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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Veröffentlicht in:Glia 1997-04, Vol.19 (4), p.286-297
Hauptverfasser: Tanaka, Junya, Markerink-Van Ittersum, Marjanne, Steinbusch, Harry W. M., de Vente, Jan
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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. 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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 &amp; development</subject><subject>Caudate Nucleus - metabolism</subject><subject>Corpus Callosum - growth &amp; development</subject><subject>Corpus Callosum - metabolism</subject><subject>Cyclic GMP - metabolism</subject><subject>Development. Senescence. 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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 &amp; development</subject><subject>Parietal Lobe - metabolism</subject><subject>Prosencephalon - growth &amp; development</subject><subject>Prosencephalon - metabolism</subject><subject>Putamen - growth &amp; 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. 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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 &amp; development</topic><topic>Caudate Nucleus - metabolism</topic><topic>Corpus Callosum - growth &amp; 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 &amp; development</topic><topic>Parietal Lobe - metabolism</topic><topic>Prosencephalon - growth &amp; development</topic><topic>Prosencephalon - metabolism</topic><topic>Putamen - growth &amp; 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 &amp; Sons, Inc</pub><pmid>9097073</pmid><doi>10.1002/(SICI)1098-1136(199704)19:4&lt;286::AID-GLIA2&gt;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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