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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 |
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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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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.</description><identifier>ISSN: 0022-3042</identifier><identifier>EISSN: 1471-4159</identifier><identifier>DOI: 10.1111/j.1471-4159.2007.04894.x</identifier><identifier>PMID: 17854387</identifier><identifier>CODEN: JONRA9</identifier><language>eng</language><publisher>Oxford, UK: Oxford, UK : Blackwell Publishing Ltd</publisher><subject>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</subject><ispartof>Journal of neurochemistry, 2007-11, Vol.103 (4), p.1396-1407</ispartof><rights>2007 INIST-CNRS</rights><rights>2007 The Authors Journal Compilation 2007 International Society for Neurochemistry</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5294-508ab9997910be3a17b246c3d909eb19dd9e1c9c9a88344fa2fc8b415e08bd1c3</citedby><cites>FETCH-LOGICAL-c5294-508ab9997910be3a17b246c3d909eb19dd9e1c9c9a88344fa2fc8b415e08bd1c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19208431$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17854387$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hansen, Raino Kristian</creatorcontrib><creatorcontrib>Christensen, Claus</creatorcontrib><creatorcontrib>Korshunova, Irina</creatorcontrib><creatorcontrib>Kriebel, Martin</creatorcontrib><creatorcontrib>Burkarth, Nadine</creatorcontrib><creatorcontrib>Kiselyov, Vladislav V</creatorcontrib><creatorcontrib>Olsen, Marianne</creatorcontrib><creatorcontrib>Østergaard, Søren</creatorcontrib><creatorcontrib>Holm, Arne</creatorcontrib><creatorcontrib>Volkmer, Hansjürgen</creatorcontrib><creatorcontrib>Walmod, Peter S</creatorcontrib><creatorcontrib>Berezin, Vladimir</creatorcontrib><creatorcontrib>Bock, Elisabeth</creatorcontrib><title>Identification of NCAM-binding peptides promoting neurite outgrowth via a heterotrimeric G-protein-coupled pathway</title><title>Journal of neurochemistry</title><addtitle>J Neurochem</addtitle><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.</description><subject>Animals</subject><subject>Bacterial diseases</subject><subject>Binding sites</subject><subject>Biochemistry</subject><subject>Biological and medical sciences</subject><subject>Brain</subject><subject>Cell adhesion & migration</subject><subject>Cell Proliferation</subject><subject>Cells, Cultured</subject><subject>Cerebellum - growth & development</subject><subject>Cerebellum - metabolism</subject><subject>Cerebellum - physiology</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Ent and stomatologic bacterial diseases</subject><subject>G-protein</subject><subject>Human bacterial diseases</subject><subject>Humans</subject><subject>Infectious diseases</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>neural cell adhesion molecule</subject><subject>Neural Cell Adhesion Molecules - antagonists & inhibitors</subject><subject>Neural Cell Adhesion Molecules - genetics</subject><subject>Neural Cell Adhesion Molecules - metabolism</subject><subject>neurite outgrowth</subject><subject>Neurites - metabolism</subject><subject>Neurites - physiology</subject><subject>Neurology</subject><subject>PC12 Cells</subject><subject>Peptides</subject><subject>Peptides - genetics</subject><subject>Peptides - metabolism</subject><subject>Peptides - physiology</subject><subject>pertussis toxin</subject><subject>Protein Binding - physiology</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Receptors, G-Protein-Coupled - antagonists & inhibitors</subject><subject>Receptors, G-Protein-Coupled - physiology</subject><subject>Signal transduction</subject><subject>Signal Transduction - physiology</subject><subject>surface plasmon resonance</subject><subject>synthetic peptides</subject><subject>Toxoids - pharmacology</subject><issn>0022-3042</issn><issn>1471-4159</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNqNkU9v0zAYhy0EYt3gK4CFxG4J_pfGPnCYKhhDYxxgZ8tx3rSu0jjYDl2_PQ6tmMQFfLFlP7_Xr_0ghCkpaR7vtiUVNS0ErVTJCKlLIqQS5cMTtPhz8BQtCGGs4ESwM3Qe45YQuhRL-hyd0VpWgst6gcJNC0NynbMmOT9g3-G71dWXonFD64Y1HmFMroWIx-B3Ps1bA0zBJcB-Suvg92mDfzqDDd5AguBTcDsIzuLrIkcSuKGwfhp7aPFo0mZvDi_Qs870EV6e5gt0__HD99Wn4vbr9c3q6rawFVOiqIg0jVKqVpQ0wA2tGyaWlreKKGioalsF1CqrjJRciM6wzsomvxyIbFpq-QW6PNbNffyYICa9c9FC35sB_BT1UgrBSEX-Cc6QpEpm8M1f4NZPYciPyMyyEqKqZkgeIRt8jAE6PeYvMeGgKdGzPb3VsyQ9S9KzPf3bnn7I0Ven-lOzg_YxeNKVgbcnwERr-i6Ywbr4yClGpOA0c--P3N71cPjvBvTnu9W8yvnXx3xnvDbrkO-4_8YI5YTIHFCc_wJ3rL-B</recordid><startdate>200711</startdate><enddate>200711</enddate><creator>Hansen, Raino