Retrograde axonal transport of signal transduction proteins in rat sciatic nerve
Neurons require a mechanism to transmit stable signals over the large distance from the nerve growth cone or terminal to the cell body, in order that information from the target tissue can be relayed to the cell body where it is required. Nerve growth factor (NGF), a target-derived neurotrophic fact...
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Veröffentlicht in: | Brain research 1995-08, Vol.690 (1), p.55-63 |
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description | Neurons require a mechanism to transmit stable signals over the large distance from the nerve growth cone or terminal to the cell body, in order that information from the target tissue can be relayed to the cell body where it is required. Nerve growth factor (NGF), a target-derived neurotrophic factor, is thought to signal over this distance by receptor mediated internalization of NGF, followed by retrograde axonal transport of the NGF-receptor complex. In this paper we show, by immunohistochemistry of rat sciatic nerve, accumulation of phosphotyrosine immunoreactivity only on the distal side of a nerve crush, suggesting axonal transport of tyrosine kinases and/or tyrosine phosphorylated proteins primarily in a retrograde direction. Furthermore, we also show retrograde axonal transport of phosphoinositide 3-kinase, ERK, MEK and MEK kinase, of which all but MEK kinase are known to be activated downstream of tyrosine receptor kinase activation. The retrograde transport of these proteins suggests that they may be involved in transmission of signals along the axon, relaying neurotrophic factor receptor activation at the nerve terminal to the nerve cell body. |
doi_str_mv | 10.1016/0006-8993(95)00587-G |
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Nerve growth factor (NGF), a target-derived neurotrophic factor, is thought to signal over this distance by receptor mediated internalization of NGF, followed by retrograde axonal transport of the NGF-receptor complex. In this paper we show, by immunohistochemistry of rat sciatic nerve, accumulation of phosphotyrosine immunoreactivity only on the distal side of a nerve crush, suggesting axonal transport of tyrosine kinases and/or tyrosine phosphorylated proteins primarily in a retrograde direction. Furthermore, we also show retrograde axonal transport of phosphoinositide 3-kinase, ERK, MEK and MEK kinase, of which all but MEK kinase are known to be activated downstream of tyrosine receptor kinase activation. The retrograde transport of these proteins suggests that they may be involved in transmission of signals along the axon, relaying neurotrophic factor receptor activation at the nerve terminal to the nerve cell body.</description><identifier>ISSN: 0006-8993</identifier><identifier>EISSN: 1872-6240</identifier><identifier>DOI: 10.1016/0006-8993(95)00587-G</identifier><identifier>PMID: 7496807</identifier><identifier>CODEN: BRREAP</identifier><language>eng</language><publisher>London: Elsevier B.V</publisher><subject>Animals ; Axonal Transport - physiology ; Biological and medical sciences ; Calcium-Calmodulin-Dependent Protein Kinases - metabolism ; ERK ; Fundamental and applied biological sciences. Psychology ; GAP-43 ; GAP-43 Protein ; Growth Substances - metabolism ; Immunohistochemistry ; Isolated neuron and nerve. Neuroglia ; MEK ; MEK kinase ; Membrane Glycoproteins - metabolism ; Nerve Growth Factors - metabolism ; Nerve Tissue Proteins - metabolism ; Neurotrophic ; Phosphatidylinositol 3-kinase ; Phosphorylation ; Protein-Serine-Threonine Kinases - metabolism ; Rats ; Rats, Wistar ; Retrograde axonal transport ; Sciatic Nerve - metabolism ; Signal transduction ; Signal Transduction - physiology ; Vertebrates: nervous system and sense organs</subject><ispartof>Brain research, 1995-08, Vol.690 (1), p.55-63</ispartof><rights>1995</rights><rights>1995 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c483t-54f3d6b866bcf9019607e8306a69e738d167d25bdbabcd23ae4d0c81b82c204b3</citedby><cites>FETCH-LOGICAL-c483t-54f3d6b866bcf9019607e8306a69e738d167d25bdbabcd23ae4d0c81b82c204b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/000689939500587G$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27903,27904,65309</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3653677$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7496807$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Johanson, Sven.O.