JIP1-Mediated JNK Activation Negatively Regulates Synaptic Plasticity and Spatial Memory

JIP1 expression in hippocampal neurons

Our initial studies were designed to examine the expression of JIP1 protein in the hippocampus. Immunohistochemical staining of tissue sections demonstrated that JIP1 is expressed in the CA1, CA3, and the dentate gyrus (DG) regions of the hippocampus (Fig. 1A). JIP1 was primarily found on dendrites (colocalization with MAP2) and to a lesser extent on cell bodies (colocalization with NeuN) of the CA1/CA3 pyramidal and DG granule neurons (Fig. 1A).

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Figure 1.

Analysis of JIP1 expression in the hippocampus. A, Fluorescent immunohistochemistry of the CA1, CA3, and DG regions of the hippocampus indicates that JIP1 (green) predominantly colocalizes with MAP2 (red) in wild-type brain sections (top), suggesting relative enrichment of the JIP1 protein in neuronal processes. Colocalization between JIP1 (green) and neuron-specific nuclear protein (NeuN; red) is sparse in the hippocampal subfields (bottom). CA1, Cornu ammonis 1; CA3, cornu ammonis 3; grDG, granular layer of DG; poDG, polymorphic layer of DG; s.l., stratum lucidem; s.l.m., stratum lacunosum moleculare; s.p., stratum pyramidale; s.r., stratum radiatum. Scale bar, 50 μm. B, Nissl stain and NeuN stain of JIP1^WT and JIP1^TA coronal hippocampal sections. Scale bar, 200 μm. C, D, Pyramidal cells of the CA1 region of JIP1^WT and JIP1^TA were stained with Nissl, NeuN, the dendritic marker MAP2, the astrocytic marker GFAP, and the inhibitory GABAergic marker GAD67 (C). The staining was quantitated (D) (mean ± SEM; n = 4; p > 0.05; Student's t test). Scale bar, 50 μm.

We next examined the hippocampal architecture of JIP1^TA and JIP1^WT mice. Qualitative analysis of Nissl-stained (Fig. 1B,C) and Golgi-stained (Fig. 2A) coronal sections did not reveal differences in hippocampus morphology between JIP1^TA and JIP1^WT mice. Moreover, analysis of basal and apical dendrites from Golgi-stained CA1 pyramidal neurons revealed no significant differences in dendritic branching, spine density, or spine type (Fig. 2A–E). In addition, the intensity and distribution of the neuronal marker NeuN (t₍₆₎ = 0.89, p = 0.41; two-tailed unpaired Student's t test), the dendritic marker MAP2 (t₍₆₎ = 0.71, p = 0.51; two-tailed unpaired Student's t test), the GABAergic interneuron marker GAD67 (t₍₆₎ = 0.27, p = 0.79; two-tailed unpaired Student's t test), and the glial marker GFAP (t₍₆₎ = 0.44, p = 0.67; two-tailed unpaired Student's t test) were similar in JIP1^TA and JIP1^WT mice (Fig. 1B–D). Collectively, these data indicate that the Thr¹⁰³Ala mutation in JIP1 did not cause detectable changes in basic hippocampus morphology.

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Figure 2.

Neuronal spine density and dendritic arborization of CA1 pyramidal neurons are similar in JIP1^WT and JIP1^TA mice. A, Representative images of apical and basal dendrites spine morphology in JIP1^TA mice and JIP1^WT littermates. Scale bar, 10 μm. B, Quantitation of basal and apical dendritic spine density (mean ± SEM; n = 5 slices from 5 mice per genotype; p > 0.05, Student's t test). C, Quantitation of different spine types in basal and apical dendrites (mean ± SEM, n = 5 slices from 5 mice per genotype; p > 0.05, Student's t test). D, E, Sholl analysis of dendritic arborization of CA1 pyramidal neurons. Values on the x-axis represent increasing distance from the soma of the pyramidal cells. Basal and apical dendrites of pyramidal cells from n = 5 slices from 5 mice per genotype were examined (mean ± SEM; p > 0.05, Student's t test).

JIP1-mediated JNK activation in the hippocampus

We have demonstrated previously that JIP1^TA mice exhibit defects in metabolic stress-induced JNK activation in adipose tissue (Morel et al., 2010). To test whether the Thr¹⁰³Ala mutation in JIP1 also caused defects in JNK activation in neural tissue, we examined a model of JIP1-dependent JNK activation (kainate excitotoxicity) in the hippocampus. Examination of the DG after short-term exposure to kainate caused JIP1-dependent JNK activation and phosphorylation of the JNK substrate cJun and JIP1-independent increased expression of cJun and cFos (Whitmarsh et al., 2001). We found that kainate caused a similar increase in cJun and cFos expression in JIP1^TA and JIP1^WT mice (Fig. 3B,C). In contrast, kainate caused increased cJun phosphorylation in JIP1^WT but not JIP1^TA mice (Fig. 3A). These data demonstrate that the Thr¹⁰³Ala mutation suppresses JIP1-mediated JNK activation in the hippocampus. Time course analysis confirmed that cJun phosphorylation in the hippocampus of kainate-stimulated JIP1^WT mice was strongly suppressed in JIP1^TA mice after exposure to kainate (two-way ANOVA: genotype F_(1,32) = 15.11, p < 0.001; time F_(3,32) = 34.26, p < 0.001; genotype × time F_(3,32) = 5.05, p = 0.005; Fig. 3D,E). These data extend our previous finding that JIP1^TA mice exhibit defects in JIP1-dependent JNK activation in adipose tissue (Morel et al., 2010) to demonstrate that JIP1^TA mice also exhibit profound defects in JIP1-mediated JNK activation in the hippocampus.

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Figure 3.

JIP1-dependent JNK activation in the hippocampus is suppressed in JIP1^TA mice. A–C, JIP1^WT and JIP1^TA mice were treated by systemic injection of kainate. At 2 h after treatment, sections of the brain were prepared and stained (green) with antibodies to pSer⁶³ cJun (A), cJun (B), or cFos (C). DNA was stained with DAPI (red). Representative sections of the DG of the hippocampus are presented. Scale bar, 75 μm. D, E, Extracts prepared from the hippocampus of JIP1^WT and JIP1^TA mice treated with kainate (0–60 min) were examined by multiplexed ELISA to measure the amount of pSer⁶³-cJun (D) and cJun (E) normalized to the amount of JNK. Data are shown as mean ± SEM. n = 5; **p < 0.01, two-way ANOVA followed by Bonferroni's post hoc test.

