Evidence map›Paper›PMID 24859003›Full record

ArticleNature cell biology2014

Actin dynamics modulate mechanosensitive immobilization of E-cadherin at adherens junctions.

W Engl, B Arasi, L L Yap, J P Thiery, V Viasnoff

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In one paragraph

Article in Nature cell biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed, 1 pooled it
–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

96 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  12. Regulation of intercellular viscosity by E-cadherin-dependent phosphorylation of EGFR in collective cell migration.Proceedings of the National Academy of Sciences of the United States of America · 2024
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  15. Characterization of early and late events of adherens junction assembly.bioRxiv : the preprint server for biology · 2024
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36 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

W EnglMechanobiology Institute, National University of Singapore, 5A Engineering Drive 1, Singapore 117411, Singapore.
B ArasiMechanobiology Institute, National University of Singapore, 5A Engineering Drive 1, Singapore 117411, Singapore.
L L YapDepartment of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, 8 Medical Drive, Singapore 117596, Singapore.
J P Thiery1] Mechanobiology Institute, National University of Singapore, 5A Engineering Drive 1, Singapore 117411, Singapore [2] Department of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, 8 Medical Drive, Singapore 117596, Singapore [3] Institute of Molecular Cell Biology, A*STAR, 61 Biopolis Drive, Singapore 138673, Singapore [4].
V Viasnoff1] Mechanobiology Institute, National University of Singapore, 5A Engineering Drive 1, Singapore 117411, Singapore [2].

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mechanical stress is increasingly being shown to be a potent modulator of cell-cell junctional morphologies in developmental and homeostatic processes. Intercellular force sensing is thus expected to be an important regulator of cell signalling and tissue integrity. In particular, the interplay between myosin contractility, actin dynamics and E-cadherin recruitment largely remains to be uncovered. We devised a suspended cell doublet assay to quantitatively assess the correlation between myosin II activity and local E-cadherin recruitment. The single junction of the doublet exhibited a stereotypical morphology, with E-cadherin accumulating into clusters of varied concentrations at the rim of the circular contact. This local recruitment into clusters derived from the sequestration of E-cadherin through a myosin-II-driven modulation of actin turnover. We exemplify how the regulation of actin dynamics provides a mechanism for the mechanosensitive response of cell contacts.

Indexed as

Cell AdhesionMechanotransduction, CellularActinsAdherens JunctionsAnimalsCadherinsCell Line, TumorCell ShapeGreen Fluorescent ProteinsMiceMyosin Type IIProtein TransportRecombinant Fusion ProteinsRNA InterferenceSarcoma 180Stress, MechanicalActinsCadherinsGreen Fluorescent ProteinsMyosin Type IIRecombinant Fusion Proteins

Identifiers

PMID24859003

What OpenQuestion holds

Textmetadata
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.