Engineered G protein coupled receptors reveal independent regulation of internalization, desensitization and acute signaling
- Kimberly Scearce-Levie†1Email author,
- Michael D Lieberman†1,
- Heather H Elliott1 and
- Bruce R Conklin1, 2
© Scearce-Levie et al; licensee BioMed Central Ltd. 2005
Received: 23 August 2004
Accepted: 11 February 2005
Published: 11 February 2005
The physiological regulation of G protein-coupled receptors, through desensitization and internalization, modulates the length of the receptor signal and may influence the development of tolerance and dependence in response to chronic drug treatment. To explore the importance of receptor regulation, we engineered a series of Gi-coupled receptors that differ in signal length, degree of agonist-induced internalization, and ability to induce adenylyl cyclase superactivation. All of these receptors, based on the kappa opioid receptor, were modified to be receptors activated solely by synthetic ligands (RASSLs). This modification allows us to compare receptors that have the same ligands and effectors, but differ only in desensitization and internalization.
Removal of phosphorylation sites in the C-terminus of the RASSL resulted in a mutant that was resistant to internalization and less prone to desensitization. Replacement of the C-terminus of the RASSL with the corresponding portion of the mu opioid receptor eliminated the induction of AC superactivation, without disrupting agonist-induced desensitization or internalization. Surprisingly, removal of phosphorylation sites from this chimera resulted in a receptor that is constitutively internalized, even in the absence of agonist. However, the receptor still signals and desensitizes in response to agonist, indicating normal G-protein coupling and partial membrane expression.
These studies reveal that internalization, desensitization and adenylyl cyclase superactivation, all processes that decrease chronic Gi-receptor signals, are independently regulated. Furthermore, specific mutations can radically alter superactivation or internalization without affecting the efficacy of acute Gi signaling. These mutant RASSLs will be useful for further elucidating the temporal dynamics of the signaling of G protein-coupled receptors in vitro and in vivo.
The specificity, diversity, and physiological importance of G protein-coupled receptors (GPCR) have made these receptors excellent drug targets. It is becoming clear that the regulation of the GPCR itself – its location, stability, and signal duration – is a key component of the signaling process [1, 2] The length of a GPCR signal can be modulated by receptor desensitization (decrease in receptor responsiveness) and receptor internalization (trafficking of receptors to endocytotic vesicles). The cell can also respond to prolonged activation by upregulating compensatory pathways. For example, prolonged signaling through a Gi-coupled receptor inhibits adenylyl cyclase (AC), while paradoxically increasing the ability of the Gs-coupled pathway to stimulate AC, a phenomenon known as AC superactivation . Such regulatory mechanisms may contribute to the development of drug tolerance and dependence, including the response to chronic opiate use .
The complex effects of drugs at multiple receptor subtypes in multiple tissues have made it difficult to isolate the relative contributions of GPCR regulation, ligand binding, effector coupling, drug metabolism, and cellular downregulation machinery. Even if two receptors couple to the same signaling pathway, the physiological effects of their activation could vary tremendously depending on the pharmacokinetics of the ligands, the cell type expressing the receptors, and the interactions with desensitization mechanisms. An engineered family of receptors that share the same ligand binding and effector coupling, yet have discrete mutations that cause them to internalize or desensitize differentially, would help pinpoint the physiological consequences of GPCR desensitization. This is especially important in the light of recent evidence showing dramatically different endocytosis and signaling profiles of mu opioid receptors (MOR) in response to different ligands [5, 6]. In addition, understanding the signals that allow transmembrane proteins to be more or less resistant to endocytosis will improve our understanding of endocytosis as a general regulatory mechanism, as it has been implicated in the regulation of signaling of growth factor receptors [7, 8] and ion channels [9–11].
