Prostaglandin E receptor EP1 forms a complex with dopamine D1 receptor and directs D1-induced cAMP production to adenylyl cyclase 7 through mobilizing G(βγ) subunits in human embryonic kidney 293T cells.

Abstract:

:The mechanism underlying the crosstalk between multiple G protein-coupled receptors remains poorly understood. We previously reported that prostaglandin E receptor EP1 facilitates dopamine D1 receptor signaling in striatal slices and promotes behavioral responses induced by D1 receptor agonists. Here, using human embryonic kidney (HEK)-293T cells expressing D1 and EP1, we have analyzed the mechanism underlying EP1-mediated facilitation of D1 receptor signaling. Fluorescent immunostaining showed that EP1 and D1 receptors are partly colocalized in the cells, and coprecipitation experiments revealed a molecular complex of EP1 and D1 receptors. Treatment of the cells with 17S,17,20-dimethyl-2,5-ethano-6-oxo-PGE₁ (ONO-DI-004), an EP1-selective agonist, enhanced cAMP production induced by D1 agonists (±)-6-chloro-2,3,4,5-tetrahydro-1-phenyl-1H-3-benzazepine hydrobromide (SKF-81297) and 6-chloro-2,3,4,5-tetrahydro-1-(3-methylphenyl)-3-(2-propenyl)-1H-3-benzazepine-7,8-diol hydrobromide (SKF-83822). Although this facilitative effect of EP1 stimulation was not affected by pharmacologic blockade of EP1-induced Ca²⁺ increase, it was blocked by overexpression of G(tα) as a G(βγ) scavenger. Consistently, depletion of adenylyl cyclase (AC) 7, a G(βγ)-sensitive AC isoform, abolished the facilitative action of EP1 on D1-induced cAMP production. Notably, neither G(tα) overexpression nor AC7 depletion affected cAMP production induced by D1 stimulation alone. In contrast, depletion of AC6, another AC isoform, reduced cAMP production induced by D1 stimulation alone, but spared its facilitation by EP1 stimulation. Collectively, these data suggest that, through complex formation with D1, EP1 signaling directs the D1 receptor through G(βγ) to be coupled to AC7, an AC isoform distinct from those used by the D1 receptor alone, in HEK-293T cells.

journal_name

Mol Pharmacol

journal_title

Molecular pharmacology

authors

Ehrlich AT,Furuyashiki T,Kitaoka S,Kakizuka A,Narumiya S

doi

10.1124/mol.113.087288

subject

Has Abstract

pub_date

2013-09-01 00:00:00

pages

476-86

issue

3

eissn

0026-895X

issn

1521-0111

pii

mol.113.087288

journal_volume

84

pub_type

杂志文章
  • Strong activation of ether-à-go-go-related gene 1 K+ channel isoforms by NS1643 in human embryonic kidney 293 and Chinese hamster ovary cells.

    abstract::Two different mechanisms leading to increased current have been described for the small-molecule human ether-à-go-go-related gene (herg) activator NS1643 [1,3-bis-(2-hydroxy-5-trifluoromethylphenyl)-urea]. On herg1a channels expressed in Xenopus laevis oocytes, it mainly acts via attenuation of inactivation and for ra...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.111.071621

    authors: Schuster AM,Glassmeier G,Bauer CK

    更新日期:2011-11-01 00:00:00

  • High-throughput screening reveals a small-molecule inhibitor of the renal outer medullary potassium channel and Kir7.1.

    abstract::The renal outer medullary potassium channel (ROMK) is expressed in the kidney tubule and critically regulates sodium and potassium balance. The physiological functions of other inward rectifying K(+) (Kir) channels expressed in the nephron, such as Kir7.1, are less well understood in part due to the lack of selective ...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.109.059840

    authors: Lewis LM,Bhave G,Chauder BA,Banerjee S,Lornsen KA,Redha R,Fallen K,Lindsley CW,Weaver CD,Denton JS

    更新日期:2009-11-01 00:00:00

  • Identification of novel small-molecule agonists for human formyl peptide receptors and pharmacophore models of their recognition.

