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RPE and IPE cells, freshly isolated from pigmented rat eyes, were exposed to several secretagogues to determine whether the lipid moiety of these cells had a characteristic distribution of sulfhydryl groups and whether the proteins in RPE and IPE cells were dissimilar. RPE cell sensitivity to N-ethylmaleimide was similar to that of other cell types. The presence of a large, detergent-resistant, cytoskeleton-associated fraction in RPE and IPE cells was examined by electron microscopy. This fraction was composed of at least two proteins having Mr = 300,000 and 100,000, respectively. Two other proteins having Mr = 55,000 and 25,000 were associated with the cytoplasmic membrane in RPE and IPE cells. Proteins present in the membrane and cytoplasmic fractions of RPE cells were also characterized by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. There were, however, no qualitative differences in the protein composition of the two cell types, and the major polypeptides present were identical. The existence of a disulfide-linked membrane complex was suggested by treatment of the plasma membranes with either N-ethylmaleimide or monensin. The inhibition of cholate transport by the addition of monensin in intact RPE cells and IPE cells further suggested the presence of a membrane complex. The effect of monensin on rhodopsin binding was examined in both RPE and IPE cells. The number of rhodopsin binding sites was shown to be decreased by treatment of both RPE and IPE cells with monensin.Determination of the genotoxicity of AgNO3 on Raphanus sativus (radish) seedlings using comet assay, chromosomal aberration, and micronucleus tests. 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