Evidence map›Paper›PMID 21966409›Full record

ArticlePloS one2011

Protein 4.1B contributes to the organization of peripheral myelinated axons.

Carmen Cifuentes-Diaz, Fabrice Chareyre, Marta Garcia, Jérôme Devaux, Michèle Carnaud, Grégoire Levasseur, Michiko Niwa-Kawakita, Sheila Harroch, Jean-Antoine Girault, Marco Giovannini and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

39 citing papers in PubMed, 58 citations in OpenAlex.

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  11. Mechanisms of node of Ranvier assembly.Nature reviews. Neuroscience · 2021
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  17. The Axonal Cytoskeleton and the Assembly of Nodes of Ranvier.The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry · 2018
    Review
  18. Review
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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 at 5 institutions in 1 country.

Carmen Cifuentes-DiazInserm, UMR-S 839, Paris, France.
Fabrice Chareyre
Marta Garcia
Jérôme Devaux
Michèle Carnaud
Grégoire Levasseur
Michiko Niwa-Kawakita
Sheila Harroch
Jean-Antoine Girault
Marco Giovannini
Laurence Goutebroze
Sorbonne Université · FRInstitut Universitaire de France · FRInstitut du Fer à Moulin · FRCentre de Recherche en Neurobiologie - Neurophysiologie de Marseille · FRInstitut Pasteur · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurons are characterized by extremely long axons. This exceptional cell shape is likely to depend on multiple factors including interactions between the cytoskeleton and membrane proteins. In many cell types, members of the protein 4.1 family play an important role in tethering the cortical actin-spectrin cytoskeleton to the plasma membrane. Protein 4.1B is localized in myelinated axons, enriched in paranodal and juxtaparanodal regions, and also all along the internodes, but not at nodes of Ranvier where are localized the voltage-dependent sodium channels responsible for action potential propagation. To shed light on the role of protein 4.1B in the general organization of myelinated peripheral axons, we studied 4.1B knockout mice. These mice displayed a mildly impaired gait and motility. Whereas nodes were unaffected, the distribution of Caspr/paranodin, which anchors 4.1B to the membrane, was disorganized in paranodal regions and its levels were decreased. In juxtaparanodes, the enrichment of Caspr2, which also interacts with 4.1B, and of the associated TAG-1 and Kv1.1, was absent in mutant mice, whereas their levels were unaltered. Ultrastructural abnormalities were observed both at paranodes and juxtaparanodes. Axon calibers were slightly diminished in phrenic nerves and preterminal motor axons were dysmorphic in skeletal muscle. βII spectrin enrichment was decreased along the axolemma. Electrophysiological recordings at 3 post-natal weeks showed the occurrence of spontaneous and evoked repetitive activity indicating neuronal hyperexcitability, without change in conduction velocity. Thus, our results show that in myelinated axons 4.1B contributes to the stabilization of membrane proteins at paranodes, to the clustering of juxtaparanodal proteins, and to the regulation of the internodal axon caliber.

Indexed as

Alternative SplicingAnimalsAxonsElectrophysiologyErythrocytesFemaleMaleMiceMice, KnockoutMicrofilament ProteinsMicroscopy, FluorescenceModels, BiologicalMutationMyelin SheathNeuronsProtein IsoformsEpb41l1 protein, ratEpb41l3 protein, mouseMicrofilament ProteinsProtein Isoforms

Identifiers

PMID21966409
PMCPMC3180372
OpenAlexW2027190540

What OpenQuestion holds

Textmetadata
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.