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1a-Adrenergic Receptors
Institute of Vascular Medicine, Peking University Third Hospital and Key Laboratory of Molecular Cardiovascular Sciences, Ministry of Education, Beijing, China
Received for publication July 4, 2005.
Accepted for publication May 11, 2006.
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Abstract |
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1A-adrenergic receptor (AR) using the yeast two-hybrid system. Whereas CUB5 did not couple to either 1B-AR or 1D-AR. It was determined that amino acids 322 to 359 of 1A-AR were the major binding region for CUB5. The direct interaction between 1A-AR cytoplasmic tail and CUB5 was discovered by glutathione S-transferase pull-down assay. We confirmed the interaction of mTLD with 1A-AR in human embryonic kidney (HEK) 293 cells by immunoprecipitation, immunofluorescence, and fluorescence resonance energy transfer. Although mTLD did not affect the density and affinity of receptors in crudely prepared membranes from HEK293 cells stably expressing 1A-AR, it significantly altered the subcellular localization of the receptors. Moreover, mTLD reduced the level of cell surface 1A-ARs, delayed the initial rate of agonist-induced receptor internalization, and facilitated agonist-induced calcium transient. We have demonstrated that mTLD interacts with 1A-AR directly, alters the subcellular localization of receptor, and influences agonist-induced 1A-AR internalization and calcium signaling.
1-Adrenergic receptors (ARs) are G-protein-coupled receptors (GPCRs) that respond to norepinephrine and epinephrine. 1-ARs can be classified into at least three subtypes, termed 1A, 1B, and 1D, according to their ligand specificity and their amino acid sequences. Although the three 1-AR subtypes all couple to the Gq/11 signaling pathway, they have distinct functional roles in mediating vascular smooth muscle contraction and cardiomyocyte hypertrophy (Zhu et al., 1997
; Autelitano and Woodcock, 1998; Grupp et al., 1998).
As the largest family of membrane proteins, GPCRs respond to extracellular stimulations and convert them to intracellular signals. In general, this transduction is defined as follows: ligand binding changes the conformation of receptor's intracellular region, which induces the interaction of receptor with heterotrimeric G-proteins and the ultimate dissociation of G and G
subunits. These activated subunits can stimulate and/or inhibit a variety of intracellular effectors. A large number of intracellular molecules other than G-proteins (non-G-proteins) could also interact with GPCR, mediate the intracellular response, or regulate the receptor's state, distribution, and function (Hall et al., 1999; Heuss and Gerber, 2000; Brzostowski and Kimmel, 2001).
ARs have been shown to associate with several non-G-proteins. The majority of them were identified for 2-AR, such as ARK, -arrestin, AKAP79/150, NHERF, and eIF-2B (Klein et al., 1997; Menard et al., 1997; Hall et al., 1998; Fraser et al., 2000; Cong et al., 2001); only a few proteins are reported to interact with 1-AR. Among them, the µ2 subunit of the AP2 clathrin adaptor complex specifically interacts with 1B-AR (Diviani et al., 2003), whereas tissue transglutaminase II (Gh) and gC1q-R interact with 1B- and 1D-AR (Chen et al., 1996; Pupo and Minneman, 2003). Neuronal nitric-oxide synthase was believed previously to interact with 1A-AR but was found to interact with all three subtypes of 1-AR and 1- and 2-ARs (Pupo and Minneman, 2002). So far, no interacting protein has been identified specifically for 1A-AR, the most important and efficient subtype of 1-AR (Zhong and Minneman, 1999; Zhong et al., 2001).
CUB5 domain, a segment of mammalian Tolloid (mTLD) (Takahara et al., 1994), has been identified as an 1A-AR coupling protein by our group (Xu et al., 2003). In the present study, we have further explored the interaction of 1A-AR and mTLD. In particular, we investigated the differential interactions of CUB5 domain with three 1-AR subtypes and the region of 1A-AR that binds to the CUB5 domain. We also assessed this interaction by glutathione S-transferase (GST)-1A-AR fusion protein pull-down assay, immunoprecipitation, immunofluorescence, and fluorescence resonance energy transfer (FRET). Moreover, the effects of mTLD on pharmacological property, localization, and signaling of 1A-AR were also investigated in this study.
