Ca2+-impermeable AMPA receptors
Ca2+-permeable AMPA receptors
excitatory postsynaptic currents
glutamate receptor 2
Abnormal influx of Ca2+ is thought to contribute to the neuronal injury associated with a number of brain disorders, and Ca2+-permeable AMPA receptors (CP-AMPARs) play a critical role in the pathological process. Despite the apparent vulnerability of fast-spiking (FS) interneurons in neurological disorders, little is known about the CP-AMPARs expressed by functionally identified FS interneurons in the developing prefrontal cortex (PFC). We investigated the development of inwardly rectifying AMPA receptor-mediated currents and their correlation with NMDA receptor-mediated currents in FS interneurons in the rat PFC. We found that 78% of the FS interneurons expressed a low rectification index, presumably Ca2+-permeable AMPARs, with only 22% exhibiting AMPARs with a high rectification index, probably Ca2+ impermeable (CI). FS interneurons with CP-AMPARs exhibited properties distinct from those expressing CI-AMPARs, although both displayed similar morphologies, passive membrane properties and AMPA currents at resting membrane potentials. The AMPA receptors also exhibited dramatic changes during cortical development with significantly more FS interneurons with CP-AMPARs and a clearly decreased rectification index during adolescence. In addition, FS interneurons with CP-AMPARs exhibited few or no NMDA currents, distinct frequency-dependent synaptic facilitation, and protracted maturation in short-term plasticity. These data suggest that CP-AMPARs in FS interneurons may play a critical role in neuronal integration and that their characteristic properties may make these cells particularly vulnerable to disruptive influences in the PFC, thus contributing to the onset of many psychiatric disorders.
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Synaptic transmissions mediated by α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) and N-methyl-d-aspartic acid (NMDA) receptors in the cortical interneurons control the feedforward and feedback inhibition in the cortical circuitry (McBain & Fisahn, 2001; Maccaferri & Dingledine, 2002; Jonas et al. 2004). Many studies in the hippocampus indicated that γ-aminobutyric acid (GABA)-ergic interneurons generally exhibit a significant proportion of glutamate receptor 2 (GluR2)-lacking AMPA receptors (McBain & Dingledine, 1993; Geiger et al. 1995; Koh et al. 1995; Toth & McBain, 1998, 2000; Isaac et al. 2007). The Ca2+ permeability of AMPARs is critically dependent on GluR2; those containing GluR2 are Ca2+ impermeable (CI-AMPARs) and have a linear current–voltage (I–V) relation, and those lacking GluR2 are Ca2+ permeable (CP-AMPARs) and strongly inwardly rectifying (Hollmann & Heinemann, 1994; Jonas & Burnashev, 1995). GluR2-lacking CP-AMPARs have recently received considerable attention because of their postulated role in synaptic plasticity (Liu & Cull-Candy, 2000; Clem & Barth, 2006; Plant et al. 2006; Adesnik & Nicoll, 2007) and neurological disorders (Tanaka et al. 2000; Cull-Candy et al. 2006; Liu et al. 2006; Isaac et al. 2007; Liu & Zukin, 2007). Although a previous study reported that fast-spiking (FS) interneurons in the rat motor cortex had a relatively small NMDA contribution (Angulo et al. 1999a), the AMPA and NMDA subtypes expressed by functionally identified neocortical interneurons remained limited (Blatow et al. 2005), particulary in the prefrontal cortex (PFC). Recent studies indicated that Ca2+ influx in the dendrites of neocortical interneurons is mainly through CP-AMPARs (Goldberg et al. 2003) and that pyramidal neurons in the somatosensory cortex lost CP-AMPARs before postnatal day (PD)16 (Kumar et al. 2002). In addition, we recently found that FS interneurons in the rat PFC exhibited distinct properties of NMDA currents, particularly during the adolescent period. In juvenile animals (PD15 − 28), most (73%) of the FS cells demonstrated both AMPA and NMDA currents; in adults (∼PD90), only ∼26% contained detectable NMDA currents (Wang & Gao, 2009). Because functional maturation of the PFC is presumably delayed and the underlying synaptic refinement process is usually not completed until late adolescence and early adulthood (Woo et al. 1997; Tseng & O’Donnell, 2007; Wang et al. 2008), it would be intriguing to identify the functional change that occurs in CP-AMPARs in the developing FS interneurons in PFC. We proposed that FS interneurons in the PFC may use CP-AMPARs for Ca2+ influx to compensate for the apparent lack of synaptic NMDA receptors. We tested this possibility by examining the rectification index (RI) of AMPAR-mediated currents in the FS interneurons at different developmental stages. We found that the AMPARs in FS interneurons with many NMDA receptors in the rat PFC displayed a clearly linear I–V relationship and paired-pulse depression. In contrast, the AMPARs in FS interneurons with no or few NMDA receptors expressed CP-AMPARs, which exhibited a significantly non-linear I–V relationship, prominent synaptic facilitation, and distinct frequency-dependent short-term plasticity. The AMPA receptors also exhibited a significantly decreased RI during adolescence.
