Airway smooth muscle prostaglandin-EP1 receptors directly modulate 2-adrenergic receptors within a unique heterodimeric complex
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1Pulmonary Division, Department of Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.
2Cardiopulmonary Genomics Program, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Abstract
Multiple and paradoxical effects of airway smooth muscle (ASM) 7-transmembrane–spanning receptors activated during asthma, or by treatment with bronchodilators such as 2–adrenergic receptor (2AR) agonists, indicate extensive receptor crosstalk. We examined the signaling of the prostanoid-EP1 receptor, since its endogenous agonist prostaglandin E2 is abundant in the airway, but its functional implications are poorly defined. Activation of EP1 failed to elicit ASM contraction in mouse trachea via this Gq-coupled receptor. However, EP1 activation markedly reduced the bronchodilatory function of 2AR agonist, but not forskolin, indicating an early pathway interaction. Activation of EP1 reduced 2AR-stimulated cAMP in ASM but did not promote or augment 2AR phosphorylation or alter 2AR trafficking. Bioluminescence resonant energy transfer showed EP1 and 2AR formed heterodimers, which were further modified by EP1 agonist. In cell membrane [35S]GTPS binding studies, the presence of the EP1 component of the dimer uncoupled 2AR from Gs, an effect accentuated by EP1 agonist activation. Thus alone, EP1 does not appear to have a significant direct effect on airway tone but acts as a modulator of the 2AR, altering Gs coupling via steric interactions imposed by the EP1:2AR heterodimeric signaling complex and ultimately affecting 2AR-mediated bronchial relaxation. This mechanism may contribute to -agonist resistance found in asthma.
See the related Commentary beginning on page 1210
Introduction
The 7-transmembrane–spanning (7-TM–spanning) receptors represent the largest signaling family in the genome. We estimate that the lung expresses 25–50 7-TM receptors in airway epithelial cells, airway smooth muscle (ASM), pulmonary vasculature, alveolar walls, and resident immune cells (1). In regard to asthma, several 7-TM receptors play established roles in bronchoconstriction (e.g., M3-muscarinic receptor) and bronchodilation (e.g., 2–adrenergic receptor [2AR]). Despite identification of the endogenous ligands and receptor localization, there are a number of 7-TM receptors expressed in the airway whose functions are unknown, or appear to function paradoxically, based on recombinantly expressed receptors in model cell systems. This lack of understanding of receptor function has impeded our ability to ascertain the role of these ligands (some of which are markedly increased in asthma) in the relaxation/contraction of ASM; thus the mechanistic basis of bronchial hyperreactivity and bronchoconstriction in asthma remains only partially understood. In many cases the basis for incomplete mechanistic information can be attributed to the nature of recombinant expression systems, which may not take into account multiple receptor subtypes, receptor/receptor interactions, crosstalk via second messengers, or subcellular localization of receptors and specific effectors.
These issues are particularly obvious when one considers the biologic actions of prostaglandin E2 (PGE2), which, via at least 4 receptor subtypes (EP1–EP4), can evoke multiple signals. By activation of the Gs-coupled EP2 receptor, PGE2 can evoke ASM relaxation (2). However, blockade of PGE2 production leads to partial reversal of 2AR desensitization in the context of inflammation (3), and thus PGE2 may promote bronchoconstriction via desensitization of 2AR function or by activation of the Gq-coupled EP1 receptor. PGE2 is produced by ASM, airway epithelial cells, and inflammatory cells and is the most abundant prostanoid in epithelial lining fluid (4-6). However, EP1-mediated signal transduction and its effect on airway responsiveness remains unclear. We show here a unique function of the EP1 receptor in ASM, which to our knowledge has not been previously described for 7-TM receptors. The EP1 receptor itself, despite its coupling to inositol 1,4,5-triphosphate (IP3) and intracellular calcium ([Ca2+]i), failed to exert the expected bronchoconstrictive response. Instead, EP1 receptor activation modulated 2AR function via formation of a heterodimeric complex that directly decreased 2AR coupling to Gs in an EP1 receptor, agonist-dependent, fashion.
Results
EP1 receptor activation in isolated and intact ASM.
The biologic actions of PGE2 are potentially mediated by multiple receptor subtypes that differentially couple to Gq, Gi, and Gs. Although a relaxant action of PGE2, mediated via the EP2 isoform in ASM, has been documented (7), the extent to which PGE2 couples to the other subtypes in ASM, particularly the potentially probronchoconstrictive Gq-coupled EP1 receptor, is not established. EP1-specific RT-PCR was carried out on murine ASM cells in culture (Figure 1A). A single product of the expected molecular size was obtained, and Southern blots with an EP1-specific oligonucleotide hybridized to the product. Sequencing further confirmed the product as the murine EP1 receptor (GenBank accession no. NM_013641). With regard to signal transduction, the EP1-specific agonist 17-phenyl trinor-PGE2 (17-PTP) was found to stimulate inositol phosphate production (Figure 1B) and [Ca2+]i transients (Figure 1C). Of note, maximal activation of the EP1 receptor by 17-PTP stimulated [Ca2+]i to a greater extent, and with greater potency, than the M3-muscarinic agonist carbachol (Figure 1D). These findings confirmed EP1 receptor expression in ASM cells and that its activation by agonists resulted in IP3 and [Ca2+]i turnover as assessed in whole cells. Because these effectors mediate 7-TM receptor contraction of ASM, the data suggested that the EP1 receptor would likely promote airway contraction.
Excised mouse tracheal ring preparations were utilized to ascertain the effects of EP1 activation on active force generation in the intact airway. However, despite its ability to stimulate IP3 and [Ca2+]i turnover in ASM, 17-PTP caused no detectable contraction of tracheal rings even at concentrations up to 10 μM (Figure 2A). Since 17-PTP did not directly effect ASM tone, we next investigated whether EP1 receptor activation could modify the response to another contractile agonist acting through Gq. For these studies, tracheal rings were pretreated with 1 μM 17-PTP for 15 minutes prior to contraction with various concentrations of acetylcholine (Figure 2A). The maximal acetylcholine response in the absence (26 ± 5.3 mN) or presence (26 ± 4.8 mN) of EP1 coactivation was not different, nor was the EC50 for the response (91 ± 11 versus 82 ± 15 μM, respectively). We next considered whether EP1 receptor activation alters ASM relaxation. The efficacy and potency of the AR agonist isoproterenol to relax acetylcholine-constricted ASM in the presence and absence of EP1 receptor activation was ascertained. Tracheal rings were first treated with vehicle or 1 μM 17-PTP for 15 minutes, contracted continuously with 10 μM acetylcholine, and exposed to increasing concentrations of isoproterenol. In the presence of vehicle, isoproterenol caused a dose-dependent relaxation with an EC50 of 23.4 ± 4.8 nM and a maximal reduction in force of 36.6% ± 2.9% (Figure 2B). However, following pretreatment with 17-PTP, a marked reduction in AR-mediated relaxation was observed, with isoproterenol evoking only 17.1% ± 2.4% relaxation (n = 6; P < 0.001; Figure 2B). Of note, the EC50 for isoproterenol was also increased under these conditions to 58.2 ± 6.1 nM (P < 0.001). As shown in Figure 2C, this same AR desensitization effect of 17-PTP was observed when tracheal rings were contracted by 60 mM KCl. The endogenous EP1 receptor agonist is PGE2, which activates other EP receptors and thus under physiologic conditions could evoke an effect that dominates airway responses over the EP1-specific phenotype we observed. We therefore studied the effect of pretreatment with 10 nM PGE2 (which evokes only 15% relaxation) using the same protocol as for 17-PTP. As shown in Figure 2D, PGE2 also evoked a loss of isoproterenol-mediated relaxation, amounting to an approximate 25% desensitization. This lower amount of desensitization (compared with 17-PTP pretreatment) may be due to the combined relaxant effect of PGE2 and isoproterenol.
Given that mouse trachea has a mixed population of 1AR and 2AR subtypes (8), the 17-PTP effect was also assessed using the relatively 2AR subtype-specific agonist formoterol. Under these conditions, 17-PTP evoked a 55% ± 5% desensitization of formoterol-mediated relaxation, indicating a 17-PTP effect on 2AR (the predominant AR subtype of human tracheal ASM). To determine whether the inhibitory effect of 17-PTP extended to other ASM relaxants, we performed analogous experiments with forskolin, which directly activates adenylyl cyclase, mimicking a Gs-coupled receptor. However, unlike the response with isoproterenol, pretreatment with 17-PTP had no effect on the maximal response or the EC50 (Figure 3A). Given that the EP1 receptor couples to Gq, we considered that second messengers generated from phospholipase C (PLC) activation may be involved in the apparent crosstalk between 2AR and EP1 receptors. However, pretreatment with the PLC inhibitors U73122 (5 μM; Figure 3B) and Et-18-OCH3 (10 μM; data not shown) failed to alter the 17-PTP effect. 2ARs have also been shown in some cells to couple to Gi (9), which may act to oppose Gs-mediated signaling. Treatment of tracheal rings with pertussis toxin, however, had no effect on the EP1-mediated 2AR desensitization (Figure 3C), indicating that enhanced Gi coupling was an unlikely mechanism. Finally, the 2AR desensitization phenotype evoked by EP1 activation was not altered by pretreatment with 100 μM of the NO inhibitor L-NAME (51.2% ± 6.8% desensitization) or 10 μM of the cyclooxygenase inhibitor indomethacin (57% ± 5% desensitization).
Desensitization of 2AR by EP1 receptor activation.
