Evidence map›Paper›PMID 29980799›Full record

ArticleCellular and molecular life sciences : CMLS2018

Dsg2 via Src-mediated transactivation shapes EGFR signaling towards cell adhesion.

Hanna Ungewiß, Vera Rötzer, Michael Meir, Christina Fey, Markus Diefenbacher, Nicolas Schlegel, Jens Waschke

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 15% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Pooled it
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  4. Review
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  11. Review
  12. Desmoglein 2 can undergo CaBiophysical journal · 2022
    Article
  13. Desmosomal Cadherins in Health and Disease.Annual review of pathology · 2022
    Review
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  15. Article
  16. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Hanna UngewißDepartment I, Institute of Anatomy and Cell Biology, Ludwig Maximilians University Munich, Pettenkoferstr. 11, 80336, Munich, Germany.
Vera RötzerDepartment I, Institute of Anatomy and Cell Biology, Ludwig Maximilians University Munich, Pettenkoferstr. 11, 80336, Munich, Germany.
Michael MeirDepartment of General, Visceral, Vascular and Paediatric Surgery, Julius-Maximilians-Universität, Oberdürrbacher Str. 6, 97080, Würzburg, Germany.
Christina FeyDepartment for Tissue Engineering and Regenerative Medicine, University Hospital Würzburg, Röntgenring 11, 97070, Würzburg, Germany.
Markus DiefenbacherDepartment of Biochemistry and Molecular Biochemistry, University of Würzburg, Am Hubland, 97074, Würzburg, Germany.
Nicolas SchlegelDepartment of General, Visceral, Vascular and Paediatric Surgery, Julius-Maximilians-Universität, Oberdürrbacher Str. 6, 97080, Würzburg, Germany.
Jens WaschkeDepartment I, Institute of Anatomy and Cell Biology, Ludwig Maximilians University Munich, Pettenkoferstr. 11, 80336, Munich, Germany. jens.waschke@med.uni-muenchen.de.
Ludwig-Maximilians-Universität München · DEUniversity of Würzburg · DEUniversitätsklinikum Würzburg · DE

Funding

Deutsche Forschungsgemeinschaft SPP1782
6 · The paper itself

Abstract

Rapidly renewing epithelial tissues such as the intestinal epithelium require precise tuning of intercellular adhesion and proliferation to preserve barrier integrity. Here, we provide evidence that desmoglein 2 (Dsg2), an adhesion molecule of desmosomes, controls cell adhesion and proliferation via epidermal growth factor receptor (EGFR) signaling. Dsg2 is required for EGFR localization at intercellular junctions as well as for Src-mediated EGFR activation. Src binds to EGFR and is required for localization of EGFR and Dsg2 to cell-cell contacts. EGFR is critical for cell adhesion and barrier recovery. In line with this, Dsg2-deficient enterocytes display impaired barrier properties and increased cell proliferation. Mechanistically, Dsg2 directly interacts with EGFR and undergoes heterotypic-binding events on the surface of living enterocytes via its extracellular domain as revealed by atomic force microscopy. Thus, our study reveals a new mechanism by which Dsg2 via Src shapes EGFR function towards cell adhesion.

Indexed as

Caco-2 CellsCell AdhesionCell Line, TumorCell ProliferationCRISPR-Cas SystemsDesmoglein 2DesmosomesErbB ReceptorsHumansIntestinal MucosaMicroscopy, Atomic Forcep38 Mitogen-Activated Protein KinasesProtein BindingSignal Transductionsrc-Family KinasesTranscriptional ActivationDesmoglein 2ErbB Receptorsp38 Mitogen-Activated Protein Kinasessrc-Family KinasesCell adhesionDesmosomal cadherinsDesmosomesIntestinal barrier

Identifiers

PMID29980799
PMCPMC11105603
OpenAlexW2821813142

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.