Nitric oxide-mediated cGMP synthesis in oligodendrocytes in the developing rat brain
We investigated the nature of cGMP‐synthesizing cells in the developing rat forebrain using cGMP‐immunocytochemistry in combination with in vitro incubation of brain slices. When brain slices of immature rats, aged between 1 and 4 weeks, were incubated with sodium nitroprusside (SNP), a nitric oxide...
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description | We investigated the nature of cGMP‐synthesizing cells in the developing rat forebrain using cGMP‐immunocytochemistry in combination with in vitro incubation of brain slices. When brain slices of immature rats, aged between 1 and 4 weeks, were incubated with sodium nitroprusside (SNP), a nitric oxide (NO) donor compound, in the presence of the phosphodiesterase inhibitor isobutylmethylxanthine (IBMX), small round cells with a few processes in and around the corpus callosum were visualized with the cGMP‐antibody. The morphology and the distribution of the cGMP‐positive cells were consistent with the criteria for oligodendrocytes. Furthermore, the cGMP‐positive cells expressed 2′3′‐cyclic nucleotide 3′‐phosphodiesterase (CNPase) and gelsolin, which are marker proteins for oligodendrocytes. Therefore, we concluded that the cGMP‐positive cells were oligodendrocytes. A subpopulation of the oligodendrocyte was found to be cGMP‐immunoreactive also when slices were incubated in the absence of SNP. Furthermore, incubation of the slice in the presence of L‐NAME, an inhibitor of NO synthase, but in the absence of SNP abolished cGMP immunostaining. In addition, some populations of neurons and astrocytes in restricted brain areas produced cGMP in response to the incubation with SNP as previously reported, whereas both ameboid and ramified microglial cells did not respond to the treatment. Atrial natriuretic peptide, a stimulator of particulate guanylyl cyclase, enhanced cGMP synthesis in astrocytes in some brain regions but not in oligodendrocytes. These findings indicate that oligodendrocytes in the immature rat brain express soluble guanylyl cyclase. No cGMP‐positive oligodendrocytes were found in the mature rat brain, suggesting that cGMP may mediate signals related to myelinogenesis in the rat brain. GLIA 19:286–297, 1997. © 1997 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/(SICI)1098-1136(199704)19:4<286::AID-GLIA2>3.0.CO;2-W |
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M. ; de Vente, Jan</creator><creatorcontrib>Tanaka, Junya ; Markerink-Van Ittersum, Marjanne ; Steinbusch, Harry W. M. ; de Vente, Jan</creatorcontrib><description>We investigated the nature of cGMP‐synthesizing cells in the developing rat forebrain using cGMP‐immunocytochemistry in combination with in vitro incubation of brain slices. When brain slices of immature rats, aged between 1 and 4 weeks, were incubated with sodium nitroprusside (SNP), a nitric oxide (NO) donor compound, in the presence of the phosphodiesterase inhibitor isobutylmethylxanthine (IBMX), small round cells with a few processes in and around the corpus callosum were visualized with the cGMP‐antibody. The morphology and the distribution of the cGMP‐positive cells were consistent with the criteria for oligodendrocytes. Furthermore, the cGMP‐positive cells expressed 2′3′‐cyclic nucleotide 3′‐phosphodiesterase (CNPase) and gelsolin, which are marker proteins for oligodendrocytes. Therefore, we concluded that the cGMP‐positive cells were oligodendrocytes. A subpopulation of the oligodendrocyte was found to be cGMP‐immunoreactive also when slices were incubated in the absence of SNP. Furthermore, incubation of the slice in the presence of L‐NAME, an inhibitor of NO synthase, but in the absence of SNP abolished cGMP immunostaining. In addition, some populations of neurons and astrocytes in restricted brain areas produced cGMP in response to the incubation with SNP as previously reported, whereas both ameboid and ramified microglial cells did not respond to the treatment. Atrial natriuretic peptide, a stimulator of particulate guanylyl cyclase, enhanced cGMP synthesis in astrocytes in some brain regions but not in oligodendrocytes. These findings indicate that oligodendrocytes in the immature rat brain express soluble guanylyl cyclase. No cGMP‐positive oligodendrocytes were found in the mature rat brain, suggesting that cGMP may mediate signals related to myelinogenesis in the rat brain. GLIA 19:286–297, 1997. © 1997 Wiley‐Liss, Inc.