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Materials and Methods |
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1A-, 1B-, and 1D-ARs and C-terminally truncated 1A-ARs in mammalian expression vectors PDT-1A,-1B,-1D, and -1ACT, and the GST-tagged 1A-AR cytoplasmic tail, GST-1A, were generous gifts from Dr. Kenneth P. Minneman (Department of Pharmacology, Emory University, Atlanta, GA). The cDNA sequence encoding the 1B- and 1D-AR cytoplasmic tail and various fragments of the 1A-AR carboxyl terminus were generated by PCR and cloned into pGBKT7 with EcoRI and BamHI sites (see Supplemental Data). PCR reactions were carried out using high-fidelity Pfx DNA polymerase (Invitrogen, Carlsbad, CA).
cDNA encoding human mTLD (P13497
[GenBank]
) was obtained from Invitrogen. For mammalian cell expression, PCR products were subcloned into pcDNA3.1 (+) with NheI and XhoI sites to generate pMT, and other HA-tagged PCR products were also subcloned into pcDNA3.1 (+) with NheI and PmeI sites to generate pMT/HA (supplemental data). The cDNA of prey 3, which encodes aa 867 to 986 of mTLD, was subcloned into pcDNA3.1 (+) with EcoRI and BamHI sites to generate HA-tagged pcP3HA, as we described previously (Xu et al., 2003). Construct EGFP-1A, expressing fused EGFP/1A-AR, was made by cutting 1A-AR cDNA with its flank EcoRI and BamHI restriction sites from PDT-1A and then cloning back into the EGFP-C2 expression vector. All constructs were confirmed with Prism 3700 DNA automatic sequencer (Applied Biosystems Inc., Foster City, CA).
Yeast Two-Hybrid. We used pretransformed MATCHMAKER two-hybrid system (Clontech, Mountain View, CA) to perform the screening. Yeast Saccharomyces cerevisiae strains AH109 and Y187 were used as the host for the in vivo interaction studies. Yeast two-hybrid analysis was carried out as described in Clontech's user manual. PGAACT, a bait plasmid containing 1A-AR aa 322 to 466 was transformed into yeast strain AH109 by the LiCl/polyethylene glycol method, and mating with human brain cDNA pretransformed yeast strain Y187. Prey plasmids were isolated from the positive colonies using the Zymoprep Yeast Plasmid Minipreparation Kit (Zymo Research, Orange, CA) and sequenced with Prism 3700 DNA automatic sequencer.
-Galactosidase activity was used to test interactions between different fusion proteins. In brief, both bait and prey plasmids were transformed into the yeast strain Y187; then, -galactosidase activities were measured by colony-lift filter assay and liquid -galactosidase assay with O-nitrophenyl glycoside (Merck and Co., Inc., Whitehouse Station, NJ).
GST Pull-Down Assay. MagneGST Pull-Down System (Promega, San Luis Obispo, CA) was used for direct interaction assays between 1A-AR and mTLD. GST-1A-AR cytoplasmic tail fusion proteins or GST proteins were lysed from 1 ml of bacterial culture, and immobilized on MagneGST Particles. Transcription/translation of aa 867 to 986 of mTLD was undertaken in vitro using TNTT7 Quick-Coupled transcription/translation reactions Master Mix (Promega, Madison, WI). Binding reactions were performed in 200 µl of binding/wash buffer (4.2 mM Na2HPO4,2mMKH2PO4, 140 mM NaCl, and 10 mM KCl, pH 7.2) for 1 h at room temperature. Particles were washed five times with the same buffer, and bound proteins were analyzed by immunoblotting.
Cell Line, Culture, and Transfection. HEK293 cells were obtained from the American Type Culture Collection (Manassas, VA) and cultured in glutamine-containing high-glucose Dulbecco's modified Eagle's medium supplemented with 10% fetal bovine serum, 1 mM sodium pyruvate, 100 mg/ml streptomycin, and 100 U/ml penicillin at 37°C under a 95% air/5% CO2 atmosphere. HEK293 cells stably transfected PDT-1A were also cultured in the same conditions except that 200 mg/ml G418 (Geneticin) was added. Lipofectamine 2000 (Invitrogen) was used in all transfection experiments.
