Astrocytic Ca2+ signals are required for the functional integrity of tripartite synapses
- Mika Tanaka†1,
- Pei-Yu Shih†1,
- Hiroshi Gomi2,
- Takamasa Yoshida1,
- Junichi Nakai1, 3,
- Reiko Ando1,
- Teiichi Furuichi1, 5,
- Katsuhiko Mikoshiba1, 4,
- Alexey Semyanov1Email author and
- Shigeyoshi Itohara1Email author
© Tanaka et al.; licensee BioMed Central Ltd. 2013
Received: 28 November 2012
Accepted: 25 January 2013
Published: 28 January 2013
Neuronal activity alters calcium ion (Ca2+) dynamics in astrocytes, but the physiologic relevance of these changes is controversial. To examine this issue further, we generated an inducible transgenic mouse model in which the expression of an inositol 1,4,5-trisphosphate absorbent, “IP3 sponge”, attenuates astrocytic Ca2+ signaling.
Attenuated Ca2+ activity correlated with reduced astrocytic coverage of asymmetric synapses in the hippocampal CA1 region in these animals. The decreased astrocytic ‘protection’ of the synapses facilitated glutamate ‘spillover’, which was reflected by prolonged glutamate transporter currents in stratum radiatum astrocytes and enhanced N-methyl-D-aspartate receptor currents in CA1 pyramidal neurons in response to burst stimulation. These mice also exhibited behavioral impairments in spatial reference memory and remote contextual fear memory, in which hippocampal circuits are involved.
Our findings suggest that IP3-mediated astrocytic Ca2+ signaling correlates with the formation of functional tripartite synapses in the hippocampus.
Astrocytes exhibit dynamic Ca2+ mobilization via an inositol 1,4,5-trisphosphate (IP3)-induced Ca2+ release (IICR)-dependent mechanism [1, 2]. The role of astrocytic Ca2+ dynamics, however, has been debated over the last decade . Some studies report intact hippocampal short-and long-term plasticity in situ in IP3 receptor (IP3R)-type 2 knockout mice, in which hippocampal astrocytes completely lack IICR [4, 5], whereas others report that these mice show no cholinergic-induced long-term potentiation (LTP) in vivo [6, 7]. In situ evidence also indicates that hippocampal LTP depends on D-serine release from astrocytes under the control of astrocytic Ca2+ signaling . A number of reports describe spontaneous or stimulation-evoked Ca2+ activity in astrocytes in vivo [9–12], but still very little is known about the in vivo significance of astrocytic Ca2+ mobilization [6, 7], especially in higher brain functions such as learning and memory. In the present study, we generated a new mouse model in which astrocytic IICR is attenuated, and examined the role of astrocytic Ca2+ signaling at the level of both the tripartite synapse and behavior.
Attenuated agonist-evoked IICR in astrocytes by IP3 buffering with a glutathione-S-transferase (GST)-IP3 sponge
We then examined whether the GST-fused IP3 sponge was expressed in the same manner as lacZ in the DTg mice. Double immunolabeling detected the GST-IP3 sponge in lacZ-positive astrocytes (Figure 1, H to J). The GST-IP3 sponge was also detected by glutathione-trapping in the brains of the DTg mice (Additional file 3: Figure S2A). Quantification of the GST-IP3 sponge in the brain (Additional file 3: Figure S2, B to E) revealed that GST-IP3 sponge expression could be repressed by doxycycline (Dox) treatment (25 μg/ml in the drinking water) initiated either before birth (indicated as “Dox”) or at 1 mo of age (indicated as “Dox*”). Each astrocyte in the DTg mice was estimated to contain approximately 3800 GST-IP3 sponge molecules (see Additional file 4: Additional Methods). When transgene expression was inhibited in DTg mice by Dox administration initiated before birth, the induced expression of lacZ did not reach the same level as that in DTg mice without Dox treatment, even 8 weeks after Dox withdrawal (data not shown). Thus, in the following experiments, we used DTg mice without Dox treatment to obtain maximal expression of the IP3 sponge for attenuation of astrocytic IICR.