To test how JIP1-mediated JNK activation contributes to a physiologically relevant response, we examined the effect of contextual fear conditioning, which was shown previously to cause transient JNK activation in the dorsal hippocampus (Sherrin et al., 2010). Immunoblot analysis using antibodies to JNK and phospho-JNK was performed to assess changes in JNK activation in dorsal hippocampal extracts from JIP1^WT and JIP1^TA mice that were subjected to single-trial contextual fear conditioning. Extracts were prepared at various times after the single trial to correspond to the consolidation phase of contextual fear (Igaz et al., 2002). JNK immunoblot analysis detects the 46 kDa (JNK1α1 and JNK1β1) and 54 kDa isoforms (JNK2α2, JNK2β2, and JNK3α2) in brain (Davis, 2000). We found that contextual fear conditioning caused an increase in 46 kDa phospho-JNK in JIP1^WT mice at 30 min (176 ± 12% of naive control mice; Bonferroni post hoc test, p < 0.001) and 60 min (127 ± 8% of naive; Bonferroni post hoc test, p = 0.09; Fig. 4). In contrast, we found that JIP1^TA mice exhibited decreased 46 kDa phospho-JNK at 30 min (75 ± 11% of naive; Bonferroni post hoc test, p = 0.011), 60 min (53 ± 7% of naive; p < 0.001) and 180 min (79 ± 6% of naive; p = 0.009) after contextual fear conditioning (two-way ANOVA: genotype F_(1,50) = 15.11, p < 0.001; time F_(4,50) = 10.42, p < 0.001; genotype × time F_(4,50) = 22.11, p < 0.001; Fig. 4). These data demonstrate that the JIP1 Thr¹⁰³Ala mutation suppresses JNK activation caused by contextual fear conditioning.

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Figure 4.

JIP1^TA mice exhibit reduced JNK activation in the dorsal hippocampus after contextual fear conditioning. Dorsal hippocampal tissue was isolated from naive mice and from mice at different times after contextual fear conditioning (FC) and examined by immunoblot analysis by probing with antibodies to phospho-JNK, JNK, and GAPDH. The amount of 46 and 54 kDa phospho-JNK was quantitated and normalized to the amount of JNK in each sample. Data are shown as mean ± SEM. n = 5; ***p < 0.001, for JIP1^TA compared with JIP1^WT mice; #p < 0.01, ##p < 0.001 compared with the naive control, two-way ANOVA, followed by Bonferroni's post hoc test.

JIP1-mediated JNK activation suppresses NMDA-dependent synaptic plasticity

JNK activation is associated with mechanistic changes in synaptic plasticity in the hippocampus (Wang et al., 2004; Chen et al., 2005; Zhu et al., 2005; Li et al., 2007; Yang et al., 2011). Therefore, synaptic plasticity may be altered by JIP1-dependent JNK activation in the context of fear conditioning (Fig. 4). We therefore examined synaptic transmission in JIP1^WT and JIP1^TA mice.

Basal synaptic transmission at Schaffer collateral–CA1 synapses in JIP1^WT and JIP1^TA mice was characterized through the I/O relationship of fEPSPs. Analysis revealed that the fEPSP slopes, plotted against the stimulation strength, were comparable in slices from JIP1^WT and JIP1^TA mice (two-way repeated-measures ANOVA: genotype F_(1,420) = 0.23, p = 0.63; amplitude F_(14,442) = 79.27, p < 0.001; genotype × amplitude F_(14,420) = 0.35, p = 0.63; Fig. 5A). Similarly, when the fEPSP slopes were plotted as a function of increasing fiber volley amplitudes, no differences between JIP1^WT and JIP1^TA mice were detected (Fig. 5B). Moreover, PPF, indicative of presynaptic plasticity (Zucker and Regehr, 2002), at Schaffer collateral–CA1 synapses from JIP1^TA mice was similar to JIP1^WT mice at several interpulse intervals (two-way repeated-measures ANOVA: genotype F_(1,223) = 0.08, p = 0.78; interval F_(6,223) = 13.56, p < 0.001; genotype × interval F_(8,208) = 0.15, p = 0.98; Fig. 5C). These data demonstrate similar basal synaptic transmission in the hippocampi of JIP1^TA and JIP1^WT mice.

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Figure 5.

The threshold for LTP induction is reduced in JIP1^TA mice. A, B, Basal synaptic transmission at Schaffer collateral–CA1 synapses, as assessed by measuring the fEPSP I/O relationship (A) and the fEPSP slope to fiber volley relationship (B), was similar in JIP1^TA slices (n = 16 slices, 13 mice) compared with slices obtained from JIP1^WT littermates (n = 16 slices, 12 mice). No statistically significant differences were found (p > 0.05, two-way repeated-measures ANOVA). C, fEPSPs from JIP1^TA (n = 16 slices, 13 mice) and JIP1^WT (n = 16 slices, 12 mice) slices exhibited similar paired pulse facilitation. No statistically significant differences were found (p > 0.05, two-way repeated-measures ANOVA). D, HFS LTP was induced by two trains of 100 Hz stimulation (separated by a 20 s interval) to the Schaffer collaterals in slices from JIP1^TA and JIP1^WT mice (n = 10 slices, 8 mice/genotype). Stimulation was delivered at time 0 (arrow). No statistically significant differences were found (p > 0.05, Student's t test). E, An intermediate stimulation LTP protocol involved 900 pulses of 10 Hz stimuli delivered at time 0. LTP induced at intermediate frequencies was significantly facilitated in slices taken from JIP1^TA mice when compared with JIP1^WT controls (n = 10 slices, 9 mice/genotype). Statistically significant differences are indicated (***p < 0.001, Student's t test). F, LTD induced by LFS (1 Hz, 900 pulses, 0–15 min time) was significantly reduced in JIP1^TA slices compared with JIP1^WT slices (n = 10 slices, 10 mice/genotype). Statistically significant differences are indicated (***p < 0.0001, Student's t test). G, LTD induced by 0.5 Hz stimulation (0.5 Hz, 900 pulses, 0–30 min time) was similar in JIP1^WT and JIP1^TA slices (n = 14 slices, 11 mice/genotype). No statistically significant differences were found (p > 0.05, Student's t test). H, Frequency–response function in JIP1^TA and JIP1^WT mice. The percentage change in synaptic strength from baseline in JIP1^TA and JIP1^WT mice at 50–60 min after stimulation at the indicated frequency is presented. Data are shown as mean ± SEM. Magnitudes of LTP/LTD were calculated as the ratio of the average fEPSPs between 50 and 60 min and average baseline fEPSPs between −20 min and 0 min. Statistically significant differences are indicated (***p < 0.001, Student's t test). I, mGluR-dependent LTP in hippocampal slices from JIP1^TA and JIP1^WT mice. mGluR-LTD was induced by incubation of JIP1^TA and JIP1^WT slices with DHPG (100 μm) for 5 min (n = 10 slices, 10 mice/genotype). Basal fEPSPs were recorded before LTD induction with DHPG. No statistically significant differences were found (p > 0.05, Student's t test). J, Depotentiation is not affected in JIP1^TA mice. HFS (100 Hz twice for 1 s with 20 s interval) followed by 1 Hz (15 min) stimulation 10 min later to the Schaffer collaterals produced similar depotentiation in slices from JIP1^TA and JIP1^WT mice (n = 10 slices, 10 mice/genotype). No statistically significant differences were found (p > 0.05, Student's t test). The insets in D–J show representative fEPSP responses obtained before and after LTP, LTD and depotentiation inducing stimuli. Calibration: 0.2 mV/10 ms.

