The Class-A GPCR Dopamine D2 Receptor Forms Transient Dimers Stabilized by Agonists: Detection by Single-Molecule Tracking
Whether class-A G-protein coupled receptors (GPCRs) exist and work as monomers or dimers has drawn extensive attention. A class-A GPCR dopamine D2 receptor (D2R) is involved in many physiological and pathological processes and diseases, indicating its critical role in proper functioning of neuronal circuits. In particular, D2R homodimers might play key roles in schizophrenia development and amphetamine-induced psychosis. Here, using single-molecule imaging, we directly tracked single D2R molecules in the plasma membrane at a physiological temperature of 37 °C, and unequivocally determined that D2R forms transient dimers with a lifetime of 68 ms in its resting state. Agonist addition prolonged the dimer lifetime by a factor of ~1.5, suggesting the possibility that transient dimers might be involved in signaling.
KeywordsDopamine receptor G protein-coupled receptor (GPCR) Plasma membrane Cultured cell Single-molecule biophysics Dimerization
G-protein-coupled receptors (GPCRs) constitute the largest protein superfamily in the human genome, including about 800 genes. They are involved in many physiological processes and are currently one of the most prominent pharmacological targets. Despite the importance of GPCRs, the fundamental question of whether GPCRs form and work as monomers, dimers, and/or greater multimers have remained unanswered [1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16]. The functional units of class-C GPCRs, including metabotropic glutamate receptor 1 [17, 18, 19, 20, 21] and GABAB receptors [22, 23, 24], are generally considered to be constitutive homo- and/or hetero-dimers. However, our knowledge about the oligomeric states of the largest class of GPCRs, the class-A group GPCRs, is quite limited. They might exist as monomers [3, 4, 16, 25], dimers [26, 27, 28, 29, 30, 31, 32], constitutive multimers  and/or dynamically interchanging monomers and dimers [34, 35, 36, 37, 38, 39], even in the ER membrane .
The first step toward resolving this issue is to determine whether class-A GPCRs form dimers and multimers in the plasma membranes (PMs) of living cells, rather than relying on in vitro experiments [34, 35, 36, 37, 38, 39], and to employ methods that can directly observe the dynamic interconversions between monomers and di-/multimers. Previously, by developing a single fluorescent-molecule imaging method, the dynamic monomer–dimer equilibrium for a GPCR, the N-formyl peptide receptor (FPR), was determined in living cells, for the first time ever for any membrane molecule . In quiescent cells before agonist stimulation of FPR, the dimer–monomer 2D-equilibrium constant was 3.6 copies/μm2, with 2D-dissociation and 2D-association rate constants of 11.0 s−1 and 3.1 [copies/μm2]−1s−1, respectively, at 37 °C. With the physiological FPR expression level of ~2.1 receptor copies/μm2 (~6000 copies/neutrophil), monomers continually convert into dimers every 150 ms, dimers dissociate into monomers in 91 ms (dimer lifetime; inverse the 2D-dissociation rate constant), and at any moment, 2500 and 3500 receptor molecules participate in transient dimers and monomers, respectively. Transient homodimers of the class-A GPCR were also found for M1 muscarinic receptor , β1-adrenergic receptor (AR), β2-AR , and dopamine D2 receptor (D2R) . Interestingly, in the case of FPR, even after stimulation of the antagonist, the monomer–dimer equilibrium was not affected .
In the present study, to advance this line of research further, we further examined whether a class-A GPCR, D2R, forms transient or prolonged dimers and whether ligation influences dimerization. We selected D2R because it plays a critical role in the development of psychosis, as illustrated by the fact that many antipsychotics act by modulating D2R. Furthermore, D2R dimerization might be involved in the pathophysiology of schizophrenia as well as in the sensitized state after exposure to amphetamine, a drug that can cause psychosis . Furthermore, D2R might play important roles in other tissues: in addition to neurons in the cerebral cortex, olfactory tubercle, and hippocampus, D2R is ubiquitously expressed in various tissues, including blood vessels, adrenal gland, heart, and kidney .
