Ternary complex with Trk, p75, and an ankyrin-rich membrane spanning protein

Neurotrophins play many critical roles in regulating neuronal plasticity, survival, and differentiation in the nervous system. Neurotrophins recognize two different receptors, the Trk receptor tyrosine kinase and the p75 neurotrophin receptor, which are associated closely. Several adaptor proteins a...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of neuroscience research 2004-10, Vol.78 (2), p.186-192
Hauptverfasser: Chang, Mi-Sook, Arevalo, Juan Carlos, Chao, Moses V.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 192
container_issue 2
container_start_page 186
container_title Journal of neuroscience research
container_volume 78
creator Chang, Mi-Sook
Arevalo, Juan Carlos
Chao, Moses V.
description Neurotrophins play many critical roles in regulating neuronal plasticity, survival, and differentiation in the nervous system. Neurotrophins recognize two different receptors, the Trk receptor tyrosine kinase and the p75 neurotrophin receptor, which are associated closely. Several adaptor proteins are associated with each receptor. An ankyrin‐rich membrane spanning protein (ARMS), originally identified as a substrate for protein kinase D (Kidins220) and as a p75 interacting protein, serves as a novel downstream target of Trk receptor tyrosine kinases. Kidins220/ARMS is co‐expressed frequently with Trk and p75 and represents the only membrane‐associated protein known to interact with both receptors. We report here that a ternary complex can be formed between Trk, p75, and Kidins220/ARMS. The extracellular domains of the TrkA and the p75 receptors are necessary for their association, whereas the juxtamembrane region of p75 was responsible for the interaction with Kidins220/ARMS. Interestingly, increasing the level of Kidins220/ARMS expression resulted in a decreased association of TrkA with p75. These findings thus suggest that Kidins220/ARMS plays an important role in regulating interactions between Trk and p75 neurotrophin receptors. © 2004 Wiley‐Liss, Inc.
doi_str_mv 10.1002/jnr.20262
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_66907243</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>66907243</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3592-d3947f31c16afcf33181bbca6956cca1cf728c0c1bfa4c1867ca981fad80d9773</originalsourceid><addsrcrecordid>eNp1kFtLxDAQhYMoul4e_APSJ0GwOkmapHkU8cqiIOvlLaRpqnHbbE120f33RnfVJ2GGefnOmZmD0C6GIwxAjl99OCJAOFlBAwxS5AUrxCoaAOWQF4DJBtqM8RUApGR0HW1gRkXJoRyg4cgGr8M8M5Oub-1H9u6mL9kojA-zXrDDTPs6darxPDifB2dess52VdDeZrHX3jv_nPVhMrXOb6O1RrfR7iznFro_PxudXubD24ur05NhbiiTJK-pLERDscFcN6ahFJe4qozmknFjNDaNIKUBg6tGFwaXXBgtS9zouoRaCkG30P7CN-19m9k4VZ2LxrZtOmoyi4pzCYIUNIEHC9CESYzBNqoPrkvvKgzqKzqVolPf0SV2b2k6qzpb_5HLrBJwvADeXWvn_zup65u7H8t8oXBxaj9-FTqMFRdUMPV4c6GeyNMQSvagGP0E0ZiG-w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>66907243</pqid></control><display><type>article</type><title>Ternary complex with Trk, p75, and an ankyrin-rich membrane spanning protein</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Chang, Mi-Sook ; Arevalo, Juan Carlos ; Chao, Moses V.</creator><creatorcontrib>Chang, Mi-Sook ; Arevalo, Juan Carlos ; Chao, Moses V.</creatorcontrib><description>Neurotrophins play many critical roles in regulating neuronal plasticity, survival, and differentiation in the nervous system. Neurotrophins recognize two different receptors, the Trk receptor tyrosine kinase and the p75 neurotrophin receptor, which are associated closely. Several adaptor proteins are associated with each receptor. An ankyrin‐rich membrane spanning protein (ARMS), originally identified as a substrate for protein kinase D (Kidins220) and as a p75 interacting protein, serves as a novel downstream target of Trk receptor tyrosine kinases. Kidins220/ARMS is co‐expressed frequently with Trk and p75 and represents the only membrane‐associated protein known to interact with both receptors. We report here that a ternary complex can be formed between Trk, p75, and Kidins220/ARMS. The extracellular domains of the TrkA and the p75 receptors are necessary for their association, whereas the juxtamembrane region of p75 was responsible for the interaction with Kidins220/ARMS. Interestingly, increasing the level of Kidins220/ARMS expression resulted in a decreased association of TrkA with p75. These findings thus suggest that Kidins220/ARMS plays an important role in regulating interactions between Trk and p75 neurotrophin receptors. © 2004 Wiley‐Liss, Inc.