Your browser doesn't support javascript.
loading
Prostaglandin E-prostanoid-3 receptor activation of cyclic AMP response element-mediated gene transcription.
Audoly, L P; Ma, L; Feoktistov, I; de Foe, S K; Breyer, M D; Breyer, R M.
Affiliation
  • Audoly LP; Department of Medicine, Division of Nephrology, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.
J Pharmacol Exp Ther ; 289(1): 140-8, 1999 Apr.
Article in En | MEDLINE | ID: mdl-10086997
The prostaglandin E-prostanoid (EP)3 receptor signals primarily through the inhibitory G protein Gi, thereby decreasing intracellular cAMP levels. To study the signal transduction properties of the rabbit EP3 receptor, five splice variants were expressed in HEK293tsA201 cells: 72A, 74A, 77A, 80A and the novel splice variant NT, which lacks the C-terminal sequence. The ability of the EP3 receptor splice variants to modulate expression of a beta-galactosidase reporter gene under the control of a promoter containing cAMP response elements (CRE) was assessed. Each splice variant induced sulprostone-mediated increase in beta-galactosidase enzymatic activity with EC50 ranging from 0.8 nM for the NT splice variant to 3.1 nM for the 77A splice variant. Substitution of either Asp338 with Ala, or Arg329 with Ala or Glu in the 77A splice variant resulted in a loss of receptor-evoked increases in beta-galactosidase activity, whereas substitution of Lys300 with alanine had no effect on signal transduction. These phenotypes correlate with the inhibition of cAMP generation by direct cAMP measurement. Signal transduction was insensitive to pretreatment of cells with pertussis toxin, suggesting that a nonGi/Go pathway is activated by the EP3 receptor. Direct measurement of second messenger levels confirmed that there was no increase in cAMP levels mediated by the 77A splice variant, however, there was a modest increase in intracellular Ca2+. Partial blockade of the reporter activity with kinase inhibitors demonstrates that CRE activation is mediated in part by a Ca2+-dependent kinase pathway. These data suggest that the EP3 receptor signals through a novel cAMP response element binding protein/CRE pathway.
Subject(s)
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Transcription, Genetic / Receptors, Prostaglandin E / Cyclic AMP / Response Elements Limits: Animals Language: En Journal: J Pharmacol Exp Ther Year: 1999 Document type: Article Affiliation country: United States Country of publication: United States
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Transcription, Genetic / Receptors, Prostaglandin E / Cyclic AMP / Response Elements Limits: Animals Language: En Journal: J Pharmacol Exp Ther Year: 1999 Document type: Article Affiliation country: United States Country of publication: United States