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  • Life and Medical Sciences  (14)
  • Glycoconjugates  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Anatomy and embryology 182 (1990), S. 611-616 
    ISSN: 1432-0568
    Keywords: Eye development ; Glycoconjugates ; Histochemistry ; Immunohistochemistry ; Lectins
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Lectin histochemical methods and immunohistochemical techniques have been utilized to investigate and partially characterize glycoconjugates in the developing eye. Peanut-lectin-binding sites associated with radial glial cells were found in the diencephalon. In the optic primordia, binding sites associated with radial glia were masked by terminal sialic acid, and only reacted with peanut lectin when pretreated with sialidase. This finding indicates that glycoconjugates associated with diencephalic radial glia contain terminal galactose-β-(1→3)N-acetyl galactosamine, but glycoconjugates associated with radial glia in the optic primordia contain sialic acid→galactose-β(1→3)N-acetyl galactosamine. The selective distribution of galactose, N-acetyl galactosamine and fucose associated with radial glial cells has also been demonstrated. We postulate that these distributions mediate the shaping of the developing eye.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 189 (1977), S. 177-185 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Polymorphonuclear leukocytes (PMN's) incubated three to eight minutes at 37°C in medium containing 1 × 10-6M of the ionophore antibiotic A23187 released their cytoplasmic granules into the extracellular medium. Transmission electron microscopy of treated cells showed microfilament bundles extending between adjacent granules within the cytoplasm and between granules and the plasma membrane. Tiny dense projections (beads) 8-12 nm in diameter were observed along segments of the cytoplasmic surface of the plasma membrane with a periodicity of 20-30 nm. These beads were observed on the plasma membrane only in the vicinity of intra- or extracytoplasmic granules. The structural relationships of the beads with the plasma membrane micro-filaments suggest they play a role in the process of ionophore-induced granule release from polymorphonuclear leukocytes.
    Additional Material: 1 Tab.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 207 (1983), S. 605-614 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Carbonic anhydrase (CA) isozyme I and isozyme II have been localized with the immunoperoxidase bridge method in cells of mouse and rat salivary glands and exorbital lacrimal glands. Immunostaining proved optimal in Carnoy fixed specimens for some sites and in Bouin fixed glands for other sites. Staining in mouse largely resembled that in rat glands, but minor species differences were observed. Serous acinar cells in the submandibular gland stained uniformly and exclusively for CA I. From 50 to 100% of the serous acinar cells in the parotid glands evidenced content of both CA I and CA II. A minor population of serous acinar cells in the mouse exorbital lacrimal gland stained for CA I and CA II, but these glands in the rat failed to stain.Immunostaining was observed in ducts in Bouin fixed glands. Some cells in striated ducts of submandibular and sublingual glands stained for CA I and CA II and other cells in these ducts were negative. Such cellular heterogeneity was also observed in excretory ducts of submandibular and sublingual glands. These findings thus demonstrate the presence of CA in two morphologically and functionally diverse cell populations in rodent salivary glands.Immunolocalization of the CA isozymes in serous acinar cells and intercalated duct cells, presumably packaged in secretory granules, implies a role for this enzyme in salivary secretions whereas localization of CA in striated and excretory ducts suggests their traditional function in fluid and electrolyte transport.
    Additional Material: 11 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 202 (1982), S. 431-443 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The distribution of complex carbohydrates has been investigated cytochemically at the light and electron microscope levels in collecting ducts of the guinea pig kidney. The dialyzed iron method demonstrated acidic complex carbohydrate ultrastructurally on the outer surface of the apical and the basolateral plasmalemma of the principal cells and in their maturing Golgi cisternae and secretory granules. Glycoconjugate in these sites stained for sulfate esters with the high iron diamine method but lacked reactivity toward the periodic acid-thiocarbohydrazide-silver proteinate (PA-T-SP) sequence for visualizing vicglycol-containing glycoprotein. Lability to testicular hyaluronidase and resistance to sialidase identified the Glycosaminoglycan (GAG) in principal cell granules and the plasmalemmae as a chondroitin sulfate. In contrast, intercalated cells of the collecting ducts failed to stain with the cationic reagents, but showed light PA-T-SP reactivity demonstrative of neutral glycoprotein in the glycocalyx of the apical plasmalemma. Immunostaining with the immunoglobulin-enzyme bridge procedure localized carbonic anhydrase selectively to the intercalated cells. The ultrastructural and cytochemical observations on the guinea pig collecting ducts implicate intercalated cells in fluid and electrolyte transport and principal cells in secretion of a chondroitin sulfate to the tubule lumen and intercellular space.
