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  • Lysosomes  (9)
  • Springer  (9)
  • 2015-2019
  • 1975-1979  (9)
  • 1970-1974
  • 1975  (9)
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Publisher
  • Springer  (9)
Years
  • 2015-2019
  • 1975-1979  (9)
  • 1970-1974
Year
  • 1
    ISSN: 1432-072X
    Keywords: Lysosomes ; α-Mannosidase ; Sporangium ; Achlya ; Cycloheximide ; Actinomycin ; Differentiation ; Morphogenesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The present paper describes intracellular changes in α-mannosidase specific activity during Ca++-induced sporangium formation in the water mold Achlya bisexualis. The enzyme, which is concentrated in a cellular fraction with lysosome-like characteristics, undergoes a four-fold increase during sporangium differentiation. Addition of cycloheximide (100 μg/ml) or actinomycin D (10 μg/ml) at any time during the developmental sequence prevents further increase in the enzyme activity. These data suggest that coincident RNA and protein synthesis are essential for the accumulation of enzyme activity. Mixing of cell extracts from different developmental stages provides evidence that activators or inhibitors of the enzyme activity are not responsible for the enzyme activity evident at the different stages.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 164 (1975), S. 279-289 
    ISSN: 1432-0878
    Keywords: Graafian follicle (Rabbit) ; Ovulation ; Ovary surface epithelium ; Lysosomes ; Electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The germinal or surface epithelium covering rabbit Graafian follicles contains occasional small, dark, lysosome-like bodies. After an ovulatory dose of human chorionic gonadotropin (HCG) such bodies gradually increase in size and number. At 8 hr after HCG there is a maximal accumulation in the apical follicle cells; then the dense bodies decrease and just prior to ovulation, 9.5 hr after HCG, only few of them remain in the attenuated surface epithelium. Most of the growing membrane-surrounded bodies probably represent lysosomes, since electron microscopy combined with cytochemistry revealed that many of them contain the lysosomal “marker” enzyme, acid phosphatase. The role of sex steroids and prostaglandins regarding lysosomal growth and labilization is discussed. The close temporal relation between disappearance of the apical surface epithelial lysosomes and disintegration of the underlying tunica albuginea gives further support to our working hypothesis that at least part of the “ovulatory enzymes” emanate from the surface epithelium. The technical assistance of Miss Ingalis Fransson, Miss Kerstin Nilsson and Mrs. Ulla-Britt Westman is greatly appreciated.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 163 (1975), S. 373-382 
    ISSN: 1432-0878
    Keywords: Parotid gland (rat) ; Isoprenalin stimulation ; Acid phosphatase ; Lysosomes ; Endocytosis of ferritin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Distribution of acid phosphatase as a marker enzyme for lysosomes was investigated in the isoprenalin stimulated rat parotid gland. The enzyme was localized in lipofuscin-like bodies as well as in non-discharged granules. The appearance of these bodies was correlated in time to the appearance of smooth vesicles and reduction of the acinar lumen. Ferritin, used as a tracer and introduced into the stimulated gland via cannulated parotid ducts, was found in smooth vesicles, vacuoles and lipofuscin-like bodies throughout the cytoplasm of the acinar cells. Very often ferritin-containing vesicles were found in the vicinity of the Golgi complex. In most cases the vesicles containing ferritin also showed acid phosphatase reaction product. A possible correlation between the lysosomal system and the process of recycling and degradation of membranes in the stimulated gland is discussed.
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  • 4
    ISSN: 1432-0878
    Keywords: Metaphyseal bone (Guinea pig) ; Osteogenic cells ; Lysosomes ; Alkaline phosphatase ; Electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary A transmission electron microscopic study of demineralized, methaphyseal bone of the young guinea pig is presented. Special attention is paid to the lysosomal system of the different cell types. Visualization of acid phosphatase and aryl sulfatase activity was used to identify tissue components as belonging thereto. The distribution of alkaline phosphatase activity, a plasma membrane marker, was also examined. Osteoblasts were distinguished by a marked development of the granular endoplasmic reticulum and the Golgi complex. Perivascular cells type A, morphologically resembled the osteoblasts, and are believed to represent an early stage in the specialization of the latter. A few lysosomes were normally found in the osteoblasts; they were less common in the type A cells. In contrast to their regular occurrence in guinea pig epiphyseal cartilage, dense bodies of lysosomal nature (“type I vesicles”) were only rarely seen in the bone matrix. Structures analogous to the type II vesicles in cartilage were, however, normally present. Their membrane showed activity of alkaline phosphatase. Possible functions of lysosomes and matrix vesicles in osteogenesis are discussed. Perivascular cells type B and chondroclasts both contained a prominent Golgi complex and large numbers of free ribosomes, mitochondria and lysosomes. In the type B cells, inclusion material of varying appearance often occurred in the lysosomes and in endocytic vesicles. The chondroclasts sometimes presented a ruffled border, with associated vacuoles and lysosomes in the subjacent cytoplasm. It is suggested that both cell types participate in the resorption of the epiphyseal cartilage. Chondroclasts presumably arise by fusion of type B cells and/or monocytic precursors from the peripheral blood. The skilled technical assistance of Mrs. Eva Lundberg and the secretarial assistance of Mrs. Inger Åhrén are gratefully acknowledged. The authors are indebted to Dr. Stanislaw Moskalewski for constructive criticism of the manuscript.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 156 (1975), S. 301-315 
    ISSN: 1432-0878