D2R homo-dimerization has been a controversial subject matter. On the one hand, constitutive dimerization was reported , but on the other hand, transient dimerization was suggested [11, 39, 43]. Meanwhile, agonist stimulation was found to reorient the fourth transmembrane helix in the constitutive dimer , suggesting that allosteric communication between the protomers of D2R dimers modulated the protomer activation . Furthermore, the presence of monomers and various multimers up to pentamers of D2R has been reported [39, 45].
Previously, using single-molecule imaging, Tabor et al.  detected transient D2R homodimers with a lifetime of ~0.5 s, which was longer than that we found for FPR (91 ms) by a factor of 5.5. It should be noted that our experiments for FPR were performed at 37 °C, whereas the result for D2R dimer lifetime by Tabor et al. was obtained at 24 °C. Meanwhile, other data of GPCR homodimer lifetimes were all conducted at lower temperatures: M1 muscarinic receptor (lifetime ~0.7 s, 8x longer than FPR dimer lifetime) at 23 °C  and β1- and β2-AR (lifetime ~5 s, 55x longer than FPR dimer lifetime) at 20.5 °C. Due to such variations, we consider that the GPCR homodimer lifetimes should be better defined, by observing them at a physiological temperature of 37 °C.
Furthermore, to investigate the physiological relevance of GPCR homodimers, the effect of agonist on the homodimer lifetime would be quite important. The results about this point reported in the literature are quite varied. No effects were detected on the homodimers of FPR [6, 35], β1- and β2-AR [30, 36, 46], M1 muscarinic receptor , 5HT2c  and 5HT4  serotonin receptor, and neurotensin receptor 1 , as well as β1–β2 AR heterodimers . On the other hand, an increase of apparent dimer fraction was observed for D2R upon agonist addition , which might be due to the agonist-induced rearrangements of the transmembrane α-helices within the D2R homodimers  (similar findings were made for CCR2  and CXCR4 ).
Here, using single fluorescent-molecule imaging-tracking, we unequivocally detected transient D2R dimers in the live-cell PM, and determined their lifetimes at 37 °C. Furthermore, we found that the D2R dimer lifetimes were prolonged after agonist stimulation.
Materials and Methods
Cell Culture, cDNA Construction, and Expression in CHO-K1 Cells
CHO-K1 cells, which do not respond to dopamine stimulation , were cultured in Ham’s F12 medium (Sigma) supplemented with 10% (v/v) FBS, 100 units/ml penicillin, and 0.1 mg/ml streptomycin. The cells were transfected with the cDNA encoding acyl-carrier protein (ACP)-tagged human D2R (cDNA encoding the short variant; Addgene) in the plasmid vector pcDNA3.1(+) (Life Technologies) using LipofectAMINE PLUS (Life Technologies), according to the manufacturer’s recommendations. Transfected cells were seeded in glass-base dishes (35-mmϕ with a glass window of 12 mmϕ, 0.12–0.17-mm-thick glass; Iwaki), and cultured for 24–48 h before use. ACP is known to be monomeric .
The treatments of the cells with agonists and neutral antagonists were performed by adding 1 ml solutions of 30 µM dopamine (Wako), 30 µM (-)-quinpirole (SIGMA-Aldrich) or 200 nM (+)-UH-232 (TOCRIS), in Hank’s balanced salt solution (HBSS, Nissui) buffered with 2 mM piperazine-N,N’-bis(ethanesulfonic acid) (PIPES) from Dojindo (Kumamoto, Japan), at pH 7.4 (P-HBSS).
Labeling of D2R with the Fluorescent Dye ATTO594
ACP-tagged D2R expressed in the PM was labeled with ATTO594 (ATTO-TECH), by incubating the cells with 2 µM ATTO594-Coenzyme A (custom-synthesized by Shinsei Kagaku, Osaka, Japan, by conjugating ATTO594-maleimide to Coenzyme A-SH [New England Biolabs]) and 1 µM phosphopantetheine transferase at ~25 °C for 20 min, which are the conditions that achieved ~95% labeling of ACP . The cells were washed with P-HBSS three times, and then the washed cells were subjected to microscopic observations. The cells exhibiting the presence of 0.4–0.8 ATTO594-ACP-D2R spots/µm2 were used for single-molecule imaging experiments.