    abstract::N-formyl peptide receptor (FPR1) and N-formyl peptide receptor-like 1 (FPRL1, now known as FPR2) are G protein-coupled receptors involved in host defense and sensing cellular dysfunction. Because of the potential for FPR1/FPR2 as a therapeutic target, our recent high-throughput screening efforts have focused on the id...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.109.060673

    authors: Kirpotina LN,Khlebnikov AI,Schepetkin IA,Ye RD,Rabiet MJ,Jutila MA,Quinn MT

    更新日期:2010-02-01 00:00:00

  • Phenylarsine oxide inhibits agonist-induced changes in photolabeling but not agonist-induced desensitization of the beta-adrenergic receptor.

    abstract::In the human lymphocyte, desensitization of the beta-adrenergic receptor-adenylate cyclase complex is associated with sequestration of the receptor as well as a change in photolabeling of beta-receptor proteins. Thus, desensitization of the lymphocyte beta-adrenergic receptor-adenylate cyclase system is associated wit...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:

    authors: Feldman RD,McArdle W,Lai C

    更新日期:1986-11-01 00:00:00

  • Conformational dynamics of Kir3.1/Kir3.2 channel activation via δ-opioid receptors.

    abstract::This study assessed how conformational information encoded by ligand binding to δ-opioid receptors (DORs) is transmitted to Kir3.1/Kir3.2 channels. Human embryonic kidney 293 cells were transfected with bioluminescence resonance energy transfer (BRET) donor/acceptor pairs that allowed us to evaluate independently reci...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.112.081950

    authors: Richard-Lalonde M,Nagi K,Audet N,Sleno R,Amraei M,Hogue M,Balboni G,Schiller PW,Bouvier M,Hébert TE,Pineyro G

    更新日期:2013-02-01 00:00:00

  • Relative substrate activities of structurally related pteridine, quinazoline, and pyrimidine analogs for mouse liver folylpolyglutamate synthetase.

    abstract::Several structurally related series of folate analogs were studied as substrates for mouse liver folylpolyglutamate synthetase (FPGS). A comparison of the kinetics of the interaction of this enzyme with folate analogs that contained the quinazoline ring in place of the pteridine ring with those of the analogous pterid...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:

    authors: Moran RG,Colman PD,Jones TR

    更新日期:1989-11-01 00:00:00

  • Level of cytosolic free calcium during acetaminophen toxicity in mouse hepatocytes.

    abstract::It has been suggested that elevated cytosolic free calcium plays a key role in acetaminophen-induced cell death. The present study has examined the effect of a toxic concentration of acetaminophen on cytosolic free calcium in single mouse hepatocytes, using the dye fura-2 and video imaging fluorescence microscopy. Cyt...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:

    authors: Harman AW,Mahar SO,Burcham PC,Madsen BW

    更新日期:1992-04-01 00:00:00

  • Molecular basis of the synergistic inhibition of platelet function by nitrovasodilators and activators of adenylate cyclase: inhibition of cyclic AMP breakdown by cyclic GMP.

    abstract::We investigated the roles of cyclic GMP and cyclic AMP in the inhibition of rabbit platelet aggregation and degranulation by two nitrovasodilators, sodium nitroprusside (SNP) and 3-morpholinosydnonimine (SIN-1; the active metabolite of molsidomine), with particular reference to the synergistic interaction of these dru...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:

    authors: Maurice DH,Haslam RJ

    更新日期:1990-05-01 00:00:00

  • Metabolic effects of rexinoids: tissue-specific regulation of lipoprotein lipase activity.

    abstract::Hypertriglyceridemia is a frequent complication accompanying the treatment of patients with either retinoids or rexinoids, [retinoid X receptor (RXR)-selective retinoids]. To investigate the cellular and molecular basis for this observation, we have studied the effects of rexinoids on triglyceride metabolism in both n...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.59.2.170

    authors: Davies PJ,Berry SA,Shipley GL,Eckel RH,Hennuyer N,Crombie DL,Ogilvie KM,Peinado-Onsurbe J,Fievet C,Leibowitz MD,Heyman RA,Auwerx J

    更新日期:2001-02-01 00:00:00

  • Long-term channel block is required to inhibit cellular transformation by human ether-à-go-go-related gene (hERG1) potassium channels.

    abstract::Both human ether-à-go-go-related gene (hERG1) and the closely related human ether-à-go-go (hEAG1) channel are aberrantly expressed in a large proportion of human cancers. In the present study, we demonstrate that transfection of hERG1 into mouse fibroblasts is sufficient to induce many features characteristic of malig...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.113.091439

    authors: Pier DM,Shehatou GS,Giblett S,Pullar CE,Trezise DJ,Pritchard CA,Challiss RA,Mitcheson JS