Our laboratory has engineered a Gi-coupled receptor that is insensitive to endogenous ligands but can still respond to the synthetic small-molecule agonist spiradoline [12, 13]. This receptor activated solely by a synthetic ligand (RASSL) was based on the kappa opioid receptor (KOR). In the original RASSLs, exchanging the second extracellular loop of the KOR with the corresponding sequence from the delta opioid receptor, and making an additional point mutation (Q297E), resulted in a receptor with 1/2,000 of the response to dynorphin and other endogenous peptides relative to the wild-type KOR. However, the response of this RASSL to spiradoline was not altered. RASSLs can be expressed in a tissue-specific manner in transgenic mice, allowing direct control of Gi-mediated physiological responses such as heart rate . It has also been recently used to help identify the mammalian sweet receptor by expressing it in mouse taste buds . To investigate the endocytosis and desensitization of GPCRs, we have since developed four new RASSLs. To visualize these RASSLs in living cells, we fused the green fluorescent protein (GFP) to the N-terminus (outer portion) of the RASSL resulting in Rog (RASSL opioid green). Given the well-documented role of the C-terminal region in the desensitization and internalization of GPCRs [1, 16–18], we made a series of C-terminal mutant RASSLs designed to desensitize and internalize at different rates.
This novel receptor system offers an opportunity to test specific hypotheses about the relationship between receptor sequence and receptor regulation, without requiring the use of multiple ligands that might have different effects on the signal and the regulation of receptors. Because RASSLs lack endogenous agonists, they allow greater control of the timing and specificity of activation than is possible with endogenous receptors. In these studies, we test how the removal of phosphorylation sites from the C-terminal regions of a Gi-coupled RASSL alters the receptor's internalization, desensitization, and induction of AC superactivation. Since it is well established that the endogenous mu and kappa opioid receptors differ in these properties, we also explore the regulation of kappa opioid RASSLs bearing specific portions of the mu opioid receptor C-terminal sequence. The cell culture experiments presented here provide a basis for in vivo studies in complex tissues such as the nervous system. Insight gained through these experiments may help explain the differences seen in vivo between different endogenous Gi-coupled receptors, improving our understanding of the contribution of receptor regulation to the physiological response to agonists and our overall understanding of GPCR signal regulation.
Rog, a GFP-tagged RASSL, signals appropriately
EC50 and Emax values for inhibition of cAMP accumulation by spiradoline
EC50 (nM spiradoline)
0.41 ± 0.08
0.41 ± 0.15
0.42 ± 0.23
0.50 ± 0.22
1 nM spiradoline pretreatment
4.32 ± 1.96
0.42 ± 0.21
2.05 ± 0.03
> 13.44 ± 5.41
64.4 ± 4.8
56.1 ± 5.1
58.0 ± 0.9
64.1 ± 4.8
1 nM spiradoline pretreatment
55.7 ± 3.7
53.3 ± 0.9
43.6 ± 1.5
51.5 ± 6.0
Rog is internalized by agonist treatment
The GFP tag on Rog allows direct observation of agonist-induced receptor internalization by confocal microscopy (Figure 2B). In untreated cells, the receptor was visible primarily on the plasma membrane. One hour after spiradoline treatment (10–100 μM), the receptor was observed in bright, punctate intracellular vesicles. Dynorphin (100 μM), in contrast, did not lead to significant internalization of the receptor (Figure 2B). An ELISA that detects only cell-surface receptors was used to quantify the extent of receptor internalization after spiradoline treatment. With increasing doses of spiradoline, fewer receptors were detected on the cell surface, culminating in an approximately 45% loss of cell-surface receptors at the maximal dose of 100 μM (Figure 2C). The same dose of spiradoline resulted in a similar 47% loss of KOR from the cell surface (not shown). The time course of internalization in response to 1 μM spiradoline was relatively rapid, with significant receptor loss apparent within 5 min (Figure 2C). Maximal receptor loss was detected approximately 20 min after agonist treatment began.
