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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...

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Autores principales: Peña, Brisa, Martinelli, Valentina, Jeong, Mark, Bosi, Susanna, Lapasin, Romano, Taylor, Matthew R. G., Long, Carlin S., Shandas, Robin, Park, Daewon, Mestroni, Luisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2016
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.
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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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