</description><identifier>ISSN: 0894-1491</identifier><identifier>EISSN: 1098-1136</identifier><identifier>DOI: 10.1002/(SICI)1098-1136(199704)19:4<286::AID-GLIA2>3.0.CO;2-W</identifier><identifier>PMID: 9097073</identifier><identifier>CODEN: GLIAEJ</identifier><language>eng</language><publisher>New York: John Wiley & Sons, Inc</publisher><subject>1-Methyl-3-isobutylxanthine - pharmacology ; 2',3'-Cyclic-Nucleotide Phosphodiesterases - biosynthesis ; Aging - metabolism ; Animals ; astrocyte ; Atrial Natriuretic Factor - pharmacology ; atrial natriuretic peptide ; Biological and medical sciences ; Caudate Nucleus - growth & development ; Caudate Nucleus - metabolism ; Corpus Callosum - growth & development ; Corpus Callosum - metabolism ; Cyclic GMP - metabolism ; Development. Senescence. Regeneration. Transplantation ; Fluorescent Antibody Technique, Indirect ; Fundamental and applied biological sciences. Psychology ; Gelsolin - biosynthesis ; guanylyl cyclase ; In Vitro Techniques ; Male ; microglia ; myelinogenesis ; Nitric Oxide - physiology ; Nitroprusside - pharmacology ; Oligodendroglia - drug effects ; Oligodendroglia - metabolism ; Parietal Lobe - growth & development ; Parietal Lobe - metabolism ; Prosencephalon - growth & development ; Prosencephalon - metabolism ; Putamen - growth & development ; Putamen - metabolism ; Rats ; Rats, Inbred Lew ; Vertebrates: nervous system and sense organs</subject><ispartof>Glia, 1997-04, Vol.19 (4), p.286-297</ispartof><rights>Copyright © 1997 Wiley‐Liss, Inc.</rights><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c5272-5322e1fcbc6f9bb087aee704da4e9143ad0584442f4d27e5a8caa30da148e9763</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%2F%28SICI%291098-1136%28199704%2919%3A4%3C286%3A%3AAID-GLIA2%3E3.0.CO%3B2-W$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2F%28SICI%291098-1136%28199704%2919%3A4%3C286%3A%3AAID-GLIA2%3E3.0.CO%3B2-W$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2617616$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9097073$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tanaka, Junya</creatorcontrib><creatorcontrib>Markerink-Van Ittersum, Marjanne</creatorcontrib><creatorcontrib>Steinbusch, Harry W. M.</creatorcontrib><creatorcontrib>de Vente, Jan</creatorcontrib><title>Nitric oxide-mediated cGMP synthesis in oligodendrocytes in the developing rat brain</title><title>Glia</title><addtitle>Glia</addtitle><description>We investigated the nature of cGMP‐synthesizing cells in the developing rat forebrain using cGMP‐immunocytochemistry in combination with in vitro incubation of brain slices. When brain slices of immature rats, aged between 1 and 4 weeks, were incubated with sodium nitroprusside (SNP), a nitric oxide (NO) donor compound, in the presence of the phosphodiesterase inhibitor isobutylmethylxanthine (IBMX), small round cells with a few processes in and around the corpus callosum were visualized with the cGMP‐antibody. The morphology and the distribution of the cGMP‐positive cells were consistent with the criteria for oligodendrocytes. Furthermore, the cGMP‐positive cells expressed 2′3′‐cyclic nucleotide 3′‐phosphodiesterase (CNPase) and gelsolin, which are marker proteins for oligodendrocytes. Therefore, we concluded that the cGMP‐positive cells were oligodendrocytes. A subpopulation of the oligodendrocyte was found to be cGMP‐immunoreactive also when slices were incubated in the absence of SNP. Furthermore, incubation of the slice in the presence of L‐NAME, an inhibitor of NO synthase, but in the absence of SNP abolished cGMP immunostaining. In addition, some populations of neurons and astrocytes in restricted brain areas produced cGMP in response to the incubation with SNP as previously reported, whereas both ameboid and ramified microglial cells did not respond to the treatment. Atrial natriuretic peptide, a stimulator of particulate guanylyl cyclase, enhanced cGMP synthesis in astrocytes in some brain regions but not in oligodendrocytes. These findings indicate that oligodendrocytes in the immature rat brain express soluble guanylyl cyclase. No cGMP‐positive oligodendrocytes were found in the mature rat brain, suggesting that cGMP may mediate signals related to myelinogenesis in the rat brain. GLIA 19:286–297, 1997. © 1997 Wiley‐Liss, Inc.