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The Journal of Neuroscience, November 15, 2001, 21(22):9027-9035

Cloning, Expression, and Regulation of a Glucocorticoid-Induced Receptor in Rat Brain: Effect of Repetitive Amphetamine

Danzhao Wang1, James P. Herman2, Laurel M. Pritchard2, 3, Rebecca H. Spitzer2, 3, Rebecca L. Ahlbrand2, 3, Gerald L. Kramer4, Frederick Petty4, Floyd R. Sallee1, 2, and Neil M. Richtand2, 3

1 Pharmacology Research Center, Children's Hospital Medical Center, Cincinnati, Ohio 45229, 2 Department of Psychiatry, University of Cincinnati College of Medicine, Cincinnati, Ohio 45267, 3 Cincinnati Veterans Affairs Medical Center, Psychiatry Service (V116A), Cincinnati, Ohio 45220, and 4 Veterans Affairs Medical Center and University of Texas Southwestern Medical Center, Dallas, Texas 75216


    ABSTRACT
TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

Behavioral sensitization to psychostimulants involves neuroadaptation of stress-responsive systems. We have identified and sequenced a glucocorticoid-induced receptor (GIR) cDNA from rat prefrontal cortex. The full-length GIR cDNA encodes a 422 amino acid protein belonging to G-protein-coupled receptor superfamily. Although the ligand for GIR is still unknown, the dendrogram construction indicates that GIR may belong to peptide receptor subfamily (e.g., substance P receptor), with more distant relationship to subfamilies of glycoprotein hormone receptors (e.g., thyrotropin receptor) and biogenic amine receptors (e.g., dopamine receptor). GIR shares 31-34% amino acid identity to the tachykinin receptors (substance P receptor, neurokinin A receptor, and neurokinin B receptor). GIR mRNA is expressed preferentially in brain, and its neuronal expression is relegated to limbic brain regions, particularly in forebrain. GIR transcript levels are increased significantly and persistently in prefrontal cortex for 7 d after discontinuation of chronic amphetamine exposure. The induction of GIR expression by amphetamine is associated with augmented behavioral activation. These findings suggest that modulation of GIR expression may be involved in behavioral sensitization, and GIR may play a role at the interface between stress and neuroadaptation to psychostimulants.

Key words: GIR; seven-transmembrane spanning receptor; mRNA; prefrontal cortex; chronic amphetamine administration; behavioral sensitization


    INTRODUCTION
TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

Behavioral sensitization is a progressive and enduring enhancement of certain behaviors after repetitive stress or stimulant drug administration. It is a useful, well studied model of behavioral plasticity (Antelman et al., 1980; Robinson and Becker, 1986; Kalivas and Duffy, 1989). After repeated, intermittent treatment with stress or stimulant drugs, sensitized behaviors may occur more intensely with a shorter latency or at a lower dose than before behavioral sensitization (Antelman et al., 1980; Segal et al., 1980). The ventral tegmental area, prefrontal cortex, and amygdala seem to mediate the initial development of sensitization to neural substrates, whereas the nucleus accumbens and more distal structures may be involved in its expression (Kalivas and Stewart, 1991; Pierce and Kalivas, 1997; Wolf, 1998). Sensitization is a long-lasting behavioral change accompanied by neuroadaptation (White and Kalivas, 1998; Nestler, 2000), a consequence of new protein synthesis depending on sustained alteration of gene expression (Karler et al., 1993; Sorg and Ulibarri, 1995; Nestler, 2000). For example, Delta FosB accumulates in the nucleus accumbens long after chronic exposure to drugs of abuse including amphetamine, cocaine, and opiates (Hope et al., 1994; Kelz et al., 1999; Kelz and Nestler, 2000), and NAC-1 mRNA expression remains elevated in the nucleus accumbens for 3 weeks after acute and repeated cocaine administration (Cha et al., 1997). These examples of neuroadaptation are relevant to the human addictive process, in which learned drug-seeking and other behaviors persist long after bouts of drug use are extinguished (Vanderschuren and Kalivas, 2000).

Mechanisms of cross-sensitization between stress and psychostimulants remain elusive, but the activation of the hypothalamic-pituitary-adrenal axis in response to stress may facilitate the development of sensitization and enhance the vulnerability to drug addiction (Koob, 1999). Substance P appears to be a pivotal neurotransmitter implicated in both stress and drug dependence models (Kramer et al., 1998; Murtra et al., 2000). The glucocorticoid-induced receptor (GIR) was originally identified as a stress-response element from a murine thymoma cDNA library treated with glucocorticoid and forskolin (Harrigan et al., 1991). GIR mRNA was further localized to limbic forebrain regions, dorsal and ventral striatum, and hypothalamic nuclei within the mouse CNS (Pesini et al., 1998). Recently, the gene structure of human GIR was described (De Moerlooze et al., 2000; Parker et al., 2000). Although it is known that GIR expression is restricted to brain and thymus and it can be induced by dexamethasone and forskolin, the ligands of this membrane receptor and its functions remain unknown (Harrigan et al., 1989, 1991; Parker et al., 2000).

