- Open Access
Involvement of the N-methyl-d-aspartate receptor GluN2D subunit in phencyclidine-induced motor impairment, gene expression, and increased Fos immunoreactivity
Molecular Brain volume 6, Article number: 56 (2013)
Noncompetitive N-methyl-d-aspartate (NMDA) receptor antagonists evoke a behavioral and neurobiological syndrome in experimental animals. We previously reported that phencyclidine (PCP), an NMDA receptor antagonist, increased locomotor activity in wildtype (WT) mice but not GluN2D subunit knockout mice. Thus, the aim of the present study was to determine whether the GluN2D subunit is involved in PCP-induced motor impairment.
PCP or UBP141 (a GluN2D antagonist) induced potent motor impairment in WT mice but not GluN2D KO mice. By contrast, CIQ, a GluN2C/2D potentiator, induced severe motor impairment in GluN2D KO mice but not WT mice, suggesting that the GluN2D subunit plays an essential role in the effects of PCP and UBP141, and an appropriate balance between GluN2C and GluN2D subunits might be needed for appropriate motor performance. The level of the GluN2D subunit in the mature mouse brain is very low and restricted. GluN2D subunits exist in brainstem structures, the globus pallidus, thalamus, and subthalamic nucleus. We found that the expression of the c-fos gene increased the most among PCP-dependent differentially expressed genes between WT and GluN2D KO mice, and the number of Fos-positive cells increased after PCP administration in the basal ganglia motor circuit in WT mice but not GluN2D KO mice.
These results suggest that the GluN2D subunit within the motor circuitry is a key subunit for PCP-induced motor impairment, which requires an intricate balance between GluN2C- and GluN2D-mediated excitatory outputs.
The N-methyl-D-aspartate (NMDA) receptor channel is involved in various physiological functions, including learning and memory. NMDA receptors are primarily composed of GluN1, GluN2 (A-D), and GluN3 subunits. The GluN1 subunit is expressed ubiquitously, whereas GluN2 subunit expression is region- and cell-specific. Additionally, the temporal expression of each subunit varies . Among the GluN2 (A-D) subunits, the physiological role of the GluN2D subunit is not fully understood because of its unique properties. In the rodent brain, the GluN2D subunit is expressed during postnatal periods. However, as the animal ages, the levels of GluN2D mRNA and protein decrease. In mature brains, significant levels of GluN2D subunits are mainly restricted to diencephalic, mesencephalic, and brainstem structures, particularly the globus pallidus, thalamus, subthalamic nucleus, and superior colliculus . GluN2D knockout (KO) mice are viable and exhibit no obvious histological abnormalities . However, these KO mice exhibit a reduction of spontaneous locomotor activity in a novel environment and less sensitivity to stress in the elevated plus maze, light–dark box, and forced swim test [2, 3].
Phencyclidine (PCP) has been extensively used as a pharmacological model of schizophrenia because of its ability to evoke the positive and negative symptoms of schizophrenia and characteristic cognitive deficits of this illness observed in humans [4, 5]. However, NMDA receptor antagonists evoke a behavioral syndrome in experimental animals characterized by hyperlocomotion and the disruption of prepulse inhibition of the startle response [6, 7]. Chronic exposure to PCP intensely affects the relative immunoreactivity of the GluN2 subunit in the frontal cortex. Following PCP treatment, GluN2D immunoreactivity and protein expression increase significantly and induce a shift to a predominance of the GluN2D subunit in the frontal cortex . However, the possible role of the GluN2D subunit in PCP-induced changes in gene expression and the brain networks involved in these changes remain unexplored.
We previously reported that the NMDA receptor antagonist PCP significantly increased extracellular levels of dopamine in the striatum and prefrontal cortex in wildtype (WT) mice but not GluN2D KO mice. Furthermore, acute and repeated administration of PCP did not increase locomotor activity in GluN2D KO mice .
In the present study, we performed the rotarod test, gene expression analyses, and Fos immunohistochemistry in WT and GluN2D KO mice to elucidate the role of the GluN2D subunit in PCP-induced behavioral and neurobiological effects. The results indicated that the GluN2D subunit of the NMDA receptor plays an important role in PCP-induced motor impairment and PCP-induced abnormal gene expression. PCP-induced motor impairment was attenuated in GluN2D KO mice by preventing PCP-induced excitation via the GluN2D subunit in the neural circuit that includes the motor loop.
Pharmacological modulation of motor performance using PCP and UBP141
Motor impairment was measured by placing WT and GluN2D KO mice on a fixed-speed rotarod (12 rpm) and monitoring their performance for 300 s, 30 min after saline or PCP administration. Saline injections did not affect motor performances. At a dose of 3 or 5 mg/kg, PCP led to motor impairment in the rotarod test (Figure 1B). PCP-injected GluN2D KO mice performed better than PCP-injected WT mice. Significant differences in motor impairment were observed between WT and GluN2D KO mice, based on Fisher’s exact test (p < 0.05 at both doses; dependence on genotype).
The UBP141 solution (3 mM) was freshly prepared and injected intracisternally under ether anesthesia. Motor impairment was measured by placing WT and GluN2D KO mice on a fixed-speed rotarod (0 rpm and 6 rpm) and monitoring their performance for 300 s, 30 min after UBP141 administration. Motor performance was maintained after vehicle injections. An intracisternal injection of 3 mM UBP141 solution (20 μl) resulted in motor impairment in seven of 10 WT mice at 0 rpm and eight of 9 WT mice at 6 rpm (Figure 1C). In contrast, UBP141 did not cause motor impairment in GluN2D KO mice at 0 rpm (n = 9) and five of eight KO mice at 6 rpm (Figure 1C). The differences in UBP141-induced motor impairment between WT and GluN2D KO mice were significant at 0 rpm and 6 rpm (Fisher’s exact test, p = 0.0031 and 0.049, respectively; dependence on genotype).
The CIQ solution and its vehicle were freshly prepared and administered in WT and GluN2D KO mice. CIQ did not cause hyperlocomotion, but it markedly reduced motor performance in 13 of 15 GluN2D KO mice (Figure 1D). In contrast, CIQ did not cause motor impairment in five of eight WT mice. The difference in CIQ-induced motor impairment between WT and GluN2D KO mice was significant (Fisher’s exact test, p = 0.0026; dependence on genotype).
