Evidence map›Paper›PMID 27254775›Full record

ArticleCell adhesion & migration2017

Desmoglein 3 regulates membrane trafficking of cadherins, an implication in cell-cell adhesion.

Hanan Moftah, Kasuni Dias, Ehsanul Hoque Apu, Li Liu, Jutamas Uttagomol, Lesley Bergmeier, Stephanie Kermorgant, Hong Wan

Open access · goldAbstract read
In one paragraph

Article in Cell adhesion & migration, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

19 citing papers in PubMed, 24 citations in OpenAlex.

  1. An Integrated Proteomics and Genomics Approach to Identify Essential Protein Kinases During Human Trophoblast Development.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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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

8 authors at 1 institution in 1 country.

Hanan Moftaha Centre for Clinical and Diagnostic Oral Sciences, Institute of Dentistry, Barts and The London, School of Medicine and Dentistry , Queen Mary University of London , Whitechapel, London , UK.
Kasuni Diasa Centre for Clinical and Diagnostic Oral Sciences, Institute of Dentistry, Barts and The London, School of Medicine and Dentistry , Queen Mary University of London , Whitechapel, London , UK.
Ehsanul Hoque Apua Centre for Clinical and Diagnostic Oral Sciences, Institute of Dentistry, Barts and The London, School of Medicine and Dentistry , Queen Mary University of London , Whitechapel, London , UK.
Li Liua Centre for Clinical and Diagnostic Oral Sciences, Institute of Dentistry, Barts and The London, School of Medicine and Dentistry , Queen Mary University of London , Whitechapel, London , UK.
Jutamas Uttagomola Centre for Clinical and Diagnostic Oral Sciences, Institute of Dentistry, Barts and The London, School of Medicine and Dentistry , Queen Mary University of London , Whitechapel, London , UK.
Lesley Bergmeiera Centre for Clinical and Diagnostic Oral Sciences, Institute of Dentistry, Barts and The London, School of Medicine and Dentistry , Queen Mary University of London , Whitechapel, London , UK.
Stephanie Kermorgantb Barts Cancer Institute, John Vane Science Center , Charterhouse Square, London , UK.
Hong Wana Centre for Clinical and Diagnostic Oral Sciences, Institute of Dentistry, Barts and The London, School of Medicine and Dentistry , Queen Mary University of London , Whitechapel, London , UK.
Queen Mary University of London · GB

Funding

Medical Research Council G0501003
6 · The paper itself

Abstract

E-cadherin mediated cell-cell adhesion plays a critical role in epithelial cell polarization and morphogenesis. Our recent studies suggest that the desmosomal cadherin, desmoglein 3 (Dsg3) cross talks with E-cadherin and regulates its adhesive function in differentiating keratinocytes. However, the underlying mechanism remains not fully elucidated. Since E-cadherin trafficking has been recognized to be a central determinant in cell-cell adhesion and homeostasis we hypothesize that Dsg3 may play a role in regulating E-cadherin trafficking and hence the cell-cell adhesion. Here we investigated this hypothesis in cells with loss of Dsg3 function through RNAi mediated Dsg3 knockdown or the stable expression of the truncated mutant Dsg3ΔC. Our results showed that loss of Dsg3 resulted in compromised cell-cell adhesion and reduction of adherens junction and desmosome protein expression as well as the cortical F-actin formation. As a consequence, cells failed to polarize but instead displayed aberrant cell flattening. Furthermore, retardation of E-cadherin internalization and recycling was consistently observed in these cells during the process of calcium induced junction assembling. In contrast, enhanced cadherin endocytosis was detected in cells with overexpression of Dsg3 compared to control cells. Importantly, this altered cadherin trafficking was found to be coincided with the reduced expression and activity of Rab proteins, including Rab5, Rab7 and Rab11 which are known to be involved in E-cadherin trafficking. Taken together, our findings suggest that Dsg3 functions as a key in cell-cell adhesion through at least a mechanism of regulating E-cadherin membrane trafficking.

Indexed as

AnimalsCadherinsCell AdhesionCell LineDesmoglein 3Epithelial CellsHumansMiceProtein TransportCadherinsDesmoglein 3DSG3 protein, humanadherens junctiondesmoglein 3desmosomeE-cadherin traffickingepithelial cellsintercellular junction

Identifiers

PMID27254775
PMCPMC5479455
OpenAlexW2419405591

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.