Given the importance of stress to models of stimulant sensitization, we evaluated this potential stress-responsive GIR gene in neuroadaptation. To explore the functions of GIR in the experimental animal models, we have cloned rat GIR cDNA, characterized its expression and regional localization in brain, and provided the first evidence about its potential role in the long-term maintenance of neuroadaptation at the genetic transcriptional level.


    MATERIALS AND METHODS
TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

Animals. Male adult Sprague Dawley rats (200-250 gm; Harlan Sprague Dawley Laboratories, Indianapolis, IN) were housed for a minimum of 2 weeks in a vivarium before use. Animals were killed by decapitation, and the brains were quickly removed and placed on ice for dissection. Dissection was performed using a coronal rodent brain matrix as described (Segal and Kuczenski, 1974). The most anterior brain region was used for assays of prefrontal cortex after removing the olfactory bulb. After dissection, brain regions were frozen in liquid nitrogen and stored at -80°C before use.

Drugs. D-amphetamine (D-AMPH) (Research Biochemicals, Natick, MA) was dissolved in 0.9% saline. Drug concentrations were calculated as the free base. All injections were subcutaneous in a final volume of 1 ml/kg body weight.

RNA preparation and reverse transcription. Total RNA was isolated from rat prefrontal cortex by single-step guanidine thiocyanate-phenol extraction using the TRI REAGENT (Molecular Research Center, Cincinnati, OH) following the manufacturer's instruction. The purified RNA was used for the rat GIR cDNA cloning, amplification of both 5' and 3' cDNA ends. The concentrations of RNA samples were determined by spectrophotometric measurements at 260 and 280 nm. First-strand cDNA was synthesized from total RNA using a random hexamer primer (Promega, Madison, WI) following the manufacturer's instruction.

PCR. A 166 bp rat cDNA fragment was isolated from medial prefrontal cortex by differential display (N. Richtand, unpublished data). Using the BLASTN program on National Center for Biotechnology Information (NCBI) web server, we found that this fragment shared 81% identity to the mouse GIR (Harrigan et al., 1991). Then we designed two oligonucleotides (primer A and primer B) within the 166 bp stretch and one oligonucleotide (MGIR1) in the transmembrane domain I of mouse GIR outside the 166 bp rat-mouse matched region. The oligonucleotides were: primer A (5'-GCATAGACAGAGCCAAGGCCA-3', 1985-2005 bp, GenBank accession number AY029071), primer B (5'-AGCAGAG-GCTGGTTCAGTCA-3', 1780-1799 bp, GenBank accession number AY029071), and MGIR1 (5'-CTCTTCGGTAATGTCCTGGTC-3', 537-557 bp, GenBank accession number M80481). Amplification was conducted with MGIR1 and primer A in a thermal cycler for 30 cycles of 94°C for 30 sec, 50°C for 30 sec, and 68°C for 2 min using Platinum Taq polymerase (Life Technologies, Bethesda, MD). One-third of the RT-PCR product was subjected to Southern blot analysis using the nested rat-specific primer B as probe. The blotted membrane was washed in 2× SSC at 60°C and exposed to Kodak X-Omat AR film at -80°C. The 1.4 kb PCR product, amplified from the prefrontal cortex and identified by Southern blot analysis, was purified by agarose gel electrophoresis and subcloned into the pGEM-T vector (Promega). Positive clones were selected by colony hybridization using primer B as probe again, and insert sequences were determined by DNA sequencing. Sequence analysis demonstrated a 97% sequence identity between the rat and mouse GIR cDNA (Harrigan et al., 1991).

5'- and 3'-rapid amplification of cDNA ends. After obtaining the partial rat GIR cDNA, 5'- and 3'-rapid amplification of cDNA ends (RACE) was performed to determine the putative leading exon and 3' noncoding region of rat GIR using the SMART RACE cDNA amplification kit (Clontech, Palo Alto, CA). Total RNA from rat prefrontal cortex was used as template to synthesize the first-strand cDNAs for 5'- and 3'-ends following the manufacturer's instruction. The first-strand 5'-RACE-ready cDNA was synthesized with 5'-RACE cDNA synthesis primer (5'-CDS) and SMART II oligonucleotide, and the first-strand 3'-RACE-ready cDNA was synthesized with 3'-RACE cDNA synthesis primer (3'-CDS) (Clontech).

The GIR-specific primers were designed from the obtained partial sequence of rat GIR: RGSP1 (5'-TTATAACAAGTGCTGCTCATG-GCAAACCAGTGG-3', 1294-1326 bp, GenBank accession number AY029071), RNGSP1 (5'-CAAAGTAGAGGGCGTTGTTGGTGTGG-3', 1264-1289 bp, GenBank accession number AY029071), RGSP2 (5'-CCTCTTCGCTCTCTGCTGGTTCCCC-3', 1201-1225 bp, GenBank accession number AY029071), and RNGSP2 (5'-CAACTGCTATGTCC-TCCTTCTGTCCAGC-3', 1228-1255 bp, GenBank accession number AY029071). The 5'-RACE amplification was performed in 50 µl of final volume using 2.5 µl of 1/100 diluted 5'-RACE-ready cDNA template, a 2 µM concentration of GIR-specific RGSP1 and Universal Primer Mix, and Advantage 2 Polymerase Mix (Clontech). The 3'-RACE amplification was performed similarly by using 3'-RACE-ready cDNA and GIR-specific RGSP2. PCR amplification was conducted in a thermal cycler for initial five cycles of 94°C for 5 sec and 72°C for 3 min, followed by five cycles of 94°C for 5 sec, 70°C for 10 sec, 72°C for 3 min, and ended with 35 cycles of 94°C for 5 sec, 68°C for 10 sec, and 72°C for 3 min. The RACE amplification products were confirmed by Southern blot analysis with nested GIR-specific oligonucleotides RNGSP1 for 5'-RACE product, and RNGSP2 for 3'-RACE product, respectively. The positive DNA fragments were gel-purified and subcloned into the pGEM-T vector (Promega). Positive clones were selected and subjected to DNA sequencing.