Brain slice preparation and physiological recording
Seventy-three Sprague–Dawley rats of either gender, aged PD15–115, were used in this study. The rats were divided into juvenile (PD15−28), adolescent (PD31−63) and adult (PD86−115) groups as previously reported (Spear, 2000; Tseng & O’Donnell, 2007; Wang & Gao, 2009). The rats were cared for according to National Institutes of Health guidelines, and the experimental protocol was approved by the Institutional Animal Care and Use Committee at Drexel University College of Medicine. The experiments also complied with the policies and regulations of ethical matters in The Journal of Physiology (Drummond, 2009). The detailed procedure can be found in our previous studies (Gao & Goldman-Rakic, 2003; Gao et al. 2003; Gao, 2007; Wang & Gao, 2009). The rats were deeply anaesthetized with Euthasol (0.2 ml kg−1, i.p.), rapidly perfused with ice-cold (< 4°C) sucrose solution containing (in mm): KCl 2.5, NaH2PO4 1.25, NaHCO3 26, CaCl2 0.5, MgSO4 7.0, and sucrose 213, and aerated with 95% O2 and 5% CO2. The rats were decapitated with a guillotine; the brains were quickly removed and placed in the same sucrose solution. Horizontal brain slices at 300 μm were made with a Vibratome (Vibratome Co., St Louis, MO, USA), and the slices were incubated in an oxygenated sucrose solution at 35°C for 1 h. The slices were incubated at room temperature until being transferred into a submerged recording chamber. The recordings were conducted with cortical slices perfused with Ringer solution containing the following ingredients (in mm): NaCl 128, KCl 2.5, NaH2PO4 1.25, CaCl2 2, MgSO4 1, NaHCO3 26, and dextrose 10, pH 7.4. Whole-cell patch clamp recordings were conducted in the PFC slices through an upright microscope (Olympus BX61, Olympus Optics, Japan) equipped with infrared differential interference contrast optics (IR-DIC). The recordings were conducted at ∼36°C. Resistance of the recording pipette (1.2 mm borosilicate glass) was ∼9 MΩ. Tips of the recording pipettes were first filled with a potassium gluconate-based intracellular solution (∼1 mm from the tip) and then backfilled with a Cs+-containing solution. The potassium gluconate solution contained (in mm): potassium gluconate 120, KCl 6, ATP-Mg 4, Na2GTP 0.3, EGTA 0.1, Hepes 10, and 0.3% biocytin, pH 7.3, 310 mosmol L−1; the Cs+ solution contained (in mm): caesium gluconate 120, QX-314 chloride 5, CsCl2 6, ATP-Mg 1, Na2GTP 0.2, Hepes 10, spermine 0.05, and 0.3% biocytin at pH 7.3 (adjusted with CsOH). With this strategy, we were able to record the action potentials immediately (usually within 1 min) after forming a giga-seal due to the presence of a K+ internal solution at the tip of the patch pipette. Then we could record AMPAR- and NMDAR-mediated currents with minimal K+ current contamination due to the delayed diffusion (∼5 min) of Cs+ ions into the recorded cell (Wang & Gao, 2009). The excitatory postsynaptic currents (EPSCs) were evoked by a bipolar electrode placed about 300 μm away from the recorded neurons (0.1 ms, 40–400 μA, 0.1 Hz) in the presence of the GABAA antagonist picrotoxin (50 μm, Sigma-Aldrich, St Louis, MO, USA). The AMPA receptor-mediated AMPA EPSCs were recorded at −60 mV for the paired-pulse stimulation, whereas the inwardly rectifying AMPA EPSCs were recorded at −60, 0 and +60 mV to calculate the RI (see ‘Data analysis’) in the presence of picrotoxin and NMDA receptor antagonist d-(−)-2-amino-5-phosphonopentanoic acid (d-APV, 50 μm, Sigma-Aldrich). The I–V relationships of AMPA EPSCs were recorded 10 min after break-in to allow sufficient time for diffusion of spermine, and measurements were made from the averages of 15 responses evoked by intracortical stimulation with membrane potentials held at 20 mV steps from −80 mV to +80 mV. The NMDA receptor-mediated currents (NMDA EPSCs) were recorded at +60 mV under conditions of bath-applied picrotoxin and the AMPA receptor antagonist 2,3-dihydroxy-6-nitro-7-sulfamoyl-benzo[f]quinoxaline-2,3-dione (NBQX) (20 μm, Sigma-Aldrich). NMDA EPSCs were confirmed by bath application of d-APV (50 μm) in some cases. To record NMDA receptor-mediated miniature EPSCs (mEPSCs), membrane potentials of FS interneurons were held either at −60 mV in Mg2+-free external solution with bath perfusion of the sodium channel blocker tetrodotoxin (TTX, 0.5 μm) and picrotoxin (100 μm), as described previously (Myme et al. 2003) or at +60 mV in the presence of picrotoxin, NBQX and TTX. The access resistance ranged from 18 to 30 MΩ, and the series resistances were constantly monitored through a test hyperpolarizing pulse (5 mV, 200 ms) applied in each sweep and were compensated at regular intervals throughout the recordings. The electric signals were recorded using MultiClamp 700B (Molecular Devices) and acquired at sampling intervals of 20–50 μs through pCLAMP 9.2 software (Molecular Devices).
Histological and morphological analyses
All slices with recorded neurons were preserved for biocytin immunostaining as previously reported (Gao et al. 2003; Gao, 2007; Wang & Gao, 2009). Briefly, slices were fixed with 4% paraformaldehyde for at least 24 h; the slices were placed in 3% H2O2 for 30 min to block the endogenous horseradish peroxidase. After thorough rinsing, reactions of an avidin/biotinylated enzyme complex (Vector Laboratories, USA) were conducted overnight, followed by the Ni-3,3-diaminobenzidine reaction. The slices were rinsed with 0.1 mm phosphate buffer (pH 7.4), mounted on glass slides, and covered with water-soluble mounting media. All labelled neurons were double-checked to determine that their documented locations and firing patterns matched, for cell type identification.
