Evidence map›Paper›PMID 29742438›Full record

ArticleCell reports2018

Homophilic and Heterophilic Interactions of Type II Cadherins Identify Specificity Groups Underlying Cell-Adhesive Behavior.

Julia Brasch, Phinikoula S Katsamba, Oliver J Harrison, Göran Ahlsén, Regina B Troyanovsky, Indrajyoti Indra, Anna Kaczynska, Benjamin Kaeser, Sergey Troyanovsky, Barry Honig and 1 more

Abstract read
In one paragraph

Article in Cell reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
–field-weighted citation impact
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

38 citing papers in PubMed.

  1. Article
  2. Article
  3. Structural Insights into Ordered Multicomponent Assemblies in Cell Junctions.Advances in experimental medicine and biology · 2026
    Review
  4. Article
  5. Nervous system-wide analysis of allScience advances · 2025
    Article
  6. Article
  7. Neurotensin modulates ovarian vascular permeability via adherens junctions.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Adhesion-Based Self-Organization in Tissue Patterning.Annual review of cell and developmental biology · 2022
    Review
  15. Article
  16. Potential Therapeutic Applications of N-Cadherin Antagonists and Agonists.Frontiers in cell and developmental biology · 2022
    Review
  17. Article
  18. Article
  19. Review
  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

11 authors.

Julia BraschZuckerman Mind Brain Behavior Institute, New York, NY 10027, USA; Department of Biochemistry and Molecular Biophysics, Columbia University, New York, NY 10032, USA.
Phinikoula S KatsambaZuckerman Mind Brain Behavior Institute, New York, NY 10027, USA; Howard Hughes Medical Institute, Columbia University, New York, NY 10032, USA.
Oliver J HarrisonZuckerman Mind Brain Behavior Institute, New York, NY 10027, USA; Department of Biochemistry and Molecular Biophysics, Columbia University, New York, NY 10032, USA.
Göran AhlsénZuckerman Mind Brain Behavior Institute, New York, NY 10027, USA; Howard Hughes Medical Institute, Columbia University, New York, NY 10032, USA.
Regina B TroyanovskyDepartment of Dermatology, The Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
Indrajyoti IndraDepartment of Dermatology, The Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
Anna KaczynskaDepartment of Biochemistry and Molecular Biophysics, Columbia University, New York, NY 10032, USA.
Benjamin KaeserDepartment of Biochemistry and Molecular Biophysics, Columbia University, New York, NY 10032, USA.
Sergey TroyanovskyDepartment of Dermatology, The Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
Barry HonigZuckerman Mind Brain Behavior Institute, New York, NY 10027, USA; Howard Hughes Medical Institute, Columbia University, New York, NY 10032, USA; Department of Biochemistry and Molecular Biophysics, Columbia University, New York, NY 10032, USA; Center for Computational Biology and Bioinformatics, Columbia University, New York, NY 10032, USA; Department of Systems Biology, Columbia University, New York, NY 10032, USA; Department of Medicine, Columbia University, New York, NY 10032, USA. Electronic address: bh6@columbia.edu.
Lawrence ShapiroZuckerman Mind Brain Behavior Institute, New York, NY 10027, USA; Department of Biochemistry and Molecular Biophysics, Columbia University, New York, NY 10032, USA. Electronic address: lss8@columbia.edu.

Funding

Inter-junctional signaling in epithelial junctional complexR01AR044016 · NIAMS · WASHINGTON UNIVERSITY · PI TROYANOVSKY, SERGEY M · 1996 to 2020
$6.8M
Cadherin Clusters and actin filamentsR01AR070166 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Sergey M Troyanovsky · 2016 to 2026
$4.1M
MOLECULAR BASIS OF CADHERIN MEDIATED CELL ADHESIONR01GM062270 · NIGMS · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI SHAPIRO, LAWRENCE S · 2001 to 2015
$3.4M
Functional and Structural Links between Cadherin, Gamma-Secretase, and NotchR01AR057992 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI TROYANOVSKY, SERGEY M · 2010 to 2014
$1.6M
Howard Hughes Medical InstituteNIAMS NIH HHS R01 AR044016NIAMS NIH HHS R01 AR057992NIAMS NIH HHS R01 AR070166NIGMS NIH HHS R01 GM062270
6 · The paper itself

Abstract

Type II cadherins are cell-cell adhesion proteins critical for tissue patterning and neuronal targeting but whose molecular binding code remains poorly understood. Here, we delineate binding preferences for type II cadherin cell-adhesive regions, revealing extensive heterophilic interactions between specific pairs, in addition to homophilic interactions. Three distinct specificity groups emerge from our analysis with members that share highly similar heterophilic binding patterns and favor binding to one another. Structures of adhesive fragments from each specificity group confirm near-identical dimer topology conserved throughout the family, allowing interface residues whose conservation corresponds to specificity preferences to be identified. We show that targeted mutation of these residues converts binding preferences between specificity groups in biophysical and co-culture assays. Our results provide a detailed understanding of the type II cadherin interaction map and a basis for defining their role in tissue patterning and for the emerging importance of their heterophilic interactions in neural connectivity.

Indexed as

Amino Acid SequenceAnimalsCadherinsCell AdhesionCell LineConserved SequenceDNA Mutational AnalysisHumansMiceMutationPhylogenyProtein BindingProtein MultimerizationCadherinscadherincell adhesioncrystal structurehemophilic specificityheterophilic specificityneural patterningsynaptic targeting

Identifiers

PMID29742438
PMCPMC6029887

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.