Direct DNA sequencing. Plasmid DNA was prepared using a Qiagen (Valencia, CA) DNA purification kit. Double-stranded DNA was directly sequenced at the University of Cincinnati DNA Core Facility and confirmed by complementary strand sequence.

Tissue distribution. Tissue-specific expression of GIR was investigated by Northern blot analysis. A rat multiple-tissue Northern blot of poly(A)+ RNA from heart, brain, spleen, lung, liver, skeletal muscle, kidney, and testis was purchased from Clontech. The rat GIR-specific cDNA probe (1201-1568 bp, GenBank accession number AY029071) was labeled by random priming with [alpha -32P]dCTP and incubated with the membrane at 68°C for 1 hr in ExpressHyb Solution (Clontech). The blot was washed once with 2× SSC containing 0.05% SDS at room temperature for 40 min and twice with 0.1× SSC containing 0.1% SDS at 50°C for 40 min, followed by exposure to Kodak X-Omat AR film at -80°C. Finally, the blot was stripped and rehybridized with a rat beta -actin cDNA probe (Clontech) as an internal standard.

In situ hybridization. Assessment of GIR mRNA expression was accomplished using probes that recognize the 368 bp stretch of GIR mRNA (complementary to the 1201-1568 bp region of rat GIR mRNA, GenBank accession number AY029071). Labeling reactions included 60 µCi of 35S-UTP (specific activity 1800 Ci/mmol), 1× transcription buffer, 15 mM dithiothreitol, 200 µM GTP, CTP, and ATP, 10 µM UTP, 40 U of placental RNase inhibitor, 1 µg of linearized plasmid DNA, and 20 U of appropriate RNA polymerase (T3 or T7; Roche Molecular Biochemicals, Indianapolis, IN). Reactions were incubated at 37°C for 90 min. The DNA template was then removed by RNase-free DNase I digestion for 15 min at 37°C, and reaction mix was diluted to 100 µl with diethylpyrocarbonate (DEPC)-treated water and ethanol precipitated with 7.5 M ammonium acetate.

Brain sections were fixed for 10 min in 4% buffered paraformaldehyde and rinsed twice in 5 mM DEPC-treated potassium PBS (KPBS), pH 7.5 (5 min), twice in KPBS and 0.2% glycine, and twice in KPBS. Sections were then acetylated by a 10 min treatment with 0.25% acetic anhydride and 0.1 M triethanolamine, pH 8.0, rinsed twice in 0.2× SSC (5 min), and dehydrated in a graded ethanol series. Labeled probes were added to a hybridization buffer containing 50% formamide, 20 mM Tris-HCl, pH 7.5, 1 mM EDTA, 335 mM NaCl, 1× Denhardt's solution, 200 µg/ml salmon sperm DNA, 150 µg/ml yeast transfer RNA, 20 mM dithiothreitol, and 10% dextran sulfate. Probes were denatured for 15 min at 65°C and 50 µl (1 × 106 cpm) of diluted probe applied to each slide. Slides were coverslipped, placed in moistened chambers, and incubated overnight at 55°C. After hybridization, coverslips were removed in 0.2× SSC and rinsed in fresh 0.2× SSC for 10 min. Sections were treated with RNase A (50 µg/ml) for 30 min at 37°C and transferred to fresh 2× SSC, then rinsed three times in 0.2× SSC (10 min per wash) followed by a 1 hr wash in 0.2× SSC at 65°C. Sections were dehydrated in a graded ethanol series, dried at room temperature, and exposed for 14-21 d to Kodak BioMAX film (Eastman Kodak, Rochester, NY). Hybridization controls included (1) sections hybridized with sense-strand probe generated from the same vector construct, and (2) sections preincubated in RNase A (50 µg/ml, 30 min, 37°C) before hybridization with antisense probe. No hybridization signal was observed after either control procedure.

GIR mRNA expression after chronic amphetamine administration. Male Sprague Dawley rats (200-250 gm; Harlan Sprague Dawley Laboratories) received subcutaneous injections of either D-AMPH (2.5 mg/kg) or saline (1 ml/kg) in their home cages once daily for 5 consecutive days (days 1-5). On day 9, 4 d after completion of this pretreatment regimen, all animals were transferred to residential activity chambers (Segal and Kuczenski, 1987; Richtand et al., 2000) and received saline injection (1 ml/kg) on days 10 and 11 to measure conditioned response to injection. On day 12, 7 d after completion of the pretreatment regimen, all rats received D-AMPH (2.5 mg/kg), and locomotor activity was determined by photobeam monitoring for 150 min after injection. Locomotor activity is expressed as crossovers, defined as the number of times the animal crosses into any of four quadrants subdividing the enclosure. All animals were killed by decapitation 4 hr after injection, and total RNA was extracted from prefrontal cortex for determination of GIR mRNA expression. In a separate experiment, rats were injected with either D-AMPH (2.5 mg/kg) or saline (1 ml/kg) for 5 consecutive days and killed by decapitation 7 d after the last injection without the final AMPH challenge. Thus, four groups were generated: SAL-AMPH (saline for 5 d and AMPH at challenge), AMPH-AMPH (AMPH for 5 d and AMPH at challenge), SAL (Saline for 5 d), and AMPH (AMPH for 5 d).

