Open AccessFormation of a protein corona on the surface of extracellular vesicles in blood plasma
Author(s) -
Tóth Eszter Á.,
Turiák Lilla,
Visnovitz Tamás,
Cserép Csaba,
Mázló Anett,
Sódar Barbara W.,
Försönits András I.,
Petővári Gábor,
Sebestyén Anna,
Komlósi Zsolt,
Drahos László,
Kittel Ágnes,
Nagy György,
Bácsi Attila,
Dénes Ádám,
Gho Yong Song,
SzabóTaylor Katalin É.,
Buzás Edit I.
Publication year - 2021
Publication title -
journal of extracellular vesicles
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.94
H-Index - 68
ISSN - 2001-3078
DOI - 10.1002/jev2.12140
Subject(s) - chemistry , blood proteins , differential centrifugation , extracellular vesicle , nanoparticle tracking analysis , cd63 , biophysics , microvesicles , biochemistry , biology , microrna , gene
In this study we tested whether a protein corona is formed around extracellular vesicles (EVs) in blood plasma. We isolated medium‐sized nascent EVs of THP1 cells as well as of Optiprep‐purified platelets, and incubated them in EV‐depleted blood plasma from healthy subjects and from patients with rheumatoid arthritis. EVs were subjected to differential centrifugation, size exclusion chromatography, or density gradient ultracentrifugation followed by mass spectrometry. Plasma protein‐coated EVs had a higher density compared to the nascent ones and carried numerous newly associated proteins. Interactions between plasma proteins and EVs were confirmed by confocal microscopy, capillary Western immunoassay, immune electron microscopy and flow cytometry. We identified nine shared EV corona proteins (ApoA1, ApoB, ApoC3, ApoE, complement factors 3 and 4B, fibrinogen α‐chain, immunoglobulin heavy constant γ2 and γ4 chains), which appear to be common corona proteins among EVs, viruses and artificial nanoparticles in blood plasma. An unexpected finding of this study was the high overlap of the composition of the protein corona with blood plasma protein aggregates. This is explained by our finding that besides a diffuse, patchy protein corona, large protein aggregates also associate with the surface of EVs. However, while EVs with an external plasma protein cargo induced an increased expression of TNF‐α, IL‐6, CD83, CD86 and HLA‐DR of human monocyte‐derived dendritic cells, EV‐free protein aggregates had no effect. In conclusion, our data may shed new light on the origin of the commonly reported plasma protein ‘contamination’ of EV preparations and may add a new perspective to EV research.