</description><identifier>ISSN: 0360-4012</identifier><identifier>EISSN: 1097-4547</identifier><identifier>DOI: 10.1002/jnr.20262</identifier><identifier>PMID: 15378608</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Amino Acid Sequence ; Animals ; Binding Sites ; Cell Line ; Humans ; Membrane Proteins - analysis ; Membrane Proteins - chemistry ; Molecular Sequence Data ; Nerve Tissue Proteins - analysis ; Nerve Tissue Proteins - chemistry ; neurotrophin ; NGF ; Protein Structure, Tertiary ; Rats ; receptor complex ; Receptor, Nerve Growth Factor ; Receptor, trkA - analysis ; Receptor, trkA - chemistry ; Receptors, Nerve Growth Factor - analysis ; Receptors, Nerve Growth Factor - chemistry</subject><ispartof>Journal of neuroscience research, 2004-10, Vol.78 (2), p.186-192</ispartof><rights>Copyright © 2004 Wiley‐Liss, Inc.</rights><rights>Copyright 2004 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3592-d3947f31c16afcf33181bbca6956cca1cf728c0c1bfa4c1867ca981fad80d9773</citedby><cites>FETCH-LOGICAL-c3592-d3947f31c16afcf33181bbca6956cca1cf728c0c1bfa4c1867ca981fad80d9773</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjnr.20262$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjnr.20262$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27922,27923,45572,45573</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15378608$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chang, Mi-Sook</creatorcontrib><creatorcontrib>Arevalo, Juan Carlos</creatorcontrib><creatorcontrib>Chao, Moses V.</creatorcontrib><title>Ternary complex with Trk, p75, and an ankyrin-rich membrane spanning protein</title><title>Journal of neuroscience research</title><addtitle>J. Neurosci. Res</addtitle><description>Neurotrophins play many critical roles in regulating neuronal plasticity, survival, and differentiation in the nervous system. Neurotrophins recognize two different receptors, the Trk receptor tyrosine kinase and the p75 neurotrophin receptor, which are associated closely. Several adaptor proteins are associated with each receptor. An ankyrin‐rich membrane spanning protein (ARMS), originally identified as a substrate for protein kinase D (Kidins220) and as a p75 interacting protein, serves as a novel downstream target of Trk receptor tyrosine kinases. Kidins220/ARMS is co‐expressed frequently with Trk and p75 and represents the only membrane‐associated protein known to interact with both receptors. We report here that a ternary complex can be formed between Trk, p75, and Kidins220/ARMS. The extracellular domains of the TrkA and the p75 receptors are necessary for their association, whereas the juxtamembrane region of p75 was responsible for the interaction with Kidins220/ARMS. Interestingly, increasing the level of Kidins220/ARMS expression resulted in a decreased association of TrkA with p75. These findings thus suggest that Kidins220/ARMS plays an important role in regulating interactions between Trk and p75 neurotrophin receptors. © 2004 Wiley‐Liss, Inc.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Binding Sites</subject><subject>Cell Line</subject><subject>Humans</subject><subject>Membrane Proteins - analysis</subject><subject>Membrane Proteins - chemistry</subject><subject>Molecular Sequence Data</subject><subject>Nerve Tissue Proteins - analysis</subject><subject>Nerve Tissue Proteins - chemistry</subject><subject>neurotrophin</subject><subject>NGF</subject><subject>Protein Structure, Tertiary</subject><subject>Rats</subject><subject>receptor complex</subject><subject>Receptor, Nerve Growth Factor</subject><subject>Receptor, trkA - analysis</subject><subject>Receptor, trkA - chemistry</subject><subject>Receptors, Nerve Growth Factor - analysis</subject><subject>Receptors, Nerve Growth Factor - chemistry</subject><issn>0360-4012</issn><issn>1097-4547</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kFtLxDAQhYMoul4e_APSJ0GwOkmapHkU8cqiIOvlLaRpqnHbbE120f33RnfVJ2GGefnOmZmD0C6GIwxAjl99OCJAOFlBAwxS5AUrxCoaAOWQF4DJBtqM8RUApGR0HW1gRkXJoRyg4cgGr8M8M5Oub-1H9u6mL9kojA-zXrDDTPs6darxPDifB2dess52VdDeZrHX3jv_nPVhMrXOb6O1RrfR7iznFro_PxudXubD24ur05NhbiiTJK-pLERDscFcN6ahFJe4qozmknFjNDaNIKUBg6tGFwaXXBgtS9zouoRaCkG30P7CN-19m9k4VZ2LxrZtOmoyi4pzCYIUNIEHC9CESYzBNqoPrkvvKgzqKzqVolPf0SV2b2k6qzpb_5HLrBJwvADeXWvn_zup65u7H8t8oXBxaj9-FTqMFRdUMPV4c6GeyNMQSvagGP0E0ZiG-w</recordid><startdate>20041015</startdate><enddate>20041015</enddate><creator>Chang, Mi-Sook</creator><creator>Arevalo, Juan Carlos</creator><creator>Chao, Moses V.