Evidence map›Paper›PMID 29217681›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2018

The Protein Tyrosine Phosphatase Shp2 Regulates Oligodendrocyte Differentiation and Early Myelination and Contributes to Timely Remyelination.

Jared T Ahrendsen, Danielle E Harlow, Lisbet T Finseth, Jennifer N Bourne, Sean P Hickey, Elizabeth A Gould, Cecilia M Culp, Wendy B Macklin

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.4field-weighted citation impact, top 35% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Genes in Axonal Regeneration.Molecular neurobiology · 2024
    Review
  4. Excitable Axonal Domains Adapt to Sensory Deprivation in the Olfactory System.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  5. Article
  6. Article
  7. Loss of Shp2 Rescues BDNF/TrkB Signaling and Contributes to Improved Retinal Ganglion Cell Neuroprotection.Molecular therapy : the journal of the American Society of Gene Therapy · 2019
    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

8 authors at 2 institutions in 1 country.

Jared T AhrendsenDepartment of Cell and Developmental Biology, and.ORCID 0000-0002-9309-6544
Danielle E HarlowDepartment of Cell and Developmental Biology, and.
Lisbet T FinsethDepartment of Cell and Developmental Biology, and.ORCID 0000-0001-6128-1828
Jennifer N BourneDepartment of Cell and Developmental Biology, and.ORCID 0000-0001-5501-0351
Sean P HickeyDepartment of Cell and Developmental Biology, and.
Elizabeth A GouldDepartment of Cell and Developmental Biology, and.
Cecilia M CulpDepartment of Cell and Developmental Biology, and.
Wendy B MacklinDepartment of Cell and Developmental Biology, and Wendy.Macklin@ucdenver.edu.ORCID 0000-0002-1252-0607
University of Colorado Denver · USWeber State University · US

Funding

Institutional Training in Otolaryngology ResearchT32DC012280 · NIDCD · UNIVERSITY OF COLORADO DENVER · PI Yuri Agrawal, Sue C. Kinnamon · 2013 to 2026
$3.4M
Signaling pathways regulating myelination in the CNSF31NS081834 · NINDS · UNIVERSITY OF COLORADO DENVER · PI AHRENDSEN, JARED TYLER · 2012 to 2014
$82k
NIDCD NIH HHS T32 DC012280NINDS NIH HHS F31 NS081834
6 · The paper itself

Abstract

Shp2 is a nonreceptor protein tyrosine phosphatase that has been shown to influence neurogenesis, oligodendrogenesis, and oligodendrocyte differentiation. Furthermore, Shp2 is a known regulator of the Akt/mammalian target of rapamycin and ERK signaling pathways in multiple cellular contexts, including oligodendrocytes. Its role during later postnatal CNS development or in response to demyelination injury has not been examined. Based on the current studies, we hypothesize that Shp2 is a negative regulator of CNS myelination. Using transgenic mouse technology, we show that Shp2 is involved in oligodendrocyte differentiation and early myelination, but is not necessary for myelin maintenance. We also show that Shp2 regulates the timely differentiation of oligodendrocytes following lysolecithin-induced demyelination, although apparently normal remyelination occurs at a delayed time point. These data suggest that Shp2 is a relevant therapeutic target in demyelinating diseases such as multiple sclerosis.

Indexed as

AnimalsCell DifferentiationFemaleMaleMiceMice, TransgenicMyelin SheathNeurogenesisOligodendrogliaProtein Tyrosine Phosphatase, Non-Receptor Type 11ZebrafishProtein Tyrosine Phosphatase, Non-Receptor Type 11myelinationoligodendrocyteremyelinationShp2

Identifiers

PMID29217681
PMCPMC5783963
OpenAlexW2775765482

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.