© 1990 Oxford University Press
other |
Screening for Immunomodulators: Effects of Xenobiotics on Macrophage Chemiluminescence in vitro
Department of Bacteriology and Center for Environmental Toxicology, University of Wisconsin Madison, Wisconsin 53706
Received June 14, 1989; accepted September 18, 1989
Screening for Immunomodulators: Effects of Xenobiotics on Macrophage Chemiluminescence in vitro. TAM, P. E., AND HINSDILL, R. D. (1990). Fundam. Appl. Toxicol. 14, 542–553. Macrophage chemiluminescence (CL) was evaluated as a primary screening assay by assessing the modulatory activity of 17 different chemicals. The chemicals were either known immuno-modulatory drugs or environmental toxicants with reported immunomodulatory activity. Elicited mouse peritoneal macrophages were exposed to the chemicals in vitro, and CL was measured in response to an opsonized yeast stimulus. Ten chemicals (hydrocortisone, dextran sulfate, di-fl-octyltin dichloride, dimethyltin dichloride, azathioprine, lambda carrageenan (1-carrageenan), lead, N-propyl gallate, gallic acid, and indomethacin) were identified as effective modulators of CL. The polyanions dextran sulfate and 1-carrageenan either suppressed or enhanced CL, depending on the experimental conditions, while the remaining modulators were inhibitory. A series of secondary assays was used to verify this modulatory activity and to explore different mechanisms of action. Each effective modulator altered only a few specific components of the more complex CL response, and the following general mechanisms were apparent. At least 2 chemicals showed distinct antioxidant activity and thus probably did not alter functional aspects of macrophage CL. Chemicals which blocked Fc receptor function delayed the peak CL of macrophages stimulated by opsonized yeast. Nine of the 10 modulators inhibited hydrogen peroxide release, but only 3 inhibited the release of superoxide. Finally, some effective modulators were chemicals known to interact with cell membranes or specific membrane receptors, and these were able to directly induce a CL response without the addition of opsonized yeast as a stimulus. Thus, macrophage CL was a simple, quantitative, yet sensitive immunotoxicologic screening assay capable of identifying many known immunomodulatory drugs. Supplementary assays were useful both in confirming the functional effects of these chemicals on CL and in delineating potential mechanisms by which modulation of CL can occur.