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Identification of NCAM-binding peptides promoting neurite outgrowth via a heterotrimeric G-protein-coupled pathway

A combinatorial library of undecapeptides was produced and utilized for the isolation of peptide binding to the fibronectin type 3 modules (F3I-F3II) of the neural cell adhesion molecule (NCAM). The isolated peptides were sequenced and produced as dendrimers. Two of the peptides (denoted ENFIN2 and...

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Published in:Journal of neurochemistry 2007-11, Vol.103 (4), p.1396-1407
Main Authors: Hansen, Raino Kristian, Christensen, Claus, Korshunova, Irina, Kriebel, Martin, Burkarth, Nadine, Kiselyov, Vladislav V, Olsen, Marianne, Østergaard, Søren, Holm, Arne, Volkmer, Hansjürgen, Walmod, Peter S, Berezin, Vladimir, Bock, Elisabeth
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creator Hansen, Raino Kristian
Christensen, Claus
Korshunova, Irina
Kriebel, Martin
Burkarth, Nadine
Kiselyov, Vladislav V
Olsen, Marianne
Østergaard, Søren
Holm, Arne
Volkmer, Hansjürgen
Walmod, Peter S
Berezin, Vladimir
Bock, Elisabeth
description A combinatorial library of undecapeptides was produced and utilized for the isolation of peptide binding to the fibronectin type 3 modules (F3I-F3II) of the neural cell adhesion molecule (NCAM). The isolated peptides were sequenced and produced as dendrimers. Two of the peptides (denoted ENFIN2 and ENFIN11) were confirmed to bind to F3I-F3II of NCAM by surface plasmon resonance. The peptides induced neurite outgrowth in primary cerebellar neurons and PC12E2 cells, but had no apparent neuroprotective properties. NCAM is known to activate different intracellular pathways, including signaling through the fibroblast growth factor receptor, the Src-related non-receptor tyrosine kinase Fyn, and heterotrimeric G-proteins. Interestingly, neurite outgrowth stimulated by ENFIN2 and ENFIN11 was independent of signaling through fibroblast growth factor receptor and Fyn, but could be inhibited with pertussis toxin, an inhibitor of certain heterotrimeric G-proteins. Neurite outgrowth induced by trans-homophilic NCAM was unaffected by the peptides, whereas knockdown of NCAM completely abrogated ENFIN2- and ENFIN11-induced neuritogenesis. These observations suggest that ENFIN2 and ENFIN11 induce neurite outgrowth in an NCAM-dependent manner through G-protein-coupled signal transduction pathways. Thus, ENFIN2 and ENFIN11 may be valuable for exploring this particular type of NCAM-mediated signaling.
doi_str_mv 10.1111/j.1471-4159.2007.04894.x
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These observations suggest that ENFIN2 and ENFIN11 induce neurite outgrowth in an NCAM-dependent manner through G-protein-coupled signal transduction pathways. Thus, ENFIN2 and ENFIN11 may be valuable for exploring this particular type of NCAM-mediated signaling.</abstract><cop>Oxford, UK</cop><pub>Oxford, UK : Blackwell Publishing Ltd</pub><pmid>17854387</pmid><doi>10.1111/j.1471-4159.2007.04894.x</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record>
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source Wiley; Free Full-Text Journals in Chemistry
subjects Animals
Bacterial diseases
Binding sites
Biochemistry
Biological and medical sciences
Brain
Cell adhesion & migration
Cell Proliferation
Cells, Cultured
Cerebellum - growth & development
Cerebellum - metabolism
Cerebellum - physiology
Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
Ent and stomatologic bacterial diseases
G-protein
Human bacterial diseases
Humans
Infectious diseases
Medical sciences
Mice
neural cell adhesion molecule
Neural Cell Adhesion Molecules - antagonists & inhibitors
Neural Cell Adhesion Molecules - genetics
Neural Cell Adhesion Molecules - metabolism
neurite outgrowth
Neurites - metabolism
Neurites - physiology
Neurology
PC12 Cells
Peptides
Peptides - genetics
Peptides - metabolism
Peptides - physiology
pertussis toxin
Protein Binding - physiology
Rats
Rats, Wistar
Receptors, G-Protein-Coupled - antagonists & inhibitors
Receptors, G-Protein-Coupled - physiology
Signal transduction
Signal Transduction - physiology
surface plasmon resonance
synthetic peptides
Toxoids - pharmacology
title Identification of NCAM-binding peptides promoting neurite outgrowth via a heterotrimeric G-protein-coupled pathway
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