MOUSE SERUM-AMYLOID-A (SAA) PROTEINS ISOLATED BY 2-DIMENSIONAL ELECTROPHORESIS - CHARACTERIZATION OF ISOTYPES AND THE EFFECT OF SEPARATE AND COMBINED ADMINISTRATIONS OF CYTOKINES, DEXAMETHASONE AND LIPOPOLYSACCHARIDE (LPS) ON SERUM LEVELS AND ISOTYPE DISTRIBUTION
Cf. Bruun et al., MOUSE SERUM-AMYLOID-A (SAA) PROTEINS ISOLATED BY 2-DIMENSIONAL ELECTROPHORESIS - CHARACTERIZATION OF ISOTYPES AND THE EFFECT OF SEPARATE AND COMBINED ADMINISTRATIONS OF CYTOKINES, DEXAMETHASONE AND LIPOPOLYSACCHARIDE (LPS) ON SERUM LEVELS AND ISOTYPE DISTRIBUTION, Clinical and experimental immunology, 111(1), 1998, pp. 231-236
Hydrophobic interaction chromatography and two-dimensional electrophor
esis were used to isolate and characterize mouse SAA, and to study the
in vivo effect of separate or combined administrations of cytokines,
dexamethasone (DEX) and LPS on mouse SAA. Four SAA spots containing pa
rtial amino acid sequence in accordance with mouse apoSAA1 and apoSAA2
/SAA(SJL/J) pi 5.9 were demonstrated in serum. One of these proteins r
epresents a previously undescribed, acidic acute-phase mouse SAA prote
in. Both DEX and interferon-gamma (IFN-gamma) proved to be capable of
increasing SAA serum levels. In contrast to what has been shown in pre
vious in vivo studies, administration of IL-6 did increase the SAA lev
els to nearly the same magnitude as IL-1, and the effect of IL-6 and L
PS on SAA production was not significantly altered by the addition of
DEX. Irrespective of the inflammatory stimuli that was administered, a
non-selective production of SAA1 and SAA2 was observed in most groups
, including the group that received IL-6. The results illustrate that
data obtained about mouse SAA are highly dependent on which models, is
olation and identification methods are used.