Construction of competitor DNA and quantitative RT-PCR. To construct the mutant template for competitive PCR, a 20 bp GIR sequence (5'-TCGCTCTCTGCTGGTTCCCC-3', 1206-1225 bp, GenBank accession number AY029071) was incorporated into the 5' end of the upstream PCR primer so that a rat GIR cDNA fragment could be amplified by RT-PCR using the chimeric upstream primer (5'-TCGCTCTCTGCTGGTTCCCCTCCCTTCATCTACTGCTGGC-3', 1327-1346 bp, GenBank accession number AY029071) and the downstream primer (5'-CGGCCACAGTGGGTTCCAC-3', 1550-1568 bp, GenBank accession number AY029071). The 262 bp PCR product was subcloned into the pGEM-T vector (Promega). The plasmid DNA was purified (Qiagen), and the competitor insert was verified by DNA sequencing. The insert (262 bp) was released by EcoRI digestion and purified by agarose gel electrophoresis. DNA concentration was determined spectrophotometrically. Serial dilutions of mutant template were prepared.

The amount of GIR mRNA was quantitated by competitive RT-PCR as described previously (Siebert and Larrick, 1992; Raeymaekers, 1999). Briefly, reverse transcription was performed with 2 µg of total RNA using a nonspecific random hexamer primer (Promega). One microliter of first-strand cDNA was mixed with known amounts of linearized competitor DNA ranging from 0.5 to 16 fg and subjected to coamplification with GIR-specific primers (5'-TCGCTCTCTGCTGGTTCCCC-3', 1206-1225 bp and 5'-CGGCCACAGTGGGTTCCAC-3', 1550-1568 bp, GenBank accession number AY029071). PCR was run for 30 cycles of 94°C for 1 min, 60°C for 50 sec, and 72°C for 1.5 min, and the PCR products were electrophoresed on 1.2% agarose gel and stained with ethidium bromide. The amount of rat GIR mRNA was determined by calculating how much of the competitor was required to achieve equal molar amounts of products as described previously (Siebert and Larrick, 1992; Raeymaekers, 1999). To do so, the intensities of ethidium bromide fluorescence bands, corresponding to the PCR products either from the GIR mRNA or from the competitor (101 bp size difference), were measured densitometrically on the computer imaging of the gels. The quantitative determination was achieved by digitization of gels with a BioImage System Quantity One (Bio-Rad, Hercules, CA) and further densitometric evaluation with the ImageQuant 1.2 software. The intensity ratios between the two bands were logarithmically plotted against the known initial input of competitor template, and the amount of GIR mRNA in the total RNA samples was calculated by extrapolating from the intersection of the curves, where the amounts of target and competitor are equal (log10 = 0) to the x-axis, as indicated by Siebert and Larrick (1992). Control PCR with water or RNA template without reverse transcription gave no amplification product (data not shown).

Statistical analysis. Group data are expressed as mean ± SEM. Statistical analysis was performed by unpaired Student's t test. Differences were considered significant at p < 0.05.


    RESULTS
TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

Identification and characterization of rat GIR cDNA

We have cloned and characterized the full-length GIR cDNA from rat prefrontal cortex by RT-PCR, 5'-RACE, and 3'-RACE. Complete sequencing of the cDNA reveals a 1266 bp open reading frame flanked by a 307 bp 5'-untranslated region and a 2100 bp 3'-untranslated region (GenBank accession number AY029071). A polyadenylation signal is present at position 3615, 16 nucleotides upstream of the poly(A) tail. A potential translation initiation site (ATG) is assigned to the methionine codon at nucleotide positions 308-310 because it matches the vertebrate consensus sequences at +4 position and is predicted to initiate translation of GIR, although it shows a suboptimal sequence at the -3 position (Kozak, 1991).

Amino acid sequence and its comparison with other receptors

Based on amino acid sequence derived from the rat GIR cDNA, this gene encodes a protein of 422 amino acids with a relative molecular mass of 48 kDa. The hydrophobicity plot of the protein sequence reveals the presence of seven distributed hydrophobic regions throughout the polypeptide, indicating that GIR belongs to the G-protein-coupled receptor superfamily (Fig. 1). The seven putative transmembrane alpha -helices of GIR consist of a continuous stretch of 17-23 uncharged amino acid residues, except that transmembrane domains II, III, and IV contain Asp116, His155, Asp167, and His203, respectively (Fig. 2A). Both Figures 1 and 2A show the hydrophobic N-terminal region with the presence of a potential signal sequence (17 residue in length) and potential signal peptidase cleavage sites (von Heijne, 1986) located at Val15 and Ala17.



