Evidence map›Paper›PMID 17606871›Full record

ArticleThe Journal of cell biology2007

Locally controlled inhibitory mechanisms are involved in eukaryotic GPCR-mediated chemosensing.

Xuehua Xu, Martin Meier-Schellersheim, Jianshe Yan, Tian Jin

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

39 citing papers in PubMed, 95 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Gradients of PI(4,5)PFrontiers in cell and developmental biology · 2022
    Article
  6. Ras inhibitor CAPRI enables neutrophil-like cells to chemotax through a higher-concentration range of gradients.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Adaptation of Living Systems.Annual review of condensed matter physics · 2018
    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

4 authors at 1 institution in 1 country.

Xuehua XuChemotaxis Signal Section, Laboratory of Immunogenetics, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD 20852, USA.
Martin Meier-Schellersheim
Jianshe Yan
Tian Jin
National Institutes of Health · US

Funding

The mechanisms underlying the GPCR-mediated chemotaxis in D. discoideumZIAAI000916 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI JIN, TIAN · 2009 to 2025
$12.3M
Immunology Team Contributions to the PSIIMZIAAI000974 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI GERMAIN, RONALD N · 2009 to 2025
$6.9M
Program in Systems Immunology and Infectious Disease ModelingZ01AI000974 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI GERMAIN, RONALD N · 2006 to 2008
$1.4M
G-protein Coupled Receptor Mediated Directional SensingZ01AI000916 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI JIN, TIAN · 2002 to 2008
$1.2M
Intramural NIH HHS
6 · The paper itself

Abstract

Gprotein-coupled receptor (GPCR) signaling mediates a balance of excitatory and inhibitory activities that regulate Dictyostelium chemosensing to cAMP. The molecular nature and kinetics of these inhibitors are unknown. We report that transient cAMP stimulations induce PIP3 responses without a refractory period, suggesting that GPCR-mediated inhibition accumulates and decays slowly. Moreover, exposure to cAMP gradients leads to asymmetric distribution of the inhibitory components. The gradients induce a stable accumulation of the PIP3 reporter PHCrac-GFP in the front of cells near the cAMP source. Rapid withdrawal of the gradient led to the reassociation of G protein subunits, and the return of the PIP3 phosphatase PTEN and PHCrac-GFP to their pre-stimulus distribution. Reapplication of cAMP stimulation produces a clear PHCrac-GFP translocation to the back but not to the front, indicating that a stronger inhibition is maintained in the front of a polarized cell. Our study demonstrates a novel spatiotemporal feature of currently unknown inhibitory mechanisms acting locally on the PI3K activation pathway.

Indexed as

Signal TransductionAnimalsCell MembraneCell PolarityChemotactic FactorsCyclic AMPDictyosteliumEukaryotic CellsFluorescence Resonance Energy TransferGreen Fluorescent ProteinsKineticsModels, BiologicalPhosphatidylinositol 3-KinasesPhosphoinositide-3 Kinase InhibitorsProtein BindingPTEN PhosphohydrolaseChemotactic FactorsCyclic AMPGreen Fluorescent ProteinsPhosphatidylinositol 3-KinasesPhosphoinositide-3 Kinase InhibitorsPTEN PhosphohydrolaseReceptors, G-Protein-Coupled

Identifiers

PMID17606871
PMCPMC2064430
OpenAlexW1970711216

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.