    Keywords: Metaphyseal bone (Guinea pig) ; Osteogenic cells ; Endocytosis ; Lysosomes ; Electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Guinea pig metaphyseal bone was exposed to horse spleen ferritin in vitro and to colloidal thorium dioxide in vivo. The cellular uptake and intracellular accumulation of these marker particles were studied ultrastructurally. In vitro, the ferritin molecules were found to spread evenly throughout the tissue. After 1–2 hours ferritin was mainly found in plasma membrane invaginations and in endocytic vesicles of varying size. At 4–6 hours a successive accumulation of the marker in secondary lysosomes could be observed. In addition to ferritin, the lysosomes and the large endocytic vesicles often contained other inclusions. In vivo, the pattern of intracellular accumulation of the marker particles was identical to that in vitro. Moreover, the presence within the cells of similar amounts of thorium dioxide after 1 and 4 days suggested that these indigestible molecules are stored intracellularly for a considerable time. In accordance therewith there were no definite signs of extrusion of labeled bodies or secretion of the exogenous marker by exocytosis. Ferritin and thorium dioxide were taken up by all cell types in the metaphysis. Both in vitro and in vivo perivascular cells type B ingested large amounts of marker particles, whereas chondroclasts, endothelial cells, perivascular cells type A and osteohlasts showed a more restricted endocytizing ability. On the basis of these observations, the functional significance of different cell types in the resorption of the epiphyseal cartilage and the formation of bone is discussed. The skilled technical assistance of Mrs. Eva Lundberg and the secretarial assistance of Mmes. Ulla Linder and Diane Setchell are gratefully acknowledged. The author is also indebted to Dr. Ulf Friberg and Dr. Stanislaw Moskalewski for constructive criticism of the manuscript.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 161 (1975), S. 541-553 
    ISSN: 1432-0878
    Keywords: Corpora lutea (Rabbit) ; Endocytosis ; Peroxidase ; Lysosomes ; Electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Horseradish peroxidase (HBP) was injected directly into the corpora lutea of rabbits on different days of pseudopregnancy. Young luteal cells have also been incubated “in vitro” in a medium containing horseradish peroxidase. In the “in vivo” experiments the 5 to 9 days old luteal cells take up far more horseradish peroxidase than the older ones (14–20 days). Different types of endocytic vacuoles, MvB's and also some DB's are already peroxidase positive shortly (15–20 min) after injection of the tracer. In the “in vitro” experiments the cells are more heavily loaded. The normal morphology of pale, dense and terminal MvB's is also described and staining with PTA at low pH provides further information on changes occurring in the MvB's. The various findings on multivesicular bodies are compared and two possible pathways for endocytic vacuoles are proposed: one to DB's the other to MvB's. The related phenomena of the uptake of material and the internalization of plasma membrane are discussed in the light of the possible function of endocytosis in luteal cells.
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  • 7
    ISSN: 1432-0878
    Keywords: Chondrocytes (Fetal guinea pig) ; Endocytosis ; Lysosomes ; Formation of cartilage ; Matrix vesicles
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Chondrocytes isolated from fetal, guinea-pig epiphyses were grown in monolayer culture, exposed to thorium dioxide particles, and studied ultrastructurally after varying intervals. The exogenous marker was ingested by endocytosis and subsequently accumulated in lysosomes. After intramuscular injection into young guinea pigs, the thorium dioxidelabeled chondrocytes formed a typical hyaline cartilage. This consisted mainly of rounded or polygonal cells with large, eccentrically located nuclei. The cytoplasm showed an extensive granular endoplasmic reticulum and a well-developed Golgi complex, suggesting active synthesis and secretion of matrix components. Among the other cytoplasmic organelles, lysosomes containing variable amounts of marker particles were observed. After 2–3 weeks the transplants showed signs of cellular degeneration and disintegration. During these processes, lysosomes remained structurally intact and, furthermore, retained the incorporated marker. Thus, thorium dioxide-labeled bodies were found in former chondrocyte lacunae and in the intercellular substance proper. In the latter location labeled bodies could be observed in close proximity to early mineral deposits. These results are discussed with special reference to the cellular origin and lysosomal nature of matrix vesicles in calcifying cartilages. The skilled technical assistance of Mrs. Eva Lundberg and Miss Karin Askfors and the secretarial assistance of Mrs. Ingrid Wäälma are gratefully acknowledged.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 156 (1975), S. 359-376 
    ISSN: 1432-0878
    Keywords: Mouse-liver ; Human-IgG ; Lysosomes ; Fluorescent antibody technique ; Electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary 1. Human IgG is stored in the form of remarkable droplets in the cytoplasm of mouse hepatocytes following intravenous injection. 2. The earliest protein uptake occurs within 1 minute after injection and droplets can be found up to 32 hours thereafter; 64 hours p.i. the foreign protein is no longer visible in hepatocytes. 3. Electron microscopy reveals that the uptake occurs by a process of “macropinocytosis”. The resulting protein droplets fuse with primary lysosomes and are transformed into phagolysosomes. 4. At the same time as the phagolysosomes are formed the IgG-droplets loose their immunological activity-as early as 2 hours after injection.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 157 (1975), S. 217-225 
    ISSN: 1432-0878
    Keywords: Ganglia ; Neurons ; Pigmented granules ; Acid phosphatase ; Lysosomes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The organization of the ganglia and the ultrastructure of the neurons of Bulla gouldiana are similar to those described for other molluscs. Acid phosphatase positive reactions were found in the large pigmented granules, small dense bodies, multivesicular bodies, and Golgi lamellae and associated vesicles. The small dense bodies and multivesicular bodies may be stages in the formation of the larger pigmented granules which are interpreted as lysosomes. Comparison is made between the pigmented granules in Bulla and the lipofuscin bodies of vertebrate neurons. The possible involvement of these pigmented granules in the hyperpolarization of Bulla and Aplysia neurons to light is discussed.
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