Evidence map›Paper›PMID 26341907›Full record

ArticleNeuroscience2015

Developmental expression and function analysis of protein tyrosine phosphatase receptor type D in oligodendrocyte myelination.

Q Zhu, Z Tan, S Zhao, H Huang, X Zhao, X Hu, Y Zhang, C B Shields, N Uetani, M Qiu

Abstract read
In one paragraph

Article in Neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 39% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
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  4. Review
  5. Review
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  7. Article
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  11. Article
  12. LAR Receptor Tyrosine Phosphatase Family in Healthy and Diseased Brain.Frontiers in cell and developmental biology · 2021
    Review
  13. Article
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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

10 authors at 3 institutions in 2 countries.

Q ZhuDepartment of Anatomical Sciences and Neurobiology, University of Louisville, Louisville, KY 40292, USA.
Z TanDepartment of Anatomical Sciences and Neurobiology, University of Louisville, Louisville, KY 40292, USA; Institute of Developmental and Regenerative Biology, Zhejiang Key Lab of Organ Development and Regeneration, College of Life Sciences, Hangzhou Normal University, China.
S ZhaoDepartment of Anatomical Sciences and Neurobiology, University of Louisville, Louisville, KY 40292, USA.
H HuangDepartment of Anatomical Sciences and Neurobiology, University of Louisville, Louisville, KY 40292, USA; Institute of Developmental and Regenerative Biology, Zhejiang Key Lab of Organ Development and Regeneration, College of Life Sciences, Hangzhou Normal University, China.
X ZhaoDepartment of Anatomical Sciences and Neurobiology, University of Louisville, Louisville, KY 40292, USA; Institute of Developmental and Regenerative Biology, Zhejiang Key Lab of Organ Development and Regeneration, College of Life Sciences, Hangzhou Normal University, China.
X HuDepartment of Anatomical Sciences and Neurobiology, University of Louisville, Louisville, KY 40292, USA.
Y ZhangNorton Neuroscience Institute, Norton Healthcare, Louisville, KY 40202, USA.
C B ShieldsNorton Neuroscience Institute, Norton Healthcare, Louisville, KY 40202, USA.
N UetaniMcGill Cancer Centre and Department of Biochemistry, McGill University, Montreal, Quebec H3G 1Y6, Canada.
M QiuDepartment of Anatomical Sciences and Neurobiology, University of Louisville, Louisville, KY 40292, USA; Institute of Developmental and Regenerative Biology, Zhejiang Key Lab of Organ Development and Regeneration, College of Life Sciences, Hangzhou Normal University, China. Electronic address: m0qiu001@louisville.edu.
University of Louisville · USNorton Healthcare · USMcGill University · CA

Funding

Transcriptional control of oligodendrocyte differentiation and myelinationR01NS037717 · NINDS · UNIVERSITY OF LOUISVILLE · PI QIU, MENGSHENG · 2000 to 2013
$3.6M
NINDS NIH HHS R01 NS037717NINDS NIH HHS R01NS37717
6 · The paper itself

Abstract

Receptor protein tyrosine phosphatases (RPTPs) are extensively expressed in the central nervous system (CNS), and have distinct spatial and temporal patterns in different cell types during development. Previous studies have demonstrated possible roles for RPTPs in axon outgrowth, guidance, and synaptogenesis. In the present study, our results revealed that protein tyrosine phosphatase, receptor type D (PTPRD) was initially expressed in mature neurons in embryonic CNS, and later in oligodendroglial cells at postnatal stages when oligodendrocytes undergo active axonal myelination process. In PTPRD mutants, oligodendrocyte differentiation was normal and a transient myelination delay occurred at early postnatal stages, indicating the contribution of PTPRD to the initiation of axonal myelination. Our results also showed that the remyelination process was not affected in the absence of PTPRD function after a cuprizone-induced demyelination in adult animals.

Indexed as

AnimalsBlotting, WesternBrainCell DifferentiationCuprizoneDemyelinating DiseasesDisease Models, AnimalEvoked Potentials, MotorImmunohistochemistryIn Situ HybridizationMice, TransgenicMotor ActivityMutationOligodendrogliaReceptor-Like Protein Tyrosine Phosphatases, Class 2Spinal CordCuprizonePtprd protein, mouseReceptor-Like Protein Tyrosine Phosphatases, Class 2axonal myelinationcorpus callosumcuprizonespinal cord

Identifiers

PMID26341907
PMCPMC4600676
OpenAlexW1260057052

What OpenQuestion holds

Textmetadata
LicenceTDM
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.