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Extracellular Vesicles as Therapeutic Agents for Cardiac Fibrosis

Heart disease remains an increasing major public health challenge in the United States and worldwide. A common end-organ feature in diseased hearts is myocardial fibrosis, which stiffens the heart and interferes with normal pump function, leading to pump failure. The development of cells for regener...

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Autores principales: Rogers, Russell G., Ciullo, Alessandra, Marbán, Eduardo, Ibrahim, Ahmed G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7255103/
https://www.ncbi.nlm.nih.gov/pubmed/32528309
http://dx.doi.org/10.3389/fphys.2020.00479
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author Rogers, Russell G.
Ciullo, Alessandra
Marbán, Eduardo
Ibrahim, Ahmed G.
author_facet Rogers, Russell G.
Ciullo, Alessandra
Marbán, Eduardo
Ibrahim, Ahmed G.
author_sort Rogers, Russell G.
collection PubMed
description Heart disease remains an increasing major public health challenge in the United States and worldwide. A common end-organ feature in diseased hearts is myocardial fibrosis, which stiffens the heart and interferes with normal pump function, leading to pump failure. The development of cells for regenerative therapy has been met with many pitfalls on its path to clinical translation. Recognizing that regenerative cells secrete therapeutically bioactive vesicles has paved the way to circumvent many failures of cell therapy. In this review, we provide an overview of extracellular vesicles (EVs), with a focus on their utility as therapeutic agents for cardiac regeneration. We also highlight the engineering potential of EVs to enhance their therapeutic application.
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spelling pubmed-72551032020-06-10 Extracellular Vesicles as Therapeutic Agents for Cardiac Fibrosis Rogers, Russell G. Ciullo, Alessandra Marbán, Eduardo Ibrahim, Ahmed G. Front Physiol Physiology Heart disease remains an increasing major public health challenge in the United States and worldwide. A common end-organ feature in diseased hearts is myocardial fibrosis, which stiffens the heart and interferes with normal pump function, leading to pump failure. The development of cells for regenerative therapy has been met with many pitfalls on its path to clinical translation. Recognizing that regenerative cells secrete therapeutically bioactive vesicles has paved the way to circumvent many failures of cell therapy. In this review, we provide an overview of extracellular vesicles (EVs), with a focus on their utility as therapeutic agents for cardiac regeneration. We also highlight the engineering potential of EVs to enhance their therapeutic application. Frontiers Media S.A. 2020-05-21 /pmc/articles/PMC7255103/ /pubmed/32528309 http://dx.doi.org/10.3389/fphys.2020.00479 Text en Copyright © 2020 Rogers, Ciullo, Marbán and Ibrahim. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Rogers, Russell G.
Ciullo, Alessandra
Marbán, Eduardo
Ibrahim, Ahmed G.
Extracellular Vesicles as Therapeutic Agents for Cardiac Fibrosis
title Extracellular Vesicles as Therapeutic Agents for Cardiac Fibrosis
title_full Extracellular Vesicles as Therapeutic Agents for Cardiac Fibrosis
title_fullStr Extracellular Vesicles as Therapeutic Agents for Cardiac Fibrosis
title_full_unstemmed Extracellular Vesicles as Therapeutic Agents for Cardiac Fibrosis
title_short Extracellular Vesicles as Therapeutic Agents for Cardiac Fibrosis
title_sort extracellular vesicles as therapeutic agents for cardiac fibrosis
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7255103/
https://www.ncbi.nlm.nih.gov/pubmed/32528309
http://dx.doi.org/10.3389/fphys.2020.00479
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