Induction of vascular endothelial growth factor receptors and phosphatidylinositol 3′-kinase/Akt signaling by global cerebral ischemia in the rat
Vascular endothelial growth factor is an angiogenic peptide that binds to tyrosine kinase receptors on target cells to activate signal transduction pathways involving phosphatidylinositol 3′-kinase and the serine–threonine protein kinase, Akt. To determine whether this signaling pathway is activated...
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creator | Jin, K.L Mao, X.O Nagayama, T Goldsmith, P.C Greenberg, D.A |
description | Vascular endothelial growth factor is an angiogenic peptide that binds to tyrosine kinase receptors on target cells to activate signal transduction pathways involving phosphatidylinositol 3′-kinase and the serine–threonine protein kinase, Akt. To determine whether this signaling pathway is activated in cerebral ischemia, we examined the expression of vascular endothelial growth factor receptors 1 and 2, and phosphatidylinositol 3′-kinase-activated phospho-Akt, in the cerebral cortex and hippocampus following transient global cerebral ischemia in the rat. Western blot analysis and immunocytochemistry demonstrated induction of vascular endothelial growth factor receptor 1 and 2 expression, and of anti-phosphatidylinositol 3′-kinase-immunoprecipitated phospho-Akt, in vulnerable regions of the cortex and hippocampus after 15
min of global ischemia and 4–72
h of reperfusion.
These findings demonstrate that vascular endothelial growth factor receptors and receptor-coupled signal transduction pathways are induced in ischemic brain
in vivo, and could therefore participate in endogenous neuroprotective responses to ischemia. |
doi_str_mv | 10.1016/S0306-4522(00)00331-6 |
format | Article |
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min of global ischemia and 4–72
h of reperfusion.
These findings demonstrate that vascular endothelial growth factor receptors and receptor-coupled signal transduction pathways are induced in ischemic brain
in vivo, and could therefore participate in endogenous neuroprotective responses to ischemia.</description><identifier>ISSN: 0306-4522</identifier><identifier>EISSN: 1873-7544</identifier><identifier>DOI: 10.1016/S0306-4522(00)00331-6</identifier><identifier>PMID: 11036205</identifier><identifier>CODEN: NRSCDN</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>angiogenesis ; Animals ; Biological and medical sciences ; Blotting, Western ; cerebral cortex ; Cerebral Cortex - enzymology ; Cerebral Cortex - metabolism ; hippocampus ; Hippocampus - enzymology ; Hippocampus - metabolism ; hypoxia ; Immunohistochemistry ; Ischemic Attack, Transient - enzymology ; Ischemic Attack, Transient - metabolism ; Male ; Medical sciences ; Neurology ; Phosphatidylinositol 3-Kinases - metabolism ; Phosphatidylinositol 3-Kinases - physiology ; Phosphorylation ; Protein-Serine-Threonine Kinases - physiology ; Proto-Oncogene Proteins - metabolism ; Proto-Oncogene Proteins - physiology ; Proto-Oncogene Proteins c-akt ; Rats ; Rats, Sprague-Dawley ; Receptor Protein-Tyrosine Kinases - biosynthesis ; Receptors, Growth Factor - biosynthesis ; Receptors, Vascular Endothelial Growth Factor ; Signal Transduction ; stroke ; Vascular diseases and vascular malformations of the nervous system</subject><ispartof>Neuroscience, 2000-01, Vol.100 (4), p.713-717</ispartof><rights>2000 IBRO</rights><rights>2001 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c389t-462c219cfb6b38c4f6a7b94a3dbb97947a5fc3dc6133570b56fc0c3748ca9d3</citedby><cites>FETCH-LOGICAL-c389t-462c219cfb6b38c4f6a7b94a3dbb97947a5fc3dc6133570b56fc0c3748ca9d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0306452200003316$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=798368$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11036205$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jin, K.L</creatorcontrib><creatorcontrib>Mao, X.O</creatorcontrib><creatorcontrib>Nagayama, T</creatorcontrib><creatorcontrib>Goldsmith, P.C</creatorcontrib><creatorcontrib>Greenberg, D.A</creatorcontrib><title>Induction of vascular endothelial growth factor receptors and phosphatidylinositol 3′-kinase/Akt signaling by global cerebral ischemia in the rat</title><title>Neuroscience</title><addtitle>Neuroscience</addtitle><description>Vascular endothelial growth factor is an angiogenic peptide that binds to tyrosine kinase receptors on target cells to activate signal transduction pathways involving phosphatidylinositol 3′-kinase and the serine–threonine protein kinase, Akt. To determine whether this signaling pathway is activated in cerebral ischemia, we examined the expression of vascular endothelial growth factor receptors 1 and 2, and phosphatidylinositol 3′-kinase-activated phospho-Akt, in the cerebral cortex and hippocampus following transient global cerebral ischemia in the rat. Western blot analysis and immunocytochemistry demonstrated induction of vascular endothelial growth factor receptor 1 and 2 expression, and of anti-phosphatidylinositol 3′-kinase-immunoprecipitated phospho-Akt, in vulnerable regions of the cortex and hippocampus after 15
min of global ischemia and 4–72
h of reperfusion.
