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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 156 (1974), S. 1-20 
    ISSN: 1432-0878
    Keywords: Exocrine pancreas ; Cell membrane regulation ; Coated vesicles, Multivesicular bodies ; Endocytosis ; Autoradiography, Electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Stimulation of secretion by pilocarpine results in a 70% loss of zymogen granules from pancreatic acinar cell during the first hr after injection of the drug. In previous work (Geuze and Poort, 1973), we found that the amount of membrane stored in the surface of the microvilli and of the numerous infoldings present in highly stimulated cells, increases during the first 2 hr and then decreases again during the 3rd hr after stimulation, concurrently with maximal endocytosis of sorbitol-[su14C]. Further observations on the fine structure of stimulated cells at various time intervals after injection of pilocarpine showed that during the first hr numerous smooth vesicles and multivesicular bodies (mvb's) appear in the apical cytoplasm, while the number of coated vesicles and their relative total volume increase significantly 3 hr after stimulation. By infusion of ferritin in the pancreatic duct system in vivo and application of cytochemical techniques (osmium impregnation, electron microscope autoradiography and acid phosphatase cytochemistry) it could be established that after stimulated exocytotic secretion, redundant apical cell membrane is withdrawn by at least two routes: 1) During the initial rapid increase of the amount of apical cell membrane, withdrawal is accomplished by interiorization of luminal invaginations into smooth endocytotic vesicles, which in turn give rise to mvb's by infolding and subsequent fission of their limiting membrane. 2) Once the bulk of stored secretion granules has been discharged, endocytotic coated vesicles become gradually more prominent as carriers for redundant cell membrane. The contents of endocytotic structures ultimately become incorporated in residual bodies, suggesting lysosomal degradation of cell membrane prior to eventual reutilization. Coated vesicles also originate by pinching off from mature Golgi cisternae and condensing vacuoles. A possible function of the coated membranes in the concentration of exportable protein within forming secretory granules is discussed.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 155 (1974), S. 135-154 
    ISSN: 1432-0878
    Keywords: Exocrine pancreas ; Frog ; Ultrastructure ; Intracellular transport ; Autoradiography
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The route by which secretory proteins are transported in the frog exocrine pancreas cell was investigated by an ultrastructural and electron microscope autoradiographic analysis of in vivo 3H-leucine labelled tissue. The ultrastructure of the cell is characteristic of serous epithelial cells and resembles that of mammalian exocrine pancreas cells very closely. Autoradiographic results revealed that the proteins, after being synthesized in the rough endoplasmic reticulum (RER), are transported through the Golgi cisternae to condensing vacuoles which subsequently change into secretory granules. The determination of the timing of this transport was complicated by a very slow turnover of leucine in the frog. Nevertheless, by a semi-quantitative approach, some time characteristics could be estimated: about 11 min after the onset of their synthesis the proteins enter the Golgi system, and about 25 min later the condensing vacuoles. Secretory granules become labelled between 60 and 120 min. These results are discussed, also in relation to the transport route and kinetics in mammalian tissue.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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