Evidence map›Paper›PMID 11950933›Full record

ArticleMolecular biology of the cell2002

Vav regulates activation of Rac but not Cdc42 during FcgammaR-mediated phagocytosis.

Jayesh C Patel, Alan Hall, Emmanuelle Caron

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
9.9field-weighted citation impact, top 1% 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

47 citing papers in PubMed, 125 citations in OpenAlex.

  1. Article
  2. Phagocytosis at a glance.Journal of cell science · 2025
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  16. Phagocytosis: A Fundamental Process in Immunity.BioMed research international · 2017
    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

3 authors at 1 institution in 1 country.

Jayesh C PatelMedical Research Council Laboratory for Molecular Cell Biology, Department of Biochemistry and Molecular Biology, University College London, London WC1E 6BT, United Kingdom.
Alan Hall
Emmanuelle Caron
MRC Laboratory for Molecular Cell Biology · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

Phagocytosis is the process whereby cells direct the spatially localized, receptor-driven engulfment of particulate materials. It proceeds via remodeling of the actin cytoskeleton and shares many of the core cytoskeletal components involved in adhesion and migration. Small GTPases of the Rho family have been widely implicated in coordinating actin dynamics in response to extracellular signals and during diverse cellular processes, including phagocytosis, yet the mechanisms controlling their recruitment and activation are not known. We show herein that in response to ligation of Fc receptors for IgG (FcgammaR), the guanine nucleotide exchange factor Vav translocates to nascent phagosomes and catalyzes GTP loading on Rac, but not Cdc42. The Vav-induced Rac activation proceeds independently of Cdc42 function, suggesting distinct roles for each GTPase during engulfment. Moreover, inhibition of Vav exchange activity or of Cdc42 activity does not prevent Rac recruitment to sites of particle attachment. We conclude that Rac is recruited to Fcgamma membrane receptors in its inactive, GDP-bound state and that Vav regulates phagocytosis through subsequent catalysis of GDP/GTP exchange on Rac.

Indexed as

AnimalsCatalysiscdc42 GTP-Binding ProteinCell LineCOS CellsMacrophagesMiceMicroscopy, FluorescenceModels, BiologicalOncogene ProteinsPhagocytosisProtein BindingProtein ConformationProto-Oncogene Proteins c-vavrac GTP-Binding ProteinsReceptors, IgGcdc42 GTP-Binding ProteinOncogene ProteinsProto-Oncogene Proteins c-vavrac GTP-Binding ProteinsReceptors, IgGrho GTP-Binding ProteinsVav1 protein, mouse

Identifiers

PMID11950933
PMCPMC102263
OpenAlexW2147897016

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.