Evidence map›Paper›PMID 24966329›Full record

ArticleThe Journal of biological chemistry2014

Antiviral responses in mouse embryonic stem cells: differential development of cellular mechanisms in type I interferon production and response.

Ruoxing Wang, Jundi Wang, Dhiraj Acharya, Amber M Paul, Fengwei Bai, Faqing Huang, Yan-Lin Guo

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.7field-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

28 citing papers in PubMed, 47 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Ruoxing WangFrom the Departments of Biological Sciences and.
Jundi WangFrom the Departments of Biological Sciences and.
Dhiraj AcharyaFrom the Departments of Biological Sciences and.
Amber M PaulFrom the Departments of Biological Sciences and.
Fengwei BaiFrom the Departments of Biological Sciences and.
Faqing HuangChemistry and Biochemistry, University of Southern Mississippi, Hattiesburg, Mississippi 39406.
Yan-Lin GuoFrom the Departments of Biological Sciences and yanlin.guo@usm.edu.
University of Southern Mississippi · US

Funding

Training and Mentoring Core P20GM103476 · NIGMS · UNIVERSITY OF SOUTHERN MISSISSIPPI · PI MICHAEL R GARRETT · 2012 to 2026
$60.2M
P38alpha in Mouse Embryonic Stem CellsR21HL082731 · NHLBI · UNIVERSITY OF SOUTHERN MISSISSIPPI · PI GUO, YAN-LIN · 2006 to 2007
$395k
Embryonic stem cell-based fibroblast model of innate immunity developmentR15GM109299 · NIGMS · UNIVERSITY OF SOUTHERN MISSISSIPPI · PI GUO, YAN-LIN · 2014 to 2014
$354k
NHLBI NIH HHS HL082731NHLBI NIH HHS R21 HL082731NIGMS NIH HHS 1R15GM109299-01A1NIGMS NIH HHS P20 GM103476NIGMS NIH HHS R15 GM109299
6 · The paper itself

Abstract

We have recently reported that mouse embryonic stem cells (mESCs) are deficient in expressing type I interferons (IFNs) in response to viral infection and synthetic viral RNA analogs (Wang, R., Wang, J., Paul, A. M., Acharya, D., Bai, F., Huang, F., and Guo, Y. L. (2013) J. Biol. Chem. 288, 15926-15936). Here, we report that mESCs are able to respond to type I IFNs, express IFN-stimulated genes, and mediate the antiviral effect of type I IFNs against La Crosse virus and chikungunya virus. The major signaling components in the IFN pathway are expressed in mESCs. Therefore, the basic molecular mechanisms that mediate the effects of type I IFNs are functional in mESCs; however, these mechanisms may not yet be fully developed as mESCs express lower levels of IFN-stimulated genes and display weaker antiviral activity in response to type I IFNs when compared with fibroblasts. Further analysis demonstrated that type I IFNs do not affect the stem cell state of mESCs. We conclude that mESCs are deficient in type I IFN expression, but they can respond to and mediate the cellular effects of type I IFNs. These findings represent unique and uncharacterized properties of mESCs and are important for understanding innate immunity development and ESC physiology.

Indexed as

AnimalsAntiviral AgentsBlotting, WesternCell LineCells, CulturedCell SurvivalChikungunya virusChlorocebus aethiopsCytokinesDose-Response Relationship, DrugEmbryonic Stem CellsFibroblastsGene ExpressionHost-Pathogen InteractionsImmunity, InnateInterferon Type IAntiviral AgentsCytokinesG1p2 protein, mouseIfnar1 protein, mouseInterferon Type IReceptor, Interferon alpha-betaUbiquitinsAntiviral ResponseDouble-stranded RNA (dsRNA)Embryonic Stem CellInnate ImmunityInterferonInterferon-stimulated GenesViral Replication

Identifiers

PMID24966329
PMCPMC4155682
OpenAlexW2080409511

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.