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Fluorescence-Based Nanoparticle Tracking Analysis and Flow Cytometry for Characterization of Endothelial Extracellular Vesicle Release

As extracellular vesicles (EVs) have become a prominent topic in life sciences, a growing number of studies are published on a regular basis addressing their biological relevance and possible applications. Nevertheless, the fundamental question of the true vesicular nature as well as possible influe...

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Autores principales: Oesterreicher, Johannes, Pultar, Marianne, Schneider, Jaana, Mühleder, Severin, Zipperle, Johannes, Grillari, Johannes, Holnthoner, Wolfgang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7731108/
https://www.ncbi.nlm.nih.gov/pubmed/33291792
http://dx.doi.org/10.3390/ijms21239278
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author Oesterreicher, Johannes
Pultar, Marianne
Schneider, Jaana
Mühleder, Severin
Zipperle, Johannes
Grillari, Johannes
Holnthoner, Wolfgang
author_facet Oesterreicher, Johannes
Pultar, Marianne
Schneider, Jaana
Mühleder, Severin
Zipperle, Johannes
Grillari, Johannes
Holnthoner, Wolfgang
author_sort Oesterreicher, Johannes
collection PubMed
description As extracellular vesicles (EVs) have become a prominent topic in life sciences, a growing number of studies are published on a regular basis addressing their biological relevance and possible applications. Nevertheless, the fundamental question of the true vesicular nature as well as possible influences on the EV secretion behavior have often been not adequately addressed. Furthermore, research regarding endothelial cell-derived EVs (EndoEVs) often focused on the large vesicular fractions comprising of microvesicles (MV) and apoptotic bodies. In this study we aimed to further extend the current knowledge of the influence of pre-isolation conditions, such as cell density and conditioning time, on EndoEV release from human umbilical vein endothelial cells (HUVECs). We combined fluorescence nanoparticle tracking analysis (NTA) and the established fluorescence-triggered flow cytometry (FT-FC) protocol to allow vesicle-specific detection and characterization of size and surface markers. We found significant effects of cell density and conditioning time on both abundance and size distribution of EndoEVs. Additionally, we present detailed information regarding the surface marker display on EVs from different fractions and size ranges. Our data provide crucial relevance for future projects aiming to elucidate EV secretion behavior of endothelial cells. Moreover, we show that the influence of different conditioning parameters on the nature of EndoEVs has to be considered.
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spelling pubmed-77311082020-12-12 Fluorescence-Based Nanoparticle Tracking Analysis and Flow Cytometry for Characterization of Endothelial Extracellular Vesicle Release Oesterreicher, Johannes Pultar, Marianne Schneider, Jaana Mühleder, Severin Zipperle, Johannes Grillari, Johannes Holnthoner, Wolfgang Int J Mol Sci Article As extracellular vesicles (EVs) have become a prominent topic in life sciences, a growing number of studies are published on a regular basis addressing their biological relevance and possible applications. Nevertheless, the fundamental question of the true vesicular nature as well as possible influences on the EV secretion behavior have often been not adequately addressed. Furthermore, research regarding endothelial cell-derived EVs (EndoEVs) often focused on the large vesicular fractions comprising of microvesicles (MV) and apoptotic bodies. In this study we aimed to further extend the current knowledge of the influence of pre-isolation conditions, such as cell density and conditioning time, on EndoEV release from human umbilical vein endothelial cells (HUVECs). We combined fluorescence nanoparticle tracking analysis (NTA) and the established fluorescence-triggered flow cytometry (FT-FC) protocol to allow vesicle-specific detection and characterization of size and surface markers. We found significant effects of cell density and conditioning time on both abundance and size distribution of EndoEVs. Additionally, we present detailed information regarding the surface marker display on EVs from different fractions and size ranges. Our data provide crucial relevance for future projects aiming to elucidate EV secretion behavior of endothelial cells. Moreover, we show that the influence of different conditioning parameters on the nature of EndoEVs has to be considered. MDPI 2020-12-04 /pmc/articles/PMC7731108/ /pubmed/33291792 http://dx.doi.org/10.3390/ijms21239278 Text en © 2020 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
Oesterreicher, Johannes
Pultar, Marianne
Schneider, Jaana
Mühleder, Severin
Zipperle, Johannes
Grillari, Johannes
Holnthoner, Wolfgang
Fluorescence-Based Nanoparticle Tracking Analysis and Flow Cytometry for Characterization of Endothelial Extracellular Vesicle Release
title Fluorescence-Based Nanoparticle Tracking Analysis and Flow Cytometry for Characterization of Endothelial Extracellular Vesicle Release
title_full Fluorescence-Based Nanoparticle Tracking Analysis and Flow Cytometry for Characterization of Endothelial Extracellular Vesicle Release
title_fullStr Fluorescence-Based Nanoparticle Tracking Analysis and Flow Cytometry for Characterization of Endothelial Extracellular Vesicle Release
title_full_unstemmed Fluorescence-Based Nanoparticle Tracking Analysis and Flow Cytometry for Characterization of Endothelial Extracellular Vesicle Release
title_short Fluorescence-Based Nanoparticle Tracking Analysis and Flow Cytometry for Characterization of Endothelial Extracellular Vesicle Release
title_sort fluorescence-based nanoparticle tracking analysis and flow cytometry for characterization of endothelial extracellular vesicle release
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7731108/
https://www.ncbi.nlm.nih.gov/pubmed/33291792
http://dx.doi.org/10.3390/ijms21239278
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