Evidence map›Paper›PMID 25502296›Full record

ArticleMolecular neurobiology2016

Immunomodulator CD200 Promotes Neurotrophic Activity by Interacting with and Activating the Fibroblast Growth Factor Receptor.

Stanislava Pankratova, Halla Bjornsdottir, Claus Christensen, Lanjun Zhang, Shizhong Li, Oksana Dmytriyeva, Elisabeth Bock, Vladimir Berezin

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular neurobiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
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  7. Review
  8. Review
  9. CD200-CD200R signaling and diseases: a potential therapeutic target?International journal of physiology, pathophysiology and pharmacology · 2019
    Review
  10. Article
  11. Article
  12. Article
  13. Microglia: Housekeeper of the Central Nervous System.Cellular and molecular neurobiology · 2018
    Review
  14. Review
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 1 institution in 1 country.

Stanislava PankratovaLaboratory of Neural Plasticity, Department of Neuroscience and Pharmacology, Panum Institute, Blegdamsvej 3, 2200, Copenhagen, Denmark. stasya@sund.ku.dk.
Halla BjornsdottirLaboratory of Neural Plasticity, Department of Neuroscience and Pharmacology, Panum Institute, Blegdamsvej 3, 2200, Copenhagen, Denmark.
Claus ChristensenLaboratory of Neural Plasticity, Department of Neuroscience and Pharmacology, Panum Institute, Blegdamsvej 3, 2200, Copenhagen, Denmark.
Lanjun ZhangLaboratory of Neural Plasticity, Department of Neuroscience and Pharmacology, Panum Institute, Blegdamsvej 3, 2200, Copenhagen, Denmark.
Shizhong LiLaboratory of Neural Plasticity, Department of Neuroscience and Pharmacology, Panum Institute, Blegdamsvej 3, 2200, Copenhagen, Denmark.
Oksana DmytriyevaLaboratory of Neural Plasticity, Department of Neuroscience and Pharmacology, Panum Institute, Blegdamsvej 3, 2200, Copenhagen, Denmark.
Elisabeth BockLaboratory of Neural Plasticity, Department of Neuroscience and Pharmacology, Panum Institute, Blegdamsvej 3, 2200, Copenhagen, Denmark.
Vladimir BerezinLaboratory of Neural Plasticity, Department of Neuroscience and Pharmacology, Panum Institute, Blegdamsvej 3, 2200, Copenhagen, Denmark.
Neurosciences Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The CD200 ligand is expressed by a variety of cell types, including vascular endothelia, kidney glomeruli, some subsets of T and B cells, and neurons in the brain and periphery. In contrast, the receptor of CD200, CD200R, has a limited expression pattern and is mainly expressed by cells of myeloid origin. A recently solved crystal structure of the CD200-CD200R ectodomain complex suggests involvement of the first immunoglobulin (Ig)-like modules in ligand-receptor binding, resulting in the inhibition of myeloid cell function. In the central nervous system, CD200 has been implicated in the suppression of microglia activation. We for the first time demonstrated that CD200 can interact with and transduce signaling through activation of the fibroblast growth factor receptor (FGFR), thereby inducing neuritogenesis and promoting neuronal survival in primary neurons. CD200-induced FGFR phosphorylation was abrogated by CD200R, whereas FGF2-induced FGFR activation was inhibited by CD200. We also identified a sequence motif located in the first Ig-like module of CD200, likely representing the minimal CD200 binding site for FGFR. The FGFR binding motif overlaps with the CD200R binding site, suggesting that they can compete for CD200 binding in cells that express both receptors. We propose that CD200 in neurons functions as a ligand of FGFR.

Indexed as

Amino Acid SequenceAnimalsAntigens, CDCells, CulturedDose-Response Relationship, DrugHippocampusImmunologic FactorsMolecular Sequence DataNerve Growth FactorsNeuronsProtein BindingProtein Structure, SecondaryRatsRats, WistarReceptors, Fibroblast Growth FactorAntigens, CDantigens, CD200Immunologic FactorsNerve Growth FactorsReceptors, Fibroblast Growth FactorCD200FGF receptorNeurite outgrowthNeuronal survival

Identifiers

PMID25502296
OpenAlexW2154685709

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.