    Additional Material: 20 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 237 (1993), S. 421-430 
    ISSN: 0003-276X
    Keywords: Organ of Corti ; Ultrastructure ; Cytoskeleton ; Gerbil ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Deiters cells in the gerbil cochlea disclosed unusual ultrastructural features. A sharp transition zone separated the cell body underlying outer hair cells into an upper compartment with numerous organelles and a lower part devoid of structures other than the microtubule stalk. Deiters cells exhibited a unique structure, the rosette complex, which consisted of a core of densely fibrillar trabeculae, enclosed in a filamentous meshwork and surrounded by tubulocisternal endoplasmic reticulum. The dense trabeculae radiated in columns downward from an apical translucent area toward a lucent zone around the nucleus. They also spread to the medial plasmalemma enveloping nerves and upward into the base of the phalanx. Frequent, small Golgi complexes bordered the tubular reticulum. The distinctive mitochondria of Deiters cells frequently paralleled the plasmalemma, revealed an elongated, often arched profile, and contained sparse, longitudinally aligned cristae. The stalk, composed of characteristic microtubule bundles resembling those in pillar cells, ascended from basal to apical plasmalemma of the cell body and into the phalanx and reticular lamina as previously described. The stalk appeared also to ramify into smaller microtubule bundles in apical cytosol penetrating the rosette complex. Nuclei in Deiters cells differed from those in hair cells in their location high in the cell and in showing chromatin dispersion indicative of more active protein synthesis. © 1993 Wiley-Liss, Inc.
    Additional Material: 18 Ill.
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  • 6
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Comparative light and electron microscopic study of nuclei in rat trigeminal neurons identified two structures which are the ultrastructural equivalent of the paranucloelar structure and the accessory body of Cajal, two nucleoplasmic structures previously demonstrated in other neurons by light microscope silver staining methods. Ultrastructural evidence indicates that the dense component of the nucleolus is converted into the paranucleolar structure, which then detaches from the nucleolar surface to lie free in the nucleoplasm as the accessory body of Cajal. The cytochemistry, ultrastructure, and antimonate reactivity of the paranucleolar structure and accessory body were identical. Both structures lacked cytochemically demonstrable DNA, RNA, or basic protein.The neuronal nuclei also contained Feulgen-positive sex chromatin bodies that adhered to the nucleolus, the nuclear membrane, or to both of these structures in specimens of female but not male rats. The ultrastructure and antimonate reactivity of these bodies closely resembled that of heterochromatin clumps but differed markedly from that of the paranucleolar structures and accessory bodies.Additional structures characterized ultrastructurally included patches, granular bodies, and flakes. These structures, like the paranucleolar structure and the accessory body of Cajal, are apparently unique to nuclei of neurons. Cytochemical methods showed that the patches contained basic protein but no nucleic acid.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 211 (1985), S. 376-390 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Parafin sections of normal human kidney were stained with a battery of ten lectin-horseradish peroxidase conjugates. Staining of proximal tubules revealed a relatively uniform distribution of glycoconjugates having bi- and/or triantennary N-linked sugar chains as well as terminal β-galactose and α-fucose in all cells. In contrast, terminal α- and β-galactose and α-fucose were localized in only some cells of the thin limbs, whereas N-linked sugar chains and terminal α-N-acetylgalactosamine occurred in all cells. In the ascending thick limbs, terminal α-N-acetylgalactosamine was found in some cells and N-linked sugar chains and terminal β-galactose were present in all cells. The distal convoluted tubules contained N-linked oligosaccharides and terminal β-galactose in all cells. Terminal α-N-acetylgalactosamine was found in some but not all profiles of distal convoluted tubules in a few kidneys. In the initial (connecting) segment of cortical collecting ducts, cells varied in their content of glycogen and glycoconjugates with terminal α-and β-galactose, α-fucose and α-N-acetylgalactosamine, but cells in this segment evidenced uniform localization of N-linked sugar chains. A similar distribution of sugars occurred in the medullary ray segment of cortical collecting ducts, except for terminal β-galactose which was present in all cells. In the medullary collecting ducts, there was also considerable cell-to-cell variation in the content and distribution of glycogen and glycoconjugates having N-linked sugar chains, terminal α-galactose, α-fucose, α-N-acetylgalactosamine, and the disaccharide galactose-(β 1 → 3)-N-acetylgalactosamine. The content and distribution of glycoconjugates in the nephron varied only slightly between kidneys from different individuals, but individual variability was extensive in the collecting ducts. The reasons for these individual differences have not been determined, however. Cellular heterogeneity of glycosubstances within the different regions of the human kidney correlates with similar findings in other mammals and implies diverse functional roles for the various types of complex carbohydrates in the kidney.