To determine whether the JIP1 Thr¹⁰³Ala mutation affects NMDAR-dependent forms of synaptic plasticity (Citri and Malenka, 2008), LTP was measured using a tetanic HFS protocol (2 trains of 1 s 100 Hz, separated by 20 s). Similar potentiation was produced in both JIP1^WT and JIP1^TA mice (Fig. 5D; fEPSPs were potentiated to 145 ± 7% for JIP1^WT and 146 ± 4% for JIP1^TA; t₍₁₈₎ = 0.12, p = 0.89; two-tailed unpaired Student's t test), indicating that the ability to induce LTP with strong stimulation was unimpaired in JIP1^TA mice. We next investigated whether the threshold stimulation for induction of LTP (Hu et al., 2007) differed between JIP1^WT and JIP1^TA mice. A 900 pulse train of 10 Hz stimulation resulted in a modest, but detectable, degree of LTP in slices obtained from JIP1^TA mice (Fig. 5E; 122 ± 4% of baseline at 50–60 min after LTP induction), though with minimal posttetanic potentiation, whereas fEPSPs in JIP1^WT slices were not potentiated (Fig. 5E; 92.1 ± 5.5% of baseline; t₍₁₈₎ = 7.61, p < 0.001; two-tailed unpaired Student's t test), with a trend toward depression. These data demonstrate that LTP could be induced at lower frequencies in JIP1^TA mice compared with JIP1^WT mice.

We also examined the induction of NMDAR-dependent LTD (Collingridge et al., 2010) in JIP1^WT and JIP1^TA mice. We found that LFS consisting of 900 single pulses at 1 Hz for 15 min generated robust LTD in JIP1^WT mice, but LTD was absent in JIP1^TA mice (Fig. 5F; JIP1^WT mice, 72 ± 2%; JIP1^TA mice, 98 ± 3%; p < 0.01; t₍₁₈₎ = 7.05, p < 0.001; two-tailed unpaired Student's t test). In view of the similar posttetanic depression (initial dip) between JIP1^WT and JIP1^TA brain slices, we determined whether JIP1^TA mice exhibit other forms of LTD. We therefore induced LTD by delivering the same number of single pulses (900) at 0.5 Hz for 30 min (Fig. 5G). This form of LTD also relies on NMDARs (Dudek and Bear, 1992), but depends to a greater degree on release of calcium from intracellular stores (Nakano et al., 2004). This LTD protocol produced equivalent depression in both JIP1^TA and JIP1^WT mice (Fig. 5G; JIP1^WT, 68 ± 3%; JIP1^TA, 66 ± 2%; t₍₂₆₎ = 0.55, p = 0.58; two-tailed unpaired Student's t test). These data indicate that disruption of JIP1-mediated JNK activation reduces the optimal frequency stimulation for LTD while enabling LTP at lower stimulation frequencies at Schaffer collateral–CA1 synapses (Fig. 5H).

Two different forms of LTD coexist at Schaffer collateral–CA1 synapses in the hippocampus, one dependent on NMDARs and another dependent on the activity of metabotropic glutamate receptors (mGluRs), specifically mGluR5 (Huber et al., 2001). Therefore, we next examined a possible effect of the JIP1^TA mutation on mGluR-dependent LTD. We found that a 5 min bath application of 100 μm DHPG (a group I mGluR agonist) to acute slices resulted in a persistent depression of Schaffer collateral-evoked responses that was comparable between JIP1^TA and JIP1^WT slices (Fig. 5I; 62 ± 1% of baseline at 60 min after drug application for JIP1^TA vs 65 ± 8% for JIP1^WT; t₍₁₈₎ = 0.68, p = 0.49; two-tailed unpaired Student's t test). These results suggest that, whereas the JIP1^TA mutation blocks the NMDAR-dependent forms of LTD, it does not affect the mGluR-dependent form.

Another important aspect of synaptic modification is synaptic depotentiation, namely that the synaptic potentiation could be subsequently reversed by LFS. In view of the finding that two trains of HFS at 100 Hz induced significant LTP in response to a 20 s intertetanus interval in both groups of mice (Fig. 5D), we used this HFS protocol followed by LFS 10 min later (900 pulses at 1 Hz) to induce depotentiation (Fig. 5J). One hour after the LFS, the evoked responses in both JIP1^WT and JIP1^TA mice dropped to the baseline level (100 ± 4% compared with baseline before the HFS for JIP1^WT, and 101 ± 3% for JIP1^TA; t₍₁₈₎ = 0.23, p = 0.82; two-tailed unpaired Student's t test), indicating effective LFS-induced depotentiation in both genotypes.

We next tested whether application of a selective inhibitor of JNK would mimic the effects of the JIP1 Thr¹⁰³Ala mutation on NMDA-receptor dependent forms of LTP and LTD. Slices were obtained from wild-type mice and exposed either to the selective JNK inhibitor JNK-in-8 (6 μm) or solvent (aCSF) for 20 min before stimulation protocols. The drug application was maintained throughout the recording period. Basal synaptic transmission was not affected by JNK-in-8, as indicated by the unchanged I/O relation (two-way repeated-measures ANOVA: genotype F_(1,308) = 0.88, p = 0.35); amplitude F_(14,308) = 61.73, p < 0.001; genotype × amplitude F_(14,308) = 0.35, p = 0.63) and unchanged PPF (two-way repeated-measures ANOVA: genotype F_(1,132) = 0.46, p = 0.56); interval F_(6,132) = 42.12, p < 0.001; genotype × interval F_(6,132) = 1.17, p = 0.11; Fig. 6A,B). In addition, inhibiting JNK activation in slices did not affect HFS LTP (Fig. 6C; 60 min after 2 × 100 Hz tetanization: 127 ± 6% of baseline for vehicle-treated slices vs 125 ± 5% for JNK-in-8-treated slices; t₍₂₂₎ = 0.25, p = 0.81; two-tailed unpaired Student's t test). However, JNK inhibition prevented the induction of LTD using the 1 Hz stimulation protocol (Fig. 6D; vehicle-treated slices, 77 ± 3%; JNK-in-8-treated slices, 101 ± 4%; p < 0.05; t₍₁₈₎ = 4.81, p < 0.001; two-tailed unpaired Student's t test). The latter result closely parallels the result obtained for the JIP1^TA slices (cf. Fig. 5F). Therefore, these data confirm that JIP1-mediated JNK activation plays an essential, but differential, role in certain forms NMDA-receptor dependent synaptic plasticity.

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Figure 6.