Activation of Gq-protein coupled receptors triggers IICR in astrocytes [4, 18]. To examine whether the agonist-evoked IICR is affected by GST-IP3 sponge expression, S-3,5-dihydroxyphenylglycine (DHPG), a selective metabotropic glutamate receptor agonist, was puff-applied to CA1 astrocytes expressing G-CaMP2 in hippocampal slices from either control or TTg mice. Ca2+ imaging of the astrocytic processes (Figure 2, G to N) revealed that the duration (Figure 2O) and area under the curve (Figure 2P) of Ca2+ events of the DHPG-evoked Ca2+ responses were both significantly attenuated in the TTg mice (F5,3418 = 19.95, P < 0.001, two-way ANOVA for Figure 2O; F5,3418 = 22.79, P < 0.001, two-way ANOVA for Figure 2P; number of cells, 13 for each genotype; number of animals, 5 for Ctrl and 4 for TTg; number of events, see Additional file 5: Table S2). Baseline Ca2+ activity without glutamate puffs was not significantly altered in TTg mice (Figure 2, O and P, No puff). These findings indicate that agonist-evoked IICRs in situ were significantly attenuated by GST-IP3 sponge expression in astrocytes.
Reduced synaptic coverage by astrocytic processes in DTg mice
Enhanced glutamate spillover at CA1-CA3 synapses in DTg mice
Changes in glutamate spillover could affect synaptic transmission and presynaptic release probability by acting on presynaptic receptors in hippocampal synapses. We detected no significant differences, however, in the input–output relationship (Additional file 7: Figure S4A) and in the paired-pulse facilitation (Additional file 7: Figure S4B) of field excitatory postsynaptic potentials in the hippocampal CA1 region of DTg mice, suggesting a lack of presynaptic changes with these stimulation protocols. Glutamate spillover during high-frequency burst stimulation could recruit additional synaptic and extrasynaptic N-methyl-D-aspartate receptors (NMDARs) [23, 24]. This process is limited by perisynaptic transporters and could thus be enhanced in DTg mice. Therefore, we compared EPSCs mediated by NMDARs (EPSCNMDAR) in response to a single stimulus and a train of 5 stimuli at 100 Hz (Figure 4D). Consistent with enhanced glutamate spillover, EPSCNMDAR induced by high frequency stimulation normalized to a single stimulus EPSCNMDAR was enhanced in DTg mice (Figure 4E, P = 0.045, unpaired t test).
Impaired spatial reference memory and remote contextual fear memory in DTg mice
In the fear-conditioning test, DTg mice and WT mice exhibited an equivalent level of contextual and cued fear memory 1 and 2 d after training (Figure 5F). When assessed for remote fear memory 30 d post-training, however, DTg mice exhibited significantly reduced contextual fear memory (Figure 5G, P = 0.019, unpaired t test), whereas DTg and WT mice froze at similar levels when assessed for cued fear memory at 31 d (Figure 5G, P = 0.156, unpaired t test). DTg mice treated with Dox showed no significant defect in the recent or remote fear-conditioning tests (Figure 5, I and J). All mice tested showed comparable footshock sensitivity (Figure 5, H and K). These data suggest that GST-IP3 sponge expression in the astrocytes of the DTg mice impairs the establishment and/or retrieval of remote contextual fear memory, which is thought to involve interaction/communication between the hippocampus and neocortex after the formation of recent memory in the hippocampus [26–28].
The IP3 sponge, a novel recombinant hyperaffinity IP3 absorbent , inhibits IICR in cultured mammalian cells, starfish oocytes, and Drosophila[13, 29, 30]. In the present study, we generated DTg mice in which the GST-IP3 sponge was expressed in astrocytes using the Tet-OFF system . This transgenic mouse system enabled us to induce the expression of the lacZ marker protein in approximately 90% of S100B-positive astrocytes in the hippocampal CA1 region of the DTg mice. Ca2+ imaging of hippocampal slices from transgenic mice expressing G-CaMP2 confirmed that agonist-evoked IICR was attenuated in the processes of GST-IP3 sponge-positive astrocytes. Thus, we obtained a mouse model in which astrocytic IICR was attenuated. Analyses of the DTg mice revealed 1) a significant reduction in the astrocyte coverage of asymmetric synapses in the hippocampal CA1 region, 2) enhanced glutamate spillover at CA1-CA3 synapses during high-frequency activity, and 3) impaired spatial reference memory and remote contextual fear memory.
