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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 710 (1994), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Anatomy and embryology 128 (1969), S. 318-328 
    ISSN: 1432-0568
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Die meisten Capillarendothelien der Hypophysenvorderlappen bei Ratten und Kaninchen zeigten auch bei wiederholter Injektion keine Vitalfärbung mit Lithiumcarmin oder Tusche, dagegen ließen sich die meisten pericapillären Zellen mit den sauren Farbstoffen, besonders mit Trypanblau, stark anfärben. Bei elektronenmikroskopischer Untersuchung findet man wenige Lysosomen im Cytoplasma der Capillarendothelien; auch ist an ihnen eine Reaktion auf die Vitalfärbung nicht deutlich zu beobachten. Die pericapillären Zellen erscheinen nach den wiederholten Injektionen des Vitalfarbstoffes vermehrt und enthalten viele kleine oder große Lysosomen im Cytoplasma; die meisten von ihnen stimmen vielleicht mit den pericapillären Histiocyten überein. Auf Grund dieser Befunde vertreten wir die Ansicht, daß die Capillarendothelien des Hypophysenvorderlappens aus der Kategorie des reticuloendothelialen Systems ausgeschlossen werden sollten. Es sind pericapilläre Histiocyten, die bei der Vitalfärbung mit sauren Farbstoffen stark hervortreten. Die Capillarendothelien haben viele Poren, die durch ein dünnes Diaphragma gedeckt werden. Das Diaphragma ist nicht trilamellar, sondern monolamellar und hat in seinem Zentrum eine ringartige Struktur. Deren Gesamtdurchmesser beträgt ca. 200 Å und ihr Durchmesser im Lichten ca. 70 Å.
    Notes: Summary Most capillary endothelial cells of the anterior pituitary of rats and rabbits are not vitally stained by acid dyes and india ink, while the pericapillary cells are intensively stained by acid dyes, especially by trypan blue. In electron micrographs, capillary endothelial cells have few lysosomes in their relatively scanty cytoplasm. These cells do not react markedly to repeated injections of acid dye whereas most pericapillary cells are increased in number and size after repeated injections of acid dye and show numerous lysosomal structures in the cytoplasm. These cells are considered to correspond to the acid dye-accumulating pericapillary cell observed by light microscopy. From these facts, the present authors emphasize that the capillary endothelial cell of the anterior pituitary should be excluded from the reticulo-endothelial system, as it is a pericapillary histiocyte that is stained vitally by acid dyes. The capillary endothelium has numerous fenestrae of 500 Å diameter, closed by a thin diaphragm. The diaphragm is not trilaminar but mono-layered and there is a dense ring-like structure in its central area. The overall diameter of the ring-like structure is about 200 Å and the light center is about 70 Å in diameter. It is suggested that the highly organized structures of the diaphragm may relate to the passage of substances such as acid dye from the capillary lumen into the pericapillary space.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-0568
    Keywords: Interrenal tissue ; Chick embryo ; Freeze fracture ; Intercellular junction ; Macula occludens
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The fine structural development of the intercellular junctions in the interrenal tissue of chick embryos and hens was studied using freezefracture and thin section images. In thin sections, junctional complex-like structures consisting of desmosomes and gap junctions are already seen between the interrenal cells in the 8 day-old embryo. In the freeze-fracture image, small gap junctions are already present between the interrenal cells of 8–10 day-old embryos. After 11 days of incubation, two types of gap junctions are noticeable; type I belongs to a common kind of the gap junction and type II is made of a group of many small rectangular or oval gap junctions and has an irregular meshwork configuration. Incomplete maculae occludentes, consisting of only a few linear arrays of membrane particles thought to be derived from type II gap junctions, appear on the plasma membrane around 15 days of incubation. Typical maculae occludentes belonging to a so-called “inverted type” are distinctly seen around 21 days. In view of the fact that the cell arangement of the interrenal tissue in the early stage of development is somewhat similar to that of a tubular gland, and that the macula occludens exists in the older embryo and adult hen, it is considered that the interrenal cell of this animal retains more or less an epithelial property originating from the mesodermal epithelium. No zonulae occludentes are recognizable between the interrenal cells throughout all the stages from embryo to adult.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Anatomy and embryology 152 (1978), S. 243-259 
