cGMP promotes neurite outgrowth and growth cone turning and improves axon regeneration on spinal cord tissue in combination with cAMP
Abstract Cyclic adenosine monophosphate (cAMP) has been intensively studied in recent years in order to elucidate its contribution in intracellular signalling mechanisms that regulate axon growth and guidance, and also to test if its activation can promote axon regeneration after injury. Cyclic guan...
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description | Abstract Cyclic adenosine monophosphate (cAMP) has been intensively studied in recent years in order to elucidate its contribution in intracellular signalling mechanisms that regulate axon growth and guidance, and also to test if its activation can promote axon regeneration after injury. Cyclic guanosine monophosphate (cGMP), however, has been given considerably less attention even though it too mediates intracellular signalling cascades activated by extracellular guidance cues. cGMP can promote neurite outgrowth in neuronal cell lines but its role in promoting growth and regeneration of primary neurons is not well established. Here, we have examined the effects of elevating cGMP activity on axon growth, guidance and regeneration in vitro. We have found that, like cAMP elevation, activation of cGMP increases rat dorsal root ganglion (DRG) neurite outgrowth on a polylysine substrate and that asymmetric cGMP elevation promotes attractive growth cone turning. When grown in an in vitro model of axon regeneration activation of cGMP alone was not sufficient to promote adult neurite outgrowth. However, when combined with cAMP elevation substantial regeneration of adult neurites is achieved, superior to that achieved with either cAMP or cGMP alone. Regeneration is enhanced still further with simultaneous application of a Nogo receptor blocking peptide, suggesting this combinatorial strategy could achieve far greater axon regeneration in vivo than targeting individual cell signalling mechanisms. |
doi_str_mv | 10.1016/j.brainres.2009.07.071 |
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Cyclic guanosine monophosphate (cGMP), however, has been given considerably less attention even though it too mediates intracellular signalling cascades activated by extracellular guidance cues. cGMP can promote neurite outgrowth in neuronal cell lines but its role in promoting growth and regeneration of primary neurons is not well established. Here, we have examined the effects of elevating cGMP activity on axon growth, guidance and regeneration in vitro. We have found that, like cAMP elevation, activation of cGMP increases rat dorsal root ganglion (DRG) neurite outgrowth on a polylysine substrate and that asymmetric cGMP elevation promotes attractive growth cone turning. When grown in an in vitro model of axon regeneration activation of cGMP alone was not sufficient to promote adult neurite outgrowth. However, when combined with cAMP elevation substantial regeneration of adult neurites is achieved, superior to that achieved with either cAMP or cGMP alone. Regeneration is enhanced still further with simultaneous application of a Nogo receptor blocking peptide, suggesting this combinatorial strategy could achieve far greater axon regeneration in vivo than targeting individual cell signalling mechanisms.</description><identifier>ISSN: 0006-8993</identifier><identifier>EISSN: 1872-6240</identifier><identifier>DOI: 10.1016/j.brainres.2009.07.071</identifier><identifier>PMID: 19646425</identifier><identifier>CODEN: BRREAP</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Aging ; Animals ; Animals, Newborn ; Axon guidance ; Axon regeneration ; Axons - physiology ; Biological and medical sciences ; cAMP ; Cells, Cultured ; cGMP ; Cyclic AMP - metabolism ; Cyclic AMP Response Element-Binding Protein - metabolism ; Cyclic GMP - metabolism ; Development. Senescence. Regeneration. Transplantation ; Fundamental and applied biological sciences. Psychology ; Ganglia, Spinal - physiology ; GPI-Linked Proteins ; Growth Cones - physiology ; Immunohistochemistry ; Myelin Proteins ; Nerve Regeneration - physiology ; Neurite outgrowth ; Neurites - physiology ; Neurology ; Neurons - physiology ; Nogo receptor ; Nogo Receptor 1 ; Phosphorylation ; Rats ; Rats, Sprague-Dawley ; Receptors, Cell Surface ; Receptors, Peptide - antagonists & inhibitors ; Spinal Cord - physiology ; Vertebrates: nervous system and sense organs</subject><ispartof>Brain research, 2009-10, Vol.1294, p.12-21</ispartof><rights>Elsevier B.V.</rights><rights>2009 Elsevier B.V.