Immunogold electron microscopic evidence of in situ formation of homo- and heteromeric purinergic adenosine A1 and P2Y2 receptors in rat brain
© Namba et al; licensee BioMed Central Ltd. 2010
Received: 27 July 2010
Accepted: 29 November 2010
Published: 29 November 2010
Purines such as adenosine and ATP are now generally recognized as the regulators of many physiological functions, such as neurotransmission, pain, cardiac function, and immune responses. Purines exert their functions via purinergic receptors, which are divided into adenosine and P2 receptors. Recently, we demonstrated that the Gi/o-coupled adenosine A1 receptor (A1R) and Gq/11-coupled P2Y2 receptor (P2Y2R) form a heteromeric complex with unique pharmacology in co-transfected human embryonic kidney cells (HEK293T). However, the heteromeric interaction of A1R and P2Y2R in situ in brain is still largely unknown.
In the present study, we visualized the surface expression and co-localization of A1R and P2Y2R in both transfected HEK293T cells and in rat brain by confocal microscopy and more precisely by immunogold electron microscopy. Immunogold electron microscopy showed the evidence for the existence of homo- and hetero-dimers among A1R and P2Y2R at the neurons in cortex, cerebellum, and particularly cerebellar Purkinje cells, also supported by co-immunoprecipitation study.
The results suggest that evidence for the existence of homo- and hetero-dimers of A1R and P2Y2R, not only in co-transfected cultured cells, but also in situ on the surface of neurons in various brain regions. While the homo-dimerization ratios displayed similar patterns in all three regions, the rates of hetero-dimerization were prominent in hippocampal pyramidal cells among the three regions.
The adenosine A1 receptor (A1R) is known to regulate Ca2+/K+ channels, adenylate cyclase, and phospholipase C by coupling to Gi/o proteins . In hippocampal astrocytes, P2Y1R- and P2Y2R-mediated Ca2+ responses differentially show two forms of activity-dependent negative feedback of synaptic transmission via the phospholipase C beta-IP3 pathway . Today, the homo- or hetero-dimers of many kinds of GPCRs have been reported . We previously demonstrated that A1R associates with P2Y1R in co-transfected HEK293T cells and in rat brain homogenates, whereby a P2Y1R agonist stimulates A1R signaling via Gi/o [4, 5]. Furthermore, in HEK293T cells co-transfected with A1R and P2Y2R, the heterodimers display synergistic increases in Ca2+ signaling, whereby simultaneous activation of the two receptors attenuates A1R signaling via Gi/o, but synergistically enhances P2Y2R signaling via Gq/11 . Also, the simultaneous activation of endogenous A1R and P2Y2R in DDT1MF-2 cells synergistically increases translocation of protein kinase C . Because A1R are widely expressed in brain , it is likely that these receptors also associate directly in situ; however, direct evidence of their dimerization or precise co-localization in brain has yet to be demonstrated. The aim of the present study is to determine whether A1R and P2Y2R associate with each other in rat brain by co-immunoprecipitation and looking for receptor complexes via immunogold electron microscopy (IEM).
Double immunostaining of A1R/P2Y2R in HEK293T cells and rat brain sections
Double immunostaining using anti-HA 3F10 mAb rat antibody (anti-HA) and anti-Myc 9E10 mAb mouse antibody (anti-Myc) in HA-A1R and Myc-P2Y2R-co-transfected HEK293T cells were performed as previously described . Cells were washed and then stained with Alexa 568-conjugated goat anti-rat IgG antibody (1:200, Invitrogen, Carlsbad, CA) for A1R or Alexa 488-conjugated goat anti-mouse IgG antibody (1:200, Invitrogen) for P2Y2R. The characterization of antibodies for rat brain sections was previously reported, although the rabbit polyclonal anti-P2Y2R antibody (anti-P2Y2R; 1 μg/ml, Alomone Labs, Jerusalem, Israel) was used instead of the rabbit polyclonal anti-P2Y1R antibody [5, 8].
