Inhibitory Effects of Cholesterol Sulfate on Progesterone Production in Human Granulosa-like Tumor Cell Line, KGN

• Published in: ENDOCRINE JOURNAL Vol. 55; no. 3; pp. 575 - 581
• Main Authors: TSUTSUMI, Ryo, HIROI, Hisahiko, MOMOEDA, Mikio, HOSOKAWA, Yumi, NAKAZAWA, Fumiko, KOIZUMI, Minako, YANO, Tetsu, TSUTSUMI, Osamu, TAKETANI, Yuji
• Format: Journal Article
• Language: English; Japanese
• Published: Japan The Japan Endocrine Society 2008
• Subjects: Cell Line, Tumor; Cholesterol Esters - pharmacology; Cholesterol Side-Chain Cleavage Enzyme - genetics; Cholesterol Side-Chain Cleavage Enzyme - metabolism; Cholesterol sulfate; Cyclic AMP - pharmacology; Down-Regulation - drug effects; Down-Regulation - genetics; Female; Ferredoxin-NADP Reductase - genetics; Ferredoxin-NADP Reductase - metabolism; Ferredoxins - genetics; Ferredoxins - metabolism; Gene Expression Regulation, Neoplastic - drug effects; Granulosa Cell Tumor - genetics; Granulosa Cell Tumor - metabolism; Granulosa Cell Tumor - pathology; Humans; KGN cells; Ovarian Neoplasms - genetics; Ovarian Neoplasms - metabolism; Ovarian Neoplasms - pathology; P450scc; Phosphoproteins - genetics; Phosphoproteins - metabolism; Progesterone; Progesterone - biosynthesis; RNA, Messenger - metabolism; StAR protein
• ISSN: 0918-8959; 1348-4540
• DOI: 10.1507/endocrj.K07-097

Cholesterol sulfate (CS) is a component of cell membranes that plays a role in stabilizing the cell membrane. We previously reported that CS increased in the endometrium during implantation, suggesting that CS plays an important role in reproduction. It has been reported that CS regulates progesterone and pregnenolone production in the placenta, adrenal glands and ovary. The regulatory mechanisms of steroid hormone production by CS, however, are still unknown. In the present study, we investigated the effect of CS on the expression of progesterone production-related genes in KGN cells, derived from human granulosa-like tumor. KGN cells were cultured with CS (10 μM) or cholesterol (10 μM) in the presence of 8-bromo-cAMP (1 mM). Progesterone levels in the culture media were measured by enzyme linked fluorescent assay at 24 h after treatment of CS and cAMP. Total RNAs were extracted for quantitative real time RT-PCR with specific primer of StAR protein, P450scc, HSD3B2, ferredoxin and ferredoxin reductase. Whole cell lysates were extracted for western blot analysis with antibody for StAR protein. Progesterone concentration in the culture medium increased to 38-fold by treatment of cAMP. CS significantly reduced progesterone concentration by 30% compared with those of cAMP treatment (p<0.05), while cholesterol did not change the progesterone concentration. CS treatment down-regulated the expression of StAR mRNA and P450scc mRNA was to 54% and 60%, respectively (p<0.05). Western blot analysis revealed that the amount of StAR protein was also reduced by CS treatment. The expression of HSD3B2 mRNA was up-regulated to 3.4-fold by treatment of cAMP. The expression of ferredoxin and ferredoxin reductase mRNA was not affected by CS treatment. These data implied that CS has an inhibitory effect on progesterone production by regulating the expression of StAR and P450scc gene expression.