The inhibitory effect of 17-PTP on isoproterenol-mediated relaxation observed in the tracheal ring studies indicated functional interplay between the EP1 and 2AR signal transduction pathways. Additionally, the absence of a significant EP1 effect on forskolin-mediated relaxation and no change in phenotype observed with PLC inhibition suggested that this interaction could potentially occur at the level of the 2AR itself. The effect of 17-PTP on isoproterenol-stimulated cAMP production was determined in isolated ASM cells. In the absence of 17-PTP, 1 μM isoproterenol stimulated cAMP to 88.0% ± 16.3% of the maximum level obtained with 10 μM forskolin. However, when cells were pretreated with 1 μM 17-PTP for 15 minutes prior to isoproterenol stimulation, cAMP production was reduced to 37.0% ± 3.9% (n = 4; P = 0.02) of the forskolin response (Figure 4A). Taken together with the tracheal ring data, these results indicated an interplay between the EP1 receptor and 2AR, with activation of the former resulting in decreased function of the latter. Two processes that we considered potential mechanisms to account for uncoupling of 2AR signal transduction within the time frame of minutes included (a) enhanced loss of cell surface receptors due to internalization and (b) enhanced isoproterenol-stimulated 2AR phosphorylation due to EP1 activation or phosphorylation of the 2AR by EP1 activation via PKC. To ascertain whether EP1 activation altered the extent or rate of agonist-mediated 2AR internalization, we performed radioligand binding on intact ASM cells with the hydrophilic radioligand [3H]-CGP-12177. Since this ligand does not enter intact cells (10), a decrease in binding occurs when surface receptors are internalized. Thus, as expected for agonist-promoted internalization of the 2AR, exposure of ASM cells to 1 μM isoproterenol caused a time-dependent decrease in [3H]-CGP-12177 binding sites of 39.1% ± 5.7% after 30 minutes (Figure 4B). Pretreatment of cells with 1 μM 17-PTP for 15 minutes had no effect on isoproterenol-stimulated internalization (37.4% ± 3.6%; n = 5). We next examined the potential for 17-PTP to promote phosphorylation of the 2AR. For the phosphorylation experiments, human embryonic kidney (HEK) cells transiently cotransfected with plasmids so as to express the EP1 receptor and FLAG-tagged 2AR were loaded with 32P-orthophosphate. Cells were treated with vehicle, isoproterenol, 17-PTP, phorbol-12-myristate-13-acetate (a positive control for PKC-mediated event), or isoproterenol plus 17-PTP. 2AR was purified by FLAG immunoprecipitation. As shown in Figure 4C, isoproterenol evoked robust phosphorylation of the 2AR, while no detectable phosphorylation over background was noted with 17-PTP exposure alone. Importantly, the extent of isoproterenol–promoted 2AR phosphorylation was not altered by 17-PTP (48 ± 4.5 relative units versus 42 ± 4.2 relative units in the presence and absence of 17-PTP, respectively; n = 5; P = NS).
2ARs and EP1 receptors form heterodimers.
Since these well-defined short-term mechanisms of receptor regulation and crosstalk were not at play during EP1-induced desensitization of 2AR, we considered an alternative hypothesis, which was that the 2 receptors formed heterodimers. We also considered whether agonist activation of the EP1 receptor directly affected the receptor/receptor interaction within the complex, altering 2AR coupling to Gs. As a screen for such a complex in ASM cells, fluorescence microscopy was carried out using 2AR- and EP1-specific primary antibodies. Secondary antibodies provided for red (2AR) and green (EP1) signals. Merged images revealed yellow signals consistent with areas of colocalization of these 2 receptors (Figure 5A). To rigorously assess the potential for heterodimer formation, bioluminescence resonant energy transfer (BRET) and coimmunoprecipitation studies were undertaken in transfected HEK 293 cells. BRET was carried out in living cells expressing 2 receptors having carboxyterminally fused Renilla luciferase (Rluc) or yellow fluorescent protein (YFP). As described in detail elsewhere (11-13), this approach takes advantage of a signal produced by the energy donor moiety (Rluc) acting on the energy acceptor (YFP) when the two are in very close proximity. As shown in Figure 5B, studies carried out in HEK 293 cells transfected to express 2AR-Rluc and EP1-YFP (see Methods) indeed revealed a BRET signal, as indicated by the perturbation of the emission spectrum at 530 nM. To verify that this represented oligomer formation, rather than a "pseudo-BRET" signal (11) due to random collisions of overexpressed receptors, studies were carried out with multiple levels of expression (altering the 2AR-Rluc/EP1-YFP ratio). As expected under conditions of dimer formation, the BRET signal saturated, with a calculated maximal ratio (BRETmax) of 0.49 ± 0.04 and a BRET50 of 2.97 ± 0.56 (Figure 5C). In contrast, in experiments utilizing cotransfections of 2AR-Rluc and a YFP fusion with the -aminobutyric acid receptor subtype bR2 (GABAb R2–YFP) a small signal was observed, as was the case with cotransfections of C-C chemokine receptor 5–Rluc (CCR5-Rluc) and 2AR-YFP (Figure 5D). These low-level signals and a lack of saturation (data not shown) were consistent with prior observations that neither the GABAb R2 nor CCR5 receptors form heterodimers with the 2AR (13, 14). We next examined whether activation of the EP1 receptor or the 2AR altered the BRET signal. As shown in Figure 5E, treatment of cotransfected cells with 17-PTP or isoproterenol for 15 minutes prior to the addition of coelenterazine h increased the BRET signal in both cases. Given that most 7-TM dimers appear to be formed intracellularly and then expressed at the cell surface (11, 12, 15, 16), and given the short-term agonist exposure used in these experiments, we do not interpret these results as representing an increased number of dimers per se. Rather, the data are consistent with a conformational change that occurs (potentially in either receptor) when one receptor is bound by its agonist, which causes the Rluc and YFP moieties to move closer together. The magnitude of the agonist-promoted increase in BRET is not trivial, in that the BRET signal is proportional to the distance between the donor and acceptor by a factor of 106 (11, 12, 15).
To further corroborate dimer formation, coimmunoprecipitation studies were carried out in HEK 293 cells transfected to express FLAG-2AR and the EP1 receptor both alone and together. Immunoprecipitation was carried out with anti-FLAG antibody, and the precipitated proteins were fractionated on SDS-PAGE followed by Western blots using a polyclonal EP1 antisera. As shown in Figure 5F, the EP1 receptor migrated at approximately 45 kDa in Western blots of cell lysates using the EP1 antisera. Upon immunoprecipitation with FLAG antibody, protein from cells transfected to express EP1 or 2AR showed no immunoreactivity with the EP1 antisera. However, when the 2 receptors were cotransfected, a band of the appropriate molecular size was observed. Of note, the high–molecular weight bands, which could represent dimers, are often not resistant to SDS and are not typically visualized (14). These coimmunoprecipitation studies are thus consistent with the BRET results, indicating the presence of the EP1:2AR heterodimer.
EP1: 2AR heterodimer formation uncouples 2AR from G
s. Taken together, the above results indicated that the EP1 receptor and the 2AR exist as an oligomeric complex, with activation of the EP1 receptor markedly desensitizing 2AR signaling and physiologic function, and that such desensitization is not due to downstream second messenger feedback. This suggested that agonist activation of the EP1 receptor within the dimer results in a steric effect on the 2AR, altering its conformation in such a way as to directly affect 2AR-Gs interaction. To examine this, we studied agonist-promoted [35S]GTPS binding in cell membranes. This provided for direct quantitation of receptor–G protein interaction by measuring GTP turnover and, since it is performed with isolated membranes, was not affected by intracellular factors. In these studies, [35S]GTPS binding was carried out by incubating membranes from cells transfected to express Gs, 2AR, and the EP1 receptor with vehicle, isoproterenol alone, or isoproterenol with 17-PTP. In other studies, Gs and 2AR were expressed without the EP1 receptor so as to ascertain 2AR coupling to Gs in the absence of the EP1:2AR dimer. Expression levels of 2AR in the 2AR and EP1 (3774 ± 815 fmol/mg) and 2AR transfections (3367 ± 185 fmol/mg) were comparable. Net isoproterenol-stimulated [35S]GTPS binding is shown in Figure 6A. Incubation with 17-PTP resulted in a significant decrease in isoproterenol-stimulated binding, amounting to an approximately 60% reduction (n = 4; P = 0.02). Interestingly, the presence of the EP1 receptor, even in the absence of its activation by agonist, decreased 2AR coupling to Gs. As shown in Figure 6A, cells expressing 2AR alone had the highest isoproterenol-stimulated [35S]GTPS binding, and as expected, 17-PTP had no effect in these cells. Additional studies were also carried out using ASM cell membranes (Figure 6B). Analogous to what was observed in the transfected cell studies, [35S]GTPS turnover was decreased when membranes were incubated with isoproterenol and 17-PTP compared with isoproterenol alone. These data then confirmed the concept of a direct interaction between the 2 receptors in the cell type of interest when the receptors were expressed at physiologic levels.
Discussion
PGE2 is a cyclooxygenase-derived product of arachidonic acid metabolism that plays a major role in regulating such diverse physiological processes as smooth muscle tone, inflammation, and pain (reviewed in ref. 17). The biological effects of PGE2 are often multifaceted and can appear contradictory to traditional signaling paradigms. As introduced earlier, some of these properties of PGE2 are due to the fact that it is an endogenous agonist for 4 receptor subtypes coupled to several signal transduction cascades. The EP1 receptor is linked to IP3 and [Ca2+]i turnover through Gq-mediated signal transduction (18), whereas the EP2 and EP4 receptors stimulate adenylyl cyclase and cAMP production through Gs (19-21). Splice variants of the EP3 receptor give rise to multiple isoforms that apparently can couple to Gi, Gs, or Gq (22, 23). Since one or more of these receptors may be expressed by a cell or tissue, the integrated response to PGE2 often represents the net effect of additive or opposing signal transduction events. Moreover, temporal and spatial changes in patterns of EP receptor expression in response to various stimuli (e.g., injury and inflammation) provide an additional level of dynamic regulation and complexity to PGE2-regulated processes in the airways. For example, recent studies of the PGE2-mediated fibroproliferative response due to intratracheal bleomycin have shown an approximately 50% decrease in fibroblast EP2 receptor mRNA without significant change in the other EP subtypes (24), whereas FITC-mediated fibrosis was associated with decreases in both EP2 and EP4 transcript expression (24).
