Evidence map›Paper›PMID 32300430›Full record

ArticleJournal of hematology2018

Functional Properties of Circulating Exosomes Mediated by Surface-Attached Plasma Proteins.

Tatiana Shtam, Stanislav Naryzhny, Arthur Kopylov, Elena Petrenko, Roman Samsonov, Roman Kamyshinsky, Yana Zabrodskaya, Daniil Nikitin, Maxim Sorokin, Anton Buzdin and 1 more

Open access · greenAbstract read
In one paragraph

Article in Journal of hematology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

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  9. Cloaked Viruses and Viral Factors in Cutting Edge Exosome-Based Therapies.Frontiers in cell and developmental biology · 2020
    Review
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

11 authors at 6 institutions in 2 countries.

Tatiana ShtamN.N.Petrov National Medical Research Center of Oncology, 197758, Leningradskaya 68, St.-Petersburg, Russia.
Stanislav NaryzhnyPetersburg Nuclear Physics Institute named by B.P. Konstantinov of National Research Centre «Kurchatov Institute», 188300, Orlova roscha 1, Gatchina, Russia.
Arthur KopylovOrekhovich Institute of Biomedical Chemistry of Russian Academy of Medical Sciences, 119121, Pogodinskaya 10, Moscow, Russia.
Elena PetrenkoOrekhovich Institute of Biomedical Chemistry of Russian Academy of Medical Sciences, 119121, Pogodinskaya 10, Moscow, Russia.
Roman SamsonovN.N.Petrov National Medical Research Center of Oncology, 197758, Leningradskaya 68, St.-Petersburg, Russia.
Roman KamyshinskyNational Research Center "Kurchatov Institute", 123098, Academician Kurchatov Square 1, Moscow, Russia.
Yana ZabrodskayaPetersburg Nuclear Physics Institute named by B.P. Konstantinov of National Research Centre «Kurchatov Institute», 188300, Orlova roscha 1, Gatchina, Russia.
Daniil NikitinEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991, 32, Vavilova Str., Moscow, Russia.
Maxim SorokinNational Research Center "Kurchatov Institute", 123098, Academician Kurchatov Square 1, Moscow, Russia.
Anton BuzdinEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991, 32, Vavilova Str., Moscow, Russia.
Anastasia MalekN.N.Petrov National Medical Research Center of Oncology, 197758, Leningradskaya 68, St.-Petersburg, Russia.
Institute of Oncology NN Petrov · RUEngelhardt Institute of Molecular Biology · RUInstitute of Biomedical Chemistry · RUPetersburg Nuclear Physics Institute · RUKurchatov Institute · RUWalsh University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundExosomes and other types of extracellular vesicles present an important component of circulating plasma. Exosomes released by endothelial and blood cells account for majority of plasma exosomal population; exosomes secreted by other cells might cross tissue-plasma barrier and reach circulating plasma as well. Definitely, exosomes of different cellular origins are different by content and function. However, exosomal surface membrane interacts with plasma components. This interaction may alter composition of exosomal surface and hence, provide these vesicles with new functional properties. This study was aimed to estimate composition and possible functional role of proteins attached on the surface of plasma exosomes.

methodsHere, extracellular vesicles from human plasma were isolated by ultracentrifugation and treated by trypsin. Trypsinized and native exosomes were analyzed by nanoparticle tracking analysis, Western blotting and quantitative high-resolution mass spectrometry.

resultsSurface-attached proteins were removed from exosomes isolated from plasma of healthy donors by incubation with serine protease (trypsin). Treatment did not impact exosomes integrity while slightly reduced hydrodynamic radius. Mass spectrometry revealed 259 exosomal proteins; among them 79 proteins were completely removed and more than half of the proteins were partially removed by trypsinization. Gene ontology functional annotation revealed mostly extracellular locations of proteins cleaved from a surface of the plasma exosomes. Moreover, proteins cleaved from the exosome surface are supposed to be implicated into integrin-linked kinase (ILK), focal adhesion kinase (FAK) and other pathways connecting cell surface with intracellular signaling cascades.

conclusionTaken together, our results demonstrate that a surface of circulating exosomes is decorated by plasma proteins, and these proteins can mask tissue-specific characteristic of the exosomal surface membrane and provide exosomes with new and uniform properties.

Indexed as

ExosomesFAK signalingILK signalingMass spectrometryPlasma proteins

Identifiers

PMID32300430
PMCPMC7155850
OpenAlexW2901851607

What OpenQuestion holds

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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.