10.1021/acs.biomac.5b01734 |
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