Evidence map›Paper›PMID 24665413›Full record

ArticleTissue barriers2013

HGF signaling regulates Claudin-3 dynamics through its C-terminal tyrosine residues.

Floor Twiss, Michiel Oldenkamp, Annemieke Hiemstra, Houjiang Zhou, Lucrèce Matheron, Shabaz Mohammed, Johan de Rooij

Open access · hybridAbstract read
In one paragraph

Article in Tissue barriers, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. The Epithelial Cell Leak Pathway.International journal of molecular sciences · 2021
    Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Actin-interacting protein 1 controls assembly and permeability of intestinal epithelial apical junctions.American journal of physiology. Gastrointestinal and liver physiology · 2015
    Article
  13. Article
  14. 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

7 authors at 3 institutions in 1 country.

Floor TwissHubrecht Institute for Developmental Biology and Stem Cell Research and University Medical Centre Utrecht; Utrecht, The Netherlands.
Michiel OldenkampHubrecht Institute for Developmental Biology and Stem Cell Research and University Medical Centre Utrecht; Utrecht, The Netherlands.
Annemieke HiemstraHubrecht Institute for Developmental Biology and Stem Cell Research and University Medical Centre Utrecht; Utrecht, The Netherlands.
Houjiang ZhouBiomolecular Mass Spectrometry and Proteomics; Bijvoet Center for Biomolecular Research and Utrecht Institute of Pharmaceutical Sciences; Utrecht University; Utrecht, The Netherlands ; The Netherlands Proteomics Centre; The Netherlands.
Lucrèce MatheronBiomolecular Mass Spectrometry and Proteomics; Bijvoet Center for Biomolecular Research and Utrecht Institute of Pharmaceutical Sciences; Utrecht University; Utrecht, The Netherlands ; The Netherlands Proteomics Centre; The Netherlands.
Shabaz MohammedBiomolecular Mass Spectrometry and Proteomics; Bijvoet Center for Biomolecular Research and Utrecht Institute of Pharmaceutical Sciences; Utrecht University; Utrecht, The Netherlands ; The Netherlands Proteomics Centre; The Netherlands.
Johan de RooijHubrecht Institute for Developmental Biology and Stem Cell Research and University Medical Centre Utrecht; Utrecht, The Netherlands.
Hubrecht Institute for Developmental Biology and Stem Cell Research · NLPharmo Institute · NLUtrecht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The hormone HGF regulates morphogenesis and regeneration of multiple organs and increased HGF signaling is strongly associated with metastatic cancer. At the cellular level, one of the distinct effects of HGF is the de-stabilization of cell-cell junctions. Several molecular mechanisms have been shown to be involved that mostly culminate at the E-cadherin adhesion complex. One of the key determinants in HGF-driven morphological changes is the actomyosin cytoskeleton whose organization and physical parameters changes upon stimulation. Here we have investigated how HGF affects the different actomyosin-associated cell-cell junction complexes, Nectin Junctions, Adherens Junctions and Tight Junctions in MDCK cells. We find that components of all complexes stay present at cell-cell contacts until their physical dissociation. We find that at cell-cell junctions, the mobility of Claudin-3, but not that of other cell-cell adhesion receptors, is affected by HGF. This depends on tyrosine residues that likely affect PDZ-domain interactions at the C-terminal tail of Claudin-3, although their phosphorylation is not directly regulated by HGF. Thus we uncovered Claudins as novel targets of HGF signaling at cell-cell junctions.

Indexed as

cell-cell junctionsClaudinHGF signalingphosphorylationTight Junctionturnover

Identifiers

PMID24665413
PMCPMC3894234
OpenAlexW2008039606

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.