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  • Autoradiography  (14)
  • Springer  (14)
  • American Institute of Physics (AIP)
  • 1970-1974  (14)
  • 1974  (14)
Collection
Publisher
  • Springer  (14)
  • American Institute of Physics (AIP)
Years
  • 1970-1974  (14)
Year
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 99 (1974), S. 255-263 
    ISSN: 1432-072X
    Keywords: Mannan Synthesis ; Saccharomyces cerevisiae ; Autoradiography ; Cell Wall ; Yeast
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The combination of high-resolution autoradiography and biochemical methods has been used to ascertain the site of mannan synthesis in the yeastSaccharomyces cerevisiae. High-resolution autoradiography has been performed under conditions when addedd-mannose-3H was incorporated exclusively into mannan. Application of “pulse-chase” labelling technique revealed that the radio-active mannose is fixed primarily in the cytoplasmic space from where it is transported into the cell wall. Additional experiments with separated membrane fractions from the same yeast strongly support the hypothesis that the plasmalemma is not directly involved in the biosynthesis of yeast mannan and that the membranes of the endoplasmic reticulum are the sites where the polymerization of mannosyl units takes place.
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  • 2
    ISSN: 1432-0878
    Keywords: Sea anemone mesoglea ; Collagen synthesis ; Epitheliomuscular cells ; Electron microscopy ; Autoradiography
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Electron microscopy and autoradiography (H3-proline) were used to determine the cell(s) responsible for collagen synthesis and lamination in the mesoglea of the sea anemone, Aiptasia diaphana. Mesogleal collagen is synthesized by the epidermal epitheliomuscular cells which contain much rough endoplasmic reticulum, and secretory vesicles attached to microtubules which cross the basal plasmalemma and anchor in the basement membrane; these cells incorporate large amounts of H3-proline. The mesogleal collagen fibers are non-striated, have clear centers, and a diameter of 200–260 Å; their walls are composed of 65 Å diameter subunit fibrils which appear to be helically oriented. Epitheliomuscular cells rest upon a subepidermal basement membrane which is composed of mesogleal collagen fibers, 65 Å subunit fibrils, and dense granules. This subepidermal basement membrane labels definitively with H3-proline, and is the region where soluble collagen precursors apparently form subunit fibrils which associate to yield mesogleal fibers. The columnar mesogleal collagen fibers are arranged to form layers: the fibers of each layer have the same longitudinal orientation, while those of adjacent layers display an approximate orthogonal arrangement. It is felt that the subepidermal basement membrane is responsible for this organization of mesogleal fibers. Mesogleal amoebocytes do not label with H3-proline and show no ultrastructural evidence of collagen secretion.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 151 (1974), S. 281-292 
    ISSN: 1432-0878
    Keywords: Adrenal cortex ; Mitochondria ; ACTH ; DNA-synthesis ; Autoradiography ; Electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The effects of a chronic ACTH administration (up to 12 consecutive days) on the 3H-thymidine uptake by the mitochondrial compartment of rat adrenal zona fasciculata were investigated by high resolution autoradiography, and compared with the changes in volume and number per cell of these organelles induced by the hormonal treatment. Up to the 9th day of treatment there is a significant increase in the tracer incorporation into adrenocortical mitochondria which is coupled with a significant increase in the volume of the organelles. After 12 days of hormone administration a significant decrease in the 3H-thymidine mitochondrial uptake is found, which is associated with a conspicuous increase in the number of mitochondria per cell and a net decrease in their average volume. The data are discussed in the light of evidence indicating that mitochondria possess a genetic apparatus largely independent of nuclear control. It is hypothesized that ACTH controls the growth and proliferation of adrenocortical mitochondria and that the mechanism of this action of ACTH involves stimulation of the mitochondrial DNA synthesis.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 152 (1974), S. 299-303 
    ISSN: 1432-0878
    Keywords: Post-capillary venules ; Mice ; Pathway of B lymphocytes ; Autoradiography
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Histological observation on the mesenteric lymph node and Peyer's patches of C3H B mice, neonatally thymectomized, lethally irradiated and reconstituted with syngeneic bone marrow cells, showed that a large number of lymphocytes appeared selectively in the restricted territory surrounding the post-capillary venules. Severe depletion of lymphocytes persisted in most of the thymus-dependent areas. Lymphocytes were also observed passing through the walls of the post-capillary venules. Autoradiographic studies on the mesenteric lymph node of recipient B mice 30 minutes after intravenous injection of cells labelled with 3H-uridine and taken from lymph nodes of donor B mice showed that B lymphocytes could penetrate the walls of the post-capillary venules from the blood into the peripheral lymphoid tissues. The post-capillary venules, which are known as the recirculating route of T lymphocytes in normal animals, are thought to be the pathway of migrating B lymphocytes in B mice.