Because PGE2 is produced endogenously within the lung and activates pathways that may both enhance and inhibit ASM contraction, it may have particular relevance in asthma. PGE2 is produced by ASM cells, bronchial and alveolar epithelial cells, fibroblasts, and inflammatory cells in the lung, and increased levels have been reported in some studies with human asthma (25, 26). Furthermore, an initial enzyme for prostanoid receptor synthesis (COX-2), as well as PGE2 precursors, are increased in asthmatic airways (27, 28). Following its discovery, PGE2 was found to relax ASM and thus has generally been considered to be a bronchoprotective prostanoid. The bronchodilatory effect of PGE2 appears to be due to activation of the EP2 receptor subtype, since PGE2-mediated bronchodilation is present in EP1-, EP3-, and EP4-null mice but absent in EP2-null mice (29). Interestingly, in nonasthmatic humans, PGE2 exerts a net bronchodilation; in asthmatics, though, the response is highly variable, sometimes resulting in significant bronchoconstriction (30). The complex nature of PGE2 action in the asthmatic milieu is further illustrated in that it may serve as an intermediary through which inflammatory cytokines can modulate other receptor systems that govern airway tone. In particular, PGE2 appears to mediate the inhibitory effects of the inflammatory cytokines TGF and interleukin-1 on 2AR signal transduction in cultured ASM (31-34). These inflammatory cytokines stimulate COX-2 and production of PGE2 by ASM, and it has been proposed that the resulting increase in cAMP production following EP2 receptor activation leads to desensitization of the 2AR (3). However, the mechanism(s) by which this inhibition occurs has not been completely elucidated, nor has the role of other EP receptor subtypes in mediating this effect been explored.
We define here a unique role for the EP1 receptor expressed on ASM cells using both molecular studies in transfected cells and ASM cells and physiologic studies in trachea. We showed that the EP1 receptor existed as a heterodimer (or higher-order oligomer) with the 2AR, and the signaling of this complex was manifested by an altered 2AR conformation and decreased functional interaction with Gs. EP1 activation by agonist further enhanced 2AR desensitization, as shown in the [35S]GTPS studies. This effect was also readily observed in ASM cells utilizing whole-cell cAMP measurements and membrane [35S]GTPS binding and manifested at the physiologic level with intact tracheal rings. Interestingly, the extent of 2AR desensitization evoked by the EP1 agonist, as assessed using these distinctly different methods, amounted to approximately 50% in all cases. In addition, the EP1 receptor, while capable of stimulating intracellular IP3 and [Ca2+]i (as assessed by global whole-cell assays), did not ultimately cause significant ASM contraction. Thus the dimer may serve not only to form a specialized signaling unit, but could also place the complex in a subcellular compartment that isolates it from activation of the downstream components of contraction. Indeed, 2ARs have been shown to be localized to caveolae, which are specialized flask-shaped invaginations of the cell membrane that promote association of the receptor with certain signal transduction elements (35). However, we note that EP1 receptor–mediated contraction has been observed in guinea pig trachea (36), suggesting that the extent of EP1-mediated tracheal contraction may depend on the species.
We have thus considered the physiologic role of the EP1 receptor in ASM as primarily one of modulating 2AR function, with no observable direct effect on contraction. To our knowledge, this "monitor-like" function has not been previously described for a 7-TM receptor with its heterodimeric partner. However, there are somewhat analogous scenarios with other receptors. For the GABAb R1 and R2 subtypes, it appears that the R1:R2 heterodimer represents a distinct signaling unit, in that the R1 subtype binds the agonist while the R2 subtype couples to G protein activation (37). Furthermore, GABAb R1 cell surface expression requires heterodimer formation with GABAb R2 in the endoplasmic reticulum (38). For the 1DAR, cell surface expression appears to be dependent on oligomeric association with the 1BAR (39). Once so expressed, each subtype can signal independently. Similarly, the 2AR can form dimers with the 1DAR and promote its expression (40). Other examples of homo-and heterodimerization function have been recently reviewed (12, 15, 16). We are unaware of a previous report of the unique function of a 7-TM receptor that we describe here.
In the current report, we utilized the physiologic readout of airway contraction and relaxation as the relevant functional signal and found that activation of the EP1 receptor had no direct physiologic action. However, we found that EP1 activation resulted in substantial loss of 2AR-mediated ASM relaxation. We demonstrated that this interaction of signal transduction networks occurred at the level of the receptors, rather than downstream effectors, and was not due to posttranslational modification of the 2AR by phosphorylation or other potential distal-pathway crosstalk mechanisms (41). Rather, formation of the EP1:2AR heterodimer was a distinct signaling complex, where the EP1 receptor modulates 2AR coupling to Gs. Using multiple approaches, the EP1-agonist dependency of the 2AR modulation was demonstrated. However, we cannot exclude the notion that the mere presence of the heterodimer acts to modulate the function of one of its members, the 2AR. Indeed, the [35S]GTPS binding studies showed that 2AR coupling to Gs was decreased when coexpressed with the EP1 receptor. However, the spontaneous switching of the EP1 receptor to the active conformation may mimic the agonist-occupied form; thus it is not unexpected that coexpression, particularly at relatively high levels, would have an agonist-occupied effect. Regardless, in the native state both receptors were expressed on ASM, and we showed that EP1 receptor activation decreased 2AR function in isolated ASM cells and in intact tissue.
In summary, we define a unique modulatory function of the EP1 receptor, which acts primarily to regulate 2AR function. In asthma, then, local concentrations of elevated PGE2 could act to quench 2AR function, resulting in decreased responsiveness to -agonist. The mechanism of this receptor interaction appears to be due to the formation of a heterodimer; thus the EP1:2AR dimer should be considered the functional signaling complex in ASM, with a unique phenotype based on steric interactions that lead to attenuated 2AR-Gs coupling.
Methods
Plasmid constructs, cells culture, and transfection.
The human 2AR cDNA was tagged at the amino terminus with the FLAG epitope and fused at the carboxyl terminus with the cDNA for Rluc, and the cDNA for the human EP1 receptor was fused at the carboxyl terminus with the cDNA for YFP, using standard techniques. The final constructs representing 2AR, FLAG-2AR, and 2AR-Rluc were in pcDNA3, and the EP1-YFP construct was in pEYFP-N1 (BD Biosciences — Clontech). Primary cultures of ASM cells were derived from explants of excised tracheas from the mice as reported previously (42) and maintained in DMEM, 10% FCS, and x1 antibiotic-antimycotic solution (Invitrogen Corp.) at 37°C in a 95% air, 5% CO2 incubator. These cells maintain the morphologic and immunohistochemical characteristics of ASM cells for at least 15 passages, although most experiments were performed with cells in passages 4–12. Both COS-7 and HEK 293 cells were similarly maintained as monolayers in DMEM supplemented with 10% FCS, 100 U/ml penicillin, and 100 mg/ml streptomycin. Transfection of these cells for BRET and [35S]GTPS binding experiments was performed using Lipofectamine (Invitrogen Corp.) by methods previously described (43).
RT-PCR.
Total RNA was extracted from freshly isolated lungs with Tri-Reagent (Molecular Research Center Inc.). An aliquot of RNA was reverse transcribed with random hexamers with murine leukemia virus reverse transcriptase (PerkinElmer) as previously described (43). Transgene cDNA was amplified with 150 nM each of a sense primer (5'-CGTGTCATTTCCTGGGTGGCT-3') and an antisense primer homologous to regions within the mouse EP1 open reading frame (5'-GTGGCTGTGGCTGAAGTGATG-3'). PCR was at 95°C for 120 seconds followed by amplification for 35 cycles at 95°C for 60 seconds and 56°C for 60 seconds and a final extension at 72°C for 7 minutes. The PCR products were detected in agarose gels stained with ethidium bromide. RNA samples not subjected to reverse transcription were used as negative controls to ensure that the observed PCR product was not the result of contaminating DNA.
Measurement of inositol phosphate production and [Ca2+]i.
Formation of [3H]-inositol phosphate was determined in intact ASM cells as previously reported (41). Briefly, near-confluent ASM cells in 12-well plates were incubated with inositol-free media containing [3H]-myoinositol (5 μCi/ml) for 24 hours at 37°C in 5% CO2 atmosphere. Cells were then washed and incubated with PBS for 30 minutes followed by a 30-minute incubation with 20 mM LiCl in PBS. The cells were treated with either PBS (basal), 1 μM PGE2, 1 μM 17-PTP, or thrombin (a positive control) for 15 minutes, after which total inositol phosphates were extracted by column chromatography with AG1-X8 resin (Bio-Rad).
To measure [Ca2+]i, murine ASM cells were seeded into black-walled, clear-based 96-well plates (Corning) at a density of approximately 80,000 cells per well and cultured overnight in 100 μl DMEM supplemented with 10% FCS as above. On the following day, the cells were incubated at 37°C for 60 minutes with the Calcium 3 indicator (Molecular Devices) that was dissolved in Hank’s balanced salt solution containing 20 mM HEPES, pH 7.4, and 2.5 mM probenecid in a final volume of 200 μl/well. The cell plates were then placed into the FlexStation II scanning fluorimeter/luminometer (Molecular Devices) to monitor fluorescence before and after the addition of 50 μl vehicle or a x5 concentration of the indicated drug (Figure 1, C and D) using an excitation wavelength of 485 nm, emission wavelength of 525 nm, and emission cutoff of 515 nm. Responses were measured as peak fluorescence intensity minus basal fluorescence intensity, with each data point in an individual experiment representing the mean of 4 replicates. Final data reported represent the mean of 4 different experiments using ASM cells derived from 2 different mice.
Radioligand binding and cAMP production.
The expression of 2ARs in membranes prepared from transiently transfected HEK 293 and COS-7 cells was quantified by radioligand binding assays using the antagonist [125I]-iodocyanopindolol as previously reported (44). To assess the rate of 2AR sequestration in ASM cells, whole-cell binding assays were performed using the hydrophilic, membrane-impermeant radioligand [3H]-CGP-12177 to determine the amount of cell-surface 2AR in the untreated cells as well as in cells treated with either isoproterenol or isoproterenol with 17-PTP (1 μM each) for periods up to 30 minutes as previously described in detail (45).
To measure cAMP production, ASM cells were seeded onto 24-well plates and maintained overnight in DMEM supplemented with 10% FCS to allow adherence. The cells were then switched to serum-free DMEM for an additional 24 hours. The cells were loaded with [3H]-adenine (2 μCi/well) for 2 hours and then washed twice with PBS to remove excess adenine. Cells were then treated with either vehicle or 17-PTP (1 μM final concentration) for 15 minutes before stimulation with either 1 μM isoproterenol or 100 μM forskolin for 15 minutes. Reactions were terminated by the addition of 50 μl concentrated HCl. After the samples were frozen and thawed once to ensure cell lysis, cAMP was eluted by alumina column chromatography. Recovered counts were corrected for adenine uptake, and column efficiency ascertained with tracer [14C]-cAMP. Each data point was determined from the mean of triplicate samples, and expressed as its percentage of the mean forskolin response for that experiment. The results shown represent the mean ± SEM of 4 separate experiments performed with cell lines derived from 2 different mice.
