Evidence map›Paper›PMID 33361424›Full record

ArticleJournal of virology2021

Diverse Populations of Extracellular Vesicles with Opposite Functions during Herpes Simplex Virus 1 Infection.

Christos Dogrammatzis, Shadia Saleh, Clayton Deighan, Maria Kalamvoki

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

32 citing papers in PubMed, 38 citations in OpenAlex.

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  16. Cell-to-cell communications of cGAS-STING pathway in tumor immune microenvironment.Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2024
    Review
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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

4 authors at 1 institution in 1 country.

Christos DogrammatzisUniversity of Kansas Medical Center, Department of Microbiology, Molecular Genetics and Immunology, Kansas City, Kansas, USA.
Shadia SalehUniversity of Kansas Medical Center, Department of Microbiology, Molecular Genetics and Immunology, Kansas City, Kansas, USA.
Clayton DeighanNanoView Biosciences, Boston, Massachusetts, USA.
Maria KalamvokiUniversity of Kansas Medical Center, Department of Microbiology, Molecular Genetics and Immunology, Kansas City, Kansas, USA mkalamvoki@kumc.edu.
University of Kansas Medical Center · US

Funding

Synthetic Chemical Biology CoreP20GM113117 · NIGMS · UNIVERSITY OF KANSAS LAWRENCE · PI OROZCO, ROBIN C. · 2016 to 2025
$23.9M
Cargo, biogenesis and functions of extracellular vesicles released during HSV-1 infectionR01AI162784 · NIAID · UNIVERSITY OF KANSAS MEDICAL CENTER · PI Maria Kalamvoki · 2021 to 2026
$2.4M
Alterations in the surfaceome of the herpes simplex virus 1 infected cells via the Cbl/CIN85 endocytic machinery and the role of the Infected Cell Protein No 0 (ICP0) in endocytosis.R21AI144883 · NIAID · UNIVERSITY OF KANSAS MEDICAL CENTER · PI KALAMVOKI, MARIA · 2020 to 2021
$421k
Immunomodulatory effects of coronavirus membrane proteins E, M, and S.R21AI158229 · NIAID · UNIVERSITY OF KANSAS MEDICAL CENTER · PI KALAMVOKI, MARIA, STEPHENS, EDWARD BRICE · 2020 to 2020
$421k
NIAID NIH HHS R01 AI162784NIAID NIH HHS R21 AI144883NIAID NIH HHS R21 AI158229NIGMS NIH HHS P20 GM113117
6 · The paper itself

Abstract

Extracellular vesicles (EVs) are released by all types of cells as a means of intercellular communication. Their significance lies in the fact that they can alter recipient cell functions, despite their limited capacity for cargo. We have previously demonstrated that herpes simplex virus 1 (HSV-1) infection influences the cargo and functions of EVs released by infected cells and that these EVs negatively impact a subsequent HSV-1 infection. In the present study, we have implemented cutting-edge technologies to further characterize EVs released during HSV-1 infection. We identified distinct EV populations that were separable through a gradient approach. One population was positive for the tetraspanin CD63 and was distinct from EVs carrying components of the endosomal sorting complexes required for transport (ESCRT). Nanoparticle tracking analysis (NTA) combined with protein analysis indicated that the production of CD63

Indexed as

Antiviral AgentsCell LineEndosomal Sorting Complexes Required for TransportExocytosisExtracellular VesiclesHerpesvirus 1, HumanHost-Pathogen InteractionsHumansMembrane ProteinsSTING ProteinTetraspanin 30TetraspaninsViral ProteinsAntiviral AgentsEndosomal Sorting Complexes Required for TransportMembrane ProteinsSTING1 protein, humanSTING ProteinTetraspanin 30TetraspaninsViral Proteinsbiogenesis of extracellular vesiclesCD63CD81ESCRTextracellular vesiclesHSV-1L-particlestetraspanins

Identifiers

PMID33361424
PMCPMC8094966
OpenAlexW3116990207

What OpenQuestion holds

Textmetadata
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.