Evidence map›Paper›PMID 20813901›Full record

ArticleBlood2010

PtdIns3P and Rac direct the assembly of the NADPH oxidase on a novel, pre-phagosomal compartment during FcR-mediated phagocytosis in primary mouse neutrophils.

Karen E Anderson, Tamara A M Chessa, Keith Davidson, Robert B Henderson, Simon Walker, Tanya Tolmachova, Katarzyna Grys, Oliver Rausch, Miguel C Seabra, Victor L J Tybulewicz and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

34 citing papers in PubMed, 65 citations in OpenAlex.

  1. Review
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  11. The Role of Macrophages inFrontiers in immunology · 2020
    Review
  12. Article
  13. Association ofJournal of immunology research · 2020
    Article
  14. 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

12 authors at 3 institutions in 1 country.

Karen E AndersonInositide Laboratory, Babraham Institute, Babraham Research Campus, Cambridge, UK.
Tamara A M Chessa
Keith Davidson
Robert B Henderson
Simon Walker
Tanya Tolmachova
Katarzyna Grys
Oliver Rausch
Miguel C Seabra
Victor L J Tybulewicz
Len R Stephens
Phillip T Hawkins
Babraham Institute · GBImperial College London · GBUCB Pharma (United Kingdom) · GB

Funding

Biotechnology and Biological Sciences Research Council BBS/E/B/0000C218Biotechnology and Biological Sciences Research Council BBS/E/B/0000M211Medical Research Council G0600840Medical Research Council G9805886Wellcome TrustWellcome Trust WT085889MA
6 · The paper itself

Abstract

The generation of reactive oxygen species (ROS) by the nicotinamide adenine dinucleotide phosphate oxidase is an important mechanism by which neutrophils kill pathogens. The oxidase is composed of a membrane-bound cytochrome and 4 soluble proteins (p67(phox), p40(phox), p47(phox), and GTP-Rac). These components form an active complex at the correct time and subcellular location through a series of incompletely understood mutual interactions, regulated, in part, by GTP/GDP exchange on Rac, protein phosphorylation, and binding to lipid messengers. We have used a variety of assays to follow the spatiotemporal assembly of the oxidase in genetically engineered primary mouse neutrophils, during phagocytosis of both serum- and immunoglobulin G-opsonized targets. The oxidase assembles directly on serum-Staphylococcus aureus-containing phagosomes within seconds of phagosome formation; this process is only partially dependent (∼ 30%) on PtdIns3P binding to p40(phox), but totally dependent on Rac1/2 binding to p67(phox). In contrast, in response to immunoglobulin G-targets, the oxidase first assembles on a tubulovesicular compartment that develops at sites of granule fusion to the base of the emerging phagosome; oxidase assembly and activation is highly dependent on both PtdIns3P-p40(phox) and Rac2-p67(phox) interactions and delivery to the phagosome is regulated by Rab27a. These results define a novel pathway for oxidase assembly downstream of FcR-activation.

Indexed as

AnimalsEnzyme ActivationHumansMiceMice, KnockoutNADPH OxidasesNeutrophilsPhagocytosisPhosphatidylinositol PhosphatesPhosphoproteinsrac GTP-Binding ProteinsReactive Oxygen SpeciesReceptors, FcNADPH Oxidasesneutrophil cytosol factor 40Kneutrophil cytosol factor 67Kphosphatidylinositol 3-phosphatePhosphatidylinositol PhosphatesPhosphoproteinsrac GTP-Binding ProteinsReactive Oxygen SpeciesReceptors, Fc

Identifiers

PMID20813901
PMCPMC3368544
OpenAlexW2086730788

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.