IICR-dependent regulation of astrocytic ensheathment of synapses provides new insight into the controversy surrounding whether astrocytic Ca2+ signaling affects neuronal functions. These findings raise intriguing possibilities regarding neuron-astrocyte interactions: when the synapse releases glutamate on metabotropic glutamate receptors in the surrounding astrocyte, the level of Ca2+ activity in astrocytic processes is maintained, providing high astrocytic coverage of the synapse. An inactive synapse would then not have astrocytic coverage, allowing for neurotransmitter diffusion in and out of the synaptic cleft. Thus, our data provide a possible mechanism for activity-dependent regulation of astrocytic coverage in the tripartite synapse.
Indeed, astrocytic processes are considered very plastic [32–37], as is astrocytic coverage of synapses [38, 39]. The dynamic motility of astrocytic processes is essential for astrocytes to modulate synaptic activity, but its regulation in vivo remains largely unknown. Glutamate causes filopodia formation in cultured hippocampal astrocytes , which is mediated by metabotropic glutamate receptors . Metabotropic glutamate receptor-activation in astrocytes in vitro [41–44] and in situ  leads to an increase in intracellular Ca2+ concentrations through the release from intracellular stores. Our results provide a link between IICR and plasticity of the astrocytic processes in vivo. The downstream cascade leading to changes in the morphology of astrocytic processes, however, remains to be clarified, and might involve regulation of the organization and assembly of the actin cytoskeleton in astrocytes . IICR in the growth cone acts on downstream effectors to regulate microtubule assembly and promote neurite extension . Microtubule networks and actin networks might contribute to the motility of peripheral astrocytic processes in vivo. Moreover, the Ca2+ concentration regulates the migration of astrocytoma cells by forming or disassembling focal adhesions [44, 45]. Local concentrations of Ca2+ are further suggested to be involved in filopodia formation by regulating focal adhesions . These mechanisms might cooperatively contribute to the structural integrity of tripartite synapses.
Several reports suggest Ca2+-dependent release of glutamate and D-serine from astrocytes [6–8, 47–49]. Both are co-agonists of NMDA receptors. Therefore, reduced Ca2+ activity in astrocytes might decrease the activation of NMDA receptors by those gliotransmitters during synaptic transmission. In contrast, we found that high-frequency stimulation in DTg mice increases the NMDA receptor current in CA1 pyramidal neurons, which correlates with enhanced glutamate spillover. Recent reports suggest that NMDA receptors located at synaptic and extrasynaptic sites have distinct functional roles [24, 50]. Spillover can actually increase the proportion of extrasynaptic NMDA receptors activated during burst firing, affecting hippocampal-based learning. In addition, glutamate spillover leads to an increase in intersynaptic crosstalk. The increased intersynaptic crosstalk could impair the independent operation of hippocampal synapses and thus affect synaptic characteristics, such as the spatial precision of synaptic inputs , which might also be important for learning and memory. We cannot exclude the possibility that glutamate spillover during burst firing increases release probability by activating presynaptic NMDA receptors, which leaves open the possibility that reduced astrocytic coverage has presynaptic effects as well as postsynaptic effects. In the present study, however, it is unlikely that presynaptic mGluRs were involved in the enhanced NMDA receptor currents. NMDA receptor currents were recorded in the presence of S-MCPG (200 μM), which blocks Type I and Type II mGluRs. Activation of Type III mGluRs by enhanced glutamate spillover decreases the release probability at CA3-CA1 synapses with Shaffer collaterals . If this were the case, the observed potentiation of the NMDA receptor current could be underestimated in GST-IP3 sponge-expressing animals. These and other effects of enhanced spillover on the hippocampal network should be addressed in future studies.
