Evidence map›Paper›PMID 34520123›Full record

ArticleJournal of extracellular vesicles2021

Formation of a protein corona on the surface of extracellular vesicles in blood plasma.

Eszter Á Tóth, Lilla Turiák, Tamás Visnovitz, Csaba Cserép, Anett Mázló, Barbara W Sódar, András I Försönits, Gábor Petővári, Anna Sebestyén, Zsolt Komlósi and 8 more

Open access · goldAbstract read
In one paragraph

Article in Journal of extracellular vesicles, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 309 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
309citing papers in PubMed, 2 pooled it
24.5field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

309 citing papers in PubMed, 2 syntheses or guidelines pooled it, 452 citations in OpenAlex.

  1. Pooled it
  2. Systematic review of changes in extracellular vesicles associated with obstructive sleep apnoea: implications for diagnosis and treatment.European respiratory review : an official journal of the European Respiratory Society · 2025
    Pooled it
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249 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors at 5 institutions in 3 countries.

Eszter Á TóthDepartment of Genetics, Cell- and Immunobiology, Semmelweis University, Budapest, Hungary.
Lilla TuriákELKH-SE Immune-Proteogenomics Extracellular Vesicle Research Group, Budapest, Hungary.
Tamás VisnovitzDepartment of Genetics, Cell- and Immunobiology, Semmelweis University, Budapest, Hungary.
Csaba CserépLaboratory of Neuroimmunology, Institute of Experimental Medicine, Eötvös Loránd Research Network, Budapest, Hungary.
Anett MázlóDepartment of Immunology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Barbara W SódarDepartment of Genetics, Cell- and Immunobiology, Semmelweis University, Budapest, Hungary.
András I FörsönitsDepartment of Genetics, Cell- and Immunobiology, Semmelweis University, Budapest, Hungary.
Gábor PetőváriTumour Biology, Tumour Metabolism Research Group, 1st Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.
Anna SebestyénTumour Biology, Tumour Metabolism Research Group, 1st Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.
Zsolt KomlósiDepartment of Genetics, Cell- and Immunobiology, Semmelweis University, Budapest, Hungary.
László DrahosELKH-SE Immune-Proteogenomics Extracellular Vesicle Research Group, Budapest, Hungary.
Ágnes KittelInstitute of Experimental Medicine, Eötvös Loránd Research Network, Budapest, Hungary.
György NagyDepartment of Genetics, Cell- and Immunobiology, Semmelweis University, Budapest, Hungary.
Attila BácsiDepartment of Immunology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Ádám DénesLaboratory of Neuroimmunology, Institute of Experimental Medicine, Eötvös Loránd Research Network, Budapest, Hungary.
Yong Song GhoDepartment of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang, Republic of Korea.
Katalin É Szabó-TaylorDepartment of Genetics, Cell- and Immunobiology, Semmelweis University, Budapest, Hungary.
Edit I BuzásDepartment of Genetics, Cell- and Immunobiology, Semmelweis University, Budapest, Hungary.ORCID 0000-0002-3744-206X
Semmelweis University · HUHUN-REN Institute of Experimental Medicine · HUImmunoGenes (Hungary) · HUUniversity of Debrecen · HUPohang University of Science and Technology · KR

Funding

European Research Council ERC-CoG 724994European Research Council H2020-ITN-2018-813294-ENTRAIN
6 · The paper itself

Abstract

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.

Indexed as

Extracellular VesiclesFemaleHumansMaleMass SpectrometryPlasmaProtein CoronaProtein Coronaaggregationblood plasmaextracellular vesiclesmass spectrometryprotein corona

Identifiers

PMID34520123
PMCPMC8439280
OpenAlexW3199740606

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.