    ISSN: 1432-0568
    Keywords: Oviduct epithelium ; Fine structure ; Cytodifferentiation ; Ciliogenesis ; Aging
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The fine structure of the oviduct epithelium of the newborn to the old mouse was studied with an electron microscope. Just after birth, epithelial cells lining the ampulla of the mouse oviduct are simple columnar in shape and of one type in fine structure. They contain numerous free ribosomes, an extremely poor rough endoplasmic reticulum, and a small Golgi complex. In the 3-day-old mouse, the epithelial cells are differentiated neither into ciliated nor secretory cells, and are characterized by the appearance of many autolysosomes and a solitary cilium. The ciliary cells differentiates 5 days after birth. Ciliogenesis is frequently observed at 5–10 days. The important role of the fibrous granules for ciliogenesis and that of the Golgi apparatus for membranogenesis of the cilia are described and discussed. The secretory cell having mucous secretory materials is differentiated at 23 days. In the epithelial cell lining the ampulla of the aged (22 to 24-month-old) mouse oviduct, large autolysosomes and vacuoles 2–6 μm in diameter occur in the ciliated cell, though cilia and other cell organelles are well preserved. In the old mouse the secretory granules almost disappear and the rough endoplasmic reticulum is strikingly dilated in the secretory cell. No features showing the transformation between the secretory cell and the ciliary one are seen in the mouse oviduct.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Anatomy and embryology 142 (1973), S. 267-281 
    ISSN: 1432-0568
    Keywords: Adrenal cortex ; Human embryo ; Cytodifferentiation ; Mitochondria ; Smooth endoplasmic reticulum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Adrenal glands of early human embryos from 20 to 150 mm (CRL) were examined with the aid of the electron microscope. 1. The outer-zone cells of these embryos were somewhat smaller than the inner-zone cells and contained club-shaped or oval mitochondria with laminar or tubular cristae in the cytoplasm. The mitochondria in the inner-zone cells were also round, oval or club-shaped; their cristae are generally tubular or laminar in 20-, 21- and 22 mm embryos, and tubular or vesicular in 68-, 78-, 95-, 115-, and 150-mm embryos. With advancing cytodifferentiation, mitochondria tended to become larger and round in shape. The mitochondrial cristae in the cortical cell were considered to be transformed from the laminar type to the tubular one and then to the vesicular one with advancing functional differentiation. 2. The elements of endoplasmic reticulum were very poor, and numerous free polysomes were distributed throughout the cytoplasm in the outer-zone cells of these embryos. Especially in 68-, 78-, 95-, 115-, and 150-mm embryos, small areas of the cytoplasm contained parallel, regularly arranged lamellar rough endoplasmic reticulum. The end of the rough element was continuous with the tubule of smooth endoplasmic reticulum. The elements of smooth endoplasmic reticulum are thought to be derived from those of rough endoplasmic reticulum. A few inner-zone cells of embryos 20–22 mm in length and most inner-zone cells of embryos 68–150 mm in length contained small areas of lamellar profiles of rough endoplasmic reticulum in a parallel arrangement in the cytoplasm. The end of each element was related to that of smooth tubular endoplasmic reticulum. The tubular smooth endoplasmic reticulum occupied most of the cytoplasm in some inner-zone cells of embryos 20–22 mm in length and in most cells of embryos 68–150 mm in length. 3. Lipid droplets were very few in both inner- and outer-zone cells of these embryos. 4. Glycogen particles were abundant in both outer- and inner-zone cells of the early embryo, and reduced in quantity with advancing cytodifferentiation. In embryos 95\2-150 mm in length glycogen particles were difficult to find in the cortical cell. 5. Small dense bodies and coated vesicles were often seen in or near the Golgi region of the inner-zone cell at all embryonic stages.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Anatomy and embryology 125 (1966), S. 132-151 
    ISSN: 1432-0568
