Abstract

Extracellular vesicles (EVs) are a highly attractive subject of biomedical research as possible carriers of nucleic acid and protein biomarkers. EVs released to body fluids enable indirect access to inner organs by so-called “liquid biopsies”. Obtaining a high-quality EV sample with minimum contaminants is crucial for proteomic analyses using LC–MS/MS or other techniques. However, the EV content in various body fluids largely differs, which may hamper subsequent analyses. Here, we present a comparison of extracellular vesicle yields from blood plasma, cerebrospinal fluid, and seminal plasma using an experimental pig model. Pigs are widely used in biomedical research as large animal models with anatomy and physiology close to those of humans and enable studies (e.g., of the nervous system) that are unfeasible in humans. EVs were isolated from body fluids by differential centrifugation followed by ultracentrifugation. EVs were characterized according to protein yields and to the quality of the isolated vesicles (e.g., size distribution, morphology, positivity for exosome markers). In our experimental setting, substantial differences in EV amounts were identified among body fluids, with the seminal plasma being the richest EV source. The yields of pellet proteins from ultracentrifugation of 1 mL of porcine body fluids may help to estimate body fluid input volumes to obtain sufficient samples for subsequent proteomic analyses.

Highlights

  • Extracellular vesicles (EVs) are membrane-enveloped particles released by cells to surrounding tissue microenvironment and body fluids

  • We analyzed the presence of small extracellular vesicles in porcine blood plasma, cerebrospinal fluid, and seminal plasma

  • Substantial differences in EV content were identified among body fluids, including up to 1000 times lower protein amount extracted from

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Summary

Introduction

Extracellular vesicles (EVs) are membrane-enveloped particles released by cells to surrounding tissue microenvironment and body fluids. According to their origin, apoptotic bodies, microvesicles, and exosomes are recognized as the major types of EVs. Because the origin is difficult to assess in already released EVs, the term “small EVs” has been suggested for vesicles below 200 nm by the International Society for Extracellular Vesicles [1]. Small EVs contain molecules of EV-producing cells, which are incorporated into the vesicles during their biogenesis [2]. The lipid composition of the small EV bilayer membrane is distinct from that of the plasma membrane of the source cell, as the EV membrane is enriched in detergent-resistant lipid rafts. The EV internal cargo consists mainly of Proteomes 2019, 7, 17; doi:10.3390/proteomes7020017 www.mdpi.com/journal/proteomes

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