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The Journal of Neuroscience, June 1, 2002, 22(11):4428-4436

Activity-Dependent Recruitment of Extrasynaptic NMDA Receptor Activation at an AMPA Receptor-Only Synapse

Beverley A. Clark and Stuart G. Cull-Candy

Department of Pharmacology, University College London, London WC1E 6BT, United Kingdom


    ABSTRACT
TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

We have identified an excitatory synapse in cerebellar molecular layer interneurons at which the level of presynaptic activity determines the receptor type involved in the postsynaptic response. When small numbers of parallel fibers are activated, EPSCs are mediated solely by AMPA receptors (AMPARs), despite our finding that NMDA receptors (NMDARs) are present in the dendrites of these cells. The EPSC kinetics are fast (tau  decay = 0.82 ± 0.05 msec at room temperature), consistent with the role these interneurons are thought to play in precisely timed inhibitory control of Purkinje cells. NMDARs are activated only when glutamate release is increased either by facilitation with brief high-frequency trains or by recruiting more presynaptic fibers with higher stimulus intensities. Under these conditions, EPSCs consist of a fast-rising AMPAR-mediated current followed by a slow component mediated by both NMDARs and AMPARs. Inhibitors of glutamate transport increase the amplitude and prolong the time course of the compound EPSCs. In contrast, the properties of fast AMPAR EPSCs resulting from the activation of few inputs remain unchanged when glutamate uptake is blocked. Our results suggest that, at these synapses, the postsynaptic density contains AMPARs alone. It is only when transmitter release is high enough for glutamate to diffuse to the extrasynaptic space and to reach concentrations sufficient to activate extrasynaptic receptors that NMDARs are involved in the postsynaptic response. We suggest that such a spatial separation of receptor types may provide a mechanism for rapid changes in EPSC properties, depending on the amount of synaptic activity.

Key words: extrasynaptic NMDA receptor; AMPA-EPSC; diffusion; glutamate transporters; parallel fiber; cerebellar interneuron


    INTRODUCTION
TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

At central glutamatergic synapses, basic properties of EPSCs are determined by the receptor subtypes present and by the amplitude and spatiotemporal profile of the transmitter concentration transient within the synaptic cleft. Functional and immunocytochemical studies have shown that many central excitatory synapses possess both AMPA receptors (AMPARs) and NMDA receptors (NMDARs) in their postsynaptic density (PSD) (Jones and Baughman, 1991; Kharazia et al., 1996; Takumi et al., 1999) and that these are coactivated by the release of a quantum of neurotransmitter (Bekkers and Stevens, 1989; Silver et al., 1992; Umemiya et al., 1999). The relative contribution of AMPARs and NMDARs to the EPSC reflects not only their different biophysical properties (including the voltage-dependent block of NMDARs by Mg2+) but also differences in receptor density and affinity.

It is well established that EPSCs are mediated by NMDARs alone at several types of central synapses ("silent synapses"; Malinow et al., 2000). In contrast, there are very few examples of synapses in which EPSCs are mediated solely by AMPARs. "AMPAR-only" EPSCs have been described so far in cultured retinal ganglion cells (Taschenberger et al., 1995) and at excitatory synaptic inputs to Purkinje cells in cerebellar slices (Perkel et al., 1990; Llano et al., 1991). The observation that Purkinje cells from rats older than ~P14 lack functional NMDARs supports this finding (Farrant and Cull-Candy, 1991; Momiyama et al., 1996). We were interested to determine whether AMPAR-only synapses occur in neurons that do express functional NMDARs. The properties of NMDARs make it likely that, even at low density, extrasynaptic NMDARs will produce a detectable current if conditions arise whereby glutamate escapes the synaptic cleft.

Isolated somatic patches from molecular layer interneurons of the cerebellum contain both NMDAR and AMPARs (Cull-Candy et al., 1998; Clark and Cull-Candy, 1999; Liu and Cull-Candy, 2000). However, it has been reported that the NMDAR-mediated component of evoked EPSCs is small at parallel fiber (PF)-to-interneuron synapses (Glitsch and Marty, 1999). Whether this weak NMDAR-component arose from direct activation of synaptic receptors or from diffusion of glutamate to extrasynaptic sites is not known. However, it is clear that high-frequency, high-intensity trains of PF stimulation can activate EPSCs with large AMPAR and NMDAR components (Carter and Regehr, 2000). We have investigated whether this NMDAR component arises from synaptic or extrasynaptic receptors and how it is influenced by synaptic activity. We find that low-frequency activation of small numbers of PFs generates EPSCs mediated solely by AMPARs. Synchronous activation of larger numbers of synapses, or facilitation of glutamate release by stimulus trains, results in NMDAR activation that is enhanced by glutamate transporter blockers. We suggest that transmitter released from one or a few PF terminals fails to activate NMDARs because they are not colocalized with AMPARs in the PSD in these cells. Facilitation or overlap of glutamate released from multiple adjacent synapses activates extrasynaptic AMPARs and NMDARs. This results in a switch in the EPSC from AMPAR-only, to one containing both AMPAR- and NMDAR-mediated components, providing a mechanism for rapid changes in EPSC properties, depending on the intensity of synaptic activity.