Immunoprecipitation and western blotting of rat brain homogenates
Eight-week-old male Wistar rats were decapitated under anesthesia (Nembutal; 30 mg/kg i.v.), and cortical, hippocampal, and cerebellar tissues were dissected out. The tissues were homogenized with a Polytron homogenizer in 50 mM Tris-acetate, pH 7.4, containing a protease inhibitor cocktail (Roche Applied Science, Manheim, Germany), and the resulting cell suspensions were centrifuged at 30,000 × g for 30 min at 4°C. The pellets were solubilized in ice-cold lysis buffer (50 mM Tris-HCl, pH 7.4, 1% Triton X-100, 300 mM NaCl and a protease inhibitor cocktail) for 60 min at 4°C. The mixture was centrifuged at 18,500 × g for 20 min at 4°C, and the supernatant pre-cleared with Protein G-Sepharose™4 Fast Flow (Amersham Bioscience, Piscataway, NJ). The lysate was incubated with rabbit polyclonal anti-A1R antibody (anti-A1R; 1 μg/ml, Sigma-Aldrich, St. Louis, MO) for 60 min at 4°C. Protein G-Sepharose was added to the mixture, and the incubation continued for an additional 120 min. Protein G-Sepharose was recovered by centrifugation and washed three times with lysis buffer. Immunoprecipitates were eluted with SDS-PAGE sample buffer, resolved by 12% SDS-PAGE, and electrotransferred to nitrocellulose membranes. Receptors on the blot were detected using anti-A1R or anti-P2Y2R, followed by horseradish peroxidase-conjugated goat anti-rabbit IgG secondary antibody (Sigma-Aldrich). The reactive bands were visualized with enhanced chemiluminescent substrates (SuperSignal West Pico, Pierce, Rockford, IL).
Pre-embedding immunogold electron microscopy (IEM) of transfected HEK293T cells
HEK293T cells expressing HA-A1R and Myc-P2Y2R were fixed with 4% PFA, and permeabilized with 0.25% Triton X-100. Cells were incubated with anti-HA and anti-Myc for 3 h at 4°C. After washing with PBS, cells were incubated with 10-nm gold particle-conjugated goat anti-rat IgG antibody (rat IgG-10, 1:1000, BBI International, Lakewood, CO) and 5-nm gold particle-conjugated goat anti-mouse IgG antibody (mouse IgG-5, 1:1000, BBI International) for 4 h at 4°C. After washing, the cells were fixed with 2.5% glutaraldehyde in 0.15 M sodium cacodylate, pH 7.4 for 2 h, washed, and postfixed with 1% osmium tetroxide for 4 h at room temperature. The cells were then dehydrated and embedding resin (Epon 812; NISSIN EM, Tokyo, Japan). Specimens were observed with an H7500 electron microscope (Hitachi, Japan). We quantified the gold staining as follows: The gene-transfected HEK293T cells with the highest numbers of total immuno-reacted gold particles were defined as 100% labeling. Because the co-transfected HEK293T cells that displayed unique pharmacology in our previous study  exhibited more than 20% hetero-dimeric gold particles, we used this number as a threshold in the current study. Thus, cells with more than 20% hetero-dimeric particles were defined as being "significantly stained", and those with 20% or less were defined as "not significantly stained".
Post-embedding immunogold electron microscopy of brain tissues
Dissected brain tissues were cut into 1.0 mm3 blocks that were then incubated with lead (II) acetate (Sigma-Aldrich) buffer for 1 h at room temperature, dehydrated through a series of graded ethanol, and embedded in LR-white (NISSIN EM). Ultra thin sections (40 nm) were mounted on 200-mesh nickel grids (NISSIN EM) and incubated in PBS containing 1% BSA for 10 min. After immunostaining with primary antibodies, each specimen was incubated with mouse IgG-5- and IgG-10-nm gold particle-conjugated goat anti-rabbit IgG antibody (rabbit IgG-10) for 6 h at 4°C. For controls, transfected HEK293T cells were embedded with LR-white under the same conditions as described above. After incubation at 4°C for 12 h with anti-HA (10 μg/ml) and anti-Myc (10 μg/ml), samples were washed with 1% BSA/PBS. After incubation with gold particle-conjugated secondary antibodies for 6 h at 4°C, sections were stained with uranyl acetate for 10 min. "Significant heteromeric staining" was defined as more than 20% of the total number of immuno-reacted gold particles at the cell surface occurring in heteromeric clusters.
Comparison of the numbers of monomers, homo-dimers, and hetero-dimers
Co-localization of A1R and P2Y2R in transfected HEK293T cells
Immunohistochemical studies in rat brain
We examined the expression of A1R and P2Y2R in brain using immunohistochemical analyses (Figure 2). The specificity of the antibodies against A1R and P2Y2R was confirmed by the immunocytochemistry of recombinant receptor-expressing cell lines, i.e. antibodies used in this study showed no cross-labeling in A1R- and P2Y2R-transfected HEK293T cells (data not shown). Prominent staining of A1R and P2Y2R were observed especially in Purkinje cells (Figure 2D-F), interposed cerebellar nuclei (Figure 2G-H), and hippocampal pyramidal cells (Figure 2J-L). Comparatively high immunoreactivities were also detected in the piriform cortex, amygdala, hypothalamus, and brainstem (data not shown). Their expressions were mainly restricted to cell bodies and neuronal dendrites. Importantly, co-localization of A1R and P2Y2R in the cerebellum was observed in cell bodies, except in the nuclear region, in the Purkinje cells and those of the interposed cerebellar lobule nucleus (Figure 2D-I). In the hippocampal region, pyramidal cell bodies, especially the cell surface membranes, in CA1, CA2, CA3, and the dentate gyrus (CA3; Figure 2J-L, others; data not shown) were intensely stained for both A1R and P2Y2R. Similar staining patterns were seen in cell bodies of neurons in the cerebral cortex (data not shown).