The action potentials recorded in current clamp mode in the first minute after membrane break-in were used to measure the resting membrane potential, input resistance, action potential (AP) threshold, AP half-width, and afterhyperpolarization. All of these parameters were used to distinguish FS interneurons from other cell types. Detailed procedures can be found in our recent report (Wang & Gao, 2009). Data were rejected for further analysis if the series resistance changed more than 20% during recordings. The amplitudes of the EPSCs were measured by averaging 30 sweeps from the onset to the peak of the EPSCs with Clampfit 9.2 software (Molecular Devices). Only the neurons that produced stable EPSCs for at least 5 min without rundown were used for further analysis. The time constant decay was obtained by fitting the recovery phase of the evoked EPSC with a single exponential function (standard exponential formula) in Clampfit 9.2. The RI for individual FS interneurons was calculated as the amplitude of AMPA-EPSC+60 mV/AMPA-EPSC−60 mV. The reversal potentials were empirically determined by a plot in which zero current crossed the x-axis (potential). The paired-pulse ratio (PPR) was determined as the peak amplitude of AMPA EPSC2/EPSC1 in 20 Hz recordings. The mEPSCs recorded in the voltage-clamp mode were analysed with Clampfit 9.2. A typical mEPSC was selected to create a sample template for event detection within a data period, and the AMPA or NMDA mEPSCs were detected with a threshold set at 3 times the value of the root mean square of the baseline noise. For the mEPSCs recorded at −60 mV in zero Mg2+ solution, the peak of an mEPSC was taken as the AMPA amplitude, whereas the NMDA current was measured 5 ms after the mEPSC peak. We chose 5 ms instead of the 18–23 ms used for pyramidal cells by Myme et al. (see Myme et al. 2003) because the decay of AMPA EPSC on the fast-spiking interneurons was usually < 5 ms (Hestrin, 1993; McBain & Dingledine, 1993; Angulo et al. 1997; Wang & Gao, 2009), whereas the EPSC decay on pyramidal neurons was ≥15 ms (Hestrin, 1993; McBain & Dingledine, 1993; Myme et al. 2003). The NMDA/AMPA ratio for mEPSCs was given as the ratio of these two currents. For the NMDA mEPSCs recorded at +60 mV, the mEPSC amplitude, frequency and 63% decay were directly measured from the averaged mEPSCs. All data were presented as mean ± standard error of the mean along with Student's t test, ANOVA, χ2 test, or Pearson rank correlations to examine the statistical significance.
FS interneurons in the rat PFC can be divided into two distinct subtypes based on the RI in AMPA-mediated EPSCs
Despite the heterogeneous nature of GABAergic interneurons in the neocortex, they are divided physiologically into FS cells and several non-FS cell types (Kawaguchi, 1995; Cauli et al. 1997; Xiang et al. 1998; Gibson et al. 1999; Gao et al. 2003). To study the development of AMPA and NMDA receptors in the prefrontal interneurons, we recorded over 200 neurons in layers 2–5. All tested cells were initially identified under infrared differential interference contrast optics by their morphology, that is, cell bodies and multipolar dendrites. The identities of the presumptive FS interneurons were further confirmed by the following parameters: biocytin-labelled morphology, high-frequency and non-adapting firing patterns (>100 Hz, Fig. 1A, B, D and E, Table 1), and narrow half-width (mean 0.55 ± 0.04 ms) of action potentials and large fast afterhyperpolarizations (15.5 ± 0.58 mV, range 9.4–22.4 mV). These parameters are widely accepted as reliable criteria for the identification of cortical interneurons, as reported in our recent study (Wang & Gao, 2009) and in numerous previous studies (Kawaguchi, 1995; Cauli et al. 1997; Xiang et al. 1998; Gibson et al. 1999; Gao et al. 2003). Because NMDA receptors exhibited few developmental changes on the non-FS interneurons (Wang & Gao, 2009), we focused on the identified FS interneurons in this study. The remaining neurons, including pyramidal neurons and non-FS interneurons, were excluded from the dataset.
|CI (RI > 0.7) n= 19 (21.8%)||CP (RI < 0.7) n= 68 (78.2%)||P value|
|Age (days)||43.9 ± 7.29||46.4 ± 3.77||0.754|
|Rectification index||1.23 ± 0.06||0.21 ± 0.02||<0.0001|
|Resting membrane potential (mV)||−66.6 ± 3.33||−67.1 ± 1.22||0.733|
|Input resistance (MΩ)||210.3 ± 30.7||191.0 ± 11.6||0.240|
|AP threshold (mV)||−35.7 ± 2.21||−33.7 ± 1.34||0.356|
|AP half-width (ms)||0.56 ± 0.02||0.55 ± 0.03||0.868|
|Afterhyperpolarization (mV)||16.2 ± 3.46||14.4 ± 1.76||0.655|
|AMPA EPSC amplitude (pA)||72.4 ± 14.2||78.6 ± 7.2||0.616|
|AMPA EPSC decay (ms)||4.25 ± 0.53||3.92 ± 0.42||0.925|
|AMPA EPSC charge (pC)||0.65 ± 0.15||0.87 ± 0.10||0.421|
|AMPA EPSC 20–80% rise time (ms)||0.65 ± 0.06||0.67 ± 0.05||0.966|
|NMDA EPSC amplitude (pA)||53.4 ± 12.05||8.87 ± 1.58||<0.0001|
|NMDA/AMPA ratio||1.02 ± 0.12||0.19 ± 0.02||<0.0001|