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  • 5
    ISSN: 1432-0878
    Keywords: Hypothalamic neurosecretory system (rat) ; Adrenal cortex ; 35S-cysteine incorporation ; Autoradiography
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The incorporation of 35S-labelled cysteine in the hypothalamic-neurohypophyseal system was studied in normal and adrenalectomized rats and in rats treated with excess hydrocortisone. Labelled cysteine was intraperitoneally administered and grain counts were made of autoradiographs produced from sections of the supraoptic and paraventricular nucleus, median eminence and neurohypophysis of animals killed 45 min., 4 hours and 24 hours after administration of the labelled substance. On the whole, lower incorporation levels of the label were noted in the adrenalectomized rats, compared with the controls. In the rats treated with excess hydrocortisone, the grain counts at 45 min and 4 hours after injection were higher and those at 24 hours were lower than those of the controls. The findings are discussed, among other things, in terms of rate of uptake vs. time and related to previous reports on the cysteine uptake and neurosecretory activity of the hypothalamic-neurosecretory sytem.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 153 (1974), S. 399-413 
    ISSN: 1432-0878
    Keywords: Spinal ganglia (Rat) ; Cell division ; Autoradiography ; Neurone morphogenesis ; Light and electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Pulse labelling with tritiated thymidine was used to determine the time of the final division of the neuroblasts which subsequently form rat lumbar dorsal root ganglion neurones. The final division occurred during a 4 day period, the maximum frequency being on day 12 of gestation. Separation of the ganglion cells into large light neurones and small dark neurones showed that the large light neurones were formed earlier than the small dark neurones. In both cases the final divisions occurred over a period of 3–4 days, but the peak rate of formation of large neurones was on day 12, and that of the small neurones was on day 13. Low power electron micrographs were used to measure mean cell diameter throughout development from day 11 of gestation until a postnatal age of 225 days. A marked increase in cell diameter occurred on day 15–15.5, about 3 days after the final cell divisions of the majority of the cells. The rate of growth increased just before birth, but no increase in mean cell diameter was found between day 21 of gestation and the third day postnatal. The growth was again rapid after this period until a plateau in cell diameter was reached about 33 days after birth.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 150 (1974), S. 443-454 
    ISSN: 1432-0878
    Keywords: Haematopoiesis ; Lymnaea stagnalis ; Amoebocytes ; Autoradiography ; Ultrastructure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary In order to investigate haematopoiesis in the freshwater pulmonate Lymnaea stagnalis, the blood cells and the connective tissue of this snail were studied by light and electron microscopy as well as by autoradiography. In the circulating blood only one type of cell, the amoebocyte, is present. Amoebocytes also occur in the connective tissue (tissue amoebocytes) as single cells, in small groups or in large accumulations. Study of the morphology and ultrastructure of blood and tissue amoebocytes shows that no differences exist between these cells, indicating that L. stagnalis does not possess a well-defined haematopoietic organ. This assumption is supported by the following observations: 1. both blood and tissue amoebocytes can act as phagocytes, 2. blood and tissue amoebocytes both have the capacity to divide (i.e. incorporate tritiated thymidine) and 3. the percentage of dividing cells in the blood and in the connective tissue is the same. These quantitative data indicate furthermore that there is no difference in the relative importance of the blood and the connective tissue in the process of haematopoiesis. Comparison of tritiated thymidine labelled cells with unlabelled amoebocytes showed that these cells do not differ with respect to their morphology and ultrastructure. Moreover, amoebocytes involved in phagocytosis and encapsulation of foreign materials or in wound healing still have the capacity to divide. The percentages of tritiated thymidine labelled amoebocytes in different snails varied considerably. It is suggested that this variation reflects differences in the physiological state of the individual snails.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 154 (1974), S. 443-470 
    ISSN: 1432-0878
    Keywords: Oocytes and T-prospermatogonia ; Rat ; Quantitative analysis ; Autoradiography
