Human granulosa-lutein cells express functional EP1 and EP2 prostaglandin receptors

被引:31
作者
Harris, TE
Squires, PE
Michael, AE
Bernal, AL
Abayasekara, DR
机构
[1] Univ London Royal Coll Vet Surg, Dept Vet Basic Sci, Reprod & Dev Grp, London NW1 0TU, England
[2] Univ Warwick, Dept Biol Sci, Coventry CV4 7AL, W Midlands, England
[3] UCL, Dept Biochem & Mol Biol, London NW3 2PF, England
[4] John Radcliffe Hosp, Nuffield Dept Obstet & Gynaecol, Oxford OX3 9DU, England
基金
英国惠康基金;
关键词
human granulosa-lutein cells; PGE(2); EP1 and EP2 receptors; cAMP; progesterone;
D O I
10.1006/bbrc.2001.5301
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Prostaglandin E(2) (PGE(2)) exerts mainly luteotrophic effects in the corpus luteum. In other tissues, PGE,, acts via specific PGE2 receptor subtypes including EP(1), which modulates intracellular calcium ([Ca(2+)](i)) and EP(2), which is coupled to cyclic AMP (cAMP) generation. We have therefore investigated the presence of functional EP1 and EP2 receptors using human granulosa-lutein (GL) cells. Reverse-transcription PCR revealed that GL cells expressed mRNA transcripts encoding both EP1 and EP2 receptors. When GL cells were challenged with ligands that can bind to both receptor subtypes (PGE2 and 16,16 dimethyl PGE) or exclusively to EP2 (butaprost), both cAMP formation and progesterone synthesis were stimulated. Furthermore, the cAMP response to these agonists could be significantly blocked by an EP1/2 antagonist AH6809 but not by an EP1-selective antagonist SC19220. Exposure of GL cells to 16,16-dm PGE(2) transiently raised [Ca(2+)](i) levels, which could be prevented by both AH6809 and SC19220. We therefore conclude that human GL cells express functional EP1 and EP2 receptors. (C) 2001 Academic Press.
引用
收藏
页码:1089 / 1094
页数:6
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