We first examined the I–V relationships of AMPA receptor-mediated EPSCs evoked by low-intensity stimulation of the intracortical fibres through an electrode placed ∼300 μm away from the recorded interneurons. It is known that CP-AMPARs can be blocked by endogenous intracellular polyamines (Bowie & Mayer, 1995; Kamboj et al. 1995; Koh et al. 1995). This intracellular block underlies inward rectification in the I−V relationship, which is presumably associated with GluR2-lacking CP-AMPARs. Although the inward rectification of CP-AMPAR channels could be lost quickly in cell-free membrane patches due to dissipation of intracellular polyamines, the loss of the rectification is prevented by adding spermine to the internal solution used to fill the patch pipette (Bowie & Mayer, 1995; Donevan & Rogawski, 1995; Koh et al. 1995). The AMPAR-mediated currents were recorded at −60, 0 and +60 mV, respectively, in the presence of picrotoxin (50 μm) and d-APV (50 μm) in bath solution and spermine (50 μm), a high-affinity antagonist of GluR2-lacking CP-AMPARs, included in the intracellular solution (Kamboj et al. 1995; Kumar et al. 2002). As shown in Fig. 1C and F, the I–V curves of the AMPA EPSCs in the individual FS interneurons were drawn, and the RIs of the EPSCs were calculated by comparing the conductance ratios of EPSC+60 mV/EPSC−60 mV. It is known that cells expressing appreciable levels of GluR2 receptors, which form CI-AMPARs with linear or outwardly rectifying I–V relationships, were usually unaffected by spermine (Toth & McBain, 1998; Kumar et al. 2002; Andersen et al. 2005). Considering the effects of the junction potential of the recording solution (about 14.9 mV), we arbitrarily set the breakup value of RI at 0.7 (Noh et al. 2005). Based on the I–V curve and the RI values (range 0.02–1.78), all recorded FS interneurons could be easily classified as either CI or CP (see Fig. 1A–F; Table 1). We found that most (68 of 87 or 78.1%) of the FS interneurons tested were CP cells exhibiting inwardly rectifying I–V curves in the presence of spermine. The RI values in most of the CP neurons were smaller than 0.5, with those in only four cells ranging from 0.51 to 0.64. In contrast, most of the CI cells had RI values ranging from 1.10 to 1.78 with the exception of four cells in which the RI values ranged from 0.76 to 0.92 (CP: n= 68, RI = 0.21 ± 0.02, range 0.01–0.64; CI: n= 19, RI = 1.23 ± 0.06, range 0.76–1.78; P < 0.0001; see inset between Fig. 1C and F). Despite the differences in RI ratios between CI and CP neurons, the other passive membrane properties such as resting membrane potential, input resistance, firing pattern, and half-width of action potentials appeared to be similar, without significant difference (P > 0.05 for all; Table 1). The other measured parameters, including amplitude, decay, charge and 20% to 80% rise time of AMPA EPSCs recorded at −60 mV were also similar between the CI and CP interneurons, without statistical difference (P > 0.05 for all; Table 1). To determine whether RI was affected by the reversal potential, the AMPA EPSCs were recorded with 20 mV steps from −80 mV to +80 mV in a subset of FS interneurons (9 cells). As shown in the I–V relationships (Fig. 1G and H), the EPSC amplitudes were normalized to −80 mV levels, and rectification differences of EPSCs between CI and CP appeared only in the positive holding potentials. The dashed lines fitting to the EPSC amplitudes in the hyperpolarized voltage range in both CI and CP cells exhibit the deviations of the EPSC amplitudes in the depolarized voltage range from the linear fit functions. I–V relationships in both CI and CP interneurons exhibited similar reversal potentials without statistical difference (P= 0.121), but a weak correlation between RI values and reversal potential was observed (Square of correlation coefficient R2= 0.389, P= 0.073; Fig. 1H). Because the series resistance was monitored and compensated periodically, these results suggested that the contribution of voltage-clamp errors to the observed differences in rectification was minimal. In another set of experiments, we tested whether inclusion of spermine (50 μm) in the pipette affects the reversal potentials of AMPAR-mediated EPSCs. We found no difference between the FS interneurons perfused with spermine and those without spermine (reversal potential with spermine 11.9 ± 3.61 vs. that without spermine 13.4 ± 2.94, n= 7 in each group, P= 0.748), in agreement with a previous report (Kumar et al. 2002). We also did not find a clear difference in the morphologies of the FS interneurons expressing CI and CP. Most of the cells identified exhibited non-pyramidal shapes, as shown in Fig. 1A and D.
Developmental changes in CI- and CP-AMPARs in the FS interneurons
Previous studies indicated that during early postnatal development, expression of GluR2 subunits is low compared with that of GluR1, but it increases rapidly during the first postnatal week (Monyer et al. 1991). Consistent with these findings, synaptic GluR2-lacking AMPARs were only detected in pyramidal neurons in the neonatal neocortex (Kumar et al. 2002; Shin et al. 2007). Because the functional maturation of the PFC is postulated to be protracted and the synaptic refinement process is not completed until early adulthood (Woo et al. 1997; Wang et al. 2008), we speculated that the changes in CP-AMPARs in the PFC may be prolonged to complement the development of prefrontal functions. To test this possibility, we examined the changes in AMPARs in the FS interneurons at different developmental stages. As shown in Fig. 2A, although the RI changes in FS neurons did not seem to be correlated with the ages of the animals (R2= 0.018, P= 0.498), we found significantly more cells expressing CP-AMPARs (increased by 22.5%) during the adolescent period (χ2= 5.76, P= 0.016); in fact, 90% of cells in this age group exhibited low RIs (Fig. 2A, arrow). This trend remained until adulthood with partial recovery (χ2= 2.38, P= 0.123 for juveniles vs. adults and χ2= 6.86, P= 0.087 between adolescents and adults). Overall, the FS interneurons exhibited a significant decrease in RI values during the adolescent period (RI = 0.57 ± 0.09 in juveniles vs. 0.31 ± 0.06 in adolescents, P= 0.021), and the RIs were recovered in adults (P= 0.449 between juveniles and adults and P= 0.211 between adolescents and adults). These results indicated that AMPARs exhibited significant changes during the adolescent period and that, unlike those found in the cortical pyramidal neurons (Kumar et al. 2002), AMPA receptors in most of the FS interneurons remained permeable to Ca2+ with few changes.
