Premium
Techniques to improve detection and analysis of extracellular vesicles using flow cytometry
Author(s) -
Inglis Heather C.,
Danesh Ali,
Shah Avani,
Lacroix Jacques,
Spinella Philip C.,
Norris Philip J.
Publication year - 2015
Publication title -
cytometry part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.316
H-Index - 90
eISSN - 1552-4930
pISSN - 1552-4922
DOI - 10.1002/cyto.a.22649
Subject(s) - flow cytometry , extracellular vesicles , lysis , chromatography , detection limit , cytometry , filtration (mathematics) , chemistry , computer science , microbiology and biotechnology , biology , mathematics , statistics
Extracellular vesicles (EVs) range in size from 50 nm to 1 µm. Flow cytometry (FCM) is the most commonly used method for analyzing EVs; however, accurate characterization of EVs remains challenging due to their small size and lack of discrete positive populations. Here we report the use of optimization techniques that are especially well‐suited for analyzing EVs from a high volume of clinical samples. Utilizing a two pronged approach that included 1) pre‐filtration of antibodies to remove aggregates, followed by 2) detergent lysis of a replicate sample to account for remaining false positive events, we were able to effectively limit false positive non‐EV events. In addition, we show that lysed samples are a useful alternative to isotypes for setting gates to exclude background fluorescence. To reduce background, we developed an approach using filters to “wash” samples post‐staining thus providing a faster alternative to ultracentrifugation and sucrose gradient fractionation. In conclusion, use of these optimized techniques enhances the accuracy and efficiency of EV detection using FCM. © 2015 International Society for Advancement of Cytometry