Evidence map›Paper›PMID 19926792›Full record

ArticleThe Journal of biological chemistry2010

Sequestering of Rac by the Yersinia effector YopO blocks Fcgamma receptor-mediated phagocytosis.

Eleanor Groves, Katrin Rittinger, Marlise Amstutz, Sara Berry, David W Holden, Guy R Cornelis, Emmanuelle Caron

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

22 citing papers in PubMed, 41 citations in OpenAlex.

  1. Evaluation of Proteomic and Lipidomic Changes inInternational journal of molecular sciences · 2022
    Article
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  7. Review
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  9. Yersinia type III effectors perturb host innate immune responses.World journal of biological chemistry · 2016
    Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Yersinia pestis: mechanisms of entry into and resistance to the host cell.Frontiers in cellular and infection microbiology · 2013
    Review
  20. Tyrosine phosphorylation and bacterial virulence.International journal of oral science · 2012
    Review
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

7 authors at 2 institutions in 2 countries.

Eleanor GrovesFrom the Centre for Molecular Microbiology and Infection, Imperial College London, London SW7 2AZ, United Kingdom. Electronic address: e.groves@imperial.ac.uk.
Katrin Rittingerthe Division of Molecular Structure, National Institute for Medical Research, The Ridgeway, London NW7 1AA, United Kingdom, and.
Marlise AmstutzInfection Biology, Biozentrum, University of Basel, Klingenbergstrasse 50/70, CH-4056 Basel, Switzerland.
Sara BerryFrom the Centre for Molecular Microbiology and Infection, Imperial College London, London SW7 2AZ, United Kingdom.
David W HoldenFrom the Centre for Molecular Microbiology and Infection, Imperial College London, London SW7 2AZ, United Kingdom.
Guy R CornelisInfection Biology, Biozentrum, University of Basel, Klingenbergstrasse 50/70, CH-4056 Basel, Switzerland.
Emmanuelle CaronFrom the Centre for Molecular Microbiology and Infection, Imperial College London, London SW7 2AZ, United Kingdom.
Imperial College London · GBUniversity of Basel · CH

Funding

Medical Research Council G0800148Medical Research Council MC_U117565398
6 · The paper itself

Abstract

Pathogenic Yersinia species neutralize innate immune mechanisms by injecting type three secretion effectors into immune cells, altering cell signaling. Our study elucidates how one of these effectors, YopO, blocks phagocytosis. We demonstrate using different phagocytic models that YopO specifically blocks Rac-dependent Fcgamma receptor internalization pathway but not complement receptor 3-dependent uptake, which is controlled by Rho activity. We show that YopO prevents Rac activation but does not affect Rac accumulation at the phagocytic cup. In addition, we show that plasma membrane localization and the guanine-nucleotide dissociation inhibitor (GDI)-like domain of YopO cooperate for maximal anti-phagocytosis. Although YopO has the same affinity for Rac1, Rac2, and RhoA in vitro, it selectively interacts with Rac isoforms in cells. This is due to the differential localization of the Rho family G proteins in resting cells; Rac isoforms partially exist as a GDI-free pool at the membrane of resting cells, whereas RhoA is trapped in the cytosol by RhoGDIalpha. We propose that YopO exploits this basic difference in localization and availability to selectively inhibit Rac-dependent phagocytosis.

Indexed as

PhagocytosisAnimalsBacterial ProteinsBinding SitesBlotting, WesternCell LineCell MembraneChlorocebus aethiopsCOS CellsGreen Fluorescent ProteinsGuanine Nucleotide Dissociation InhibitorsHumansMacrophagesMiceMicroscopy, ConfocalMutationBacterial ProteinsFc gamma receptor IIAGDP dissociation inhibitor 1Green Fluorescent ProteinsGuanine Nucleotide Dissociation InhibitorsProtein Serine-Threonine Kinasesrac1 GTP-Binding ProteinReceptors, IgGrhoA GTP-Binding ProteinYopO protein, Yersinia enterocolitica

Identifiers

PMID19926792
PMCPMC2823549
OpenAlexW1978946613

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.