Evidence map›Paper›PMID 24591580›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

Sequential breakdown of 3-phosphorylated phosphoinositides is essential for the completion of macropinocytosis.

Masashi Maekawa, Shimpei Terasaka, Yasuhiro Mochizuki, Katsuhisa Kawai, Yuka Ikeda, Nobukazu Araki, Edward Y Skolnik, Tomohiko Taguchi, Hiroyuki Arai

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
–field-weighted citation impact
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

60 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Phafins Are More Than Phosphoinositide-Binding Proteins.International journal of molecular sciences · 2023
    Review
  12. Phosphoinositides as membrane organizers.Nature reviews. Molecular cell biology · 2022
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  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

9 authors.

Masashi MaekawaDepartment of Health Chemistry and Pathological Cell Biology Laboratory, Graduate School of Pharmaceutical Sciences, University of Tokyo, Tokyo 113-0033, Japan.
Shimpei Terasaka
Yasuhiro Mochizuki
Katsuhisa Kawai
Yuka Ikeda
Nobukazu Araki
Edward Y Skolnik
Tomohiko Taguchi
Hiroyuki Arai

Funding

TRIM27 is a new negative regulator of CD4 T cells and Mast cells.R01GM099873 · NIGMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI SKOLNIK, EDWARD Y · 2012 to 2015
$1.5M
New Signaling pathways that positively and negatively regulate CD4 T cells via thR01AI080583 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI SKOLNIK, EDWARD Y · 2008 to 2014
$1.0M
NIAID NIH HHS R01 AI080583NIAID NIH HHS R01AI080583NIGMS NIH HHS R01 GM099873
6 · The paper itself

Abstract

Macropinocytosis is a highly conserved endocytic process by which extracellular fluid and solutes are internalized into cells. Macropinocytosis starts with the formation of membrane ruffles at the plasma membrane and ends with their closure. The transient and sequential emergence of phosphoinositides PI(3,4,5)P3 and PI(3,4)P2 in the membrane ruffles is essential for macropinocytosis. By making use of information in the Caenorhabditis elegans mutants defective in fluid-phase endocytosis, we found that mammalian phosphoinositide phosphatase MTMR6 that dephosphorylates PI(3)P to PI, and its binding partner MTMR9, are required for macropinocytosis. INPP4B, which dephosphorylates PI(3,4)P2 to PI(3)P, was also found to be essential for macropinocytosis. These phosphatases operate after the formation of membrane ruffles to complete macropinocytosis. Finally, we showed that KCa3.1, a Ca(2+)-activated K(+) channel that is activated by PI(3)P, is required for macropinocytosis. We propose that the sequential breakdown of PI(3,4,5)P3 → PI(3,4)P2 → PI(3)P → PI controls macropinocytosis through specific effectors of the intermediate phosphoinositides.

Indexed as

AnimalsCaenorhabditis elegansCell LineDNA PrimersHumansMicroscopy, Electron, ScanningMicroscopy, FluorescencePhosphatidylinositol PhosphatesPhosphoric Monoester HydrolasesPhosphorylationPinocytosisProtein Tyrosine Phosphatases, Non-ReceptorReverse Transcriptase Polymerase Chain ReactionRNA InterferenceRNA, Small InterferingDNA PrimersMTMR6 protein, humanphosphatidylinositol-3,4-bisphosphate 4-phosphatasePhosphatidylinositol PhosphatesPhosphoric Monoester HydrolasesProtein Tyrosine Phosphatases, Non-ReceptorRNA, Small Interfering

Identifiers

PMID24591580
PMCPMC3964036

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.