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Combination human umbilical cord perivascular and endothelial colony forming cell therapy for ischemic cardiac injury
Cell-based therapeutics are promising interventions to repair ischemic cardiac tissue. However, no single cell type has yet been found to be both specialized and versatile enough to heal the heart. The synergistic effects of two regenerative cell types including endothelial colony forming cells (ECF...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10457300/ https://www.ncbi.nlm.nih.gov/pubmed/37626067 http://dx.doi.org/10.1038/s41536-023-00321-3 |
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author | Iqbal, Farwah Johnston, Alexander Wyse, Brandon Rabani, Razieh Mander, Poonam Hoseini, Banafshe Wu, Jun Li, Ren-Ke Gauthier-Fisher, Andrée Szaraz, Peter Librach, Clifford |
author_facet | Iqbal, Farwah Johnston, Alexander Wyse, Brandon Rabani, Razieh Mander, Poonam Hoseini, Banafshe Wu, Jun Li, Ren-Ke Gauthier-Fisher, Andrée Szaraz, Peter Librach, Clifford |
author_sort | Iqbal, Farwah |
collection | PubMed |
description | Cell-based therapeutics are promising interventions to repair ischemic cardiac tissue. However, no single cell type has yet been found to be both specialized and versatile enough to heal the heart. The synergistic effects of two regenerative cell types including endothelial colony forming cells (ECFC) and first-trimester human umbilical cord perivascular cells (FTM HUCPVC) with endothelial cell and pericyte properties respectively, on angiogenic and regenerative properties were tested in a rat model of myocardial infarction (MI), in vitro tube formation and Matrigel plug assay. The combination of FTM HUCPVCs and ECFCs synergistically reduced fibrosis and cardiomyocyte apoptosis, while promoting favorable cardiac remodeling and contractility. These effects were in part mediated by ANGPT2, PDGF-β, and VEGF-C. PDGF-β signaling-dependent synergistic effects on angiogenesis were also observed in vitro and in vivo. FTM HUCPVCs and ECFCs represent a cell combination therapy for promoting and sustaining vascularization following ischemic cardiac injury. |
format | Online Article Text |
id | pubmed-10457300 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104573002023-08-27 Combination human umbilical cord perivascular and endothelial colony forming cell therapy for ischemic cardiac injury Iqbal, Farwah Johnston, Alexander Wyse, Brandon Rabani, Razieh Mander, Poonam Hoseini, Banafshe Wu, Jun Li, Ren-Ke Gauthier-Fisher, Andrée Szaraz, Peter Librach, Clifford NPJ Regen Med Article Cell-based therapeutics are promising interventions to repair ischemic cardiac tissue. However, no single cell type has yet been found to be both specialized and versatile enough to heal the heart. The synergistic effects of two regenerative cell types including endothelial colony forming cells (ECFC) and first-trimester human umbilical cord perivascular cells (FTM HUCPVC) with endothelial cell and pericyte properties respectively, on angiogenic and regenerative properties were tested in a rat model of myocardial infarction (MI), in vitro tube formation and Matrigel plug assay. The combination of FTM HUCPVCs and ECFCs synergistically reduced fibrosis and cardiomyocyte apoptosis, while promoting favorable cardiac remodeling and contractility. These effects were in part mediated by ANGPT2, PDGF-β, and VEGF-C. PDGF-β signaling-dependent synergistic effects on angiogenesis were also observed in vitro and in vivo. FTM HUCPVCs and ECFCs represent a cell combination therapy for promoting and sustaining vascularization following ischemic cardiac injury. Nature Publishing Group UK 2023-08-25 /pmc/articles/PMC10457300/ /pubmed/37626067 http://dx.doi.org/10.1038/s41536-023-00321-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Iqbal, Farwah Johnston, Alexander Wyse, Brandon Rabani, Razieh Mander, Poonam Hoseini, Banafshe Wu, Jun Li, Ren-Ke Gauthier-Fisher, Andrée Szaraz, Peter Librach, Clifford Combination human umbilical cord perivascular and endothelial colony forming cell therapy for ischemic cardiac injury |
title | Combination human umbilical cord perivascular and endothelial colony forming cell therapy for ischemic cardiac injury |
title_full | Combination human umbilical cord perivascular and endothelial colony forming cell therapy for ischemic cardiac injury |
title_fullStr | Combination human umbilical cord perivascular and endothelial colony forming cell therapy for ischemic cardiac injury |
title_full_unstemmed | Combination human umbilical cord perivascular and endothelial colony forming cell therapy for ischemic cardiac injury |
title_short | Combination human umbilical cord perivascular and endothelial colony forming cell therapy for ischemic cardiac injury |
title_sort | combination human umbilical cord perivascular and endothelial colony forming cell therapy for ischemic cardiac injury |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10457300/ https://www.ncbi.nlm.nih.gov/pubmed/37626067 http://dx.doi.org/10.1038/s41536-023-00321-3 |
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