Coimmunoprecipitation Assay. HEK293 cells were transfected and cultured for 48 h. Immunoprecipitation was performed as described previously (Vazquez-Prado et al., 2000) with minor modifications. In brief, cells were washed with ice-cold PBS and lysed for 1 h on ice in lysis buffer (10 mM Tris-HCl, pH 7.4, 50 mM NaCl, 5 mM EDTA, 1% Triton X-100, and 0.05% SDS) supplemented with 50 mM sodium fluoride, 100 mM sodium orthovanadate, 10 mM sodium pyrophosphate, 20 mg/ml aprotinin, 20 mg/ml leupeptin, and 100 mg/ml phenylmethylsulfonyl fluoride. Cell lysates were centrifuged at 12,700g for 15 min, and the supernatants were incubated overnight at 4°C with the anti-Flag M2 affinity resin (Sigma-Aldrich.) or anti-c-myc antibodies (Santa Cruz Biotechnology, Inc., Santa Cruz, CA) plus protein G resin (Sigma-Aldrich). After four washes with lysis buffer without protease inhibitors, the immune complexes were denatured by boiling in 2x loading buffer and analyzed by immunoblotting. Anti-1A-AR antibodies (Santa Cruz Biotechnology), anti-mTLD antibodies, and Supersignal West Pico Chemiluminent (Pierce Biotechnology, Inc.) were used to detect proteins.
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1A and pMT/HA. Twenty-four hours after transfection, cells were fixed in 4% formaldehyde for 10 min and permeated with 0.1% Triton X-100 for 10 min. The fixed cells were incubated with anti-HA monoclonal antibodies (1:100 dilutions; Santa Cruz Biotechnology) overnight at 4°C and then with a TRITC-conjugated anti-mouse antibody (1:200 dilution; Invitrogen) for 1 h. The distributions of 1A-AR and mTLD were examined with a confocal laser-scanning microscope system (TCS SP2; Leica, Wetzlar, Germany) with a 40x oil immersion objective lens. Fluorescence of TRITC was then excited continuously for 5 min to bleach the TRITC signal irreversibly. Images of the EGFP fluorescence were acquired before and after photobleaching. The extent of FRET was assessed by calculating the ratio of the EGFP fluorescence before (DA) and after (D) photobleaching, using the equation E = D/DA. Nine to ten cells from three individual experiments were selected, and the D/DA of intracellular areas was averaged.
Radioligand Binding. HEK293 cells stably transfected PDT-1A were plated in 10-cm dishes and transfected with pcDNA3.1/LacZ or pMT. Forty-eight hours after transfection, cells were washed with PBS, pH 7.6, and harvested. After centrifugation and homogenization with a Polytron homogenizer (Kinematica, Basel, Switzerland), cell membranes were collected by centrifugation at 20,000g for 20 min and resuspended in PBS. Radioligand binding sites were measured by saturation analysis of specific binding of the 1A-AR antag-onist radioligand 125I-BE2254 (15-500 pM). Nonspecific binding was defined as binding in the presence of phentolamine at 100 µM.
Whole-Cell ELISA. HEK293 cells stably transfected with PDT-1A were plated in poly-D-lysine-coated 24-well plates and transfected with pcDNA3.1/LacZ or pMT. Forty-eight hours later, cells were incubated with DMEM containing phenylephrine (10 µM) for 0 to 60 min at 37°C. The transfected cells were then fixed in 2% formaldehyde for 10 min without permeating the cells. Changes in surface receptor density were subsequently determined by ELISA, taking advantage of the FLAG-tag in 1A-AR. Cells were labeled with the anti-FLAG M2 antibody (1:1000 dilution; Sigma-Aldrich) followed by anti-mouse antibody (1:1000 dilution; Jackson ImmunoResearch, West Grove, PA). Antibody labeling was detected by incubation with O-phenylenediamine (Sigma-Aldrich, Inc.), and absorbance was read at 490 nm.
Intracellular Calcium Measurement. PDT-1A stably transfected HEK293 cells were transfected with pcDNA3.1/LacZ or pMT. Twenty-four hours after transfection and a further8hof serum starvation, cells were loaded with calcium indicator, fluo-4AM (In-vitrogen), as described previously (Wang et al., 2001). Fluorescence was visualized by Zeiss LSM510 confocal microscope (Oberkochen, Germany) equipped with an argon laser (488 nm) and 40x, 1.3 numerical aperture oil immersion objective lens. Images were acquired at sampling rates of 10 s/image, and phenylephrine (10 µM) was added after the first three images were acquired. The digital images were analyzed with IDL image-processing software (ver. 5.4; RSI, Boulder, CO). Four to five cells were selected, and the average fluorescence density of intracellular areas was measured to indicate calcium level. All the data were normalized by fluorescent density before stimulation.
