The production of collagenase by adherent mononuclear cells cultured from human peripheral blood

Mononuclear cells were isolated from human peripheral blood by Ficoll‐Hypaque centrifugation, and the cells adherent to plastic substrata were cultured in serum‐free media supplemented with lactalbumin hydrolysate. These cell cultures, which consisted predominantly of monocyte‐macrophages as judged by nonspecific esterase staining, accumulated collagenase in the medium. This collagenase resembled other vertebrate collagenases in that it cleaved native triple‐helical type I collagen at a locus 3/4‐length away from the amino‐terminal end of the molecule. The collagenase activity was inhibited by Na2EDTA, dithiothreitol, and fetal calf serum, while the addition of Ca++ or N‐ethylmaleimide enhanced the enzyme activity. The accumulation of collagenase in the culture media was markedly enhanced by the incubation of cells with concanavalin A or phorbol myristic acetate. In the presence of cycloheximide, the levels of collagenase activity were markedly reduced, suggesting that active protein synthesis was required to express the enzyme activity. In additional experiments, monocytes were further purified by counterflow centrifugation‐elutriation. The collagenase production was markedly increased in cultures enriched in monocyte‐macrophages and devoid of polymorphonuclear leukocytes. The accumulation of collagenase in monocyte cultures incubated for 48 hours in the presence of concanavalin A or phorbol myristic acetate was of the same order of magnitude as in parallel cultures containing the same number of polymorphonuclear leukocytes purified by Ficoll‐Hypaque centrifugation and Plasmagel sedimentation. The demonstration of collagenase activity in the monocyte cultures appears to reflect the increased diversity of monocyte functions which may play an important role in the tissue damage in chronic inflammatory diseases such as rheumatoid arthritis.