Altered gene expression in GluN2D KO mice in response to PCP
We explored the alterations in gene expression in GluN2D KO mice that could be responsible for the differential behavioral responses to PCP. We first performed a preliminary cDNA array experiment using mRNA derived from the striata in WT and GluN2D KO mice with or without PCP treatment. Compared with saline-injected WT mice, saline-injected GluN2D KO mice showed increased expression of 247 transcripts (Figure 2A; KOS/WS). An injection of PCP (10 mg/kg, s.c.) in WT mice and KO mice increased the expression of 193 and 46 transcripts, respectively (Figure 2A; WPCP/WS or KOPCP/KOS). The expression of a large number of genes was increased in the saline-injected GluN2D KO and PCP-injected WT mice. Both groups shared 36% and 46% of the increased transcripts, respectively. However, the increased gene expression pattern in PCP-injected GluN2D KO mice (KOPCP/KOS) differed from PCP-injected WT mice (WPCP/WS). Interestingly, 47 and 24 of the transcripts that showed increased expression in PCP-injected WT mice (WPCP/WS) and saline-injected GluN2D KO mice (KOS/WS), respectively, showed an opposite trend in PCP-injected GluN2D KO mice (Figure 2A). Figure 2B illustrates the relationship between the effect of PCP in WT and KO mice. Each control consisted of a WT or KO mouse. Linear regression analysis showed that the data fit a straight line (r = −0.564). The expression ratios of all of the transcripts demonstrated a weak inverse relationship in response to PCP between WT and KO mice. The probes in this cDNA array contain many interesting genes but do not fully cover genes. Therefore, we next used a commercial array (MouseRef-8 BeadChip with greater than 24,000 probes) provided by Illumina.
We utilized WT and GluN2D KO mouse striata to profile the DEGs following PCP administration in WT and GluN2D KO mice. Total RNAs from the striata of WT and GluN2D KO mice obtained 2 h after an injection of saline or PCP (10 mg/kg, s.c.) were analyzed using a microarray-based screen with Illumina MouseRef-8. An Additional file 1: Table S1 shows this in more detail [see Additional file 1: Table S1]. This comparative analysis revealed the differential expression profiles of 51 genes following PCP administration, with 40 genes upregulated more than 1.3-fold and 11 genes downregulated less than 0.7-fold in WT and GluN2D KO mice. The two genotypes were found to share only 18% of the genes in the PCP-induced increase in the expression profile. Correlation analysis revealed that the PCP-induced increase in gene expression in WT and GluN2D KO mice was inversely associated (r = −0.46).
Real-time qRT-PCR analyses
To validate the microarray data, the RNA levels of some of the candidate DEGs were analyzed by qRT-PCR. From the DNA array results using the striata, 23 genes that were upregulated more than 1.3-fold or downregulated less than 0.7-fold in WT and GluN2D KO mice were chosen. The qRT-PCR results (Table 1) confirmed the microarray data for both the upregulation and downregulation of the selected genes. The expression of Hace1, Osbpl8, Smpd4, and Slc17 in the striatum in GluN2D KO mice was significantly increased. Among the 23 genes, 17 were upregulated, and one was downregulated with PCP treatment. Several of these 17 genes in GluN2D KO mice showed significantly altered expression in response to PCP compared with their expression profiles in WT mice.
Similarly, we evaluated total RNA derived from pooled frontal cortices in the qRT-PCR analyses (Table 2). Using the same primer sets that we used for the striatum, 13 genes were found to be upregulated by PCP treatment. As a result, we found four candidate genes from the cDNA array and confirmed their expression using real-time RT-PCR. These four genes are not involved in the MouseRef-8 BeadChip. Furthermore, we found 23 candidate genes from the MouseRef-8 BeadChip with greater than 24,000 probes.
The gene expression data shown in Tables 1 and 2 were uploaded into MetaCore 5.0 software (GeneGo pathway analysis). Graphical representations of the molecular relationships between genes were generated in a network built by the auto expand path algorithm, allowing 50 nodes (Figure 3). The network analysis of the 16 genes in Figure 3 showed that eight genes were directly linked to nuclear factor-κB (NF-κB; Figure 3A). Downstream of NF-κB was indirectly linked to 14-3-3 as one node and then from 14-3-3 spread to EGR4 or DSIPI and Sestrin 1. However, significantly altered processes for KOPCP/KOS were not indicated. Similarly, 12 genes in the frontal cortex (Table 2) generated a network (Figure 3B). This network included TXNIP (an oxidative stress mediator), REDD1 (which promotes neuronal cell death), and GADD45γ (which is involved in the regulation of growth and apoptosis). These analyses indicated that PCP is a stress factor that induces stress responses and is involved in apoptosis in WT mice. Among the PCP-induced changes in gene expressions, Fos was most distinguishable between WT and GluN2D KO mice. Therefore, we chose Fos for the immunohistochemical analysis.
Induction of Fos by PCP administration
Photomicrographs and semiquantitative analyses of Fos expression are shown in Figures 4 and 5. PCP (10 mg/kg, s.c.) markedly increased the density of Fos-positive cells in the motor cortex and cingulate cortex and moderately increased the density of Fos-positive cells in the subthalamic nucleus, and thalamus in WT mice (Figures 4EG and 5EF). However, the Fos ratio was scarcely increased in the striatum (Figure 5). Two-way ANOVA of the Fos data in the motor cortex indicated a significant effect of PCP treatment (effect of PCP, F1,15 = 10.59, p = 0.0053; PCP-genotype interaction, F1,15 = 7.18, p = 0.017). Further, post hoc testing by Scheffe’s test revealed that PCP significantly increased Fos density in the motor cortex of WT mice (p = 0.0006). In the cingulate cortex and subthalamic nucleus, two-way ANOVA indicated a significant effect of PCP treatment (cingulate cortex, F1,16 = 29.17, p = 0.0001; subthalamic nucleus, F1,16 = 11.44, p = 0.0038, respectively. no PCP-genotype interaction). Due to unequal variance, we used Kruskal-Wallis nonparametric test. It indicated that PCP significantly increased Fos density in the cingulate cortex (p = 0.024) and the subthalamic nucleus (p = 0.046) of WT mice. Additionally, two-way ANOVA of Fos-data in the thalamus indicated a significant PCP-genotype interaction (F1,12 = 10.74, p = 0.0066) and followed by Scheffe’s test, a significant increase in GluN2D KO mice treated with saline compared to WT mice (p = 0.0255) (Figure 4G). Two-way ANOVA of Fos-data in the striatum indicated no main effect and no PCP-genotype interaction and followed by Scheffe’s test, a significant increase in GluN2D KO mice treated with saline compared to WT mice (p = 0.0240) (Figure 5G). In the present study, the PCP-induced increase in the number of Fos-positive cells was suppressed to varying degrees in the observed brain areas in GluN2D KO mice.