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1A-AR via Yeast Two-Hybrid Assay. To identify proteins interacting with 1A-AR, we screened a human brain cDNA library, using the yeast two-hybrid assay with the cytoplasmic tail (aa 322-466) of 1A-AR as bait. More than 2 x 107 colonies were screened, and positive colonies were identified by monitoring the activation of reporter genes HIS3, ADE2, and MEL1. Plasmids containing prey cDNA from each positive colony were isolated and sequenced. Of the nine positive colonies obtained, six prey plasmids were identified. As shown in Fig. 1, top, the cDNA of prey 3 encodes aa 867 to 986, the CUB5 domain, of protein mTLD.
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1-AR in yeast two-hybrid system. We found that only yeast cells transformed with CUB5 cDNA constructs and cytoplasmic tail of 1A-AR cDNA constructs showed an obvious activation of reporter gene -galactosidase, which was consistent with the yeast two-hybrid assay screening results. No such interaction was detected between the CUB5 domain and cytoplasmic tail of either 1B-AR or 1D-AR (Fig. 1, bottom).
Amino Acid Residues 322 to 359 of 1A-AR Are Important for Interaction with CUB5. As mentioned above, the whole cytoplasmic tail of 1A-AR was used as bait in the yeast two hybrid screen. To localize the CUB5 domain interaction on 1A-AR C terminus, a series of truncations of 1A-AR cytoplasmic tail, illustrated in Fig. 2, were screened against CUB5 domain. Both X-Gal colony-lift filter assay and liquid -galactosidase assay yielded similar results (Fig. 2). Truncations of the carboxyl end of 1A-AR were quite tolerated, displaying positive interactions with CUB5. Only a small fragment, containing residues 360 to 398, did not interact with CUB5. Truncations from the amino terminus of the 1A-AR cytoplasmic tail narrowed the region for interaction with CUB5 domain to residues 322 to 359.
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1A-AR in Vitro and Vivo. To examine whether mTLD can directly interact with 1A-AR, purified GST-1A-AR-cytoplasmic-tail fusion proteins from bacterial cells and in vitro synthesized CUB5 domains were subject to GST pull-down assay. The bound proteins were fractionated by SDS-polyacrylamide gel electrophoresis and detected by Western blotting. As shown in Fig. 3, the CUB5 domains bound to GST-1A-AR-cytoplasmic-tail fusion proteins but not to GST alone.
To confirm the interaction between 1A-AR and mTLD in vivo, 1A-AR and mTLD were transiently expressed in HEK293 cells, lysed, and immunoprecipitated by their antibodies, respectively. In immunoblots of cell lysate, bands corresponding to 1A-AR (
50 kDa) and mTLD were revealed by their respective antibodies in transfected but not in untransfected cells (Fig. 4). Immunoprecipitating 1A-AR with anti-Flag M2 affinity resin resulted in coimmunoprecipitation of mTLD, as revealed by the specific 150-kDa band detected in immunoprecipitates of cotransfected cells. This band was not present in immunoprecipitates from HEK293 cells expressing 1A-AR or mTLD alone. Conversely, reverse immunoprecipitating mTLD also showed coimmunoprecipitation of 1A-AR (Fig. 4). Thus, in HEK293 cells, mTLD interacted specifically with 1A-AR.
Likewise, in HEK293 cells transiently expressing 1A-AR and CUB5 domain, immunoprecipitating 1A-AR with antiFlag M2 affinity resin also resulted in coimmunoprecipitation of CUB5 (Fig. 4C). Moreover, the CUB5 coimmunoprecipitated by the C-terminally truncated 1A-AR was less than 5% of that by full-length 1A-AR, confirming that the binding to CUB5 domain was mostly contributed by the C terminus of 1A-AR.