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  		Figure 1.   Hydropathy analysis. Plot of hydrophobicity and hydrophilicity of the rat GIR protein. Eight hydrophobic domains, including a putative signal sequence (S) and seven transmembrane spans (I-VII) are predicted.



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  		Figure 2.   Amino acid sequence of rat GIR and its comparison with other receptors. A, The amino acid sequences of rat GIR, mouse GIR, human GIR, rat substance P receptor (NK1R), rat neurokinin B receptor (NK3R), and rat neurokinin A receptor (NK2R) are aligned for best homology. Transmembrane domains (TM) of the rat GIR are predicted and labeled. Signal peptide is predicted and boxed. black-triangle indicates potential glycosylation sites,  indicates potential protein kinase C phosphorylation sites, and open circle  indicates potential protein kinase A phosphorylation sites. black-square indicates Cys residues, * indicates Asp residues, and and  indicates His residues. B, Relatedness of GIR to other members of the seven transmembrane receptor family. A dendrogram was constructed by Pileup (GCG program) of the amino acid sequences representing the cloned members of the seven transmembrane family receptors (TSHR, thyrotropin receptor; LHR, lutropin receptor; NY4R, neuropeptide Y4 receptor; NY1R, neuropeptide Y1 receptor; GIR, glucocorticoid-induced receptor; NK1R, substance P receptor; NK3R, neurokinin B receptor; NK2R, neurokinin A receptor; OPRK, Kapp-type opioid receptor; D3R, dopamine D3 receptor; D2R, dopamine D2 receptor; D5R, dopamine D5 receptor; D1R, dopamine D1 receptor; beta 2AR, adrenergic beta 2 receptor; beta 1AR, adrenergic beta 1 receptor; STE2, yeast alpha  factor receptor).

The primary amino acid sequence of rat GIR was blasted in the GenBank database, and revealed a significant similarity to other G-protein-coupled receptors (Fig. 2A). Overall, the rat GIR shares the highest sequence identities with mouse (97%) and human GIR (88%) and limited but close identities with rat substance P receptor (NK-1R, 33.7%), neurokinin A receptor (NK-2R, 31.3%), and neurokinin B receptor (NK-3R, 34.3%). The rat GIR shows sequence identities to the transmembrane domains I (50%), II (38%), III (27%), IV (33%), V (36%), VI (43%), and VII (70%) of substance P receptor, with an overall identity of 42.4% in the transmembrane domain regions. It also shows significant sequence identities to the first (33%), second (53%), and third intracellular loops (31%), with more limited sequence identities to the N terminus (22%), first (25%), second (27%), and third extracellular loops (8%) as well as the C terminus (20%) of substance P receptor. Figure 2A shows the alignment of these receptors illustrating several conserved regions in their amino acid sequences. The rat GIR has several structural characteristics common to the members of the G-protein-coupled receptor superfamily. Four potential N-linked glycosylation sites are identified as Asn38, Asn45, Asn66, and Asn133 according to the consensus sequence of Asn-X-Ser/Thr. Three of them are located in the N terminus, and one is in the first extracellular loop. Several consensus sites for possible phosphorylation by protein kinase C and protein kinase A exist in the third intracellular loop and C terminus, respectively. Several cysteine residues are identified in the intracellular and extracellular loops as well as C terminus, respectively. In comparison with the mouse GIR, the rat GIR has a deletion involving one amino acid residue at position 40 in the N terminus. A dendrogram was constructed using the Wisconsin Package version 10, Genetics Computer Group (GCG, Madison, WI), and the clusters of GIR and tachykinin receptors are closely related as compared with the other members in the G-protein-coupled receptor superfamily (Fig. 2B).



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  		Figure 3.   Expression of GIR in adult rat tissues by Northern blot analysis. Poly(A)+ RNA (2 µg) from various rat tissues was hybridized with probes specific to rat GIR (top panel) and beta -actin (bottom panel) on a nylon membrane. The origin of each RNA is shown at the top, and the molecular mass of standard markers (in kilobases) is shown on the left. GIR expression is detected in brain. No detectable hybridization signal is seen in heart, spleen, lung, liver, skeletal muscle, kidney, and testis. The blot was stripped and rehybridized with a beta -actin probe.

Tissue distribution of rat GIR

The tissue distribution of GIR expression in rats was examined by Northern blot analysis. A major mRNA species was detected in brain by Northern blot analysis using rat GIR cDNA as probe (Fig. 3). The expression was not detected in peripheral tissues, including heart, spleen, lung, liver, skeletal muscle, kidney, and testis (Fig. 3).

