Evidence map›Paper›PMID 15800180›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2005

Adherens junctions in myelinating Schwann cells stabilize Schmidt-Lanterman incisures via recruitment of p120 catenin to E-cadherin.

Nicolas Tricaud, Claire Perrin-Tricaud, Juan L Brusés, Urs Rutishauser

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

40 citing papers in PubMed, 78 citations in OpenAlex.

  1. Article
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  5. Review
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  10. Wallerian demyelination: chronicle of a cellular cataclysm.Cellular and molecular life sciences : CMLS · 2017
    Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Label-free imaging of Schwann cell myelination by third harmonic generation microscopy.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  17. PMP22 is critical for actin-mediated cellular functions and for establishing lipid rafts.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
    Article
  18. Article
  19. 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

4 authors at 1 institution in 1 country.

Nicolas TricaudCell Biology Program, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA.
Claire Perrin-Tricaud
Juan L Brusés
Urs Rutishauser
Memorial Sloan Kettering Cancer Center · US

Funding

Cell Interactions in Synapes Formation and FunctionR01NS040300 · NINDS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI BRUSES, JUAN L · 2001 to 2005
$1.2M
NINDS NIH HHS NS40300NINDS NIH HHS R01 NS040300
6 · The paper itself

Abstract

Schwann cell myelin contains highly compacted layers of membrane as well as noncompacted regions with a visible cytoplasm. One of these cytoplasmic compartments is the Schmidt-Lanterman incisure, which spirals through the compacted layers and is believed to help sustain the growth and function of compact myelin. Incisures contain adherens junctions (AJs), the key components of which are E-cadherin, its cytoplasmic partners called catenins, and F-actin. To explore in vivo the role of cadherin and catenins in incisures, E-cadherin mutant proteins that completely replace endogenous cadherin have been delivered to the cells using adenovirus. When the introduced cadherin lacked its extracellular domain, association of p120 catenin (p120ctn) with the cadherin did not occur, and incisures disappeared. Remarkably, the additional replacement of two phosphorylatable tyrosines by phenylalanine in the cytoplasmic tail of the mutant cadherin restored both p120ctn binding and incisure architecture, indicating that p120ctn recruitment is critical for incisures maintenance and might be regulated by phosphorylations. In addition, the ability of the p120ctn/cadherin complex to support incisures was blocked by mutation of the Rho GTPase regulatory region of the p120ctn, and downregulation of Rac1 activity at the junction reversed this inhibition. Because Rho GTPases regulate the state of the actin filaments, these findings suggest that one role of p120ctn in incisures is to organize the cytoskeleton at the AJ. Finally, developmental studies of Schwann cells demonstrated that p120ctn recruitment from the cytoplasm to the AJ occurs before the appearance of Rac1 GTPase and F-actin at the junction.

Indexed as

2',3'-Cyclic-Nucleotide PhosphodiesterasesAdenoviridaeAdherens JunctionsAge FactorsAnimalsAnimals, NewbornAxonsbeta CateninBlotting, WesternCadherinsCateninsCell Adhesion MoleculesCell CountCHO CellsCloning, MolecularConnexins2',3'-Cyclic-Nucleotide Phosphodiesterasesbeta CateninCadherinsCateninsCell Adhesion MoleculesConnexinsDelta CateninDNA-Binding ProteinsGje1 protein, mouseGreen Fluorescent ProteinsNerve Tissue ProteinsPhosphoproteinsrac1 GTP-Binding ProteinRag2 protein, mouserho GTP-Binding ProteinsTyrosine

Identifiers

PMID15800180
PMCPMC6724905
OpenAlexW2059892947

What OpenQuestion holds

Textmetadata
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.