Evidence map›Paper›PMID 9852580›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience1998

Neurite outgrowth stimulated by neural cell adhesion molecules requires growth-associated protein-43 (GAP-43) function and is associated with GAP-43 phosphorylation in growth cones.

K F Meiri, J L Saffell, F S Walsh, P Doherty

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
5.1field-weighted citation impact, top 3% 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

51 citing papers in PubMed, 241 citations in OpenAlex.

  1. Article
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  6. Accumulation of PSA-NCAM marks nascent neurodegeneration in the dorsal hippocampus after neonatal hypoxic-ischemic brain injury in mice.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2021
    Article
  7. Review
  8. FGF/FGFR signaling in health and disease.Signal transduction and targeted therapy · 2020
    Review
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  11. 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

4 authors at 2 institutions in 2 countries.

K F MeiriDepartment of Pharmacology, State University of New York Health Science Center, Syracuse, New York 13210, USA.
J L Saffell
F S Walsh
P Doherty
Guy's Hospital · GBState University of New York · US

Funding

GAP-43 FUNCTION BY GENETIC MANIPULATIONR01NS033118 · NINDS · UPSTATE MEDICAL UNIVERSITY · PI MEIRI, KARINA F · 1995 to 2005
$1.4M
SIGNAL TRANSDUCTION IN THE NEURONAL GROWTH CONER01NS026091 · NINDS · UPSTATE MEDICAL UNIVERSITY · PI MEIRI, KARINA F · 1994 to 2001
$79k
SIGNAL TRANSDUCTION IN THE NEURONAL GROWTH CONER29NS026091 · NINDS · UPSTATE MEDICAL UNIVERSITY · PI MEIRI, KARINA F · 1988 to 1992
–
NINDS NIH HHS NS 26091NINDS NIH HHS NS 33118NINDS NIH HHS R01 NS033118Wellcome Trust
6 · The paper itself

Abstract

The mechanisms whereby cell adhesion molecules (CAMs) promote axonal growth and synaptic plasticity are poorly understood. Here we show that the neurite outgrowth stimulated by NCAM-mediated fibroblast growth factor (FGF) receptor activation in cerebellar granule cells is associated with increased GAP-43 phosphorylation on serine-41. In contrast, neither NCAM nor FGF was able to stimulate neurite outgrowth in similar neurons from mice in which the GAP-43 gene had been deleted by homologous recombination. Integrin-mediated neurite outgrowth was unaffected by GAP-43 deletion. Both neurite outgrowth and rapid phosphorylation of GAP-43 in isolated growth cones required the first three Ig domains of a NCAM-Fc chimera and were stimulated maximally at 5 micrograms/ml (approximately 50 nM). Likewise, GAP-43 phosphorylation in isolated growth cones also was stimulated by an L1-Fc chimera. Both neurite outgrowth and NCAM-stimulated GAP-43 phosphorylation were inhibited by antibodies to the FGF receptor and a diacylglycerol lipase inhibitor (RHC80267) that blocks the production of arachidonic acid in response to activation of the FGF receptor. Direct activation of the FGF receptor and the arachidonic acid cascade with either basic FGF or melittin also resulted in increased GAP-43 phosphorylation. These data suggest that the stimulation of neurite outgrowth by NCAM requires GAP-43 function and that GAP-43 phosphorylation in isolated growth cones occurs via an FGF receptor-dependent increase in arachidonic acid.

Indexed as

3T3 CellsAnimalsAntibodiesCells, CulturedCoculture TechniquesCyclohexanonesFibroblast Growth FactorsGAP-43 ProteinGrowth ConesMiceMice, KnockoutNeural Cell Adhesion MoleculesNeuritesPhosphorylationReceptors, Fibroblast Growth FactorRecombinant Fusion Proteins1,6-bis(cyclohexyloximinocarbonyl)hexaneAntibodiesCyclohexanonesFibroblast Growth FactorsGAP-43 ProteinNeural Cell Adhesion MoleculesReceptors, Fibroblast Growth FactorRecombinant Fusion Proteins

Identifiers

PMID9852580
PMCPMC6793360
OpenAlexW1906779471

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.