    更新日期:2014-08-01 00:00:00

  • Multiple actions of propofol on alphabetagamma and alphabetadelta GABAA receptors.

    abstract::GABAA receptors are predominantly composed of alphabetagamma and alphabetadelta isoforms in the brain. It has been proposed that alphabetagamma receptors mediate phasic inhibition, whereas alphabetadelta receptors mediate tonic inhibition. Propofol (2,6-di-isopropylphenol), a widely used anesthetic drug, exerts its ef...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.104.003426

    authors: Feng HJ,Macdonald RL

    更新日期:2004-12-01 00:00:00

  • The effects of pertussis toxin on autoreceptor-mediated inhibition of dopamine synthesis in the rat striatum.

    abstract::Activation of synthesis-modulating dopamine autoreceptors by dopamine or its agonists has been shown to inhibit dopamine synthesis in the rat striatum. However, systemic administration of the direct-acting dopamine agonist apomorphine failed to inhibit dopamine synthesis in striata from rats that had received local un...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:

    authors: Bean AJ,Shepard PD,Bunney BS,Nestler EJ,Roth RH

    更新日期:1988-12-01 00:00:00

  • Different types of receptor interaction of peptide and nonpeptide angiotensin II antagonists revealed by receptor binding and functional studies.

    abstract::The pharmacological effects of angiotensin II (AII) are potently inhibited by several peptide and recently synthesized nonpeptide AII receptor antagonists. The interaction of sarcosine1, isoleucine8-AII (sarile), sarcosine1,O-methyltyrosine4-AII (sarmesin), and the nonpeptide AII antagonists 2-n-butyl-4-chloro-5- hydr...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:

    authors: Wienen W,Mauz AB,Van Meel JC,Entzeroth M

    更新日期:1992-06-01 00:00:00

  • Novel angiotensin II antagonists distinguish amphibian from mammalian angiotensin II receptors expressed in Xenopus laevis oocytes.

    abstract::Angiotensin II (AII) stimulates rapid increases in cytosolic Ca2+ concentrations in Xenopus laevis oocytes after binding to specific receptors located in the surrounding follicular cells. In follicular oocytes, the peptide AII receptor antagonists saralasin (IC50 = 25 nM) and CGP 42112A (IC50 = 400 nM) were orders of ...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:

    authors: Ji H,Sandberg K,Catt KJ

    更新日期:1991-02-01 00:00:00

  • Activation of retinoic acid receptors by dihydroretinoids.

    abstract::Vitamin A-derived metabolites act as ligands for nuclear receptors controlling the expression of a number of genes. Stereospecific saturation of the C(13)-C(14) double bond of all-trans-retinol by the enzyme, retinol saturase (RetSat), leads to the production of (R)-all-trans-13,14-dihydroretinol. In liver and adipose...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.109.060038

    authors: Moise AR,Alvarez S,Domínguez M,Alvarez R,Golczak M,Lobo GP,von Lintig J,de Lera AR,Palczewski K

    更新日期:2009-12-01 00:00:00

  • Chronic selegiline administration transiently decreases tyrosine hydroxylase activity and mRNA in the rat nigrostriatal pathway.

    abstract::Selegiline, a selective monoamine oxidase type B inhibitor, is beneficial in the treatment of Parkinson's disease. However, this beneficial effect is only transient, and patients must ultimately resort to treatment with standard levodopa therapy. We studied the effects of chronic selegiline treatment on the rat nigros...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:

    authors: Vrana SL,Azzaro AJ,Vrana KE

    更新日期:1992-05-01 00:00:00

  • Regulation of the cellular localization and signaling properties of the alpha(1B)- and alpha(1D)-adrenoceptors by agonists and inverse agonists.

    abstract::The regulation of the cellular distribution and intracellular signaling properties of the alpha(1B)- and alpha(1D)- adrenoceptor (alpha(1)-AR) subtypes was examined in stably transfected Rat 1 fibroblasts. In unstimulated cells, alpha(1B)-AR expression was noted primarily on the cell surface. Treatment with phenylephr...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.57.4.659

    authors: McCune DF,Edelmann SE,Olges JR,Post GR,Waldrop BA,Waugh DJ,Perez DM,Piascik MT

