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  • 1
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 207 (1983), S. 539-546 
    ISSN: 0003-276X
    Schlagwort(e): Life and Medical Sciences ; Cell & Developmental Biology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Medizin
    Notizen: The tridimensional structure of rough endoplasmic reticulum was examined with both high and low voltage electron microscopes in large ventral horn cells of rat spinal cord, by combining stereoscopic techniques with the use of thick sections selectively impregnated with heavy metal salts. In all neurons examined Nissl bodies appeared as well defined clusters of densely stained and profusely anastomosed plate-, ribbon-, and thread-like cisternae. Plate-like cisternae were variable in size, often showed a shallow curvature, and usually ran in short parallel arrays, separated from one another by fairly constant intervals. All gave rise at their edges to several ribbon-like extensions which occasionally decreased in width distally, turning into thin, thread-like cisternae. Characteristically, these ribbon-like structures would emerge at an angle from their plate of origin and smoothly curve away from the plane of the plate to merge with ribbons or threads arising from adjacent or more distant plates. Most plate-like cisternae were found at the periphery of Nissl bodies and tended to be oriented parallel to their surface. In contrast, the center of Nissl bodies was almost exclusively occupied by a complex network of ribbon-and thread-like cisternae. It is suggested that the basic plate/ribbon association here described in spinal motoneurons might be a constant feature of Nissl body architecture in various neuronal types, while the size, orientation, and relative proportion of plate-like cisternae may vary according to the metabolic state and/or functional specialization of the cells.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 243 (1995), S. 283-293 
    ISSN: 0003-276X
    Schlagwort(e): Secretion pathway ; Yeasts species ; Golgi apparatus ; Secretion granules ; Life and Medical Sciences ; Cell & Developmental Biology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Medizin
    Notizen: Background: In the yeast Saccharomyces cerevisiae, the Golgi apparatus consists of discrete units distributed throughout the cytoplasm. When such units are examined in three dimensions, in relatively thick sections prepared for the electron microscope, they usually appear as small tubular networks with a stained material accumulating in dilations located at the junctions of membranous tubules. To see whether such tubular networks are observed in other yeast species, the three-dimensional structure of organelles in eight additional yeast strains, endowed with diverse biological properties, are examined.Methods: Yeast strains were grown at 24°C in YPD medium (2% Bactopeptone, 1% Bactoyeast extract, and 2% glucose). Cells that were examined by electron microscopy came from exponentially growing cultures grown in a shaking water bath and maintained at a OD 600 (optical density at 600 nm) of 0.5. Cells were fixed in a fixative containing 2% glutaraldehyde in 0.1 M cacodylate buffer pH 7.4 and 0.8 M sorbitol. They were then treated for 15 min in 1% sodium metaperiodate and postfixed for 1 hr in potassium ferrocyanide-osmic acid. They were preembedded in agarose prior to dehydration and finally embedded in Epon. In these conditions, the preservation of cell organelles was improved and the cytoplasmic retraction from the cell wall was minimized. Photographs of sections tilted at ± 15° from the 0° position of the goniometric stage were used to prepare stereopairs from which the three-dimensional configuration of the organelles was visualized.Results: In all yeast strains, tubular networks appeared as separate elements or units dispersed throughout the cytoplasm. Each unit consisted of anastomosed membranous tubules. In some strains such as Saccharomyces cerevisiae, Zygosaccharomyces rouxii, or Saccharomyces pombe, such units appeared mainly as polygonal networks of intensely stained membranous tubules. Along these networks, distensions filled with stained material were similar in size to nearby secretory granules, suggesting that the latter formed by fragmentation of the tubular networks. In Hansenula polymorpha, Pichia pastoris, and Debaryomyces hansenii, networks of anastomosed tubules were closely superposed to each other and formed parallel arrays reminiscent of the stacks of Golgi saccules seen in mammalian cells. However, in contrast to what is usually found in the latter, the layers making up the parallel arrays in yeasts, were clearly continuous to each other. In other strains, i.e., Kluyveromyces lactis, Candida albicans, and Candida parapsilosis, the situation was intermediate and their cytoplasm contained only arrays of small size with two or at most three superposed layers of membranous tubules. Small vesicles in the 30-50 nm range were rarely encountered in most yeast strains.Conclusions: It is therefore concluded that tubular networks, presumably Golgi in nature, are present in all yeasts examined so far. Yet, in some strains, these tubular networks may be arranged in parallel arrays or stacks. © 1995 Wiley-Liss, Inc.