Tracheal ring contractility studies.
Studies of mouse tracheal ring contractility were performed as reported previously in detail (41). Briefly, tracheas were excised and dissected free of surrounding tissues and cut into rings of 5 mm in length. The rings were mounted on stainless steel wires connected to isometric force transducers and immersed in a physiologic saline solution (118 mM NaCl, 11 mM glucose, 4.73 mM KCl, 1.2 mM MgCl2, 0.026 mM EDTA, 1.2 mM KH2PO4, 2.5 mM CaCl2, and 25 mM NaH2CO3) at 37°C and bubbled with 95% O2 and 5% CO2, maintaining a pH of 7.40. Each tracheal ring was stretched to a tension of 5 mN, which we have previously determined to be an optimal passive tension for maximizing active force (42). Following a period of equilibration for 30 minutes, the indicated agents (Figures 2 and 3) were added to the bath, and the maximal response over the next 5 minutes was recorded. Cumulative concentration-isometric force curves were generated for the responses using standard curve-fitting techniques. Pretreatments of equilibrated rings included 1 μM 17-PTP for 15 minutes, 10 nM PGE2 for 15 minutes, 10 μg/ml pertussis toxin for 4 hours, 100 μM L-NAME for 30 minutes, 10 μM indomethacin for 30 minutes, 5 μM U73112 for 15 minutes, and 10 μM Et-18-OCH3 for 30 minutes. All mouse studies were reviewed and approved by the University of Cincinnati College of Medicine Animal Care and Use Committee.
Receptor phosphorylation.
Whole-cell phosphorylation experiments were performed as previously described (46), with minor modifications. HEK 293 cells cotransfected with the 2AR-FLAG and EP1-YFP constructs were plated in 100-mm dishes. Forty-eight hours after transfection, the media was changed to serum- and phosphate-free DMEM containing 500 μCi/ml 32P-orthophosphate. After incubation for 2 hours at 37°C in 95% air and 5% CO2, the cells were treated with vehicle, 1 μM isoproterenol, 100 nM phorbol-12-myristate-13-acetate, 1 μM 17-PTP, or 1 μM isoproterenol plus 1 μM 17-PTP for 15 minutes. The cells were then washed 4 times with ice-cold PBS and solubilized by rotating for 2 hours at 4°C in solubilization buffer, which consisted of 1% Triton X-100 (Sigma-Aldrich), 0.05% SDS, 0.5 mM EGTA, 1 mM EDTA, the phosphatase inhibitors sodium pyrophosphate and NaF (both at 10 mM), and the protease inhibitors leupeptin, aprotinin, benzamidine and soybean trypsin inhibitor (5 μg/ml each) in PBS. The lysates were centrifuged at 20,000 g for 10 minutes at 4°C to remove unsolubilized material. 2AR-FLAG was immunoprecipitated by incubating the solubilized lysate overnight at 4°C with an anti-FLAG antibody preconjugated to agarose beads (Sigma-Aldrich). After washing the beads 4 times with ice-cold solubilization buffer, the tagged receptor was eluted with 3x FLAG peptide (Sigma-Aldrich). The eluate was fractionated by 10% SDS-PAGE, and the resultant signal from the dried gel was quantified by a GE Healthcare phosphorimager. Data was expressed as relative units from the pixel densities using ImageQuant software (version 1.2).
BRET measurements.
BRET assays were carried out with the Flexstation II scanning fluorimeter/luminometer (Molecular Devices) using methods similar to that previously reported by Bouvier et al. (14). HEK 293 cells either transfected with 2AR-Rluc alone or cotransfected with receptor-YFP fusion constructs were detached 48 hours after transfection and seeded onto 96-well plates at a density of approximately 80,000 cells/well in PBS containing 0.1% glucose. To determine the full spectrum of emission, light-emission acquisition (420–560 nm) was started 5 minutes after coelenterazine h (5 μM final concentration) was added. Emission values recorded at 475 nm and 530 nm after addition of coelenterazine h were used to determine the BRET ratio for each well. In some experiments, the transfected cells were treated with either isoproterenol or 17-PTP for 15 minutes prior to addition of coelenterazine h. The net BRET signal for each condition, performed in triplicate, was calculated by dividing the 530-nm emission of receptor-YFP by the 475-nm emission of the receptor-Rluc after subtracting the background signal determined from cells transfected with the receptor-Rluc construct alone using the formula [(Em530 – Em475) x CF]/EM475, where CF represents Em530/Em475, the ratio of the signals from cells expressing receptor-Rluc alone. Maximal BRET levels (BRETmax) were obtained by cotransfecting increasing levels of receptor-YFP constructs with a constant quantity of the 2AR-Rluc construct. BRETmax and BRET50 were derived from fitting these data to a 1-site hyperbolic function.
Immunoprecipitation and Western blotting.
HEK 293 cells expressing the EP1 receptor, FLAG-tagged 2AR, or both were solubilized for 2 hours at 4°C in RIPA buffer (1x PBS, 1% IGEPA, 0.5% sodium deoxycholate, and 0.1% SDS) containing protease inhibitors. The solubilized lysates were cleared by centrifugation at 10,000 g, and a portion of the cleared sample was removed for protein determination and Western blot analysis. The remainder was incubated with M2 anti-FLAG affinity matrix (Sigma-Aldrich) overnight at 4°C. The resin was then collected by centrifugation, washed 3 times with Tris-buffered saline, and eluted with 2x Laemelli loading buffer. For Western blot analysis, whole cell lysates and immunoprecipitated samples were fractionated on 8% polyacrylamide gels and transferred to PVDF membranes. Blots were blocked with 5% nonfat milk and incubated overnight at 4°C with a polyclonal anti-EP1 antibody (Cayman Chemical Co.) diluted 1:200. The blots were then washed, incubated with anti-rabbit IgG antibody diluted 1:6,500 at room temperature for 1 hour, and detected by enhanced chemiluminesence.
[35S]GTP S binding.
[35S]GTPS binding assays were performed as described previously (47) with modifications that include a Gs immunoprecipitation step (48). HEK 293 cells were cotransfected with plasmid vectors encoding human Gs and either 2AR alone or 2AR plus the EP1 receptor. Studies with ASM cells were carried out without transfections utilizing endogenous expression of the receptors and Gs. For the binding reaction, partially purified cell membrane protein (75 μg) was incubated for 15 minutes at 30°C in a binding buffer (10 mM HEPES, pH 7.4, 3 mM MgCl2, and 50 mM NaCl) that included 50 nCi [35S]GTPS and 10 μM guanosine diphosphate in a total volume of 100 μl. Basal (vehicle) and agonist-stimulated (1 μM isoproterenol) conditions were each determined in the absence and presence of 1 μM 17-PTP. Parallel assays containing unlabeled GTPS (100 μM) were used to define nonspecific binding. The reactions were stopped by addition of cold solubilization buffer (10 mM HEPES, pH 7.4, 50 mM NaCl, 5 mM EDTA, and 0.5% Triton-X) and rotated for 2 hours at 4°C. After centrifugation at 20,000 g for 15 minutes, the supernatant was incubated overnight with 1 μg Gs antibody (Santa Cruz Biotechnology Inc.) and 20 μl protein A–conjugated agarose beads. The beads were washed 3 times with phosphorylation solubilization buffer, and the bound radioactivity was measured in a liquid scintillation counter. Under these conditions, nonspecific binding was typically <10% of the total. Agonist-stimulated binding was derived by subtracting the counts of basal samples from the counts of the isoproterenol-treated samples. Each data point within an experiment was determined from triplicate samples.
Immunofluorescence microscopy.
Murine ASM cells were passed to Lab-Tek chamber slides (Nunc) and grown overnight. After the media was aspirated, the cells were washed with PBS and then fixed with cold methanol for 4 minutes. Cells were then placed in blocking buffer composed of PBS containing 10% donkey serum and 1% Triton-X for 30 minutes at room temperature. The blocking buffer was removed, and cells were incubated overnight at room temperature in PBS containing 1% Triton-X, a 1:50 dilution of a rabbit anti-EP1 antibody (Santa Cruz Biotechnology Inc.), and a 1:200 dilution of a chicken anti-2AR antibody (Abcam). Primary antibody was not added to the negative controls. After incubation, the buffer containing the primary antibodies was aspirated, and the cells were washed with PBS containing 0.1% Triton-X. Cells were then incubated with secondary antibodies for 2–4 hours with 0.1% Triton-X in PBS containing a 1:200 dilution of a Cy2-conjugated donkey anti-rabbit antibody and a 1:800 dilution of a Cy3-conjugated donkey anti-chicken antibody. Cells were then washed with PBS and mounted with Gelmount (Biomeda) to reduce fading. Fluorescent images were captured electronically using the appropriate filter sets on a Zeiss Axioplan II Microscope System at a magnification of x200.
Statistics.
Concentration-response and BRET data were fit by nonlinear functions using the Prism software program (version 4.0; GraphPad Software). Statistical comparisons were by paired or unpaired Student’s t tests as appropriate, with P < 0.05 considered significant. Data are represented as mean ± SEM of the indicated number of experiments.
Acknowledgments
This work was supported by NIH grants HL071609 (to D.W. McGraw) and HL045967 (to S.B. Liggett). The authors thank Michel Bouvier for providing constructs, Cheryl Theiss for assistance with cell culture, and Esther Getz Moses for manuscript preparation.
Footnotes
Nonstandard abbreviations used: AR, adrenergic receptor; ASM, airway smooth muscle; BRET, bioluminescence resonant energy transfer; [Ca2+]i, intracellular calcium; GABAb R2, -aminobutyric acid receptor subtype bR2; HEK, human embryonic kidney; IP3, inositol 1,4,5-triphosphate; PGE2, prostaglandin E2; 17-PTP, 17-phenyl trinor-PGE2; Rluc, Renilla luciferase; 7-TM, 7-transmembrane; YFP, yellow fluorescent protein.
