Induction of guanosine triphosphate-cyclohydrolase by follicle-stimulating hormone enhances interleukin-1β-stimulated nitric oxide synthase activity in granulosa cells

• Published in: Endocrinology (Philadelphia) Vol. 138; no. 1; pp. 162 - 168
• Main Authors: TABRAUE, C, DIAZ PENATE, R, GALLARDO, G, HERNANDEZ, I, QUINTANA, J, LOPEZ BLANCO, F, GONZALES REYES, J, FANJUL, L. F, RUIZ DE GALARRETA, C. M
• Format: Journal Article
• Language: English
• Published: Bethesda, MD Endocrine Society 1997
• Subjects: Animals; Biological and medical sciences; Biopterins - analogs & derivatives; Biopterins - physiology; Cells, Cultured; Enzyme Induction; Female; Follicle Stimulating Hormone - pharmacology; Fundamental and applied biological sciences. Psychology; Granulosa Cells - enzymology; GTP Cyclohydrolase - biosynthesis; GTP Cyclohydrolase - genetics; Hormone metabolism and regulation; Interleukin-1 - pharmacology; Mammalian female genital system; Nitric Oxide Synthase - biosynthesis; Nitric Oxide Synthase - genetics; Rats; Rats, Sprague-Dawley; RNA, Messenger - analysis; Vertebrates: reproduction; Rat; Enzyme; Induction; Cytokine; Rodentia; Interleukin 1β; Biosynthesis; Gonadotropin; Synthase; Glycoprotein hormone; Vertebrata; Mammalia; Adenohypophyseal hormone; Enzymatic activity; Animal; Nitric oxide; Hormonal regulation; FSH; Granulosa
• ISSN: 0013-7227; 1945-7170
• DOI: 10.1210/endo.138.1.4854

In cultured granulosa cells, interleukin-1 beta (IL-1 beta) induced a time-dependent (16-72 h) and dose-related (0.3-30 ng/ml) stimulation of nitric oxide (NO) synthase (NOS) activity, as determined by the catalytic conversion of [3H]arginine to [3H]citrulline and NO2- accumulation in the culture medium. Although FSH alone failed to stimulate NOS activity, concomitant treatment with the gonadotropin (200 ng/ ml) or the cell-permeant cAMP analog (Bu)2cAMP (0.5 mM) markedly enhanced IL-1 beta-induced NO generation in cultured granulosa cells. The effect of IL-1 beta on citrulline biosynthesis and NO2- accumulation was abrogated by the NOS inhibitor NG-methyl-L-arginine or the IL-1-receptor antagonist protein. In contrast bacterial endotoxin (lipopolysaccharide), interferon-gamma, or tumor necrosis factor-alpha, which are well known inducers of inducible NOS (iNOS) in a variety of immunocompetent and nonimmunocompetent cell types, failed to increase [3H]citrulline formation or NO2- accumulation in untreated or FSH-stimulated cells. As demonstrated by reverse transcriptase-PCR analysis, IL-1 beta-stimulated NO generation was accompanied by a time-dependent increase in messenger RNA levels for iNOS and GTP-cyclohydrolase (GTPCH), the rate-limiting step for de novo tetrahydrobiopterin (BH4) biosynthesis. Treatment with FSH augmented only GTPCH messenger RNA expression, and a more than additive GTPCH signal was observed when cells were simultaneously challenged with IL-1 beta and FSH. Treatment with the GTPCH inhibitor 2,4-diamino-6-hydroxypyrimidine prevented IL-1 beta-induced NOS activity in untreated or FSH-stimulated cells, and this inhibition was completely reversed by sepiapterin, a substrate for BH4 biosynthesis, via an alternative pterin salvage pathway present in many cell types. As BH4 is an essential cofactor for NOS catalytic activity, these observations strongly suggest that FSH-induced biosynthesis of endogenous BH4 is essential for full iNOS biosynthetic capacity in IL-1 beta-stimulated granulosa cells.