Induction of c-fos mRNA by UBP141, CIQ, and PCP with dantrolene administration determined by qRT-PCR
The levels of c-fos mRNA were examined by qRT-PCR in the striatum and thalamus in WT and GluN2D KO mice. Intracisternal injection of UBP141 enhanced c-fos expression in the thalamus and striatum in WT mice (F1,11 = 7.102, p = 0.016, and F1,11 = 4.585, p = 0.048, respectively) but not in GluN2D KO mice (Figure 6A). We then used CIQ, a potentiator of NR2C/2D subunits. CIQ markedly enhanced c-fos expression in the thalamus and striatum in both WT and GluN2D KO mice (Figure 6B). In the thalamus and striatum, two-way ANOVA indicated a significant effect of CIQ treatment (F1,19 = 112.59, p < 0.0001, and F1,19 = 197.01, p < 0.0001, respectively).
In the present study, we found substantial genotype-dependent differences in PCP-induced c-fos expression. This difference might have been secondary to PCP’s differential genotypic effects on hyperlocomotion. Therefore, we injected mice with dantrolene before PCP administration to investigate the effect of hyperlocomotion on c-fos expression stimulated by PCP. Dantrolene acts as muscle relaxant and is used for malignant hyperthermia. The therapeutic action of dantrolene appears to be attributable to its ability to bind to an amino-terminal sequence of skeletal ryanodine receptors . Dantrolene completely blocked PCP-induced hyperlocomotion in WT mice (n =3). Dantrolene itself did not increase c-fos expression except in the thalamus in GluN2D KO mice (Figure 6C). Dantrolene did not inhibit PCP-induced c-fos expression in the thalamus or striatum in WT mice or thalamus in GluN2D KO mice (Figure 6C, D). Therefore, the substantial genotype differences in PCP-induced c-fos expression were not secondary to PCP’s differential genotypic effects on hyperlocomotion. In addition, Numeric data of Figure 6(A-D) and these actin data are shown in Additional file 2: Table S2.
The pharmacological activity of acute PCP administration in mice can be broadly classified into three symptoms: cognitive dysfunction, hyperlocomotion, and motor impairment. In the present study, we focused on motor impairment caused by PCP. The main findings were that PCP-induced motor impairment was markedly reduced in GluN2D KO mice compared with WT mice. The PCP-induced enhanced expression of c-fos, one of the most potent PCP-dependent DEGs between the two genotypes, was suppressed in several areas of the motor circuit in GluN2D KO mice. These findings indicate that ablation of the GluN2D subunit blocks the PCP-dependent abnormal neuronal activation in the motor circuit and prevents motor impairment. Thus, GluN2D subunit-containing NMDA receptors appear to play a key role in PCP-induced motor impairment.
PCP-induced motor impairment is attributable to blockade of the GluN2D subunit
Although PCP is a nonselective blocker of GluN2(A-D)-containing NMDA receptors , PCP-induced motor impairment was reduced in GluN2D KO mice, suggesting that systemic PCP administration resulted in motor impairment mainly by blocking the GluN2D subunit. Watanabe et al. reported that the expression of GluN2D subunit mRNA is clearly detectable in the diencephalon and brainstem in the embryonic brain, but GluN2D subunit expression is nearly abolished in the mature rodent brain . In the present study, the striatum had low expression levels of the GluN2D subunit. Interestingly, rather low levels of the GluN2D subunit play an important role in PCP-induced abnormal behaviors.
Ablation of the GluN2D subunit did not produce motor impairment in mature GluN2D KO mice, but change in gene expression remained. In the striatum of GluN2D KO mice, we found increased expression of four genes: Slc17, Hace1, Smpd4, and Osbpl8. Among these genes, the expression of vGluT2 (Slc17), which encodes a transporter of cytosol glutamate into synaptic vesicles, was strongly increased in the striatum but not frontal cortex in mature GluN2D KO mice. Mice that heterozygously lack vglut2 have been reported to show an increased locomotor response to amphetamine and increased sensitivity to the startle-disrupting effects of MK-801 . However, because acute and repeated PCP administration does not increase locomotor activity in GluN2D KO mice , the increased expression of vGluT2 in the striatum in GluN2D KO mice may negatively regulate PCP-induced locomotor activity. The other three genes, Hace1, Smpd4, and Osbpl8, have not yet been investigated with regard to motor impairment.
To investigate the role of the GluN2D subunit in PCP-induced motor impairment while avoiding the effects of GluN2D subunit ablation during development, we used the GluN2C/2D-selective antagonist UBP141 for the rotarod test. UBP141 is a competitive glutamate binding site antagonist, displaying seven-fold higher selectivity for GluN2D-containing receptors over GluN2B- or GluN2A-containing receptors . In the present study, UBP141 induced severe motor impairment in WT mice but not GluN2D KO mice, suggesting that the blockade of GluN2D-containing NMDA receptors caused motor impairment without developmental adaptations. Although the affinities of UBP141 for the GluN2C and GluN2D subunits are within a similar range, UBP141 likely inhibits the GluN2C subunit as well as the GluN2D subunit. The finding that UBP141 did not induce severe motor impairment in GluN2D KO mice suggests that inhibition of GluN2C subunit-containing NMDA receptors may not be involved in motor impairment. If so, then the inhibition of GluN2C subunit-containing NMDA receptors by PCP does not appear to play a significant role in PCP-induced motor impairment. Therefore, the inhibition of the GluN2D subunit by PCP appeared to participate in PCP-induced motor impairment in WT mice.
