Evidence map›Paper›PMID 31308397›Full record

ArticleScientific reports2019

Perturbation of ubiquitin homeostasis promotes macrophage oxidative defenses.

Marie-Eve Charbonneau, Karla D Passalacqua, Susan E Hagen, Hollis D Showalter, Christiane E Wobus, Mary X D O'Riordan

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

15 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Almost 50 Years of Monomeric Extracellular Ubiquitin (eUb).Pharmaceuticals (Basel, Switzerland) · 2024
    Review
  5. Article
  6. Article
  7. Epithelial sodium channels in macrophage migration and polarization: role of proinflammatory cytokines TNFα and IFNγ.American journal of physiology. Regulatory, integrative and comparative physiology · 2022
    Article
  8. Review
  9. Review
  10. Article
  11. Ubiquitin-related processes and innate immunity in C. elegans.Cellular and molecular life sciences : CMLS · 2021
    Review
  12. Functions of ROS in Macrophages and Antimicrobial Immunity.Antioxidants (Basel, Switzerland) · 2021
    Review
  13. Article
  14. Review
  15. Article
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.

Marie-Eve CharbonneauDepartment of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan, 48109, United States of America.
Karla D PassalacquaDepartment of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan, 48109, United States of America.
Susan E HagenDepartment of Medicinal Chemistry, College of Pharmacy, University of Michigan, Ann Arbor, Michigan, 48109, United States of America.
Hollis D ShowalterDepartment of Medicinal Chemistry, College of Pharmacy, University of Michigan, Ann Arbor, Michigan, 48109, United States of America.
Christiane E WobusDepartment of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan, 48109, United States of America.
Mary X D O'RiordanDepartment of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan, 48109, United States of America. oriordan@umich.edu.
University of Michigan–Ann Arbor · US

Funding

Targeting host deubiquitinases for broad spectrum anti-infective therapyR33AI102106 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI O'RIORDAN, MARY · 2014 to 2016
$1.4M
Targeting host deubiquitinases for broad spectrum anti-infective therapyR21AI102106 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI O'RIORDAN, MARY, WOBUS, CHRISTIANE · 2012 to 2013
$423k
NIAID NIH HHS R21 AI102106NIAID NIH HHS R33 AI102106
6 · The paper itself

Abstract

The innate immune system senses microbial ligands through pattern recognition and triggers downstream signaling cascades to promote inflammation and immune defense mechanisms. Emerging evidence suggests that cells also recognize alterations in host processes induced by infection as triggers. Protein ubiquitination and deubiquitination are post-translational modification processes essential for signaling and maintenance of cellular homeostasis, and infections can cause global alterations in the host ubiquitin proteome. Here we used a chemical biology approach to perturb the cellular ubiquitin proteome as a simplified model to study the impact of ubiquitin homeostasis alteration on macrophage function. Perturbation of ubiquitin homeostasis led to a rapid and transient burst of reactive oxygen species (ROS) that promoted macrophage inflammatory and anti-infective capacity. Moreover, we found that ROS production was dependent on the NOX2 phagocyte NADPH oxidase. Global alteration of the ubiquitin proteome also enhanced proinflammatory cytokine production in mice stimulated with a sub-lethal dose of LPS. Collectively, our findings suggest that major changes in the host ubiquitin landscape may be a potent signal to rapidly deploy innate immune defenses.

Indexed as

AnimalsFemaleHomeostasisImmunity, InnateInflammationMacrophagesMiceMice, Inbred C57BLNADPH OxidasesOxidation-ReductionOxidative StressPhagocytesRAW 264.7 CellsReactive Oxygen SpeciesSignal TransductionUbiquitinNADPH OxidasesReactive Oxygen SpeciesUbiquitin

Identifiers

PMID31308397
PMCPMC6629656
OpenAlexW2958933207

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.