Abstract

Experimental conditions known to alter the shape, permeability and organization of cells were used to find out their effects on tyrosine aminotransferase (TAT) in rat liver epithelial cell lines. To produce a more spheroidal morphology for non-malignant cells than that obtainable on plastic, floating collagen and poly(2-hydroxyethylmethacrylate) (poly(HEMA)), were used as substrata. Under these experimental conditions the basal level of TAT activity increased 1.5–2.5-fold. When monolayer cultures were permeabilized by the use of a hypertonic salt solution, the basal activity increased 4–5-fold. TAT activity was also elevated in hepatoma cells cultured in anchorage-independent conditions. The enzyme was not inducible by dexamethasone (DEX) under any of these culture conditions, and the lack of induction was not due to the absence of receptors for this hormone. These studies have shown that the production of TAT, one of the characteristics of adult liver, has persisted in a number of rat epithelial cell lines derived from normal, malignant or regenerating liver and its activity was influenced by the different culture conditions employed.

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