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1A-AR. To characterize the mTLD-1A-AR association in vivo, EGFP-fused 1A-AR and HA-tagged mTLD were transfected into HEK293 cells to allow the subcellular localization of these proteins to be determined using an immunofluorescence assay. As shown in Fig. 5, in cells expressing EGFP-fused 1A-AR alone, fluorescence was observed both on the cell surface and intracellularly (Fig. 5A), which was consistent with previous reports (Chalothorn et al., 2002). When mTLD and 1A-AR were coexpressed, the subcellular localization of 1A-AR was significantly altered. The EGFP fluorescence signal of 1A-AR accumulated predominantly in certain cytoplasmic compartments colocalizing with mTLD (Fig. 5, B, C, and D). However, if the cells were stimulated with 10-5 M phenylephrine for 5 min before fixation, colocalization of 1A-AR with mTLD was evident on the cell surface and the cytoplasmic compartment, although the fluorescence signal of 1A-AR was still concentrated in the cytoplasm (Fig. 5, E, F, and G). To validate whether a direct interaction happens between these two molecules, FRET between EGFP-fused 1A-AR (donor fluorescence) and immunofluorescence stained mTLD (acceptor fluorescence) was measured by acceptor photobleaching method. As shown in Fig. 5H, in the absence of mTLD, EGFP signal declined 16.9 ± 3.6% after 5 min of continuous activation of TRITC signal, because EGFP fluorescence could also be excited and inactivated during the process. In the presence of mTLD, however, the fluorescence of the donor in the cells increased 26.7 ± 5.4% after photobleaching of acceptor fluorescence, which indicates a tight intermolecular association between 1A-AR and mTLD in HEK 293 cells.
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1A-AR in immunofluorescence assay, we compared the number of cell surface 1A-AR in HEK293 cells stably transfected with PDT-1A in the presence or absence of mTLD (Fig. 6A) using whole-cell ELISA assays. As shown in Fig. 6B, the presence of mTLD reduced the number of cell surface 1A-AR by 44 ± 6% (P < 0.001, n = 8) compared with cells transfected with a control vector, pcDNA3.1/LacZ. In addition, we examined the time course of 1A-AR internalization in response to phenylephrine (10 µM). As shown in Fig. 6C, in the control group (pcDNA3.1/LacZ transfected), there was a rapid agonist-induced internalization of cell surface receptor with a 63 ± 2% (n = 8) reduction after 1 h; in the mTLD group, the time course of 1A-AR internalization was somewhat delayed. The number of cell surface receptors initially increased after 5 min of agonist stimulation and decreased by 58 ± 5% (n = 8) between 5 and 60 min of agonist exposure.
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1A-AR. To study the effect of mTLD on the pharmacological properties of 1A-AR, crude membranes were prepared from HEK293 cells expressing 1A-AR with and without concomitant expression of mTLD. The density and affinity of 1A-AR binding sites were then determined by saturation analysis of the specific binding of the antagonist radioligand 125I-BE2254. As shown in Fig. 7, the presence of mTLD had no effects on the density of 1A-AR. There was no significant difference in Bmax between LacZ-coexpressing and mTLD-coexpressing groups (1030 ± 65 versus 1048 ± 119 fmol/mg, respectively; both n = 4). Furthermore, there was no significant difference in the affinity of 1A-AR to the radioligand 125I-BE2254 in the presence of LacZ or mTLD (272 ± 26 versus 352 ± 69 pM, respectively; both n = 4). These results indicated that the interaction of mTLD with 1A-AR does not affect the pharmacological properties of the receptor, although mTLD pulled considerable receptors into intracellular compartment.
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1A-AR signaling function, the dynamics of intracellular calcium concentration ([Ca2+]i) in response to 1A-AR activation was examined with a calcium indicator, fluo-4. In 1A-AR and LacZ cotransfected cells, we detected a sharp, high-amplitude, and phasic [Ca2+]i change approximately 2 to 3 min after 10 µM phenylephrine stimulation (Fig. 8, A and C). The calcium transient diminished slowly and displayed an exponential decay with a time constant of 4.5 min (Fig. 8D). In contrast to LacZ cotransfected control cells, in the presence of mTLD, the phasic [Ca2+]i response was initiated immediately after receptor activation. However, the maximum amplitude of the [Ca2+]i response was relative smaller (Fig. 8, B and C), only approximately 58% of control group, although the attenuation of the calcium transient was also shown as exponential decay with a time constant of 4.6 min (Fig. 8E). We also studied the effect of mTLD on intracellular calcium response to angiotensin-II type 1 receptor (AT1R) and 1-AR activation. Quantification of [Ca2+]i demonstrated that in response to 1-AR activation, intracellular calcium increased slowly, and progressively (Supplemental Data, Fig A). Intracellular calcium in response to AT1R activation occurred immediately after receptor activation (Supplemental Data, Fig B). In both experiments, calcium response was not affected by mTLD. |
Discussion |
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; Fraser et al., 2000; Cong et al., 2001). The interactions of GPCRs with various cellular proteins are likely to mediate or regulate the intracellular signaling of receptor, providing explanation for the distinct functions by close-related subtypes within the same family.
