Evidence map›Paper›PMID 10704450›Full record

ArticleThe Journal of cell biology2000

Schwann cell myelination requires timely and precise targeting of P(0) protein.

X Yin, G J Kidd, L Wrabetz, M L Feltri, A Messing, B D Trapp

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

28 citing papers in PubMed, 72 citations in OpenAlex.

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  12. Interplay between LXR and Wnt/β-catenin signaling in the negative regulation of peripheral myelin genes by oxysterols.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2011
    Article
  13. Article
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  15. Cholesterol regulates the endoplasmic reticulum exit of the major membrane protein P0 required for peripheral myelin compaction.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2009
    Article
  16. P0 protein is required for and can induce formation of schmidt-lantermann incisures in myelin internodes.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2008
    Article
  17. Article
  18. Immune cells contribute to myelin degeneration and axonopathic changes in mice overexpressing proteolipid protein in oligodendrocytes.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2006
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  19. Different intracellular pathomechanisms produce diverse Myelin Protein Zero neuropathies in transgenic mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2006
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  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

6 authors at 3 institutions in 2 countries.

X YinDepartment of Neurosciences, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA.
G J Kidd
L Wrabetz
M L Feltri
A Messing
B D Trapp
Cleveland Clinic · USSan Raffaele University of Rome · ITUniversity of Wisconsin–Madison · US

Funding

Molecular Mechanisms of Schwann Cell MyelinationR37NS038186 · NINDS · CLEVELAND CLINIC LERNER COM-CWRU · PI TRAPP, BRUCE D · 2002 to 2008
$2.8M
MOLECULAR MECHANISMS OF SCHWANN CELL MYELINATIONR01NS038186 · NINDS · CLEVELAND CLINIC LERNER COM-CWRU · PI TRAPP, BRUCE D · 1999 to 2014
$2.5M
IONIC CHANNELS IN MYELINATED NERVESR01NS023375 · NINDS · UNIVERSITY OF WISCONSIN MADISON · PI CHIU, SHING YAN · 1986 to 2004
$1.7M
NINDS NIH HHS NS-23375NINDS NIH HHS NS-38186NINDS NIH HHS R01 NS023375NINDS NIH HHS R01 NS038186NINDS NIH HHS R37 NS038186
6 · The paper itself

Abstract

This report investigated mechanisms responsible for failed Schwann cell myelination in mice that overexpress P(0) (P(0)(tg)), the major structural protein of PNS myelin. Quantitative ultrastructural immunocytochemistry established that P(0) protein was mistargeted to abaxonal, periaxonal, and mesaxon membranes in P(0)(tg) Schwann cells with arrested myelination. The extracellular leaflets of P(0)-containing mesaxon membranes were closely apposed with periodicities of compact myelin. The myelin-associated glycoprotein was appropriately sorted in the Golgi apparatus and targeted to periaxonal membranes. In adult mice, occasional Schwann cells myelinated axons possibly with the aid of endocytic removal of mistargeted P(0). These results indicate that P(0) gene multiplication causes P(0) mistargeting to mesaxon membranes, and through obligate P(0) homophilic adhesion, renders these dynamic membranes inert and halts myelination.

Indexed as

AgingAnimalsAxonsCell MembraneEndosomesGene AmplificationGolgi ApparatusImmunohistochemistryMiceMice, TransgenicMicroscopy, ElectronMyelin-Associated GlycoproteinMyelin P0 ProteinMyelin SheathRNA, MessengerSchwann CellsMyelin-Associated GlycoproteinMyelin P0 ProteinRNA, Messenger

Identifiers

PMID10704450
PMCPMC2174550
OpenAlexW2109723536

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.