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Intravenous delivery of adeno-associated virus 9-encoded IGF-1Ea propeptide improves post-infarct cardiac remodelling

The insulin-like growth factor Ea propeptide (IGF-1Ea) is a powerful enhancer of cardiac muscle growth and regeneration, also blocking age-related atrophy and beneficial in multiple skeletal muscle diseases. The therapeutic potential of IGF-1Ea compared with mature IGF-1 derives from its local actio...

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Autores principales: Gallego-Colon, Enrique, Villalba, Maria, Tonkin, Joanne, Cruz, Francisco, Bernal, Juan Antonio, Jimenez-Borregureo, Luis J, Schneider, Michael D, Lara-Pezzi, Enrique, Rosenthal, Nadia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5744701/
https://www.ncbi.nlm.nih.gov/pubmed/29302333
http://dx.doi.org/10.1038/npjregenmed.2016.1
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author Gallego-Colon, Enrique
Villalba, Maria
Tonkin, Joanne
Cruz, Francisco
Bernal, Juan Antonio
Jimenez-Borregureo, Luis J
Schneider, Michael D
Lara-Pezzi, Enrique
Rosenthal, Nadia
author_facet Gallego-Colon, Enrique
Villalba, Maria
Tonkin, Joanne
Cruz, Francisco
Bernal, Juan Antonio
Jimenez-Borregureo, Luis J
Schneider, Michael D
Lara-Pezzi, Enrique
Rosenthal, Nadia
author_sort Gallego-Colon, Enrique
collection PubMed
description The insulin-like growth factor Ea propeptide (IGF-1Ea) is a powerful enhancer of cardiac muscle growth and regeneration, also blocking age-related atrophy and beneficial in multiple skeletal muscle diseases. The therapeutic potential of IGF-1Ea compared with mature IGF-1 derives from its local action in the area of synthesis. We have developed an adeno-associated virus (AAV) vector for IGF-1Ea delivery to the heart to treat mice after myocardial infarction and examine the reparative effects of local IGF-1Ea production on left ventricular remodelling. A cardiotropic AAV9 vector carrying a cardiomyocyte-specific IGF-1Ea-luciferase bi-cistronic gene expression cassette (AAV9.IGF-1Ea) was administered intravenously to infarcted mice, 5 h after ischemia followed by reperfusion (I/R), as a model of myocardial infarction. Virally encoded IGF-1Ea in the heart improved global left ventricular function and remodelling, as measured by wall motion and thickness, 28 days after delivery, with higher viral titers yielding better improvement. The present study demonstrates that single intravenous AAV9-mediated IGF-1Ea Gene Therapy represents a tissue-targeted therapeutic approach to prevent the adverse remodelling after myocardial infarct.
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spelling pubmed-57447012018-01-04 Intravenous delivery of adeno-associated virus 9-encoded IGF-1Ea propeptide improves post-infarct cardiac remodelling Gallego-Colon, Enrique Villalba, Maria Tonkin, Joanne Cruz, Francisco Bernal, Juan Antonio Jimenez-Borregureo, Luis J Schneider, Michael D Lara-Pezzi, Enrique Rosenthal, Nadia NPJ Regen Med Article The insulin-like growth factor Ea propeptide (IGF-1Ea) is a powerful enhancer of cardiac muscle growth and regeneration, also blocking age-related atrophy and beneficial in multiple skeletal muscle diseases. The therapeutic potential of IGF-1Ea compared with mature IGF-1 derives from its local action in the area of synthesis. We have developed an adeno-associated virus (AAV) vector for IGF-1Ea delivery to the heart to treat mice after myocardial infarction and examine the reparative effects of local IGF-1Ea production on left ventricular remodelling. A cardiotropic AAV9 vector carrying a cardiomyocyte-specific IGF-1Ea-luciferase bi-cistronic gene expression cassette (AAV9.IGF-1Ea) was administered intravenously to infarcted mice, 5 h after ischemia followed by reperfusion (I/R), as a model of myocardial infarction. Virally encoded IGF-1Ea in the heart improved global left ventricular function and remodelling, as measured by wall motion and thickness, 28 days after delivery, with higher viral titers yielding better improvement. The present study demonstrates that single intravenous AAV9-mediated IGF-1Ea Gene Therapy represents a tissue-targeted therapeutic approach to prevent the adverse remodelling after myocardial infarct. Nature Publishing Group 2016-06-09 /pmc/articles/PMC5744701/ /pubmed/29302333 http://dx.doi.org/10.1038/npjregenmed.2016.1 Text en Copyright © 2016 Published in partnership with the Australian Regenerative Medicine Institute http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Gallego-Colon, Enrique
Villalba, Maria
Tonkin, Joanne
Cruz, Francisco
Bernal, Juan Antonio
Jimenez-Borregureo, Luis J
Schneider, Michael D
Lara-Pezzi, Enrique
Rosenthal, Nadia
Intravenous delivery of adeno-associated virus 9-encoded IGF-1Ea propeptide improves post-infarct cardiac remodelling
title Intravenous delivery of adeno-associated virus 9-encoded IGF-1Ea propeptide improves post-infarct cardiac remodelling
title_full Intravenous delivery of adeno-associated virus 9-encoded IGF-1Ea propeptide improves post-infarct cardiac remodelling
title_fullStr Intravenous delivery of adeno-associated virus 9-encoded IGF-1Ea propeptide improves post-infarct cardiac remodelling
title_full_unstemmed Intravenous delivery of adeno-associated virus 9-encoded IGF-1Ea propeptide improves post-infarct cardiac remodelling
title_short Intravenous delivery of adeno-associated virus 9-encoded IGF-1Ea propeptide improves post-infarct cardiac remodelling
title_sort intravenous delivery of adeno-associated virus 9-encoded igf-1ea propeptide improves post-infarct cardiac remodelling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5744701/
https://www.ncbi.nlm.nih.gov/pubmed/29302333
http://dx.doi.org/10.1038/npjregenmed.2016.1
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