    Additional Material: 17 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 240 (1994), S. 149-156 
    ISSN: 0003-276X
    Keywords: Cochlea ; Supporting cells ; Morphology ; Ion transport ; Ultrastructure ; Gerbil ; Outer tunnel ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: The mammalian cochlea contains beneath and lateral to outer hair cells, several types of supporting cells. The function of these cells has not been explained beyond providing a structural base.Methods: The supporting cells of gerbil cochlea were examined by electron microscopy with a view to elucidating their biologic activity on the basis of cytologic structure.Results: Ultrastructural examination differentiated the laterally located Hensen cells from their medial neighbor connected to the third Deiters cell. The later cell formed a cover to the outer tunnel between Hensen and Deiters cells, appeared not to reach the basilar membrane, and exhibited a denser cytosol and more mitochondria, compared to Hensen cells. In these respects the cell observed here to cover the outer tunnel, corresponded with the tectal cell described by Henson et al. (1983) in the mustache bat, but not heretofore documented in other animals.Conclusions: This distinctive cell in the gerbil differend in displaying unique villus-like structures which projected from the basomedial surface and are referred to as fimbriae. The fimbriae and interspersed filopodia largely filled outer tunnel space and expanded the cell's basal surface. The amplification of basal plasmalemma by fimbriae and their content of mitochondria testify to a role for the tectal cell in ion resorption and an influence on ion content and volume of outer tunnel fluid. © 1994 Wiley-Liss, Inc.
    Additional Material: 10 Ill.
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  • 9
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Efferent reproductive ducts of male mice, including ductuli efferentes, epididymis, and vas deferens, were fixed and embedded in paraffin, and sections were stained with a battery of lectin-horseradish peroxidase conjugates to localize specific sugars or sugar sequences in glycoconjugates. Cilia and the apical surfaces of ciliated cells in the ductuli efferentes stained intensely with lectin specific for sialic acid and terminal α-N-acetyl-D-galactosamine. Flask cells and clear cells in the epididymis reacted positively and similarly with most lectins used, providing evidence that these cell types are related. In contrast, disparities in lectin staining suggest that flask cells and clear cells are a cell type distinct from principal cells. Basal cells were not present in the ductuli efferentes but formed a continuous layer in the epididymis and vas deferens. Basal cells contained oligosaccharides terminated by sialic acid and α-D-galactose and varying amounts of terminal β-D-galactose and α-N-acetyl-D-galactosamine. Basal cells also stained variably with lectins specific for the core region of complex type N-glycosidic side chains. The basal cells varied structurally, having long spinous apical processes approaching or reaching the lumen in region I of the epididymis and being low cuboidal or squamoid and lacking apical processes in epididymal regions II-V and in the vas deferens. The contiguous nature of the basal cells and the presence of glycoconjugates bearing terminal α-galactosyl residues in all basal cells suggest a possible role for these cells in a regulatory influence on transepithelial movement of fluid and/or ions in the epididymis and vas deferens.
    Additional Material: 10 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    American Journal of Anatomy 159 (1980), S. 307-329 
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Ultrastructural and complex-carbohydrate cytochemical studies were carried out on guinea pig gastric mucosa to assess the histochemical properties of the secretions of different gastric epithelial cells and to investigate the differentiation, origin, and renewal of certain cell types. The observations disclosed heterogeneity or variability of the secretory granules within individual mucigenic cells and zymogen cells. The cytochemical methods also served in characterizing and distinguishing five cell types in the gastric glands, including the isthmus cell, a mucous cell considered comparable to the mucous neck cell, the chief cell, and forms transitional between the isthmus and mucous cells and the mucous and zymogenic cells. The several cell types differed widely in the cytochemical properties of the secretory granules and the apical plasmalemma, and each had a distinctive distribution in the gastric gland. Cytochemical staining observed here provided evidence on synthesis and intracellular metamorphosis of mucous droplets and on formation of glycocalyx.
    Additional Material: 45 Ill.
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