</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c483t-2380b3fbdfb0bc5d4d7c49d3e892e728dfbfbb9ea5bf08e72e41490878b7fee33</citedby><cites>FETCH-LOGICAL-c483t-2380b3fbdfb0bc5d4d7c49d3e892e728dfbfbb9ea5bf08e72e41490878b7fee33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.brainres.2009.07.071$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22361611$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19646425$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Murray, Andrew J</creatorcontrib><creatorcontrib>Peace, Andrew G</creatorcontrib><creatorcontrib>Shewan, Derryck A</creatorcontrib><title>cGMP promotes neurite outgrowth and growth cone turning and improves axon regeneration on spinal cord tissue in combination with cAMP</title><title>Brain research</title><addtitle>Brain Res</addtitle><description>Abstract Cyclic adenosine monophosphate (cAMP) has been intensively studied in recent years in order to elucidate its contribution in intracellular signalling mechanisms that regulate axon growth and guidance, and also to test if its activation can promote axon regeneration after injury. Cyclic guanosine monophosphate (cGMP), however, has been given considerably less attention even though it too mediates intracellular signalling cascades activated by extracellular guidance cues. cGMP can promote neurite outgrowth in neuronal cell lines but its role in promoting growth and regeneration of primary neurons is not well established. Here, we have examined the effects of elevating cGMP activity on axon growth, guidance and regeneration in vitro. We have found that, like cAMP elevation, activation of cGMP increases rat dorsal root ganglion (DRG) neurite outgrowth on a polylysine substrate and that asymmetric cGMP elevation promotes attractive growth cone turning. When grown in an in vitro model of axon regeneration activation of cGMP alone was not sufficient to promote adult neurite outgrowth. However, when combined with cAMP elevation substantial regeneration of adult neurites is achieved, superior to that achieved with either cAMP or cGMP alone. Regeneration is enhanced still further with simultaneous application of a Nogo receptor blocking peptide, suggesting this combinatorial strategy could achieve far greater axon regeneration in vivo than targeting individual cell signalling mechanisms.</description><subject>Aging</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Axon guidance</subject><subject>Axon regeneration</subject><subject>Axons - physiology</subject><subject>Biological and medical sciences</subject><subject>cAMP</subject><subject>Cells, Cultured</subject><subject>cGMP</subject><subject>Cyclic AMP - metabolism</subject><subject>Cyclic AMP Response Element-Binding Protein - metabolism</subject><subject>Cyclic GMP - metabolism</subject><subject>Development. Senescence. Regeneration. Transplantation</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Ganglia, Spinal - physiology</subject><subject>GPI-Linked Proteins</subject><subject>Growth Cones - physiology</subject><subject>Immunohistochemistry</subject><subject>Myelin Proteins</subject><subject>Nerve Regeneration - physiology</subject><subject>Neurite outgrowth</subject><subject>Neurites - physiology</subject><subject>Neurology</subject><subject>Neurons - physiology</subject><subject>Nogo receptor</subject><subject>Nogo Receptor 1</subject><subject>Phosphorylation</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors, Cell Surface</subject><subject>Receptors, Peptide - antagonists & inhibitors</subject><subject>Spinal Cord - 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>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUsFu1DAQjRCILoVfqHKBnrKM7WwSXxBVBQWpFZWAs2U7k8VL4iy209IP4L-ZdANIHEAayZ7Re29G8ybLThisGbDq5W5tgnY-YFxzALmGmoI9yFasqXlR8RIeZisAqIpGSnGUPYlxR6kQEh5nR0xWZVXyzSr7YS-urvN9GIcxYcw9TsElzMcpbcN4m77k2rf58rWjxzxNwTu_va-7gYg3RNPfR58H3KLHoJOjhCLundc9sUKbJxfjhLnzlA6G6vegWzernl1dP80edbqP-Gx5j7PPb998On9XXH64eH9-dlnYshGp4KIBIzrTdgaM3bRlW9tStgIbybHmDdU7YyTqjemgoQqWrJTQ1I2pO0QhjrPTgy7N_W3CmNTgosW-1x7HKapalLABCTUhX_wTyRmTooZZsjoAbRhjDNipfXCDDneKgZqtUjv1yyo1W6WgpmBEPFk6TGbA9g9t8YYAzxeAjlb3XdDeuvgbx7moWMVmodcHHNLmbhwGFa1Db7F1AW1S7ej-P8urvyRs77yjrl_xDuNuJNPJF8VU5ArUx_mw5ruiVbEN7Uz8BOmaza0</recordid><startdate>20091006</startdate><enddate>20091006</enddate><creator>Murray, Andrew J</creator><creator>Peace, Andrew G</creator><creator>Shewan, Derryck 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>20091006</creationdate><title>cGMP promotes neurite outgrowth and growth cone turning and improves axon regeneration on spinal cord tissue in combination with cAMP</title><author>Murray, Andrew J ; Peace, Andrew G ; Shewan, Derryck