Evidence map›Paper›PMID 18824569›Full record

ArticleThe Journal of cell biology2008

Tre1 GPCR initiates germ cell transepithelial migration by regulating Drosophila melanogaster E-cadherin.

Prabhat S Kunwar, Hiroko Sano, Andrew D Renault, Vitor Barbosa, Naoyuki Fuse, Ruth Lehmann

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

46 citing papers in PubMed, 84 citations in OpenAlex.

  1. Harnessing the Power ofCold Spring Harbor perspectives in biology · 2026
    Review
  2. Heterotypic intercellular adhesion tunes efficiency of cell-on-cell migration.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Hedgehog and Drosophila germ cell migration.Development (Cambridge, England) · 2025
    Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. The Journal of cell biology · 2018
    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

6 authors at 3 institutions in 2 countries.

Prabhat S KunwarHoward Hughes Medical Institute, New York University School of Medicine, New York, NY 10016, USA.
Hiroko Sano
Andrew D Renault
Vitor Barbosa
Naoyuki Fuse
Ruth Lehmann
Howard Hughes Medical Institute · USKyoto University · JPNew York University · US

Funding

Germ Cell Migration in Drosophila.R01HD041900 · NICHD · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI LEHMANN, RUTH · 2001 to 2012
$3.5M
UW Multidisciplinary Clinical Research Training (RMI)K12HD049100 · NICHD · UNIVERSITY OF WASHINGTON · PI DEYO, RICHARD A · 2004 to 2004
$1.3M
Howard Hughes Medical InstituteNICHD NIH HHS HD49100NICHD NIH HHS K12 HD049100NICHD NIH HHS R01 HD041900
6 · The paper itself

Abstract

Despite significant progress in identifying the guidance pathways that control cell migration, how a cell starts to move within an intact organism, acquires motility, and loses contact with its neighbors is poorly understood. We show that activation of the G protein-coupled receptor (GPCR) trapped in endoderm 1 (Tre1) directs the redistribution of the G protein Gbeta as well as adherens junction proteins and Rho guanosine triphosphatase from the cell periphery to the lagging tail of germ cells at the onset of Drosophila melanogaster germ cell migration. Subsequently, Tre1 activity triggers germ cell dispersal and orients them toward the midgut for directed transepithelial migration. A transition toward invasive migration is also a prerequisite for metastasis formation, which often correlates with down-regulation of adhesion proteins. We show that uniform down-regulation of E-cadherin causes germ cell dispersal but is not sufficient for transepithelial migration in the absence of Tre1. Our findings therefore suggest a new mechanism for GPCR function that links cell polarity, modulation of cell adhesion, and invasion.

Indexed as

AnimalsCadherinsCell AdhesionCell MovementCell PolarityDrosophila melanogasterDrosophila ProteinsEmbryo, NonmammalianEpitheliumFemaleGerm CellsHeterotrimeric GTP-Binding ProteinsMembrane Transport ProteinsMicroscopy, ElectronMutationProtein SubunitsCadherinsDrosophila Proteinsgbb protein, DrosophilaHeterotrimeric GTP-Binding ProteinsMembrane Transport ProteinsProtein SubunitsReceptors, G-Protein-CoupledTransforming Growth Factor betaTre1 protein, Drosophilatud protein, Drosophila

Identifiers

PMID18824569
PMCPMC2557050
OpenAlexW2172152017

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.