Macrophage tumour cell lines (PUS-1.8, P388Dl) produced detectable granulocyte macrophage colonystimulating (CSF-2) activity measured using a factor-dependent cell line FDC-PI. The production of CSF-2 was enhanced by endotoxin and inhibited by serum, and correlated inversely with [3H]TdR incorporation. mRNA isolated from PU5-1.8 or P388D 1 cells initiated CSF-2 production when injected into Xenopus laevis oocytes. The specific activity in this assay was unaltered in mRNA isolated from endotoxin-treated cells.The results suggest that endotoxin acts at a post-transcriptional level.