Regional localization of GIR mRNA in rat forebrain

In situ hybridization analysis was performed to assess GIR mRNA expression in rat forebrain (Figs. 4, 5, Table 1). Hybridizations revealed high levels of GIR expression in scattered hippocampal neurons (Fig. 4A), the nucleus of the lateral olfactory tract (Fig. 4B), and midline thalamic nuclei (nucleus reuniens of the thalamus, zona incerta) (Fig. 4C). Positive signal was also observed in the dorsolateral septum and tenia tecta. Significant hybridization signal was also observed in all regions of neocortex and in limbic cortical regions, notably including infralimbic, prelimbic, and anterior cingulate regions comprising the rodent prefrontal cortical system (Fig. 4D,E). Significant positive hybridization was also observed in the olfactory bulbs, posterior divisions of the bed nucleus of the stria terminalis, and the ventromedial and ventrobasal complexes of the thalamus. Low levels of GIR mRNA could be detected in neuroendocrine regulatory regions of the hypothalamus, including the medial preoptic area, paraventricular nucleus, supraoptic nucleus, and suprachiasmatic nucleus. Low but definitely detectable levels of GIR mRNA were observed in the nucleus accumbens shell (Fig. 5). In no case was positive hybridization observed in sections hybridized with sense-strand probes or sections pretreated with RNaseA.



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  		Figure 4.   Expression of GIR mRNA in the forebrain of the rat (A-F ). A, GIR mRNA is expressed in scattered neurons throughout the hippocampal formation. B, The highest levels of GIR mRNA are detected in the nucleus of the lateral nucleus of the olfactory tract (NOT). C, Signal is also observed in several diencephalic nuclei, including the anteromedial thalamic nucleus and nucleus reuniens. D, Dense GIR mRNA expression is observed in scattered cells of the cerebral cortex, including the medial prefrontal region. E, High-power photomicrograph of prefrontal cortex GIR hybridization, illustrating confinement of grains to neuronal nuclei (arrows). F, Localization of GIR mRNA in caudate putamen; weak labeling is observed in widely scattered cells throughout the structure. Scale bars: A, B, D, F, 100 µm; C, 200 µm; E, 25 µm.



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  		Figure 5.   Expression of GIR mRNA in caudate nucleus and nucleus accumbens of mouse (A) and rat (B). The same probe was used for panels A and B. A, Note extensive GIR mRNA in the caudate putamen (Caudate) and nucleus accumbens (NAcc) of the mouse. B, Weak, but positive hybridization signal is observed in the shell of the nucleus accumbens (NAcc). No signal is observed in the caudate putamen (Caudate) at this magnification.


                              
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  		Table 1.   Distribution of GIR mRNA in rat telencephalon and diencephalon

Notably, GIR mRNA expression in the caudate putamen was confined to widely scattered neurons (Fig. 4F), and expression in nucleus accumbens was quite weak and limited to the shell region. This distribution stands in marked contrast to anatomical localization of GIR mRNA in mouse, which showed rich expression throughout the striatum and nucleus accumbens using the same rat cRNA probe (Fig. 5, compare A,B).

Response of rat GIR expression to chronic amphetamine administration

Because of longstanding neurochemical changes in prefrontal cortex after repetitive AMPH (Hamamura and Fibiger, 1993) and abundant GIR expression in this brain region (Fig. 4D,E), we determined the effect of amphetamine on GIR expression in this brain region after chronic amphetamine administration. The expression levels of GIR mRNA in rat prefrontal cortex after behavioral sensitization to amphetamine were quantitatively determined by competitive RT-PCR. The representative competitive PCR image is shown in Figure 6A. The GIR mRNA levels were calculated from the linear regression plot of the ratio plotted logarthmically against the initial input of competitor DNA, as shown in Figure 6B. In the experiment with amphetamine administration for 5 d followed by a challenge injection 7 d after drug ceased, the GIR mRNA levels in prefrontal cortex of AMPH-AMPH rats were significantly increased by 1.31-fold compared with SAL-AMPH rats (2.97 ± 0.26 vs 2.27 ± 0.22 fg/100 ng total RNA; n = 6; p < 0.05) (Fig. 6B). Animal behavior was also determined following this amphetamine treatment regimen. In agreement with earlier studies (Segal and Kuczenski, 1994), amphetamine pretreatment resulted in robust behavioral sensitization under these conditions, as evidenced by the significant decrease in locomotion of AMPH-AMPH rats at 12-60 min after injection during the focused stereotypy phase of AMPH response (50.20 ± 12.63 vs 286.00 ± 27.57 crossovers/12-60 min; n = 6; p < 0.0001) and increased locomotion at 60-150 min during the post-stereotypy locomotion phase of AMPH response (496.67 ± 70.28 vs 312.25 ± 29.17 crossovers/60-150 min; n = 6; P < 0.05) (Fig. 6C).



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  		Figure 6.   Effects of amphetamine on rat GIR expression in prefrontal cortex quantitatively determined by competitive PCR analysis and on locomotion activities measured by cumulative numbers of crossovers. A, Representative competitive PCR image. B, GIR mRNA levels calculated from linear regression plot of the ratio plotted logarithmically against initial amount of input competitor DNA. Values are expressed as mean ± SEM (n = 6). SEs are represented by bars.  denotes SAL-AMPH rats. black-square denotes AMPH-AMPH rats. C, Cumulative numbers of crossovers measured during the 12-60 min and the 60-150 min periods after challenge injection. Values are expressed as mean ± SEM (n = 6). SEs are represented by bars.  denotes SAL-AMPH rats. black-square denotes AMPH-AMPH rats. D, Bar graph represents the increased levels of GIR mRNA in prefrontal cortex after withdrawal from chronic amphetamine exposure in a separate experiment without amphetamine challenge. Values are expressed as mean ± SEM (n = 6). SEs are represented by bars.  denotes SAL rats.  denotes AMPH rats.

