DAP12. is a recently cloned, immunoreceptor tyrosine-based activation motif
-bearing transmembrane adapter molecule that is associated with the NK-acti
vating receptors, Previous reports showed that the DAP12 message could be d
etected not only in NK cells but also in granulocytes, monocytes, dendritic
cells, and macrophages, In this study we found a significant level of DAP1
2 protein expression in macrophage-related cell lines and organs. Additiona
lly, we observed increased expression of DAP12, after LPS-induced different
iation of M1 cells into macrophages, To examine the role of DAP12 in the my
eloid cell lineage, we established M1 FLAG-DAP12 transfectants (FDAP-M1) an
d demonstrated the marked;morphological changes in FDAP-M1 cells caused by
signaling through DAP12 Cell surface phenotypic analysis showed up-regulati
on of macrophage markers CD11b, 2,4G2, and adhesion molecule B7-2, Addition
ally, after stimulation through DAP12, phosphorylated FLAG -DAP12 could be
immunoprecipitated using anti-phosphotyrosine mAbs, Collectively, these fin
dings indicate that direct DAP12 signaling has an important role in macroph
age differentiation.