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Spatiotemporal expression patterns of sialoglycoconjugates during nephron morphogenesis and their regional and cell type-specific distribution in adult rat kidney

dc.contributor.authorPaulson, James C.en_US
dc.contributor.authorGoldstein, Irwin J.en_US
dc.contributor.authorToma, Valeriuen_US
dc.contributor.authorWinter, Harry C.en_US
dc.contributor.authorRoth, Jürgenen_US
dc.contributor.authorZuber, Christianen_US
dc.date.accessioned2006-09-11T18:55:47Z
dc.date.available2006-09-11T18:55:47Z
dc.date.issued2003-08en_US
dc.identifier.citationZuber, Christian; Paulson, James C.; Toma, Valeriu; Winter, Harry C.; Goldstein, Irwin J.; Roth, Jürgen; (2003). "Spatiotemporal expression patterns of sialoglycoconjugates during nephron morphogenesis and their regional and cell type-specific distribution in adult rat kidney." Histochemistry and Cell Biology 120(2): 143-160. <http://hdl.handle.net/2027.42/47395>en_US
dc.identifier.issn1432-119Xen_US
dc.identifier.issn0948-6143en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/47395
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=12898273&dopt=citationen_US
dc.description.abstractThe expression of α2,6- and α2,3-linked sialic acids on N -glycans was studied in embryonic, postnatal, and adult rat kidney. Histochemistry and blotting using Polyporus squamosus and Sambucus nigra lectins for α2,6-linked sialic acids and the Maackia amurensis lectin for α2,3-linked sialic acids were performed and sialyltransferase activity was assayed. N -glycans with α2,6- and α2,3-linked sialic acid were differently expressed in the two embryonic anlagen and early stages of nephron. Metanephrogenic mesenchyme was positive for α2,3-linked sialic acid but not for the α2,6-linked one, which became detectable initially in the proximal part of S-shaped bodies. Collecting ducts were positive for α2,6-linked sialic acid, whereas α2,3-linked sialic acid was restricted to their ampullae. Although positive in embryonic kidney, S1 and S2 of proximal tubules became unreactive for α2,3-linked sialic acid in postnatal and adult kidneys. In adult kidney, intercalated but not principal cells of collecting ducts were reactive for α2,3-linked sialic acid. In contrast, α2,6-linked sialic acids were detected in all cells of adult kidney nephron. Blot analysis revealed a different but steady pattern of bands reactive for α2,6- and α2,3-linked sialic acid in embryonic, postnatal, and adult kidney. Activity of α2,6 and α2,3 sialyltransferases was highest in embryonic kidney and decreased over postnatal to adult kidney with the activity of α2,6 sialyltransferase always being three to fourfold that of α2,3 sialyltransferase. Thus, α2,6- and α2,3-linked sialic acids are differently expressed in embryonic anlagen and mesenchyme-derived early stages of nephron and show regional and cell type-specific differences in adult kidney.en_US
dc.format.extent2220945 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlagen_US
dc.subject.otherSialic Aciden_US
dc.subject.otherKidney Developmenten_US
dc.subject.otherLifeSciencesen_US
dc.subject.otherPolyporus Squamosus Lectinen_US
dc.subject.otherHistochemistryen_US
dc.subject.otherKidneyen_US
dc.subject.otherSialyltransferaseen_US
dc.subject.otherMaackia Amurensis Lectinen_US
dc.titleSpatiotemporal expression patterns of sialoglycoconjugates during nephron morphogenesis and their regional and cell type-specific distribution in adult rat kidneyen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Biological Chemistry, School of Medicine, University of Michigan, Ann Arbor, Michigan, 48109-0606, USAen_US
dc.contributor.affiliationumDepartment of Biological Chemistry, School of Medicine, University of Michigan, Ann Arbor, Michigan, 48109-0606, USAen_US
dc.contributor.affiliationotherThe Scripps Research Institute, Department of Molecular Biology, La Jolla, CA 92037, USAen_US
dc.contributor.affiliationotherDivision of Cell and Molecular Pathology, Department of Pathology, University of Zürich, Schmelzbergstrasse 12, 8091, Zürich, Switzerlanden_US
dc.contributor.affiliationotherDivision of Cell and Molecular Pathology, Department of Pathology, University of Zürich, Schmelzbergstrasse 12, 8091, Zürich, Switzerlanden_US
dc.contributor.affiliationotherDivision of Cell and Molecular Pathology, Department of Pathology, University of Zürich, Schmelzbergstrasse 12, 8091, Zürich, Switzerlanden_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid12898273en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/47395/1/418_2003_Article_553.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/s00418-003-0553-0en_US
dc.identifier.sourceHistochemistry and Cell Biologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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