Evidence map›Paper›PMID 14610056›Full record

ArticleThe Journal of cell biology2003

Cellular levels of p120 catenin function as a set point for cadherin expression levels in microvascular endothelial cells.

Kanyan Xiao, David F Allison, Kathleen M Buckley, Margaret D Kottke, Peter A Vincent, Victor Faundez, Andrew P Kowalczyk

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 209 papers.

0numbers the graph read from it
0cells of the map it votes in
209citing papers in PubMed
8.9field-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

209 citing papers in PubMed, 402 citations in OpenAlex.

  1. Article
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  9. Review
  10. Article
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  12. Engineering the Interactions of Classical Cadherin Cell-Cell Adhesion Proteins.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Review
  13. Article
  14. Article
  15. CD93 maintains endothelial barrier function by limiting the phosphorylation and turnover of VE-cadherin.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2023
    Article
  16. Review
  17. Review
  18. IRF6 Regulates the Delivery of E-Cadherin to the Plasma Membrane.The Journal of investigative dermatology · 2022
    Article
  19. Article
  20. Article

149 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 2 countries.

Kanyan XiaoDepartment of Dermatology, School of Medicine, Emory University, Atlanta, GA 30322, USA.
David F Allison
Kathleen M Buckley
Margaret D Kottke
Peter A Vincent
Victor Faundez
Andrew P Kowalczyk
Emory University · USAlbany Medical Center Hospital · USInstitute of Cell Biology · UA

Funding

Role of p0071 in Cutaneous Intercellular JunctionsR01AR048266 · NIAMS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI ANDREW P. KOWALCZYK · 2002 to 2026
$8.2M
UV light and the cutaneous neurosensory systemP30AR042687 · NIAMS · EMORY UNIVERSITY · PI CAUGHMAN, STEWART W · 1994 to 2003
$2.5M
NIAMS NIH HHS 1R01AR048266NIAMS NIH HHS P30 AR042687NIAMS NIH HHS P30AR042687NIAMS NIH HHS R01 AR048266
6 · The paper itself

Abstract

The mechanisms by which catenins regulate cadherin function are not fully understood, and the precise function of p120 catenin (p120ctn) has remained particularly elusive. In microvascular endothelial cells, p120ctn colocalized extensively with cell surface VE-cadherin, but failed to colocalize with VE-cadherin that had entered intracellular degradative compartments. To test the possibility that p120ctn binding to VE-cadherin regulates VE-cadherin internalization, a series of approaches were undertaken to manipulate p120ctn availability to endogenous VE-cadherin. Expression of VE-cadherin mutants that competed for p120ctn binding triggered the degradation of endogenous VE-cadherin. Similarly, reducing levels of p120ctn using siRNA caused a dramatic and dose-related reduction in cellular levels of VE-cadherin. In contrast, overexpression of p120ctn increased VE-cadherin cell surface levels and inhibited entry of cell surface VE-cadherin into degradative compartments. These results demonstrate that cellular levels of p120ctn function as a set point mechanism that regulates cadherin expression levels, and that a major function of p120ctn is to control cadherin internalization and degradation.

Indexed as

Antigens, CDCadherin 5CadherinsCateninsCell AdhesionCell Adhesion MoleculesCell LineDelta CateninEndocytosisEndothelium, VascularFeedback, PhysiologicalHumansMutationPhosphoproteinsProtein BindingProtein TransportAntigens, CDCadherin 5CadherinsCateninsCell Adhesion MoleculesCTNND1 protein, humanDelta CateninPhosphoproteinsRNA, Small Interfering

Identifiers

PMID14610056
PMCPMC2173638
OpenAlexW1934202741

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.