Concerning changes in long-term plasticity in DTg mice, we found that there were no significant differences in long-term potentiation (LTP), long-term depression (LTD), and depotentiation induced by conventional protocols in situ (i.e., 2 tetanic stimulations , 5 theta-burst stimulations (TBS) , and 3 TBS for LTP ; low-frequency stimulation (LFS)  and paired pulse-LFS  for LTD; and 2 tetanic stimulations followed by LFS for depotentiation ; data not shown). Despite these findings, our results indicate that enhanced glutamate spillover in the hippocampus correlates with impaired learning and memory in DTg mice, very likely by perturbing the independent operation of hippocampal synapses . Indeed, if LTP can be effectively triggered, but in the ‘wrong’ population of synapses, the memory still can be potentially affected.
The normal recent context fear memory in DTg mice contrasts with the impaired spatial reference memory in these mice. This discrepancy can be reconciled by the fact that spatial reference memory evaluated in the water maze is not associated with contextual fear memory [56–58] and each of these distinct types of memories have different underlying mechanisms . Although the impairment of remote contextual fear memory in DTg mice indicates miscommunication between the hippocampus and cortical areas [26–28], our result does not exclude the possibility that the anterior cingulate cortex, in which GST-IP3 sponge expression in the astrocytes was also observed (Figure 1C and data not shown), is solely responsible for the phenotype [27, 60, 61].
Generation of GST-IP 3 sponge-TetO-nls-LacZ (Tg1) and GLT-1-tTA (Tg2) transgenic mice
All experimental protocols were approved by the RIKEN Institutional Animal Care and Use Committee. For the Tg1 DNA construct, coding sequences of the GST-IP3 sponge  and nls-LacZ , together with splicing signals derived from the pMSG vector (GE Healthcare), were inserted downstream of the bidirectional tetracycline-Operator (TetO) element-dependent promoters of the pBI Tet vector (Clontech). For the Tg2 DNA construct, the tTA coding sequence from the pTet-Off vector (Clontech), with splicing signals derived from the pMSG vector (GE Healthcare), was inserted using a Red/ET Recombination system (Gene Bridges) into a bacterial artificial chromosome clone, RP23-361H22 (BAC PAC Resources), containing the GLT-1 (Slc1a2) gene to replace the first ATG of the GLT-1 coding region. These constructs were digested away from the prokaryotic sequence, purified, and individually injected into the pronuclei of C57BL/6-fertilized embryos to generate transgenic offspring. Each founder line was backcrossed with C57BL/6 mice and maintained in this genetic background.
Astrocyte Ca2+ imaging with G-CaMP2
Transverse hippocampal slices were prepared from 5- to 6-mo-old Ctrl mice carrying tetO-G-CaMP2 and GLT-1-tTA (Tg2), and TTg mice carrying GST-IP 3 sponge-TetO-nls-LacZ (Tg1), tetO-G-CaMP2 and GLT-1-tTA (Tg2) in accordance with RIKEN regulations. Animals were anesthetized with 2-bromo-2-chloro-1,1,1-trifluroethane and decapitated. The brain was exposed, chilled with ice-cold solution containing (in mM): 75 sucrose, 87 NaCl, 2.5 KCl, 0.5 CaCl2, 1.25 NaH2PO4, 7 MgCl2, 25 NaHCO3, 1 Na-ascorbate, and 11 D-glucose. Hippocampi from both hemispheres were isolated and placed in an agar block. Transverse slices (350-400 μm) were cut with a vibrating microtome (Microm HM 650V, Thermo Fisher Scientific Inc.) and left to recover for 30 min at 34°C and then at room temperature for 1 h in an interface chamber with storage solution containing (in mM): 127 NaCl, 2.5 KCl, 1.25 NaH2PO4, 1 MgCl2, 1 CaCl2, 25 NaHCO3, and 25 D-glucose. The slices were then transferred to the recording chamber and continuously perfused with recording solution containing (in mM): 127 NaCl, 2.5 KCl, 1.25 NaH2PO4, 1 MgCl2, 2 CaCl2, 25 NaHCO3, and 25 D-glucose. All solutions were saturated with 95% O2 and 5% CO2. Osmolarity was adjusted to 300 ± 5 mOsm.