Rog-A is resistant to agonist-induced internalization
Rog-μ more readily internalizes in response to spiradoline
Since the mu opioid receptor (MOR) internalizes more readily than the KOR, we made Rog-μ, a chimeric receptor in which the entire intracellular portion of the C-terminus was replaced with the corresponding MOR sequence (Figure 1). Rog-μ was expected to internalize to a greater extent than Rog in response to spiradoline. Confocal microscopy showed nearly complete internalization of Rog-μ after one hour of treatment with 10 μM spiradoline (Figure 3A, right). A cell-surface ELISA revealed 25–30% internalization of Rog-μ at low doses of spiradoline, ranging from 0.01 to 0.1 μM (Figure 3C). Little internalization of Rog or Rog-A has been observed at these doses (Figures 3B and 3C). At higher doses of spiradoline, no difference in internalization between Rog and Rog-μ was observed. ANOVA indicated a main effect of drug dose (F9,52 = 55.79, p < 0.0001) and an interaction between receptor type and drug dose (F9,52 = 3.89, p < 0.0008). Post-hoc Scheffé analysis shows significant differences between Rog and Rog-μ at 0.01 μM (p = .024) and 0.1 μM (p = .016) doses of spiradoline. When cells were treated with 1 μM spiradoline for differing lengths of time, there was no detectable difference in the time course of internalization of Rog and Rog-μ (Figure 3C). ANOVA indicated a main effect of time (F11,48 = 53.20, p < 0.0001), with no effect of receptor type. There was also no difference in cAMP inhibition after spiradoline activation of Rog and Rog-μ (Table 1).
Constitutive internalization of Rog-μA
Since cell-surface expression of a GPCR can be stabilized by the addition of antagonist [21, 22], we examined the effect of the KOR antagonist norBNI on cell-surface expression of Rog-μA. Antagonist treatment nearly doubled the amount of Rog-μA detected in the membrane (Figure 4A; p < 0.005; F1,6 = 27.00). It also increased the cell-surface expression of Rog-μ, but to a lesser degree (p < 0.05, F1,6 = 11.54). In contrast, it had no effect on the cell-surface expression of Rog. The increase in membrane expression of Rog-μA after antagonist treatment was confirmed by confocal microscopy. Under basal conditions, little Rog-μA was seen in the plasma membrane, although the receptor was readily detected in other areas of the cell (Figure 4B). After overnight treatment with 10 μM norBNI, most of the Rog-μA was seen in the plasma membrane (Figure 4B). In contrast, untreated Rog receptors were primarily located in the plasma membrane (Figures 2B, 4B), and norBNI treatment had little effect on their localization (Figure 4B). These experiments suggest that Rog-μA may be constitutively downregulated and rapidly cycled in and out of the plasma membrane.
Rog-A is more resistant to desensitization
In addition to regulation by internalization, a GPCR signal can be modulated by desensitization: uncoupling from the signaling effectors after continuous agonist stimulation. To explore desensitization directly, we briefly pretreated each RASSL with 1 nM spiradoline for 15 min, and examined inhibition of cAMP accumulation in response to a variety of doses of spiradoline. The low pretreatment dose had caused no receptor internalization detectable by ELISA-based assays. Pretreatment reduced the responsiveness of Rog receptors to spiradoline (Figure 5A, Table 1). The same maximal inhibition of cAMP accumulation was observed, but the dose response curve was shifted approximately 10-fold, with the EC50 for Rog shifting from 0.41 nM to 4.32 nM spiradoline after spiradoline pretreatment. Pretreatment of Rog-A with the same dose of spiradoline, however, did not significantly affect the response of the cells to subsequent treatment (Figure 5A, Table 1). The EC50 for spiradoline after 1 nM spiradoline pretreatment of Rog-A was 0.42 nM, compared to 0.41 nM for vehicle-treated cells. Spiradoline pretreatment shifted the EC50 of Rog-μ to 2.05 nM (Figure 5A, Table 1). Notably, the maximal response of pretreated Rog-μ-expressing cells was less than half that of untreated cells, indicating a decreased efficacy of Rog-μ signaling through the Gi pathway. Spiradoline pretreatment strongly reduced the response of Rog-μA to further spiradoline treatment (Figure 5A, Table 1). In fact, it appears that the response to spiradoline in pretreated Rog-μA cells is so low that the dose range tested (up to 100 nM) does not yield a maximal inhibition of cAMP, and no sigmoidal dose-response curve can be fitted to these data. Therefore, we cannot calculate an accurate EC50 for desensitized Rog-μA receptors. However, assuming that the maximal response occurs at doses higher than 100 nM spiradoline, we can estimate that the EC50 would be at least 13.44 nM. This indicates that Rog-μ and Rog-μA receptors desensitize readily. For these receptors, the dose of spiradoline required to achieve the EC50 is significantly lower than the dose required to internalize the cell-surface receptors (Figures 4, 5). While only a fraction of the total surface receptor pool needs to be activated to activate Gi maximally, a much larger fraction of the receptor population must be internalized before it can be accurately measured.