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Normal thyroid glands of White-Leghorn chick embryo, ranging in age from 6 to 17 days of incubation were studied with the light as well as electron microscope. 1. By light microscopy, the thyroid tissue from 6 to 10 days of incubation consists of the epithelial cell cord and the loose mesenchyme, and the PAS-positive droplets begin to be found distinctly throughout the epithelial cell cord in a 9 day-old embryo. 2. By electron microscopy, the thyroid cell of a 7 day-old chick embryo is characterized by numerous abundant polysomes. Though a few mitochondria and small Golgi area are noticed, the rough-surfaced endoplasmic reticulum is very poor. This structure is developed more and more with increase of incubating days. 3. In an 8 day- (rarely in a 7 day-) old embryo, the primitive follicle lumen appears between two epithelial cells. Fairly long microvilli are well developed and a terminal bar forms a ring at the edge of the lumen. Around the lumen are numerous small vesicles considered to be derived from the Golgi field. The developmental endoplasmic reticulum, the Golgi apparatus lying near the lumen, numerous vesicles which might be derived from the Golgi region, a central flagellum projecting from the epithelial cell, and an appearances of the terminal bar are considered to be important elements in making up the primitive follicle lumen. In a few cases, the primitive follicle lumen has a shallow intracellular bay or extension which could be interpreted as an intracellular follicle lumen. 4. A few small dense granules suggesting lysosomes appear at 8 days (rarely at 7 days) of incubation in or near the Golgi region. 5. A few large intracellular less dense droplets are first found near the primitive follicle lumen at 10 days of incubation. It is not yet solved whether this droplet is a secretory substance or a resorbed one. 6. By mitosis of the epithelial cells and fusion of the follicle lumens, the primitive follicle lumen enlarges with increase of days. The loose mesenchyme begins to penetrate into the epithelial cell cord to make up each follicle at 10–11 days of incubation, and the typical follicle is mostly completed at 14 days of incubation. 7. All the mesenchyme cells including the endothelial cell and connective tissue cell are characterized by abundant polysomes and poorly developed cytomembrane system. The rough-surfaced endoplasmic reticulum is developed more and more with incubating days in the endothelial as well as connective tissue cells. Rerely, a round cell, high in electron density, suggesting an erythroblast is seen in contact with the endothelial cell in 7–9 days old embryos.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1432-0568
    Keywords: Liver ; Sinusoid ; Kupffer cell ; Phagocytosis ; Rabbit
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The fine structure and functional properties of Kupffer's stellate cells and endothelial cells of the hepatic sinusoid of normal and experimental rabbits were studied using light as well as electron microscopy. (1) By light microscopy, it is clear that only the Kupffer cell ingests erythrocytes injected, while the endothelial cell is almost flattened, even after short-term (3 days) or long-term (10, 22 days) injection of a large dose of heterogenous erythrocytes. Both types of cell are easily distinguishable from each other in the liver of the saline solution-perfused animal. The numerical ratio of Kupffer cells to endothelial cells in normal and experimental animals is always constant (about 4:6). (2) Electron microscopically, the Kupffer cell is characterized by welldeveloped cytoplasmic protrusions such as numerous microvilli and pseudopods, while the endothelial cell is almost flat and smooth on its surface. All the Kupffer cells take up the heterogeneous erythrocytes injected, by phagocytosis. There is a distance of 20–30 nm between the plasma membrane of the Kupffer cell and that of the phagocytized erythrocyte, when the erythrocyte is caught by the Kupffer cell. Filamentous dense materials suggesting fuzzy coats of both plasma membranes are seen in the space. The Kupffer cell cytoplasm in contact with the erythrocyte sometimes shows microtubules running parallel or obliquely to the plasma membrane. No infiltrations of lymphocytes and plasma cells are observed in the liver of the experimental animals. No phagocytotic features are seen in any of the endothelial cells, though coated pits, small vesicles, and small lysosomelike dense bodies are found to be increased in number in the long-term erythrocyte-injected animal. (3) Staphylococci aureus, when injected, are also phagocytized