Large and small macromolecular activators of phagocytosis from platele
ts (l-MAPP and s-MAPP, respectively), which function via the neutrophi
lic Fc gamma receptors (Fc gamma R) were refined from platelet release
products by gel filtration and affinity chromatography,vith the use o
f an anti transferrin antibody column and the mechanism of phagocytosi
s activation was investigated. Flow cytometry revealed that l-MAPP and
s-MAPP did not increase the expression of neutrophilic Fc gamma RII (
CD32) and Fc gamma RIII (CD16) antigens, whereas rosette formation of
neutrophils with rabbit IgG-sensitized sheep erythrocytes (EA) in the
presence of anti Fc gamma R antibodies suggested that both MAPPs incre
ase the binding ability of Fc gamma RII, On the other hand, the enhanc
ing effect of l-MAPP and s-MAPP on neutrophilic phagocytosis disappear
ed with the increase in phagocytosis by the phosphate-buffered saline
control neutrophils when they were centrifuged with EA before incubati
on for phagocytosis. The enhanced phagocytosis, both by the two MAPPs
and centrifugation, was canceled by treatment of the neutrophils with
anti-CD32 Fab. The phagocytosis activatory effects of MAPP on neutroph
ils were canceled by anti-CD71 monoclonal antibody but not by transfer
rin.