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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Inflammation research 25 (1988), S. 360-367 
    ISSN: 1420-908X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract α2Macroglobulin is a proteinase inhibitor which is converted from its native form into an electrophoretically “fast” form by reaction with a proteinase or methylamine. All α2M “fast” forms bind to a specific high-affinity receptor on macrophages. α2M “fast” forms inhibit the interferon-γ (IFN)-induced increase in macrophage Ia expression. This study examined whether α2M-proteinase complexes alter prostaglandin (PG) E2 synthesis, and whether PGE2 mediates α2M “fast” forms effects on macrophage Ia expression. Culture with α2M “fast” forms increased PGE2 accumulation in the medium over control values in a dose-dependent manner. Culture with IFN alone did not increase PGE2 levels, but potentiated the effect of α2M-proteinase complexes on PGE2 levels. Inhibition of PGE2 synthesis did not alter the PGE2 did suppress IFN-induced Ia expression. Thus, α2M-proteinase complexes increase macrophage PGE2 synthesis, but increased synthesis of PGE2 or other cyclooxygenase products is not the mediator of antagonism of IFN-induced Ia expression by α2M-proteinase complexes.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Cancer immunology immunotherapy 7 (1980), S. 225-233 
    ISSN: 1432-0851
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary NaIO4 treatment of mouse adherent peritoneal cells or lymphocyte-free cloned macrophages enhances their cytotoxic and tumoricidal activity. 5×10−3 M NaIO4 treatment of nontumoricidal BCG-activated macrophages renders them completely tumoricidal, whereas the same treatment of stimulated (peptone-normal) macrophages renders them weakly tumoricidal. Addition of LPS in nanogram quantities too low to enhance tumor cell killing by untreated peptone-normal macrophages causes NaIO4-treated peptone-normal macrophages to be maximally tumoricidal. The activating action of NaIO4, MAF, or LPS can be potently, but inconsistently, blocked or reversed by the reducing agent NaBH4 or the aldehyde-reacting agent dimedone. NaIO4 treatment of lymphocyte-free macrophage colonies does not make them cytotoxic, but NaIO4-treated colony macrophages are cytotoxic for tumor cells when cultured in 10 ng/ml LPS (an amount of LPS inadequate to render untreated colony macrophages cytotoxic). Supernatants of NaIO4-treated adherent peritoneal cells contain MAF activity. Thus, the NaIO4-induced enhancement of peritoneal cell tumoricidal activity may result from both direct NaIO4 activating effects on macrophages and indirect NaIO4 effects through NaIO4-induced MAF production.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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