Handling and storage of human body fluids for analysis of extracellular vesicles

Type:
Peer-reviewed article
Authors: 
Y. Yuana, A.N. B&buml;ing, A.E. Grootemaat, E. van der Pol, C.M. Hau, P. Czimar, E. Buhr, A. Sturk, and R. Nieuwland
Date:
Published November 11, 2015
Journal:
Journal of Extracellular Vesicles
Volume:
4
Pagination: 
29260: 1-12
DOI:
10.3402/jev.v4.29260
Keywords:
Erythrocyte, guideline, plasma, saliva, urine, platelet, cell-derived vesicles
Attachment: 
Yuana 2015 JEV Handling.pdf (4,336 kB)

Abstract

Because procedures of handling and storage of body fluids affect numbers and composition of extracellular vesicles (EVs), standardization is important to ensure reliable and comparable measurements of EVs in a clinical environment. We aimed to develop standard protocols for handling and storage of human body fluids for EV analysis. Conditions such as centrifugation, single freezethaw cycle, effect of time delay between blood collection and plasma preparation and storage were investigated. Plasma is the most commonly studied body fluid in EV research. We mainly focused on EVs originating from platelets and erythrocytes and investigated the behaviour of these 2 types of EVs independently as well as in plasma samples of healthy subjects. EVs in urine and saliva were also studied for comparison. All samples were analysed simultaneously before and after freezethawing by resistive pulse sensing, nanoparticle tracking analysis, conventional flow cytometry (FCM) and transmission (scanning) electron microscopy. Our main finding is that the effect of centrifugation markedly depends on the cellular origin of EVs. Whereas erythrocyte EVs remain present as single EVs after centrifugation, platelet EVs form aggregates, which affect their measured concentration in plasma. Single erythrocyte and platelet EVs are present mainly in the range of 100-200 nm, far below the lower limit of what can be measured by conventional FCM. Furthermore, the effects of single freezethaw cycle, time delay between blood collection and plasma preparation up to 1 hour and storage up to 1 year are insignificant (p>0.05) on the measured concentration and diameter of EVs from erythrocyte and platelet concentrates and EVs in plasma, urine and saliva. In conclusion, in standard protocols for EV studies, centrifugation to isolate EVs from collected body fluids should be avoided. Freezing and storage of collected body fluids, albeit their insignificant effects, should be performed identically for comparative EV studies and to create reliable biorepositories.

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