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Morphological basis of nitric oxide production and its correlation with the polysialylated precursor cells in the dentate gyrus of the adult guinea pig hippocampus
Neurogenesis in the hippocampus persist throughout life and precursors of neurons reside in the granule cell layer of the dentate gyrus. Until now, the role of nitric oxide (NO) in the phenomenon has been unclear. By using specific antibodies and a confocal laser scanning microscope, the localizatio...
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Published in: | Anatomical Science International 2003-06, Vol.78 (2), p.98-103 |
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description | Neurogenesis in the hippocampus persist throughout life and precursors of neurons reside in the granule cell layer of the dentate gyrus. Until now, the role of nitric oxide (NO) in the phenomenon has been unclear. By using specific antibodies and a confocal laser scanning microscope, the localization of NO synthase (NOS) was examined in the dentate gyrus of the adult guinea pig in relation with the neuronal precursor marker highly polysialylated neural cell adhesion molecule (PSA‐N‐CAM). Observation of single immunolabeled sections has revealed that both the PSA‐N‐CAM‐ and most NOS‐positive cells were localized in the granule cell layer of the dentate gyrus. The former were small in size and showed a punctate, clustered immunoreaction with an irregular cellular margin, whereas the latter showed somewhat diverse cellular profiles. Some NOS‐positive neurons had elliptical‐like morphology with elongated dendrites, whereas others were small, irregularly shaped and mostly lacking dendritic spines. Double immunolabeling has revealed that NOS‐immunoreactivity intermingled, as well as colocalized, with that of PSA‐N‐CAM, particulary in the granule cell layer. The doubly stained cells were morphologically indistinguishable from PSA‐N‐CAM single positive cells. These results not only suggest the role of NO production in adult hippocampal neurogenesis, but also indicate that some PSA‐N‐CAM‐expressing neuronal precursors produce NO. |
doi_str_mv | 10.1046/j.0022-7722.2003.00045.x |
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T. M. Shariful ; Kuraoka, Akio ; Kawabuchi, Masaru</creator><creatorcontrib>Islam, A. T. M. Shariful ; Kuraoka, Akio ; Kawabuchi, Masaru</creatorcontrib><description>Neurogenesis in the hippocampus persist throughout life and precursors of neurons reside in the granule cell layer of the dentate gyrus. Until now, the role of nitric oxide (NO) in the phenomenon has been unclear. By using specific antibodies and a confocal laser scanning microscope, the localization of NO synthase (NOS) was examined in the dentate gyrus of the adult guinea pig in relation with the neuronal precursor marker highly polysialylated neural cell adhesion molecule (PSA‐N‐CAM). Observation of single immunolabeled sections has revealed that both the PSA‐N‐CAM‐ and most NOS‐positive cells were localized in the granule cell layer of the dentate gyrus. The former were small in size and showed a punctate, clustered immunoreaction with an irregular cellular margin, whereas the latter showed somewhat diverse cellular profiles. Some NOS‐positive neurons had elliptical‐like morphology with elongated dendrites, whereas others were small, irregularly shaped and mostly lacking dendritic spines. Double immunolabeling has revealed that NOS‐immunoreactivity intermingled, as well as colocalized, with that of PSA‐N‐CAM, particulary in the granule cell layer. The doubly stained cells were morphologically indistinguishable from PSA‐N‐CAM single positive cells. These results not only suggest the role of NO production in adult hippocampal neurogenesis, but also indicate that some PSA‐N‐CAM‐expressing neuronal precursors produce NO.