by the Kupffer cell in the same way as erythrocytes and fuse with lysosomes in the cytoplasm. (4) Injected India ink particles are ingested into the coated pits of both types of cell by micropinocytosis. These coated pits become smooth vesicles and fuse with one another to form large vacuoles containing the India ink particles in the cytoplasm. (5) Both Kupffer cell and endothelial cell are stained with vital dyes, which are also considered to be ingested by micropinocytosis. (6) From the above facts it is concluded that the Kupffer cell is not derived from the endothelial cell. Both types of cell have a micropinocytotic activity, and only the Kupffer cell has a phagocytotic activity; neither India ink injection nor vital staining of the acid dye are suitable methods for detecting this phagocytotic activity. The hepatic sinusoidal region might not be a site where immunological reactions take place, though the blood stream is here cleansed of foreign materials and bacteria.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Histochemistry and cell biology 43 (1975), S. 283-290 
    ISSN: 1432-119X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Intracellular dense bodies, cytoplasmic matrices, and luminal colloids in the thyroid follicle of cyclostomes, hagfish and lamprey were examined to identify the distribution of iodine using an energy dispersive X-ray microanalyzer attached to a scanning transmission electron microscope. High level of iodine was detected only in the large dense body of the hagfishes, while it was too slight in quantity to detect by this method in the cytoplasmic matrix as well as in the luminal colloid. In the adult lamprey thyroid, an appreciable amount of iodine was detected in a few large dense bodies. In mice and rats, it is very hard to detect iodine in the luminal colloid, intracellular colloid droplet, and in the lysosomal dense granule by this method, though these structures have been well known to contain a fairly large amount of iodine which is combined with thyroglobulin. These facts mean that intracellular dense bodies in the thyroid follicular epithelium of the cyclostome, especially of the hagfish have an extremely larger amount of iodine. These bodies are considered to be secondary lysosomes or residual bodies containing reabsorbed colloid materials which are highly condensed.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Histochemistry and cell biology 51 (1977), S. 321-326 
    ISSN: 1432-119X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The adenylate cyclase activity in the theca folliculi of the mouse Graafian follicle was investigated using the electron microscopic cytochemistry. Deposits of reaction product are recognized on the plasma membrane of the fibroblast, theca cell and transitional cell from the fibroblast-like cell to the theca cell (partially or incompletely differentiated theca cell) after incubation with adenylyl-imidodiphosphate (AMP-PNP) as an effective substrate for adenylate cyclase. This fact indicates that these cells have the receptor on the plasma membrane, and the adenylate cyclase-cyclic AMP system is important for the steroid secretion or the collagen fiber production. It is difficult to clarify by this method the relationship between the adenylate cyclase activity and the functional differentiation of the theca cell.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Histochemistry and cell biology 38 (1974), S. 5-18 
    ISSN: 1432-119X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary An endogenous peroxidase activity is demonstrated in acinar cells of the salivary gland and epithelial cells of the colonic crypt of normal rats and mice using electron microscopic histochemistry. The main site of the enzymatic activity is cisternae of the rough endoplasmic reticulum including those of the nuclear envelope, while the intensity of the activity is greatly variable among cell types. Some vesicular and cisternal elements of the Golgi apparatus and secretory granules exhibit the reaction, but it is not consistent in all cells with the peroxidase-positive endoplasmic reticulum. It is very interesting that the peroxidase activity is positive in the rough endoplasmic reticulum-Golgi complex-secretory granule system (EGG system) of the cells located at the beginning and the end of the digestive tract. This suggests a peroxidase-dependent anti-infectious mechanism. Some large and small membrane-limited non-secretory granules and mitochondria also reacted.
    Type of Medium: Electronic Resource
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