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Human Heart Explant-Derived Extracellular Vesicles: Characterization and Effects on the In Vitro Recellularization of Decellularized Heart Valves

Extracellular vesicles (EVs) are particles released from different cell types and represent key components of paracrine secretion. Accumulating evidence supports the beneficial effects of EVs for tissue regeneration. In this study, discarded human heart tissues were used to isolate human heart-deriv...

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Autores principales: Leitolis, Amanda, Suss, Paula Hansen, Roderjan, João Gabriel, Angulski, Addeli Bez Batti, da Costa, Francisco Diniz Affonso, Stimamiglio, Marco Augusto, Correa, Alejandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6471048/
https://www.ncbi.nlm.nih.gov/pubmed/30875722
http://dx.doi.org/10.3390/ijms20061279
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author Leitolis, Amanda
Suss, Paula Hansen
Roderjan, João Gabriel
Angulski, Addeli Bez Batti
da Costa, Francisco Diniz Affonso
Stimamiglio, Marco Augusto
Correa, Alejandro
author_facet Leitolis, Amanda
Suss, Paula Hansen
Roderjan, João Gabriel
Angulski, Addeli Bez Batti
da Costa, Francisco Diniz Affonso
Stimamiglio, Marco Augusto
Correa, Alejandro
author_sort Leitolis, Amanda
collection PubMed
description Extracellular vesicles (EVs) are particles released from different cell types and represent key components of paracrine secretion. Accumulating evidence supports the beneficial effects of EVs for tissue regeneration. In this study, discarded human heart tissues were used to isolate human heart-derived extracellular vesicles (hH-EVs). We used nanoparticle tracking analysis (NTA) and transmission electron microscopy (TEM) to physically characterize hH-EVs and mass spectrometry (MS) to profile the protein content in these particles. The MS analysis identified a total of 1248 proteins. Gene ontology (GO) enrichment analysis in hH-EVs revealed the proteins involved in processes, such as the regulation of cell death and response to wounding. The potential of hH-EVs to induce proliferation, adhesion, angiogenesis and wound healing was investigated in vitro. Our findings demonstrate that hH-EVs have the potential to induce proliferation and angiogenesis in endothelial cells, improve wound healing and reduce mesenchymal stem-cell adhesion. Last, we showed that hH-EVs were able to significantly promote mesenchymal stem-cell recellularization of decellularized porcine heart valve leaflets. Altogether our data confirmed that hH-EVs modulate cellular processes, shedding light on the potential of these particles for tissue regeneration and for scaffold recellularization.
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spelling pubmed-64710482019-04-26 Human Heart Explant-Derived Extracellular Vesicles: Characterization and Effects on the In Vitro Recellularization of Decellularized Heart Valves Leitolis, Amanda Suss, Paula Hansen Roderjan, João Gabriel Angulski, Addeli Bez Batti da Costa, Francisco Diniz Affonso Stimamiglio, Marco Augusto Correa, Alejandro Int J Mol Sci Article Extracellular vesicles (EVs) are particles released from different cell types and represent key components of paracrine secretion. Accumulating evidence supports the beneficial effects of EVs for tissue regeneration. In this study, discarded human heart tissues were used to isolate human heart-derived extracellular vesicles (hH-EVs). We used nanoparticle tracking analysis (NTA) and transmission electron microscopy (TEM) to physically characterize hH-EVs and mass spectrometry (MS) to profile the protein content in these particles. The MS analysis identified a total of 1248 proteins. Gene ontology (GO) enrichment analysis in hH-EVs revealed the proteins involved in processes, such as the regulation of cell death and response to wounding. The potential of hH-EVs to induce proliferation, adhesion, angiogenesis and wound healing was investigated in vitro. Our findings demonstrate that hH-EVs have the potential to induce proliferation and angiogenesis in endothelial cells, improve wound healing and reduce mesenchymal stem-cell adhesion. Last, we showed that hH-EVs were able to significantly promote mesenchymal stem-cell recellularization of decellularized porcine heart valve leaflets. Altogether our data confirmed that hH-EVs modulate cellular processes, shedding light on the potential of these particles for tissue regeneration and for scaffold recellularization. MDPI 2019-03-14 /pmc/articles/PMC6471048/ /pubmed/30875722 http://dx.doi.org/10.3390/ijms20061279 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Leitolis, Amanda
Suss, Paula Hansen
Roderjan, João Gabriel
Angulski, Addeli Bez Batti
da Costa, Francisco Diniz Affonso
Stimamiglio, Marco Augusto
Correa, Alejandro
Human Heart Explant-Derived Extracellular Vesicles: Characterization and Effects on the In Vitro Recellularization of Decellularized Heart Valves
title Human Heart Explant-Derived Extracellular Vesicles: Characterization and Effects on the In Vitro Recellularization of Decellularized Heart Valves
title_full Human Heart Explant-Derived Extracellular Vesicles: Characterization and Effects on the In Vitro Recellularization of Decellularized Heart Valves
title_fullStr Human Heart Explant-Derived Extracellular Vesicles: Characterization and Effects on the In Vitro Recellularization of Decellularized Heart Valves
title_full_unstemmed Human Heart Explant-Derived Extracellular Vesicles: Characterization and Effects on the In Vitro Recellularization of Decellularized Heart Valves
title_short Human Heart Explant-Derived Extracellular Vesicles: Characterization and Effects on the In Vitro Recellularization of Decellularized Heart Valves
title_sort human heart explant-derived extracellular vesicles: characterization and effects on the in vitro recellularization of decellularized heart valves
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6471048/
https://www.ncbi.nlm.nih.gov/pubmed/30875722
http://dx.doi.org/10.3390/ijms20061279
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