Evidence map›Paper›PMID 30121936›Full record

ArticleMolecular neurobiology2019

TIMP-1 Promotes Oligodendrocyte Differentiation Through Receptor-Mediated Signaling.

Alexandra M Nicaise, Kasey M Johnson, Cory M Willis, Rosa M Guzzo, Stephen J Crocker

Open access · greenAbstract read
In one paragraph

Article in Molecular neurobiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

27 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. The TIMP protein family: diverse roles in pathophysiology.American journal of physiology. Cell physiology · 2024
    Review
  9. Astrocytic TIMP-1 regulates production of Anastellin, an inhibitor of oligodendrocyte differentiation and FTY720 responses.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. FunctionalNeural regeneration research · 2022
    Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  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

5 authors at 1 institution in 1 country.

Alexandra M NicaiseDepartment of Neuroscience, University of Connecticut School of Medicine, 263 Farmington Ave, Farmington, CT, 06030, USA.
Kasey M JohnsonDepartment of Neuroscience, University of Connecticut School of Medicine, 263 Farmington Ave, Farmington, CT, 06030, USA.
Cory M WillisDepartment of Neuroscience, University of Connecticut School of Medicine, 263 Farmington Ave, Farmington, CT, 06030, USA.
Rosa M GuzzoDepartment of Neuroscience, University of Connecticut School of Medicine, 263 Farmington Ave, Farmington, CT, 06030, USA.
Stephen J CrockerDepartment of Neuroscience, University of Connecticut School of Medicine, 263 Farmington Ave, Farmington, CT, 06030, USA. crocker@uchc.edu.ORCID http://orcid.org/0000-0003-4529-1385
University of Connecticut · US

Funding

Regulation of Microgliosis in Globoid Cell LeukodystrophyR56NS099359 · NINDS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI CROCKER, STEPHEN J · 2017 to 2017
$574k
Proteomic and Functional Analyses of Astrocyte ExosomesR21NS087578 · NINDS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI CROCKER, STEPHEN J, VELLA, ANTHONY T · 2015 to 2016
$428k
National Institute of Neurological Disorders and Stroke R56 NS099359National Multiple Sclerosis Society RG-5001-A3NINDS NIH HHS R21 NS087578
6 · The paper itself

Abstract

The extracellular protein tissue inhibitor of metalloproteinase (TIMP)-1 is both a matrix metalloproteinase (MMP) inhibitor and a trophic factor. Mice lacking TIMP-1 exhibit delayed central nervous system myelination during postnatal development and impaired remyelination following immune-mediated injury in adulthood. We have previously determined that the trophic action of TIMP-1 on oligodendrocyte progenitor cells (OPCs) to mature into oligodendrocytes is independent of its MMP inhibitory function. However, the mechanism by which TIMP-1 promotes OPC differentiation is not known. To address this gap in our understanding, herein, we report that TIMP-1 signals via a CD63/β1-integrin receptor complex to activate Akt (protein kinase B) to promote β-catenin signaling in OPCs. The regulation of β-catenin by TIMP-1 to promote OPC differentiation was counteracted, but not abrogated, by canonical signaling evoked by Wnt7a. These data provide a previously uncharacterized trophic action of TIMP-1 to regulate oligodendrocyte maturation via a CD63/β1-integrin/Akt pathway mechanism. These findings contribute to our emerging understanding on the role of TIMP-1 as a growth factor expressed to promote CNS myelination during development and induced in the adult to promote myelin repair.

Indexed as

Cell DifferentiationSignal TransductionAnimalsbeta CateninCells, CulturedEnzyme ActivationIntegrin beta1OligodendrogliaProtein DomainsProto-Oncogene Proteins c-aktRats, Sprague-DawleyTetraspanin 30Tissue Inhibitor of Metalloproteinase-1Wnt Proteinsbeta CateninIntegrin beta1Proto-Oncogene Proteins c-aktTetraspanin 30Tissue Inhibitor of Metalloproteinase-1Wnt ProteinsAkt/PKBAstrocyteMetalloproteinaseOligodendrocyte progenitor cellTetraspaninWnt7aβ-Catenin

Identifiers

PMID30121936
PMCPMC6379156
OpenAlexW2886214589

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.