Inhibition of JNK signaling mimics the effect of JIP1 (Thr¹⁰³Ala) mutation on NMDAR-dependent LTD. A, B, JNK-in-8 treatment did not affect baseline synaptic transmission or PPF in wild-type slices. I/O curves, as assessed by the fEPSP slope to fiber volley relationship, were similar in vehicle-treated slices (n = 12 slices) compared with wild-type slices treated with JNK-in-8 (n = 12 slices; A). fEPSPs from vehicle-treated slices (n = 12 slices) and JNK-in-8 treated (n = 12 slices) slices exhibited similar PPF (B; p > 0.05, two-way repeated-measures ANOVA). C, HFS-LTP was induced with a pair of 100 Hz tetani in the presence of either vehicle (n = 12) or 6 μm JNK-in-8 (n = 12). LTP was unaffected by JNK inhibition. (p > 0.05, Student's t test). D, LFS-LTD was induced (1 Hz, 900 pulses) in the presence of either vehicle (n = 10) or 6 μm JNK-in-8 (n = 10). LTD was impaired by JNK inhibition (***p < 0.001, Student's t test). The insets in C and D show representative fEPSP responses obtained before and after LTP/LTD-inducing stimuli. Calibration: 0.2 mV/10 ms.

JIP1^TA mice exhibit increased NMDAR signaling

It is established that JIP scaffold proteins influence NMDAR activity (Kennedy et al., 2007). The induction of synaptic plasticity at lower stimulation frequencies detected in JIP1^TA mice compared with JIP1^WT mice (Fig. 6) may therefore be mediated by changes in NMDAR signaling. Indeed, we found increased expression of NMDAR subunits GluN1 (t₍₈₎ = 2.66, p = 0.029; two-tailed unpaired Student's t test), GluN2A (t₍₈₎ = 2.85, p = 0.037; two-tailed unpaired Student's t test), and GluN2B proteins (t₍₈₎ = 2.65, p = 0.027; two-tailed unpaired Student's t test; but not mRNA) in the whole hippocampus of JIP1^TA mice compared with JIP1^WT mice (Fig. 7A–C). Control studies detected no differences in the expression of the AMPAR subunits GluA1 and GluA2 (Fig. 7A). The increased expression of NMDAR subunits was also detected in hippocampal synaptoneurosomes (Fig. 7D) and by increased cell surface detection of GluN1 by immunofluorescence analysis of hippocampal neurons (t₍₁₆₎ = 2.85, p = 0.012; two-tailed unpaired Student's t test; Fig. 7E,F) cultured from JIP1^TA mice compared with JIP1^WT mice. These changes were associated with biochemical evidence of increased NMDAR activity through assessment of downstream signaling changes, including increased GluN2B Tyr¹⁴⁷² phosphorylation (Salter and Kalia, 2004; Fig. 7A), increased cFos mRNA expression (t₍₉₎ = 3.31, p = 0.009; two-tailed unpaired Student's t test; Bading et al., 1993; Fig. 7G), ERK phosphorylation (t₍₈₎ = 3.11, p = 0.017; two-tailed unpaired Student's t test; Xia et al., 1996; Fig. 7H), and CREB phosphorylation (t₍₈₎ = 5.25, p = 0.008; two-tailed unpaired Student's t test; Ginty et al., 1993; Fig. 7H). Control experiments demonstrated that the expression of KIF17, a microtubule motor that transports GluN2B vesicles and regulates synaptic plasticity (Yin et al., 2011, 2012), was similar in JIP1^WT and JIP1^TA mice (Fig. 7H). Together, these data indicate that JIP1^TA mice may exhibit increased NMDAR signaling in the hippocampus compared with JIP1^WT mice.

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Figure 7.

The JIP1^TA mutation promotes increased NMDAR expression and activity. A–C, Lysates prepared from the hippocampi of JIP1^TA and JIP1^WT mice were examined by immunoblot analysis by probing with antibodies to NMDA and AMPAR subunits, SAP102, JIP1, and β-tubulin (A). The number of NMDAR subunits in the hippocampus was determined and normalized to the amount of β-tubulin in each sample (B, mean ± SEM, n = 5; **p < 0.01, Student's t test). The amount of NMDAR subunit mRNA in the hippocampus was measured by qRT-PCR and normalized to the amount of Gapdh mRNA in each sample (C, mean ± SEM, n = 5; p > 0.05, Student's t test). D, Enrichment of NMDAR subunits in the synaptoneurosome fraction of the hippocampus of JIP1^WT and JIP1^TA mice was examined by immunoblot analysis. E, F, Primary JIP1^WT and JIP1^TA hippocampal neurons were fixed and processed for immunofluorescence analysis under nonpermeabilized (left) and permeabilized (right) conditions. GluN1 surface and intracellular expression was examined by confocal microscopy (E). Quantitation of the cell surface expression of GluN1 in JIP1^TA and JIP1^WT hippocampal neurons was performed using ImageJ software (F). Data are shown as mean ± SEM; n = 8∼10; **p < 0.01, Student's t test. G, The expression of cJun and cFos mRNA in the hippocampus of JIP1^WT and JIP1^TA mice was normalized to the amount of Gapdh in each sample (mean ± SEM, n = 5∼6). Statistically significant differences are indicated (**p < 0.01, Student's t test). H, Lysates prepared from the hippocampus of JIP1^WT and JIP1^TA mice were examined by immunoblot analysis with antibodies to phospho-ERK, ERK, phospho-CREB, CREB, KIF17, and β-Tubulin. The amount of phospho-ERK and phospho-CREB was quantitated (mean ± SEM, n = 5). Statistically significant differences are indicated (**p < 0.01, Student's t test).

To test functionally whether NMDAR signaling was increased in JIP1^TA mice compared with JIP1^WT mice, we examined EPSCs via whole-cell recordings of CA1 pyramidal cells in acute hippocampus slices. For CA1 pyramidal cells held under voltage clamp at −70 mV, the response to Schaffer collateral stimulation is primarily mediated by AMPARs. The NMDAR-mediated component of EPSCs is readily distinguished from the AMPAR component by measuring current responses at a membrane potential of +50 mV ∼30 ms after stimulation, when ∼90% of the AMPAR response has decayed (Liao et al., 1995; Myme et al., 2003). We found that the average NMDAR-mediated peak EPSC was 1.6-fold larger in JIP1^TA mice compared with JIP1^WT mice (t₍₃₁₎ = 2.41, p = 0.022; two-tailed unpaired Student's t test; Fig. 8A,B), whereas the average peak amplitude of the AMPAR-mediated EPSCs were similar in JIP1^TA and JIP1^WT mice (t₍₃₁₎ = 0.28, p = 0.77; two-tailed unpaired Student's t test; Fig. 8A,C). These findings were reflected in the NMDAR/AMPAR peak current ratio calculated for each cell tested. JIP1^WT mice had a NMDA/AMPAR ratio of 37 ± 4%, whereas JIP1^TA mice yielded a significantly larger ratio of 50 ± 4% (t₍₃₁₎ = 2.21, p = 0.038; two-tailed unpaired Student's t test; Fig. 8D). This analysis demonstrated that NMDAR signaling is increased in JIP1^TA hippocampal neurons compared with those of JIP1^WT mice. To confirm this conclusion, we examined NMDAR-stimulated gene expression in primary JIP1^TA and JIP1^WT hippocampal neurons. We found that NMDA-induced expression of brain-derived neurotrophic factor (Bdnf) mRNA (Ghosh et al., 1994; Tabuchi et al., 2000) and cFos mRNA (Bading et al., 1993; Xia et al., 1996) by JIP1^TA neurons were increased when compared with JIP1^WT neurons ([two-way ANOVA: genotype F_(1,29) = 70.26, p < 0.001; time F_(2,29) = 39.7, p < 0.001; genotype × time F_(2,29) = 14.91, p < 0.001; for Bdnf mRNA]; [two-way ANOVA: genotype F_(1,30) = 17.67, p < 0.001; time F_(2,30) = 182.1, p < 0.001; genotype × time F_(2,30) = 7,98, p < 0.001; for cFos mRNA]; Fig. 8E,F). Together, these data indicate that the increased NMDA-mediated signaling detected in the JIP1^TA hippocampus is due to enhanced NMDAR activity in individual neurons.