Kristian</creator><creator>Christensen, Claus</creator><creator>Korshunova, Irina</creator><creator>Kriebel, Martin</creator><creator>Burkarth, Nadine</creator><creator>Kiselyov, Vladislav V</creator><creator>Olsen, Marianne</creator><creator>Østergaard, Søren</creator><creator>Holm, Arne</creator><creator>Volkmer, Hansjürgen</creator><creator>Walmod, Peter S</creator><creator>Berezin, Vladimir</creator><creator>Bock, Elisabeth</creator><general>Oxford, UK : Blackwell Publishing Ltd</general><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QR</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>200711</creationdate><title>Identification of NCAM-binding peptides promoting neurite outgrowth via a heterotrimeric G-protein-coupled pathway</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5294-508ab9997910be3a17b246c3d909eb19dd9e1c9c9a88344fa2fc8b415e08bd1c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Animals</topic><topic>Bacterial diseases</topic><topic>Binding sites</topic><topic>Biochemistry</topic><topic>Biological and medical sciences</topic><topic>Brain</topic><topic>Cell adhesion & migration</topic><topic>Cell Proliferation</topic><topic>Cells, Cultured</topic><topic>Cerebellum - growth & development</topic><topic>Cerebellum - metabolism</topic><topic>Cerebellum - physiology</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>Ent and stomatologic bacterial diseases</topic><topic>G-protein</topic><topic>Human bacterial diseases</topic><topic>Humans</topic><topic>Infectious diseases</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>neural cell adhesion molecule</topic><topic>Neural Cell Adhesion Molecules - antagonists & inhibitors</topic><topic>Neural Cell Adhesion Molecules - genetics</topic><topic>Neural Cell Adhesion Molecules - metabolism</topic><topic>neurite outgrowth</topic><topic>Neurites - metabolism</topic><topic>Neurites - physiology</topic><topic>Neurology</topic><topic>PC12 Cells</topic><topic>Peptides</topic><topic>Peptides - genetics</topic><topic>Peptides - metabolism</topic><topic>Peptides - physiology</topic><topic>pertussis toxin</topic><topic>Protein Binding - physiology</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Receptors, G-Protein-Coupled - antagonists & inhibitors</topic><topic>Receptors, G-Protein-Coupled - physiology</topic><topic>Signal transduction</topic><topic>Signal Transduction - physiology</topic><topic>surface plasmon resonance</topic><topic>synthetic peptides</topic><topic>Toxoids - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hansen, Raino Kristian</creatorcontrib><creatorcontrib>Christensen, Claus</creatorcontrib><creatorcontrib>Korshunova, Irina</creatorcontrib><creatorcontrib>Kriebel, Martin</creatorcontrib><creatorcontrib>Burkarth, Nadine</creatorcontrib><creatorcontrib>Kiselyov, Vladislav V</creatorcontrib><creatorcontrib>Olsen, Marianne</creatorcontrib><creatorcontrib>Østergaard, Søren</creatorcontrib><creatorcontrib>Holm, Arne</creatorcontrib><creatorcontrib>Volkmer, Hansjürgen</creatorcontrib><creatorcontrib>Walmod, Peter S</creatorcontrib><creatorcontrib>Berezin, Vladimir</creatorcontrib><creatorcontrib>Bock, Elisabeth</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of neurochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hansen, Raino Kristian</au><au>Christensen, Claus</au><au>Korshunova, Irina</au><au>Kriebel, Martin</au><au>Burkarth, Nadine</au><au>Kiselyov, Vladislav V</au><au>Olsen, Marianne</au><au>Østergaard, Søren</au><au>Holm, Arne</au><au>Volkmer, Hansjürgen</au><au>Walmod, Peter S</au><au>Berezin, Vladimir</au><au>Bock, Elisabeth</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of NCAM-binding peptides promoting neurite outgrowth via a heterotrimeric G-protein-coupled pathway</atitle><jtitle>Journal of neurochemistry</jtitle><addtitle>J Neurochem</addtitle><date>2007-11</date><risdate>2007</risdate><volume>103</volume><issue>4</issue><spage>1396</spage><epage>1407</epage><pages>1396-1407</pages><issn>0022-3042</issn><eissn>1471-4159</eissn><coden>JONRA9</coden><abstract>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.</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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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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