Conflict of interest: The authors have declared that no conflict of interest exists.
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2Cardiopulmonary Genomics Program, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Abstract
Multiple and paradoxical effects of airway smooth muscle (ASM) 7-transmembrane–spanning receptors activated during asthma, or by treatment with bronchodilators such as 2–adrenergic receptor (2AR) agonists, indicate extensive receptor crosstalk. We examined the signaling of the prostanoid-EP1 receptor, since its endogenous agonist prostaglandin E2 is abundant in the airway, but its functional implications are poorly defined. Activation of EP1 failed to elicit ASM contraction in mouse trachea via this Gq-coupled receptor. However, EP1 activation markedly reduced the bronchodilatory function of 2AR agonist, but not forskolin, indicating an early pathway interaction. Activation of EP1 reduced 2AR-stimulated cAMP in ASM but did not promote or augment 2AR phosphorylation or alter 2AR trafficking. Bioluminescence resonant energy transfer showed EP1 and 2AR formed heterodimers, which were further modified by EP1 agonist. In cell membrane [35S]GTPS binding studies, the presence of the EP1 component of the dimer uncoupled 2AR from Gs, an effect accentuated by EP1 agonist activation. Thus alone, EP1 does not appear to have a significant direct effect on airway tone but acts as a modulator of the 2AR, altering Gs coupling via steric interactions imposed by the EP1:2AR heterodimeric signaling complex and ultimately affecting 2AR-mediated bronchial relaxation. This mechanism may contribute to -agonist resistance found in asthma.
See the related Commentary beginning on page 1210
Introduction
The 7-transmembrane–spanning (7-TM–spanning) receptors represent the largest signaling family in the genome. We estimate that the lung expresses 25–50 7-TM receptors in airway epithelial cells, airway smooth muscle (ASM), pulmonary vasculature, alveolar walls, and resident immune cells (1). In regard to asthma, several 7-TM receptors play established roles in bronchoconstriction (e.g., M3-muscarinic receptor) and bronchodilation (e.g., 2–adrenergic receptor [2AR]). Despite identification of the endogenous ligands and receptor localization, there are a number of 7-TM receptors expressed in the airway whose functions are unknown, or appear to function paradoxically, based on recombinantly expressed receptors in model cell systems. This lack of understanding of receptor function has impeded our ability to ascertain the role of these ligands (some of which are markedly increased in asthma) in the relaxation/contraction of ASM; thus the mechanistic basis of bronchial hyperreactivity and bronchoconstriction in asthma remains only partially understood. In many cases the basis for incomplete mechanistic information can be attributed to the nature of recombinant expression systems, which may not take into account multiple receptor subtypes, receptor/receptor interactions, crosstalk via second messengers, or subcellular localization of receptors and specific effectors.
These issues are particularly obvious when one considers the biologic actions of prostaglandin E2 (PGE2), which, via at least 4 receptor subtypes (EP1–EP4), can evoke multiple signals. By activation of the Gs-coupled EP2 receptor, PGE2 can evoke ASM relaxation (2). However, blockade of PGE2 production leads to partial reversal of 2AR desensitization in the context of inflammation (3), and thus PGE2 may promote bronchoconstriction via desensitization of 2AR function or by activation of the Gq-coupled EP1 receptor. PGE2 is produced by ASM, airway epithelial cells, and inflammatory cells and is the most abundant prostanoid in epithelial lining fluid (4-6). However, EP1-mediated signal transduction and its effect on airway responsiveness remains unclear. We show here a unique function of the EP1 receptor in ASM, which to our knowledge has not been previously described for 7-TM receptors. The EP1 receptor itself, despite its coupling to inositol 1,4,5-triphosphate (IP3) and intracellular calcium ([Ca2+]i), failed to exert the expected bronchoconstrictive response. Instead, EP1 receptor activation modulated 2AR function via formation of a heterodimeric complex that directly decreased 2AR coupling to Gs in an EP1 receptor, agonist-dependent, fashion.
Results
EP1 receptor activation in isolated and intact ASM.
The biologic actions of PGE2 are potentially mediated by multiple receptor subtypes that differentially couple to Gq, Gi, and Gs. Although a relaxant action of PGE2, mediated via the EP2 isoform in ASM, has been documented (7), the extent to which PGE2 couples to the other subtypes in ASM, particularly the potentially probronchoconstrictive Gq-coupled EP1 receptor, is not established. EP1-specific RT-PCR was carried out on murine ASM cells in culture (Figure 1A). A single product of the expected molecular size was obtained, and Southern blots with an EP1-specific oligonucleotide hybridized to the product. Sequencing further confirmed the product as the murine EP1 receptor (GenBank accession no. NM_013641). With regard to signal transduction, the EP1-specific agonist 17-phenyl trinor-PGE2 (17-PTP) was found to stimulate inositol phosphate production (Figure 1B) and [Ca2+]i transients (Figure 1C). Of note, maximal activation of the EP1 receptor by 17-PTP stimulated [Ca2+]i to a greater extent, and with greater potency, than the M3-muscarinic agonist carbachol (Figure 1D). These findings confirmed EP1 receptor expression in ASM cells and that its activation by agonists resulted in IP3 and [Ca2+]i turnover as assessed in whole cells. Because these effectors mediate 7-TM receptor contraction of ASM, the data suggested that the EP1 receptor would likely promote airway contraction.
Excised mouse tracheal ring preparations were utilized to ascertain the effects of EP1 activation on active force generation in the intact airway. However, despite its ability to stimulate IP3 and [Ca2+]i turnover in ASM, 17-PTP caused no detectable contraction of tracheal rings even at concentrations up to 10 μM (Figure 2A). Since 17-PTP did not directly effect ASM tone, we next investigated whether EP1 receptor activation could modify the response to another contractile agonist acting through Gq. For these studies, tracheal rings were pretreated with 1 μM 17-PTP for 15 minutes prior to contraction with various concentrations of acetylcholine (Figure 2A). The maximal acetylcholine response in the absence (26 ± 5.3 mN) or presence (26 ± 4.8 mN) of EP1 coactivation was not different, nor was the EC50 for the response (91 ± 11 versus 82 ± 15 μM, respectively). We next considered whether EP1 receptor activation alters ASM relaxation. The efficacy and potency of the AR agonist isoproterenol to relax acetylcholine-constricted ASM in the presence and absence of EP1 receptor activation was ascertained. Tracheal rings were first treated with vehicle or 1 μM 17-PTP for 15 minutes, contracted continuously with 10 μM acetylcholine, and exposed to increasing concentrations of isoproterenol. In the presence of vehicle, isoproterenol caused a dose-dependent relaxation with an EC50 of 23.4 ± 4.8 nM and a maximal reduction in force of 36.6% ± 2.9% (Figure 2B). However, following pretreatment with 17-PTP, a marked reduction in AR-mediated relaxation was observed, with isoproterenol evoking only 17.1% ± 2.4% relaxation (n = 6; P < 0.001; Figure 2B). Of note, the EC50 for isoproterenol was also increased under these conditions to 58.2 ± 6.1 nM (P < 0.001). As shown in Figure 2C, this same AR desensitization effect of 17-PTP was observed when tracheal rings were contracted by 60 mM KCl. The endogenous EP1 receptor agonist is PGE2, which activates other EP receptors and thus under physiologic conditions could evoke an effect that dominates airway responses over the EP1-specific phenotype we observed. We therefore studied the effect of pretreatment with 10 nM PGE2 (which evokes only 15% relaxation) using the same protocol as for 17-PTP. As shown in Figure 2D, PGE2 also evoked a loss of isoproterenol-mediated relaxation, amounting to an approximate 25% desensitization. This lower amount of desensitization (compared with 17-PTP pretreatment) may be due to the combined relaxant effect of PGE2 and isoproterenol.
Given that mouse trachea has a mixed population of 1AR and 2AR subtypes (8), the 17-PTP effect was also assessed using the relatively 2AR subtype-specific agonist formoterol. Under these conditions, 17-PTP evoked a 55% ± 5% desensitization of formoterol-mediated relaxation, indicating a 17-PTP effect on 2AR (the predominant AR subtype of human tracheal ASM). To determine whether the inhibitory effect of 17-PTP extended to other ASM relaxants, we performed analogous experiments with forskolin, which directly activates adenylyl cyclase, mimicking a Gs-coupled receptor. However, unlike the response with isoproterenol, pretreatment with 17-PTP had no effect on the maximal response or the EC50 (Figure 3A). Given that the EP1 receptor couples to Gq, we considered that second messengers generated from phospholipase C (PLC) activation may be involved in the apparent crosstalk between 2AR and EP1 receptors. However, pretreatment with the PLC inhibitors U73122 (5 μM; Figure 3B) and Et-18-OCH3 (10 μM; data not shown) failed to alter the 17-PTP effect. 2ARs have also been shown in some cells to couple to Gi (9), which may act to oppose Gs-mediated signaling. Treatment of tracheal rings with pertussis toxin, however, had no effect on the EP1-mediated 2AR desensitization (Figure 3C), indicating that enhanced Gi coupling was an unlikely mechanism. Finally, the 2AR desensitization phenotype evoked by EP1 activation was not altered by pretreatment with 100 μM of the NO inhibitor L-NAME (51.2% ± 6.8% desensitization) or 10 μM of the cyclooxygenase inhibitor indomethacin (57% ± 5% desensitization).
Desensitization of 2AR by EP1 receptor activation.
