Evidence map›Paper›PMID 22513089›Full record

ArticleMolecular biology of the cell2012

Conformational epitopes at cadherin calcium-binding sites and p120-catenin phosphorylation regulate cell adhesion.

Yuliya I Petrova, MarthaJoy M Spano, Barry M Gumbiner

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
2.7field-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

53 citing papers in PubMed, 81 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Functions of p120-catenin in physiology and diseases.Frontiers in molecular biosciences · 2024
    Review
  9. Engineering the Interactions of Classical Cadherin Cell-Cell Adhesion Proteins.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Review
  10. Review
  11. Article
  12. Molecular mechanism for strengthening E-cadherin adhesion using a monoclonal antibody.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  13. Article
  14. Mechanical disruption of E-cadherin complexes with epidermal growth factor receptor actuates growth factor-dependent signaling.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  15. Article
  16. Inside-out regulation of E-cadherin conformation and adhesion.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  17. Article
  18. Sorting of cadherin-catenin-associated proteins into individual clusters.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  19. Enhanced endothelial barrier function by monoclonal antibody activation of vascular endothelial cadherin.American journal of physiology. Heart and circulatory physiology · 2021
    Article
  20. 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

3 authors at 1 institution in 1 country.

Yuliya I PetrovaDepartment of Cell Biology, University of Virginia School of Medicine, Charlottesville, VA 22908, USA.
MarthaJoy M Spano
Barry M Gumbiner
University of Virginia · US

Funding

BIOCHEMISTRY AND REGULATION OF CADHERIN ACTIVITYR01GM052717 · NIGMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI GUMBINER, BARRY M. · 1996 to 2011
$4.2M
Cadherin Regulation of Epithelial BarriersR01GM106659 · NIGMS · UNIVERSITY OF VIRGINIA · PI GUMBINER, BARRY M. · 2013 to 2016
$1.8M
NIGMS NIH HHS GM52717-14SNIGMS NIH HHS R01 GM052717NIGMS NIH HHS R01 GM106659NIGMS NIH HHS R01 GM52717
6 · The paper itself

Abstract

We investigated changes in cadherin structure at the cell surface that regulate its adhesive activity. Colo 205 cells are nonadhesive cells with a full but inactive complement of E-cadherin-catenin complexes at the cell surface, but they can be triggered to adhere and form monolayers. We were able to distinguish the inactive and active states of E-cadherin at the cell surface by using a special set of monoclonal antibodies (mAbs). Another set of mAbs binds E-cadherin and strongly activates adhesion. In other epithelial cell types these activating mAbs inhibit growth factor-induced down-regulation of adhesion and epithelial morphogenesis, indicating that these phenomena are also controlled by E-cadherin activity at the cell surface. Both types of mAbs recognize conformational epitopes at different interfaces between extracellular cadherin repeat domains (ECs), especially near calcium-binding sites. Activation also induces p120-catenin dephosphorylation, as well as changes in the cadherin cytoplasmic domain. Moreover, phospho-site mutations indicate that dephosphorylation of specific Ser/Thr residues in the N-terminal domain of p120-catenin mediate adhesion activation. Thus physiological regulation of the adhesive state of E-cadherin involves physical and/or conformational changes in the EC interface regions of the ectodomain at the cell surface that are mediated by catenin-associated changes across the membrane.

Indexed as

Amino Acid SequenceAnimalsAntibodies, MonoclonalBinding SitesCadherinsCalciumCateninsCell AdhesionCell Line, TumorCell MembraneDelta CateninDogsDown-RegulationEpitheliumEpitope MappingEpitopesAntibodies, MonoclonalCadherinsCalciumCateninsDelta CateninEpitopesIntercellular Signaling Peptides and ProteinsMutant Proteins

Identifiers

PMID22513089
PMCPMC3364174
OpenAlexW2131736508

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.