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Concise Review: The Regenerative Journey of Pericytes Toward Clinical Translation

Coronary artery disease (CAD) is the single leading cause of death worldwide. Advances in treatment and management have significantly improved patient outcomes. On the other hand, although mortality rates have decreased, more people are left with sequelae that require additional treatment and hospit...

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Autores principales: Cathery, William, Faulkner, Ashton, Maselli, Davide, Madeddu, Paolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6175115/
https://www.ncbi.nlm.nih.gov/pubmed/29732653
http://dx.doi.org/10.1002/stem.2846
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author Cathery, William
Faulkner, Ashton
Maselli, Davide
Madeddu, Paolo
author_facet Cathery, William
Faulkner, Ashton
Maselli, Davide
Madeddu, Paolo
author_sort Cathery, William
collection PubMed
description Coronary artery disease (CAD) is the single leading cause of death worldwide. Advances in treatment and management have significantly improved patient outcomes. On the other hand, although mortality rates have decreased, more people are left with sequelae that require additional treatment and hospitalization. Moreover, patients with severe nonrevascularizable CAD remain with only the option of heart transplantation, which is limited by the shortage of suitable donors. In recent years, cell‐based regenerative therapy has emerged as a possible alternative treatment, with several regenerative medicinal products already in the clinical phase of development and others emerging as competitive preclinical solutions. Recent evidence indicates that pericytes, the mural cells of blood microvessels, represent a promising therapeutic candidate. Pericytes are abundant in the human body, play an active role in angiogenesis, vessel stabilization and blood flow regulation, and possess the capacity to differentiate into multiple cells of the mesenchymal lineage. Moreover, early studies suggest a robustness to hypoxic insult, making them uniquely equipped to withstand the ischemic microenvironment. This review summarizes the rationale behind pericyte‐based cell therapy and the progress that has been made toward its clinical application. We present the different sources of pericytes and the case for harvesting them from tissue leftovers of cardiovascular surgery. We also discuss the healing potential of pericytes in preclinical animal models of myocardial ischemia (MI) and current practices to upgrade the production protocol for translation to the clinic. Standardization of these procedures is of utmost importance, as lack of uniformity in cell manufacturing may influence clinical outcome. Stem Cells 2018;36:1295–1310
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spelling pubmed-61751152018-10-15 Concise Review: The Regenerative Journey of Pericytes Toward Clinical Translation Cathery, William Faulkner, Ashton Maselli, Davide Madeddu, Paolo Stem Cells Regenerative Medicine Coronary artery disease (CAD) is the single leading cause of death worldwide. Advances in treatment and management have significantly improved patient outcomes. On the other hand, although mortality rates have decreased, more people are left with sequelae that require additional treatment and hospitalization. Moreover, patients with severe nonrevascularizable CAD remain with only the option of heart transplantation, which is limited by the shortage of suitable donors. In recent years, cell‐based regenerative therapy has emerged as a possible alternative treatment, with several regenerative medicinal products already in the clinical phase of development and others emerging as competitive preclinical solutions. Recent evidence indicates that pericytes, the mural cells of blood microvessels, represent a promising therapeutic candidate. Pericytes are abundant in the human body, play an active role in angiogenesis, vessel stabilization and blood flow regulation, and possess the capacity to differentiate into multiple cells of the mesenchymal lineage. Moreover, early studies suggest a robustness to hypoxic insult, making them uniquely equipped to withstand the ischemic microenvironment. This review summarizes the rationale behind pericyte‐based cell therapy and the progress that has been made toward its clinical application. We present the different sources of pericytes and the case for harvesting them from tissue leftovers of cardiovascular surgery. We also discuss the healing potential of pericytes in preclinical animal models of myocardial ischemia (MI) and current practices to upgrade the production protocol for translation to the clinic. Standardization of these procedures is of utmost importance, as lack of uniformity in cell manufacturing may influence clinical outcome. Stem Cells 2018;36:1295–1310 John Wiley and Sons Inc. 2018-05-31 2018-09 /pmc/articles/PMC6175115/ /pubmed/29732653 http://dx.doi.org/10.1002/stem.2846 Text en © 2018 The Authors Stem Cells published by Wiley Periodicals, Inc. on behalf of AlphaMed Press This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Regenerative Medicine
Cathery, William
Faulkner, Ashton
Maselli, Davide
Madeddu, Paolo
Concise Review: The Regenerative Journey of Pericytes Toward Clinical Translation
title Concise Review: The Regenerative Journey of Pericytes Toward Clinical Translation
title_full Concise Review: The Regenerative Journey of Pericytes Toward Clinical Translation
title_fullStr Concise Review: The Regenerative Journey of Pericytes Toward Clinical Translation
title_full_unstemmed Concise Review: The Regenerative Journey of Pericytes Toward Clinical Translation
title_short Concise Review: The Regenerative Journey of Pericytes Toward Clinical Translation
title_sort concise review: the regenerative journey of pericytes toward clinical translation
topic Regenerative Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6175115/
https://www.ncbi.nlm.nih.gov/pubmed/29732653
http://dx.doi.org/10.1002/stem.2846
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