Perineal Nets of Proteoglycans and Glycoproteins in Albino Rat Hippocampus
Identifieur interne : 001190 ( Istex/Corpus ); précédent : 001189; suivant : 001191Perineal Nets of Proteoglycans and Glycoproteins in Albino Rat Hippocampus
Auteurs : W. Mubarak ; M. N. Saleh ; R. Sayed ; A. Ohtsuka ; T. Taguchi ; T. MurakamiSource :
- Anatomia, Histologia, Embryologia [ 0340-2096 ] ; 2005-12.
Abstract
Perineuronal nets (PNs) of condensed extracellular matrix (ECM) have been shown to characterize the microenvironment of individual neurons and the chemoarchitecture of some brain regions. In the present study, PNs in the hippocampus were visualized with a cationic iron colloid method for sulphated proteoglycan content and a plant lectin from Vicia villosa agglutinin (VVA) for N‐acetylgalactosamine containing glycoconjugates. The ECM molecules were organized in reticular coats (PNs) around non‐pyramidal cells in the Ammons horn (Corneu Ammons, CA) and subicular region, in addition to pyramidal neurons located in CA2 and CA3 regions. CA2 stratum pyramidale exhibited the most intense staining of its PNs and a diffuse intervening neutrophil labelling, while CA3 region showed a graded fashion of staining intensity. The subiculum displayed intensely stained perineuronal coats. Notably, the hippocampal perineuronal nets revealed overlapped staining characteristics with both staining methods. However, cell coats of the subicular neurons showed various degrees of labelling characteristics with both markers. It is suggested that the PNs in the hippocampus are correlated with the fast spiking inhibitory GABAergic neurons and their target pyramidal cells, and this is important to keep the excitatory elements under control and therefore control the information processes within the hippocampus.
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DOI: 10.1111/j.1439-0264.2005.00669_78.x
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In the present study, PNs in the hippocampus were visualized with a cationic iron colloid method for sulphated proteoglycan content and a plant lectin from Vicia villosa agglutinin (VVA) for N‐acetylgalactosamine containing glycoconjugates. The ECM molecules were organized in reticular coats (PNs) around non‐pyramidal cells in the Ammons horn (Corneu Ammons, CA) and subicular region, in addition to pyramidal neurons located in CA2 and CA3 regions. CA2 stratum pyramidale exhibited the most intense staining of its PNs and a diffuse intervening neutrophil labelling, while CA3 region showed a graded fashion of staining intensity. The subiculum displayed intensely stained perineuronal coats. Notably, the hippocampal perineuronal nets revealed overlapped staining characteristics with both staining methods. However, cell coats of the subicular neurons showed various degrees of labelling characteristics with both markers. It is suggested that the PNs in the hippocampus are correlated with the fast spiking inhibitory GABAergic neurons and their target pyramidal cells, and this is important to keep the excitatory elements under control and therefore control the information processes within the hippocampus.</div></front></TEI><istex><corpusName>wiley</corpusName><author><json:item><name>W. Mubarak</name><affiliations><json:string>Section of Human Morphology, Graduate School of Medicine and Dentistry, Okayama University, Japan</json:string><json:string>Department of Anatomy, Faculty of Medicine, Assiut University, Egypt</json:string></affiliations></json:item><json:item><name>M. N. Saleh</name><affiliations><json:string>Section of Human Morphology, Graduate School of Medicine and Dentistry, Okayama University, Japan</json:string></affiliations></json:item><json:item><name>R. 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It is suggested that the PNs in the hippocampus are correlated with the fast spiking inhibitory GABAergic neurons and their target pyramidal cells, and this is important to keep the excitatory elements under control and therefore control the information processes within the hippocampus.</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Perineal Nets of Proteoglycans and Glycoproteins in Albino Rat Hippocampus</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Abstracts</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Perineal Nets of Proteoglycans and Glycoproteins in Albino Rat Hippocampus</title></titleInfo><name type="personal"><namePart type="given">W.