CIQ selectively potentiates GluN2C and GluN2D subunit. The EC50 values for the potentiation of GluN2C- and GluN2D-containing receptors are 2.7 and 2.8 μM, respectively . CIQ induced motor impairment in GluN2D KO mice but not WT mice, suggesting that CIQ-induced motor impairment is not caused by simple potentiation of the GluN2C subunit but rather by an imbalance of potentiation of the GluN2C subunit and GluN2D subunit. The GluN2C subunit mainly exists in the cerebellum, and GluN2D subunit exists in the thalamus, globus pallidus, and subthalamic nucleus. Therefore, the potentiation of the GluN2C or GluN2D subunit may affect different neural circuits.
Induction of c-fos by inhibition of the GluN2D subunit or potentiation of the GluN2C subunit
UBP141 administration increased c-fos expression in the thalamus and striatum in WT mice but not GluN2D KO mice. Although UBP141 inhibits GluN2D and GluN2C at similar concentrations (2.2-fold selectivity) in vitro, UBP141 is able to inhibit GluN2C subunit-containing NMDA receptors in GluN2D KO mice. However, UBP141 did not increase c-fos mRNA in GluN2D KO mice (Figure 6A). In contrast, CIQ, a potentiator of GluN2C/2D subunits, induced c-fos expression to a similar extent in WT and KO mice (Figure 6B). Therefore, CIQ likely potentiated GluN2C subunit-containing NMDA receptors in GluN2D KO mice. These results suggest that potentiation of the GluN2C subunit and inhibition of the GluN2D subunit induce neural excitation. However, the mechanisms of c-fos induction by these compounds can be different. UBP-141 has a similar mechanism of action as PCP. That is, UBP-141 blocks the GluN2D subunit-containing NMDA receptor complex in the GABA neurons. The suppression of GABA neurons then disinhibits glutamatergic neurons, and activated glutamatergic neurons induce neural excitation. CIQ enhanced the function of the NMDA receptor complex by acting on GluN2C/2D subunits. In the basal ganglia and cerebellum, direct potentiation of the GluN2C/2D subunit-containing NMDA receptor complex in glutamatergic neurons may induce c-fos expression in the thalamus and subsequently in the striatum. Thus, these increases in c-fos induction by UBP141 or CIQ are likely attributable to the activation of different neural circuits.
CIQ potentiated the function of GluN2C/2D subunit-containing NMDA receptors in WT mice but potentiated only the GluN2C subunit in GluN2D KO mice. In the present study, we found that the inhibition of GluN2D subunit-containing NMDA receptors in the motor loop or potentiation of GluN2C subunit-containing NMDA receptors likely in the cerebellum loop induced motor impairment. These two neural circuits (i.e., the basal ganglia and cerebellum) are well known to be important for cooperative movements (Figure 7). The balance between the GluN2C subunit-rich cerebellum loop and GluN2D subunit-containing basal ganglia circuit would be needed for appropriate motor performance.
PCP-induced c-fos expression and basal ganglia circuitry
The immunohistochemical analysis of Fos revealed that the PCP-induced increase in the number of Fos-positive cells was suppressed in the observed brain areas in GluN2D KO mice, including the striatum, thalamus, motor cortex, and subthalamic nucleus (Figures 4 and 5). However, the numbers of Fos-positive cells in the striatum and thalamus of saline-treated GluN2D KO mice were significantly increased compared with WT mice (Figure 4(G) and Figure 5(G), respectively). There is a possibility that the existence of a ceiling effect in GluN2D KO mice might mask the PCP-induced increases in GluN2D KO mice. Nevertheless, the measurements of c-fos mRNA by qRT-PCR indicated no significant increase in the thalamus or striatum in GluN2D KO mice (Figure 6). Therefore, the suppression of PCP-induced c-fos expression in KO mice was unlikely attributable to the ceiling effect. Changes in c-fos mRNA are more quickly linked to neural excitation than Fos protein expression. These c-fos mRNA results suggested that PCP-induced excitation in the thalamus and striatum in GluN2D KO mice was suppressed as well as in other areas of the motor loop (i.e., subthalamic nucleus and motor cortex) in GluN2D KO mice. On the other hand, the observed genotypic differences in the expression of c-fos and activation of Fos might be secondary to PCP’s differential genotypic effects on hyperlocomotion. To delineate this issue, we used the skeletal ryanodine receptor blocker dantrolene as a muscle relaxant to relieve mice from PCP-induced hyperlocomotion. Dantrolene itself did not inhibit basal c-fos expression or PCP-induced c-fos expression in WT mice (Figure 6C, D) without PCP-induced hyperlocomotion. Thus, these results indicate that the genotypic difference in PCP-induced c-fos expression was not secondary to hyperlocomotion in WT mice.
These brain areas, including the striatum, thalamus, motor cortex, and subthalamic nucleus, are components of the basal ganglia circuitry that mediates various motor functions, such as movement control, behavioral performance, and motivational processes [17–21]. A standard model of the basal ganglia circuitry suggests that direct projections from the subthalamic nucleus to output structures play a major role in motor function regulation [22–24]. Interestingly, NMDA receptors in the subthalamic nucleus and globus pallidus are mainly composed of GluN1 and GluN2D subunits . Therefore, genetic ablation of the GluN2D subunit likely results in the severe loss of NMDA receptor function in the subthalamic nucleus and globus pallidus in GluN2D KO mice. Acute PCP administration (2 mg/kg) increased extracellular glutamate levels in the prefrontal cortex . Considering that motor and prefrontal cortical areas provide a major source of glutamatergic excitatory inputs to the subthalamic nucleus [27–29], activated glutamatergic inputs to NMDA receptors via the subthalamic nucleus would be attenuated in GluN2D KO mice. Therefore, the mechanisms responsible for resistance against PCP-induced motor impairment in GluN2D KO mice may involve dysfunction of NMDA receptors in basal ganglia circuitry caused by a lack of GluN2D subunits.
PCP-induced changes in the expression of genes related to cellular stress are attenuated by genetic ablation of the GluN2D subunit
Egr4, which displays a neural-specific pattern of expression, is rapidly upregulated by neuronal activity [30–32]. Interestingly, the expression of Egr4 (NGFI-C) was potently decreased by PCP administration in the thalamus and striatum in GluN2D KO mice (Tables 1 and 2). In contrast, Egr4 expression in the frontal cortex in WT mice was increased by PCP administration. These results suggest that PCP administration induced differential neuronal activation in WT and GluN2D KO mice.