</creatorcontrib><creatorcontrib>Crouch, Michael.F.</creatorcontrib><creatorcontrib>Hendry, Ian A.</creatorcontrib><title>Retrograde axonal transport of signal transduction proteins in rat sciatic nerve</title><title>Brain research</title><addtitle>Brain Res</addtitle><description>Neurons require a mechanism to transmit stable signals over the large distance from the nerve growth cone or terminal to the cell body, in order that information from the target tissue can be relayed to the cell body where it is required. Nerve growth factor (NGF), a target-derived neurotrophic factor, is thought to signal over this distance by receptor mediated internalization of NGF, followed by retrograde axonal transport of the NGF-receptor complex. In this paper we show, by immunohistochemistry of rat sciatic nerve, accumulation of phosphotyrosine immunoreactivity only on the distal side of a nerve crush, suggesting axonal transport of tyrosine kinases and/or tyrosine phosphorylated proteins primarily in a retrograde direction. Furthermore, we also show retrograde axonal transport of phosphoinositide 3-kinase, ERK, MEK and MEK kinase, of which all but MEK kinase are known to be activated downstream of tyrosine receptor kinase activation. The retrograde transport of these proteins suggests that they may be involved in transmission of signals along the axon, relaying neurotrophic factor receptor activation at the nerve terminal to the nerve cell body.</description><subject>Animals</subject><subject>Axonal Transport - physiology</subject><subject>Biological and medical sciences</subject><subject>Calcium-Calmodulin-Dependent Protein Kinases - metabolism</subject><subject>ERK</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>GAP-43</subject><subject>GAP-43 Protein</subject><subject>Growth Substances - metabolism</subject><subject>Immunohistochemistry</subject><subject>Isolated neuron and nerve. Neuroglia</subject><subject>MEK</subject><subject>MEK kinase</subject><subject>Membrane Glycoproteins - metabolism</subject><subject>Nerve Growth Factors - metabolism</subject><subject>Nerve Tissue Proteins - metabolism</subject><subject>Neurotrophic</subject><subject>Phosphatidylinositol 3-kinase</subject><subject>Phosphorylation</subject><subject>Protein-Serine-Threonine Kinases - metabolism</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Retrograde axonal transport</subject><subject>Sciatic Nerve - metabolism</subject><subject>Signal transduction</subject><subject>Signal Transduction - physiology</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0006-8993</issn><issn>1872-6240</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1LAzEQhoMotX78A4UcRPSwmmx283ERpGgVBEX0HLLJrES2m5qkov_erS096mmYmWeGlwehI0ouKKH8khDCC6kUO1P1OSG1FMV0C42pFGXBy4pso_EG2UV7Kb0PLWOKjNBIVIpLIsbo6RlyDG_ROMDmK_SmwzmaPs1DzDi0OPm3zcwtbPahx_MYMvg-Yd_jaDJO1pvsLe4hfsIB2mlNl-BwXffR6-3Ny-SueHic3k-uHwpbSZaLumqZ443kvLGtIlRxIkAywg1XIJh0lAtX1o1rTGNdyQxUjlhJG1naklQN20enq79Dmo8FpKxnPlnoOtNDWCQtBFclo-xfkHJVC1GVA1itQBtDShFaPY9-ZuK3pkQvjeulTr3UqVWtf43r6XB2vP6_aGbgNkdrxcP-ZL03yZquHUxanzYY4zXjYoldrTAYpH16iHrQCr0F5yPYrF3wf-f4AZSgnVA</recordid><startdate>19950828</startdate><enddate>19950828</enddate><creator>Johanson, Sven.O.</creator><creator>Crouch, Michael.F.</creator><creator>Hendry, Ian A.