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Figure 8.

Increased synaptic NMDAR activity in hippocampal slices from JIP1^TA mice. A, Whole-cell voltage-clamp traces depicting typical EPSCs elicited by stimulating the Schaffer collaterals while recording CA1 pyramidal cells from JIP1^WT and JIP1^TA hippocampal slices. Strong blockade of NMDARs at a holding potential of −70 mV by magnesium isolates the AMPA component (bottom traces). The +50 mV upper traces primarily represent the NMDA component because the traces were recorded 30–50 ms after stimulation when ∼90% of the AMPAR response had decayed. The traces show the increase in the NMDAR-mediated component for the JIP1^TA group relative to JIP1^WT, whereas AMPAR mediated responses were not different. Traces depicted are averages of 20 sweeps for both NMDA and AMPAR-mediated components of JIP1^WT recorded from the same pyramidal neuron; 10 and 15 sweeps were used to produce the averages depicted for the NMDA and AMPAR-mediated components recorded from a JIP1^TA pyramidal neuron. B, C, Comparison of average NMDA and AMPAR currents. NMDAR-mediated currents (B) were significantly greater in the JIP1^TA group compared with the JIP1^WT group (mean ± SEM; n = 16 ∼ 17 cells; *p < 0.05, Student's t test), whereas average AMPAR-mediated currents (C) did not differ. D, NMDA to AMPAR current ratios were evaluated on a cell-by-cell basis. The JIP1^TA ratios (I_NMDA/I_AMPA) were larger than ratios measured from neurons in the JIP1^WT group (mean ± SEM; n = 16 ∼ 17 cells; *p < 0.05, Student's t test). E, F, NMDA-stimulated gene expression in primary cultures of JIP1^WT and JIP1^TA hippocampal neurons was studied by treating neurons with 100 μm NMDA plus 10 μm glycine. The expression of Bdnf (E) and cFos (F) mRNA was quantitated by qRT-PCR and normalized to Gapdh (mean ± SEM; n = 5∼6; ***p < 0.001, two-way ANOVA followed by Bonferroni's post hoc test).

JIP1-mediated JNK activation in locomotor, sensory and emotional responses

To address the possibility that increased NMDAR signaling in JIP1^TA mice compared with JIP1^WT mice may cause behavioral changes, we first performed a battery of basic behavioral tests of CNS function on JIP1^WT and JIP1^TA mice. We found that anxiety-related behavior was increased in JIP1^TA mice. For example, JIP1^TA mice in an elevated plus maze spent less time in the open arms, compared with JIP1^WT mice (t₍₁₈₎ = 2.79, p = 0.012; two-tailed unpaired Student's t test), with no changes in locomotor activity (t₍₁₈₎ = 0.76, p = 0.45; two-tailed unpaired Student's t test; Fig. 9A–C). Moreover, JIP1^TA mice spent significantly less time in the center (t₍₁₈₎ = 5.40, p < 0.001; two-tailed unpaired Student's t test) and more in the periphery (t₍₁₈₎ = 6.46, p < 0.001; two-tailed unpaired Student's t test) during an open-field test compared with JIP1^WT animals (Fig. 9D,E). Consistent with previous reports (Grillon et al., 1998), elevated anxiety in JIP1^TA mice was accompanied by an enhancement of the startle response to strong acoustic stimuli (two-way repeated-measures ANOVA: genotype F_(1,42) = 5.42, p = 0.035; stimulus F_(3,42) = 105.42, p < 0.001; genotype × stimulus = 9.25, p < 0.001; Fig. 9F). No changes in sensorimotor gating (pre-pulse inhibition) were observed (two-way repeated-measures ANOVA: genotype F_(1,28) = 0.13, p = 0.722; Fig. 9G). We also found that “fast” improvement in motor coordination on the accelerating rotarod was comparable between JIP1^WT and JIP1^TA mice. However, during the second day of rotarod training JIP1^TA mice did not display improved “slow” skill learning, unlike JIP1^WT mice, as indicated by significant genotype × trial interaction value (two-way repeated-measures ANOVA: genotype F_(1,98) = 4.84, p = 0.045), trial F_(7,98) = 7.73, p < 0.001; genotype × trial F_(7,98) = 3.34, p = 0.003; Fig. 9H). Together, these data demonstrate that JIP1^TA mice have normal sensory and motor activity and attention function. However, JIP1^TA mice displayed increased levels of anxiety-related behaviors and altered skill learning.

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Figure 9.

JIP1^TA mice display normal locomotor function, motor coordination, elevated anxiety-like behavior, and increased acoustic startle response. A–C, Results of elevated plus maze test. JIP1^TA mice show decreased time spent in open arms (A) and increased time spent in closed arms (B) relative to wild-type mice, indicative of elevated anxiety-like behaviors. In addition, JIP1^TA mice show normal activity as measured by total distance traveled (C). Data are shown as mean ± SEM. n = 10; **p < 0.01, Student's t test. D, E, Open-field test. JIP1^TA mice show increased anxiety-like behavior in an open-field test. Mice were allowed to explore an open field for 5 min. JIP1^TA mice spent more time in the periphery (D) and less time in the center region of the open field (E), both indicators of increased levels of anxiety-like behavior in this test. Data are shown as mean ± SEM. n = 10; ***p < 0.001, Student's t test. F, JIP1^TA mice showed an increased acoustic startle response for the 110 dB acoustic startle stimulus compared with JIP1^WT mice (mean ± SEM; n = 8; *p < 0.05, two-way repeated-measures ANOVA followed by Bonferroni's post hoc comparisons tests). G, No significant differences in PPI for the 74, 80, and 86 dB pre-pulse sound levels followed by a 110 dB startle stimulus were observed between JIP1^TA and JIP1^WT mice (mean ± SEM; n = 8; p > 0.05, two-way repeated-measures ANOVA followed by Bonferroni's post hoc test. H, JIP1^TA mice have normal balance and motor coordination, but impaired skill learning on the rotarod. Mice received four trials on day 1 (trials 1–4) and day 2 (trials 5–8). The duration of balance or latency to fall (4–40 rpm over 5 min) was recorded. Mice were trained on day 1 to establish baseline performance and retested 24 h later to measure skill learning. Both JIP1^TA and JIP1^WT mice exhibited increased skill in maintaining balance on the rotarod over the first four trials on day 1. On day 2, JIP1^TA mice failed to display motor coordination achieved after the day 1, indicative of impaired motor learning in the rotarod task. Data are shown as mean ± SEM; n = 8; *p < 0.05, two-way repeated-measures ANOVA followed by Bonferroni's post hoc test.