</description><subject>1-Methyl-3-isobutylxanthine - pharmacology</subject><subject>2',3'-Cyclic-Nucleotide Phosphodiesterases - biosynthesis</subject><subject>Aging - metabolism</subject><subject>Animals</subject><subject>astrocyte</subject><subject>Atrial Natriuretic Factor - pharmacology</subject><subject>atrial natriuretic peptide</subject><subject>Biological and medical sciences</subject><subject>Caudate Nucleus - growth & development</subject><subject>Caudate Nucleus - metabolism</subject><subject>Corpus Callosum - growth & development</subject><subject>Corpus Callosum - metabolism</subject><subject>Cyclic GMP - metabolism</subject><subject>Development. Senescence. Regeneration. Transplantation</subject><subject>Fluorescent Antibody Technique, Indirect</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gelsolin - biosynthesis</subject><subject>guanylyl cyclase</subject><subject>In Vitro Techniques</subject><subject>Male</subject><subject>microglia</subject><subject>myelinogenesis</subject><subject>Nitric Oxide - physiology</subject><subject>Nitroprusside - pharmacology</subject><subject>Oligodendroglia - drug effects</subject><subject>Oligodendroglia - metabolism</subject><subject>Parietal Lobe - growth & development</subject><subject>Parietal Lobe - metabolism</subject><subject>Prosencephalon - growth & development</subject><subject>Prosencephalon - metabolism</subject><subject>Putamen - growth & development</subject><subject>Putamen - metabolism</subject><subject>Rats</subject><subject>Rats, Inbred Lew</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0894-1491</issn><issn>1098-1136</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkttu00AQhi0EKqHwCEi-QKi9cNiTvd5wkCKXBkuhQaKQy9FmPS5bHDvsOtC8Pesmyg1IvRrNYT_9M_9G0XtKxpQQ9ubsa1mU55SoPKGUZ2dUKUnEOVUT8Y7l2WQyLS-S2bycsg98TMbF4i1Llo-i0fHF42hEciUSKhR9Gj3z_pYQGhJ5Ep0oEmCSj6LrK9s7a-LuzlaYrLGyuscqNrPPX2K_a_sf6K2PbRt3jb3pKmwr15ldj_e10I0r_I1Nt7HtTex0H6-ctu3z6EmtG48vDvE0-nb58br4lMwXs7KYzhOTMsmSlDOGtDYrk9VqtSK51Ihhx0oLVFRwXZE0F0KwWlRMYqpzozUnlaYiRyUzfhq93nM3rvu1Rd_D2nqDTaNb7LYeZK54ylL64CBNleA0U_yo1LjOe4c1bJxda7cDSmCwBWCwBYYjw3Bk2NsSAggItgAEW-DeFuBAoFgAg2XgvjwI2K7CkY_Ugw-h_-rQ197opna6NdYfx1hGZUaHhb_vx_7YBnf_aHtA2v-U7QsBnOzB1vd4dwRr9xMyyWUKy6sZ5Jd5-E9LCRf8L9RBw8k</recordid><startdate>199704</startdate><enddate>199704</enddate><creator>Tanaka, Junya</creator><creator>Markerink-Van Ittersum, Marjanne</creator><creator>Steinbusch, Harry W. M.</creator><creator>de Vente, Jan</creator><general>John Wiley & Sons, Inc</general><general>Wiley-Liss</general><scope>BSCLL</scope><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>199704</creationdate><title>Nitric oxide-mediated cGMP synthesis in oligodendrocytes in the developing rat brain</title><author>Tanaka, Junya ; Markerink-Van Ittersum, Marjanne ; Steinbusch, Harry W. M. ; de Vente, Jan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5272-5322e1fcbc6f9bb087aee704da4e9143ad0584442f4d27e5a8caa30da148e9763</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>1-Methyl-3-isobutylxanthine - pharmacology</topic><topic>2',3'-Cyclic-Nucleotide Phosphodiesterases - biosynthesis</topic><topic>Aging - metabolism</topic><topic>Animals</topic><topic>astrocyte</topic><topic>Atrial Natriuretic Factor - pharmacology</topic><topic>atrial natriuretic peptide</topic><topic>Biological and medical sciences</topic><topic>Caudate Nucleus - growth & development</topic><topic>Caudate Nucleus - metabolism</topic><topic>Corpus Callosum - growth & development</topic><topic>Corpus Callosum - metabolism</topic><topic>Cyclic GMP - metabolism</topic><topic>Development. Senescence. Regeneration. Transplantation</topic><topic>Fluorescent Antibody Technique, Indirect</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gelsolin - biosynthesis</topic><topic>guanylyl cyclase</topic><topic>In Vitro Techniques</topic><topic>Male</topic><topic>microglia</topic><topic>myelinogenesis</topic><topic>Nitric Oxide - physiology</topic><topic>Nitroprusside - pharmacology</topic><topic>Oligodendroglia - drug effects</topic><topic>Oligodendroglia - metabolism</topic><topic>Parietal Lobe - growth & development</topic><topic>Parietal Lobe - metabolism</topic><topic>Prosencephalon - growth & development</topic><topic>Prosencephalon - metabolism</topic><topic>Putamen - growth & development</topic><topic>Putamen - metabolism</topic><topic>Rats</topic><topic>Rats, Inbred Lew</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tanaka, Junya</creatorcontrib><creatorcontrib>Markerink-Van Ittersum, Marjanne</creatorcontrib><creatorcontrib>Steinbusch, Harry W. M.