In the course of screening for immunomodulators, we found a significan
t blastogenic activity specific for splenic B cells in the extracts of
safflower (Carthamus tinctorius L.). Active fractions termed SF1 and
SF2 were purified from dried petals of safflower by boiling water extr
action, ethanol precipitation and Sepharose CL-2B column chromatograph
y. The elution profiles of the gel filtration indicated that the molec
ular weight of SF1 and SF2 was estimated to be more than 100 kD. Major
components of SF1 and SF2 seem to be polysaccharides, and structural
analysis of alditol acetate derivatives by GC-MS revealed some differe
nces between SF1 and SF2 in the sugar component. Biological activities
of SF1 and SF2 on B cells and macrophages were examined in comparison
with lipopolysaccharides (LPS). SF1 and SF2 induced both the prolifer
ation and the IgM production of B cells to the equivalent level as tho
se induced by LPS. In macrophages, SF1 and SF2 effectively stimulated
the production of NO. However, SF1 stimulated the production of IL-1,
IL-6, and TNF as much as LPS, while SF2 induced them only weakly or no
t at all. Thus, these results suggest that SF1 and SF2 activate B cell
s and macrophages in different mechanisms.