FS interneurons with CP-AMPA receptors express significantly fewer NMDA receptors
We recently reported that subpopulations of FS interneurons in the PFC expressed no NMDA receptors or gradually lost NMDA receptors during PFC development (Wang & Gao, 2009). We hypothesized that the NMDA receptors in the FS interneurons may be gradually replaced by CP-AMPARs to complement the need for Ca2+ influx during synaptic transmission. To test this possibility, we systematically examined the correlation between CP-AMPARs and NMDA receptors in the FS interneurons. The FS interneurons were identified by their firing patterns, and the AMPA EPSCs were recorded at −60, 0 and +60 mV, respectively, in the presence of picrotoxin and d-APV to examine the RI values. Then, the neurons were washed with picrotoxin and NBQX for 20 min to allow the complete recovery and isolation of NMDA EPSCs. In some cases, we recorded the NMDA EPSCs first in the presence of picrotoxin and NBQX and then, after a 20 min washout, recorded AMPA EPSCs at −60, 0 and +60 mV, respectively, in the presence of picrotoxin and d-APV. The entire process of recordings took about 35 min; stimulus intensity was kept constant during the recordings. It should be noted that although extracellular application of spermine potentiated NMDA currents in the presence of saturating concentrations of glycine (Benveniste & Mayer, 1993; Williams, 1997), no evidence suggested that intracellular spermine affected NMDA receptor channels (Williams, 1997). In addition, most of the FS interneurons expressed a significantly higher proportion of NR2A subunits (Kinney et al. 2006; Xi et al. 2009a,b), whereas spermine had no effect on the affinity of NR1A/NR2A receptors for NMDA (Williams, 1994). Indeed, under both conditions, we found that the amplitudes of either AMPA- or NMDA-EPSCs were comparable, so we pooled the data. In the FS interneurons reliably recorded for NMDA EPSCs, we found that most (18 of 19 or 94.7%) of the CI cells expressed NMDA EPSCs ranging from 7.9 to 195.6 pA, except for one cell, which expressed no NMDA current (mean 53.4 ± 12.05 pA). In contrast, the FS interneurons expressing CP-AMPARs contained either few (32/68 or 47.1%, range 0.3–36.4 pA) or no (36/68 or 52.9%) NMDA EPSCs. Accordingly, the amplitudes of NMDA EPSCs (mean 8.87 ± 1.59 pA) and of the NMDA/AMPA ratios in the FS interneurons with CP-AMPARs were significantly lower than those in the CI cells (P < 0.0001 for both; Fig. 3A–D). Further analysis indicated that the amplitudes of NMDA EPSCs exhibited a bimodal distribution and were clearly correlated with RI values (n= 87, R2= 0.464, P < 0.0001), with CP interneurons displaying significantly less NMDA current than CI interneurons (Fig. 3E). Overall, the amplitudes of NMDA EPSCs in FS interneurons were significantly lower in the adolescent period; they were very much, but not significantly, lower (due to large variability) in adult rats compared with those in juveniles (mean amplitude of NMDA currents was 31.3 ± 6.73 pA in juveniles vs. 10.9 ± 2.34 pA in adolescents and 14.0 ± 9.80 pA in adults, P= 0.0037 between juveniles and adolescents, P= 0.071 between juveniles and adults, and P= 0.707 between adolescents and adults, Fig. 3F). Among the CP cells, NMDA EPSCs progressively decreased, and, in the adult animals, more and more CP interneurons expressed no NMDA currents (χ2= 7.41, P= 0.007, Fig. 3G). This result is similar to that from our previous studies, which included all (both CI and CP) FS interneurons (see Fig. 2D in Wang & Gao, 2009).
To further confirm the expression of NMDA receptors in FS interneurons with CI and CP AMPARs, NMDA receptor-mediated mEPSCs were recorded in two different sets of experiments. As shown in Fig. 4A–D, the AMPAR-mediated EPSCs in the FS interneurons were first recorded at −60, 0 and +60 mV, respectively, in the presence of picrotoxin (50 μm) and d-APV (50 μm) to determine the RI in order to identify CI and CP cells (Fig. 4A). The cells were then held at a membrane potential of −60 mV in a Mg2+-free external solution with bath perfusion of TTX (0.5 μm) and picrotoxin (100 μm) to record the mEPSCs. Under these conditions, mEPSCs with both AMPAR- and NMDAR-mediated components were readily observed (Fig. 4B). The mEPSCs in the FS interneurons with CI AMPARs (n= 6) displayed significantly slower decay than those in the CP cells (P < 0.05; Fig. 4B). Although the amplitudes in AMPA mEPSCs in CI and CP cells were similar (P= 0.948), the amplitudes of NMDA mEPSCs were significantly different (P= 0.036; Fig. 4C). Therefore, the CI cells expressed significantly higher NMDA/AMPA ratios compared with those with CP AMPARs (n= 5, P < 0.005). The RI values were also significantly correlated with the NMDA/AMPA ratios (R2= 0.847, P= 0.0001; Fig. 4D). These data further confirm that FS interneurons with lower RI values express fewer NMDA receptors. To further determine whether NMDA receptors are actually lost in some FS interneurons, we conducted another set of experiments with membrane potentials held at +60 mV to record the NMDA mEPSCs in the presence of picrotoxin, NBQX and TTX. In the 15 FS interneurons recorded from rats aged PD55–63, nine cells exhibited no NMDA mEPSCs whereas the remaining six cells displayed clear NMDA currents (Fig. 4E and F). The NMDA mEPSCs were averaged at 12.6 ± 1.44 pA in amplitude, 0.30 ± 0.10 Hz in frequency, and 31.9 ± 2.47 ms in decay. These results indicate that the contribution of NMDA receptors at glutamatergic synapses onto interneurons is small or negligible, in agreement with results from a previous study of interneurons in the amygdala (Mahanty & Sah, 1998).
