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Highly purified extracellular vesicles from human cardiomyocytes demonstrate preferential uptake by human endothelial cells

Extracellular vesicles (EVs) represent a promising cell-free alternative for treatment of cardiovascular diseases. Nevertheless, the lack of standardised and reproducible isolation methods capable of recovering pure, intact EVs presents a significant obstacle. Additionally, there is significant inte...

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Autores principales: Zwi-Dantsis, Limor, Winter, Charles W., Kauscher, Ulrike, Ferrini, Arianna, Wang, Brian, Whittaker, Thomas E., Hood, Steve R., Terracciano, Cesare M., Stevens, Molly M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7610784/
https://www.ncbi.nlm.nih.gov/pubmed/32969445
http://dx.doi.org/10.1039/d0nr04278a
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author Zwi-Dantsis, Limor
Winter, Charles W.
Kauscher, Ulrike
Ferrini, Arianna
Wang, Brian
Whittaker, Thomas E.
Hood, Steve R.
Terracciano, Cesare M.
Stevens, Molly M.
author_facet Zwi-Dantsis, Limor
Winter, Charles W.
Kauscher, Ulrike
Ferrini, Arianna
Wang, Brian
Whittaker, Thomas E.
Hood, Steve R.
Terracciano, Cesare M.
Stevens, Molly M.
author_sort Zwi-Dantsis, Limor
collection PubMed
description Extracellular vesicles (EVs) represent a promising cell-free alternative for treatment of cardiovascular diseases. Nevertheless, the lack of standardised and reproducible isolation methods capable of recovering pure, intact EVs presents a significant obstacle. Additionally, there is significant interest in investigating the interactions of EVs with different cardiac cell types. Here we established a robust technique for the production and isolation of EVs harvested from an enriched (>97% purity) population of human induced pluripotent stem cell (iPSC)-derived cardiomyocytes (CMs) with size exclusion chromatography. Utilizing an advanced fluorescence labelling strategy, we then investigated the interplay of the CM-EVs with the three major cellular components of the myocardium (fibroblasts, cardiomyocytes and endothelial cells) and identified that cardiac endothelial cells show preferential uptake of these EVs. Overall, our findings provide a great opportunity to overcome the translational hurdles associated with the isolation of intact, non-aggregated human iPSC-CM EVs at high purity. Furthermore, understanding in detail the interaction of the secreted EVs with their surrounding cells in the heart may open promising new avenues in the field of EV engineering for targeted delivery in cardiac regeneration.
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spelling pubmed-76107842021-05-14 Highly purified extracellular vesicles from human cardiomyocytes demonstrate preferential uptake by human endothelial cells Zwi-Dantsis, Limor Winter, Charles W. Kauscher, Ulrike Ferrini, Arianna Wang, Brian Whittaker, Thomas E. Hood, Steve R. Terracciano, Cesare M. Stevens, Molly M. Nanoscale Article Extracellular vesicles (EVs) represent a promising cell-free alternative for treatment of cardiovascular diseases. Nevertheless, the lack of standardised and reproducible isolation methods capable of recovering pure, intact EVs presents a significant obstacle. Additionally, there is significant interest in investigating the interactions of EVs with different cardiac cell types. Here we established a robust technique for the production and isolation of EVs harvested from an enriched (>97% purity) population of human induced pluripotent stem cell (iPSC)-derived cardiomyocytes (CMs) with size exclusion chromatography. Utilizing an advanced fluorescence labelling strategy, we then investigated the interplay of the CM-EVs with the three major cellular components of the myocardium (fibroblasts, cardiomyocytes and endothelial cells) and identified that cardiac endothelial cells show preferential uptake of these EVs. Overall, our findings provide a great opportunity to overcome the translational hurdles associated with the isolation of intact, non-aggregated human iPSC-CM EVs at high purity. Furthermore, understanding in detail the interaction of the secreted EVs with their surrounding cells in the heart may open promising new avenues in the field of EV engineering for targeted delivery in cardiac regeneration. 2020-10-14 2020-09-24 /pmc/articles/PMC7610784/ /pubmed/32969445 http://dx.doi.org/10.1039/d0nr04278a Text en https://creativecommons.org/licenses/by/3.0/This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (https://creativecommons.org/licenses/by/3.0/) .
spellingShingle Article
Zwi-Dantsis, Limor
Winter, Charles W.
Kauscher, Ulrike
Ferrini, Arianna
Wang, Brian
Whittaker, Thomas E.
Hood, Steve R.
Terracciano, Cesare M.
Stevens, Molly M.
Highly purified extracellular vesicles from human cardiomyocytes demonstrate preferential uptake by human endothelial cells
title Highly purified extracellular vesicles from human cardiomyocytes demonstrate preferential uptake by human endothelial cells
title_full Highly purified extracellular vesicles from human cardiomyocytes demonstrate preferential uptake by human endothelial cells
title_fullStr Highly purified extracellular vesicles from human cardiomyocytes demonstrate preferential uptake by human endothelial cells
title_full_unstemmed Highly purified extracellular vesicles from human cardiomyocytes demonstrate preferential uptake by human endothelial cells
title_short Highly purified extracellular vesicles from human cardiomyocytes demonstrate preferential uptake by human endothelial cells
title_sort highly purified extracellular vesicles from human cardiomyocytes demonstrate preferential uptake by human endothelial cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7610784/
https://www.ncbi.nlm.nih.gov/pubmed/32969445
http://dx.doi.org/10.1039/d0nr04278a
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