</creator><general>Elsevier B.V</general><general>Elsevier</general><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>7TK</scope><scope>7X8</scope></search><sort><creationdate>19950828</creationdate><title>Retrograde axonal transport of signal transduction proteins in rat sciatic nerve</title><author>Johanson, Sven.O. ; Crouch, Michael.F. ; Hendry, Ian A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c483t-54f3d6b866bcf9019607e8306a69e738d167d25bdbabcd23ae4d0c81b82c204b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Animals</topic><topic>Axonal Transport - physiology</topic><topic>Biological and medical sciences</topic><topic>Calcium-Calmodulin-Dependent Protein Kinases - metabolism</topic><topic>ERK</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>GAP-43</topic><topic>GAP-43 Protein</topic><topic>Growth Substances - metabolism</topic><topic>Immunohistochemistry</topic><topic>Isolated neuron and nerve. Neuroglia</topic><topic>MEK</topic><topic>MEK kinase</topic><topic>Membrane Glycoproteins - metabolism</topic><topic>Nerve Growth Factors - metabolism</topic><topic>Nerve Tissue Proteins - metabolism</topic><topic>Neurotrophic</topic><topic>Phosphatidylinositol 3-kinase</topic><topic>Phosphorylation</topic><topic>Protein-Serine-Threonine Kinases - metabolism</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Retrograde axonal transport</topic><topic>Sciatic Nerve - metabolism</topic><topic>Signal transduction</topic><topic>Signal Transduction - physiology</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Johanson, Sven.O.</creatorcontrib><creatorcontrib>Crouch, Michael.F.</creatorcontrib><creatorcontrib>Hendry, Ian A.</creatorcontrib><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>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Johanson, Sven.O.</au><au>Crouch, Michael.F.</au><au>Hendry, Ian A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Retrograde axonal transport of signal transduction proteins in rat sciatic nerve</atitle><jtitle>Brain research</jtitle><addtitle>Brain Res</addtitle><date>1995-08-28</date><risdate>1995</risdate><volume>690</volume><issue>1</issue><spage>55</spage><epage>63</epage><pages>55-63</pages><issn>0006-8993</issn><eissn>1872-6240</eissn><coden>BRREAP</coden><abstract>Neurons require a mechanism to transmit stable signals over the large distance from the nerve growth cone or terminal to the cell body, in order that information from the target tissue can be relayed to the cell body where it is required. Nerve growth factor (NGF), a target-derived neurotrophic factor, is thought to signal over this distance by receptor mediated internalization of NGF, followed by retrograde axonal transport of the NGF-receptor complex. In this paper we show, by immunohistochemistry of rat sciatic nerve, accumulation of phosphotyrosine immunoreactivity only on the distal side of a nerve crush, suggesting axonal transport of tyrosine kinases and/or tyrosine phosphorylated proteins primarily in a retrograde direction. Furthermore, we also show retrograde axonal transport of phosphoinositide 3-kinase, ERK, MEK and MEK kinase, of which all but MEK kinase are known to be activated downstream of tyrosine receptor kinase activation. The retrograde transport of these proteins suggests that they may be involved in transmission of signals along the axon, relaying neurotrophic factor receptor activation at the nerve terminal to the nerve cell body.</abstract><cop>London</cop><cop>Amsterdam</cop><cop>New York, NY</cop><pub>Elsevier B.V</pub><pmid>7496807</pmid><doi>10.1016/0006-8993(95)00587-G</doi><tpages>9</tpages></addata></record> |
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subjects | Animals Axonal Transport - physiology Biological and medical sciences Calcium-Calmodulin-Dependent Protein Kinases - metabolism ERK Fundamental and applied biological sciences. Psychology GAP-43 GAP-43 Protein Growth Substances - metabolism Immunohistochemistry Isolated neuron and nerve. Neuroglia MEK MEK kinase Membrane Glycoproteins - metabolism Nerve Growth Factors - metabolism Nerve Tissue Proteins - metabolism Neurotrophic Phosphatidylinositol 3-kinase Phosphorylation Protein-Serine-Threonine Kinases - metabolism Rats Rats, Wistar Retrograde axonal transport Sciatic Nerve - metabolism Signal transduction Signal Transduction - physiology Vertebrates: nervous system and sense organs |
title | Retrograde axonal transport of signal transduction proteins in rat sciatic nerve |
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