Evidence map›Paper›PMID 17135401›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2006

CD47 promotes neuronal development through Src- and FRG/Vav2-mediated activation of Rac and Cdc42.

Takaaki Murata, Hiroshi Ohnishi, Hideki Okazawa, Yoji Murata, Shinya Kusakari, Yuriko Hayashi, Motoaki Miyashita, Hiroshi Itoh, Per-Arne Oldenborg, Nobuhiko Furuya and 1 more

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

44 citing papers in PubMed, 83 citations in OpenAlex.

  1. Article
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  7. Article
  8. Deciphering the role of CD47 in cancer immunotherapy.Journal of advanced research · 2024
    Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. CD47: role in the immune system and application to cancer therapy.Cellular oncology (Dordrecht, Netherlands) · 2020
    Review
  15. Article
  16. Article
  17. 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

11 authors at 3 institutions in 2 countries.

Takaaki MurataLaboratory of Biosignal Sciences, Institute for Molecular and Cellular Regulation, Gunma University, Maebashi, Gunma 371-8512, Japan.
Hiroshi Ohnishi
Hideki Okazawa
Yoji Murata
Shinya Kusakari
Yuriko Hayashi
Motoaki Miyashita
Hiroshi Itoh
Per-Arne Oldenborg
Nobuhiko Furuya
Takashi Matozaki
Gunma University · JPNara Institute of Science and Technology · JPUmeå University · SE

Funding

INTEGRIN ASSOCIATED PROTEIN (IAP) IG DOMAIN FUNCTIONR01GM057573 · NIGMS · WASHINGTON UNIVERSITY · PI FRAZIER, WILLIAM A · 1998 to 2006
$1.9M
NIGMS NIH HHS GM57573-06NIGMS NIH HHS R01 GM057573
6 · The paper itself

Abstract

The development of axons and dendrites is controlled by small GTP-binding proteins of the Rho family, but the upstream signaling mechanisms responsible for such regulation remain unclear. We have now investigated the role of the transmembrane protein cluster of differentiation 47 (CD47) in this process with hippocampal neurons. CD47-deficient neurons manifested markedly impaired development of dendrites and axons, whereas overexpression of CD47 promoted such development. Interaction of SH2 domain-containing protein tyrosine phosphatase substrate-1 (SHPS-1) with CD47 also induced the formation of dendritic filopodia and spines. These effects of CD47 were prevented by inhibition of either cell division cycle 42 (Cdc42) or Rac. In CD47-deficient neurons, autophosphorylation of Src was markedly reduced. In addition, overexpression of CD47 promoted the autophosphorylation of Src. Inhibition of Src family kinases indeed prevented CD47-promoted dendritic development. Inhibition of either FGD1-related Cdc42-guanine nucleotide exchange factor (GEF) (FRG) or Vav2, which is a GEF for Cdc42 and Rac and is activated by Src, also prevented the effects of CD47 on dendritic development. These results indicate that CD47 promotes development of dendrites and axons in hippocampal neurons in a manner dependent, at least in part, on activation of Cdc42 and Rac mediated by Src as well as by FRG and Vav2.

Indexed as

AnimalsCD47 Antigencdc42 GTP-Binding ProteinCells, CulturedGuanine Nucleotide Exchange FactorsHippocampusHumansMiceMice, KnockoutNeuronsProteinsProto-Oncogene Proteins c-vavrac GTP-Binding Proteinssrc-Family KinasesCD47 AntigenCd47 protein, mousecdc42 GTP-Binding ProteinFgd1 protein, mouseGuanine Nucleotide Exchange FactorsProteinsProto-Oncogene Proteins c-vavrac GTP-Binding Proteinssrc-Family KinasesVav2 protein, mouse

Identifiers

PMID17135401
PMCPMC6674889
OpenAlexW2066551977

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.