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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Calcified tissue international 25 (1978), S. 233-240 
    ISSN: 1432-0827
    Keywords: Bone ; Bone resorption ; Albumin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary A fraction (brA), which causes resorption of fetal rat bones in vitro, has been concentrated from bovine serum albumin by anion exchange column chromatography on DEAE Sephadex. This active fraction has also been prepared using DEAE Sephadex A-50 by a batch method with a 0.09M NaCl, 0.1M TRIS buffer, pH 8.35. BrA was 10–30 times more potent than the original albumin. The retained material, which constitutes the bulk of the protein and has less activity than the original albumin, elutes with 0.45M NaCl. Similar treatment of serumα,β or γ globulins does not yield brA. Further enhancement of the bone resorbing activity of brA can be obtained with (NH4)2SO4 fractionation or extraction with CH3OH∶CHCl3. Heating at 55° C for 2 h or at 100° C for 10 min does not affect the activity; overnight incubation with protease destroys the bone resorbing effect. The bone resorbing activity is not removed by dialysis and does not correlate with the protease activity of the fraction. The action of brA is inhibited by 3 mM PO4, 1 μg/ml calcitonin or glucagon, 10−7 M dexamethasone or 0.02 μg/ml actinomycin D. The bone resorbing activity of brA is partially inhibited by 10−7–10−5 M indomethacin. PTH did not elicit bone resorption when added to cultures incubated in chemically defined medium supplemented with 0.1 mg/ml brA. However, brA did not inhibit PTH-induced resorption.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Calcified tissue international 34 (1982), S. 31-36 
    ISSN: 1432-0827
    Keywords: Bone resorption ; Osteoclasts ; A23187 ; Ionophore
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary Morphologic effects of the ionophore A23187 were compared with those of PTH and 1,25(OH)2 vitamin D3 on fetal rat limb bone cultures. All three treatments resulted in loss of bone and the appearance of multinucleate osteoclasts. Only PTH caused proliferation of fibroblast-like cells within the marrow cavity. Cleanly dissected (“stripped”) bones were unresponsive to A23187 and exhibited many dead and dying cells after 48 h in culture with this agent; in contrast, stripped bones were responsive to PTH. All three treatments showed a similar time course of appearance of osteoclasts. The results indicate that all three agents promote osteoclast formation. There are several possible explanations for the differential effects of A23187 and PTH in stripped bones, including the possibility that the cells of the periosteum are required for the action of A23187 but not of PTH.
    Type of Medium: Electronic Resource
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