Evidence map›Paper›PMID 29093447›Full record

ArticleNature communications2017

E-cadherin integrates mechanotransduction and EGFR signaling to control junctional tissue polarization and tight junction positioning.

Matthias Rübsam, Aaron F Mertz, Akiharu Kubo, Susanna Marg, Christian Jüngst, Gladiola Goranci-Buzhala, Astrid C Schauss, Valerie Horsley, Eric R Dufresne, Markus Moser and 4 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 115 papers.

0numbers the graph read from it
0cells of the map it votes in
115citing papers in PubMed
9.2field-weighted citation impact, top 1% 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

115 citing papers in PubMed, 209 citations in OpenAlex.

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  8. Beyond the membrane: rethinking EGFR signaling in physiology and cancer.Cellular and molecular life sciences : CMLS · 2026
    Review
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55 more citing papers are in PubMed but not listed here.

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

14 authors at 7 institutions in 3 countries.

Matthias RübsamDepartment of Dermatology, University of Cologne, Cologne, 50931, Germany.
Aaron F MertzDepartment of Physics, Yale University, New Haven, CT, 06520, USA.
Akiharu KuboDepartment of Dermatology, Keio University School of Medicine, Tokyo, 160-8582, Japan.
Susanna MargHannover Medical School, 30625, Hannover, Germany.
Christian JüngstCologne Excellence Cluster for Stress Responses in Ageing-associated diseases (CECAD), Cologne, 50931, Germany.ORCID http://orcid.org/0000-0002-6586-7129
Gladiola Goranci-BuzhalaDepartment of Dermatology, University of Cologne, Cologne, 50931, Germany.
Astrid C SchaussCologne Excellence Cluster for Stress Responses in Ageing-associated diseases (CECAD), Cologne, 50931, Germany.
Valerie HorsleyDepartment of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, CT, 06520, USA.
Eric R DufresneDepartment of Physics, Yale University, New Haven, CT, 06520, USA.
Markus MoserMax Planck Institute for Biochemistry, Am Klopferspitz 18, Martinsried, 82152, Germany.
Wolfgang ZieglerHannover Medical School, 30625, Hannover, Germany.ORCID http://orcid.org/0000-0003-4529-1916
Masayuki AmagaiDepartment of Dermatology, Keio University School of Medicine, Tokyo, 160-8582, Japan.ORCID http://orcid.org/0000-0003-3314-7052
Sara A WickströmCologne Excellence Cluster for Stress Responses in Ageing-associated diseases (CECAD), Cologne, 50931, Germany.
Carien M NiessenDepartment of Dermatology, University of Cologne, Cologne, 50931, Germany. carien.niessen@uni-koeln.de.
Cologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases · DEYale University · USKeio University · JPMedizinische Hochschule Hannover · DEUniversity of Cologne · DEMax Planck Institute of Biochemistry · DETH Köln - University of Applied Sciences · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Generation of a barrier in multi-layered epithelia like the epidermis requires restricted positioning of functional tight junctions (TJ) to the most suprabasal viable layer. This positioning necessitates tissue-level polarization of junctions and the cytoskeleton through unknown mechanisms. Using quantitative whole-mount imaging, genetic ablation, and traction force microscopy and atomic force microscopy, we find that ubiquitously localized E-cadherin coordinates tissue polarization of tension-bearing adherens junction (AJ) and F-actin organization to allow formation of an apical TJ network only in the uppermost viable layer. Molecularly, E-cadherin localizes and tunes EGFR activity and junctional tension to inhibit premature TJ complex formation in lower layers while promoting increased tension and TJ stability in the granular layer 2. In conclusion, our data identify an E-cadherin-dependent mechanical circuit that integrates adhesion, contractile forces and biochemical signaling to drive the polarized organization of junctional tension necessary to build an in vivo epithelial barrier.

Indexed as

Mechanotransduction, CellularActin CytoskeletonActinsAdherens JunctionsAnimalsCadherinsCell DifferentiationCell ProliferationEpidermisErbB ReceptorsMiceMice, KnockoutMicroscopy, Atomic ForceSignal TransductionTight JunctionsActinsCadherinsCdh1 protein, mouseEGFR protein, mouseErbB Receptors

Identifiers

PMID29093447
PMCPMC5665913
OpenAlexW2765175699

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.