However, there are few reports about coupling of 1A-AR with non-G-proteins. In this study, aa 867 to 986 of mTLD, which is located in the CUB5 domain of mTLD (Takahara et al., 1994), was identified as an 1A-AR-interacting protein. We confirmed the interaction of full-length mTLD with 1A-AR in HEK293 cells and showed that the presence of mTLD alters the localization, agonist-induced internalization, and calcium signaling of 1A-AR without affecting its pharmacological properties and intracellular signaling function.
In this study, the ability of the CUB5 domain to bind to two other 1-AR subtypes was also investigated. Results indicate that the CUB5 domain specifically interacts with the C tail of 1A-AR but not that of 1B- and 1D-AR. This may arise from the poor homology in this region (less than 10%) among the three subtypes (Weinberg et al., 1994). Our results also indicate that a discrete sequence in the cytoplasmic tail of 1A-AR, as demonstrated by the tight binding activity of aa 322 to 359 and halved binding ability of aa 399 to 467, interacted with the CUB5 domain.
So far, the function of the CUB domain remains poorly understood. Some investigators have proposed that CUB domains may be involved in protein-protein interactions (Bond and Beynon, 1995). Recent studies have shed some light on this field; for instance, the CUB1 domain of mTLD was critical for secretion, CUB2 domain was essential for the enzyme activity of the protein (Hartigan et al., 2003), and in the present studies, CUB5 domain was identified to bind to 1A-AR.
Our results demonstrated that 1A-AR not only interacted with the CUB5 domain directly but also associated with full-length mTLD. mTLD, the longer splice variant of BMP-1 (Takahara et al., 1994; Kessler et al., 1996), and BMP-1 share 702 identical amino acids, but mTLD has an additional EGF-like domain and two CUB domains, including the CUB5 domain. To date, most studies on mTLD or BMP-1 have concentrated on identifying their substrates. mTLD (or BMP-1) is able to cleave several precursors of extracellular matrix proteins including procollagens, biglycan, prolysyl oxidase and the chain of laminin-5 (Amano et al., 2000; Scott et al., 2000; Sasaki et al., 2001; Colombo et al., 2003). Little has been known about intracellular function of either mTLD or BMP-1. Only one study showed that intracellular BMP-1 is first synthesized as an inactive pro-BMP-1 and stored in the endoplasmic reticulum and early Golgi compartment (Leighton and Kadler, 2003). Because of the high homology with BMP-1, we hypothesized that mTLD may be processed in a manner similar to that of BMP-1. It is tempting to speculate that mTLD may be synthesized as an inactive form and stored in the endoplasmic reticulum and early Golgi compartments before secretion. Therefore, the intracellular abundance of mTLD made it possible to interact with 1A-AR inside the cells. According to a recent study (Morris et al., 2004), 1A-AR internalizes constitutively, and the surface receptor density is maintained by receptor recycling. This led to speculation that an internal pool of 1A-ARs recycles to allow for continuous agonist-induced signaling. In the same study, this constitutive trafficking was shown to be partially blocked by the Golgi-disturbing agent monensin, implying that the Golgi system is also a potential trafficking system. However, whether mTLD is involved in 1A-AR trafficking through the Golgi system remains unclear.
