The Journal of Clinical Endocrinology & Metabolism · 1994 · 69 citations · 0 references
Life SciencesBiochemistryEndocrinologyCell SignalingHormone BiochemistrySteroid BiochemistryGonadal SteroidogenesisGrowth Factor SignalingHormone BiosynthesisSteroid BiosynthesisSteroid MetabolismSteroidogenic Enzymes17 Beta-hydroxysteroid Dehydrogenases17-Beta Hydroxysteroid Dehydrogenase3 Alpha-hydroxysteroid Dehydrogenase3 Beta-hydroxysteroid DehydrogenaseDehydroepiandrosterone SynthesisGonadal Steroid BiosynthesisGranulosa Cell SteroidogenesisGrowth Factors
In this report we examined the effects of growth factors and phorbol esters on steroid hydroxylase activity in cultured human thecal and granulosa-lutein cells. Treatment of thecal cells with epidermal growth factor (EGF), fibroblast growth factor (FGF), transforming growth factor-beta (TGF beta), and tetradecanoyl phorbol acetate (TPA) resulted in the inhibition of forskolin- and dibutyryl cAMP-stimulated 17 alpha-hydroxylase activity and 17 alpha-hydroxyprogesterone and dehydroepiandrosterone production. In contrast, cAMP-stimulated 3 beta-hydroxysteroid dehydrogenase (3 beta HSD) activity was enhanced by FGF and TGF beta, and treatment with EGF enhanced cAMP-stimulated progesterone production. cAMP stimulated 3 beta HSD activity was unaffected by TPA (10 nmol/L) treatment, yet TPA inhibited cAMP-stimulated progesterone production. Basal 3 beta HSD activity and progesterone production were inhibited by TPA. In contrast to the inhibitory actions of EGF, FGF, and TGF beta on 17 alpha-hydroxylase expression, insulin and insulin-like growth factor-I enhanced forskolin-stimulated 17 alpha-hydroxylase activity. In granulosa-lutein cells, forskolin-stimulated aromatase activity was suppressed by EGF, FGF, and TPA. TGF beta had no effect on forskolin-stimulated aromatase activity. EGF, FGF, and TGF beta did not affect forskolin-stimulated progesterone production, whereas treatment with TPA inhibited cAMP-stimulated progesterone secretion. These data suggest that growth factors may differentially regulate cAMP-dependent processes in human thecal and granulosa cells of the developing follicle.