Improved extinction-resistant contextual fear memory in JIP1^TA mice

Contextual fear conditioning triggers JIP1-dependent JNK activation in the hippocampus (Fig. 4). Moreover, JNK activation in the hippocampus is implicated in some forms of hippocampus-dependent memory (Sherrin et al., 2011). We therefore compared JIP1^WT and JIP1^TA mice to determine whether JIP1-mediated JNK activation is required for the behavioral response to contextual fear conditioning. The mice received either “weak” (0.4 mA shock) or “strong” (0.8 mA shock) training and were then reexposed to the chamber 24 h later to assess long-term fear memory (Shalin et al., 2006). The two training procedures were used to adjust for nociceptive sensitivity and also to test whether a “weak” stimulation protocol similar to one that facilitated synaptic plasticity (cf. Fig. 5E) results in enhanced hippocampal memory in JIP1^TA mice. JIP1^TA and JIP1^WT mice showed no differences in freezing or activity during the exploration period before the foot-shock (data not shown), or after the 0.8mA foot-shock delivery (t₍₁₉₎ = 0.46, p = 0.65; two-tailed unpaired Student's t test; Fig. 10A, right). Significantly enhanced contextual freezing of JIP1^TA mice compared with JIP1^WT controls was found 24 h after “strong” training (Fig. 10A, left; mean percentage freezing: JIP1^TA = 85 ± 3%; JIP1^WT = 59 ± 4%; t₍₁₉₎ = 5.11, p < 0.001; two-tailed unpaired Student's t test). This enhancement of contextual fear was more pronounced in JIP1^TA mice when the “weak” paradigm was used (Fig. 10B; mean percentage freezing: JIP1^TA = 81 ± 4%; JIP1^WT = 44 ± 5%; t₍₂₆₎ = 5.26, p < 0.001; two-tailed unpaired Student's t test). We next investigated short-term memory by testing JIP1^TA and JIP1^WT mice immediately or 1 h after the “strong” conditioning paradigm. We found that JIP1^TA and JIP1^WT mice displayed similar responses in the both contextual tests (t₍₂₀₎ = 0.18, p = 0.85; 0 h after conditioning, two-tailed unpaired Student's t test; t₍₂₆₎ = 0.11, p = 0.75; 1 h after conditioning, two-tailed unpaired Student's t test; Fig. 10A, left). Therefore, JIP1^TA and JIP1^WT mice did not differ in exploration activity, nociceptive reaction to electric shock, postshock freezing response, or short-term fear memory. These findings also indicate that the increased anxiety phenotype observed with the JIP1^TA mice does not appear to fundamentally affect shock-induced and postshock behaviors, including contextual fear conditioning and learning (see also Fig. 11). Nevertheless, JIP1^TA mice exhibited increased long-term fear memory compared with JIP1^WT mice (Fig. 10A,B).

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Figure 10.

JIP1^TA mice display enhanced contextual fear and impaired fear extinction. A, “Strong” (0.8 mA electric shock) training demonstrated that JIP1^TA and JIP1^WT littermate mice exhibited similar contextual freezing when tested immediately after training or 1 h later, but the JIP1^TA mice froze more than JIP1^WT mice at 24 h after training (left). Foot-shock reactivity during fear-conditioning training did not significantly differ between JIP1^TA and JIP1^WT mice (right). Data are shown as mean ± SEM. n = 10 ∼ 11; ***p < 0.001, Student's t test. B, “Weak” (0.4 mA electric shock) training demonstrated that JIP1^TA mice (n = 14) exhibited contextual freezing that was similar to the “strong” training schedule, but JIP1^WT mice (n = 14) displayed significantly less contextual fear conditioning at 24 h after training. Data are shown as mean ± SEM. n = 14; ***p < 0.001, Student's t test. C, JIP1^TA and JIP1^WT littermate mice were infused with vehicle or the selective NMDAR antagonist APV (10 μg/ml) before “strong” (0.8 mA) contextual fear conditioning. The following day, there was a similar impairment in both genotypes in freezing levels to the conditioning context. Data are shown as mean ± SEM. n = 10; ***p < 0.001 vs JIP1^{WT+ veh}; n.s.; JIP1^{WT+ APV} vs JIP1^{TA+ APV}; two-way ANOVA followed by Bonferroni's post hoc test. D, JIP1^TA and JIP1^WT littermate mice were trained by “strong” (0.8 mA electric shock) contextual fear conditioning. Extinction began 24 h later and consisted of daily 3 min reexposures of mice to the conditioning context in the absence of shock. When compared with JIP1^WT littermates, JIP1^TA mice showed increased freezing behavior throughout extinction days 1–7 (E1–E7), indicating impaired extinction process in JIP1^TA mice. Data are shown as mean ± SEM. n = 10; *p < 0.05, ***p < 0.001; two-way repeated-measures ANOVA followed by Bonferroni's post hoc test. E, “Weak” (0.4 mA electric shock; left) and “strong” (0.8 mA; right) cued fear training, consisting of a single pair of cue (tone) and shock, demonstrated that JIP1^TA and JIP1^WT mice exhibited enhanced conditioned freezing to a cue (tone) when tested 24 h after training. Data are shown as mean ± SEM. n = 11; *p < 0.05, **p < 0.01, Student's t test.

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Figure 11.

JIP1^TA mice exhibit enhanced acquisition and reversal learning in the MWM test. A–C, JIP1^TA and JIP1^WT littermate mice learned the visible platform task (day 1 and 2), as indicated by reductions in escape time during training. The mice were then trained to find a hidden platform during the next 7 d. JIP1^TA mice showed faster escape latencies at days 6–9 of training compared with JIP1^WT littermates (A). A first probe test (day 10) was conducted 24 h after the completion of training. No significant differences in percentage time spent in the target quadrant (T) between JIP1^TA and JIP1^WT mice were observed (B). The mice were then subjected to 2 d of additional training (days 11–12) and a second probe trial was performed 24 h later. No significant differences between JIP1^TA and JIP1^WT mice were observed during second probe trial (C). Data are shown as mean ± SEM. n = 14; *p < 0.05, f(two-way repeated-measures ANOVA, followed by Bonferroni's post hoc test. D–F, Twenty-four hours after the second probe test, the platform was moved to the opposite quadrant in the pool and mice were trained for four trials (day 14, reversal learning). In this new setting, JIP1^TA mice displayed shorter escape time to find newly placed platform (NT) compared with JIP1^WT littermate mice (E). The probe test for reversal training was conducted 24 h after the completion of new platform training (day 15). Analysis of the time spent in the quadrants revealed that JIP1^TA mice spent significantly more time in the NT than JIP1^WT mice (F). Data are shown as mean ± SEM. n = 14; *p < 0.05, ***p < 0.001, two-way repeated-measures ANOVA (E) and two-way ANOVA (F) followed by Bonferroni's post hoc tests.