</description><identifier>ISSN: 1447-6959</identifier><identifier>ISSN: 0022-7722</identifier><identifier>EISSN: 1447-073X</identifier><identifier>DOI: 10.1046/j.0022-7722.2003.00045.x</identifier><identifier>PMID: 12828422</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>adult hippocampus ; Animals ; Cell adhesion molecules ; Cell Differentiation - physiology ; Cell Size - physiology ; Dendrites - metabolism ; Dendrites - ultrastructure ; Dendritic spines ; Dentate gyrus ; Dentate Gyrus - cytology ; Dentate Gyrus - growth & development ; Dentate Gyrus - metabolism ; Female ; guinea pig ; Guinea Pigs ; highly polysialylated neural cell adhesion molecule ; Hippocampus ; immunocytochemistry ; Immunohistochemistry ; Immunoreactivity ; Localization ; Male ; Microscopy, Confocal ; Neural cell adhesion molecule ; Neural Cell Adhesion Molecule L1 - metabolism ; Neural stem cells ; Neurogenesis ; Neurons - cytology ; Neurons - metabolism ; Nitrergic Neurons - metabolism ; Nitrergic Neurons - ultrastructure ; Nitric oxide ; Nitric Oxide - biosynthesis ; Nitric Oxide Synthase - metabolism ; Nitric-oxide synthase ; Sialic Acids - metabolism ; Stem Cells - cytology ; Stem Cells - metabolism</subject><ispartof>Anatomical Science International, 2003-06, Vol.78 (2), p.98-103</ispartof><rights>Japanese Association of Anatomists 2003.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4295-9adefa0261463fab25932b00cb7a48bdf22606b8af131d4d5d56b2abc5818d903</citedby><cites>FETCH-LOGICAL-c4295-9adefa0261463fab25932b00cb7a48bdf22606b8af131d4d5d56b2abc5818d903</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12828422$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Islam, A. T. M. Shariful</creatorcontrib><creatorcontrib>Kuraoka, Akio</creatorcontrib><creatorcontrib>Kawabuchi, Masaru</creatorcontrib><title>Morphological basis of nitric oxide production and its correlation with the polysialylated precursor cells in the dentate gyrus of the adult guinea pig hippocampus</title><title>Anatomical Science International</title><addtitle>Anat Sci Int</addtitle><description>Neurogenesis in the hippocampus persist throughout life and precursors of neurons reside in the granule cell layer of the dentate gyrus. Until now, the role of nitric oxide (NO) in the phenomenon has been unclear. By using specific antibodies and a confocal laser scanning microscope, the localization of NO synthase (NOS) was examined in the dentate gyrus of the adult guinea pig in relation with the neuronal precursor marker highly polysialylated neural cell adhesion molecule (PSA‐N‐CAM). Observation of single immunolabeled sections has revealed that both the PSA‐N‐CAM‐ and most NOS‐positive cells were localized in the granule cell layer of the dentate gyrus. The former were small in size and showed a punctate, clustered immunoreaction with an irregular cellular margin, whereas the latter showed somewhat diverse cellular profiles. Some NOS‐positive neurons had elliptical‐like morphology with elongated dendrites, whereas others were small, irregularly shaped and mostly lacking dendritic spines. Double immunolabeling has revealed that NOS‐immunoreactivity intermingled, as well as colocalized, with that of PSA‐N‐CAM, particulary in the granule cell layer. The doubly stained cells were morphologically indistinguishable from PSA‐N‐CAM single positive cells. These results not only suggest the role of NO production in adult hippocampal neurogenesis, but also indicate that some PSA‐N‐CAM‐expressing neuronal precursors produce NO.