Evidence map›Paper›PMID 24478351›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2014

Novel roles for osteopontin and clusterin in peripheral motor and sensory axon regeneration.

Megan C Wright, Ruifa Mi, Emmalynn Connor, Nicole Reed, Alka Vyas, Manula Alspalter, Giovanni Coppola, Daniel H Geschwind, Thomas M Brushart, Ahmet Höke

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

47 citing papers in PubMed, 79 citations in OpenAlex.

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  16. Review
  17. Unleashing Intrinsic Growth Pathways in Regenerating Peripheral Neurons.International journal of molecular sciences · 2022
    Review
  18. Article
  19. Article
  20. Involvement of Denervated Midbrain-Derived Factors in the Formation of Ectopic Cortico-Mesencephalic Projection after Hemispherectomy.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    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

10 authors at 2 institutions in 1 country.

Megan C WrightDepartments of Neurology, Neuroscience, and Orthopedics, The Johns Hopkins School of Medicine, Baltimore, Maryland 21287, and Departments of Neurology and Psychiatry, University of California, Los Angeles, Los Angeles, California 90095.
Ruifa Mi
Emmalynn Connor
Nicole Reed
Alka Vyas
Manula Alspalter
Giovanni Coppola
Daniel H Geschwind
Thomas M Brushart
Ahmet Höke
Johns Hopkins University · USUniversity of California, Los Angeles · US

Funding

MOTOR/SENSORY SPECIFICITY--MECHANISMS AND AUGMENTATIONR01NS034484 · NINDS · JOHNS HOPKINS UNIVERSITY · PI BRUSHART, THOMAS M · 1997 to 2013
$4.5M
NINDS NIH HHS R01 NS034484
6 · The paper itself

Abstract

Previous studies demonstrated that Schwann cells (SCs) express distinct motor and sensory phenotypes, which impact the ability of these pathways to selectively support regenerating neurons. In the present study, unbiased microarray analysis was used to examine differential gene expression in denervated motor and sensory pathways in rats. Several genes that were significantly upregulated in either denervated sensory or motor pathways were identified and two secreted factors were selected for further analysis: osteopontin (OPN) and clusterin (CLU) which were upregulated in denervated motor and sensory pathways, respectively. Sciatic nerve transection induced upregulation of OPN and CLU and expression of both returned to baseline levels with ensuing regeneration. In vitro analysis using exogenously applied OPN induced outgrowth of motor but not sensory neurons. CLU, however, induced outgrowth of sensory neurons, but not motor neurons. To assess the functional importance of OPN and CLU, peripheral nerve regeneration was examined in OPN and CLU(-/-) mice. When compared with OPN(+/+) mice, motor neuron regeneration was reduced in OPN(-/-) mice. Impaired regeneration through OPN(-/-) peripheral nerves grafted into OPN(+/+) mice indicated that loss of OPN in SCs was responsible for reduced motor regeneration. Sensory neuron regeneration was impaired in CLU(-/-) mice following sciatic nerve crush and impaired regeneration nerve fibers through CLU(-/-) nerve grafts transplanted into CLU(+/+) mice indicated that reduced sensory regeneration is likely due to SC-derived CLU. Together, these studies suggest unique roles for SC-derived OPN and CLU in regeneration of peripheral motor and sensory axons.

Indexed as

AnimalsCells, CulturedCholine O-AcetyltransferaseClusterinDenervationDisease Models, AnimalFemaleGene Expression RegulationGreen Fluorescent ProteinsMiceMice, TransgenicMotor NeuronsNerve Fibers, MyelinatedNerve RegenerationNeural ConductionNeuromuscular JunctionCholine O-AcetyltransferaseClusterinenhanced green fluorescent proteinGreen Fluorescent ProteinsOsteopontin

Identifiers

PMID24478351
PMCPMC3905142
OpenAlexW2079800084

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.