Evidence map›Paper›PMID 11950931›Full record

ArticleMolecular biology of the cell2002

Phosphoinositides regulate membrane-dependent actin assembly by latex bead phagosomes.

Hélène Defacque, Evelyne Bos, Boyan Garvalov, Cécile Barret, Christian Roy, Paul Mangeat, Hye-Won Shin, Vladimir Rybin, Gareth Griffiths

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 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

32 citing papers in PubMed, 70 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Expression and Functional Role of TRPV4 in Bone Marrow-Derived CD11cInternational journal of molecular sciences · 2019
    Article
  5. Osmotic activation of a CaPhysiological reports · 2017
    Article
  6. Review
  7. Article
  8. Phosphatidylinositol 4-phosphate and phosphatidylinositol 3-phosphate regulate phagolysosome biogenesis.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Mammalian septins are required for phagosome formation.Molecular biology of the cell · 2008
    Article
  20. Four distinct pathways of hemoglobin uptake in the malaria parasite Plasmodium falciparum.Proceedings of the National Academy of Sciences of the United States of America · 2008
    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

9 authors at 2 institutions in 2 countries.

Hélène DefacqueEuropean Molecular Biology Laboratory, 69012 Heidelberg, Germany.
Evelyne Bos
Boyan Garvalov
Cécile Barret
Christian Roy
Paul Mangeat
Hye-Won Shin
Vladimir Rybin
Gareth Griffiths
European Molecular Biology Laboratory · DECentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Actin assembly on membrane surfaces is an elusive process in which several phosphoinositides (PIPs) have been implicated. We have reconstituted actin assembly using a defined membrane surface, the latex bead phagosome (LBP), and shown that the PI(4,5)P(2)-binding proteins ezrin and/or moesin were essential for this process (). Here, we provide several lines of evidence that both preexisting and newly synthesized PI(4,5)P(2), and probably PI(4)P, are essential for phagosomal actin assembly; only these PIPs were routinely synthesized from ATP during in vitro actin assembly. Treatment of LBP with phospholipase C or with adenosine, an inhibitor of type II PI 4-kinase, as well as preincubation with anti-PI(4)P or anti-PI(4,5)P(2) antibodies all inhibited this process. Incorporation of extra PI(4)P or PI(4,5)P(2) into the LBP membrane led to a fivefold increase in the number of phagosomes that assemble actin. An ezrin mutant mutated in the PI(4,5)P(2)-binding sites was less efficient in binding to LBPs and in reconstituting actin assembly than wild-type ezrin. Our data show that PI 4- and PI 5-kinase, and under some conditions also PI 3-kinase, activities are present on LBPs and can be activated by ATP, even in the absence of GTP or cytosolic components. However, PI 3-kinase activity is not required for actin assembly, because the process was not affected by PI 3-kinase inhibitors. We suggest that the ezrin-dependent actin assembly on the LBP membrane may require active turnover of D4 and D5 PIPs on the organelle membrane.

Indexed as

PhagocytosisBinding SitesCell MembraneCells, CulturedChromatography, High Pressure LiquidChromatography, Thin LayerCytoskeletal ProteinsEnzyme InhibitorsEzrinFluorescent Antibody TechniqueLatexMicroscopy, FluorescenceMutationPhagosomesPhosphatidylinositolsPhosphoinositide-3 Kinase InhibitorsCytoskeletal ProteinsEnzyme InhibitorsEzrinLatexPhosphatidylinositolsPhosphoinositide-3 Kinase InhibitorsPhosphoproteinsType C Phospholipases

Identifiers

PMID11950931
PMCPMC102261
OpenAlexW2096501489

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.