Evidence map›Paper›PMID 27798242›Full record

ArticleMolecular biology of the cell2017

The VE-cadherin cytoplasmic domain undergoes proteolytic processing during endocytosis.

Wenji Su, Andrew P Kowalczyk

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

43 citing papers in PubMed, 56 citations in OpenAlex.

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  15. Calpain and Cardiometabolic Diseases.International journal of molecular sciences · 2023
    Review
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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

2 authors at 1 institution in 1 country.

Wenji SuGraduate Program in Biochemistry, Cell and Developmental Biology, Emory University, Atlanta, GA 30322.
Andrew P KowalczykDepartment of Cell Biology, Emory University, Atlanta, GA 30322 akowalc@emory.edu.
Emory University · US

Funding

Role of p0071 in Cutaneous Intercellular JunctionsR01AR048266 · NIAMS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI ANDREW P. KOWALCZYK · 2002 to 2026
$8.2M
Cadherin Regulation in Dermal Endothelial CellsR01AR050501 · NIAMS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI KOWALCZYK, ANDREW P. · 2004 to 2021
$6.6M
NIAMS NIH HHS R01 AR048266NIAMS NIH HHS R01 AR050501
6 · The paper itself

Abstract

VE-cadherin trafficking to and from the plasma membrane has emerged as a critical mechanism for regulating cadherin surface levels and adhesion strength. In addition, proteolytic processing of cadherin extracellular and cytoplasmic domains has been reported to regulate cadherin adhesion and signaling. Here we provide evidence that VE-cadherin is cleaved by calpain upon entry into clathrin-enriched domains. This cleavage event occurs between the β-catenin and p120-binding domains within the cadherin cytoplasmic tail. Of interest, VE-cadherin mutants that are resistant to endocytosis are similarly resistant to cleavage. Furthermore, p120-catenin overexpression blocks cadherin internalization and cleavage, coupling entry into the endocytic pathway with proteolytic processing. Of importance, the cleavage of the VE-cadherin tail alters the postendocytic trafficking itinerary of the cadherin, resulting in a higher turnover rate due to decreased recycling and increased degradation. In conclusion, this study identifies a novel proteolytic event that regulates the trafficking of VE-cadherin after endocytosis.

Indexed as

AnimalsAntigens, CDbeta CateninCadherin 5CadherinsCalpainCateninsCell AdhesionCell MembraneCell MovementCells, CulturedChlorocebus aethiopsClathrinCOS CellsDelta CateninEndocytosisAntigens, CDbeta CateninCadherin 5CadherinsCalpainCateninsClathrinDelta CateninPhosphoproteins

Identifiers

PMID27798242
PMCPMC5221631
OpenAlexW2541175714

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.