PCP caused selective increases in the expression of several genes in WT mice, including Ddit4 (REDD1), Bag-3, Txnip, and Sesn1. These genes are related to cellular stress. For example, REDD1 (also known as RTP801/Dig2/DDIT4) is a critical transducer of cellular responses to energy depletion through the TSC-mTOR pathway. Mammalian REDD1 is induced following DNA damage through both p53-dependent and -independent mechanisms . Recently, Jin et al. (2011) found that TXNIP inhibited mTOR activity by binding to and stabilizing the Redd1 protein . In response to stress, p53 transcribes a group of critical negative regulators of these two pathways, including Sestrin1. BAG-3, a key component of the proteostasis machinery, is induced under oxidative stress and upon proteasome inhibition [35–37]. BAG-3 triggers the recruitment of the autophagic ubiquitin adaptor p62 and thus facilitates substrate degradation through the autophagosome lysosome pathway . Therefore, the PCP-induced increases in the gene expression of Sestrin 1, Bag-3, and Ddit4 (REDD1) in WT mice are related to cellular stress, DNA damage, and the autophagosome lysosome pathway. The lack of increased expression of these genes in GluN2D KO mice after PCP administration suggests that ablation of the GluN2D subunit may prevent PCP-induced cellular stress in the striatum and frontal cortex.
In the present study, we found that PCP-induced motor impairment was reduced in GluN2D KO mice. Although the GluN2D subunit population is rather low and restricted in the mature brain, we conclude that the GluN2D subunit plays an important role in PCP-induced motor impairment and gene expression.
Materials and methods
Phencyclidine (Shionogi Pharmaceutical Co. Ltd., Osaka, Japan) was dissolved in saline. UBP141 (Abcam Biochemicals; http://www.ascentscientific.com/; accessed June 7, 2013) was dissolved in twice an equal molar amount of NaOH solution, diluted with saline, and neutralized to pH 8.0. Prof. Stephen F. Traynelis kindly provided CIQ to us. CIQ was dissolved in dimethylacetamide, and four volumes of PEG-400 were then added and gently mixed. Finally, five volumes of 5% glucose solution were added. After preparation, the CIQ solution was immediately used. Dantrolene (Sigma-Aldrich, St. Louis, MO, USA) was freshly dissolved in warm water (50°C) by sonication.
The experimental protocols were approved by the Animal Use and Care Committee of the Tokyo Metropolitan Institute of Medical Science. The mice were housed 5–6 per cage with free access to food and water and maintained on a 12 h/12 h light/dark cycle.
Three-month-old homozygous GluN2D mutant and WT mice of both sexes were obtained by crossing F11 heterozygous GluN2D mutant mice (+/−) on a 99.99% pure C57BL/6 genetic background . WT and homozygous KO mice were genotyped by polymerase chain reaction (PCR) using two internal primers (one targeted at the neomycin-resistant gene [NEO] insertion in the KO construct and one targeted at the WT gene) and one external primer, generating two products that identified the WT and KO genes. Polymerase chain reaction using Go Taq DNA polymerase (Promega, Madison, WI, USA) was performed on ear DNA eluted after overnight digestion by proteinase K. The forward primer (5′-GAG ATT GAG ATG CTG GAG CGG CTG-3′) and WT primer (5′-CGG CGG TGG CGG GGG TTT GGC-3′) produced a 455-base pair (bp) band, whereas the forward primer and NEO primer (5′-GTG GAT GTG GAA TGT GTG CGA GGC-3′) produced a 184-bp band. The PCR amplification products were electrophoretically separated on 2% agarose gels, and the bands were visualized under ultraviolet illumination.
A commercially available rotarod apparatus was used (KN-75, Natsume Seisakusho Co., Ltd, Tokyo, Japan). During the training phase, the mice underwent a training session on the apparatus for five training trials, in which the rod (3 cm diameter) was maintained at a constant speed for 300 s. The rod was kept stationary for the first trial and held at 6 rotations per minute (rpm) for two trials. The rod was then rotated at 12 rpm for two training trials, with a 3-h intertrial interval (ITI). The mice that were able to stay on the rod at 12 rpm for more than 200 s were evaluated in the test phase the next day (day 2 in Figure 1A). After the training phase, 93.3% and 90.9% of the WT and GluN2D KO mice, respectively, had proceeded to the test phase.
During the test phase, two trials were conducted with a 3-h ITI. In the first trial, the mice were placed on the rod that rotated at 12 rpm, at which time a timer was started and maintained for 300 s (day 3 in Figure 1A). The second trial was performed 30 min after PCP (3 mg/kg, subcutaneously [s.c.]) and CIQ (20 mg/kg, intraperitoneally [i.p.]) administration at 12 rpm or UBP141 administration (24.3 μg, 20 μl of 3 mM per mouse, intracisternally [i.c.], under diethyl ether anesthesia) at 0 rpm. The second trial lasted 300 s. The latency to fall from the rod was recorded for each of the two successive trials. For the animal studies, Fisher’s exact test was used to compare the data.
Tissue preparation, RNA isolation, probe labeling, and microarray hybridization
Preliminary experiment: Gene expression analyses using cDNA array
WT and GluN2D KO mice were injected with saline or PCP (10 mg/kg, s.c.). Two hours after the injection, the striata from 10 mice per treatment group (a total of 160 mice were used) were quickly dissected on ice and immediately frozen at −80°C. The precise procedure for the cDNA array experiments is described elsewhere . This developed a cDNA array system that utilized mouse KIAA-homologous cDNA (mKIAA) clones (http://www.kazusa.or.jp/rouge/; accessed July 7, 2013). KIAA clones were originally obtained from a human cDNA sequencing project to accumulate protein-coding sequence information on unidentified human genes. Although unidentified mKIAA genes are interesting, the expression data of newly identified mKIAA genes is not suitable for pathway analysis.
Experiment 1. Gene expression analyses using Illumina DNA array
WT and GluN2D KO mice were injected with saline or PCP (10 mg/kg, s.c.). Four groups, consisting of saline-treated WT, saline-treated GluN2D KO, PCP-treated WT, and PCP-treated GluN2D KO mice, were prepared. One group included four samples. One sample is prepared with more than three mice. We used 16 samples and the16 cDNA arrays. Total RNA was isolated with TRIzol reagent (Invitrogen, Carlsbad, CA, USA) and purified using the RNeasy Mini Kit according to the manufacturer’s instructions (Qiagen, Valencia, CA, USA). RNA was quantified by measuring the optical density at 260 nm using a spectrophotometer (Beckman, Fullerton, CA, USA).