Co-immunoprecipitation of A1R and P2Y2R from rat brain
Immunogold electron microscopic observations of HA-A1R and Myc-P2Y2R expressed in HEK293T cells
Immunogold electron microscopic observations of A1R and P2Y2R expressed in rat brain
We incubated post-embedded, primary antibody-stained rat brain tissues with secondary antibodies labeled with mouse IgG-5 for A1R and rabbit IgG-10 for P2Y2R. As negative controls, tissues were stained with only secondary antibodies conjugated with different sized gold particles; no significant immunoreactivities were observed under the experimental conditions used in this study (data not shown). As in the transfected HEK293T cells, we observed clusters of different-sized gold particles at cytoplasmic membranes in cell bodies, indicating the presence of heteromeric complexes of endogenous A1R and P2Y2R in rat brain (Figure 4E-G). Significant immunoreactivity was detected in Purkinje cells (Figure 4F) and hippocampal pyramidal cells (Figure 4G). Hetero- and homo-dimers were detected in significant numbers at the cell surface in both transfected HEK293T cells and native brains.
Comparison of the frequencies of monomers, homo-dimers, and hetero-dimers
We counted gold particles on the surfaces of cells in the cortex, cerebellum, and hippocampus and classified them as monomers (A1R or P2Y2R), homo-dimers (A1R-A1R or P2Y2R-P2Y2R), or hetero-dimers (A1R-P2Y2R). While the homo-dimerization ratios (A1R-A1R/P2Y2R-P2Y2R) displayed similar patterns in all three regions (Figure 1A-C), the rates of hetero-dimerization were prominent in hippocampal pyramidal cells among the three regions.
The present study provides the first detailed evidence of an interaction between endogenous A1R and P2Y2R in brains using co-immunoprecipitation and IEM. The homo-dimerization of A1R was previously analyzed in our laboratory by computational prediction, co-immunoprecipitation, and BRET analysis . In the present study, we might suggest the existence of homo-dimers (A1R-A1R and P2Y2R-P2Y2R) using IEM. Very interestingly, the percentage of A1R homo-dimers was higher than that of P2Y2R in both rat brain and transfected HEK293T cells (Figure 1). By contrast, the ratios of heteromeric gold-particle clusters were different in the cortex, hippocampus, and cerebellum. Importantly, both homo-dimeric and hetero-dimeric gold-particles were much fewer at inner cytoplasmic membranes than at the cell surface (data not shown). In general, most GPCRs dimers have been observed on the cell surface [10, 11]. Total numbers of hetero-dimers observed on the cell surface and in the cytoplasm were obviously different (data not shown) and may reflect the process of receptor maturation and association of the A1R-P2Y2R complex.
In the hippocampal region, the strong presence of hetero-dimers coincided with the relative signal intensity of the co-immunoprecipitation band (Figure 3D lane 3). In the previously reported electron microscopic analysis of A1R and P2Y1R co-localization in hippocampus, the A1R density was relatively higher than that of P2Y1R at the presynaptic membrane . They suggested that the hetero-dimerization or cross-talk of A1R and P2Y1R is involved in regulation of glutamate release. The relative distributions of immunoreactivities for GABAB R2 and GABAB R1 were also different in the basal ganglia and globus pallidus/substantia nigra, which suggests the possible co-existence and hetero-dimerization of two types of receptors at various pre-/postsynaptic sites . From the present study, it can be speculated that the A1R/P2Y2R hetero-oligomer might be responsible for down regulation, via hippocampal Ca2+ secretion, of synaptic functions . The abundant formation of A1R/P2Y2R hetero-oligomers in hippocampus revealed in this study supports the idea that the unique signal transduction generated by hetero-dimerization, including the enhancement of Ca2+ signaling via Gq/11, observed in transfected cells also occurs in hippocampus.
List of abbreviations
G protein-coupled Receptor
A1 adenosine receptor
P2Y1 purinergic receptor
P2Y2 purinergic receptor
immunogold electron microscopy
We thank Masumi Ichikawa and Kyoko Ajiki at the Tokyo Metropolitan Institute for Neuroscience for their help with the electron microscopy. This work was supported by grants-in-aid from the Ministry of Education, Culture, Sports, Science, and Technology of Japan; Grant number: 16300125, 00041830, 00041830
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