Evidence map›Paper›PMID 23857584›Full record

ArticleThe Journal of biological chemistry2013

FcγR-driven release of IL-6 by macrophages requires NOX2-dependent production of reactive oxygen species.

Anthony M Franchini, Danielle Hunt, J Andres Melendez, James R Drake

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

26 citing papers in PubMed, 50 citations in OpenAlex.

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  12. Article
  13. Role of p40FEBS open bio · 2021
    Article
  14. Article
  15. Akt3 induces oxidative stress and DNA damage by activating the NADPH oxidase via phosphorylation of p47Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  16. 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 2 institutions in 1 country.

Anthony M FranchiniFrom the Center for Immunology and Microbial Disease, Albany Medical College, Albany, New York 12208 and.
Danielle HuntFrom the Center for Immunology and Microbial Disease, Albany Medical College, Albany, New York 12208 and.
J Andres Melendezthe College of Nanoscale Science and Engineering, University at Albany-State University of New York, Albany, New York 12203.
James R DrakeFrom the Center for Immunology and Microbial Disease, Albany Medical College, Albany, New York 12208 and. Electronic address: DrakeJ@mail.amc.edu.
Albany Medical Center Hospital · USAlbany State University · US

Funding

TLR2/NLR Signal Regulation of Protective Immunity to F. TularensisP01AI056320 · NIAID · ALBANY MEDICAL COLLEGE · PI METZGER, DENNIS W · 2003 to 2016
$22.9M
NIAID NIH HHS P01 AI056320
6 · The paper itself

Abstract

Activation of the FcγR via antigen containing immune complexes can lead to the generation of reactive oxygen species, which are potent signal transducing molecules. However, whether ROS contribute to FcγR signaling has not been studied extensively. We set out to elucidate the role of NADPH oxidase-generated ROS in macrophage activation following FcγR engagement using antigen-containing immune complexes. We hypothesized that NOX2 generated ROS is necessary for propagation of downstream FcγR signaling and initiation of the innate immune response. Following exposure of murine bone marrow-derived macrophages (BMDMs) to inactivated Francisella tularensis (iFt)-containing immune complexes, we observed a significant increase in the innate inflammatory cytokine IL-6 at 24 h compared with macrophages treated with Ft LVS-containing immune complexes. Ligation of the FcγR by opsonized Ft also results in significant ROS production. Macrophages lacking the gp91(phox) subunit of NOX2 fail to produce ROS upon FcγR ligation, resulting in decreased Akt phosphorylation and a reduction in the levels of IL-6 compared with wild type macrophages. Similar results were seen following infection of BMDMs with catalase deficient Ft that fail to scavenge hydrogen peroxide. In conclusion, our findings demonstrate that ROS participate in elicitation of an effective innate immune in response to antigen-containing immune complexes through FcγR.

Indexed as

AnimalsBacterial ProteinsBone Marrow CellsCatalaseFrancisella tularensisHydrogen PeroxideImmunity, InnateInterleukin-6MacrophagesMembrane GlycoproteinsMiceMice, KnockoutNADPH Oxidase 2NADPH OxidasesProto-Oncogene Proteins c-aktReceptors, IgGBacterial ProteinsCatalaseCybb protein, mouseHydrogen PeroxideInterleukin-6Membrane GlycoproteinsNADPH Oxidase 2NADPH OxidasesProto-Oncogene Proteins c-aktReceptors, IgGAktFC ReceptorsFrancisella tularensisMacrophagesNADPH OxidaseReactive Oxygen Species (ROS)

Identifiers

PMID23857584
PMCPMC3757174
OpenAlexW2096604171

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.