FS interneurons with CI- and CP-AMPA receptors exhibit different characteristics in short-term plasticity
Previous studies indicated that activity-dependent relief from polyamine block of postsynaptic CP-AMPARs in the interneurons either reduces the rate of paired-pulse depressions in a frequency-dependent manner or induces facilitation of a synaptic response that would otherwise be depressed (Rozov et al. 1998; Rozov & Burnashev, 1999; Toth et al. 2000). In addition, the firing rates of prefrontal neurons during working memory tasks in both primates (Funahashi et al. 1989; Miller et al. 1996) and rats (Fujisawa et al. 2008) range from 2 to 40 Hz and are averaged at 15–25 Hz. We therefore examined whether CI and CP interneurons would have different synaptic responses at the physiological firing rates observed in vivo. We applied 20 Hz (50 ms interstimulus interval) paired-pulse stimulation to test the short-term synaptic response in the two kinds of synapses. When the paired-pulse protocol was applied, AMPAR-mediated EPSCs at CI and CP synapses exhibited considerably different responses. We observed both paired-pulse facilitation (PPF) and depression (PPD) among the 54 FS interneurons tested (Fig. 5A), primarily consistent with results from previous studies (Rozov et al. 1998; Angulo et al. 1999a, 2003; Toth et al. 2000). Among these FS interneurons, however, a majority (38 of 54, 70.4%) of the cells expressed PPF with a PPR of 1.37 ± 0.05, whereas the remaining cells expressed PPD with a significantly lower PPR (16/54 or 29.6%, PPR = 0.84 ± 0.03, P < 0.0001; Fig. 5B). The FS interneurons expressing PPF and PPD were again seemingly age-independent overall (χ2= 2.14, P= 0.342; Fig. 5C), but the relative ratio of FS interneurons expressing PPF increased by 21% during the adolescent period (χ2= 9.15, P= 0.0025 between juvenile and adolescent; χ2= 9.95, P= 0.0016 between adolescent and adult; χ2= 0.018, P= 0.892 between juvenile and adult). This change supports the significant increase of FS interneurons expressing CP-AMPARs described in Fig. 2A and B. The PPRs are slightly correlated with the age of the animal (n= 54, R2= 0.131, P < 0.01; Fig. 5D), with a significantly higher average PPR in adult animals compared with that in juvenile animals (1.57 ± 0.28 in adults versus 1.15 ± 0.05 in juveniles, t= 2.61, P= 0.013; Fig. 5D). Further analysis indicated that both PPF and PPD synapses were observed in CI (n= 6) and CP (n= 13) FS interneurons that were recorded in rats aged PD17–36 (Fig. 5E). We noted a weak negative correlation between PPR and RI (R2=−0.410, P= 0.130). Among these interneurons, we observed more PPD in CI neurons and more PPF in CP cells, with a significant difference between the two groups (χ2= 5.48, P= 0.019). These results were consistent with those from a previous study in the hippocampus (Toth et al. 2000). In addition, we found that the paired-pulse responses were correlated with the distribution of NMDA receptors in both CI and CP FS interneurons. The FS interneurons expressing PPD exhibited significantly more NMDA receptors compared with FS interneurons expressing PPF, and a majority of the PPF synapses contained no NMDA receptors (χ2= 4.59, P= 0.032; Fig. 5F and G).
Facilitating synapses, but not depressing synapses, are sensitive to spermine in the FS interneurons
Previous studies indicated that relief of block by intracellular polyamines was both use- and voltage-dependent (Bowie et al. 1998; Rozov et al. 1998), and CP-AMPARs were endowed with a postsynaptic mechanism for the short-term enhancement of synaptic gain (Rozov & Burnashev, 1999; Shin et al. 2005). We therefore examined whether polyamine analogous spermine would affect short-term plasticity at synapses expressing facilitation and depression in the FS interneurons. Paired-pulse stimulation at 20 Hz (50 ms interstimulus interval) was applied to identify synapses as either PPF or PPD in the presence or absence of spermine (50 μm) in the recording pipette. The EPSCs were recorded at −60 mV, and PPRs were calculated in the same cell at different times after the membrane break-in in whole-cell recordings. Under these conditions, we found that, when spermine was not included in the intracellular solution, the PPRs in both synapses expressing PPF and PPD were relatively stable without significant changes (n= 4 in each group, P > 0.05, Fig. 6A and B). However, spermine significantly increased the PPRs in the FS interneurons initially expressing PPF but had little or no effect on PPRs in the FS cells expressing PPD. As shown in Fig. 6, the PPRs in the FS cells expressing PPF were gradually and significantly increased from 1.17 ± 0.06 at baseline level (mean of the EPSCs at the first 4 min after membrane break-in) to 1.67 ± 0.13 at 15 min after break-in (n= 5, P= 0.020; Fig. 6A). In contrast, the PPD synapses exhibited no clear change in the PPRs (0.75 ± 0.08 at 4 min versus 0.81 ± 0.09 at 15 min; n= 4, P= 0.275; Fig. 6B). These results are in agreement with those from previous studies in which polyamine-dependent facilitation occurred only in the neurons expressing CP-AMPARs, including multipolar interneurons (Rozov et al. 1998; Rozov & Burnashev, 1999; Toth et al. 2000) and immature pyramidal neurons (Shin et al. 2005, 2007). Furthermore, our data also support the proposition that spermine-dependent facilitation involves a postsynaptic mechanism in the FS cells expressing PPF because spermine was included in the intracellular solution (Rozov & Burnashev, 1999; Shin et al. 2005). Polyamines are known to modulate PKC activity, which in turn enhances the phosphorylation of AMPARs and thus influences AMPAR function, particularly CP-AMPARs (Shin et al. 2007).