These findings demonstrate that vascular endothelial growth factor receptors and receptor-coupled signal transduction pathways are induced in ischemic brain
in vivo, and could therefore participate in endogenous neuroprotective responses to ischemia.</description><subject>angiogenesis</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Blotting, Western</subject><subject>cerebral cortex</subject><subject>Cerebral Cortex - enzymology</subject><subject>Cerebral Cortex - metabolism</subject><subject>hippocampus</subject><subject>Hippocampus - enzymology</subject><subject>Hippocampus - metabolism</subject><subject>hypoxia</subject><subject>Immunohistochemistry</subject><subject>Ischemic Attack, Transient - enzymology</subject><subject>Ischemic Attack, Transient - metabolism</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Neurology</subject><subject>Phosphatidylinositol 3-Kinases - metabolism</subject><subject>Phosphatidylinositol 3-Kinases - physiology</subject><subject>Phosphorylation</subject><subject>Protein-Serine-Threonine Kinases - physiology</subject><subject>Proto-Oncogene Proteins - metabolism</subject><subject>Proto-Oncogene Proteins - physiology</subject><subject>Proto-Oncogene Proteins c-akt</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptor Protein-Tyrosine Kinases - biosynthesis</subject><subject>Receptors, Growth Factor - biosynthesis</subject><subject>Receptors, Vascular Endothelial Growth Factor</subject><subject>Signal Transduction</subject><subject>stroke</subject><subject>Vascular diseases and vascular malformations of the nervous system</subject><issn>0306-4522</issn><issn>1873-7544</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtuFDEQhi1ERIbAEUCWkBAsmtjtR3evoigKECkSi7C3_OppE4_d2O6g2eUOuUmOxElwMqOwTG2qpPrqof8H4B1GXzDC_PgKEcQbytr2E0KfESIEN_wFWOG-I03HKH0JVk_IIXid8y9Ug1HyChxijAhvEVuBu4tgFl1cDDCO8EZmvXiZoA0mlsl6Jz1cp_inTHCUusQEk9V2rkWGMhg4TzHPkyzObL0LMbsSPSR_b--baxdktsen1wVmtw6yttdQbeHaR1WXapusSrVwWU924yR0AdaLMMnyBhyM0mf7dp-PwNXX859n35vLH98uzk4vG036oTSUt7rFgx4VV6TXdOSyUwOVxCg1dAPtJBs1MZpjQliHFOOjRpp0tNdyMOQIfNxtnVP8vdhcxKb-Yr2XwcYli64llDPKKsh2oE4x52RHMSe3kWkrMBIPXohHL8SD0AIh8eiF4HXu_f7AojbW_J_ai1-BD3ugyi79mGTQLj9x3dAT3lfqZEfZKsWNs0lk7WzQ1rjqRREmumce-Qe2cqnS</recordid><startdate>20000101</startdate><enddate>20000101</enddate><creator>Jin, K.L</creator><creator>Mao, X.O</creator><creator>Nagayama, T</creator><creator>Goldsmith, P.C</creator><creator>Greenberg, D.A</creator><general>Elsevier Ltd</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>7X8</scope></search><sort><creationdate>20000101</creationdate><title>Induction of vascular endothelial growth factor receptors and phosphatidylinositol 3′-kinase/Akt signaling by global cerebral ischemia in the rat</title><author>Jin, K.L ; Mao, X.O ; Nagayama, T ; Goldsmith, P.C ; Greenberg, D.A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c389t-462c219cfb6b38c4f6a7b94a3dbb97947a5fc3dc6133570b56fc0c3748ca9d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>angiogenesis</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Blotting, Western</topic><topic>cerebral cortex</topic><topic>Cerebral Cortex - enzymology</topic><topic>Cerebral Cortex - metabolism</topic><topic>hippocampus</topic><topic>Hippocampus - enzymology</topic><topic>Hippocampus - metabolism</topic><topic>hypoxia</topic><topic>Immunohistochemistry</topic><topic>Ischemic Attack, Transient - enzymology</topic><topic>Ischemic Attack, Transient - metabolism</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Neurology</topic><topic>Phosphatidylinositol 3-Kinases - metabolism</topic><topic>Phosphatidylinositol 3-Kinases - physiology</topic><topic>Phosphorylation</topic><topic>Protein-Serine-Threonine Kinases - physiology</topic><topic>Proto-Oncogene Proteins - metabolism</topic><topic>Proto-Oncogene