We then tested whether contextual fear memory is affected differentially in JIP1^TA and JIP1^WT mice after antagonism of the NMDARs. JIP1^TA and JIP1^WT mice were implanted with cannulae into the dorsal hippocampus and subjected to contextual fear conditioning. A selective NMDAR antagonist, APV (10 μg/ml; 0.5 ml) or solvent (aCSF) was infused into the dorsal hippocampus 15 min before training. Both JIP1^TA and JIP1^WT mice given APV showed substantially reduced freezing to context compared with mice that received aCSF before conditioning (two-way ANOVA: genotype F_(1,36) = 8.76, p = 0.0054; treatment F_(1,36) = 143.06, p < 0.001; genotype × treatment = 5.29, p = 0.027; Fig. 10C). However, no differences between APV-treated JIP1^TA mice and APV-treated JIP1^WT mice were observed (Bonferroni post hoc test: p = 0.62; Fig. 10C), indicating that the memory-facilitating effects observed in JIP1^TA were mediated via activation of NMDARs. Together, these experiments show that blockade of JIP1-mediated JNK activation can improve contextual learning induced by a relatively mild learning protocol and that enhanced NMDAR function is required for this facilitatory effect of JIP1^TA mutation on learning.

Previous studies have demonstrated that activation of hippocampal NMDAR regulates fear extinction (Szapiro et al., 2003; Suzuki et al., 2004; Leaderbrand et al., 2014) and that NMDAR blockade can prevent fear extinction in a variety of fear-related tasks (Santini et al., 2001; Sotres-Bayon et al., 2007). Therefore, we extended our cognitive evaluation of JIP1^TA mice by assessing contextual fear extinction to further assess the link of JIP1-JNK activation through NMDARs. Conditioned JIP1^TA and JIP1^WT mice were subjected to brief (3 min) daily extinction trials by nonreinforced placement in the training context for 7 d after contextual conditioning. During the extinction trials, JIP1^TA mice exhibited almost unchanged freezing responses, indicating nearly fully impaired extinction compared with JIP1^WT mice (repeated-measures ANOVA: genotype F_(1,108) = 388.76, p < 0.001; time F_(6,108) = 36.26, p < 0.001; F_(6,108) genotype × time = 25.35, p < 0.001; Fig. 10D). Overall, these results indicate that the enhanced contextual fear observed in JIP1^TA mice is strongly resistant to extinction.

Finally, cue-dependent fear conditioning was assessed in JIP1^TA mice and JIP1^WT controls. As with contextual fear conditioning, mice received either a “strong” or a “weak” training protocol, both consisting of a single pairing of tone and shock at 0.8 and 0.4 mA, respectively. In both protocols, JIP1^TA mice, compared with JIP1^WT controls, displayed significantly more freezing when reexposed to the tone 24 h after training (Fig. 10E, left; mean percentage freezing: “weak” cued test- JIP1^TA = 66 ± 3%; JIP1^WT = 44 ± 4%; t₍₂₀₎ = 3.71, p = 0.01; two-tailed unpaired Student's t test; Fig. 10E, right; mean percentage freezing: “strong” cued test- JIP1^TA = 70 ± 3%; JIP1^WT = 55 ± 4%; t₍₂₀₎ = 2.65, p = 0.015; two-tailed unpaired Student's t test), indicating that JIP1^TA mice display memory enhancement in the fear learning tasks in a manner involving both amygdala- and hippocampus-dependent memory systems.

Improved spatial learning in JIP1^TA mice

We next tested JIP1^TA and JIP1^WT mice using the MWM protocol, a hippocampus-dependent spatial memory task (Morris et al., 1982). During the hippocampus-independent visible portion of the training, both JIP1^TA and JIP1^WT mice readily learned to find the marked platform (Fig. 11A). Mice were then trained to swim to a hidden platform located in a fixed location of the pool (Fig. 11A,D; target quadrant, T). JIP1^TA mice had significantly decreased escape latencies compared with JIP1^WT mice on days 6–9 and day 12 of training (two-way repeated-measures ANOVA: genotype F_(1,208) = 11.03, p = 0.0049; time F_(8,208) = 21.01, p < 0.001; genotype × time F_(8,208) = 0.74, p = 0.65; Fig. 11A). However, JIP1^TA and JIP1^WT mice did not differ in the time spent in the platform-containing quadrant during probe trials on day 10 (Fig. 11B; 36 ± 3% of time in quadrant T for JIP1^TA; 35 ± 2% JIP1^WT; t₍₂₆₎ = 0.27, p = 0.783; two-tailed unpaired Student's t test) and day 13 (Fig. 11C; 38 ± 5% of time in quadrant T for JIP1^TA mice; 36 ± 3% JIP1^WT mice; t₍₂₆₎ = 0.34, p = 0.734; two-tailed unpaired Student's t test). Although JIP1^TA mice did not display preference for the target quadrant during probe trials, the decrease in escape latency during training suggests that the presence of the JIP1 Thr¹⁰³Ala mutation appears to affect gradual learning of the hidden platform MWM task moderately.

To test whether JIP1^TA mice display enhanced fast spatial learning, we performed a reversal of the hidden platform in the MWM. The hidden platform was moved to the opposite quadrant of the pool (new target quadrant, NT) and the mice were trained to swim to this new location for four trials separated by 15–20 min (Fig. 11D). JIP1^TA mice learned significantly faster to swim to the new platform location compared with control mice (two-way repeated-measures ANOVA: genotype F_(1,78) = 16.37, p = 0.0012; time F_(3,78) = 1.98, p = 0.13; genotype × time F_(3,78) = 1.86, p = 0.15; Fig. 11E). Moreover, the JIP1^TA mice displayed increased preference for the NT during a probe trial given on probe day 15 (Fig. 11F; time spent in NT: 41 ± 2% for JIP1^TA; 23 ± 4% for JIP1^WT; t₍₂₆₎ = 4.02, p < 0.001; two-tailed unpaired Student's t test). This enhancement in spatial reversal learning of the new platform location was accompanied by a decrease in the percentage of time JIP1^TA mice spent searching for the platform in the previously correct quadrant (O; t₍₂₆₎ = 2.34, p = 0.028; two-tailed unpaired Student's t test; Fig. 11F). These data indicate that the Thr¹⁰³Ala mutation in JIP1 allows for improved fast spatial learning.