AC superactivation is independent of receptor internalization
Chronic treatment of cells expressing Gi-coupled receptors with agonist results in a compensatory increase in the activity of AC and, therefore, an increased accumulation of cAMP in response to the same dose of forskolin . We examined the development of this AC superactivation in cell lines transiently expressing the RASSL variants. Forskolin (10 μM) stimulates twice as much cAMP in Rog-expressing cells treated with 10 nM spiradoline for 18 hours, compared to cells acutely treated with forskolin alone (Figure 5B; p < 0.005, F1,10 = 17.72). A similar degree of superactivation was seen in cells transfected with the wild-type KOR, indicating the same cellular response to prolonged Gi signaling through both Rog and KOR. Overnight treatment of Rog-A-expressing cells with spiradoline, followed by stimulation with 10 μM forskolin, resulted in a slightly smaller increase in cAMP (Figure 5B; p < 0.05, F1,10 = 9.52). Notably, cells expressing Rog-μ and Rog-μA receptors showed no evidence of AC superactivation after 18 h of spiradoline pretreatment. These data show that receptors that desensitize and internalize more readily at the receptor level, such as Rog-μ and Rog-μA, do not induce compensations in an opposing signaling pathway.
Although little internalization of these RASSLs has been observed at these low doses of spiradoline, we wanted to ensure that the AC superactivation data could not be explained by differences in receptor internalization. Therefore, we performed an analysis of cell-surface receptor expression in parallel with the cAMP response experiment. Cells were plated and treated with 10 nM spiradoline for 18 hours exactly as described above. Then the cells were fixed and a cell-surface ELISA was performed. In general, 7–10% of the receptors were internalized by this treatment, but there were no significant differences between receptor types (Figure 5C). ANOVA showed a significant treatment effect (F1,18 = 8.22, p < 0.01), but no effect of receptor type (p > 0.99).
We have engineered a series of RASSLs that inhibit cAMP after acute activation by spiradoline with equal efficacy but differ dramatically in cellular location and responses to chronic drug treatment.
Mutation of phosphorylation sites on the C-terminus to alanines resulted in a receptor that was relatively resistant to internalization in the presence of moderate doses of agonist (Rog-A, Figure 3) and showed no significant desensitization after pretreatment with a low dose of agonist (Figure 5A). This is consistent with recent findings that mutation of a single serine to alanine is sufficient to block internalization and desensitization of the KOR, since this mutation removes a residue that is required for G protein receptor kinase (GRK2) phosphorylation . While these studies highlight the importance of GRK phosphorylation of GPCRs in mediating receptor internalization and desensitization, it is notable that partial internalization of Rog-A was still detected in response to higher doses of spiradoline, indicating that the receptor can be internalized through different mechanisms. Reports of GPCR endocytosis in the absence of GRK phosphorylation [24–26] suggest that the removal of C-terminal phosphorylation sites may reduce the affinity of the receptor for proteins that mediate endocytosis without preventing the protein-protein interactions that are essential for internalization.
Rog-μ, the MOR/KOR chimeric mutant, was more sensitive to agonist-induced desensitization (Figure 5A) and internalization (Figure 3) than Rog. This is consistent with observations that the MOR internalizes and desensitizes more readily than the KOR. Surprisingly, mutation of C-terminal phosphorylation sites on the MOR/KOR chimera to form Rog-μA did not inhibit desensitization (Figure 5A). Rog-μA has low basal surface expression, although the GFP-tagged receptor can be seen throughout the cell (Figure 4B). It is unlikely that the extracellular mutations in Rog-μA are responsible for the unusual internalization pattern of this receptor. The extracellular mutations in Rog-μA are identical to the ones in Rog, which was shown to reach the cell surface and respond to agonist the same as GFP-tagged wild-type KOR (Figure 2). The intracellular pool of Rog-μA is not due to receptor misfolding or abnormal sorting, because some receptor was detected on the membrane (Figure 4A) and the receptor showed normal agonist-induced signaling (Figure 5A, Table 1). The observation that the addition of an antagonist can "rescue" the low cell-surface expression of Rog-μA (Figure 4A) further suggests that misfolding is not responsible for the decrease in cell surface expression.
