Evidence map›Paper›PMID 33804769›Full record

ArticleInternational journal of molecular sciences2021

Exosomes from COVID-19 Patients Carry Tenascin-C and Fibrinogen-β in Triggering Inflammatory Signals in Cells of Distant Organ.

Subhayan Sur, Mousumi Khatun, Robert Steele, T Scott Isbell, Ranjit Ray, Ratna B Ray

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
3.7field-weighted citation impact, top 5% 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

45 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
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  8. The Role of Extracellular Vesicles in Pandemic Viral Infections.Journal of microbiology (Seoul, Korea) · 2024
    Review
  9. Specific Binding of Alzheimer's Aβ Peptides to Extracellular Vesicles.International journal of molecular sciences · 2024
    Article
  10. Extracellular Vesicles: The Invisible Heroes and Villains of COVID-19 Central Neuropathology.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Review
  11. Article
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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

6 authors at 1 institution in 1 country.

Subhayan SurDepartment of Pathology, Saint Louis University, St. Louis, MO 63104, USA.
Mousumi KhatunDepartment of Pathology, Saint Louis University, St. Louis, MO 63104, USA.
Robert SteeleDepartment of Pathology, Saint Louis University, St. Louis, MO 63104, USA.
T Scott IsbellDepartment of Pathology, Saint Louis University, St. Louis, MO 63104, USA.
Ranjit RayDepartment of Internal Medicine, Saint Louis University, St. Louis, MO 63104, USA.
Ratna B RayDepartment of Pathology, Saint Louis University, St. Louis, MO 63104, USA.ORCID 0000-0003-4477-6292
Saint Louis University · US

Funding

Research Institute of Saint Louis University (T.S.I and R.R) and Pathology Department Seed Grant to RBR 319052; 270441
6 · The paper itself

Abstract

SARS-CoV-2 infection can cause cytokine storm and may overshoot immunity in humans; however, it remains to be determined whether virus-induced soluble mediators from infected cells are carried by exosomes as vehicles to distant organs and cause tissue damage in COVID-19 patients. We took an unbiased proteomic approach for analyses of exosomes isolated from plasma of healthy volunteers and COVID-19 patients. Our results revealed that tenascin-C (TNC) and fibrinogen-β (FGB) are highly abundant in exosomes from COVID-19 patients' plasma compared with that of healthy normal controls. Since TNC and FGB stimulate pro-inflammatory cytokines via the Nuclear factor-κB (NF-κB) pathway, we examined the status of tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), and C-C motif chemokine ligand 5 (CCL5) expression upon exposure of hepatocytes to exosomes from COVID-19 patients and observed significant increase compared with that from healthy subjects. Together, our results demonstrate that TNC and FGB are transported through plasma exosomes and potentially trigger pro-inflammatory cytokine signaling in cells of distant organ.

Indexed as

AgedCell LineChemokine CCL5COVID-19ExosomesFemaleFibrinogenHepatocytesHumansInflammationInterleukin-6MaleMass SpectrometryMicroscopy, Electron, TransmissionMiddle AgedNF-kappa BBBeta fibrinogenCCL5 protein, humanChemokine CCL5FibrinogenIL6 protein, humanInterleukin-6NF-kappa BProteomeTenascinTNC protein, humanTNF protein, humanTumor Necrosis Factor-alphaCOVID-19cytokinesexosomesfibrinogen-βmass spectrometrypathogenesistenascin-C

Identifiers

PMID33804769
PMCPMC8003878
OpenAlexW3136968974

What OpenQuestion holds

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LicenceCC BY
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.