Gene expression profiling for 16 different RNA samples was performed using microarray platforms from Illumina (San Diego, CA, USA). For the Illumina platform, we used the multi-sample MouseRef-8 BeadChip format with greater than 24,000 probes that simultaneously profile eight samples on a single chip. Briefly, 500 ng of total RNA was labeled using an Illumina TotalPrep RNA Amplification Kit (Life Technologies, Carlsbad, CA, USA). Double-stranded cDNA was synthesized using T7-oligo (dT) primers followed by an in vitro transcription reaction to amplify antisense-RNA (aRNA). Biotin was incorporated into the synthesized aRNA target. The biotinylated cRNA target was hybridized to the MouseRef-8 BeadChip. Hybridization, washing, and scanning were performed according to the manufacturer’s instructions following overnight hybridization. The chips were scanned using a BeadScan (Illumina) at a multiplier setting of “2.” The microarray images were recorded, and gene expression data were automatically extracted according to the manufacturer’s default settings. Raw microarray intensity data were provided using differential expression algorithms (Illumina). Additional calculations were performed within a Microsoft Excel spreadsheet. For each probe, intensity data were used in t-tests to obtain p-values and fold changes. Genes with a fold change > 1.3 or < 0.7 and between-group differences with p < 0.05 were considered to be differentially expressed genes (DEGs; . The pathway analyses of statistically significant genes were performed using MetaCore software (GeneGo, St. Joseph, MI, USA). The figures in the text are adaptations based on the figures created by MetaCore software.
To confirm the cDNA array results, quantitative reverse-transcription PCR (qRT-PCR) was performed. Purified mRNA (0.5 μg) was reverse-transcribed with random nonamers using the SuperScript III first-strand synthesis system according to the manufacturer’s instructions (Invitrogen). To evaluate gene expression, real-time qRT-PCR was performed using the SYBR-green-based real-time qRT-PCR assay. Using the primers identified by Lasergene (DNASTAR, Madison, WI, USA), qRT-PCR was performed. First-strand cDNA from the pooled mRNA was used as a template in a 25-μl PCR reaction with 200 nM primers and the Power SYBR Green PCR Master Mix (Applied Biosystems, Warrington, UK). Forty-five cycles of PCR were performed with an Applied Biosystems 7300 Real Time PCR System (Applied Biosystems). The levels of all of the cDNAs generated from the mRNA by reverse transcription were calculated using the standard curve method for quantification and normalized to actin transcript levels.
To confirm the Illumina DNA array results, qRT-PCR experiments were performed using LightCycler 480 and LightCycler 480 Probes Master (Roche, Indianapolis, IN, USA) according to the manufacturer’s protocol. Sequences for gene-specific primers that corresponded to the PCR targets were obtained using LightCycler Probe Design software (Roche). The primers were synthesized and purified by high-performance liquid chromatography by Nihon Gene Research Laboratories (Sendai, Japan). Quantitative PCR values were normalized to actin levels.
To examine c-fos mRNA levels by qRT-PCR, the mice were injected with UBP141, CIQ, and control vehicles similarly to the procedure used in the rotarod test but without behavioral testing. Two hours after injection, the thalamus and striatum from each mouse were quickly dissected on ice and immediately frozen at −80°C. Similarly, the mice first received dantrolene (5 mg/kg, i.p.) and then injected with PCP (10 mg/kg, s.c.) 15 min later. Two hours after the PCP injection, the thalamus and striatum from each mouse were quickly dissected on ice and immediately frozen at −80°C. Total RNA was separately extracted from each tissue. The qRT-PCR experiments were performed using LightCycler 480 and LightCycler 480 Probes Master (Roche, Indianapolis, IN, USA) according to the manufacturer’s protocol.
All of the animals were deeply anesthetized with an overdose of sodium pentobarbital (50 mg/kg, i.p.; Nembutal, Dainippon-Sumitomo, Osaka, Japan) and transcardially perfused with 50 ml phosphate-buffered saline (PBS), followed by ice-cold 4% paraformaldehyde in 0.1 M phosphate buffer (PB; pH 7.4). The brains were quickly removed from the skull and post-fixed overnight in the same fixative. After post-fixation, the brains were cryoprotected in 20% sucrose in PB (0.1 M, pH 7.4) for 2 days at 4°C and serially sectioned (50-μM thickness) using a Leica VT1000 P vibratome (Leica Microsystems). For the immunohistochemical visualization of Fos expression, coronal brain sections were pretreated for 15 min at room temperature with a 1% hydrogen peroxide solution to remove peroxidases. The sections were blocked for 2 h at room temperature in 4% goat serum solution (0.05% Tween-20/Tris-buffered saline), followed by incubation for 48 h at 4ºC in the primary Fos antibody (anti-Fos; 1:10,000; Ab-5, Calbiochem) in PBS with 4% normal goat serum. Immunoreactivity was visualized using ImmPRESS reagent (Vector Labs, Burlingame, CA, USA) with 3,3′-diaminobenzidine/nickel as the chromogen. Control and experimental tissues from each group were processed in parallel. No staining was observed in the brain sections with omission of either the primary or secondary antibody.
The number of Fos-positive neurons within the confines of each anatomically demarcated nucleus was evaluated using bright-field microscopy at 20× magnification. Based on Fos expression and its relevance to motor function, the following brain regions were selected for counting Fos-immunoreactive cells: striatum (0.98 mm), thalamus (−2.06 mm), paraventricular thalamic nucleus (−1.46), cingulate cortex and motor cortex (1.7 mm), and subthalamic nucleus (−2.18 mm). Bregma-based coordinates  are shown in parentheses after each brain region. The analyses of Fos-immunoreactive nuclei were performed using a Keyence microscope system (Keyence BZ-8100, Woodcliff Lake, NJ, USA). Twenty to 30 photographs (one photograph was extracted from five superimposed photographs at different depths) per coronal slice were taken in the selected regions. Full-image reconstruction of the entire slice was performed using Keyence BZ-8100. The areas that contained the striatum and other brain areas were cut off using Adobe Photoshop Elements software and transferred to NIH ImageJ software to automatically count Fos-labeled cells in the region of interest as defined by the template. The number of Fos-positive cells was normalized to the area (mm2).
