Abstract

Cells originating from the human fetal liver and grown as a primary monolayer culture for 4 to 11 days contain an enzyme system that metabolizes benzo(α) pyrene. The basal level of the enzyme varied about three-fold. The activity was increased from 1.4- to 5.1-fold by the exposure of cells for 24 hours to benz(α) anthracene, the magnitude of increase depending on the amount of inducer, on the individual cell batch studied and on the stage of cell growth. Also 3-methylcholanthrene, but not benzo(α)pyrene, induced the enzyme activity in fetal liver cell cultures at concentrations used. Fibroblast cultures derived from the human fetal lung or skin exhibited less benzo(α)pyrene metabolism and the inducibility of the enzyme activity was less marked than in hepatic cell cultures.

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