Single Fluorescent-Molecule Video Imaging, Detection of Colocalization-Codiffusion, and Determination of Dimer Lifetimes
Single molecules of the fluorescently-labeled ACP-D2R expressed in the bottom PM were observed at 37 °C, using a home-built objective-lens-type total internal reflection microscope based on an Olympus IX-70 inverted microscope [53, 54], with a 100x objective lens (numerical aperture of 1.49; Olympus UAPON100XOTIRF). Fluorescent images were projected onto a two-stage microchannel plate intensifier (C8600-03, Hamamatsu Photonics), coupled to a scientific complementary metal–oxide–semiconductor camera operated at 30 or 250 Hz (C11440-22CU, Hamamatsu Photonics). The acquired image sequence was directly recorded on a solid-state drive installed on a personal computer. Fluorescent spots were identified by using a home-made computer program, as described previously .
Colocalization of two fluorescent spots (molecules) of the same color (the same ATTO594 probe) was detected when the two fluorescent molecules became localized within 220 nm from each other [35, 54]. An image-correlation analysis revealed a threshold value of 220 nm for detecting one or two peaks (for Alexa594 and DY547, 219 ± 9.0 nm, Kasai et al. ). Obviously, a scale of 220 nm is much greater than the molecular scale. Therefore, in addition to the colocalization due to the specific direct/indirect molecular binding as well as the entrapment in the same nano-domain, the incidental approaches of molecules within 220 nm, termed “incidental colocalization”, will often occur. However, although unassociated molecules may track together by chance over a short distance, the probability of this occurring for multiple frames is small, and therefore, longer colocalization durations imply the presence of molecular interactions between the two molecules, rather than incidental approaches within 220 nm (see the Results section). A similar method for detecting colocalization-codiffusion has been proposed .
Each time a colocalization-codiffusion event of D2R molecules was detected, its duration was measured, and after many such colocalization events were observed, a histogram showing the distribution of colocalization durations was obtained. The histogram could be fitted by a single exponential function, which provided a decay constant (lifetime; τ observed). This value was then corrected for the photobleaching lifetime (τ bleaching) to obtain the duration of apparent colocalization (τ apparent colocalization), using the equation [τ observed −1−2τ bleaching −1]−1 = τ apparent colocalization [35, 57]. (In our previous work , by comparing the results obtained by recordings at a 4-ms time resolution, we showed that τ observed of 110 ms could be determined precisely by 33-ms-resolution observations [normal video rate]. Therefore, we employed normal-video-rate observations in the present study.)
In principle, since the histogram of individual dimer durations should include the contributions of both specific and incidental colocalization events, the durations of which are described by complex functions. Nevertheless, we found that the incidental colocalization duration distribution could be quite-well described by a single exponential function with an incidental colocalization lifetime of 19 ± 0.66 ms, using a monomer reference molecule, ACP linked to the transmembrane domain of the low-density lipoprotein receptor, called ACP-TM . Furthermore, as described in the previous paragraph, the distribution of colocalization durations could be fitted by a single exponential function, probably due to the insufficient time resolution and/or poor signal-to-noise ratios, suggesting that its lifetime, τ apparent colocalization, closely represents the distribution of the sum of the durations of the following three events: duration from the encounter of two molecules within the distance of 220 nm until the binding of two molecules (duration 1), that of actual binding of two molecules (duration 2), and that from the separation of two molecules until they become separated over the distance of 220 nm (duration 3). Therefore, at the time resolution and signal-to-noise ratio of the present instrument, the best estimate of the binding duration of the two molecules would be τ apparent colocalization minus incidental colocalization lifetime of 19 ± 0.66 ms (assuming that this lifetime is close to the sum of duration 1 and duration 3). The pure incidental colocalization events are not included in this argument, because the fitting was performed from the second bin (33 ms and longer), which excludes the majority of incidental events.
