Evidence map›Paper›PMID 26046627›Full record

ArticlePloS one2015

Mechanosensitive Adaptation of E-Cadherin Turnover across adherens Junctions.

Simon de Beco, Jean-Baptiste Perney, Sylvie Coscoy, François Amblard

Abstract read
In one paragraph

Article in PloS one, 2015. 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
–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

20 citing papers in PubMed.

  1. bioRxiv : the preprint server for biology · 2026
    Article
  2. Review
  3. Article
  4. Shaping epithelial lumina under pressure.Biochemical Society transactions · 2024
    Review
  5. Article
  6. Mechanics of cell-cell junctions.Biophysical journal · 2023
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Integration of Cadherin Adhesion and Cytoskeleton atCold Spring Harbor perspectives in biology · 2017
    Review
  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.

Simon de BecoLaboratoire de Physico-Chimie, Centre de Recherche, Institut Curie, Paris, France; Centre National de la Recherche Scientifique, Unité Mixte de Recherche 168, Paris, France; Université Pierre et Marie Curie, Paris, France.
Jean-Baptiste PerneyLaboratoire de Physico-Chimie, Centre de Recherche, Institut Curie, Paris, France; Centre National de la Recherche Scientifique, Unité Mixte de Recherche 168, Paris, France; Université Pierre et Marie Curie, Paris, France.
Sylvie CoscoyLaboratoire de Physico-Chimie, Centre de Recherche, Institut Curie, Paris, France; Centre National de la Recherche Scientifique, Unité Mixte de Recherche 168, Paris, France; Université Pierre et Marie Curie, Paris, France.
François AmblardLaboratoire de Physico-Chimie, Centre de Recherche, Institut Curie, Paris, France; Centre National de la Recherche Scientifique, Unité Mixte de Recherche 168, Paris, France; Université Pierre et Marie Curie, Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the natural and technological world, multi-agent systems strongly depend on how the interactions are ruled between their individual components, and the proper control of time-scales and synchronization is a key issue. This certainly applies to living tissues when multicellular assemblies such as epithelial cells achieve complex morphogenetic processes. In epithelia, because cells are known to individually generate actomyosin contractile stress, each individual intercellular adhesive junction line is subjected to the opposed stresses independently generated by its two partner cells. Contact lines should thus move unless their two partner cells mechanically match. The geometric homeostasis of mature epithelia observed at short enough time-scale thus raises the problem to understand how cells, if considered as noisy individual actuators, do adapt across individual intercellular contacts to locally balance their time-average contractile stress. Structural components of adherens junctions, cytoskeleton (F-actin) and homophilic bonds (E-cadherin) are quickly renewed at steady-state. These turnovers, if they depend on forces exerted at contacts, may play a key role in the mechanical adaptation of epithelia. Here we focus on E-cadherin as a force transducer, and we study the local regulation and the mechanosensitivity of its turnover in junctions. We show that E-cadherin turnover rates match remarkably well on either side of mature intercellular contacts, despite the fact that they exhibit large fluctuations in time and variations from one junction to another. Using local mechanical and biochemical perturbations, we find faster turnover rates with increased tension, and asymmetric rates at unbalanced junctions. Together, the observations that E-cadherin turnover, and its local symmetry or asymmetry at each side of the junction, are mechanosensitive, support the hypothesis that E-cadherin turnover could be involved in mechanical homeostasis of epithelia.

Indexed as

Adherens JunctionsAnimalsCadherinsCytoskeletonDogsEndocytosisFluorescence Recovery After PhotobleachingMadin Darby Canine Kidney CellsMicroscopy, FluorescenceRecombinant Fusion ProteinsTime FactorsCadherinsRecombinant Fusion Proteins

Identifiers

PMID26046627
PMCPMC4457789

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Registered trials

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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.