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Cloning and functional pharmacology of two corticotropin-releasing factor receptors from a teleost fish

Pohl, Sigrun; Darlison, Mark G.; Clarke, W.Craig; Lederis, Karl; Richter, Dietmar

Authors

Sigrun Pohl

Mark G. Darlison

W.Craig Clarke

Karl Lederis

Dietmar Richter



Abstract

Although it is well established that fish possess corticotropin-releasing factor (CRF) and a CRF-like peptide, urotensin I, comparatively little is known about the pharmacology of their cognate receptors. Here we report the isolation and functional expression of two complementary {DNAs} (cDNAs), from the chum salmon Oncorhynchus keta, which encode orthologues of the mammalian and amphibian {CRF} type 1 (CRF1) and type 2 (CRF2) receptors. Radioligand competition binding experiments have revealed that the salmon {CRF1} and {CRF2} receptors bind urotensin I with ∼8-fold higher affinity than rat/human CRF. These two peptides together with two related CRF-like peptides, namely, sauvagine and urocortin, were also tested in cAMP assays; for cells expressing the salmon {CRF1} receptor, {EC50} values for the stimulation of cAMP production were between 4.5±1.8 and 15.3±3.1 nM. For the salmon {CRF2} receptor, the corresponding values were: rat/human CRF, 9.4±0.4 nM; urotensin I, 21.2±2.1 nM; sauvagine, 0.7±0.1 nM; and urocortin, 2.2±0.7 nM. We have also functionally coupled the O. keta {CRF1} receptor, in Xenopus laevis oocytes, to the endogenous Ca2+-activated chloride conductance by co-expression with the G-protein α subunit, Gα16. The {EC50} value for channel activation by rat/human {CRF} (11.2±2.6 nM) agrees well with that obtained in cAMP assays (15.3±3.1 nM). We conclude that although sauvagine is 13- and 30-fold more potent than rat/human {CRF} and urotensin I, respectively, in activating the salmon {CRF2} receptor, neither receptor appears able to discriminate between the native ligands {CRF} and urotensin I.

Journal Article Type Article
Acceptance Date Sep 7, 2001
Online Publication Date Sep 27, 2001
Publication Date Nov 2, 2001
Deposit Date Jul 26, 2016
Journal European Journal of Pharmacology
Print ISSN 0014-2999
Publisher Elsevier
Peer Reviewed Peer Reviewed
Volume 430
Issue 2-3
Pages 193-202
DOI https://doi.org/10.1016/S0014-2999%2801%2901391-7
Keywords Adenylate cyclase, Corticotropin-releasing factor receptor, Gα16, Urocortin, Urotensin I, Xenopus oocyte expression,
Public URL http://researchrepository.napier.ac.uk/Output/316432