</description><subject>adult hippocampus</subject><subject>Animals</subject><subject>Cell adhesion molecules</subject><subject>Cell Differentiation - physiology</subject><subject>Cell Size - physiology</subject><subject>Dendrites - metabolism</subject><subject>Dendrites - ultrastructure</subject><subject>Dendritic spines</subject><subject>Dentate gyrus</subject><subject>Dentate Gyrus - cytology</subject><subject>Dentate Gyrus - growth & development</subject><subject>Dentate Gyrus - metabolism</subject><subject>Female</subject><subject>guinea pig</subject><subject>Guinea Pigs</subject><subject>highly polysialylated neural cell adhesion molecule</subject><subject>Hippocampus</subject><subject>immunocytochemistry</subject><subject>Immunohistochemistry</subject><subject>Immunoreactivity</subject><subject>Localization</subject><subject>Male</subject><subject>Microscopy, Confocal</subject><subject>Neural cell adhesion molecule</subject><subject>Neural Cell Adhesion Molecule L1 - metabolism</subject><subject>Neural stem cells</subject><subject>Neurogenesis</subject><subject>Neurons - cytology</subject><subject>Neurons - metabolism</subject><subject>Nitrergic Neurons - metabolism</subject><subject>Nitrergic Neurons - ultrastructure</subject><subject>Nitric oxide</subject><subject>Nitric Oxide - biosynthesis</subject><subject>Nitric Oxide Synthase - metabolism</subject><subject>Nitric-oxide synthase</subject><subject>Sialic Acids - metabolism</subject><subject>Stem Cells - cytology</subject><subject>Stem Cells - metabolism</subject><issn>1447-6959</issn><issn>0022-7722</issn><issn>1447-073X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNqNkcuKFDEUhgtRnIu-ggQEd9WTnCRVqYWLYRh1YNSFCu5CKkl1p0lXyqTCdD-PL2qqu0Fw5Son53z_ufBXFSJ4RTBrbrYrjAHqtgVYAca0fDHjq_2z6pIw1ta4pT-fn-Om491FdZXSFmPScUJfVhcEBAgGcFn9_hzitAk-rJ1WHvUquYTCgEY3R6dR2Dtj0RSDyXp2YURqNMjNCekQo_XqmHty8wbNm8IFf0hO-UMpWFNkVueYQkTaep-QG4-UseNc6mh9iPk4a0kqk_2M1tmNVqHJrdHGTVPQajfl9Kp6MSif7Ovze139-HD__e5T_fj148Pd7WOtGXS87pSxg8LQENbQQfXAOwo9xrpvFRO9GQAa3PRCDYQSwww3vOlB9ZoLIkyH6XX17tS33Psr2zTLnUvL6mq0ISfZUga8ZbSAb_8BtyHHsewmoRUtcCEYL5Q4UTqGlKId5BTdTsWDJFguNsqtXGyUi41ysVEebZT7In1zHpD7nTV_hWffCvD-BDw5bw__3Vjefnv4UiL6B6uPr3s</recordid><startdate>200306</startdate><enddate>200306</enddate><creator>Islam, A. T. M. Shariful</creator><creator>Kuraoka, Akio</creator><creator>Kawabuchi, Masaru</creator><general>Blackwell Publishing Ltd</general><general>Springer Nature B.V</general><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>K9.</scope><scope>7X8</scope></search><sort><creationdate>200306</creationdate><title>Morphological basis of nitric oxide production and its correlation with the polysialylated precursor cells in the dentate gyrus of the adult guinea pig hippocampus</title><author>Islam, A. T. M. Shariful ; Kuraoka, Akio ; Kawabuchi, Masaru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4295-9adefa0261463fab25932b00cb7a48bdf22606b8af131d4d5d56b2abc5818d903</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>adult hippocampus</topic><topic>Animals</topic><topic>Cell adhesion molecules</topic><topic>Cell Differentiation - physiology</topic><topic>Cell Size - physiology</topic><topic>Dendrites - metabolism</topic><topic>Dendrites - ultrastructure</topic><topic>Dendritic spines</topic><topic>Dentate gyrus</topic><topic>Dentate Gyrus - cytology</topic><topic>Dentate Gyrus - growth & development</topic><topic>Dentate Gyrus - metabolism</topic><topic>Female</topic><topic>guinea pig</topic><topic>Guinea Pigs</topic><topic>highly polysialylated neural cell adhesion molecule</topic><topic>Hippocampus</topic><topic>immunocytochemistry</topic><topic>Immunohistochemistry</topic><topic>Immunoreactivity</topic><topic>Localization</topic><topic>Male</topic><topic>Microscopy, Confocal</topic><topic>Neural cell adhesion molecule</topic><topic>Neural Cell Adhesion Molecule L1 - metabolism</topic><topic>Neural stem cells</topic><topic>Neurogenesis</topic><topic>Neurons - cytology</topic><topic>Neurons - metabolism</topic><topic>Nitrergic Neurons - metabolism</topic><topic>Nitrergic Neurons - ultrastructure</topic><topic>Nitric oxide</topic><topic>Nitric