    Zusätzliches Material: 20 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 232 (1992), S. 25-35 
    ISSN: 0003-276X
    Schlagwort(e): Life and Medical Sciences ; Cell & Developmental Biology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Medizin
    Notizen: In order to analyse, at the electron microscope level, the three-dimensional configuration of the trans compartment of the Golgi apparatus rat dorsal root ganglia were treated to demonstrate cytidine monophosphatase (CMPase) activity. The localization of enzymatic activity in the Golgi apparatus varied according to cell types. In type A and C cell, CMPase was exclusively located in the transmost sacculotubular element, whereas in type B cells all the saccules of the stacks forming the Golgi ribbon and the trans-Golgi networks were impregnated. Numerous dense bodies seen at proximity were also CMPase positive. In 3 μm thick sections of type A cells examined at low magnification, the impregnated element was scattered throughout the cytoplasm and never formed a continuous structure. In type B cells, the strongly reactive trans-Golgi networks did not follow the entire length of the impregnated Golgi ribbon but were preferentially located in the concavity of its arched portions. At higher magnification and in all cell types some tubular portions of the trans-Golgi networks took the apperance of spheroidal cage-like structures, the CMPase positive anastomotic tubules forming the bars of the cage. Anastomotic tubules separated from the trans-Golgi networks formed fenestrated spheres, while nearby CMPase-reactive dense bodies exhibited a paler hilus. These observations were taken to indicate that in ganglion cells, some CMPase positive dense bodies, presumably lysosomes, formed by fragmentation of the trans-Golgi networks.
    Zusätzliches Material: 16 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    American Journal of Anatomy 151 (1978), S. 191-211 
    ISSN: 0002-9106
    Schlagwort(e): Life and Medical Sciences ; Cell & Developmental Biology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Medizin
    Notizen: The endoplasmic reticulum (ER) was stained selectively by a sequence of uranyl acetate, lead and copper citrate, according to the method of Thiéry and Rambourg ('76), and then investigated in 0.5 to 2.0-μm-thick sections with the transmission electron microscope. Examination of photographic stereopairs allowed a three-dimensional visualization of the ER at various steps of spermiogenesis.During the Golgi and cap phases of spermiogenesis (steps 1-7, classification of Leblond and Clermont, '52a), the ER is distributed throughout the cytoplasm as a three-dimensional network of spherical and tubular cisternae connected by narrow tubules. In addition, a close network of tubular cisternae is located along the convex surface of the Golgi apparatus and lines the plasma membrane. Where the cell membrane joins that of another spermatid to form an intercellular bridge, this network extends across the bridge.During the acrosome phase (steps 8-14), the cytoplasm contains an abundant ER that shows the following modifications: (A) Along the inside and outside of the caudal tube the cisternae form long tubes or plates which run adjacent and parallel to the microtubules. These cisternae are connected by delicate lateral anastomoses; (B) Along the flagellum the ER forms a “fenestrated sleeve” made up of a close network of tubular cisternae; (C) Similar networks are organized as “fenestrated spherules” enclosing large vesicles seen throughout the cytoplasm; (D) At a short distance from the flagellum, the ER cisternae are continuous with a stack of annulate lamellae and an aggregate of radially arranged collapsed cisternae called the “radial body”.During the last or maturation phase (steps 15-19), the ER regresses. Thus, during the final steps in the formation of the flagellum, the ER network fragments and then most of the cisternae disappear from the cytoplasm. The “radial body” is the last element of the ER to be dissolved. Thus the ER undergoes extensive structural modifications during spermiogenesis, suggesting an active contribution of this organelle to the differentiation of the spermatid into a spermatozoon.
    Zusätzliches Material: 16 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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