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Neoinnervation and neovascularization of acellular pericardial-derived scaffolds in myocardial infarcts

Engineered bioimplants for cardiac repair require functional vascularization and innervation for proper integration with the surrounding myocardium. The aim of this work was to study nerve sprouting and neovascularization in an acellular pericardial-derived scaffold used as a myocardial bioimplant....

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Autores principales: Gálvez-Montón, Carolina, Fernandez-Figueras, M. Teresa, Martí, Mercè, Soler-Botija, Carolina, Roura, Santiago, Perea-Gil, Isaac, Prat-Vidal, Cristina, Llucià-Valldeperas, Aida, Raya, Ángel, Bayes-Genis, Antoni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4529715/
https://www.ncbi.nlm.nih.gov/pubmed/26205795
http://dx.doi.org/10.1186/s13287-015-0101-6
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author Gálvez-Montón, Carolina
Fernandez-Figueras, M. Teresa
Martí, Mercè
Soler-Botija, Carolina
Roura, Santiago
Perea-Gil, Isaac
Prat-Vidal, Cristina
Llucià-Valldeperas, Aida
Raya, Ángel
Bayes-Genis, Antoni
author_facet Gálvez-Montón, Carolina
Fernandez-Figueras, M. Teresa
Martí, Mercè
Soler-Botija, Carolina
Roura, Santiago
Perea-Gil, Isaac
Prat-Vidal, Cristina
Llucià-Valldeperas, Aida
Raya, Ángel
Bayes-Genis, Antoni
author_sort Gálvez-Montón, Carolina
collection PubMed
description Engineered bioimplants for cardiac repair require functional vascularization and innervation for proper integration with the surrounding myocardium. The aim of this work was to study nerve sprouting and neovascularization in an acellular pericardial-derived scaffold used as a myocardial bioimplant. To this end, 17 swine were submitted to a myocardial infarction followed by implantation of a decellularized human pericardial-derived scaffold. After 30 days, animals were sacrificed and hearts were analyzed with hematoxylin/eosin and Masson’s and Gallego’s modified trichrome staining. Immunohistochemistry was carried out to detect nerve fibers within the cardiac bioimplant by using β(III) tubulin and S100 labeling. Isolectin B4, smooth muscle actin, CD31, von Willebrand factor, cardiac troponin I, and elastin antibodies were used to study scaffold vascularization. Transmission electron microscopy was performed to confirm the presence of vascular and nervous ultrastructures. Left ventricular ejection fraction (LVEF), cardiac output (CO), stroke volume, end-diastolic volume, end-systolic volume, end-diastolic wall mass, and infarct size were assessed by using magnetic resonance imaging (MRI). Newly formed nerve fibers composed of several amyelinated axons as the afferent nerve endings of the heart were identified by immunohistochemistry. Additionally, neovessel formation occurred spontaneously as small and large isolectin B4-positive blood vessels within the scaffold. In summary, this study demonstrates for the first time the neoformation of vessels and nerves in cell-free cardiac scaffolds applied over infarcted tissue. Moreover, MRI analysis showed a significant improvement in LVEF (P = 0.03) and CO (P = 0.01) and a 43 % decrease in infarct size (P = 0.007). ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13287-015-0101-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-45297152015-08-09 Neoinnervation and neovascularization of acellular pericardial-derived scaffolds in myocardial infarcts Gálvez-Montón, Carolina Fernandez-Figueras, M. Teresa Martí, Mercè Soler-Botija, Carolina Roura, Santiago Perea-Gil, Isaac Prat-Vidal, Cristina Llucià-Valldeperas, Aida Raya, Ángel Bayes-Genis, Antoni Stem Cell Res Ther Short Report Engineered bioimplants for cardiac repair require functional vascularization and innervation for proper integration with the surrounding myocardium. The aim of this work was to study nerve sprouting and neovascularization in an acellular pericardial-derived scaffold used as a myocardial bioimplant. To this end, 17 swine were submitted to a myocardial infarction followed by implantation of a decellularized human pericardial-derived scaffold. After 30 days, animals were sacrificed and hearts were analyzed with hematoxylin/eosin and Masson’s and Gallego’s modified trichrome staining. Immunohistochemistry was carried out to detect nerve fibers within the cardiac bioimplant by using β(III) tubulin and S100 labeling. Isolectin B4, smooth muscle actin, CD31, von Willebrand factor, cardiac troponin I, and elastin antibodies were used to study scaffold vascularization. Transmission electron microscopy was performed to confirm the presence of vascular and nervous ultrastructures. Left ventricular ejection fraction (LVEF), cardiac output (CO), stroke volume, end-diastolic volume, end-systolic volume, end-diastolic wall mass, and infarct size were assessed by using magnetic resonance imaging (MRI). Newly formed nerve fibers composed of several amyelinated axons as the afferent nerve endings of the heart were identified by immunohistochemistry. Additionally, neovessel formation occurred spontaneously as small and large isolectin B4-positive blood vessels within the scaffold. In summary, this study demonstrates for the first time the neoformation of vessels and nerves in cell-free cardiac scaffolds applied over infarcted tissue. Moreover, MRI analysis showed a significant improvement in LVEF (P = 0.03) and CO (P = 0.01) and a 43 % decrease in infarct size (P = 0.007). ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13287-015-0101-6) contains supplementary material, which is available to authorized users. BioMed Central 2015-05-27 /pmc/articles/PMC4529715/ /pubmed/26205795 http://dx.doi.org/10.1186/s13287-015-0101-6 Text en © Gálvez-Montón et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Short Report
Gálvez-Montón, Carolina
Fernandez-Figueras, M. Teresa
Martí, Mercè
Soler-Botija, Carolina
Roura, Santiago
Perea-Gil, Isaac
Prat-Vidal, Cristina
Llucià-Valldeperas, Aida
Raya, Ángel
Bayes-Genis, Antoni
Neoinnervation and neovascularization of acellular pericardial-derived scaffolds in myocardial infarcts
title Neoinnervation and neovascularization of acellular pericardial-derived scaffolds in myocardial infarcts
title_full Neoinnervation and neovascularization of acellular pericardial-derived scaffolds in myocardial infarcts
title_fullStr Neoinnervation and neovascularization of acellular pericardial-derived scaffolds in myocardial infarcts
title_full_unstemmed Neoinnervation and neovascularization of acellular pericardial-derived scaffolds in myocardial infarcts
title_short Neoinnervation and neovascularization of acellular pericardial-derived scaffolds in myocardial infarcts
title_sort neoinnervation and neovascularization of acellular pericardial-derived scaffolds in myocardial infarcts
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4529715/
https://www.ncbi.nlm.nih.gov/pubmed/26205795
http://dx.doi.org/10.1186/s13287-015-0101-6
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