Activated microglia cells express argininosuccinate synthetase and argininosuccinate lyase in the rat brain after transient ischemia

Argininosuccinate-synthetase (ASS), argininosuccinate-lyase (ASL) and nitric oxide synthase (NOS) act in the l-arginine-NO- l-citrulline cycle. In the rat brain, ASS is expressed in neurons, ASL in neurons and astroglia in the striatum, both are co-expressed with nNOS in medium-sized neurons. Microg...

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Veröffentlicht in:Experimental neurology 2007-11, Vol.208 (1), p.100-109
Hauptverfasser: Bizzoco, Elisa, Faussone-Pellegrini, Maria Simonetta, Vannucchi, Maria Giuliana
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Vannucchi, Maria Giuliana
description Argininosuccinate-synthetase (ASS), argininosuccinate-lyase (ASL) and nitric oxide synthase (NOS) act in the l-arginine-NO- l-citrulline cycle. In the rat brain, ASS is expressed in neurons, ASL in neurons and astroglia in the striatum, both are co-expressed with nNOS in medium-sized neurons. Microglia cells express iNOS and ASS after activation but no information is available on ASL and on ASS/ASL/iNOS co-expression in this glial population. The present aim was to ascertain, by immunohistochemistry, whether the microglia cells of the rat striatum and fronto-parietal cortex express ASL and ASS in control conditions and after transient ischemia induced by middle cerebral artery occlusion, and whether ASL and ASS are co-expressed with iNOS. The study was conducted 24, 72 and 144 h after reperfusion in two groups of ischemic rats with different tissue damage and survival. ASS and ASL are not expressed by microglia cells in controls while are present in most of the activated microglia cells in the ischemic rats. In those animals with longer survival, ASS and ASL were no more detectable at 144 h, while, in the animals with shorter survival, they were co-expressed with iNOS, but only at 72 h. In the cortex, at variance with the striatum, almost all of nNOS-positive neurons co-expressed ASS and ASL. In conclusion, only activated microglia cells express ASS and ASL, this expression precedes that of iNOS and does not necessarily imply its appearance. Therefore, local factors such as the NO produced by nNOS/ASS/ASL-positive neurons, could influence ASS/ASL-positive microglia cells avoiding or allowing the induction, in these cells, of iNOS.
doi_str_mv 10.1016/j.expneurol.2007.07.018
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In those animals with longer survival, ASS and ASL were no more detectable at 144 h, while, in the animals with shorter survival, they were co-expressed with iNOS, but only at 72 h. In the cortex, at variance with the striatum, almost all of nNOS-positive neurons co-expressed ASS and ASL. In conclusion, only activated microglia cells express ASS and ASL, this expression precedes that of iNOS and does not necessarily imply its appearance. 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In those animals with longer survival, ASS and ASL were no more detectable at 144 h, while, in the animals with shorter survival, they were co-expressed with iNOS, but only at 72 h. In the cortex, at variance with the striatum, almost all of nNOS-positive neurons co-expressed ASS and ASL. In conclusion, only activated microglia cells express ASS and ASL, this expression precedes that of iNOS and does not necessarily imply its appearance. 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Faussone-Pellegrini, Maria Simonetta ; Vannucchi, Maria Giuliana</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c430t-fe4df8c76e870a3818c12b153b66e174f7586a9aaf4a48cf311958b20519b4c33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Animals</topic><topic>Argininosuccinate Lyase - analysis</topic><topic>Argininosuccinate Lyase - metabolism</topic><topic>Argininosuccinate lyase, ASL</topic><topic>Argininosuccinate Synthase - analysis</topic><topic>Argininosuccinate Synthase - metabolism</topic><topic>Argininosuccinate synthetase, ASS</topic><topic>Biological and medical sciences</topic><topic>Brain - enzymology</topic><topic>Cerebral Infarction - etiology</topic><topic>Cerebral Infarction - pathology</topic><topic>Corpus striatum</topic><topic>Corpus Striatum - chemistry</topic><topic>Corpus Striatum - pathology</topic><topic>Focal transient ischemia</topic><topic>Frontal Lobe - chemistry</topic><topic>Frontal Lobe - pathology</topic><topic>Fronto-parietal cortex</topic><topic>Inducible nitric oxide synthase, iNOS</topic><topic>Ischemic Attack, Transient - complications</topic><topic>Ischemic Attack, Transient - enzymology</topic><topic>Ischemic Attack, Transient - pathology</topic><topic>Ischemic Attack, Transient - physiopathology</topic><topic>l-arginine-NO- l-citrulline cycle</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microglia - chemistry</topic><topic>Microglia - enzymology</topic><topic>Microglia - pathology</topic><topic>Microglia cells</topic><topic>Neurologic Examination</topic><topic>Neurology</topic><topic>Neuronal cells</topic><topic>Neurons - chemistry</topic><topic>Neurons - pathology</topic><topic>Nitric Oxide Synthase Type I - analysis</topic><topic>Parietal Lobe - chemistry</topic><topic>Parietal Lobe - pathology</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Vascular diseases and vascular malformations of the nervous system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bizzoco, Elisa</creatorcontrib><creatorcontrib>Faussone-Pellegrini, Maria Simonetta</creatorcontrib><creatorcontrib>Vannucchi, Maria Giuliana</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>Experimental neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bizzoco, Elisa</au><au>Faussone-Pellegrini, Maria Simonetta</au><au>Vannucchi, Maria Giuliana</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Activated microglia cells express argininosuccinate synthetase and argininosuccinate lyase in the rat brain after transient ischemia</atitle><jtitle>Experimental neurology</jtitle><addtitle>Exp Neurol</addtitle><date>2007-11-01</date><risdate>2007</risdate><volume>208</volume><issue>1</issue><spage>100</spage><epage>109</epage><pages>100-109</pages><issn>0014-4886</issn><eissn>1090-2430</eissn><coden>EXNEAC</coden><abstract>Argininosuccinate-synthetase (ASS), argininosuccinate-lyase (ASL) and nitric oxide synthase (NOS) act in the l-arginine-NO- l-citrulline cycle. In the rat brain, ASS is expressed in neurons, ASL in neurons and astroglia in the striatum, both are co-expressed with nNOS in medium-sized neurons. Microglia cells express iNOS and ASS after activation but no information is available on ASL and on ASS/ASL/iNOS co-expression in this glial population. The present aim was to ascertain, by immunohistochemistry, whether the microglia cells of the rat striatum and fronto-parietal cortex express ASL and ASS in control conditions and after transient ischemia induced by middle cerebral artery occlusion, and whether ASL and ASS are co-expressed with iNOS. The study was conducted 24, 72 and 144 h after reperfusion in two groups of ischemic rats with different tissue damage and survival. ASS and ASL are not expressed by microglia cells in controls while are present in most of the activated microglia cells in the ischemic rats. In those animals with longer survival, ASS and ASL were no more detectable at 144 h, while, in the animals with shorter survival, they were co-expressed with iNOS, but only at 72 h. In the cortex, at variance with the striatum, almost all of nNOS-positive neurons co-expressed ASS and ASL. In conclusion, only activated microglia cells express ASS and ASL, this expression precedes that of iNOS and does not necessarily imply its appearance. Therefore, local factors such as the NO produced by nNOS/ASS/ASL-positive neurons, could influence ASS/ASL-positive microglia cells avoiding or allowing the induction, in these cells, of iNOS.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><pmid>17900569</pmid><doi>10.1016/j.expneurol.2007.07.018</doi><tpages>10</tpages></addata></record>
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subjects Animals
Argininosuccinate Lyase - analysis
Argininosuccinate Lyase - metabolism
Argininosuccinate lyase, ASL
Argininosuccinate Synthase - analysis
Argininosuccinate Synthase - metabolism
Argininosuccinate synthetase, ASS
Biological and medical sciences
Brain - enzymology
Cerebral Infarction - etiology
Cerebral Infarction - pathology
Corpus striatum
Corpus Striatum - chemistry
Corpus Striatum - pathology
Focal transient ischemia
Frontal Lobe - chemistry
Frontal Lobe - pathology
Fronto-parietal cortex
Inducible nitric oxide synthase, iNOS
Ischemic Attack, Transient - complications
Ischemic Attack, Transient - enzymology
Ischemic Attack, Transient - pathology
Ischemic Attack, Transient - physiopathology
l-arginine-NO- l-citrulline cycle
Male
Medical sciences
Microglia - chemistry
Microglia - enzymology
Microglia - pathology
Microglia cells
Neurologic Examination
Neurology
Neuronal cells
Neurons - chemistry
Neurons - pathology
Nitric Oxide Synthase Type I - analysis
Parietal Lobe - chemistry
Parietal Lobe - pathology
Rats
Rats, Wistar
Vascular diseases and vascular malformations of the nervous system
title Activated microglia cells express argininosuccinate synthetase and argininosuccinate lyase in the rat brain after transient ischemia
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