Influence of macrophage products on the release of plasminogen activator, collagenase, β-glucuronidase and prostaglandin E2 by articular chondrocytes

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Abstract
The effects of products of mononucelar phagocytes on the secretory activity of chondrocytes were studied. The primary confluent cultures of rabbit articular chondrocytes were exposed to standard medium alone or enriched with conditioned medium obtained from cultures of rabbit peritoneal macrophages, the mouse macrophage cell line P388D1 or human blood mononuclear cells. Four markers of release were assessed: the neutral proteinases plasminogen activator and collagenase, the acid hydrolase .beta.-glucuronidase and prostaglandin [PG] E2; the kinetics of their changes were also monitored. Chondrocytes that were cultured in standard medium secreted large amounts of plasminogen activator, some .beta.-glucuronidase, but no collagenase, and released only minor amounts of PG E2. The addition of conditioned medium from rabbit macrophages induced a rapid release of large quantities of PG E2 and an abundant secretion of collagenase, while abolishing or strongly decreasing plasminogen activator secretion. .beta.-glucuronidase secretion was markedly enhanced. The decrease in secretion of plasminogen activator appeared to reflect a diminished production, since no evidence was found for the generation of inhibitors or for an accelerated extracellular breakdown of the enzyme. Conditioned media of the mouse and human mononuclear cells influenced the secretory activities of rabbit articular chondrocytes in a similar way, suggesting that the factor (or factors) acting on chondrocytes is produced by a variety of macrophages and that its action is not species-restricted. The time course and concentration-dependence of the effects observed indicate that the secretion of plasminogen activator and collagenase are influenced in a strictly reciprocal fashion by the macrophage products. The release of PG E2 paralleled that of collagenase.