Hippocampal slices were transferred to the recording chamber mounted on the stage of the Olympus BX-61 equipped with differential interference contrast optics and a water immersion objective lens (60x, NA = 0.9, Olympus) superfused with artificial cerebrospinal fluid (ACSF). A mode-locked tunable 720–930 nm laser Chameleon XR (Coherent) was used as the excitation source. Fluorescence was collected using photomultiplier tubes (Hamamatsu). Serial scanning of slices was tuned to an 890-nm wavelength at 1 Hz and emitted green fluorescence was collected through a 495–540 nm bandpass filter. Astrocytes were selected for data analysis if they emitted G-CaMP2 fluorescence, and spontaneous Ca2+ transients were recorded during the first 5 min of each recording. Cells with frequent (> 0.0167 Hz) somatic Ca2+ activity were excluded. Stimulation-induced Ca2+ transients were initiated by pressure-ejection of 200 μM DHPG in ACSF containing 50 μM Alexa594 (Molecular Probes) through a glass micropipette (2–3 μm diameter). The puff pipette was always kept 30 μm away from and 100 μm above the recorded astrocyte. Two 5-min long recordings were made for a long puff time (500 ms) and a short puff time (100 ms) in a random sequence. DHPG was applied four times at 1-min intervals at 1 min after the beginning of each 5-min long recording period.
Post-calcium imaging immunohistochemistry and confocal imaging
To confirm the expression of G-CaMP2 and the GST-IP3 sponge in the recorded astrocytes, slices from TTg mice were fixed with 4% paraformaldehyde immediately after recording and then processed for immunostaining using the anti-GFP antibody (for G-CaMP2) and anti-β-galactosidase as described in the Additional Methods (Additional file 4). Confocal images were acquired with an Olympus FV1000 confocal microscope. Astrocytes that showed double immunolabeling were recorded through 10x and 20x objectives and a single scan was performed by alternating the excitation wavelengths between 543 nm (G-CaMP2) and 488 nm (lacZ). Acquired images were analyzed using FluoView (Olympus) and ImageJ (a public domain Java image processing program by Wayne Rasband).
Data analysis for two-photon Ca2+ imaging
Two-photon Ca2+ imaging data was analyzed using a custom-written algorithm in MATLAB (MathWorks). Statistical analysis was performed with SPSS (IBM). Time series of fluorescence changes were standardized along the time axis pixel-by-pixel with subtraction of the mean and division of the SD. The images at each time were then flattened by Gaussian filter (4 pixels, σ = 2.0) to reduce the shot noise of the imaging device. We calculated the SD of the filtered image stacks along the time axis pixel-by-pixel and detected changeable areas that exceeded a criterion (from mean + 10SD to + 12SD). Those areas were denoised and smoothed by morphologic operations, and then identified as regions of interest (ROIs). The soma area was distinguished from process regions that we used as ROIs. The standardized time series were rescaled to original fluorescence changes pixel-by-pixel with multiplication of the original SD and addition of the original mean. We created time traces by pixel-averaging within each ROI. The mean and SD of time points less than median + 1SD was defined as the baseline and base SD of the time trace, respectively. Time traces were smoothed by low-pass filter (cutoff frequency, 0.2 Hz). Ca2+ events were identified as follows: We set two criteria to identify Ca2+ events: baseline + 1-base SD line (first criterion) and baseline + 2-base SD line (second criterion). Traces with peaks larger than the second criterion were considered candidate events. If the trace fell below the first criterion before and after the peak, the first points were defined as the start and end points of one event, respectively. Time duration from the start to the end point was defined as one event duration. The fractional change in fluorescence intensity was defined as ΔF/F0 = (F – F0) / F0, where F0 was the baseline and F is the time trace. Event areas were computed with summation of ΔF/F0 during the event duration. Durations and event areas of individual Ca2+ events were averaged over events, trials, and samples under each puff condition. The durations and event areas were tested using two-way ANOVA and multiple comparisons with Bonferroni’s correction.