The inhibitory effect of 17-PTP on isoproterenol-mediated relaxation observed in the tracheal ring studies indicated functional interplay between the EP1 and 2AR signal transduction pathways. Additionally, the absence of a significant EP1 effect on forskolin-mediated relaxation and no change in phenotype observed with PLC inhibition suggested that this interaction could potentially occur at the level of the 2AR itself. The effect of 17-PTP on isoproterenol-stimulated cAMP production was determined in isolated ASM cells. In the absence of 17-PTP, 1 μM isoproterenol stimulated cAMP to 88.0% ± 16.3% of the maximum level obtained with 10 μM forskolin. However, when cells were pretreated with 1 μM 17-PTP for 15 minutes prior to isoproterenol stimulation, cAMP production was reduced to 37.0% ± 3.9% (n = 4; P = 0.02) of the forskolin response (Figure 4A). Taken together with the tracheal ring data, these results indicated an interplay between the EP1 receptor and 2AR, with activation of the former resulting in decreased function of the latter. Two processes that we considered potential mechanisms to account for uncoupling of 2AR signal transduction within the time frame of minutes included (a) enhanced loss of cell surface receptors due to internalization and (b) enhanced isoproterenol-stimulated 2AR phosphorylation due to EP1 activation or phosphorylation of the 2AR by EP1 activation via PKC. To ascertain whether EP1 activation altered the extent or rate of agonist-mediated 2AR internalization, we performed radioligand binding on intact ASM cells with the hydrophilic radioligand [3H]-CGP-12177. Since this ligand does not enter intact cells (10), a decrease in binding occurs when surface receptors are internalized. Thus, as expected for agonist-promoted internalization of the 2AR, exposure of ASM cells to 1 μM isoproterenol caused a time-dependent decrease in [3H]-CGP-12177 binding sites of 39.1% ± 5.7% after 30 minutes (Figure 4B). Pretreatment of cells with 1 μM 17-PTP for 15 minutes had no effect on isoproterenol-stimulated internalization (37.4% ± 3.6%; n = 5). We next examined the potential for 17-PTP to promote phosphorylation of the 2AR. For the phosphorylation experiments, human embryonic kidney (HEK) cells transiently cotransfected with plasmids so as to express the EP1 receptor and FLAG-tagged 2AR were loaded with 32P-orthophosphate. Cells were treated with vehicle, isoproterenol, 17-PTP, phorbol-12-myristate-13-acetate (a positive control for PKC-mediated event), or isoproterenol plus 17-PTP. 2AR was purified by FLAG immunoprecipitation. As shown in Figure 4C, isoproterenol evoked robust phosphorylation of the 2AR, while no detectable phosphorylation over background was noted with 17-PTP exposure alone. Importantly, the extent of isoproterenol–promoted 2AR phosphorylation was not altered by 17-PTP (48 ± 4.5 relative units versus 42 ± 4.2 relative units in the presence and absence of 17-PTP, respectively; n = 5; P = NS).
2ARs and EP1 receptors form heterodimers.
Since these well-defined short-term mechanisms of receptor regulation and crosstalk were not at play during EP1-induced desensitization of 2AR, we considered an alternative hypothesis, which was that the 2 receptors formed heterodimers. We also considered whether agonist activation of the EP1 receptor directly affected the receptor/receptor interaction within the complex, altering 2AR coupling to Gs. As a screen for such a complex in ASM cells, fluorescence microscopy was carried out using 2AR- and EP1-specific primary antibodies. Secondary antibodies provided for red (2AR) and green (EP1) signals. Merged images revealed yellow signals consistent with areas of colocalization of these 2 receptors (Figure 5A). To rigorously assess the potential for heterodimer formation, bioluminescence resonant energy transfer (BRET) and coimmunoprecipitation studies were undertaken in transfected HEK 293 cells. BRET was carried out in living cells expressing 2 receptors having carboxyterminally fused Renilla luciferase (Rluc) or yellow fluorescent protein (YFP). As described in detail elsewhere (11-13), this approach takes advantage of a signal produced by the energy donor moiety (Rluc) acting on the energy acceptor (YFP) when the two are in very close proximity. As shown in Figure 5B, studies carried out in HEK 293 cells transfected to express 2AR-Rluc and EP1-YFP (see Methods) indeed revealed a BRET signal, as indicated by the perturbation of the emission spectrum at 530 nM. To verify that this represented oligomer formation, rather than a "pseudo-BRET" signal (11) due to random collisions of overexpressed receptors, studies were carried out with multiple levels of expression (altering the 2AR-Rluc/EP1-YFP ratio). As expected under conditions of dimer formation, the BRET signal saturated, with a calculated maximal ratio (BRETmax) of 0.49 ± 0.04 and a BRET50 of 2.97 ± 0.56 (Figure 5C). In contrast, in experiments utilizing cotransfections of 2AR-Rluc and a YFP fusion with the -aminobutyric acid receptor subtype bR2 (GABAb R2–YFP) a small signal was observed, as was the case with cotransfections of C-C chemokine receptor 5–Rluc (CCR5-Rluc) and 2AR-YFP (Figure 5D). These low-level signals and a lack of saturation (data not shown) were consistent with prior observations that neither the GABAb R2 nor CCR5 receptors form heterodimers with the 2AR (13, 14). We next examined whether activation of the EP1 receptor or the 2AR altered the BRET signal. As shown in Figure 5E, treatment of cotransfected cells with 17-PTP or isoproterenol for 15 minutes prior to the addition of coelenterazine h increased the BRET signal in both cases. Given that most 7-TM dimers appear to be formed intracellularly and then expressed at the cell surface (11, 12, 15, 16), and given the short-term agonist exposure used in these experiments, we do not interpret these results as representing an increased number of dimers per se. Rather, the data are consistent with a conformational change that occurs (potentially in either receptor) when one receptor is bound by its agonist, which causes the Rluc and YFP moieties to move closer together. The magnitude of the agonist-promoted increase in BRET is not trivial, in that the BRET signal is proportional to the distance between the donor and acceptor by a factor of 106 (11, 12, 15).
To further corroborate dimer formation, coimmunoprecipitation studies were carried out in HEK 293 cells transfected to express FLAG-2AR and the EP1 receptor both alone and together. Immunoprecipitation was carried out with anti-FLAG antibody, and the precipitated proteins were fractionated on SDS-PAGE followed by Western blots using a polyclonal EP1 antisera. As shown in Figure 5F, the EP1 receptor migrated at approximately 45 kDa in Western blots of cell lysates using the EP1 antisera. Upon immunoprecipitation with FLAG antibody, protein from cells transfected to express EP1 or 2AR showed no immunoreactivity with the EP1 antisera. However, when the 2 receptors were cotransfected, a band of the appropriate molecular size was observed. Of note, the high–molecular weight bands, which could represent dimers, are often not resistant to SDS and are not typically visualized (14). These coimmunoprecipitation studies are thus consistent with the BRET results, indicating the presence of the EP1:2AR heterodimer.
EP1: 2AR heterodimer formation uncouples 2AR from G
s. Taken together, the above results indicated that the EP1 receptor and the 2AR exist as an oligomeric complex, with activation of the EP1 receptor markedly desensitizing 2AR signaling and physiologic function, and that such desensitization is not due to downstream second messenger feedback. This suggested that agonist activation of the EP1 receptor within the dimer results in a steric effect on the 2AR, altering its conformation in such a way as to directly affect 2AR-Gs interaction. To examine this, we studied agonist-promoted [35S]GTPS binding in cell membranes. This provided for direct quantitation of receptor–G protein interaction by measuring GTP turnover and, since it is performed with isolated membranes, was not affected by intracellular factors. In these studies, [35S]GTPS binding was carried out by incubating membranes from cells transfected to express Gs, 2AR, and the EP1 receptor with vehicle, isoproterenol alone, or isoproterenol with 17-PTP. In other studies, Gs and 2AR were expressed without the EP1 receptor so as to ascertain 2AR coupling to Gs in the absence of the EP1:2AR dimer. Expression levels of 2AR in the 2AR and EP1 (3774 ± 815 fmol/mg) and 2AR transfections (3367 ± 185 fmol/mg) were comparable. Net isoproterenol-stimulated [35S]GTPS binding is shown in Figure 6A. Incubation with 17-PTP resulted in a significant decrease in isoproterenol-stimulated binding, amounting to an approximately 60% reduction (n = 4; P = 0.02). Interestingly, the presence of the EP1 receptor, even in the absence of its activation by agonist, decreased 2AR coupling to Gs. As shown in Figure 6A, cells expressing 2AR alone had the highest isoproterenol-stimulated [35S]GTPS binding, and as expected, 17-PTP had no effect in these cells. Additional studies were also carried out using ASM cell membranes (Figure 6B). Analogous to what was observed in the transfected cell studies, [35S]GTPS turnover was decreased when membranes were incubated with isoproterenol and 17-PTP compared with isoproterenol alone. These data then confirmed the concept of a direct interaction between the 2 receptors in the cell type of interest when the receptors were expressed at physiologic levels.
Discussion
PGE2 is a cyclooxygenase-derived product of arachidonic acid metabolism that plays a major role in regulating such diverse physiological processes as smooth muscle tone, inflammation, and pain (reviewed in ref. 17). The biological effects of PGE2 are often multifaceted and can appear contradictory to traditional signaling paradigms. As introduced earlier, some of these properties of PGE2 are due to the fact that it is an endogenous agonist for 4 receptor subtypes coupled to several signal transduction cascades. The EP1 receptor is linked to IP3 and [Ca2+]i turnover through Gq-mediated signal transduction (18), whereas the EP2 and EP4 receptors stimulate adenylyl cyclase and cAMP production through Gs (19-21). Splice variants of the EP3 receptor give rise to multiple isoforms that apparently can couple to Gi, Gs, or Gq (22, 23). Since one or more of these receptors may be expressed by a cell or tissue, the integrated response to PGE2 often represents the net effect of additive or opposing signal transduction events. Moreover, temporal and spatial changes in patterns of EP receptor expression in response to various stimuli (e.g., injury and inflammation) provide an additional level of dynamic regulation and complexity to PGE2-regulated processes in the airways. For example, recent studies of the PGE2-mediated fibroproliferative response due to intratracheal bleomycin have shown an approximately 50% decrease in fibroblast EP2 receptor mRNA without significant change in the other EP subtypes (24), whereas FITC-mediated fibrosis was associated with decreases in both EP2 and EP4 transcript expression (24).