</namePart><namePart type="family">Mubarak</namePart><affiliation>Section of Human Morphology, Graduate School of Medicine and Dentistry, Okayama University, Japan</affiliation><affiliation>Department of Anatomy, Faculty of Medicine, Assiut University, Egypt</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">M. N.</namePart><namePart type="family">Saleh</namePart><affiliation>Section of Human Morphology, Graduate School of Medicine and Dentistry, Okayama University, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">R.</namePart><namePart type="family">Sayed</namePart><affiliation>Section of Human Morphology, Graduate School of Medicine and Dentistry, Okayama University, Japan</affiliation><affiliation>Department of Anatomy and Histology, Faculty of Veterinary Medicine, Assiut University, Egypt</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">A.</namePart><namePart type="family">Ohtsuka</namePart><affiliation>Section of Human Morphology, Graduate School of Medicine and Dentistry, Okayama University, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T.</namePart><namePart type="family">Taguchi</namePart><affiliation>Department of Radiological Technology, Faculty of Health Sciences, School of Medicine, Okayama University, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T.</namePart><namePart type="family">Murakami</namePart><affiliation>Section of Human Morphology, Graduate School of Medicine and Dentistry, Okayama University, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="abstract" displayLabel="abstract"></genre><originInfo><publisher>Blackwell Verlag GmbH</publisher><place><placeTerm type="text">Berlin, Germany</placeTerm></place><dateIssued encoding="w3cdtf">2005-12</dateIssued><copyrightDate encoding="w3cdtf">2005</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><internetMediaType>text/html</internetMediaType></physicalDescription><abstract lang="en">Perineuronal nets (PNs) of condensed extracellular matrix (ECM) have been shown to characterize the microenvironment of individual neurons and the chemoarchitecture of some brain regions. In the present study, PNs in the hippocampus were visualized with a cationic iron colloid method for sulphated proteoglycan content and a plant lectin from Vicia villosa agglutinin (VVA) for N‐acetylgalactosamine containing glycoconjugates. The ECM molecules were organized in reticular coats (PNs) around non‐pyramidal cells in the Ammons horn (Corneu Ammons, CA) and subicular region, in addition to pyramidal neurons located in CA2 and CA3 regions. CA2 stratum pyramidale exhibited the most intense staining of its PNs and a diffuse intervening neutrophil labelling, while CA3 region showed a graded fashion of staining intensity. The subiculum displayed intensely stained perineuronal coats. Notably, the hippocampal perineuronal nets revealed overlapped staining characteristics with both staining methods. However, cell coats of the subicular neurons showed various degrees of labelling characteristics with both markers. It is suggested that the PNs in the hippocampus are correlated with the fast spiking inhibitory GABAergic neurons and their target pyramidal cells, and this is important to keep the excitatory elements under control and therefore control the information processes within the hippocampus.</abstract><relatedItem type="host"><titleInfo><title>Anatomia, Histologia, Embryologia</title></titleInfo><genre type="journal">journal</genre><identifier type="ISSN">0340-2096</identifier><identifier type="eISSN">1439-0264</identifier><identifier type="DOI">10.1111/(ISSN)1439-0264</identifier><identifier type="PublisherID">AHE</identifier><part><date>2005</date><detail type="volume"><caption>vol.</caption><number>34</number></detail><detail type="supplement"><caption>Suppl. no.</caption><number>s1</number></detail><extent unit="pages"><start>34</start><end>35</end></extent></part></relatedItem><identifier type="istex">232F695A5B1A658395AF4E8076C68157BE60097B</identifier><identifier type="DOI">10.1111/j.1439-0264.2005.00669_78.x</identifier><identifier type="ArticleID">AHE669_78_78</identifier><recordInfo><recordContentSource>WILEY</recordContentSource><recordOrigin>Blackwell Verlag GmbH</recordOrigin></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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