M5, a phosphoinositol-linked human myelomonocytic activation-associated antigen

Abstract

SUMMARY: When investigating the previously described monoclonal antibody (MoAb) VIM-5, raised against THP1 cells and binding to human monocytes and granulocytes, we found that the antigen detected by this antibody, designated M5, becomes very strongly expressed on monocytes after overnight culture with phorbol myristate acetate (PMA) or lipopolysaccharide (LPS) but not with recombinant human interferon-gamma (rhIFN-γ). Granulocytes stimulated with formyl-methionyl-leucyl-phenylalinine (FMLP) become negative for binding VIM-5. Immature granulocytes from bone marrow do not express M5, thus its expression on granulocytes is differentiation linked. The antigen bound by VIM-S is sensitive to hydrolysis by phosphoinositol-specific phospholipase C (PI-PLC). The immunoprecipitated MS antigen on monocytes is a broad band, with a peak of 50 kD (unreduced) and two bands of S3 kD and 44 kD (reduced). We have therefore detected an antigen that is up-regulated on stimulated monocytes but, conversely, down-regulated on FMLP-stimulated granulocytes.