Because PGE2 is produced endogenously within the lung and activates pathways that may both enhance and inhibit ASM contraction, it may have particular relevance in asthma. PGE2 is produced by ASM cells, bronchial and alveolar epithelial cells, fibroblasts, and inflammatory cells in the lung, and increased levels have been reported in some studies with human asthma (25, 26). Furthermore, an initial enzyme for prostanoid receptor synthesis (COX-2), as well as PGE2 precursors, are increased in asthmatic airways (27, 28). Following its discovery, PGE2 was found to relax ASM and thus has generally been considered to be a bronchoprotective prostanoid. The bronchodilatory effect of PGE2 appears to be due to activation of the EP2 receptor subtype, since PGE2-mediated bronchodilation is present in EP1-, EP3-, and EP4-null mice but absent in EP2-null mice (29). Interestingly, in nonasthmatic humans, PGE2 exerts a net bronchodilation; in asthmatics, though, the response is highly variable, sometimes resulting in significant bronchoconstriction (30). The complex nature of PGE2 action in the asthmatic milieu is further illustrated in that it may serve as an intermediary through which inflammatory cytokines can modulate other receptor systems that govern airway tone. In particular, PGE2 appears to mediate the inhibitory effects of the inflammatory cytokines TGF and interleukin-1 on 2AR signal transduction in cultured ASM (31-34). These inflammatory cytokines stimulate COX-2 and production of PGE2 by ASM, and it has been proposed that the resulting increase in cAMP production following EP2 receptor activation leads to desensitization of the 2AR (3). However, the mechanism(s) by which this inhibition occurs has not been completely elucidated, nor has the role of other EP receptor subtypes in mediating this effect been explored.
We define here a unique role for the EP1 receptor expressed on ASM cells using both molecular studies in transfected cells and ASM cells and physiologic studies in trachea. We showed that the EP1 receptor existed as a heterodimer (or higher-order oligomer) with the 2AR, and the signaling of this complex was manifested by an altered 2AR conformation and decreased functional interaction with Gs. EP1 activation by agonist further enhanced 2AR desensitization, as shown in the [35S]GTPS studies. This effect was also readily observed in ASM cells utilizing whole-cell cAMP measurements and membrane [35S]GTPS binding and manifested at the physiologic level with intact tracheal rings. Interestingly, the extent of 2AR desensitization evoked by the EP1 agonist, as assessed using these distinctly different methods, amounted to approximately 50% in all cases. In addition, the EP1 receptor, while capable of stimulating intracellular IP3 and [Ca2+]i (as assessed by global whole-cell assays), did not ultimately cause significant ASM contraction. Thus the dimer may serve not only to form a specialized signaling unit, but could also place the complex in a subcellular compartment that isolates it from activation of the downstream components of contraction. Indeed, 2ARs have been shown to be localized to caveolae, which are specialized flask-shaped invaginations of the cell membrane that promote association of the receptor with certain signal transduction elements (35). However, we note that EP1 receptor–mediated contraction has been observed in guinea pig trachea (36), suggesting that the extent of EP1-mediated tracheal contraction may depend on the species.
We have thus considered the physiologic role of the EP1 receptor in ASM as primarily one of modulating 2AR function, with no observable direct effect on contraction. To our knowledge, this "monitor-like" function has not been previously described for a 7-TM receptor with its heterodimeric partner. However, there are somewhat analogous scenarios with other receptors. For the GABAb R1 and R2 subtypes, it appears that the R1:R2 heterodimer represents a distinct signaling unit, in that the R1 subtype binds the agonist while the R2 subtype couples to G protein activation (37). Furthermore, GABAb R1 cell surface expression requires heterodimer formation with GABAb R2 in the endoplasmic reticulum (38). For the 1DAR, cell surface expression appears to be dependent on oligomeric association with the 1BAR (39). Once so expressed, each subtype can signal independently. Similarly, the 2AR can form dimers with the 1DAR and promote its expression (40). Other examples of homo-and heterodimerization function have been recently reviewed (12, 15, 16). We are unaware of a previous report of the unique function of a 7-TM receptor that we describe here.
In the current report, we utilized the physiologic readout of airway contraction and relaxation as the relevant functional signal and found that activation of the EP1 receptor had no direct physiologic action. However, we found that EP1 activation resulted in substantial loss of 2AR-mediated ASM relaxation. We demonstrated that this interaction of signal transduction networks occurred at the level of the receptors, rather than downstream effectors, and was not due to posttranslational modification of the 2AR by phosphorylation or other potential distal-pathway crosstalk mechanisms (41). Rather, formation of the EP1:2AR heterodimer was a distinct signaling complex, where the EP1 receptor modulates 2AR coupling to Gs. Using multiple approaches, the EP1-agonist dependency of the 2AR modulation was demonstrated. However, we cannot exclude the notion that the mere presence of the heterodimer acts to modulate the function of one of its members, the 2AR. Indeed, the [35S]GTPS binding studies showed that 2AR coupling to Gs was decreased when coexpressed with the EP1 receptor. However, the spontaneous switching of the EP1 receptor to the active conformation may mimic the agonist-occupied form; thus it is not unexpected that coexpression, particularly at relatively high levels, would have an agonist-occupied effect. Regardless, in the native state both receptors were expressed on ASM, and we showed that EP1 receptor activation decreased 2AR function in isolated ASM cells and in intact tissue.
In summary, we define a unique modulatory function of the EP1 receptor, which acts primarily to regulate 2AR function. In asthma, then, local concentrations of elevated PGE2 could act to quench 2AR function, resulting in decreased responsiveness to -agonist. The mechanism of this receptor interaction appears to be due to the formation of a heterodimer; thus the EP1:2AR dimer should be considered the functional signaling complex in ASM, with a unique phenotype based on steric interactions that lead to attenuated 2AR-Gs coupling.
Methods
Plasmid constructs, cells culture, and transfection.
The human 2AR cDNA was tagged at the amino terminus with the FLAG epitope and fused at the carboxyl terminus with the cDNA for Rluc, and the cDNA for the human EP1 receptor was fused at the carboxyl terminus with the cDNA for YFP, using standard techniques. The final constructs representing 2AR, FLAG-2AR, and 2AR-Rluc were in pcDNA3, and the EP1-YFP construct was in pEYFP-N1 (BD Biosciences — Clontech). Primary cultures of ASM cells were derived from explants of excised tracheas from the mice as reported previously (42) and maintained in DMEM, 10% FCS, and x1 antibiotic-antimycotic solution (Invitrogen Corp.) at 37°C in a 95% air, 5% CO2 incubator. These cells maintain the morphologic and immunohistochemical characteristics of ASM cells for at least 15 passages, although most experiments were performed with cells in passages 4–12. Both COS-7 and HEK 293 cells were similarly maintained as monolayers in DMEM supplemented with 10% FCS, 100 U/ml penicillin, and 100 mg/ml streptomycin. Transfection of these cells for BRET and [35S]GTPS binding experiments was performed using Lipofectamine (Invitrogen Corp.) by methods previously described (43).
RT-PCR.
Total RNA was extracted from freshly isolated lungs with Tri-Reagent (Molecular Research Center Inc.). An aliquot of RNA was reverse transcribed with random hexamers with murine leukemia virus reverse transcriptase (PerkinElmer) as previously described (43). Transgene cDNA was amplified with 150 nM each of a sense primer (5'-CGTGTCATTTCCTGGGTGGCT-3') and an antisense primer homologous to regions within the mouse EP1 open reading frame (5'-GTGGCTGTGGCTGAAGTGATG-3'). PCR was at 95°C for 120 seconds followed by amplification for 35 cycles at 95°C for 60 seconds and 56°C for 60 seconds and a final extension at 72°C for 7 minutes. The PCR products were detected in agarose gels stained with ethidium bromide. RNA samples not subjected to reverse transcription were used as negative controls to ensure that the observed PCR product was not the result of contaminating DNA.
Measurement of inositol phosphate production and [Ca2+]i.
Formation of [3H]-inositol phosphate was determined in intact ASM cells as previously reported (41). Briefly, near-confluent ASM cells in 12-well plates were incubated with inositol-free media containing [3H]-myoinositol (5 μCi/ml) for 24 hours at 37°C in 5% CO2 atmosphere. Cells were then washed and incubated with PBS for 30 minutes followed by a 30-minute incubation with 20 mM LiCl in PBS. The cells were treated with either PBS (basal), 1 μM PGE2, 1 μM 17-PTP, or thrombin (a positive control) for 15 minutes, after which total inositol phosphates were extracted by column chromatography with AG1-X8 resin (Bio-Rad).
To measure [Ca2+]i, murine ASM cells were seeded into black-walled, clear-based 96-well plates (Corning) at a density of approximately 80,000 cells per well and cultured overnight in 100 μl DMEM supplemented with 10% FCS as above. On the following day, the cells were incubated at 37°C for 60 minutes with the Calcium 3 indicator (Molecular Devices) that was dissolved in Hank’s balanced salt solution containing 20 mM HEPES, pH 7.4, and 2.5 mM probenecid in a final volume of 200 μl/well. The cell plates were then placed into the FlexStation II scanning fluorimeter/luminometer (Molecular Devices) to monitor fluorescence before and after the addition of 50 μl vehicle or a x5 concentration of the indicated drug (Figure 1, C and D) using an excitation wavelength of 485 nm, emission wavelength of 525 nm, and emission cutoff of 515 nm. Responses were measured as peak fluorescence intensity minus basal fluorescence intensity, with each data point in an individual experiment representing the mean of 4 replicates. Final data reported represent the mean of 4 different experiments using ASM cells derived from 2 different mice.
Radioligand binding and cAMP production.
The expression of 2ARs in membranes prepared from transiently transfected HEK 293 and COS-7 cells was quantified by radioligand binding assays using the antagonist [125I]-iodocyanopindolol as previously reported (44). To assess the rate of 2AR sequestration in ASM cells, whole-cell binding assays were performed using the hydrophilic, membrane-impermeant radioligand [3H]-CGP-12177 to determine the amount of cell-surface 2AR in the untreated cells as well as in cells treated with either isoproterenol or isoproterenol with 17-PTP (1 μM each) for periods up to 30 minutes as previously described in detail (45).
To measure cAMP production, ASM cells were seeded onto 24-well plates and maintained overnight in DMEM supplemented with 10% FCS to allow adherence. The cells were then switched to serum-free DMEM for an additional 24 hours. The cells were loaded with [3H]-adenine (2 μCi/well) for 2 hours and then washed twice with PBS to remove excess adenine. Cells were then treated with either vehicle or 17-PTP (1 μM final concentration) for 15 minutes before stimulation with either 1 μM isoproterenol or 100 μM forskolin for 15 minutes. Reactions were terminated by the addition of 50 μl concentrated HCl. After the samples were frozen and thawed once to ensure cell lysis, cAMP was eluted by alumina column chromatography. Recovered counts were corrected for adenine uptake, and column efficiency ascertained with tracer [14C]-cAMP. Each data point was determined from the mean of triplicate samples, and expressed as its percentage of the mean forskolin response for that experiment. The results shown represent the mean ± SEM of 4 separate experiments performed with cell lines derived from 2 different mice.