</creatorcontrib><creatorcontrib>de Vente, Jan</creatorcontrib><collection>Istex</collection><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>Glia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tanaka, Junya</au><au>Markerink-Van Ittersum, Marjanne</au><au>Steinbusch, Harry W. M.</au><au>de Vente, Jan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nitric oxide-mediated cGMP synthesis in oligodendrocytes in the developing rat brain</atitle><jtitle>Glia</jtitle><addtitle>Glia</addtitle><date>1997-04</date><risdate>1997</risdate><volume>19</volume><issue>4</issue><spage>286</spage><epage>297</epage><pages>286-297</pages><issn>0894-1491</issn><eissn>1098-1136</eissn><coden>GLIAEJ</coden><abstract>We investigated the nature of cGMP‐synthesizing cells in the developing rat forebrain using cGMP‐immunocytochemistry in combination with in vitro incubation of brain slices. When brain slices of immature rats, aged between 1 and 4 weeks, were incubated with sodium nitroprusside (SNP), a nitric oxide (NO) donor compound, in the presence of the phosphodiesterase inhibitor isobutylmethylxanthine (IBMX), small round cells with a few processes in and around the corpus callosum were visualized with the cGMP‐antibody. The morphology and the distribution of the cGMP‐positive cells were consistent with the criteria for oligodendrocytes. Furthermore, the cGMP‐positive cells expressed 2′3′‐cyclic nucleotide 3′‐phosphodiesterase (CNPase) and gelsolin, which are marker proteins for oligodendrocytes. Therefore, we concluded that the cGMP‐positive cells were oligodendrocytes. A subpopulation of the oligodendrocyte was found to be cGMP‐immunoreactive also when slices were incubated in the absence of SNP. Furthermore, incubation of the slice in the presence of L‐NAME, an inhibitor of NO synthase, but in the absence of SNP abolished cGMP immunostaining. In addition, some populations of neurons and astrocytes in restricted brain areas produced cGMP in response to the incubation with SNP as previously reported, whereas both ameboid and ramified microglial cells did not respond to the treatment. Atrial natriuretic peptide, a stimulator of particulate guanylyl cyclase, enhanced cGMP synthesis in astrocytes in some brain regions but not in oligodendrocytes. These findings indicate that oligodendrocytes in the immature rat brain express soluble guanylyl cyclase. No cGMP‐positive oligodendrocytes were found in the mature rat brain, suggesting that cGMP may mediate signals related to myelinogenesis in the rat brain. GLIA 19:286–297, 1997. © 1997 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>John Wiley & Sons, Inc</pub><pmid>9097073</pmid><doi>10.1002/(SICI)1098-1136(199704)19:4<286::AID-GLIA2>3.0.CO;2-W</doi><tpages>12</tpages></addata></record> |
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subjects | 1-Methyl-3-isobutylxanthine - pharmacology 2',3'-Cyclic-Nucleotide Phosphodiesterases - biosynthesis Aging - metabolism Animals astrocyte Atrial Natriuretic Factor - pharmacology atrial natriuretic peptide Biological and medical sciences Caudate Nucleus - growth & development Caudate Nucleus - metabolism Corpus Callosum - growth & development Corpus Callosum - metabolism Cyclic GMP - metabolism Development. Senescence. Regeneration. Transplantation Fluorescent Antibody Technique, Indirect Fundamental and applied biological sciences. Psychology Gelsolin - biosynthesis guanylyl cyclase In Vitro Techniques Male microglia myelinogenesis Nitric Oxide - physiology Nitroprusside - pharmacology Oligodendroglia - drug effects Oligodendroglia - metabolism Parietal Lobe - growth & development Parietal Lobe - metabolism Prosencephalon - growth & development Prosencephalon - metabolism Putamen - growth & development Putamen - metabolism Rats Rats, Inbred Lew Vertebrates: nervous system and sense organs |
title | Nitric oxide-mediated cGMP synthesis in oligodendrocytes in the developing rat brain |
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