© 1991 Oxford University Press
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Modulation of lnterleukin-2-Driven Proliferation of Human Large Granular Lymphocytes by Carbaryl, an Anticholinesterase Insecticide1,2
*Department of Pharmaceutical Sciences, College of Pharmacy, University of Nebraska Medical Center 600 South 42nd Street, Omaha, Nebraska 68198-6025
Institute of Agriculture and Natural Resources 101 Natural Resources Hall, Lincoln, Nebraska 68583-0818
Received September 5, 1990; accepted January 28, 1991
Modulation of Interieukin-2-Driven Proliferation of Human Large Granular Lymphocytes by Carbaryl, an Anticholinesterase Insecticide. Bavari, S., Casale, G. P., Gold, R. E., and Vitzthum, E. F. (1991). Fundam. Appl. Toxicol. 17,61-74. Studies in other laboratories have provided evidence that the interleukin-2 (IL2) signaling pathway in lymphocytes includes essential, serine proteases. Since the anticholinesterase (antiCHE) insecticides are potent serine hydrolase (esterase and protease) inhibitors, we assessed the ability of carbaryl (CA, a widely used antiCHE insecticide) and a-naphthol (NA, a major metabolite of carbaryl) to modulate IL2-driven proliferation of large granular lymphocytes (LGL) purified from human peripheral blood. These cells express nearly all of the natural killer (NK.) activity of human peripheral Wood. NK cells are normal lymphocytes that respond to IL2 by proliferating and increasing their tumoricidal activity on a per cell basis. Cultures of purified LGL, initiated in the presence of human recombinant IL2, were harvested on culture Day 4, then proliferation was measured as [3H]thymidine incorporation. When added only at the time cultures were initiated, CA inhibited incorporation 10-32%, 35-53%, and 54-57% at 0.5, 5.0, and 50 mm, respectively. In contrast, NA had no effect at 0.5 and 5.0 mm, but was inhibitory (16-17%) at 50 mm. Reexposure to CA or NA, during the incorporation assay, had little effect on the observed inhibition profiles. Chemically induced changes in cell number during an 8-day culture period reflected the chemically induced changes in [3H]thymidine incorporation. Neither CA nor NA produced cell death. Quantitation of both CA and NA by HPLC indicated a rapid loss of CA (ca. 95% in 24 hr) and a much slower loss of NA from the culture medium. CA inhibited human LGL proliferation at concentrations producing little or no inhibition of serum CHE, an indicator of exposure to antiCHE insecticides.