In a separate experiment with chronic amphetamine exposure but no challenge injection, the expression levels of GIR were quantitatively determined by competitive RT-PCR 7 d after an identical 5 d pretreatment regimen with amphetamine or saline. A similar upregulation of GIR mRNA was observed 7 d after amphetamine ceased. The GIR mRNA levels in prefrontal cortex of AMPH rats were significantly increased by 1.70-fold compared with SAL rats (3.65 ± 0.22 vs 2.15 ± 0.33 fg/100 ng total RNA; n = 6; p < 0.05) (Fig. 6D).


    DISCUSSION
TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

We have identified a stress-responsive receptor, GIR, from prefrontal cortex of rat brain. The deduced amino acid sequence suggests that GIR is a member of the G-protein-coupled receptor superfamily and shares the identity to tachykinin receptors (31-34%). GIR is expressed preferentially in the brain and has demonstrated a responsive alteration on gene expression to amphetamine treatment. Moreover, the increased levels of GIR mRNA persist 7 d after withdrawal from chronic amphetamine administration. Regulation of GIR mRNA expression may represent a long-lasting effect at the molecular level in neuroadaptation to psychostimulants.

The structural analysis of rat GIR, a G-protein-coupled receptor, suggests some important clues to its potential pharmacological and physiological functions. The putative protein kinase C site and protein kinase A sites in the third intracellular loop are often called the "G-protein-loop" because of their importance in G-protein coupling (Strader et al., 1994), suggesting that phosphorylation may modulate the functional activity of GIR. The role of putative protein kinase C sites in the C terminus of rat GIR remains to be studied because similar phosphorylation sites in the C terminus of beta -adrenergic receptor have been shown to play a pivotal role in regulating receptor desensitization (Bouvier et al., 1989; Clark et al., 1989). Similar to the beta -adrenergic receptor, a potential disulfide bond linking Cys143 in the first extracellular loop and Cys223 in the second extracellular loop of rat GIR may help to maintain the active conformation of the receptor and is important for ligand receptor interaction (Dohlman et al., 1990). The highly conserved Cys362 in the C terminus of rat GIR may function as a target site for palmitoylation, and the palmityl group may anchor the cytoplasmic tail of the receptor to the plasma membrane to control the structure of this receptor (O'Dowd et al., 1989; Strader et al., 1994).

Rat GIR is an orphan receptor, however, it shows close sequence identity to the rat substance P receptor (33.7%) with divergent similarity in different regions. For example, the most conserved portions of these two receptors are the transmembrane domain I (50%), the second intracellular loop (53%), and the transmembrane domain VII (70%), and the least conserved is the third extracellular loop (8%). Although the endogenous ligand for GIR is unknown, the primary sequence identity between GIR and substance P receptor in the transmembrane segments (42.4% overall) suggests that GIR may be a member of the same subfamily as substance P receptor (Strader et al., 1994). Construction of a dendrogram supports the notion that GIR may belong to the peptide receptor subfamily (e.g., substance P receptor), with more distant relationship to the subfamilies of glycoprotein hormone receptors (e.g., thyrotropin receptor) and biogenic amine receptors (e.g., dopamine receptor) (Strader et al., 1994). Notably there is a conserved Asp residue (Asp167 in rat GIR) on the edge of the transmembrane domain III of GIR, which is seen as well in substance P, neurokinin B, and neurokinin A receptors. Because the highly conserved Asp residue in the transmembrane domain III has only been reported for the biogenic amine receptors with a primary function of interacting with the biogenic amines (Strader et al., 1987, 1994), the potential role of this region in determining ligand specificity in the peptide receptor subfamily should be investigated. The Asp116 residue, found in the transmembrane domain II of rat GIR, is conserved in G-protein-coupled receptors and appears to be involved in transduction of the agonist-binding signals to stimulate an interaction with the appropriate G-protein (Strader et al., 1994).

The dominant expression of GIR occurs in brain, which agrees with findings for both mouse and human GIR mRNA expression (Harrigan et al., 1991; Parker et al., 2000). Within brain, GIR mRNA is expressed neuronally, as demonstrated by in situ hybridization with intense staining localized to nucleus of the lateral olfactory tract, hippocampus, neocortex, and limbic cortical regions. Of particular interest, very high levels of GIR mRNA were observed in the nucleus of the lateral olfactory tract, responsible for relay of olfactory information to piriform cortex and amygdala. High levels of GIR were also observed in the midline thalamic nuclei and in dorsolateral septum, which have reciprocal connections with limbic cortex and hippocampus, and in the hippocampus itself, a critical component of learning and memory integration (Jakab and Leranth, 1995; Price, 1995; Shipley et al., 1995). Positive hybridization signal was also observed in limbic cortical structures, including the infralimbic, prelimbic, and anterior cingulate cortices, as well as the limbic (shell) region of the nucleus accumbens. Together, these data suggest a prominent role for GIR in limbic circuits regulating memory, stress, and reward.

