Evidence map›Paper›PMID 12045182›Full record

ArticleThe Journal of cell biology2002

Genetic analysis of the role of G protein-coupled receptor signaling in electrotaxis.

Min Zhao, Tian Jin, Colin D McCaig, John V Forrester, Peter N Devreotes

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

38 citing papers in PubMed, 106 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Electrotaxis of Dictyostelium discoideum, Migration in an Electric Field.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  6. The aerotaxis ofFrontiers in cell and developmental biology · 2023
    Article
  7. Article
  8. Article
  9. The Dynamics of Aerotaxis in a Simple Eukaryotic Model.Frontiers in cell and developmental biology · 2021
    Article
  10. Using Live-Cell Imaging and Synthetic Biology to Probe Directed Migration inFrontiers in cell and developmental biology · 2021
    Review
  11. Article
  12. Article
  13. Article
  14. Expression of integrins to control migration direction of electrotaxis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Electric Pulses Can Influence Galvanotaxis ofBioMed research international · 2018
    Article
  20. Excitable Signal Transduction Networks in Directed Cell Migration.Annual review of cell and developmental biology · 2017
    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

5 authors at 3 institutions in 2 countries.

Min ZhaoDepartment of Biomedical Sciences, University of Aberdeen, Aberdeen AB25 2ZD, United Kingdom. m.zhao@abdn.ac.uk
Tian Jin
Colin D McCaig
John V Forrester
Peter N Devreotes
University of Aberdeen · GBJohns Hopkins Medicine · USJohns Hopkins University · 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
G-protein Coupled Receptor Mediated Directional SensingZ01AI000916 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI JIN, TIAN · 2002 to 2008
$1.2M
Wellcome Trust
6 · The paper itself

Abstract

Cells display chemotaxis and electrotaxis by migrating directionally in gradients of specific chemicals or electrical potential. Chemotaxis in Dictyostelium discoideum is mediated by G protein-coupled receptors. The unique Gbeta is essential for all chemotactic responses, although different chemoattractants use different receptors and Galpha subunits. Dictyostelium amoebae show striking electrotaxis in an applied direct current electric field. Perhaps electrotaxis and chemotaxis share similar signaling mechanisms? Null mutation of Gbeta and cAMP receptor 1 and Galpha2 did not abolish electrotaxis, although Gbeta-null mutations showed suppressed electrotaxis. By contrast, G protein signaling plays an essential role in chemotaxis. G protein-coupled receptor signaling was monitored with PHcrac-green fluorescent protein, which translocates to inositol phospholipids at the leading edge of cells during chemotaxis. There was no intracellular gradient of this protein during electrotaxis. However, F-actin was polymerized at the leading edge of cells during electrotaxis. We conclude that reception and transduction of the electrotaxis signal are largely independent of G protein-coupled receptor signaling and that the pathways driving chemotaxis and electrotaxis intersect downstream of heterotrimeric G proteins to invoke cytoskeletal elements.

Indexed as

Cell MovementElectrophysiologyActinsAnimalsBiological TransportDictyosteliumGreen Fluorescent ProteinsGTP-Binding ProteinsIn Vitro TechniquesLuminescent ProteinsMutationPhosphatidylinositolsReceptors, Cell SurfaceReceptors, Cyclic AMPSignal TransductionActinsGreen Fluorescent ProteinsGTP-Binding ProteinsLuminescent ProteinsPhosphatidylinositolsReceptors, Cell SurfaceReceptors, Cyclic AMP

Identifiers

PMID12045182
PMCPMC2174050
OpenAlexW1976669405

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.