Proteins - physiology</topic><topic>Proto-Oncogene Proteins c-akt</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptor Protein-Tyrosine Kinases - biosynthesis</topic><topic>Receptors, Growth Factor - biosynthesis</topic><topic>Receptors, Vascular Endothelial Growth Factor</topic><topic>Signal Transduction</topic><topic>stroke</topic><topic>Vascular diseases and vascular malformations of the nervous system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jin, K.L</creatorcontrib><creatorcontrib>Mao, X.O</creatorcontrib><creatorcontrib>Nagayama, T</creatorcontrib><creatorcontrib>Goldsmith, P.C</creatorcontrib><creatorcontrib>Greenberg, D.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>MEDLINE - Academic</collection><jtitle>Neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jin, K.L</au><au>Mao, X.O</au><au>Nagayama, T</au><au>Goldsmith, P.C</au><au>Greenberg, D.A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Induction of vascular endothelial growth factor receptors and phosphatidylinositol 3′-kinase/Akt signaling by global cerebral ischemia in the rat</atitle><jtitle>Neuroscience</jtitle><addtitle>Neuroscience</addtitle><date>2000-01-01</date><risdate>2000</risdate><volume>100</volume><issue>4</issue><spage>713</spage><epage>717</epage><pages>713-717</pages><issn>0306-4522</issn><eissn>1873-7544</eissn><coden>NRSCDN</coden><abstract>Vascular endothelial growth factor is an angiogenic peptide that binds to tyrosine kinase receptors on target cells to activate signal transduction pathways involving phosphatidylinositol 3′-kinase and the serine–threonine protein kinase, Akt. To determine whether this signaling pathway is activated in cerebral ischemia, we examined the expression of vascular endothelial growth factor receptors 1 and 2, and phosphatidylinositol 3′-kinase-activated phospho-Akt, in the cerebral cortex and hippocampus following transient global cerebral ischemia in the rat. Western blot analysis and immunocytochemistry demonstrated induction of vascular endothelial growth factor receptor 1 and 2 expression, and of anti-phosphatidylinositol 3′-kinase-immunoprecipitated phospho-Akt, in vulnerable regions of the cortex and hippocampus after 15
min of global ischemia and 4–72
h of reperfusion.
These findings demonstrate that vascular endothelial growth factor receptors and receptor-coupled signal transduction pathways are induced in ischemic brain
in vivo, and could therefore participate in endogenous neuroprotective responses to ischemia.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>11036205</pmid><doi>10.1016/S0306-4522(00)00331-6</doi><tpages>5</tpages></addata></record> |
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subjects | angiogenesis Animals Biological and medical sciences Blotting, Western cerebral cortex Cerebral Cortex - enzymology Cerebral Cortex - metabolism hippocampus Hippocampus - enzymology Hippocampus - metabolism hypoxia Immunohistochemistry Ischemic Attack, Transient - enzymology Ischemic Attack, Transient - metabolism Male Medical sciences Neurology Phosphatidylinositol 3-Kinases - metabolism Phosphatidylinositol 3-Kinases - physiology Phosphorylation Protein-Serine-Threonine Kinases - physiology Proto-Oncogene Proteins - metabolism Proto-Oncogene Proteins - physiology Proto-Oncogene Proteins c-akt Rats Rats, Sprague-Dawley Receptor Protein-Tyrosine Kinases - biosynthesis Receptors, Growth Factor - biosynthesis Receptors, Vascular Endothelial Growth Factor Signal Transduction stroke Vascular diseases and vascular malformations of the nervous system |
title | Induction of vascular endothelial growth factor receptors and phosphatidylinositol 3′-kinase/Akt signaling by global cerebral ischemia in the rat |
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