Literature DB >> 9844004

Nerve growth factor acutely reduces chemical transmission by means of postsynaptic TrkA-like receptors in squid giant synapse.

H Moreno1, M Nadal, E Leznik, M Sugimori, I Lax, J Schlessinger, R Llinás.   

Abstract

Tyrosine phosphorylation has been shown to be an important modulator of synaptic transmission in both vertebrates and invertebrates. Such findings hint toward the existence of extracellular ligands capable of activating this widely represented signaling mechanism at or close to the synapse. Examples of such ligands are the peptide growth factors which, on binding, activate receptor tyrosine kinases. To gain insight into the physiological consequences of receptor tyrosine kinase activation in squid giant synapse, a series of growth factors was tested in this preparation. Electrophysiological, pharmacological, and biochemical analysis demonstrated that nerve growth factor (NGF) triggers an acute and specific reduction of the postsynaptic potential amplitude, without affecting the presynaptic spike generation or presynaptic calcium current. The NGF target is localized at a postsynaptic site and involves a new TrkA-like receptor. The squid receptor crossreacts with antibodies generated against mammalian TrkA, is tyrosine phosphorylated in response to NGF stimulation, and is blocked by specific pharmacological inhibitors. The modulation described emphasizes the important role of growth factors on invertebrate synaptic transmission.

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Year:  1998        PMID: 9844004      PMCID: PMC24564          DOI: 10.1073/pnas.95.25.14997

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  42 in total

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Authors:  J Schlessinger; A Ullrich
Journal:  Neuron       Date:  1992-09       Impact factor: 17.173

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Authors:  A Riccio; B A Pierchala; C L Ciarallo; D D Ginty
Journal:  Science       Date:  1997-08-22       Impact factor: 47.728

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Authors:  N Q McDonald; M V Chao
Journal:  J Biol Chem       Date:  1995-08-25       Impact factor: 5.157

4.  Shc binding to nerve growth factor receptor is mediated by the phosphotyrosine interaction domain.

Authors:  I Dikic; A G Batzer; P Blaikie; A Obermeier; A Ullrich; J Schlessinger; B Margolis
Journal:  J Biol Chem       Date:  1995-06-23       Impact factor: 5.157

5.  Tissue-specific alternative splicing generates two isoforms of the trkA receptor.

Authors:  P A Barker; C Lomen-Hoerth; E M Gensch; S O Meakin; D J Glass; E M Shooter
Journal:  J Biol Chem       Date:  1993-07-15       Impact factor: 5.157

6.  Dror, a potential neurotrophic receptor gene, encodes a Drosophila homolog of the vertebrate Ror family of Trk-related receptor tyrosine kinases.

Authors:  C Wilson; D C Goberdhan; H Steller
Journal:  Proc Natl Acad Sci U S A       Date:  1993-08-01       Impact factor: 11.205

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Authors:  M Barbacid
Journal:  J Neurobiol       Date:  1994-11

8.  Nerve growth factor (NGF) induces sprouting of specific neurons of the snail, Lymnaea stagnalis.

Authors:  R L Ridgway; N I Syed; K Lukowiak; A G Bulloch
Journal:  J Neurobiol       Date:  1991-06

9.  Nerve growth factor mediates signal transduction through trk homodimer receptors.

Authors:  S Jing; P Tapley; M Barbacid
Journal:  Neuron       Date:  1992-12       Impact factor: 17.173

10.  PC12 cells overexpressing the insulin receptor undergo insulin-dependent neuronal differentiation.

Authors:  I Dikic; J Schlessinger; I Lax
Journal:  Curr Biol       Date:  1994-08-01       Impact factor: 10.834

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  3 in total

1.  Protection of crayfish glial cells but not neurons from photodynamic injury by nerve growth factor.

Authors:  A V Lobanov; A B Uzdensky
Journal:  J Mol Neurosci       Date:  2009-04-18       Impact factor: 3.444

2.  Disruption of fast axonal transport is a pathogenic mechanism for intraneuronal amyloid beta.

Authors:  G Pigino; G Morfini; Y Atagi; A Deshpande; C Yu; L Jungbauer; M LaDu; J Busciglio; S Brady
Journal:  Proc Natl Acad Sci U S A       Date:  2009-03-24       Impact factor: 11.205

3.  A new invertebrate member of the p53 gene family is developmentally expressed and responds to polychlorinated biphenyls.

Authors:  Kathryn Jessen-Eller; Jill A Kreiling; Gail S Begley; Marjorie E Steele; Charles W Walker; Raymond E Stephens; Carol L Reinisch
Journal:  Environ Health Perspect       Date:  2002-04       Impact factor: 9.031

  3 in total

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