Tracheal ring contractility studies.
Studies of mouse tracheal ring contractility were performed as reported previously in detail (41). Briefly, tracheas were excised and dissected free of surrounding tissues and cut into rings of 5 mm in length. The rings were mounted on stainless steel wires connected to isometric force transducers and immersed in a physiologic saline solution (118 mM NaCl, 11 mM glucose, 4.73 mM KCl, 1.2 mM MgCl2, 0.026 mM EDTA, 1.2 mM KH2PO4, 2.5 mM CaCl2, and 25 mM NaH2CO3) at 37°C and bubbled with 95% O2 and 5% CO2, maintaining a pH of 7.40. Each tracheal ring was stretched to a tension of 5 mN, which we have previously determined to be an optimal passive tension for maximizing active force (42). Following a period of equilibration for 30 minutes, the indicated agents (Figures 2 and 3) were added to the bath, and the maximal response over the next 5 minutes was recorded. Cumulative concentration-isometric force curves were generated for the responses using standard curve-fitting techniques. Pretreatments of equilibrated rings included 1 μM 17-PTP for 15 minutes, 10 nM PGE2 for 15 minutes, 10 μg/ml pertussis toxin for 4 hours, 100 μM L-NAME for 30 minutes, 10 μM indomethacin for 30 minutes, 5 μM U73112 for 15 minutes, and 10 μM Et-18-OCH3 for 30 minutes. All mouse studies were reviewed and approved by the University of Cincinnati College of Medicine Animal Care and Use Committee.
Receptor phosphorylation.
Whole-cell phosphorylation experiments were performed as previously described (46), with minor modifications. HEK 293 cells cotransfected with the 2AR-FLAG and EP1-YFP constructs were plated in 100-mm dishes. Forty-eight hours after transfection, the media was changed to serum- and phosphate-free DMEM containing 500 μCi/ml 32P-orthophosphate. After incubation for 2 hours at 37°C in 95% air and 5% CO2, the cells were treated with vehicle, 1 μM isoproterenol, 100 nM phorbol-12-myristate-13-acetate, 1 μM 17-PTP, or 1 μM isoproterenol plus 1 μM 17-PTP for 15 minutes. The cells were then washed 4 times with ice-cold PBS and solubilized by rotating for 2 hours at 4°C in solubilization buffer, which consisted of 1% Triton X-100 (Sigma-Aldrich), 0.05% SDS, 0.5 mM EGTA, 1 mM EDTA, the phosphatase inhibitors sodium pyrophosphate and NaF (both at 10 mM), and the protease inhibitors leupeptin, aprotinin, benzamidine and soybean trypsin inhibitor (5 μg/ml each) in PBS. The lysates were centrifuged at 20,000 g for 10 minutes at 4°C to remove unsolubilized material. 2AR-FLAG was immunoprecipitated by incubating the solubilized lysate overnight at 4°C with an anti-FLAG antibody preconjugated to agarose beads (Sigma-Aldrich). After washing the beads 4 times with ice-cold solubilization buffer, the tagged receptor was eluted with 3x FLAG peptide (Sigma-Aldrich). The eluate was fractionated by 10% SDS-PAGE, and the resultant signal from the dried gel was quantified by a GE Healthcare phosphorimager. Data was expressed as relative units from the pixel densities using ImageQuant software (version 1.2).
BRET measurements.
BRET assays were carried out with the Flexstation II scanning fluorimeter/luminometer (Molecular Devices) using methods similar to that previously reported by Bouvier et al. (14). HEK 293 cells either transfected with 2AR-Rluc alone or cotransfected with receptor-YFP fusion constructs were detached 48 hours after transfection and seeded onto 96-well plates at a density of approximately 80,000 cells/well in PBS containing 0.1% glucose. To determine the full spectrum of emission, light-emission acquisition (420–560 nm) was started 5 minutes after coelenterazine h (5 μM final concentration) was added. Emission values recorded at 475 nm and 530 nm after addition of coelenterazine h were used to determine the BRET ratio for each well. In some experiments, the transfected cells were treated with either isoproterenol or 17-PTP for 15 minutes prior to addition of coelenterazine h. The net BRET signal for each condition, performed in triplicate, was calculated by dividing the 530-nm emission of receptor-YFP by the 475-nm emission of the receptor-Rluc after subtracting the background signal determined from cells transfected with the receptor-Rluc construct alone using the formula [(Em530 – Em475) x CF]/EM475, where CF represents Em530/Em475, the ratio of the signals from cells expressing receptor-Rluc alone. Maximal BRET levels (BRETmax) were obtained by cotransfecting increasing levels of receptor-YFP constructs with a constant quantity of the 2AR-Rluc construct. BRETmax and BRET50 were derived from fitting these data to a 1-site hyperbolic function.
Immunoprecipitation and Western blotting.
HEK 293 cells expressing the EP1 receptor, FLAG-tagged 2AR, or both were solubilized for 2 hours at 4°C in RIPA buffer (1x PBS, 1% IGEPA, 0.5% sodium deoxycholate, and 0.1% SDS) containing protease inhibitors. The solubilized lysates were cleared by centrifugation at 10,000 g, and a portion of the cleared sample was removed for protein determination and Western blot analysis. The remainder was incubated with M2 anti-FLAG affinity matrix (Sigma-Aldrich) overnight at 4°C. The resin was then collected by centrifugation, washed 3 times with Tris-buffered saline, and eluted with 2x Laemelli loading buffer. For Western blot analysis, whole cell lysates and immunoprecipitated samples were fractionated on 8% polyacrylamide gels and transferred to PVDF membranes. Blots were blocked with 5% nonfat milk and incubated overnight at 4°C with a polyclonal anti-EP1 antibody (Cayman Chemical Co.) diluted 1:200. The blots were then washed, incubated with anti-rabbit IgG antibody diluted 1:6,500 at room temperature for 1 hour, and detected by enhanced chemiluminesence.
[35S]GTP S binding.
[35S]GTPS binding assays were performed as described previously (47) with modifications that include a Gs immunoprecipitation step (48). HEK 293 cells were cotransfected with plasmid vectors encoding human Gs and either 2AR alone or 2AR plus the EP1 receptor. Studies with ASM cells were carried out without transfections utilizing endogenous expression of the receptors and Gs. For the binding reaction, partially purified cell membrane protein (75 μg) was incubated for 15 minutes at 30°C in a binding buffer (10 mM HEPES, pH 7.4, 3 mM MgCl2, and 50 mM NaCl) that included 50 nCi [35S]GTPS and 10 μM guanosine diphosphate in a total volume of 100 μl. Basal (vehicle) and agonist-stimulated (1 μM isoproterenol) conditions were each determined in the absence and presence of 1 μM 17-PTP. Parallel assays containing unlabeled GTPS (100 μM) were used to define nonspecific binding. The reactions were stopped by addition of cold solubilization buffer (10 mM HEPES, pH 7.4, 50 mM NaCl, 5 mM EDTA, and 0.5% Triton-X) and rotated for 2 hours at 4°C. After centrifugation at 20,000 g for 15 minutes, the supernatant was incubated overnight with 1 μg Gs antibody (Santa Cruz Biotechnology Inc.) and 20 μl protein A–conjugated agarose beads. The beads were washed 3 times with phosphorylation solubilization buffer, and the bound radioactivity was measured in a liquid scintillation counter. Under these conditions, nonspecific binding was typically <10% of the total. Agonist-stimulated binding was derived by subtracting the counts of basal samples from the counts of the isoproterenol-treated samples. Each data point within an experiment was determined from triplicate samples.
Immunofluorescence microscopy.
Murine ASM cells were passed to Lab-Tek chamber slides (Nunc) and grown overnight. After the media was aspirated, the cells were washed with PBS and then fixed with cold methanol for 4 minutes. Cells were then placed in blocking buffer composed of PBS containing 10% donkey serum and 1% Triton-X for 30 minutes at room temperature. The blocking buffer was removed, and cells were incubated overnight at room temperature in PBS containing 1% Triton-X, a 1:50 dilution of a rabbit anti-EP1 antibody (Santa Cruz Biotechnology Inc.), and a 1:200 dilution of a chicken anti-2AR antibody (Abcam). Primary antibody was not added to the negative controls. After incubation, the buffer containing the primary antibodies was aspirated, and the cells were washed with PBS containing 0.1% Triton-X. Cells were then incubated with secondary antibodies for 2–4 hours with 0.1% Triton-X in PBS containing a 1:200 dilution of a Cy2-conjugated donkey anti-rabbit antibody and a 1:800 dilution of a Cy3-conjugated donkey anti-chicken antibody. Cells were then washed with PBS and mounted with Gelmount (Biomeda) to reduce fading. Fluorescent images were captured electronically using the appropriate filter sets on a Zeiss Axioplan II Microscope System at a magnification of x200.
Statistics.
Concentration-response and BRET data were fit by nonlinear functions using the Prism software program (version 4.0; GraphPad Software). Statistical comparisons were by paired or unpaired Student’s t tests as appropriate, with P < 0.05 considered significant. Data are represented as mean ± SEM of the indicated number of experiments.
Acknowledgments
This work was supported by NIH grants HL071609 (to D.W. McGraw) and HL045967 (to S.B. Liggett). The authors thank Michel Bouvier for providing constructs, Cheryl Theiss for assistance with cell culture, and Esther Getz Moses for manuscript preparation.
Footnotes
Nonstandard abbreviations used: AR, adrenergic receptor; ASM, airway smooth muscle; BRET, bioluminescence resonant energy transfer; [Ca2+]i, intracellular calcium; GABAb R2, -aminobutyric acid receptor subtype bR2; HEK, human embryonic kidney; IP3, inositol 1,4,5-triphosphate; PGE2, prostaglandin E2; 17-PTP, 17-phenyl trinor-PGE2; Rluc, Renilla luciferase; 7-TM, 7-transmembrane; YFP, yellow fluorescent protein.
Conflict of interest: The authors have declared that no conflict of interest exists.
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