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Single-step isolation of extracellular vesicles by size-exclusion chromatography

TLDR
SEC efficiently isolates extracellular vesicles with a diameter larger than 70 nm from platelet-free supernatant of platelet concentrates to improve studies on the dimensional, structural and functional properties of extraceocytes.
Abstract
Background: Isolation of extracellular vesicles from plasma is a challenge due to the presence of proteins and lipoproteins. Isolation of vesicles using differential centrifugation or density-gradient ultracentrifugation results in co-isolation of contaminants such as protein aggregates and incomplete separation of vesicles from lipoproteins, respectively. Aim: To develop a single-step protocol to isolate vesicles from human body fluids. Methods: Platelet-free supernatant, derived from platelet concentrates, was loaded on a sepharose CL-2B column to perform size-exclusion chromatography (SEC; n=3). Fractions were collected and analysed by nanoparticle tracking analysis, resistive pulse sensing, flow cytometry and transmission electron microscopy. The concentrations of high-density lipoprotein cholesterol (HDL) and protein were measured in each fraction. Results: Fractions 9–12 contained the highest concentrations of particles larger than 70 nm and platelet-derived vesicles (46%±6 and 61%±2 of totals present in all collected fractions, respectively), but less than 5% of HDL and less than 1% of protein (4.8%±1 and 0.65%±0.3, respectively). HDL was present mainly in fractions 18–20 (32%±2 of total), and protein in fractions 19–21 (36%±2 of total). Compared to the starting material, recovery of platelet-derived vesicles was 43%±23 in fractions 9–12, with an 8-fold and 70-fold enrichment compared to HDL and protein. Conclusions: SEC efficiently isolates extracellular vesicles with a diameter larger than 70 nm from platelet-free supernatant of platelet concentrates. Application SEC will improve studies on the dimensional, structural and functional properties of extracellular vesicles. Keywords: extracellular vesicles; isolation; lipoproteins; plasma; protein; size-exclusion chromatography (Published: 8 September 2014) Citation: Journal of Extracellular Vesicles 2014, 3 : 23430 - http://dx.doi.org/10.3402/jev.v3.23430 To access the supplementary material to this article, please see Supplementary files under Article Tools online.

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References
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Journal ArticleDOI

Isolation and Characterization of Exosomes from Cell Culture Supernatants and Biological Fluids

TL;DR: This unit describes different approaches for exosome purification from various sources, and discusses methods to evaluate the purity and homogeneity of the purified exosomes preparations.
Journal ArticleDOI

B lymphocytes secrete antigen-presenting vesicles.

TL;DR: It is demonstrated by immunoelectron microscopy that the limiting membrane of MIICs can fuse directly with the plasma membrane, resulting in release from the cells of internal MHC class II-containing vesicles, suggesting a role for exosomes in antigen presentation in vivo.
Journal ArticleDOI

MicroRNAs are transported in plasma and delivered to recipient cells by high-density lipoproteins

TL;DR: Evidence that high-density lipoprotein (HDL) transports endogenous miRNAs and delivers them to recipient cells with functional targeting capabilities is presented, indicating that HDL participates in a mechanism of intercellular communication involving the transport and delivery of miRNA.
Journal ArticleDOI

Classification, Functions, and Clinical Relevance of Extracellular Vesicles

TL;DR: Evidence is accumulating that vesicles are cargo containers used by eukaryotic cells to exchange biomolecules as transmembrane receptors and genetic information, and they have a myriad of potential clinical applications, ranging from biomarkers to anticancer therapy.
Journal ArticleDOI

Separation of plasma lipoproteins by density-gradient ultracentrifugation.

TL;DR: The method employs a discontinuous salt gradient and separates VLDL, LDL, and HDL as verified by cellulose acetate- and immuno-electrophoresis and offers some advantages for research applications.
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