JNK binding is required for JIP1-mediated NMDAR regulation of learning and memory

To confirm that JIP1-mediated JNK activation plays a critical role in NMDAR-dependent, hippocampus-dependent learning and memory, we tested an independent mouse model of defective JIP1-mediated JNK activation: JIP1 lacking the JNK binding domain (JBD). To create a mouse model lacking the JBD of JIP1 (JIP1^ΔJBD mice), the core of the JBD (Leu¹⁶⁰-Asn¹⁶¹-Leu¹⁶²) mediating a hydrophobic interaction of JIP1 with JNK (Whitmarsh et al., 2001; Heo et al., 2004) was replaced with Gly¹⁶⁰-Arg¹⁶¹-Gly¹⁶² in JIP^ΔJBD mice (Fig. 12A,B). Immunoblot analysis of brain extracts from JIP1^WT and JIP1^ΔJBD mice indicated similar levels of JIP1 protein expression (Fig. 12C). To establish that the ΔJBD mutation blocks JIP1-mediated JNK activation in vivo, we compared kainate-induced excitotoxicity in the hippocampus of JIP1^WT and JIP1^ΔJBD mice. This analysis demonstrated that kainate caused similar increases in cJun expression in the DG of JIP1^WT and JIP1^ΔJBD mice, but kainate-stimulated cJun phosphorylation was markedly suppressed in JIP1^ΔJBD mice compared with JIP1^WT mice (Fig. 12D,E). These data confirm that JIP1^ΔJBD mice represent a model of defective JIP1-mediated JNK signaling.

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Figure 12.

Suppression of kainate-induced JNK activity in the hippocampus of JIP1^ΔJBD mice. A, B, A targeting vector was designed to replace JIP1 residues Leu¹⁶⁰-Asn¹⁶¹-Leu¹⁶² with Gly¹⁶⁰-Arg¹⁶¹-Gly¹⁶² in exon 3 of the Jip1 gene by homologous recombination in ES cells. The floxed Neo^R cassette inserted in intron 3 and used for selection was deleted with Cre recombinase. H, HindIII restriction enzyme. C, Lysates prepared from the cerebral cortex of Jip1^+/+ (WT) and Jip1^ΔJBD/ΔJBD (ΔJBD) mice were examined by immunoblot analysis using antibodies to JIP1 and β-Tubulin. D, E, JIP1^WT and JIP^ΔJBD mice were treated without and with kainate. Representative sections of the DG stained (green) with antibodies to phospho-cJun (D) or cJun (E) are presented. DNA was stained with DAPI (red). Scale bar, 75 μm.

We then examined contextual and cued fear conditioning to assess the effect of the JIP1^ΔJBD mutation on learning and memory. The JIP1^ΔJBD mice displayed a significantly increased conditioned freezing response in both learning tasks compared with the JIP1^WT mice when tested at 24 h after training (Fig. 13A, left: mean percentage contextual freezing; JIP1^WT = 58 ± 3%; JIP1^ΔJBD = 89 ± 3%; t₍₁₈₎ = 6.30, p < 0.001; two-tailed unpaired Student's t test; Fig. 13A, right: mean percentage cued freezing; JIP1^WT = 51 ± 1%; JIP1^ΔJBD = 69 ± 6%; t₍₂₀₎ = 2.97, p = 0.007; two-tailed unpaired Student's t test), a result very similar to that observed for the JIP1^TA mice (Fig. 10). JIP1^ΔJBD mice exhibited enhanced learning in the MWM (two-way repeated-measures ANOVA: genotype F_(1,162) = 26.04, p < 0.001; time F_(8,162) = 126.7, p < 0.001; genotype × time _(8,162) = 1.75, p = 0.84), and spent significantly more time in the target quadrant compared with control JIP1^WT mice when subjected to probe trials on day 9 (t₍₁₈₎ = 4.02, p < 0.001; Fig. 13C, left; 41 ± 2% of time in quadrant T for JIP1^ΔJBD; 32 ± 1% of time in quadrant T for JIP1^WT) and day 13 (Fig. 13C, right; 48 ± 4% of time in quadrant T for JIP1^ΔJBD; 36 ± 3% of time in quadrant T for JIP1^WT; t₍₁₈₎ = 2.44, p = 0.027; two-tailed unpaired Student's t test). This was an unexpected finding because JIP1^TA mice did not show enhanced memory retention in the hidden platform MWM task (cf. Fig. 11B,C). The larger phenotype in the JIP1^ΔJBD mice in the MWM compared with the JIP1^TA mice may result from a greater effect of the JNK-binding site mutation on JIP1-mediated JNK activation than the mutation of the T103 phosphorylation site on JIP1.

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Figure 13.

Disruption of the JBD (ΔJBD) on JIP1 causes enhanced associative learning. A, Contextual and cued fear conditioning of JIP1^ΔJBD and JIP1^WT mice consisted of one exposure to cue (context + tone) and 0.8 mA shock (mean ± SEM; n = 10∼11; **p < 0.01, Student's t test ***p < 0.001, Student's t test). B, C, MWM tests of mean latencies to escape to a visible (days 1–2) or a hidden platform (days 3–12) are presented for JIP1^ΔJBD or JIP1^WT mice (B). Probe trials were performed on days 9 and 13 of water maze training (C). JIP1^ΔJBD mice spent significantly longer time in the target quadrant compared with JIP1^WT littermates (mean ± SEM; n = 10; *p < 0.05; **p < 0.01; ***p < 0.001, two-way repeated-measures ANOVA (B) and two-way ANOVA (C) followed by Bonferroni's post hoc tests). D, The water maze platform was moved to the opposite quadrant in the pool and mice were trained for four trials (day 14, reversal learning). The probe test for reversal training was conducted 24 h after the completion of new platform training (day 15). Analysis of the time spent in the quadrants during the probe trial revealed that JIP1^ΔJBD mice spent significantly more time in the NT than JIP1^WT mice (mean ± SEM; n = 10; ***p < 0.001, two-way ANOVA followed by Bonferroni's post hoc test). E, Hippocampus lysates of JIP1^WT, JIP1^TA, and JIP1^ΔJBD mice were examined by immunoblot analysis by probing with antibodies to NMDAR subunits and β-Tubulin. F, The amount of phospho-ERK in hippocampus lysates of naive JIP1^WT and JIP1^ΔJBD mice was quantified by multiplexed ELISA and normalized to the amount of ERK2 in each sample. Data are shown as mean ± SEM. n = 5; *p < 0.05, Student's t test.

We then examined reversal learning by moving the hidden platform to the opposite quadrant (Fig. 13D, left). Similar to JIP1^TA mice, the JIP1^ΔJBD mice showed shorter latencies than control mice in finding the new platform location during a 1 d trial period (data not shown). Moreover, JIP1^ΔJBD mice spent significantly more time in the NT compared with JIP1^WT control mice (Fig. 13D, right; mean percentage of time spent in the NT was 49 ± 3%, for JIP1^ΔJBD; 28 ± 4% for JIP1^WT; t₍₁₈₎ = 4.21, p < 0.001; two-tailed unpaired Student's t test). Furthermore, like JIP1^TA mice, we found significantly increased expression of GluN1, GluN2A, and GluN2B in the hippocampus of JIP1^ΔJBD mice compared with hippocampi from JIP1^WT mice (Fig. 13E) and increased ERK activation (t₍₈₎ = 2.57, p = 0.033; two-tailed unpaired Student's t test; Fig. 13F).

Together, these analyses of JIP1^TA and JIP1^ΔJBD mice confirm that loss of JIP1-mediated JNK activation enhances NMDA-dependent hippocampus-dependent memory.