Facilitating synapses, but not depressing synapses, on FS interneurons exhibit frequency-dependent change of PPR
Previous studies indicated that synapses expressing CP-AMPARs might display short-term plasticity through postsynaptic mechanisms instead of through well-recognized presynaptic mechanisms seen in most of the synapses (Dobrunz & Stevens, 1997; Zucker & Regehr, 2002) because intracellular-loaded spermine affected the PPR (Rozov et al. 1998; Rozov & Burnashev, 1999; Toth et al. 2000; Shin et al. 2005). We therefore wondered whether the synapses expressing PPF and PPD displayed different frequency-dependent paired-pulse plasticity in FS interneurons in the PFC. Paired-pulse stimulation at different frequencies from 1 Hz to 100 Hz was applied in individual FS interneurons to record AMPA EPSCs at −60 mV in the presence of picrotoxin (50 μm) and d-APV (50 μm). No spermine was included in the pipette solution for Fig. 7A–F. Under these conditions, we found that EPSCs in facilitating FS interneurons showed a significant frequency-dependent change of the second EPSCs relative to the first EPSCs. The synapses expressed PPF at frequencies higher than 10 Hz (100 ms interval) but PPD at lower frequencies, e.g. 2 Hz, and completely recovered at 1 Hz (1000 ms interval), with a PPR of ∼1.0. For example, the PPR at 20 Hz was significantly higher than that at 2 Hz in the facilitating synapses (PPR = 1.27 ± 0.13 at 20 Hz versus 0.84 ± 0.03 at 2 Hz, n= 5, P= 0.031; *P < 0.05 between 20 Hz and 10, 5 and 1 Hz; see Fig. 7A–C). In contrast to the FS interneurons expressing facilitation, the synapses exhibiting PPD continued to express depression, independent of frequency changes in the depressing FS interneuron. Both the first and second EPSCs in response to paired-pulse stimulation at different frequencies were relatively stable, without clear change in PPRs (PPR = 0.83 ± 0.07 in 20 Hz versus 0.79 ± 0.09 in 2 Hz, n= 6, P= 0.552; P > 0.05 between 20 Hz and 10, 5 and 1 Hz; Fig. 7D–F). These results are interesting because FS interneurons with CI-AMPARs are likely to display PPD, whereas FS interneurons with CP-AMPARs exhibit apparently more PPF. Although the direct role of CP-AMPARs in the switch of PPR in the PPF synapse remains unclear, these data indicate that FS interneurons expressing CP-AMPARs play a differential role in the neuronal integration of pyramidal neurons in the neocortex (Geiger et al. 1997; Angulo et al. 1999b; Sun et al. 2005).
We have investigated the developmental changes in CP-AMPARs and their correlation with NMDA receptors in FS interneurons in the developing rat PFC. We found that most (∼78%) of the FS interneurons exhibit CP-AMPARs, with only one-quarter of them expressing CI-AMPARs. Although these FS interneurons displayed similar passive membrane properties, AMPAR-mediated currents at resting membrane potentials and morphologies, the FS interneurons with CP-AMPARs exhibited many distinct physiological properties, including few NMDA receptors and prominent frequency-dependent short-term facilitation. The AMPA EPSCs in FS interneurons also displayed a significant decrease in RI value and an increase in PPF during adolescence.
AMPARs exist as both CP and CI channels, and the presence of GluR2 subunits renders heteromeric AMPAR assemblies impermeable to Ca2+ (i.e. CI) (Adesnik & Nicoll, 2007). Considerable interest has centred on GluR2-lacking CP-AMPARs in the past decade because they confer novel properties on synapses and they are expressed in restricted cell populations or under certain physiological and pathological conditions (Liu & Cull-Candy, 2000; Bellone & Luscher, 2006; Clem & Barth, 2006; Cull-Candy et al. 2006; Plant et al. 2006; Isaac et al. 2007). The roles of such receptors in synaptic function and plasticity have been studied in hippocampal interneurons (McBain & Dingledine, 1993; Geiger et al. 1995; Koh et al. 1995; Toth & McBain, 1998, 2000; Isaac et al. 2007), neocortical pyramidal neurons (Kumar et al. 2002; Shin et al. 2007), and interneurons (Jonas et al. 1994; Rozov et al. 1998; Rozov & Burnashev, 1999). Although our findings supported some aspects of the results from these studies, we systematically reported for the first time the developmental changes in CP-AMPARs and their correlation with NMDA receptors in the functionally identified FS interneurons in the PFC. These findings are important because FS interneurons exhibited distinct developmental changes in NMDA receptors compared with other non-FS interneurons such as regular spiking and low-threshold spiking cells in the PFC (Wang & Gao, 2009). These data confirmed our propositions that, during prefrontal cortical development, NMDA receptors are gradually lost and that Ca2+ influx in FS interneurons occurs mainly through CP-AMPARs. Indeed, synaptic plasticity in FS interneurons with CP-AMPARs was usually NMDA independent (Mahanty & Sah, 1998; Laezza et al. 1999; Toth et al. 2000; Lei & McBain, 2002; Topolnik et al. 2005; Lamsa et al. 2007; Lu et al. 2007). In addition, we found that most of the FS interneurons with CP-AMPARs displayed comprehensible short-term facilitation compared with those expressing CI-AMPARs, which expressed more short-term depression. Because facilitating synapses in the FS interneurons are spermine-sensitive with clear voltage- (Toth et al. 2000; Laezza & Dingledine, 2004) and frequency-dependence (Rozov et al. 1998; Rozov & Burnashev, 1999; Sun et al. 2005), the CP and CI interneurons would have distinct roles in integrating neuronal activity in pyramidal neurons (Geiger et al. 1997; Angulo et al. 1999a; McBain & Fisahn, 2001; Pouille & Scanziani, 2001; Maccaferri & Dingledine, 2002; Jonas et al. 2004). Furthermore, unlike an apparent switch from depression in young rats (3 weeks old) to facilitation in older rats (5 weeks old) in FS interneurons in the rat motor cortex (Angulo et al. 1999b), FS interneurons in the PFC exhibited a relatively large number of PPF synapses in all age groups without significant age differences, except during the adolescent period from PD30 to PD60 (Spear, 2000; Tseng & O’Donnell, 2007). The CP-AMPAR change in adolescence is important because this period is marked by profound neuropsychological changes and by the onset of schizophrenia and other psychiatric disorders (Lewis, 1997; Spear, 2000). Indeed, a recent study reported that prefrontal cortical interneurons were more sensitive to dopaminergic modulation during adolescence (Tseng & O’Donnell, 2007). The CP-AMPARs on FS interneurons in the PFC are also clearly different from those reported in layer 5 pyramidal neurons in the rat neocortex in which GluR2-deficient CP-AMPARs were found only in rats younger than PD16 (Kumar et al. 2002; Shin et al. 2005). These results indicate that FS interneurons in the PFC undergo a developmental process in CP-AMPARs distinctly different from that of pyramidal neurons in the somatosensory cortex (Kumar et al. 2002; Shin et al. 2007) and FS interneurons in the rat motor cortex (Angulo et al. 1999b). A delayed maturation of function and receptor channels appears to be prominent in FS interneurons in the rat PFC, as shown in previous studies (Tseng & O’Donnell, 2007; Wang et al. 2008).
FS interneurons control the inhibitory action in pyramidal neurons (Cauli et al. 1997; Xiang et al. 1998; Gibson et al. 1999; Pouille & Scanziani, 2001). The dynamic properties of CP-AMPARs, evident in different forms of short- and long-term plasticity (Rozov et al. 1998; Rozov & Burnashev, 1999; Lei et al. 2002; Lei & McBain, 2004; Isaac et al. 2007; Lamsa et al. 2007), are also relevant to various neurological conditions (Liu & Zukin, 2007; Mahajan & Ziff, 2007). Changes in the expression of CP-AMPARs can alter synaptic properties or Ca2+-dependent signalling cascades or can lead to injury of selectively vulnerable neurons (Tanaka et al. 2000; Cull-Candy et al. 2006). Previous studies indicate that the subunit composition of AMPARs is dynamically remodelled in a cell- and synapse-specific manner in response to neuronal activity (Liu & Cull-Candy, 2000; Ju et al. 2004), sensory experience (Clem & Barth, 2006; Griffiths et al. 2008), and neuronal insults (Tanaka et al. 2000; Noh et al. 2005; Cull-Candy et al. 2006). Evidence exists that, even in cells expressing high levels of GluR2, a functionally relevant population of GluR2-lacking CP-AMPARs can be surface expressed under certain conditions (Ju et al. 2004; Clem & Barth, 2006; Plant et al. 2006). Thus, understanding the regulation of GluR2-lacking CP-AMPARs is of particular importance.
The prefrontal cortex is a region of the brain involved not only in normal cognitive function such as working memory and decision making but also in many psychiatric disorders. CP-AMPARs are preferentially expressed in discrete neuronal subpopulations, and their numbers appear to be upregulated (due to decrease of GluR2) in schizophrenia (Eastwood et al. 1995; Beneyto & Meador-Woodruff, 2006) and other psychiatric disorders such as drug addiction (Bellone & Luscher, 2006; Conrad et al. 2008; Van den Oever et al. 2008). Because of the close correlation between Ca2+ permeability and inward rectification in cortical neurons (Itazawa et al. 1997; Liu & Zukin, 2007), these cells are extremely sensitive to detrimental stimulations that would evoke abnormal Ca2+ influx under certain pathological conditions. Furthermore, because of its protracted functional maturation, it is expected that the underlying synaptic refinement process in these interneurons is not completed until late adolescence and early adulthood (Woo et al. 1997; Tseng & O’Donnell, 2007; Wang et al. 2008), which would greatly increase the chance of neuronal injury under extremely stressful conditions such as drug intervention (Spear, 2000; Conrad et al. 2008). In summary, because of the distinct physiological properties, FS interneurons expressing CP-AMPARs play different roles in integrating neuronal information within the prefrontal cortical circuit during normal and pathophysiological activities. They also show distinct vulnerability to disruptive influences such as psychostimulants, NMDA receptor antagonists, and other agents associated with Ca2+ influx due to high Ca2+ permeability. Therefore, understanding the detailed functions of CP-AMPARs in FS interneurons will help elaborate the functional vulnerability of these cells in the pathological process of psychiatric disorders.
W.-J.G. conceived the study, supervised the project, and wrote the manuscript. H.-X.W. carried out the experiments and data analysis. H.-X.W. also contributed to the manuscript preparation.
We thank Dr Jeremy Cohen for comments on the manuscript and Ms Pamela Fried at DUCOM Academic Publishing Services for editorial work. This study was supported by a grant from Drexel University College of Medicine, NARSAD young investigator awards, and the National Institutes of Health (R21MH232307 and R01MH232395) to W.-J. Gao. The NIH had no role in the study design; in the collection, analysis, and interpretation of the data; in the writing of the report; or in the decision to submit the paper for publication. The authors have no financial conflict of interest to disclose.