Although we tracked the signal intensities as well as the (x, y)-coordinates of single molecules, we used the signal intensity information only for the purpose of confirming colocalization. In our single-molecule tracking with the signal intensity, we hardly observed any spots exhibiting two-step photobleaching. This observation excludes the possibility that we missed fluorescent spots of dimers that last for very long durations (if we had tracked colocalization using only the (x, y)-coordinates of single molecules, long lasting dimers might appear like single molecules, and thus we might miss the long-lasting dimers). Meanwhile, even when two fluorescent spots partially overlapped, although the signal intensities of such spots might appear to be those of dimers, the two molecules were often found to be separated from each other by a distance longer than 220 nm (thus, no colocalization, and thus no binding), and therefore, simple intensity measurements were not useful for unequivocally detecting colocalization.
D2R Molecules Exhibited Transient Colocalization-Codiffusion
All single-molecule tracking experiments were performed at 37 °C, at a time resolution of 33 ms (video rate) or 4 ms. D2R conjugated at its N-terminus with ACP was expressed in CHO cells, which do not express endogenous dopamine receptors, and D2R in the PM was fluorescently labeled by covalently conjugating ATTO594. This method allowed almost complete fluorescent labeling of D2R (>95%, George et al. ). The expression levels of D2R in the PM were adjusted to 0.4–0.8 copies/µm2.
Durations of Colocalization-Codiffusion of Two D2R Molecules
Since each fluorescent spot representing a single fluorescent molecule is much larger than the molecule itself (~500 nm vs. ~5 nm in diameter), even unassociated molecules become colocalized without molecular interactions and might track together by chance over a short distance. However, the probability of such incidental codiffusion events occurring for multiple frames is small, and therefore, longer colocalization implies the occurrence of molecular interactions between two molecules. Previously, we employed a monomer-reference molecule, ACP linked to the transmembrane domain of the low-density lipoprotein receptor, ACP-TM, and found that the duration of incidental colocalization-codiffusion of ACP-TM is 19 ± 0.66 ms .
The decay constant was corrected for the photobleaching lifetime of the fluorescent probe ATTO594 (2.98 ± 0.29 s; Fig. 2b), providing 87.4 (87 ms for two significant digits) ± 4.7 ms after correction for its photobleaching lifetime. For further discussions of the colocalization lifetimes, see Materials and Methods (Single fluorescent-molecule video imaging, detection of colocalization-codiffusion, and determination of dimer lifetimes).
D2R Forms Homodimers, with a Lifetime of 68 ms
Summary of the homodimer lifetimes of D2R before and after the addition of agonist or neutral antagonist
Dimer lifetime (ms)
# of events
P (vs. D2R before ligation)
68.4 ± 4.8
+Dopamine (natural agonist)
98.6 ± 8.3
103.5 ± 9.3
+UH-232 (neutral antagonist)
70.5 ± 11.0
We previously found that the FPR homodimer lifetime was ~ 90 ms. Therefore, the lifetime of the transient homodimers of D2R is comparable to that of FPR homodimers, but slightly (25%) shorter. Previously, using single-molecule imaging at a lower frame rate (19.32 frames per second vs. 30 frames per second employed here), Tabor et al.  detected transient D2R homodimers with a lifetime of ~0.5 s at 24 °C, which was longer than that found here (68 ms at 37 °C) by a factor of 7.4.
We hardly detected any oligomers greater than dimers under the expression levels employed here (0.4–0.8 ATTO594-ACP-D2R spots/µm2 in the PM). At much higher expression levels, oligomers might form. To the best of our knowledge, the physiological expression levels of D2R have not been reported.
Agonist Stimulation Slightly Stabilized Transient Dimers, in Contrast to a Neutral Antagonist
The effects of agonists on the D2R homodimer lifetime was investigated by incubating the cells expressing D2R in the presence of agonists (15 µM dopamine or 15 µM quinpirole) , or a neutral antagonist (0.1 µM UH-232)  for 20–120 s. This incubation time was selected because intracellular Ca2+ mobilization was detected within 20 s after agonist addition (15 µM; no intracellular Ca2+ mobilization was found after the addition of a neutral agonist, UH-232, for 2 min).
