Prostaglandin E-2 (PGE(2)) exerts mainly luteotrophic effects in the corpus
luteum. In other tissues, PGE,, acts via specific PGE2 receptor subtypes i
ncluding EP1, which modulates intracellular calcium ([Ca2+](i)) and EP2, wh
ich is coupled to cyclic AMP (cAMP) generation. We have therefore investiga
ted the presence of functional EP1 and EP2 receptors using human granulosa-
lutein (GL) cells. Reverse-transcription PCR revealed that GL cells express
ed 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 AH6
809 but not by an EP1-selective antagonist SC19220. Exposure of GL cells to
16,16-dm PGE(2) transiently raised [Ca2+](i) levels, which could be preven
ted by both AH6809 and SC19220. We therefore conclude that human GL cells e
xpress functional EP1 and EP2 receptors. (C) 2001 Academic Press.