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

dc.contributor.authorOesterreicher, Johannes
dc.contributor.authorPultar, Marianne
dc.contributor.authorSchneider, Jaana
dc.contributor.authorMühleder, Severin
dc.contributor.authorZipperle, Johannes
dc.contributor.authorGrillari, Johannes
dc.contributor.authorHolnthoner, Wolfgang
dc.contributor.funderAustrian Research Promotion Agency
dc.contributor.funderFWF Austrian Science Fund
dc.contributor.funderParticle Metrix
dc.date.accessioned2021-04-12T07:45:40Z
dc.date.available2021-04-12T07:45:40Z
dc.date.issued2020-12-04
dc.description.abstractAs 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.es_ES
dc.description.peerreviewedes_ES
dc.description.sponsorshipThis research was funded by the Austrian Research promotion agency and Particle Metrix. Severin Mühleder was funded by the Austrian Science Fund (FWF) project J4358.es_ES
dc.format.number23es_ES
dc.format.volume21es_ES
dc.identifier.citationInt J Mol Sci. 2020; 21(23):9278es_ES
dc.identifier.doi10.3390/ijms21239278es_ES
dc.identifier.e-issn1422-0067es_ES
dc.identifier.journalInternational journal of molecular scienceses_ES
dc.identifier.pubmedID33291792es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/12602
dc.language.isoenges_ES
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)es_ES
dc.relation.publisherversionhttps://doi.org/10.3390/ijms21239278es_ES
dc.repisalud.institucionCNICes_ES
dc.repisalud.orgCNICCNIC::Grupos de investigación::Genética Molecular de la Angiogénesises_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.meshFlow Cytometryes_ES
dc.subject.meshFluorescencees_ES
dc.subject.meshNanoparticleses_ES
dc.subject.meshBiomarkerses_ES
dc.subject.meshCell Cyclees_ES
dc.subject.meshCell Fractionationes_ES
dc.subject.meshCell Trackinges_ES
dc.subject.meshCell-Derived Microparticleses_ES
dc.subject.meshCells, Culturedes_ES
dc.subject.meshEndothelial Cellses_ES
dc.subject.meshExtracellular Vesicleses_ES
dc.subject.meshHuman Umbilical Vein Endothelial Cellses_ES
dc.subject.meshHumanses_ES
dc.subject.meshParticle Sizees_ES
dc.titleFluorescence-Based Nanoparticle Tracking Analysis and Flow Cytometry for Characterization of Endothelial Extracellular Vesicle Release.es_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication

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