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<metadata xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/"><dc:title>Comprehensive phenotyping of extracellular vesicles in plasma of healthy humans - insights into cellular origin and biological variation</dc:title><dc:creator>Holcar,	Marija	(Avtor)
	</dc:creator><dc:creator>Marić,	Ivica	(Avtor)
	</dc:creator><dc:creator>Tertel,	Tobias	(Avtor)
	</dc:creator><dc:creator>Goričar,	Katja	(Avtor)
	</dc:creator><dc:creator>Čegovnik Primožič,	Urška	(Avtor)
	</dc:creator><dc:creator>Černe,	Darko	(Avtor)
	</dc:creator><dc:creator>Giebel,	Bernd	(Avtor)
	</dc:creator><dc:creator>Lenassi,	Metka	(Avtor)
	</dc:creator><dc:subject>biological variation</dc:subject><dc:subject>blood</dc:subject><dc:subject>extracellular vesicles</dc:subject><dc:subject>helathy humans</dc:subject><dc:subject>plasma</dc:subject><dc:description>Despite immense interest in biomarker applications of extracellular vesicles (EVs) from blood, our understanding of circulating EVs under physiological conditions in healthy humans remains limited. Using imaging and multiplex bead-based flow cytometry, we comprehensively quantified circulating EVs with respect to their cellular origin in a large cohort of healthy blood donors. We assessed coefficients of variations to characterize their biological variation and explored demographic, clinical, and lifestyle factors contributing to observed variation. Cell-specific circulating EV subsets show a wide range of concentrations that do not correlate with cell-of-origin concentrations in blood, suggesting steady-state EV subset concentrations are regulated by complex mechanisms, which differ even for EV subsets from the same cell type. Interestingly, tetraspanin+ circulating EVs largely originate from platelets and to a lesser extent from lymphocytes. Principal component analysis (PCA) and association analyses demonstrate high biological inter-individual variation in circulating EVs across healthy humans, which are only partly explained by the influence of sex, menopausal status, age and smoking on specific circulating EV and/or tetraspanin+ circulating EV subsets. No global influence of the explored subject's factors on circulating EVs was detected. Our findings provide the first comprehensive, quantitative data towards the cell-origin atlas of plasma EVs, with important implications in the clinical use of EVs as biomarkers.</dc:description><dc:date>2025</dc:date><dc:date>2026-04-15 13:42:29</dc:date><dc:type>Neznano</dc:type><dc:identifier>28982</dc:identifier><dc:identifier>UDK: 616.1:577</dc:identifier><dc:identifier>ISSN pri članku: 2001-3078</dc:identifier><dc:identifier>DOI: 10.1002/jev2.70039</dc:identifier><dc:identifier>COBISS_ID: 225240067</dc:identifier><dc:language>sl</dc:language></metadata>
