Evidence map›Paper›PMID 34306313›Full record

ArticleOxidative medicine and cellular longevity2021

Ligase Pellino3 Regulates Macrophage Action and Survival in Response to VSV Infection in RIG-I-Dependent Path.

Patryk Reniewicz, Anna Kula, Edyta Makuch, Michał Ochnik, Tomasz Lipiński, Jakub Siednienko

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 43% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Review
  3. IFNβ-InducedInternational journal of molecular sciences · 2022
    Article
  4. 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

6 authors at 2 institutions in 1 country.

Patryk ReniewiczBioengineering Research Group, Łukasiewicz Research Network-PORT Polish Center for Technology Development, Wroclaw 54-066, Poland.ORCID https://orcid.org/0000-0002-6881-4831
Anna KulaBioengineering Research Group, Łukasiewicz Research Network-PORT Polish Center for Technology Development, Wroclaw 54-066, Poland.ORCID https://orcid.org/0000-0003-4168-7016
Edyta MakuchBioengineering Research Group, Łukasiewicz Research Network-PORT Polish Center for Technology Development, Wroclaw 54-066, Poland.ORCID https://orcid.org/0000-0001-7971-0109
Michał OchnikLaboratory of Virology, Ludwik Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wroclaw 53-114, Poland.ORCID https://orcid.org/0000-0002-9509-1544
Tomasz LipińskiBioengineering Research Group, Łukasiewicz Research Network-PORT Polish Center for Technology Development, Wroclaw 54-066, Poland.ORCID https://orcid.org/0000-0002-4601-6361
Jakub SiednienkoBioengineering Research Group, Łukasiewicz Research Network-PORT Polish Center for Technology Development, Wroclaw 54-066, Poland.ORCID https://orcid.org/0000-0003-2358-5876
Łukasiewicz Research Network – PORT Polish Center for Technology Development · PLLudwik Hirszfeld Institute of Immunology and Experimental Therapy · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sensing of viral particles and elements that initiate mechanisms of immune response is an intrinsic ability of mammalian cells. Regulatory cytokines and antiviral mediators are released after triggering of complex signaling cascades in response to interaction of pathogen particles with pattern recognition receptors (PRRs) leading to the production of interferons (IFN) and proinflammatory cytokines. Viral RNA in the cytoplasm constitute a potent danger molecule that recognition is performed by RIG-I-like receptors, the most common group of receptors in mammalian cells, capable to recognize a foreign RNA. It is known that the E3 ubiquitin ligase Pellino3 plays an important role in antibacterial and antiviral response, but its involvement in the RLR pathways remains poorly understood. In this study, we investigate the molecular mechanisms of the innate immune response in BMDMs (immortalized macrophages from mouse bone marrow) during VSV infection. Here, we present evidence that the activation of the RIG-I/Pellino3/ERK1/2 pathway in BMDMs is crucial for the protection against VSV. We demonstrate that during infection, viral particles replicate in Pellino3 knockout BMDMs more effectively than in wild-type cells. Increased viral replication resulting in cell lysis and death is aid by impaired synthesis of IFN-I and inflammatory cytokines as a consequence of disturbances in the ERK1/2 pathway regulation.

Indexed as

AnimalsCytokinesImmunity, InnateInterferonsMacrophage ActivationMacrophagesMiceRNA, ViralSignal TransductionUbiquitin-Protein LigasesVirus ReplicationCytokinesInterferonsPELI3 protein, mouseRNA, ViralUbiquitin-Protein Ligases

Identifiers

PMID34306313
PMCPMC8266459
OpenAlexW3175697928

What OpenQuestion holds

Textmetadata
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.