There are several potential mechanisms for the increase in cell-surface expression after antagonist treatment. One possibility is that the antagonist, norBNI, acts as a molecular chaperone, entering the cell, binding to the receptor in intracellular compartments, and bringing it to the membrane. Ligands can act as pharmacological chaperones for the delta opioid receptor, facilitating receptor maturation and export from the endoplasmic reticulum . However, there are no reports that the norBNI antagonist is cell-permeable. Another possibility is that norBNI acts as an inverse agonist, stabilizing cell-surface receptors in an "off" conformation, making them inaccessible to GRKs and arrestins, which usually interact only with active receptors. This would suggest that in the absence of norBNI, Rog-μA may be constitutively active. However, the receptor still signals robustly in response to spiradoline (Figure 5A), so it cannot be fully active in the absence of ligand. It is also possible that, under basal conditions, Rog-μA has a higher than normal affinity for GRK or arrestin, but not the G proteins. This would result in constitutive turnover – the receptor constantly cycling in and out of the membrane – in the absence of constitutive signaling. The idea that this receptor is especially sensitive to the desensitization and internalization machinery is borne out by the observation of extensive desensitization in response to pretreatment with a low dose of agonist (Figure 5A). It will be interesting to investigate the physiological consequences of this apparent constitutive internalization and rapid desensitization in animal models.
Although most of the C-terminal sequence of Rog-μA is derived from the MOR, the MOR does not exhibit either constitutive turnover or abnormally low membrane expression. There is some evidence for partial basal internalization of the similar Rog-μ receptor (Figure 4A), although Rog-μ appears to be expressed predominantly at the cell surface under basal conditions. Since Rog-μ and Rog-μA differ at only five amino acids, some of those five residues must be responsible for the increased turnover of Rog-μA. Although phosphorylation of T394 has been reported to be required for desensitization of the MOR , subsequent reports have shown that mutating T394 to alanine facilitates the internalization and resensitization of the receptor . This suggests that phosphorylation of T394 may be a membrane retention signal and that the T394A mutation in Rog-μA is responsible for the constitutive endocytosis observed in this study. Mutagenesis of individual amino acids in this region may allow the identification of the specific residue(s) responsible for the constitutive internalization of Rog-μA.
The differences in AC superactivation between our RASSLs indicate another layer of complexity in GPCR signaling. Previous studies suggest an inverse correlation between the ability of an opioid receptor to undergo ligand-activated endocytosis and its ability to induce AC superactivation by chronic signaling . The induction of superactivation by Rog is consistent with this idea. Rog-μ, which internalizes and desensitizes readily, failed to induce any AC superactivation after chronic activation (Figure 5B). Similarly, Rog-μA, which may undergo constitutive endocytosis, did not induce AC superactivation after chronic administration of spiradoline. However, Rog-A, which was predicted to have enhanced superactivation due to its resistance to endocytosis, had levels of superactivation comparable to those seen with Rog. It is possible that Rog induces maximal superactivation, and the cell cannot respond to Rog-A signaling with any additional superactivation. Our results indicate that internalization does not directly induce AC superactivation. The dose of spiradoline (10 nM over 18 hours) used to induce strong AC superactivation in these experiments causes only minimal internalization of all of the receptors (Figure 5C). Moreover, there is no significant difference in degree of internalization among the different receptor types, although they show profound differences in superactivation. This suggests that the cellular mechanisms underlying AC superactivation and receptor internalization are independent.