Expression of GIR mRNA is also observed in forebrain effector systems mediating anxiety and neuroendocrine control. The bed nucleus of the stria terminalis is involved in coordinating behavioral and neuroendocrine responses to fearful stimuli (Henke, 1984; Casada and Dafny, 1991; Gray et al., 1993). The preoptic area, arcuate nucleus, paraventricular nucleus, and supraoptic nucleus are involved in neuroendocrine and autonomic nervous system integration (Swanson, 1987). As such, GIR circuitry may modulate behavioral and physiological interpretation of environmental information at the level of both associative and effector systems.

The expression of GIR mRNA is marked by a pronounced species difference between mouse and rat (Pesini et al., 1998). Most notable is the differential distribution of GIR in striatum and cortex. In mouse, GIR is highly expressed in targets of the nigrostriatal and mesolimbic dopamine system, including the neostriatum, nucleus accumbens, and olfactory tubercle. This finding suggests that in mouse, GIR may play a role in modulation of dopaminergic neurotransmission. The lack of GIR transcripts in the nucleus of the lateral olfactory tract, ventral thalamus, and cortex suggests a less pronounced involvement of this receptor in aspects of limbic integration in murine species. However, GIR is highly expressed in hippocampus of both species, allowing for a similar role of this receptor in modulating hippocampal function.

The persistent upregulation of GIR mRNA found in amphetamine-sensitized rat brain long after drug discontinuation is of importance because the regulation of gene expression is believed to be the molecular basis for stable neuroadaptation to chronic drug exposure (Nestler, 2000). In contrast to transient gene alterations, the persistent gene alterations are responsible for maintenance and expression of behavioral sensitization (White and Kalivas, 1998). Although extensive efforts have been made to search for candidate genes for stable neuroadaptation, only Delta FosB and NAC-1 have been reported to be persistently altered in nucleus accumbens after drug discontinuation (Cha et al., 1997; Kelz et al., 1999; Kelz and Nestler, 2000). In a similar manner, GIR mRNA is also increased after chronic exposure to amphetamine. Importantly, once induced, this increased GIR mRNA expression persists in brain for at least 7 d after amphetamine withdrawal. The sustained GIR mRNA upregulation is correlated with behavioral sensitization, as observed by increased locomotor activity and augmented stereotyped motion. Because prefrontal cortex is known to be critical in the induction of behavioral sensitization leading to increased locomotor activity (Wolf et al., 1995; Kalivas and Nakamura, 1999), a persistent modulation of GIR expression may be involved in the stable neuroadaptation to drugs of abuse.

One possible mechanism for amphetamine-induced GIR mRNA upregulation could be the transcriptional regulation involving nuclear transcription factors or steroid hormones. Behavioral sensitization to amphetamine is accompanied by an enhanced CREB phosphorylation, alterations in the expression of transcription factors, particularly Delta FosB, and the activation of the hypothalamic-pituitary-adrenal axis (Hope et al., 1994; Turgeon et al., 1997; Koob, 1999; Nestler, 2000). Preliminary observations in rat amygdalar neuronal cells have shown an upregulation of GIR mRNA induced by dexamethasone or forskolin ( D. Wang and F. Sallee, unpublished results), in agreement with similar observations in mouse T lymphocytes (Harrigan et al., 1989). These findings support the hypothesis that glucocorticoid and cAMP are involved in the regulation of GIR gene expression. Further promoter analysis of the GIR gene expression may explain how the GIR gene could be regulated by cAMP, Delta FosB-containing AP-1 complex, or steroid hormones.

In separate experiments, the amphetamine withdrawal group (AMPH) (Fig. 6D) and amphetamine challenge group (AMPH---AMPH) (Fig. 6B) had qualitatively similar increases in GIR mRNA expression that were not quantitatively equivalent (3.65 ± 0.22 vs 2.97 ± 0.26 fg/100 ng total RNA, respectively). Interanimal variability in male Sprague Dawley rats in response to repetitive AMPH has been previously described (Segal et al., 1987) and may account for the observed differences. Alternatively, the observation that the amphetamine withdrawal group (AMPH) and amphetamine challenge group (AMPH-AMPH) were not equivalent in GIR mRNA upregulation might reflect differential regulation of transcription factors in response to acute versus chronic psychostimulant administration. This phenomenon has been previously reported, whereby chronic cocaine exposure resulted in desensitization of immediate early genes induced by a subsequent cocaine challenge (Hope et al., 1992, 1998; Graybiel et al., 1995; Nye et al., 1995). This observation suggests that there might be specific transcription factors controlling GIR gene expression in response to acute versus chronic amphetamine administration. Further investigation needs to be performed to better elicit the molecular mechanisms surrounding the potential roles of GIR in adaptation to psychostimulants.


    FOOTNOTES

Received April 4, 2001; revised Aug. 10, 2001; accepted Aug. 31, 2001.

This work was supported by Department of Veterans Affairs VISN 10 Research Initiative Program Grant, a National Alliance for Research on Schizophrenia and Depression Young Investigator Award, and National Institute of Mental Health Grant 49698. We thank Dr. Lei Yu for critical reading of this manuscript, Dr. John W. Kasckow for generous gift of immortalized rat amygdalar neuronal cells, and Mr. Chad Price for assistance in the GCG software.

Correspondence should be addressed to Dr. Floyd R. Sallee, Pharmacology Research Center, Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229. E-mail: salleefr{at}emailuc.edu.


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DISCUSSION
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