Parametric or nonparametric analysis of variance (ANOVA) and appropriate post hoc tests were used to assess the effects of treatments, depending on the initial analyses of distribution normality. Correlation analyses were performed using Pearson’s coefficient. In the rotarod test, the data after 300 s were not recorded because the measurement of motor performance concluded at 300 s. To analyze the results from the rotarod test, Fisher’s exact test was used. Statistical significance was set at p < 0.05.
Watanabe M, Inoue Y, Sakimura K, Mishina M: Developmental changes in distribution of NMDA receptor channel subunit mRNAs. Neuroreport. 1992, 3: 1138-1140. 10.1097/00001756-199212000-00027.
Ikeda K, Araki K, Takayama C, Inoue Y, Yagi T, Aizawa S, Mishina M: Reduced spontaneous activity of mice defective in the epsilon 4 subunit of the NMDA receptor channel. Brain Res Mol Brain Res. 1995, 33: 61-71. 10.1016/0169-328X(95)00107-4.
Miyamoto Y, Yamada K, Noda Y, Mori H, Mishina M, Nabeshima T: Lower sensitivity to stress and altered monoaminergic neuronal function in mice lacking the NMDA receptor epsilon 4 subunit. J Neurosci. 2002, 22: 2335-2342.
Selemon LD, Goldman-Rakic PS: The reduced neuropil hypothesis: a circuit based model of schizophrenia. Biol Psychiatry. 1999, 45: 17-25. 10.1016/S0006-3223(98)00281-9.
Krystal JH, D’Souza DC, Mathalon D, Perry E, Belger A, Hoffman R: NMDA receptor antagonist effects, cortical glutamatergic function, and schizophrenia: toward a paradigm shift in medication development. Psychopharmacology (Berl). 2003, 169: 215-233. 10.1007/s00213-003-1582-z.
Geyer M, Krebs-Thomson K, Braff D, Swerdlow N: Pharmacological studies of prepulse inhibition models of sensorimotor gating deficits in schizophrenia: a decade in review. Psychopharmacology (Berlin). 2001, 156: 117-154. 10.1007/s002130100811.
Carlsson M, Carlsson A: The NMDA antagonist MK-801 causes marked locomotor stimulation in monoamine-depleted mice. J Neural Transm. 1989, 75: 221-226. 10.1007/BF01258633.
Lindahl JS, Keifer J: Glutamate receptor subunits are altered in forebrain and cerebellum in rats chronically exposed to the NMDA receptor antagonist phencyclidine. Neuropsychopharmacology. 2004, 29: 2065-2073. 10.1038/sj.npp.1300485.
Hagino Y, Kasai S, Han W, Yamamoto H, Nabeshima T, Mishina M, Ikeda K: Essential role of NMDA receptor channel epsilon4 subunit (GluN2D) in the effects of phencyclidine, but not methamphetamine. PLoS One. 2010, 5: e13722-10.1371/journal.pone.0013722.
Franklin K, Paxinos G: The Mouse Brain in Stereotaxic Coordinates. 2007, Amsterdam: Academic Press/Elsevier, 3
Kobayashi S, Yano M, Suetomi T, Ono M, Tateishi H, Mochizuki M, Xu X, Uchinoumi H, Okuda S, Yamamoto T, et al: Dantrolene, a therapeutic agent for malignant hyperthermia, markedly improves the function of failing cardiomyocytes by stabilizing interdomain interactions within the ryanodine receptor. J Am Coll Cardiol. 2009, 53: 1993-2005. 10.1016/j.jacc.2009.01.065.
Traynelis SF, Wollmuth LP, McBain CJ, Menniti FS, Vance KM, Ogden KK, Hansen KB, Yuan H, Myers SJ, Dingledine R: Glutamate receptor ion channels: structure, regulation, and function. Pharmacol Rev. 2010, 62: 405-496. 10.1124/pr.109.002451.
Naert A, Callaerts-Vegh Z, Moechars D, Meert T, D’Hooge R: Vglut2 haploinsufficiency enhances behavioral sensitivity to MK-801 and amphetamine in mice. Progress in Neuro-Psychopharmacology and Biological Psychiatry. 2011, 35: 1316-1321. 10.1016/j.pnpbp.2011.03.023.
Costa B, Feng B, Tsintsadze T, Morley R, Irvine M, Tsintsadze V, Lozovaya N, Jane D, Monaghan D: N-methyl-D-aspartate (NMDA) receptor NR2 subunit selectivity of a series of novel piperazine-2,3-dicarboxylate derivatives: preferential blockade of extrasynaptic NMDA receptors in the rat hippocampal CA3-CA1 synapse. J Pharmacol Exp Ther. 2009, 331: 618-626. 10.1124/jpet.109.156752.
Mullasseril P, Hansen KB, Vance KM, Ogden KK, Yuan H, Kurtkaya NL, Santangelo R, Orr AG, Le P, Vellano KM, Liotta DC, Traynelis SF:A subunit-selective potentiator of NR2C- and NR2D-containing NMDA receptors. Nat Commun. 2010, 1: 90-
Kringelbach ML, Jenkinson N, Owen SL, Aziz TZ:Translational principles of deep brain stimulation. Nat Rev Neurosci. 2007, 8: 623-635. 10.1038/nrn2196.
Hamada I, DeLong MR:Excitotoxic acid lesions of the primate subthalamic nucleus result in transient dyskinesias of the contralateral limbs. J Neurophysiol. 1992, 68: 1850-1858.
Baunez C, Nieoullon A, Amalric M:In a rat model of parkinsonism, lesions of the subthalamic nucleus reverse increases of reaction time but induce a dramatic premature responding deficit. J Neurosci. 1995, 15: 6531-6541.
Baunez C, Amalric M, Robbins TW:Enhanced food-related motivation after bilateral lesions of the subthalamic nucleus. J Neurosci. 2002, 22: 562-568.
Baunez C, Robbins TW:Bilateral lesions of the subthalamic nucleus induce multiple deficits in an attentional task in rats. Eur J Neurosci. 1997, 9: 2086-2099. 10.1111/j.1460-9568.1997.tb01376.x.
Dybdal D, Gale K:Postural and anticonvulsant effects of inhibition of the rat subthalamic nucleus. J Neurosci. 2000, 20: 6728-6733.