Using laser-scanning confocal microscopy and whole-cell ELISA, we showed that 1A-AR localized on the cell surface and intracellular compartment in HEK293 cells, an observation consistent with earlier studies (Hirasawa et al., 1997; Chalothorn et al., 2002). In mTLD and 1A-AR cotransfected HEK293 cells, the interaction between 1A-AR and mTLD induced the internalization and accumulation of receptors. Moreover, mTLD influenced the time course of 1A-AR inter-nalization after agonist exposure. In the absence of mTLD, there was a rapid agonist-induced internalization of cell surface receptor, a finding in agreement with previous studies in HEK293 cells (Chalothorn et al., 2002). In the presence of mTLD, the time course of 1A-AR internalization in response to agonist was different. The number of cell surface receptors initially increased during the first 5 min of agonist stimulation and then decreased by 58% by 60 min. Therefore, the results were consistent with the internalization pattern of 1A-AR in rat-1 fibroblast cells (Price et al., 2002). Price et al. (2002) observed that although the number of cell-surface wild-type 1-AR showed little increase in the early stages of agonist stimulation, the number of carboxyl-terminally truncated mutant 1-AR T348 increased significantly during the same period. Given that fibroblasts express mTLD naturally, whereas there was no mTLD expression at the mRNA level in HEK293 cells (data not shown), and considering our results that amino acid residues 322 to 359 are the primary binding region to CUB5 domain of mTLD, conflicting results of 1A-AR internalization from different groups are expected. The naturally expressed mTLD participates in the internalization of 1A-AR in fibroblasts, similar to what we observed in mTLD-transfected HEK293 cells. Partial deletion of the receptor's cytoplasmic tail would expose the primary binding region and tighten the interaction of mTLD and 1A-AR, thereby enhancing the influence of mTLD on the localization of 1A-AR.
On the other hand, phosphorylation, desensitization, internalization, and down-regulation of the receptor in response to agonist exposure would occur within seconds to hours after stimulation. Whereas arrestins have been implicated in mediating the internalization of a variety of GPCRs, the effects of -arrestin on 1A-AR are not clear. gC1q-R is a cellular protein that interacts with 1B- and 1D-AR, and regulates the cellular localization and expression of 1B-AR. Thus, it is interesting that mTLD expression alters the subcellular localization and internalization of 1A-AR as shown in the present study.
Our results suggest that mTLD did not alter the density or affinity of 1A-AR, although it altered the subcellular localization of the receptor. Thus, receptor internalization does not alter the conformation of 1A-AR, or at least does not alter the conformation of the ligand-binding region. It has been reported that 1D-ARs mainly localize intracellularly in a perinuclear orientation (Chalothorn et al., 2002) and that this fraction of the receptors can still respond well to agonist stimulation (McCune et al., 2000; Waldrop et al., 2002). Therefore, it is possible that internalized 1A-AR is still localized in certain intracellular membrane structures and preserves the receptor structure and ligand binding properties.
We observed an enhanced intracellular calcium response to 1A-AR activation in the presence of mTLD, although the time course of calcium transient decay was not altered. In addition, the effect of mTLD on intracellular calcium response to 1A-AR activation was not observed on two other GPCRs, AT1R and 1-AR. Although the physiological mechanism of calcium signaling flux remains to be investigated, it seems clear that mTLD plays an important role in the early response of 1A-AR to agonist by ensuring a rapid reaction after receptor activation.
In conclusion, we have demonstrated that mTLD is a novel and specific intracellular partner of 1A-AR, and the interaction of these two proteins influences the localization, internalization, and calcium signaling function of 1A-AR. The precise mechanism of mTLD's effects on 1A-AR is an important target for further investigation.
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Acknowledgements |
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1-AR cDNAs. We also thank Prof. K. P. Minneman and Dr. Xiaojun Du (Baker Heart Research Institute, Melbourne, Australia) for review and advice on this article. |
Footnotes |
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ABBREVIATIONS: AR, adrenergic receptor; GPCR, G-protein-coupled receptor; mTLD, mammalian Tolloid; FRET, fluorescence resonance energy transfer; GST, glutathione S-transferase; PCR, polymerase chain reaction; HA, hemagglutinin; aa, amino acids; AT1R, angiotensin II type 1 receptor; EGFP, enhanced green fluorescent protein; HEK, human embryonic kidney; TRITC, tetramethylrhodamine B isothiocyanate; PBS, phosphate-buffered saline; BE2254, 2-[[2-(4-hydroxy-3-iodo-phenyl)ethylamino]methyl]tetralin-1-one; ELISA, enzyme-linked immunosorbent assay.
The online version of this article (available at http://molpharm.aspetjournals.org) contains supplemental material. 
Address correspondence to: Youyi Zhang, Institute of Vascular Medicine, Peking University Third Hospital, No.49 Huayuan North Road, Haidian District, Beijing, P.R. China 100083. E-mail: zhangyy{at}bjmu.edu.cn
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