Mice were deeply anesthetized by intraperitoneal injection of sodium pentobarbital (0.1 mg/g body weight). After transcardial perfusion with 10 ml saline solution, the brains were fixed by perfusion with 100 ml 2% paraformaldehyde and 2.5% glutaraldehyde in 0.1 M cacodylate buffer (pH 7.3) at 4°C. Brain tissues were dissected into small blocks (~3-mm thick) and postfixed in the same fixative overnight at 4°C. Tissue blocks were coronally sliced (200-μm thick) on a DTK-100 microslicer (Dosaka) and postfixed with 1% osmium tetroxide in 0.1 M cacodylate buffer at 4°C for 1 h. Tissue slices were stained with 1% uranyl acetate at room temperature for 1 h and then dehydrated, infiltrated, and embedded in plastic resin. Semi-thin (590-nm thick) sections were cut with an Ultratrim Diatome (Nisshin EM) on an Ultracut E Ultramicrotome (Reichert-Jung) and stained with 0.25% toluidine blue. Stained sections were viewed with a BX50 microscope (Olympus) and corresponding small areas (~0.5 x 1.0 mm) of the hippocampal CA1 region in each sample were trimmed. Ultrathin (90-nm-thick) sections were cut with an Ultra 45° Diatome (Nisshin EM) on an ultramicrotome, stained with 4% uranyl acetate and then with 0.4% lead citrate, and subjected to electron microscopy analysis in a JEM 1010 (JEOL Company) at an acceleration voltage of 80 kV. Electron micrographs were obtained from the middle one-third of the CA1 stratum radiatum of the dorsal hippocampus (approximately coronal section 300) . Electron microscopy pictures at a magnification of 15,000x were scanned at a resolution of 720 dpi with an ES-2200 image scanner (Epson) to acquire the digital image and synaptic morphology was analyzed.
Astrocytic coverage of synapses and synaptic density
Asymmetric synapses, representing excitatory terminals of Schaffer collaterals, were evaluated in the stratum radiatum subfield of the CA1 region. Astrocytic coverage of synapses was classified into two types: synapses without astrocytic contact and synapses with astrocytic contact. Percentages of each type of synapse and the synaptic density (number of synapses/μm2 neuropil) were assessed using 20 electron micrographs from two mice of each genotype (5-mo-old for Figure 3C and 11-mo-old for Figure 3D), two sample blocks per animal, and five randomly selected pictures per sample block.
Recording of STCs in hippocampal astrocytes
Hippocampal slices were prepared from 4- to 5-week-old WT and DTg mice as described above.
Whole-cell recording from astrocytes
Whole-cell recordings were made with a Multiclamp 700B amplifier (Axon Instruments). The patch pipettes (3–7 MΩ) were filled with solution containing (in mM) 135 KCH3SO3, 10 HEPES, 10 Na-phosphocreatine, 4 MgCl2, 4 Na-ATP, and 0.4 Na-GTP; 290 mOsm, pH 7.2. Picrotoxin (100 μM), 2,3-dioxo-6-nitro-1,2,3,4-tetrahydrobenzo[f]quinoxaline-7-sulfonamide (NBQX, 25 μM), DL-2-amino-5-phosphonopentanoic acid (50 μM), and 8-cyclopentyltheophylline (4 μM) were added to recording ACSF to block GABAA, AMPA/kainate, NMDA, and adenosine receptors, respectively. Astrocytes in the CA1 stratum radiatum were identified by their small cell bodies, low input resistance, and very negative resting membrane potential . The cells were voltage-clamped at their resting membrane potential. The current recordings were filtered at 2 kHz, digitized at 10 kHz with a PCI-6221 A/D board (National Instruments), and recorded with WinWCP software (Strathclyde University, Glasgow, UK). STCs were evoked with a bipolar stimulating electrode placed in the stratum radiatum. Access resistance was monitored throughout each experiment. Experiments were excluded from the data analysis when the access resistance changed by more than 20%.
The first response to paired stimulation was scaled to the response elicited by a single stimulus, and then the response to the single stimulus was subtracted from the scaled response to the paired stimulation. The response to the single stimulus was then subtracted from the pure second response. The difference represented the STC without the potassium current . The STC was used to estimate the rise and decay time of the baseline transporter current.
In an experiment with a series of stimuli, three different stimulation patterns were used: a single stimulus, 4 stimuli, and 5 stimuli. To compare the kinetics of the response to the 1st and 5th stimuli, the response to 4 stimuli was subtracted from the response to 5 stimuli. The pure 5th response was used for further analysis.
