Evidence map›Paper›PMID 21956105›Full record

ArticleThe Journal of biological chemistry2011

Cooperation of p40(phox) with p47(phox) for Nox2-based NADPH oxidase activation during Fcγ receptor (FcγR)-mediated phagocytosis: mechanism for acquisition of p40(phox) phosphatidylinositol 3-phosphate (PI(3)P) binding.

Takehiko Ueyama, Junya Nakakita, Takashi Nakamura, Takeshi Kobayashi, Toshihiro Kobayashi, Jeonghyun Son, Megumi Sakuma, Hirofumi Sakaguchi, Thomas L Leto, Naoaki Saito

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

25 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
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  9. The Host Autophagy DuringFrontiers in microbiology · 2020
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  13. Article
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  18. The clearance of dying cells: table for two.Cell death and differentiation · 2016
    Review
  19. Article
  20. 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

10 authors at 4 institutions in 2 countries.

Takehiko UeyamaLaboratory of Molecular Pharmacology, Biosignal Research Center, Kobe University, Kobe 657-8501, Japan. tueyama@kobe-u.ac.jp
Junya Nakakita
Takashi Nakamura
Takeshi Kobayashi
Toshihiro Kobayashi
Jeonghyun Son
Megumi Sakuma
Hirofumi Sakaguchi
Thomas L Leto
Naoaki Saito
Kobe University · JPNagoya University · JPKyoto Prefectural University of Medicine · JPNational Institutes of Health · US

Funding

NOX family NADPH oxidases: roles in innate immunity and inflammatory diseaseZIAAI000614 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI LETO, THOMAS · 2009 to 2024
$16.2M
Intramural NIH HHS
6 · The paper itself

Abstract

During activation of the phagocyte (Nox2-based) NADPH oxidase, the cytoplasmic Phox complex (p47(phox)-p67(phox)-p40(phox)) translocates and associates with the membrane-spanning flavocytochrome b(558). It is unclear where (in cytoplasm or on membranes), when (before or after assembly), and how p40(phox) acquires its PI(3)P-binding capabilities. We demonstrated that in addition to conformational changes induced by H(2)O(2) in the cytoplasm, p40(phox) acquires PI(3)P-binding through direct or indirect membrane targeting. We also found that p40(phox) is essential when p47(phox) is partially phosphorylated during FcγR-mediated oxidase activation; however, p40(phox) is less critical when p47(phox) is adequately phosphorylated, using phosphorylation-mimicking mutants in HEK293(Nox2/FcγRIIa) and RAW264.7(p40/p47KD) cells. Moreover, PI binding to p47(phox) is less important when the autoinhibitory PX-PB1 domain interaction in p40(phox) is disrupted or when p40(phox) is targeted to membranes. Furthermore, we suggest that high affinity PI(3)P binding of the p40(phox) PX domain is critical during its accumulation on phagosomes, even when masked by the PB1 domain in the resting state. Thus, in addition to mechanisms for directly acquiring PI(3)P binding in the cytoplasm by H(2)O(2), p40(phox) can acquire PI(3)P binding on targeted membranes in a p47(phox)-dependent manner and functions both as a "carrier" of the cytoplasmic Phox complex to phagosomes and an "adaptor" of oxidase assembly on phagosomes in cooperation with p47(phox), using positive feedback mechanisms.

Indexed as

PhagocytosisAnimalsCell MembraneEndosomesEnzyme ActivationGlassHEK293 CellsHumansHydrogen PeroxideImmunoglobulin GMembrane GlycoproteinsMiceMutationNADPH Oxidase 2NADPH OxidasesPhagosomesCYBB protein, humanFc gamma receptor IIAHydrogen PeroxideImmunoglobulin GMembrane GlycoproteinsNADPH Oxidase 2NADPH Oxidasesneutrophil cytosol factor 40Kneutrophil cytosol factor 67Kneutrophil cytosolic factor 1phosphatidylinositol 3-phosphatePhosphatidylinositol PhosphatesPhosphoproteinsReactive Oxygen SpeciesReceptors, IgG

Identifiers

PMID21956105
PMCPMC3220462
OpenAlexW2156732178

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.