Analysis of extracellular vesicle microRNA profiles reveals distinct blood and lymphatic endothelial cell origins

Extracellular vesicles (EVs) are crucial mediators of cell‐to‐cell communication in physiological and pathological conditions. Specifically, EVs released from the vasculature into blood were found to be quantitatively and qualitatively different in diseases compared to healthy states. However, our u...

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Published inJournal of extracellular biology Vol. 3; no. 1; pp. e134 - n/a
Main Authors Pultar, Marianne, Oesterreicher, Johannes, Hartmann, Jaana, Weigl, Moritz, Diendorfer, Andreas, Schimek, Katharina, Schädl, Barbara, Heuser, Thomas, Brandstetter, Marlene, Grillari, Johannes, Sykacek, Peter, Hackl, Matthias, Holnthoner, Wolfgang
Format Journal Article
LanguageEnglish
Published United States John Wiley and Sons Inc 01.01.2024
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Summary:Extracellular vesicles (EVs) are crucial mediators of cell‐to‐cell communication in physiological and pathological conditions. Specifically, EVs released from the vasculature into blood were found to be quantitatively and qualitatively different in diseases compared to healthy states. However, our understanding of EVs derived from the lymphatic system is still scarce. In this study, we compared the mRNA and microRNA (miRNA) expression in blood vascular (BEC) and lymphatic (LEC) endothelial cells. After characterization of the EVs by fluorescence‐triggered flow cytometry, nanoparticle tracking analysis and cryo‐transmission electron microscopy (cryo‐TEM) we utilized small RNA‐sequencing to characterize miRNA signatures in the EVs and identify cell‐type specific miRNAs in BEC and LEC. We found miRNAs specifically enriched in BEC and LEC on the cellular as well as the extracellular vesicle level. Our data provide a solid basis for further functional in vitro and in vivo studies addressing the role of EVs in the blood and lymphatic vasculature.
Bibliography:Marianne Pultar and Johannes Oesterreicher contributed equally to this study.
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ISSN:2768-2811
2768-2811
DOI:10.1002/jex2.134