Epidermal growth factor and gonadotropin‐releasing hormone inhibit cyclic AMP–dependent luteinizing hormone receptor formation in ovarian granulosa cells
Authors:
- 1 January 1983
- journal article
- research article
- Published by Wiley in Journal of Cellular Biochemistry
- Vol. 21 (3) , 209-217
Abstract
The induction of luteinizing hormone (LH) receptors was studied in granulosa cells prepared from the ovaries of hypophysectomized diethylstilbestrol‐treated immature rats. Incubation of granulosa cells for 48 h with increasing concentrations of follicle‐stimulating hormone (FSH) or choleragen caused parallel rises in cAMP levels and LH receptors. These observations, with the finding that 8‐Bromo‐cAMP also induced LH receptor formation, indicate that hormonal stimulation of LH binding sites is mediated by cAMP. Peptide hormones that inhibited FSH‐stimulated cAMP production, such as epidermal growth factor (EGF) and a gonadotropin‐releasing hormone agonist (GnRHa), also prevented LH receptor formation. GnRHa and EGF had negligible effects on FSH‐stimulated cAMP production from 0 to 24 h of culture, but reduced cAMP accumulation by 80% and 90%, respectively, from 24 to 48 h when the majority of LH receptors appeared. FSH‐sensitive adenylate cyclase activity, as measured by the conversion of (3H)‐ATP to (3H)‐cAMP, was inhibited by GnRHa and EGF at 48 h of culture. EGF and GnRHa also reversed the inhibition of ectophosphodiesterase activity caused by FSH in granulosa cells between 48 and 72 h of culture. Both EGF and GnRHa inhibited induction of LH receptors by 8‐Bromo‐cAMP, suggesting that their effects are also on cAMP action. Addition of GnRHa, but not EGF, between 36 and 48 h of culture completely prevented further increases in LH receptors induced by 8‐Bromo‐cAMP, indicating that the inhibitory action of GnRHa can be initiated at later times during granulosa cell differentiation, whereas full expression of EGF action requires a longer period. These results demonstrate that EGF and GnRH inhibit FSH‐induced LH receptor formation in the granulosa cell by reducing hormone‐dependent cAMP production and also by impairing the ability of cAMP to stimulate LH receptor formation.Keywords
This publication has 21 references indexed in Scilit:
- Gonadotropin-Releasing Hormone: Regulation of Adenosine 3′,5′-Monophosphate in Ovarian Granulosa CellsScience, 1981
- The induction of ovarian LH‐receptors by FSH is mediated by cyclic AMPFEBS Letters, 1981
- Hormonal regulation of cytodifferentiation and intercellular communication in cultured granulosa cells.Proceedings of the National Academy of Sciences, 1981
- Growth Factors Modulate Gonadotropin Receptor Induction in Granulosa Cell CulturesScience, 1981
- Direct Inhibitory Effect of Gonadotropin-Releasing Hormone upon Follicle-Stimulating Hormone Induction of Luteinizing Hormone Receptor and Aromatase Activity in Rat Granulosa Cells*Endocrinology, 1980
- FSH induction of functional LH receptors in granulosa cells cultured in a chemically defined mediumNature, 1979
- Cell Communication and Specific Adhesion in the Microorganism Dictyostelium1979
- Factors influencing the effect of hormones on the accumulation of cyclic AMP in cultured human astrocytoma cellsMetabolism, 1975
- Gonadotrophin binding sites of the rat testisBiochimica et Biophysica Acta (BBA) - General Subjects, 1972
- Structure of the porcine LH- and FSH-releasing hormone. I. The proposed amino acid sequenceBiochemical and Biophysical Research Communications, 1971