Evidence map›Paper›PMID 22291039›Full record

ArticleThe Journal of cell biology2012

The cytoskeletal adapter protein 4.1G organizes the internodes in peripheral myelinated nerves.

Aleksandra Ivanovic, Ido Horresh, Neev Golan, Ivo Spiegel, Helena Sabanay, Shahar Frechter, Shinichi Ohno, Nobuo Terada, Wiebke Möbius, Jack Rosenbluth and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.1field-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

31 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Differential Contribution of Cadm1-Cadm3 Cell Adhesion Molecules to Peripheral Myelinated Axons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Expression of Protein 4.1 Family in Breast Cancer: Database Mining for 4.1 Family Members in Malignancies.Medical science monitor : international medical journal of experimental and clinical research · 2019
    Article
  12. Article
  13. Article
  14. Article
  15. In focus in HCB.Histochemistry and cell biology · 2017
    Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. The Nodes of Ranvier: Molecular Assembly and Maintenance.Cold Spring Harbor perspectives in biology · 2015
    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

12 authors at 4 institutions in 4 countries.

Aleksandra IvanovicDepartment of Molecular Neurobiology and 2 Department of Neurogenetics, Max Planck Institute of Experimental Medicine, D-37075 Göttingen, Germany.
Ido Horresh
Neev Golan
Ivo Spiegel
Helena Sabanay
Shahar Frechter
Shinichi Ohno
Nobuo Terada
Wiebke Möbius
Jack Rosenbluth
Nils Brose
Elior Peles
Weizmann Institute of Science · ILMax Planck Institute of Experimental Medicine · DEUniversity of Yamanashi · JPNew York University · US

Funding

Pathology of dysmyelination and demyelinationR01NS037475 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ROSENBLUTH, JACK · 1998 to 2013
$3.3M
Role of three novel CAMs in myelinating gliaR01NS050220 · NINDS · WEIZMANN INSTITUTE OF SCIENCE · PI PELES, ELIOR · 2005 to 2015
$1.6M
NINDS NIH HHS NS37475NINDS NIH HHS NS50220NINDS NIH HHS R01 NS037475NINDS NIH HHS R01 NS050220
6 · The paper itself

Abstract

Myelinating Schwann cells regulate the localization of ion channels on the surface of the axons they ensheath. This function depends on adhesion complexes that are positioned at specific membrane domains along the myelin unit. Here we show that the precise localization of internodal proteins depends on the expression of the cytoskeletal adapter protein 4.1G in Schwann cells. Deletion of 4.1G in mice resulted in aberrant distribution of both glial adhesion molecules and axonal proteins that were present along the internodes. In wild-type nerves, juxtaparanodal proteins (i.e., Kv1 channels, Caspr2, and TAG-1) were concentrated throughout the internodes in a double strand that flanked paranodal junction components (i.e., Caspr, contactin, and NF155), and apposes the inner mesaxon of the myelin sheath. In contrast, in 4.1G(-/-) mice, these proteins "piled up" at the juxtaparanodal region or aggregated along the internodes. These findings suggest that protein 4.1G contributes to the organization of the internodal axolemma by targeting and/or maintaining glial transmembrane proteins along the axoglial interface.

Indexed as

AnimalsAxonsCell Adhesion Molecules, NeuronalChlorocebus aethiopsCOS CellsMiceMice, KnockoutMicrofilament ProteinsMyelin SheathNerve Fibers, MyelinatedPeripheral NervesCell Adhesion Molecules, NeuronalEpb4.1l2 protein, mouseMicrofilament Proteins

Identifiers

PMID22291039
PMCPMC3275379
OpenAlexW2096917532

What OpenQuestion holds

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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.