    更新日期:2000-04-01 00:00:00

  • The effect of thiopurine methyltransferase expression on sensitivity to thiopurine drugs.

    abstract::Although the thiopurine drugs 6-mercaptopurine (6-MP) and 6-thioguanine (6-TG) are well established agents for the treatment of leukemia, controversies remain regarding their main mode of action. Previous evidence has suggested that although 6-TG exerts a cytotoxic effect through incorporation of 6-thioguanine nucleot...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.62.1.102

    authors: Coulthard SA,Hogarth LA,Little M,Matheson EC,Redfern CP,Minto L,Hall AG

    更新日期:2002-07-01 00:00:00

  • Activation of TRPA1 channels by the fatty acid amide hydrolase inhibitor 3'-carbamoylbiphenyl-3-yl cyclohexylcarbamate (URB597).

    abstract::As a member of the transient receptor potential (TRP) ion channel superfamily, the ligand-gated ion channel TRPA1 has been implicated in nociceptive function and pain states. The endogenous ligands that activate TRPA1 remain unknown. However, various agonists have been identified, including environmental irritants (e....

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.106.033621

    authors: Niforatos W,Zhang XF,Lake MR,Walter KA,Neelands T,Holzman TF,Scott VE,Faltynek CR,Moreland RB,Chen J

    更新日期:2007-05-01 00:00:00

  • Effects of n-dodecylguanidine on A-type potassium channels: role of external surface charges in channel gating.

    abstract::n-Dodecylguanidine (C12-G) is an amphipathic compound with a guanidine moiety, which is positively charged at physiological pH, and a hydrophobic side chain. Its effects on an A-type K+ channel clone (rKv1.4) expressed in Xenopus oocytes were examined. C12-G caused a concentration-dependent (1-20 microM) positive shif...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:

    authors: Yao JA,Saxena NC,Ziai MR,Ling S,Tseng GN

    更新日期:1995-07-01 00:00:00

  • Evidence for a second receptor for prostacyclin on human airway epithelial cells that mediates inhibition of CXCL9 and CXCL10 release.

    abstract::Herein we provide evidence for the coexpression of two distinct prostacyclin (PGI(2)) receptors (IP) on BEAS-2B human airway epithelial cells. IP receptor heterogeneity initially was suggested by the finding that the rank orders of potency of PGI(2) and three structurally similar analogs [taprostene, iloprost, 15-deox...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.110.069674

    authors: Wilson SM,Sheddan NA,Newton R,Giembycz MA

    更新日期:2011-03-01 00:00:00

  • A single amino acid, glu146, governs the substrate specificity of a human dopamine sulfotransferase, SULT1A3.

    abstract::Sulfation, catalyzed by members of the sulfotransferase (SULT) superfamily, exerts considerable influence over the biological activity of numerous endogenous and xenobiotic chemicals. In humans, catecholamines such as dopamine are extensively sulfated, and a SULT isoform (SULT1A3 or the monoamine-sulfating form of phe...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.54.6.942

    authors: Dajani R,Hood AM,Coughtrie MW

    更新日期:1998-12-01 00:00:00

  • Inactivation of multiple hepatic cytochrome P-450 isozymes in rats by allylisopropylacetamide: mechanistic implications.

    abstract::In vivo administration of the porphyrogenic agent allylisopropylacetamide (AIA) to phenobarbital-pretreated rats results in marked loss of hepatic cytochrome P-450 content. Using isozyme-selective functional markers, we now show that such loss reflects inactivation of several phenobarbital-inducible and constitutive i...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:

    authors: Bornheim LM,Underwood MC,Caldera P,Rettie AE,Trager WF,Wrighton SA,Correia MA

    更新日期:1987-08-01 00:00:00

  • Potent inhibition of aldehyde dehydrogenase-2 by diphenyleneiodonium: focus on nitroglycerin bioactivation.

    abstract::Aldehyde dehydrogenase-2 (ALDH2) catalyzes vascular bioactivation of the antianginal drug nitroglycerin (GTN) to yield nitric oxide (NO) or a related species that activates soluble guanylate cyclase (sGC), resulting in cGMP-mediated vasodilation. Accordingly, established ALDH2 inhibitors attenuate GTN-induced vasorela...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.113.086835

    authors: Neubauer R,Neubauer A,Wölkart G,Schwarzenegger C,Lang B,Schmidt K,Russwurm M,Koesling D,Gorren AC,Schrammel A,Mayer B

