Evidence map›Paper›PMID 26272917›Full record

ArticleJournal of cell science2015

The NMDA receptor functions independently and as an LRP1 co-receptor to promote Schwann cell survival and migration.

Elisabetta Mantuano, Michael S Lam, Masataka Shibayama, W Marie Campana, Steven L Gonias

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cell science, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

36 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
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  6. Protein quality control ofFrontiers in cellular neuroscience · 2022
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  7. A Soluble PrPJournal of immunology (Baltimore, Md. : 1950) · 2022
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  9. Gene Expression Profile ofFrontiers in medicine · 2022
    Article
  10. Review
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  13. Review
  14. Article
  15. Review
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  17. Article
  18. A soluble derivative of PrPThe Journal of biological chemistry · 2020
    Article
  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 2 institutions in 2 countries.

Elisabetta MantuanoDepartment of Pathology, University of California San Diego, La Jolla, CA 92093, USA Department of Experimental Medicine, Sapienza University of Rome, Rome 00161, Italy.
Michael S LamDepartment of Pathology, University of California San Diego, La Jolla, CA 92093, USA.
Masataka ShibayamaDepartment of Anesthesiology, University of California San Diego, La Jolla, CA 92093, USA.
W Marie CampanaDepartment of Anesthesiology, University of California San Diego, La Jolla, CA 92093, USA The Program in Neuroscience, University of California San Diego, La Jolla, CA 92093, USA.
Steven L GoniasDepartment of Pathology, University of California San Diego, La Jolla, CA 92093, USA sgonias@ucsd.edu.
University of California, San Diego · USSapienza University of Rome · IT

Funding

REGULATION OF UROKINASE RECEPTOR ACTIVITY BY LRPR01HL060551 · NHLBI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI GONIAS, STEVEN L. · 1999 to 2014
$4.0M
LRP-1 is a multifunctional regulator during peripheral nerve injury and pain.R01NS057456 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CAMPANA, WENDY M. · 2008 to 2012
$1.7M
NHLBI NIH HHS HL-060551NHLBI NIH HHS R01 HL060551NINDS NIH HHS NS-057456NINDS NIH HHS R01 NS057456
6 · The paper itself

Abstract

NMDA receptors (NMDA-Rs) are ionotropic glutamate receptors, which associate with LDL-receptor-related protein-1 (LRP1) to trigger cell signaling in response to protein ligands in neurons. Here, we demonstrate for the first time that the NMDA-R is expressed by rat Schwann cells and functions independently and with LRP1 to regulate Schwann cell physiology. The NR1 (encoded by GRIN1) and NR2b (encoded by GRIN2B) NMDA-R subunits were expressed by cultured Schwann cells and upregulated in sciatic nerves following crush injury. The ability of LRP1 ligands to activate ERK1/2 (also known as MAPK3 and MAPK1, respectively) and promote Schwann cell migration required the NMDA-R. NR1 gene silencing compromised Schwann cell survival. Injection of the LRP1 ligands tissue-type plasminogen activator (tPA, also known as PLAT) or MMP9-PEX into crush-injured sciatic nerves activated ERK1/2 in Schwann cells in vivo, and the response was blocked by systemic treatment with the NMDA-R inhibitor MK801. tPA was unique among the LRP1 ligands examined because tPA activated cell signaling and promoted Schwann cell migration by interacting with the NMDA-R independently of LRP1, albeit with delayed kinetics. These results define the NMDA-R as a Schwann cell signaling receptor for protein ligands and a major regulator of Schwann cell physiology, which may be particularly important in peripheral nervous system (PNS) injury.

Indexed as

AnimalsCells, CulturedDizocilpine MaleateLow Density Lipoprotein Receptor-Related Protein-1MAP Kinase Signaling SystemMatrix Metalloproteinase 9Peripheral Nerve InjuriesRatsRats, Sprague-DawleyReceptors, N-Methyl-D-AspartateRNA InterferenceSchwann CellsSciatic NerveSignal TransductionTissue Plasminogen ActivatorDizocilpine MaleateLow Density Lipoprotein Receptor-Related Protein-1Matrix Metalloproteinase 9Mmp9 protein, ratReceptors, N-Methyl-D-AspartateTissue Plasminogen ActivatorLRP1MMP9NMDA receptorPeripheral nerveSchwann cellTissue-type plasminogen activatorα2-macroglobulin

Identifiers

PMID26272917
PMCPMC4594737
OpenAlexW2223721909

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.