AC superactivation has been attributed to upregulation of AC proteins induced by Gβγ protein subunits interacting directly with GRK2/3 proteins [29, 30]. Therefore, the same mutations that prolong Rog-A signaling and inhibit endocytosis may also prevent the receptor from interacting with GRK2/3 proteins and subsequently activating Gβγ-mediated signaling events. Alterations in desensitization characteristics are unlikely to alter AC superactivation because of the drastic differences in time course underlying these distinct phenomena. Receptor desensitization happens on a scale of minutes, while AC superactivation is the result of much longer term chronic receptor activation. Therefore, a decrease in Gi signaling due to a more desensitized receptor is unlikely to have a significant effect on AC superactivation over the much longer time course used in these experiments. The additional possibility exists that altering C-terminal residues on the RASSL could increase the ability of receptors to couple to Go, resulting in perceived changes in AC superactivation . However, if this were the case, one would expect to see a shift in the dose response curve for cAMP inhibition between Rog, Rog-A, Rog-μ and Rog-μA that is not observed in any of our experiments. Further studies with this engineered receptor system in vivo may clarify the complex relationship between ligand dependent endocytosis, interaction of a GPCR C-terminus with GRK2/3, desensitization, and superactivation of AC.
The ability of these RASSLs to induce different degrees of AC superactivation may have important physiological consequences in vivo. Interestingly, when a RASSL with a C-terminus corresponding to the wild-type human KOR was expressed at high levels in the hearts of transgenic mice, the mice developed a lethal cardiomyopathy . One possible explanation is that basal signaling of the RASSL in mouse heart may increase Gs signaling through AC superactivation. Gs signaling has long been associated with heart failure, so AC superactivation may be responsible for the cardiomyopathy. Rog-μ and Rog-μA, RASSLs that do not induce superactivation, could be used to test this hypothesis and to study the consequences of AC superactivation in other tissues.
Internalized opioid receptors can be either degraded or recycled back to the membrane. The receptors that return to the membrane are stripped of arrestin, phosphates, and ligand, and are resensitized to ligand. Recent evidence demonstrates that the C-terminus is crucial for directing internalized receptors either into the degradative lysosomal pathway or back to the plasma membrane [27, 33]. We expect that several of our engineered RASSLs should also differ in their post-endocytotic fate.
It is likely that the complex mechanisms governing GPCR endocytosis, recycling, desensitization and AC superactivation will be regulated differently in different cell types. The RASSLs described here exhibit similar properties in several different mammalian cell lines we tested (rat1a, CHO and HEK293), but their properties may change in specific cell types or under specific physiological conditions. One potentially fruitful avenue for future investigations would be to target different RASSLs to particular cell types in vivo. This would allow a thorough investigation of the interplay between receptor sequence and cell-type specific mechanisms of receptor regulation.
The development of a toolbox of engineered RASSLs that differ in internalization and desensitization raises several possibilities for future research and clinical investigations. Growing evidence points to a link between receptor dynamics and the potential for drugs to elicit tolerance or dependence, especially for opioid receptors [28, 34]. Here, we present a system that allows the same drug to activate different receptors that have small, well-defined variations in sequence. The efficacy and potency of spiradoline is similar for Rog, Rog-A, Rog-μ and Rog-μA (Table 1); only the desensitization and internalization responses vary. Specifically, agonist-induced internalization is reduced in Rog-A and enhanced in Rog-μ, while Rog-μA shows agonist-independent internalization. Rog-A shows no desensitization after a brief spiradoline pretreatment, while the same treatment reduces the potency of spiradoline at Rog-μA and reduces efficacy at Rog-μ. Longer spiradoline pretreatment induces normal AC superactivation at Rog-A, but does not affect the AC response in Rog-μ or Rog-μA cells.
A family of engineered GPCRs that do not respond to endogenous ligands has enormous potential for selectively controlling G protein signaling in specific tissues without interfering with endogenous processes. Rog-A, a long-signaling RASSL, has several interesting implications for in vivo signal engineering. The basic RASSL, Ro2, shows rapid and extensive physiological desensitization , making it difficult to use in any therapeutic context where repeated activation of the receptor would be necessary. Rog-A, with its reduced desensitization, could allow continued physiological efficacy of repeated drug treatments. Comparison of the regulation and signaling of Rog, Rog-A, Rog-μ, Rog-μA, and future variants will contribute to the growing understanding of how GPCR signals are dynamically modulated. Study of these RASSLs in vivo will help solidify the elusive links between the receptor amino acid sequence, cell biology, and complex physiology.
