Evidence map›Paper›PMID 32901019›Full record

ArticleNature communications2020

Collectively stabilizing and orienting posterior migratory forces disperses cell clusters in vivo.

B Lin, J Luo, R Lehmann

Abstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
  2. Harnessing the Power ofCold Spring Harbor perspectives in biology · 2026
    Review
  3. Hedgehog and Drosophila germ cell migration.Development (Cambridge, England) · 2025
    Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Generation ofmicroPublication biology · 2025
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Profile of Ruth Lehmann.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  16. Article
  17. Dissection and Live-Imaging of the Late Embryonic Drosophila Gonad.Journal of visualized experiments : JoVE · 2020
    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

3 authors.

B LinHHMI and Kimmel Center for Biology and Medicine of the Skirball Institute, Department of Cell Biology, New York University School of Medicine, New York, NY, USA. Benjamin.lin@nyulangone.org.ORCID http://orcid.org/0000-0003-1095-8725
J LuoHHMI and Kimmel Center for Biology and Medicine of the Skirball Institute, Department of Cell Biology, New York University School of Medicine, New York, NY, USA.
R LehmannHHMI and Kimmel Center for Biology and Medicine of the Skirball Institute, Department of Cell Biology, New York University School of Medicine, New York, NY, USA. Lehmann@wi.mit.edu.ORCID http://orcid.org/0000-0002-8454-5651

Funding

Germ Cell Migration in Drosophila.R37HD041900 · NICHD · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI LEHMANN, RUTH · 2013 to 2021
$2.6M
Howard Hughes Medical InstituteNICHD NIH HHS R37 HD041900
6 · The paper itself

Abstract

Individual cells detach from cohesive ensembles during development and can inappropriately separate in disease. Although much is known about how cells separate from epithelia, it remains unclear how cells disperse from clusters lacking apical-basal polarity, a hallmark of advanced epithelial cancers. Here, using live imaging of the developmental migration program of Drosophila primordial germ cells (PGCs), we show that cluster dispersal is accomplished by stabilizing and orienting migratory forces. PGCs utilize a G protein coupled receptor (GPCR), Tre1, to guide front-back migratory polarity radially from the cluster toward the endoderm. Posteriorly positioned myosin-dependent contractile forces pull on cell-cell contacts until cells release. Tre1 mutant cells migrate randomly with transient enrichment of the force machinery but fail to separate, indicating a temporal contractile force threshold for detachment. E-cadherin is retained on the cell surface during cell separation and augmenting cell-cell adhesion does not impede detachment. Notably, coordinated migration improves cluster dispersal efficiency by stabilizing cell-cell interfaces and facilitating symmetric pulling. We demonstrate that guidance of inherent migratory forces is sufficient to disperse cell clusters under physiological settings and present a paradigm for how such events could occur across development and disease.

Indexed as

AnimalsAnimals, Genetically ModifiedBiomechanical PhenomenaBody PatterningCadherinsCell AdhesionCell MovementDrosophila melanogasterDrosophila ProteinsEmbryonic Germ CellsMicroscopy, Fluorescence, MultiphotonMyosin Type IIrho GTP-Binding ProteinsSignal TransductionSingle-Cell AnalysisCadherinsDrosophila ProteinsMyosin Type IIRho1 protein, Drosophilarho GTP-Binding Proteinsshg protein, Drosophila

Identifiers

PMID32901019
PMCPMC7479147

What OpenQuestion holds

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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.