A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c483t-2380b3fbdfb0bc5d4d7c49d3e892e728dfbfbb9ea5bf08e72e41490878b7fee33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Aging</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Axon guidance</topic><topic>Axon regeneration</topic><topic>Axons - physiology</topic><topic>Biological and medical sciences</topic><topic>cAMP</topic><topic>Cells, Cultured</topic><topic>cGMP</topic><topic>Cyclic AMP - metabolism</topic><topic>Cyclic AMP Response Element-Binding Protein - metabolism</topic><topic>Cyclic GMP - metabolism</topic><topic>Development. Senescence. Regeneration. Transplantation</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Ganglia, Spinal - physiology</topic><topic>GPI-Linked Proteins</topic><topic>Growth Cones - physiology</topic><topic>Immunohistochemistry</topic><topic>Myelin Proteins</topic><topic>Nerve Regeneration - physiology</topic><topic>Neurite outgrowth</topic><topic>Neurites - physiology</topic><topic>Neurology</topic><topic>Neurons - physiology</topic><topic>Nogo receptor</topic><topic>Nogo Receptor 1</topic><topic>Phosphorylation</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptors, Cell Surface</topic><topic>Receptors, Peptide - antagonists & inhibitors</topic><topic>Spinal Cord - physiology</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Murray, Andrew J</creatorcontrib><creatorcontrib>Peace, Andrew G</creatorcontrib><creatorcontrib>Shewan, Derryck 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>Murray, Andrew J</au><au>Peace, Andrew G</au><au>Shewan, Derryck A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>cGMP promotes neurite outgrowth and growth cone turning and improves axon regeneration on spinal cord tissue in combination with cAMP</atitle><jtitle>Brain research</jtitle><addtitle>Brain Res</addtitle><date>2009-10-06</date><risdate>2009</risdate><volume>1294</volume><spage>12</spage><epage>21</epage><pages>12-21</pages><issn>0006-8993</issn><eissn>1872-6240</eissn><coden>BRREAP</coden><abstract>Abstract Cyclic adenosine monophosphate (cAMP) has been intensively studied in recent years in order to elucidate its contribution in intracellular signalling mechanisms that regulate axon growth and guidance, and also to test if its activation can promote axon regeneration after injury. Cyclic guanosine monophosphate (cGMP), however, has been given considerably less attention even though it too mediates intracellular signalling cascades activated by extracellular guidance cues. cGMP can promote neurite outgrowth in neuronal cell lines but its role in promoting growth and regeneration of primary neurons is not well established. Here, we have examined the effects of elevating cGMP activity on axon growth, guidance and regeneration in vitro. We have found that, like cAMP elevation, activation of cGMP increases rat dorsal root ganglion (DRG) neurite outgrowth on a polylysine substrate and that asymmetric cGMP elevation promotes attractive growth cone turning. When grown in an in vitro model of axon regeneration activation of cGMP alone was not sufficient to promote adult neurite outgrowth. However, when combined with cAMP elevation substantial regeneration of adult neurites is achieved, superior to that achieved with either cAMP or cGMP alone. Regeneration is enhanced still further with simultaneous application of a Nogo receptor blocking peptide, suggesting this combinatorial strategy could achieve far greater axon regeneration in vivo than targeting individual cell signalling mechanisms.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>19646425</pmid><doi>10.1016/j.brainres.2009.07.071</doi><tpages>10</tpages></addata></record> |
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subjects | Aging Animals Animals, Newborn Axon guidance Axon regeneration Axons - physiology Biological and medical sciences cAMP Cells, Cultured cGMP Cyclic AMP - metabolism Cyclic AMP Response Element-Binding Protein - metabolism Cyclic GMP - metabolism Development. Senescence. Regeneration. Transplantation Fundamental and applied biological sciences. Psychology Ganglia, Spinal - physiology GPI-Linked Proteins Growth Cones - physiology Immunohistochemistry Myelin Proteins Nerve Regeneration - physiology Neurite outgrowth Neurites - physiology Neurology Neurons - physiology Nogo receptor Nogo Receptor 1 Phosphorylation Rats Rats, Sprague-Dawley Receptors, Cell Surface Receptors, Peptide - antagonists & inhibitors Spinal Cord - physiology Vertebrates: nervous system and sense organs |
title | cGMP promotes neurite outgrowth and growth cone turning and improves axon regeneration on spinal cord tissue in combination with cAMP |
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