Construction of mutant receptors
All receptors were based on the human kappa-opioid RASSL called Ro2 . The GFP-tagged version of the RASSL has been named "Rog" for RASSL opioid with GFP tag. Rog was made by inserting the coding sequence for emerald GFP (Packard) at the N-terminus of the receptor, after a FLAG tag (DYKDDDDV) and the first eight amino acids of the RASSL. To create Rog-A, two serines and two threonines in the C-terminal region of the receptor were mutated to alanines (Figure 1). In the human kappa opioid receptor (KOR), the mutated residues correspond to S356A, T357A, S358A and T363A. The exact location of those residues in our RASSL construct, and the complete sequence of all RASSL variants can be found on our web site http://www.ConklinLab.org. For both Rog-μ and Rog-μA, the final 35 amino acids (345–380) of Rog were replaced by 47 C-terminal residues from the rat mu opioid receptor (MOR). Rog-μA contains the following additional modifications to the rat MOR C-terminus: T383A, E388Q, E391Q, E393Q and T394A. For each receptor, a schematic design and a C-terminal amino acid sequence alignment is shown in Figure 1. All constructs were sequenced to verify the mutations.
Expression of RASSLs in mammalian cells
HEK293 cells were grown in culture to 60–80% confluence and then transfected using Lipofectamine Plus (Invitrogen, Carlsbad, CA). The RASSL construct contained a cytomegalovirus promoter to drive mammalian expression, and a neomycin-resistance gene to allow selection of stable cell lines. Experiments on transiently transfected cells were performed approximately 48 h after transfection. To create stable cell lines, transfected cells were selected with G418 (500 μg/ml, Invitrogen) for 10–14 days. Individual colonies showing green fluorescence were selected and grown under maintenance doses of G418 (250 μg/ml). Receptor expression was confirmed visually by fluorescence microscopy, and by an enzyme-linked immunoadsorbent assay (ELISA, see below).
Cell-surface expression of receptors was confirmed by an ELISA that detects only extracellular FLAG tag, which labels the N terminus of all RASSLs. This assay therefore quantifies only receptors that are in the membrane at the time of labeling, without providing detailed localization data about those receptors. Cells were plated at 100,000 cells/well on to 24-well plates coated with poly-d-lysine. Cultured cells were fixed in 4% paraformaldehyde for 10 min at 4°C, washed in phosphate-buffered saline (PBS), and then incubated in 1 μg/ml M1 anti-FLAG antibody (Sigma, St. Louis, MO) for 1 h at room temperature. They were washed again in PBS with 1 mM CaCl2 and incubated for 30 min at room temperature in secondary antibody (1:1000 goat anti-mouse conjugated with horseradish peroxidase, Biorad, Chicago, IL), then washed three times in PBS plus CaCl2. To develop the reaction, 0.25 ml of 2,2-azino-bis(3-ethylbenzthiazoline-6-sulfonic acid) liquid substrate (Sigma) was added to each well. After 15–60 min, 200 μl from each well was transferred to a 96-well plate and the optical density was read at 410 nm. To quantify agonist-induced internalization, cells were treated with various doses of spiradoline in medium for 10–120 min. The medium was removed and the cells were fixed and processed as described above. Vehicle treated cells on each plate were used to calculate a "maximum" cell-surface expression for that plate. All other treatment conditions on that plate were then normalized to this maximum to determine "percent internalization." Each experiment included 3–6 replicates per condition and was repeated at least 3 times. After values for cell-surface expression of each receptor were calculated and normalized, receptor expression was compared using two-way ANOVA (StatView v. 5.0, SAS Institute, Cary, NC). For dose response studies, receptor and dose were independent factors. For time course studies, receptor and length of treatment were independent factors.
