We have studied the role of macrophages as stromal elements in long-te
rm cultures of murine bone marrow cells. Normal ectopic macrophages we
re collected from the lung and co-cultured in various ratios with bone
marrow cells in Dexter suspension cultures. At weekly intervals, vari
ous parameters of the cultures were evaluated and compared with contro
ls. Increased numbers of macrophages in the bone marrow caused a delay
in the formation of the confluent stroma, with distinct differences i
n the pattern of hematopoietic foci in the stroma. Cytologic analysis
of nucleated cells in the nonadhering fraction showed that the monocyt
ic macrophages were the eventual line of differentiation in all cultur
es; however, this phenomenon was accelerated in cultures containing va
rious fractions of macrophages. There was a dose-dependent reduction i
n the number of myeloid progenitors in the nonadhering and adhering fr
actions of macrophage-enriched cultures with respect to controls. This
effect was mediated through both humoral factors released in the cult
ure and direct interaction between macrophages and bone marrow cells.
The results indicate that elevation of the number of macrophages in th
e bone marrow could result in an impaired process of hematopoiesis.