Oxide - biosynthesis</topic><topic>Nitric Oxide Synthase - metabolism</topic><topic>Nitric-oxide synthase</topic><topic>Sialic Acids - metabolism</topic><topic>Stem Cells - cytology</topic><topic>Stem Cells - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Islam, A. T. M. Shariful</creatorcontrib><creatorcontrib>Kuraoka, Akio</creatorcontrib><creatorcontrib>Kawabuchi, Masaru</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Anatomical Science International</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Islam, A. T. M. Shariful</au><au>Kuraoka, Akio</au><au>Kawabuchi, Masaru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Morphological basis of nitric oxide production and its correlation with the polysialylated precursor cells in the dentate gyrus of the adult guinea pig hippocampus</atitle><jtitle>Anatomical Science International</jtitle><addtitle>Anat Sci Int</addtitle><date>2003-06</date><risdate>2003</risdate><volume>78</volume><issue>2</issue><spage>98</spage><epage>103</epage><pages>98-103</pages><issn>1447-6959</issn><issn>0022-7722</issn><eissn>1447-073X</eissn><abstract>Neurogenesis in the hippocampus persist throughout life and precursors of neurons reside in the granule cell layer of the dentate gyrus. Until now, the role of nitric oxide (NO) in the phenomenon has been unclear. By using specific antibodies and a confocal laser scanning microscope, the localization of NO synthase (NOS) was examined in the dentate gyrus of the adult guinea pig in relation with the neuronal precursor marker highly polysialylated neural cell adhesion molecule (PSA‐N‐CAM). Observation of single immunolabeled sections has revealed that both the PSA‐N‐CAM‐ and most NOS‐positive cells were localized in the granule cell layer of the dentate gyrus. The former were small in size and showed a punctate, clustered immunoreaction with an irregular cellular margin, whereas the latter showed somewhat diverse cellular profiles. Some NOS‐positive neurons had elliptical‐like morphology with elongated dendrites, whereas others were small, irregularly shaped and mostly lacking dendritic spines. Double immunolabeling has revealed that NOS‐immunoreactivity intermingled, as well as colocalized, with that of PSA‐N‐CAM, particulary in the granule cell layer. The doubly stained cells were morphologically indistinguishable from PSA‐N‐CAM single positive cells. These results not only suggest the role of NO production in adult hippocampal neurogenesis, but also indicate that some PSA‐N‐CAM‐expressing neuronal precursors produce NO.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>12828422</pmid><doi>10.1046/j.0022-7722.2003.00045.x</doi><tpages>6</tpages></addata></record> |
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subjects | adult hippocampus Animals Cell adhesion molecules Cell Differentiation - physiology Cell Size - physiology Dendrites - metabolism Dendrites - ultrastructure Dendritic spines Dentate gyrus Dentate Gyrus - cytology Dentate Gyrus - growth & development Dentate Gyrus - metabolism Female guinea pig Guinea Pigs highly polysialylated neural cell adhesion molecule Hippocampus immunocytochemistry Immunohistochemistry Immunoreactivity Localization Male Microscopy, Confocal Neural cell adhesion molecule Neural Cell Adhesion Molecule L1 - metabolism Neural stem cells Neurogenesis Neurons - cytology Neurons - metabolism Nitrergic Neurons - metabolism Nitrergic Neurons - ultrastructure Nitric oxide Nitric Oxide - biosynthesis Nitric Oxide Synthase - metabolism Nitric-oxide synthase Sialic Acids - metabolism Stem Cells - cytology Stem Cells - metabolism |
title | Morphological basis of nitric oxide production and its correlation with the polysialylated precursor cells in the dentate gyrus of the adult guinea pig hippocampus |
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