Evidence map›Paper›PMID 20027292›Full record

ArticlePloS one2009

A protocadherin-cadherin-FLRT3 complex controls cell adhesion and morphogenesis.

Xuejun Chen, Eunjin Koh, Michael Yoder, Barry M Gumbiner

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

33 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Enhanced endothelial barrier function by monoclonal antibody activation of vascular endothelial cadherin.American journal of physiology. Heart and circulatory physiology · 2021
    Article
  5. Cadherin cis and trans interactions are mutually cooperative.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  6. FLRTing Neurons in Cortical Migration During Cerebral Cortex Development.Frontiers in cell and developmental biology · 2020
    Review
  7. Article
  8. Article
  9. Development (Cambridge, England) · 2017
    Article
  10. Article
  11. Article
  12. Article
  13. Aberrant expression and functions of protocadherins in human malignant tumors.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Review
  14. Allosteric Regulation of E-Cadherin Adhesion.The Journal of biological chemistry · 2015
    Article
  15. Article
  16. Article
  17. Nuclear signaling from cadherin adhesion complexes.Current topics in developmental biology · 2015
    Review
  18. Review
  19. Article
  20. Review
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

4 authors at 1 institution in 1 country.

Xuejun ChenDepartment of Cell Biology, University of Virginia Health Sciences Center, Charlottesville, Virginia, USA.
Eunjin Koh
Michael Yoder
Barry M Gumbiner
University of Virginia · US

Funding

UVA Digestive Health Research CenterP30DK067629 · NIDDK · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI PIZARRO, THERESA TORRES · 2004 to 2008
$5.6M
BIOCHEMISTRY AND REGULATION OF CADHERIN ACTIVITYR01GM052717 · NIGMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI GUMBINER, BARRY M. · 1996 to 2011
$4.2M
NIDDK NIH HHS P30 DK067629NIGMS NIH HHS R01 GM052717NIGMS NIH HHS R01GM52717
6 · The paper itself

Abstract

backgroundParaxial protocadherin (PAPC) and fibronectin leucine-rich domain transmembrane protein-3 (FLRT3) are induced by TGFbeta signaling in Xenopus embryos and both regulate morphogenesis by inhibiting C-cadherin mediated cell adhesion. PRINCIPAL

findingsWe have investigated the functional and physical relationships between PAPC, FLRT3, and C-cadherin. Although neither PAPC nor FLRT3 are required for each other to regulate C-cadherin adhesion, they do interact functionally and physically, and they form a complex with cadherins. By itself PAPC reduces cell adhesion physiologically to induce cell sorting, while FLRT3 disrupts adhesion excessively to cause cell dissociation. However, when expressed together PAPC limits the cell dissociating and tissue disrupting activity of FLRT3 to make it effective in physiological cell sorting. PAPC counteracts FLRT3 function by inhibiting the recruitment of the GTPase RND1 to the FLRT3 cytoplasmic domain. CONCLUSIONS/SIGNIFICANCE: PAPC and FLRT3 form a functional complex with cadherins and PAPC functions as a molecular "governor" to maintain FLRT3 activity at the optimal level for physiological regulation of C-cadherin adhesion, cell sorting, and morphogenesis.

Indexed as

MorphogenesisAnimalsCadherinsCell AdhesionCHO CellsCricetinaeCricetulusEmbryo, NonmammalianFlow CytometryGene Knockdown TechniquesHumansImmunoprecipitationMembrane ProteinsProtein BindingProtein TransportProtocadherinsCadherinsCDH3 protein, XenopusFLRT3 protein, XenopusMembrane ProteinsPcdh8 protein, XenopusProtocadherinsrho GTP-Binding ProteinsRnd1 protein, XenopusXenopus Proteins

Identifiers

PMID20027292
PMCPMC2791867
OpenAlexW1964497830

What OpenQuestion holds

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LicenceCC BY
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.