Rat hepatocytes have previously been reported to possess prostaglandin E₂ receptors of the EP₃-type (EP₃-receptors) that inhibit glucagonstimulated glycogenolysis by decreasing cAMP. Here, the isolation of a functional EP₃ϐ receptor cDNA clone from a rat hepatocyte cDNA library is reported. This clone can be translated into a 362-amino-acid protein, that displays over 95% homology to the EP₃ϐ receptor from mouse mastocytoma. The amino- and carboxy-terminal region of the protein are least conserved. Transiently transfected HEK 293 cells expressed a single binding site for PGE₂ with an apparent Kd of 15 nM. PGE₂ > PGF₂α > PGD₂ competed for [³H]PGE₂ binding sites as did the EP₃ receptor agonists M&B 28767 = sulprostone > misoprostol but not the EP₁ receptor antagonist SC 19220. In stably transfected CHO cells M&B 28767 > sulprostone = PGE₂ > misoprostol > PGF₂α inhibited the forskolin-elicited cAMP formation. Thus, the characteristics of the EP₃ϐ receptor of rat hepatocytes closely resemble those of the EP₃ϐ receptor of mouse mastocytoma.
Identifer | oai:union.ndltd.org:Potsdam/oai:kobv.de-opus-ubp:4583 |
Date | January 1994 |
Creators | Neuschäfer-Rube, Frank, DeVries Christa, Hänecke, Kristina, Jungermann, Kurt, Püschel, Gerhard |
Publisher | Universität Potsdam, Mathematisch-Naturwissenschaftliche Fakultät. Institut für Ernährungswissenschaft |
Source Sets | Potsdam University |
Language | English |
Detected Language | English |
Type | Postprint |
Format | application/pdf |
Source | FEBS Letters 351 (1994), 1, p. 119-122, DOI 10.1016/0014-5793(94)00837-X, ISSN 0014-5793 |
Rights | http://opus.kobv.de/ubp/doku/urheberrecht.php |
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