Alexander GE, Crutcher MD:Functional architecture of basal ganglia circuits: neural substrates of parallel processing. Trends Neurosci. 1990, 13: 266-271. 10.1016/0166-2236(90)90107-L.
DeLong MR:Primate models of movement disorders of basal ganglia origin. Trends Neurosci. 1990, 13: 281-285. 10.1016/0166-2236(90)90110-V.
Parent A, Hazrati LN:Functional anatomy of the basal ganglia. II. The place of subthalamic nucleus and external pallidum in basal ganglia circuitry. Brain Res Brain Res Rev. 1995, 20: 128-154. 10.1016/0165-0173(94)00008-D.
Standaert DG, Testa CM, Young AB, Penney JB:Organization of N-methyl-D-aspartate glutamate receptor gene expression in the basal ganglia of the rat. J Comp Neurol. 1994, 343: 1-16. 10.1002/cne.903430102.
Amitai N, Kuczenski R, Behrens MM, Markou A:Repeated phencyclidine administration alters glutamate release and decreases GABA markers in the prefrontal cortex of rats. Neuropharmacology. 2012, 62: 1422-1431. 10.1016/j.neuropharm.2011.01.008.
Afsharpour S:Topographical projections of the cerebral cortex to the subthalamic nucleus. J Comp Neurol. 1985, 236: 14-28. 10.1002/cne.902360103.
Canteras NS, Shammah-Lagnado SJ, Silva BA, Ricardo JA:Afferent connections of the subthalamic nucleus: a combined retrograde and anterograde horseradish peroxidase study in the rat. Brain Res. 1990, 513: 43-59. 10.1016/0006-8993(90)91087-W.
Bevan MD, Francis CM, Bolam JP:The glutamate-enriched cortical and thalamic input to neurons in the subthalamic nucleus of the rat: convergence with GABA-positive terminals. J Comp Neurol. 1995, 361: 491-511. 10.1002/cne.903610312.
Crosby S, Puetz J, Simburger K, Fahrner T, Milbrandt J:The early response gene NGFI-C encodes a zinc finger transcriptional activator and is a member of the GCGGGGGCG (GSG) element-binding protein family. Mol Cell Biol. 1991, 11: 3835-3841.
Crosby S, Veile R, Donis-Keller H, Baraban J, Bhat R, Simburger K, Milbrandt J:Neural-specific expression, genomic structure, and chromosomal localization of the gene encoding the zinc-finger transcription factor NGFI-C. Proc Natl Acad Sci U S A. 1992, 89: 4739-4743. 10.1073/pnas.89.10.4739.
Honkaniemi J, Sharp F:Prolonged expression of zinc finger immediate-early gene mRNAs and decreased protein synthesis following kainic acid induced seizures. Eur J Neurosci. 1999, 11: 10-17. 10.1046/j.1460-9568.1999.00401.x.
Ellisen LW, Ramsayer KD, Johannessen CM, Yang A, Beppu H, Minda K, Oliner JD, McKeon F, Haber DA:REDD1, a developmentally regulated transcriptional target of p63 and p53, links p63 to regulation of reactive oxygen species. Mol Cell. 2002, 10: 995-1005. 10.1016/S1097-2765(02)00706-2.
Jin HO, Seo SK, Kim YS, Woo SH, Lee KH, Yi JY, Lee SJ, Choe TB, Lee JH, An S, et al:TXNIP potentiates Redd1-induced mTOR suppression through stabilization of Redd1. Oncogene. 2011, 30: 3792-3801. 10.1038/onc.2011.102.
Arndt V, Dick N, Tawo R, Dreiseidler M, Wenzel D, Hesse M, Furst DO, Saftig P, Saint R, Fleischmann BK, et al:Chaperone-assisted selective autophagy is essential for muscle maintenance. Curr Biol. 2010, 20: 143-148. 10.1016/j.cub.2009.11.022.
Dikshit P, Jana NR:The co-chaperone CHIP is induced in various stresses and confers protection to cells. Biochem Biophys Res Commun. 2007, 357: 761-765. 10.1016/j.bbrc.2007.04.018.
Jacobs AT, Marnett LJ:HSF1-mediated BAG3 expression attenuates apoptosis in 4-hydroxynonenal-treated colon cancer cells via stabilization of anti-apoptotic Bcl-2 proteins. J Biol Chem. 2009, 284: 9176-9183. 10.1074/jbc.M808656200.
Yamamoto H, Imai K, Takamatsu Y, Kamegaya E, Kishida M, Hagino Y, Hara Y, Shimada K, Yamamoto T, Sora I, et al:Methamphetamine modulation of gene expression in the brain: analysis using customized cDNA microarray system with the mouse homologues of KIAA genes. Brain Res Mol Brain Res. 2005, 137: 40-46. 10.1016/j.molbrainres.2005.02.028.
Liao G, Wen Z, Irizarry K, Huang Y, Mitsouras K, Darmani M, Leon T, Shi L, Bi X:Abnormal gene expression in cerebellum of Npc1−/− mice during postnatal development. Brain Res. 2010, 1325: 128-140.
We would like to acknowledge especially Prof. Stephen F. Traynelis and Dr. Kasper B. Hansen for providing CIQ. This work was supported by Grants-in-Aid from the MEXT of Japan (20390162, 23390377, and 24659549), MHLW of Japan (H21-3jigan-ippan-011 and H22-Iyaku-015), Smoking Research Foundation, and Foundation for Promotion of Material Science and Technology of Japan (MST).
The authors declare no competing financial interests.
HY designed the research; HY, EK, WS, RH, TY, YH, and YT performed the research; HY, EK, WS, RH, TY, HK, and KI analyzed the data; HY, TY, HK, MM, and KI prepared the manuscript. All authors read and approved the final manuscript.
Electronic supplementary material
Additional file 2: Table S2:Numerical data of Figure 6 ( c-fos/actin ) and these reference data ( actin ). Two hours after the injection of (A) UBP141 (3 mM, 20 μl, i.c.), (B) CIQ (20 mg/kg, i.p.), (C, D) Dantrolene (5 mg/kg, i.p.) and PCP (10 mg/kg, s.c), c-fos and actin expressions were measured using qRT-PCR analyses. The ratio of c-fos/actin transcripts and its reference actin transcripts are shown as the mean ± SEM fold change from saline controls in WT mice. (XLSX 19 KB)
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