Whether a class-A GPCR D2R forms dimers, and if so, whether the dimers are transient or constitutive dimers, have been controversial subjects [42, 43]. In the present research, our single-molecule imaging-tracking at a time resolution of 33 ms unequivocally showed that D2R forms transient homodimers with a lifetime of 68 ms at 37 °C. This result is quite consistent with a homodimer lifetime of 90 ms for FPR observed by us at 37 °C . Meanwhile, the D2R homodimer lifetime was found to be much longer (~0.5 s) at 24 °C , a factor of 7.4 longer than that found here. Other class-A GPCRs, M1 muscarinic receptor and β1- and β2-AR, were also found to form transient homodimers with longer lifetimes of 0.7 s at 23 °C  and 5 s at 20.5 °C , respectively. Taken together, transient homodimerization is likely to be a general physical property of the class-A GPCRs, and thus homodimers may play some important roles in GPCR signaling and/or regulation. In addition, because temperature strongly affects the homodimer lifetime of D2R (between a lower temperature of 24 °C and the physiological temperature of 37 °C) and probably those of other GPCRs, the activation energy for homodimer formation is quite large (Q10 for D2R is likely to be much greater than 3, and that for β1- and β2-AR might reach 30 or more).
Furthermore, we found that the two agonists for D2R both prolonged the homodimer lifetime, whereas the neutral antagonist did not. The increase in the homodimer lifetime by the agonist binding was only by a factor of ~1.5, but if each subunit of the dimer participates in the downstream signaling, then the signal emitted by the D2R homodimer would increase by a factor of 2.3 (1.5 × 1.5). These results are quite consistent with the finding by Tabor et al. , in which agonist addition increased apparent dimer fraction of D2R. In previous analyses, the addition of agonists for FPR  and β1- and β2-AR  did not change the homodimer lifetimes, and therefore, this is the first example in which the dimer lifetime was increased by agonist addition. Although the biological significance of these differences among GPCRs is not clear, our results are consistent with the findings reported by Wang et al. , in which schizophrenia, an amphetamine-induced sensitized state, and acute amphetamine exposure were found to enhance dimerization of D2R without altering its expression levels.
Meanwhile, a pull-down assay after chemical crosslinking revealed that another class-A GPCR, CCR2, was monomeric before stimulation, but agonist addition induced dimer formation . Further studies on the effects of agonists on GPCR homodimerization are required, based on the present understanding that class-A GPCRs are likely to form transient homodimers with lifetimes shorter than 100 ms.
This research was supported in part by Grants-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology (MEXT) of the Japanese government to R.S.K. and A.K. This research was supported in part by Grants-in-Aid for scientific research from the Japan Society for the Promotion of Science (Wakate B and Kiban C to R. S. K. [26870292, 17K07333, respectively], Kiban B to T. K. F. [16H04775], and Kiban A and S to A. K. [24247029 and 16H06386, respectively]), Grants-in-Aid for Innovative Areas from the Ministry of Education, Culture, Sports, Science and Technology (MEXT) of Japan to R. S. K. (24115511) and to T. K. F. (26115707 and 15H01212) and a grant from Core Research for Evolutional Science and Technology (CREST) project of “Creation of Fundamental Technologies for Understanding and Control of Biosystem Dynamics” of Japan Science and Technology Agency (JST) to A. K. (JPMJCR14W2). WPI-iCeMS of Kyoto University is supported by the World Premiere Research Center Initiative (WPI) of the MEXT.
RSK and AK conceived this research, designed the experiments, and wrote the paper. RSK, SVI, and RMA performed the experiments and analyses. TKF developed the analysis software. All authors participated in the revisions of the manuscript and approved the final version of the manuscript.
Compliance with Ethical Standards
Conflict of Interest
The authors declare that they have no competing interests.
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