    更新日期:2013-09-01 00:00:00

  • A novel metabotropic glutamate receptor 5 positive allosteric modulator acts at a unique site and confers stimulus bias to mGlu5 signaling.

    abstract::Metabotropic glutamate receptor 5 (mGlu5) is a target for the treatment of central nervous system (CNS) disorders, such as schizophrenia and Alzheimer's disease. Furthermore, mGlu5 has been shown to play an important role in hippocampal synaptic plasticity, specifically in long-term depression (LTD) and long-term pote...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.112.082891

    authors: Noetzel MJ,Gregory KJ,Vinson PN,Manka JT,Stauffer SR,Lindsley CW,Niswender CM,Xiang Z,Conn PJ

    更新日期:2013-04-01 00:00:00

  • Enantioselective effects of hydroxy metabolites of bupropion on behavior and on function of monoamine transporters and nicotinic receptors.

    abstract::Bupropion is an atypical antidepressant that also has usefulness as a smoking-cessation aid. Because hydroxybupropion, a major metabolite of bupropion, is believed to contribute to its antidepressant activity, this metabolite may also contribute to the smoking-cessation properties of bupropion. This study investigated...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.104.001313

    authors: Damaj MI,Carroll FI,Eaton JB,Navarro HA,Blough BE,Mirza S,Lukas RJ,Martin BR

    更新日期:2004-09-01 00:00:00

  • Structural Asymmetry of Phosphodiesterase-9A and a Unique Pocket for Selective Binding of a Potent Enantiomeric Inhibitor.

    abstract::Phosphodiesterase-9 (PDE9) inhibitors have been studied as potential therapeutics for treatment of central nervous system diseases and diabetes. Here, we report the discovery of a new category of PDE9 inhibitors by rational design on the basis of the crystal structures. The best compound, (S)-6-((1-(4-chlorophenyl)eth...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.115.099747

    authors: Huang M,Shao Y,Hou J,Cui W,Liang B,Huang Y,Li Z,Wu Y,Zhu X,Liu P,Wan Y,Ke H,Luo HB

    更新日期:2015-11-01 00:00:00

  • Selective block of late currents in the DeltaKPQ Na(+) channel mutant by pilsicainide and lidocaine with distinct mechanisms.

    abstract::The congenital long QT syndrome is an inherited disorder characterized by a delay in cardiac repolarization, leading to lethal cardiac arrhythmias such as torsade de pointes. One form of this disease involves mutations in the voltage-dependent cardiac Na(+) channel, which includes an in-frame deletion of three amino a...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:

    authors: Ono K,Kaku T,Makita N,Kitabatake A,Arita M

    更新日期:2000-02-01 00:00:00

  • Effects of active and inactive phospholipase D2 on signal transduction, adhesion, migration, invasion, and metastasis in EL4 lymphoma cells.

    abstract::The phosphatidylcholine-using phospholipase D (PLD) isoform PLD2 is widely expressed in mammalian cells and is activated in response to a variety of promitogenic agonists. In this study, active and inactive hemagglutinin-tagged human PLD2 (HA-PLD2) constructs were stably expressed in an EL4 cell line lacking detectabl...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.107.040105

    authors: Knoepp SM,Chahal MS,Xie Y,Zhang Z,Brauner DJ,Hallman MA,Robinson SA,Han S,Imai M,Tomlinson S,Meier KE

    更新日期:2008-09-01 00:00:00

  • Cellular resistance to the antitumor DNA topoisomerase II inhibitor S16020-2: importance of the N-[2(Dimethylamino)ethyl]carbamoyl side chain.

    abstract::The new olivacine derivative S16020-2 (NSC-659687) is a DNA topoisomerase II inhibitor endowed with a remarkable antitumor activity against various experimental tumors. In vitro physicochemical properties of this compound, in particular its interaction with DNA and DNA topoisomerase II, were very similar to those of e...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.58.4.709

    authors: Le Mée S,Chaminade F,Delaporte C,Markovits J,Saucier JM,Jacquemin-Sablon A

    更新日期:2000-10-01 00:00:00