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Description / Table of Contents: Zusammenfassung Bei der Ratte findet die sexuelle Differenzierung der Gonade zwischen dem 14. und 15. Tag post conceptionem (p.c.) statt. Während dieser Zeit teilen sich die Oogonien und deren Parallelpopulation—die M-prospermatogonien (multiplying prospermatogonia) oder I-Gonocyten—sehr häufig. Um den 17. Tag p.c. tritt die letzte Generation der Oogonien bzw. der M-prospermatogonien in die Mitose. Die Mitosen bilden häufig “synchronisierte Gruppen”. Die postmitotischen Kerne ihrer Tochterzellen—der Oocyten und der T 1 prospermatogonien (primary transitional prospermatogonia) oder II-Gonocyten—sind klein. Ihr Chromatin ist in Form gröberer Schollen der Kernmembran angelagert. Auf diese Weise kommt das typische “krustenförmige” Aussehen bzw. die Ähnlichkeit mit den Prophasen der Oogonien und M-prospermatogonien zustande. Die Oocyten durchlaufen zunächst die G1-phase (etwa 10 Std Dauer) und treten dann—am Ende des Präleptotänstadiums—in die S-phase. Dann passieren sie die verschiedenen Stadien der meiotischen Prophase und treten vom 3. Tag post partum (p.p.) ab in das Dictyotänstadium. Die T1-prospermatogonien hingegen befinden sich etwa 10 Tage lang in der G1-phase, ohne wesentliche morphologische Veränderungen aufzuweisen. Vom 4. Tag p.p. an durchlaufen sie die S-Phase. Die S-Phasen-Dauer (D-S) beider Zellarten beträgt 11.5 Std und wurde durch Doppelmarkierung mit 14C- und 3H-Thymidin bestimmt. Als am besten geeignete Termine für die Bestimmung der D-S erwiesen sich bei den Oocyten der 18. Tag p.c. und bei den T1-prospermatogonien der 5. Tag p.p. Zu diesen beiden Zeitpunkten war die Anzahl der in die S-phase ein-und austretenden Oocyten bzw. T1-prospermatogonien gleich, die Zellen in S-phase befanden sich im “steady state”. Das Kernvolumen der Oogonien und M-prospermatogonien ist etwa doppelt so groß wie das der postmitotischen Oocyten und T1-prospermatogonien. Bis zum 5. Tage p.p. nimmt das Kernvolumen der Oocyten und T1-prospermatogonien um etwa das Fünffache zu. Der Degenerationsindex der Oocyten liegt wesentlich höher als der der T1-prospermatogonien; er ist postnatal besonders hoch. Aus den T1-prospermatogonien gehen am 4. und 5. Tage p.p. durch Teilung die T 2-prospermatogonien (secondary transitional prospermatogonia) hervor. Die Kerne dieses Zelltyps sind etwas kleiner also die der T1-prospermatogonien. Die T2-prospermatogonien treten am 6. Tage p.p. in die Mitose; es entstehen die ersten A-spermatogonien.
    Notes: Summary In the rat (Wistar-WU) sexual differentiation of the gonads occurs between days 14 and 15 post conception (p.c.). At this time the oogonia and their parallel population — the M-prospermatogonia (I-gonocytes)—divide rapidly. On about day 17 p.c., the last generation of oogonia and M-prospermatogonia, frequently arranged in synchronized clusters, enters mitosis. The postmitotic nuclei of their daughter cells—oocytes and T 1-prospermatogonia (II-gonocytes)—are small; coarse flakes of chromatin are associated with the nuclear membrane causing the typical “crustlike” appearance and the similarity with the prophases of oogonia and M-prospermatogonia. After the oocytes have passed a G1-phase of approximately 10 hr, they enter the S-phase at the end of the preleptotene stage. Then they pass the different stages of the meiotic prophase until they enter the dictyate stage from 3 day post partum (p.p.) onwards. The T1-prospermatogonia, on the other hand, spend a long G1-phase of about 10 days without any conspicuous morphological change before entering the S-phase from day 4 p.p. onwards. The duration of the S-pbase (D-S) of both cell types—oocytes and T1-prospermatogonia—as determined by the double labeling method with 14C- and 3H-thymidine is found to be 11.5 hr. The most favourable time for determining the D-S was day 18 p.c. for the oocytes and day 5 p.p. for the T1-prospermatogonia. On these two days the balance was reached between the cells entering and leaving the S-phase. The nuclear volumes of the postmitotic oocytes and T1-prospermatogonia are approximately half the size of those of their precursors. Until day 5 p.p. the nuclear volumes of the oocytes and T1-prospermatogonia increase about fivefold. The degeneration index of the oocytes is considerably higher than that of the T1-prospermatogonia; postnatally it is especially high. T 2 prospermatogonia arise by mitosis of the T1-prospermatogonia on day 4 and 5 p.p. The nuclei of this cell type are smaller than those of T1-prospermatogonia. T2-prospermatogonia enter mitosis on day 6 p.p and give rise to A-spermatogonia.
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  • 9
    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.
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  • 10
    ISSN: 1432-0878
    Keywords: Retinal projections ; (Tupaia glis) ; Axonal transport ; Synapse ; Autoradiography
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Retinal projections were studied in the tree shrew, Tupaia glis, by means of thaw-mount autoradiography. In this technique, unfixed and unembedded frozen sections are directly mounted on photographic emulsion coated slides. Loss of radiolabeled material through tissue processing is avoided, probably resulting in increased discriminatory sensitivity. Together with multiple injections of precursor cocktail it is possible to demonstrate at the light microscopic level (1) fibers in passage and axon terminals simultaneously, and (2) preferentially labeled axon terminals in the projection field as areas of greater grain density.
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