Neuronal NMDA current
Hippocampal slices were prepared from 4- to 5-week-old WT and DTg mice as described above.
Whole-cell recording from CA1 pyramidal neurons
Whole-cell patch-clamp recordings of CA1 pyramidal neurons were made in ACSF containing picrotoxin (100 μM), CGP52432 (5 μM), S-MCPG (200 μM), and NBQX (25 μM) to isolate NMDA EPSCs. For this experiment, the pipette solution contained (in mM): 130 CsCH3SO3, 8 CsCl, 10 HEPES, 4 Mg-ATP, 0.4 Na2-GTP, 10 Na2-phosphocreatine, and 5 QX-314, pH 7.2; osmolarity was 290 mOsm. To evoke NMDA EPSCs, one bipolar stimulating electrode was positioned on the Schaffer collateral pathway, and a stimulus was generated every 30 s by a constant-current stimulator (Digitimer). Experiments were always started 15 min after breaking the seal to provide for sufficient diffusion of the intracellular channel inhibitors. Whole-cell NMDA currents in response to Schaffer collateral stimulation were measured in voltage-clamp mode at +40 mV. Series resistance was monitored before each step by measuring the peak current in response to a −3 mV voltage step. Cells with unstable series resistance (> 20% change) were excluded from further analysis.
All experiments were performed by an investigator blind to the mouse genotype.
Morris water maze test
The experiments were conducted with 5-mo-old male mice. The Morris water maze test was performed as previously described with some modifications . Mice were given 4 trials per day for 7 consecutive days in the hidden platform task. A randomly selected starting point along the rim of the maze was used for each of the four trials. A probe test was performed on day 8 after the acquisition session. In the probe test, the platform was removed from the tank and each mouse was allowed to swim for 60 s. On day 10, mice were tested in a visible platform task for 3 consecutive days. In the visible platform task, the platform was made visible by attaching a black cubic landmark to the platform. Mouse movement in the water maze was recorded by a video camera and analyzed using NIH image WM software (O’Hara &Co.).
Contextual and cued fear-conditioning test
The experiments were conducted with 5.5-mo-old male mice. A fear-conditioning shock chamber (10 x 10 x 10 cm) was used. Each mouse was placed into the conditioning chamber and allowed to explore for 2 min. The mouse then received two tone-shock pairings with a 60-s interstimulus interval. Each tone-shock pairing comprised an auditory cue (80 dB white noise, 30 s long) that co-terminated with an electric footshock (0.75 mA, 2 s long). The mice were left in the conditioning chamber after the last tone-shock pairing for 1 min. The 24-h contextual test was performed 24 h after the conditioning session. Mice were returned to the same conditioning chamber and their behavior was monitored for 5 min without tone or shock. The cued test was performed 24 h after the contextual test. Another testing chamber with different properties (shape, floor type, and wall color of the surrounding environment) was used. The mice were placed in the chamber and allowed to explore for 2 min. The same tone used in the conditioning session was given for 3 min. The remote contextual fear test was repeated 30 d after the conditioning session, and the remote cued test was also repeated 24 h later. The freezing behavior of the mice was monitored using a video camera and images were processed with NIH Image FZ software (O’Hara &Co.).
Footshock sensitivity test
After the remote fear memory test, footshock sensitivity was examined by giving mice electrical shocks of increasing intensity, ranging from 0.05 mA to 1 mA, and monitoring their behavior (flinching, vocalization, small jump, and big jump).
Acknowledgements: We thank A. Lebedinskiy for preliminary experiments; C. Nishioka, Y. Kobayashi, and H. Goto for technical assistance; Y. Sano and H. Matsukawa for advice on the experiments; the BSI RRC for animal care and technical assistance; and C. Yokoyama for his comments. This work was supported, in part, by the Japan Society for the Promotion of Science (JSPS) through a Grant-in-Aid for Scientific Research (C) Grant Number 22500369 to MT and the “Funding Program for World-Leading Innovative R&D on Science and Technology (FIRST Program),” initiated by the Council for Science and Technology Policy (CSTP).
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