cAMP accumulation assay
The degree of cAMP inhibition in spiradoline-treated HEK-293 cells transiently expressing RASSL variants was measured with the CatchPoint cAMP ELISA kit (Molecular Devices, Sunnyvale, CA). Cells were plated at 5 × 104/well into 96-well plates coated with poly-d-lysine. The next day, cells were rinsed in Krebs-Ringer bicarbonate buffer with glucose (KRBG, Sigma). Cells were then incubated in pre-stimulation buffer containing a phosphodiesterase inhibitor (0.75 mM 3-isobutyl-1-methylxanthine in KRBG buffer) for 10 min at room temperature to inhibit cAMP degradation. cAMP production was stimulated by the addition of 50 μM forskolin to all cells. At the same time, various doses of spiradoline in PBS were added to cells to establish a dose-response curve. After a 15-min drug treatment at 37°C, the cells were lysed and cAMP accumulation was assayed according to the CatchPoint protocol. Inhibition of cAMP by spiradoline was determined by comparison to cells treated with forskolin alone. For each experiment, 3–6 wells per condition were averaged, and EC50 and percent inhibition values for each receptor were determined by fitting curves for each independent experiment using SOFTmax PRO v. 4.0.1 (Molecular Devices). Data for 3–8 independent experiments were averaged to determine the EC50 and maximum cAMP inhibition for each receptor and condition. For desensitization assays, a pretreatment dose (1 nM) of spiradoline diluted in sterile PBS was added to the cells, which were then incubated for 10 min at 37°C. The cells were rinsed 4 times in KRBG and then stimulated and assayed for cAMP as described above. AC superactivation was determined by measuring forskolin-stimulated (10 μM) cAMP after treatment with either 10 nM spiradoline or vehicle for 18 h. AC superactivation data were expressed as a percent increase in forskolin-stimulated cAMP relative to vehicle-pretreated cells expressing the same receptor. Conditions and receptors were compared using a two-way ANOVA with receptor and treatment condition as independent factors.
HEK293 cells stably expressing receptor constructs were plated at a density of 500,000 cells/ml onto glass Labtek II chamber slides (Fisher Scientific, Pittsburgh, PA) coated with poly-d-lysine. The following day, the cells were treated with agonist (spiradoline or dynorphin A 1–13) for typically one hour, or antagonist (NorBNI) overnight and briefly washed in PBS. The PBS was removed and replaced with 1 ml of cold 4% paraformaldehyde in PBS. The cells were fixed at room temperature for 10 min, washed with PBS, and then mounted in Vectashield (Vector Laboratories, Burlingame, CA) under cover slips. For confocal imaging on a Bio-Rad MRC 600 microscope, typical images were taken with a 40–60× oil immersion objective lens, subject to 5× Kalman filtering. The microscope operator was blind to both cell line and treatment condition.
Fluorometric imaging plate reader (FLIPR) assay
All receptors tested were transiently transfected using Lipofectamine into CHO cells in conjunction with the chimeric G protein Gqi5  in a 5:1 molar ratio of DNA. Gqi5 is a chimeric G protein alpha subunit that has the Gαq wild-type sequence except for the C-terminal 5 residues, which were changed to the corresponding Gαi sequence. This allows Gi-coupled receptors to signal through the Gq pathway, resulting in a signal that can be detected using calcium-sensitive reagents. The following day, the cells were plated in a 96-well plate (50,000 cells per well) and allowed to grow for 24 h before being incubated with the calcium-sensitive dye fura-3 for 1 h. The assay was performed as described  using a range of dilutions of either spiradoline or dynorphin A 1–13 peptide (Sigma). All experiments were performed in triplicate.
The authors are grateful for valuable technical assistance from David Sanan (confocal microscopy), Jin Liao (FLIPR assay), Sam Davis (assembly of receptor constructs), and Taeryn Kim (ELISA assays and cell culture). We also thank Drs. Lennart Mucke, Nathalie Cotte, Kam Dahlquist, Supriya Srinivasan, Whit Tingley and Alex Zambon for their insightful discussions and careful reading of this manuscript. Gary Howard, Stephen Ordway and Bethany Taylor provided editorial assistance in revision and preparation of this manuscript. This work was supported by NIH HL6064 (BRC) and a NIDA NRSA fellowship (KSL).
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