Phenotypic and functional changes associated with
tumor-bearing host (TBH) macrophages (M phi) are partly responsible for immunosuppression during
tumor growth. Flow cytofluorometric analyses revealed differences in cell-cycle kinetics between normal host (NH) and TBH M phi that were stimulated at specific receptors. Receptor-
ligand interactions were induced by
antibodies against Mac-1, -2, -3, and Ia receptors and changes in
DNA synthesis were measured over a 12-h time course by incorporation of
propidium iodide. TBH M phi showed higher
DNA synthesis than NH M phi over this time course irrespective of the receptor induced. NH M phi stimulated at the
Mac-1 receptor demonstrated higher
DNA synthesis than control NH M phi although TBH M phi stimulated at this receptor and control TBH M phi failed to show any differences. Both NH and TBH M phi exhibited small, short-term decreases in
DNA synthesis when stimulated at the Mac-2 receptor. TBH M phi that were stimulated at the
Mac-3 receptor demonstrated higher
DNA synthesis than their control counterparts while NH M phi stimulated at this receptor and control NH M phi showed identical levels of
DNA synthesis. No differences in
DNA synthesis were found among normal or TBH M phi that were stimulated through Ia. Differences in
DNA synthesis did not appear to be attributable to differences in receptor expression. Further analysis of Mac-1 and
Mac-3 stimulated cells revealed that
DNA synthesis in NH M phi stimulated at the
Mac-1 receptor returned to control levels at 48 h.(ABSTRACT TRUNCATED AT 250 WORDS)