Evidence map›Paper›PMID 37480844›Full record

ArticleDevelopmental cell2023

An E-cadherin-actin clutch translates the mechanical force of cortical flow for cell-cell contact to inhibit epithelial cell locomotion.

Ivar Noordstra, Mario Díez Hermoso, Lilian Schimmel, Alexis Bonfim-Melo, Denni Currin-Ross, Cao Nguyen Duong, Joseph Mathew Kalappurakkal, Richard G Morris, Dietmar Vestweber, Satyajit Mayor and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Developmental cell, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
8.1field-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

20 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. Article
  3. E-Cadherin: A conductor of cellular signaling.Current opinion in cell biology · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. A Hierarchical Mechanotransduction System: From Macro to Micro.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Review
  17. Review
  18. Article
  19. Article
  20. Mechanics of cell-cell junctions.Biophysical journal · 2023
    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

13 authors at 6 institutions in 4 countries.

Ivar NoordstraCentre for Cell Biology of Chronic Disease, Institute for Molecular Bioscience, The University of Queensland, St. Lucia, Brisbane, QLD 4072, Australia.
Mario Díez HermosoInstitute for Bioengineering of Catalonia (IBEC), the Barcelona Institute of Technology (BIST), 08028 Barcelona, Spain.
Lilian SchimmelCentre for Cell Biology of Chronic Disease, Institute for Molecular Bioscience, The University of Queensland, St. Lucia, Brisbane, QLD 4072, Australia.
Alexis Bonfim-MeloCentre for Cell Biology of Chronic Disease, Institute for Molecular Bioscience, The University of Queensland, St. Lucia, Brisbane, QLD 4072, Australia.
Denni Currin-RossCentre for Cell Biology of Chronic Disease, Institute for Molecular Bioscience, The University of Queensland, St. Lucia, Brisbane, QLD 4072, Australia; School of Physics & EMBL Australia Node in Single Molecule Science, School of Biomedical Sciences, University of New South Wales, Sydney, NSW 2052, Australia.
Cao Nguyen DuongDepartment of Vascular Biology, Max Planck Institute for Molecular Biomedicine, 48149 Münster, Germany.
Joseph Mathew KalappurakkalNational Centre for Biological Science, Tata Institute for Fundamental Research, Bangalore 560065, India.
Richard G MorrisSchool of Physics & EMBL Australia Node in Single Molecule Science, School of Biomedical Sciences, University of New South Wales, Sydney, NSW 2052, Australia.
Dietmar VestweberDepartment of Vascular Biology, Max Planck Institute for Molecular Biomedicine, 48149 Münster, Germany.
Satyajit MayorNational Centre for Biological Science, Tata Institute for Fundamental Research, Bangalore 560065, India.
Emma GordonCentre for Cell Biology of Chronic Disease, Institute for Molecular Bioscience, The University of Queensland, St. Lucia, Brisbane, QLD 4072, Australia.
Pere Roca-CusachsInstitute for Bioengineering of Catalonia (IBEC), the Barcelona Institute of Technology (BIST), 08028 Barcelona, Spain; Universitat de Barcelona, 08036 Barcelona, Spain. Electronic address: proca@ibecbarcelona.eu.
Alpha S YapCentre for Cell Biology of Chronic Disease, Institute for Molecular Bioscience, The University of Queensland, St. Lucia, Brisbane, QLD 4072, Australia. Electronic address: a.yap@uq.edu.au.
University of Queensland · AUMax Planck Institute for Molecular Biomedicine · DENational Centre for Biological Sciences · INInstitute for Bioengineering of Catalonia · ESUniversitat de Barcelona · ESUNSW Sydney · AU

Funding

DBT-Wellcome Trust India Alliance IA/M/15/1/502018Wellcome Trust
6 · The paper itself

Abstract

Adherens junctions (AJs) allow cell contact to inhibit epithelial migration yet also permit epithelia to move as coherent sheets. How, then, do cells identify which contacts will inhibit locomotion? Here, we show that in human epithelial cells this arises from the orientation of cortical flows at AJs. When the leader cells from different migrating sheets make head-on contact with one another, they assemble AJs that couple together oppositely directed cortical flows. This applies a tensile signal to the actin-binding domain (ABD) of α-catenin, which provides a clutch to promote lateral adhesion growth and inhibit the lamellipodial activity necessary for migration. In contrast, AJs found between leader cells in the same migrating sheet have cortical flows aligned in the same direction, and no such mechanical inhibition takes place. Therefore, α-catenin mechanosensitivity in the clutch between E-cadherin and cortical F-actin allows cells to interpret the direction of motion via cortical flows and signal for contact to inhibit locomotion.

Indexed as

ActinsLocomotionalpha CateninCadherinsEpithelial CellsHumansActinsalpha CateninCadherinsclutchcontact inhibition of locomotioncortical flowE-cadherin adhesionmechanical tensionα-catenin

Identifiers

PMID37480844
PMCPMC7616453
OpenAlexW4385077548

What OpenQuestion holds

Textmetadata
LicenceTDM
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.