Evidence map›Paper›PMID 12802064›Full record

ArticleMolecular biology of the cell2003

Receptor-mediated regulation of PI3Ks confines PI(3,4,5)P3 to the leading edge of chemotaxing cells.

Yi Elaine Huang, Miho Iijima, Carole A Parent, Satoru Funamoto, Richard A Firtel, Peter Devreotes

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 101 papers.

0numbers the graph read from it
0cells of the map it votes in
101citing papers in PubMed
7.7field-weighted citation impact, top 2% 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

101 citing papers in PubMed, 234 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Gradients of PI(4,5)PFrontiers in cell and developmental biology · 2022
    Article
  11. Article
  12. Article
  13. Review
  14. Using Live-Cell Imaging and Synthetic Biology to Probe Directed Migration inFrontiers in cell and developmental biology · 2021
    Review
  15. Article
  16. IQGAP-related protein IqgC suppresses Ras signaling during large-scale endocytosis.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  17. Article
  18. Article
  19. Review
  20. Article

41 more citing papers are in PubMed but not listed here.

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

6 authors at 3 institutions in 1 country.

Yi Elaine HuangDepartment of Cell Biology, Johns Hopkins University, School of Medicine, Baltimore, Maryland 21205, USA.
Miho Iijima
Carole A Parent
Satoru Funamoto
Richard A Firtel
Peter Devreotes
Johns Hopkins University · USUniversity of California San Diego · USNational Institutes of Health · US

Funding

Temporal and Spatial Signaling in ChemotaxisR01GM034933 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI DEVREOTES, PETER N · 1987 to 2015
$8.8M
SIGNAL TRANSDUCTION AND CELL MIGRATIONZ01BC010418 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI PARENT, CAROLE · 2000 to 2008
$2.5M
NIGMS NIH HHS GM34933NIGMS NIH HHS R01 GM034933PHS HHS 29007
6 · The paper itself

Abstract

Recent studies have demonstrated that PH domains specific for PI(3,4,5)P3 accumulate at the leading edge of a number of migrating cells and that PI3Ks and PTEN associate with the membrane at the front and back, respectively, of chemotaxing Dictyostelium discoideum cells. However, the dependence of chemoattractant induced changes in PI(3,4,5)P3 on PI3K and PTEN activities have not been defined. We find that bulk PI(3,4,5)P3 levels increase transiently upon chemoattractant stimulation, and the changes are greater and more prolonged in pten- cells. PI3K activation increases within 5 s of chemoattractant addition and then declines to a low level of activity identically in wild-type and pten- cells. Reconstitution of the PI3K activation profile can be achieved by mixing membranes from stimulated pi3k1-/pi3k2- cells with cytosolic PI3Ks from unstimulated cells. These studies show that significant control of chemotaxis occurs upstream of the PI3Ks and that regulation of the PI3Ks and PTEN cooperate to shape the temporal and spatial localization of PI(3,4,5)P3.

Indexed as

AnimalsCell MembraneChemotaxisDictyosteliumGuanosine 5'-O-(3-Thiotriphosphate)Phosphatidylinositol 3-KinasesPhosphatidylinositolsPhosphoric Monoester HydrolasesProtein KinasesPTEN PhosphohydrolaseTumor Suppressor ProteinsGuanosine 5'-O-(3-Thiotriphosphate)Phosphatidylinositol 3-KinasesPhosphatidylinositolsphosphoinositide-3,4,5-triphosphatePhosphoric Monoester HydrolasesProtein KinasesPTEN PhosphohydrolaseTumor Suppressor ProteinsYakA protein, Dictyostelium discoideum

Identifiers

PMID12802064
PMCPMC165086
OpenAlexW2168711416

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.