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  • 1
    ISSN: 1600-0765
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Culture filtrate of Bacteroides gingivalis was tested in vitro for its effect on the proteoglycan synthesis (35S-sulfate incorporation) of chick embryonic chondrocytes. The chondrocytes were cultured in high density aggregates. The culture medium (M 199 with 10% fetal calf serum) was supplemented with 20% culture filtrate, 20% heat inactivated culture filtrate (100°C, 10 min), or 20% of a low molecular fraction (M 〈 1000) of the culture filtrate. Control aggregates were cultured with 20% bacterial medium added to the culture medium. Exposure of chondrocytes to culture filtrate resulted in a rapid reduction of the synthesis of proteoglycans within 5 hours. After 24 hours of culture proteoglycan synthesis was decreased by 80%. The small amount of proteoglycans still synthesized was mainly deposited into the medium whereas in control aggregates most proteoglycans were deposited around the cells. Protein synthesis was not changed and DNA synthesis was slightly increased by the culture filtrate. When after 24 hours of culture the medium with culture filtrate was replaced by control medium, this resulted in a rapid and total repair of the proteoglycan synthesis. The effect of culture filtrate on the proteoglycan synthesis did not change after heat inactivation or using the low molecular fraction, indicating that small, non-proteinous molecules are responsible for the described effects.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1420-9071
    Keywords: Quail chorio-allantoic-membrane ; shell-less cultures ; chimera-technique
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary A technique is described for in vitro culture of the quail embryo from the 1st to the 18th day of development. The embryos are cultured in Teflon hammocks, suspended in glass supports and kept in a humidified atmosphere at 36.5°C. The quail CAM is used as support and cell source for developing non-quail cartilage and bone. The quail cells can be identified histologically and easily recognized by Feulgen-staining which is demonstrated in the presence of quail chondro- or osteoclasts in a mouse long bone rudiment cultured on the CAM.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1572-9699
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 98 (1979), S. 299-306 
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Intermittent compressive (IC) forces (96 mm Hg, 0.3 Hz) inhibit by 35-60% the serum stimulated increase in ornithine decarboxylase activity (ODC) in chick embryo epiphyseal cartilage cells and rat chondrosarcoma cells. IC had no effect on mouse fibroblast L-cells ODC. The dose-response pattern of the IC effect indicated an all-or-none response with a threshold at 80 mm Hg, a pressure roughly equivalent to the in vivo weight bearing force. The km of the cartilage cell ODC, measured at four hours, was about 0.1 mM and was not affected by IC. The Vmax, on the other hand, was significantly reduced by IC which is consistent with less enzyme or non-competitive inhibition. IC also produced a significant increase in cAMP levels in both cartilage explants and isolated cells in the presence and absence of serum and a significant reduction in 3H-thymidine incorporation into DNA. The findings show that cellular cAMP, on one hand, and ODC and DNA synthesis, on the other hand, change in opposite directions following exposure to serum and/or IC. Investigation of the IC effect on DNA synthesis in serum-deprived synchronized cartilage cells revealed that IC reduced the number of cells going into S but did not lengthen the G1 phase. Exposure to IC early in G1 (0-13 hours) produced the full effect, whereas IC application between 13 to 24 hours (pre S) had no effect. IC had no effect on 3H-thymidine incorporation in L-cells.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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