Detailed Characterization of Small Extracellular Vesicles from Different Cell Types Based on Tetraspanin Composition by ExoView R100 Platform

Small extracellular vesicles (sEV) hold enormous potential as biomarkers, drug carriers, and therapeutic agents. However, due to previous limitations in the phenotypic characterization of sEV at the single vesicle level, knowledge of cell type-specific sEV signatures remains sparse. With the introdu...

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Veröffentlicht in:International journal of molecular sciences 2022-08, Vol.23 (15), p.8544
Hauptverfasser: Breitwieser, Kai, Koch, Leon F., Tertel, Tobias, Proestler, Eva, Burgers, Luisa D., Lipps, Christoph, Adjaye, James, Fürst, Robert, Giebel, Bernd, Saul, Meike J.
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container_issue 15
container_start_page 8544
container_title International journal of molecular sciences
container_volume 23
creator Breitwieser, Kai
Koch, Leon F.
Tertel, Tobias
Proestler, Eva
Burgers, Luisa D.
Lipps, Christoph
Adjaye, James
Fürst, Robert
Giebel, Bernd
Saul, Meike J.
description Small extracellular vesicles (sEV) hold enormous potential as biomarkers, drug carriers, and therapeutic agents. However, due to previous limitations in the phenotypic characterization of sEV at the single vesicle level, knowledge of cell type-specific sEV signatures remains sparse. With the introduction of next-generation sEV analysis devices, such as the single-particle interferometric reflectance imaging sensor (SP-IRIS)-based ExoView R100 platform, single sEV analyses are now possible. While the tetraspanins CD9, CD63, and CD81 were generally considered pan-sEV markers, it became clear that sEV of different cell types contain several combinations and amounts of these proteins on their surfaces. To gain better insight into the complexity and heterogeneity of sEV, we used the ExoView R100 platform to analyze the CD9/CD63/CD81 phenotype of sEV released by different cell types at a single sEV level. We demonstrated that these surface markers are sufficient to distinguish cell-type-specific sEV phenotypes. Furthermore, we recognized that tetraspanin composition in some sEV populations does not follow a random pattern. Notably, the tetraspanin distribution of sEV derived from mesenchymal stem cells (MSCs) alters depending on cell culture conditions. Overall, our data provide an overview of the cell-specific characteristics of sEV populations, which will increase the understanding of sEV physiology and improve the development of new sEV-based therapeutic approaches.
doi_str_mv 10.3390/ijms23158544
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subjects Antibodies
CD63 antigen
CD81 antigen
CD9 antigen
Cell culture
Chemical compounds
Composition
Drug carriers
Drug delivery
Extracellular vesicles
Fibroblasts
Flow cytometry
Genotype & phenotype
Heterogeneity
Lymphocytes
Mesenchyme
Microscopy
Pharmacology
Phenotypes
Populations
Proteins
Stem cells
Surface markers
Vesicles
title Detailed Characterization of Small Extracellular Vesicles from Different Cell Types Based on Tetraspanin Composition by ExoView R100 Platform
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