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</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>7X8</scope></search><sort><creationdate>20041015</creationdate><title>Ternary complex with Trk, p75, and an ankyrin-rich membrane spanning protein</title><author>Chang, Mi-Sook ; Arevalo, Juan Carlos ; Chao, Moses V.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3592-d3947f31c16afcf33181bbca6956cca1cf728c0c1bfa4c1867ca981fad80d9773</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Binding Sites</topic><topic>Cell Line</topic><topic>Humans</topic><topic>Membrane Proteins - analysis</topic><topic>Membrane Proteins - chemistry</topic><topic>Molecular Sequence Data</topic><topic>Nerve Tissue Proteins - analysis</topic><topic>Nerve Tissue Proteins - chemistry</topic><topic>neurotrophin</topic><topic>NGF</topic><topic>Protein Structure, Tertiary</topic><topic>Rats</topic><topic>receptor complex</topic><topic>Receptor, Nerve Growth Factor</topic><topic>Receptor, trkA - analysis</topic><topic>Receptor, trkA - chemistry</topic><topic>Receptors, Nerve Growth Factor - analysis</topic><topic>Receptors, Nerve Growth Factor - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chang, Mi-Sook</creatorcontrib><creatorcontrib>Arevalo, Juan Carlos</creatorcontrib><creatorcontrib>Chao, Moses V.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of neuroscience research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chang, Mi-Sook</au><au>Arevalo, Juan Carlos</au><au>Chao, Moses V.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ternary complex with Trk, p75, and an ankyrin-rich membrane spanning protein</atitle><jtitle>Journal of neuroscience research</jtitle><addtitle>J. Neurosci. Res</addtitle><date>2004-10-15</date><risdate>2004</risdate><volume>78</volume><issue>2</issue><spage>186</spage><epage>192</epage><pages>186-192</pages><issn>0360-4012</issn><eissn>1097-4547</eissn><abstract>Neurotrophins play many critical roles in regulating neuronal plasticity, survival, and differentiation in the nervous system. Neurotrophins recognize two different receptors, the Trk receptor tyrosine kinase and the p75 neurotrophin receptor, which are associated closely. Several adaptor proteins are associated with each receptor. An ankyrin‐rich membrane spanning protein (ARMS), originally identified as a substrate for protein kinase D (Kidins220) and as a p75 interacting protein, serves as a novel downstream target of Trk receptor tyrosine kinases. Kidins220/ARMS is co‐expressed frequently with Trk and p75 and represents the only membrane‐associated protein known to interact with both receptors. We report here that a ternary complex can be formed between Trk, p75, and Kidins220/ARMS. The extracellular domains of the TrkA and the p75 receptors are necessary for their association, whereas the juxtamembrane region of p75 was responsible for the interaction with Kidins220/ARMS. Interestingly, increasing the level of Kidins220/ARMS expression resulted in a decreased association of TrkA with p75. These findings thus suggest that Kidins220/ARMS plays an important role in regulating interactions between Trk and p75 neurotrophin receptors. © 2004 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>15378608</pmid><doi>10.1002/jnr.20262</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0360-4012
ispartof Journal of neuroscience research, 2004-10, Vol.78 (2), p.186-192
issn 0360-4012
1097-4547
language eng
recordid cdi_proquest_miscellaneous_66907243
source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Amino Acid Sequence
Animals
Binding Sites
Cell Line
Humans
Membrane Proteins - analysis
Membrane Proteins - chemistry
Molecular Sequence Data
Nerve Tissue Proteins - analysis
Nerve Tissue Proteins - chemistry
neurotrophin
NGF
Protein Structure, Tertiary
Rats
receptor complex
Receptor, Nerve Growth Factor
Receptor, trkA - analysis
Receptor, trkA - chemistry
Receptors, Nerve Growth Factor - analysis
Receptors, Nerve Growth Factor - chemistry
title Ternary complex with Trk, p75, and an ankyrin-rich membrane spanning protein
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-09T16%3A24%3A58IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Ternary%20complex%20with%20Trk,%20p75,%20and%20an%20ankyrin-rich%20membrane%20spanning%20protein&rft.jtitle=Journal%20of%20neuroscience%20research&rft.au=Chang,%20Mi-Sook&rft.date=2004-10-15&rft.volume=78&rft.issue=2&rft.spage=186&rft.epage=192&rft.pages=186-192&rft.issn=0360-4012&rft.eissn=1097-4547&rft_id=info:doi/10.1002/jnr.20262&rft_dat=%3Cproquest_cross%3E66907243%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=66907243&rft_id=info:pmid/15378608&rfr_iscdi=true