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

Coronal or transverse cerebellar slices (200 µm) were cut from 18-d-old Sprague Dawley rats, as described previously (Barbour et al., 1994). Slicing and incubation solutions were adapted from Mann-Metzer and Yarom (1999) and consisted of (in mM): 85 NaCl, 2.5 KCl, 0.5 CaCl2, 4 MgCl2, 25 NaHCO3, 1.25 NaH2PO4, 75 sucrose, and 25 glucose, bubbled with 95% O2 and 5%CO2. Slices were maintained at 32°C for 1 hr, and the slicing solution was gradually replaced (1.3 ml/min) with extracellular solution containing (in mM): 125 NaCl, 2.5 KCl, 2 CaCl2, 1 MgCl2, 25 NaHCO3, 1.25 NaH2PO4, and 25 glucose. Slices were transferred to the recording chamber and, unless stated otherwise, perfused for 30 min (1.5 ml/min) with a nominally Mg2+-free extracellular solution before making recordings. All experiments were performed at 24 ± 0.5°C in the presence of 100 µM picrotoxin and 10 µM glycine, unless stated otherwise. In experiments in which 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX; Tocris Cookson, Bristol, UK) was used to block non-NMDA receptors, the glycine concentration was increased to 50 µM to minimize the effect on the glycine site of the NMDA receptor (Lester et al., 1989). All chemicals were obtained from Sigma-Aldrich (Dorset, UK) unless otherwise stated.

Recording synaptic currents. Whole-cell recordings were made from visually identified stellate cells (Häusser and Clark, 1997) using an Axopatch200B amplifier (Axon Instruments, Union City, CA). Slices were viewed with an upright microscope (Axioskop FS1; Zeiss, Welwyn Garden City, UK) using infrared-differential interference contrast optics (Stuart et al., 1993). Electrodes of 3-5 MOmega were pulled from thick-walled borosilicate glass (GC-150F; Harvard Apparatus Ltd, Edenbridge, UK), coated with Sylgard resin (Dow Corning 184) and fire polished. These were filled with an intracellular solution of (in mM): 125 CsCl, 10 HEPES, 10 BAPTA, 10 TEACl, 1 QX314, 2 Na2ATP, 2 MgATP, 0.3 Na3GTP, and 0.5 CaCl2, adjusted to pH 7.25 with CsOH, giving a final osmolarity of 285 ± 5 mOsmol/l. A 10 mM concentration of BAPTA was included to minimize the calcium-dependent inactivation of NMDA receptors (Rosenmund et al., 1995). Series resistance was monitored continuously throughout experiments and ranged from 6 to 15 MOmega . For series resistances >10 MOmega , partial compensation (60-75%) was used by means of the amplifier compensation circuit. Data were filtered at 5 kHz and digitized at 33 kHz. PF inputs to stellate cells were stimulated (<200 µsec, ± biphasic pulses) using a patch electrode (3-5 MOmega ) placed in the molecular layer at least 100 µm away from the recording electrode. Interstimulus intervals were 5-10 sec. "Low-intensity stimulation" (8-15 V) was used in some experiments. This was the threshold voltage required to activate the smallest possible number of PFs, with a failure rate of >30%. Even at this intensity, there was a significant amount of release asynchrony. To evaluate the involvement of NMDA receptors in EPSCs evoked by low-intensity stimulation, average EPSCs were constructed from events selected to avoid a contribution of release asynchrony to the EPSC time course. EPSC decays were fitted (t = 0 at the peak) with one or two exponentials, and the weighted tau (tau w) was calculated according to: tau w = (tau 1 * a1) + (tau 2 * a2), where a1 and a2 are the relative amplitudes of the two exponential components.

Ionophoresis of glutamate. Pipettes for ionophoresis were pulled from thin-walled borosilicate filamented glass using a Livingstone-type puller (Narishige, Tokyo, Japan). Electrodes had resistances of 30-50 MOmega when filled with 100 mM sodium glutamate. Current pulses of between -30 and -90 nA and of 5-25 msec duration were required to eject glutamate. No retaining current was needed. To identify the dendrites and axons of interneurons and to map responses to glutamate, cells were filled via the patch electrode with the fluorescent dye Alexa Fluor 594 hydrazide (25 µM; Molecular Probes, Eugene, OR). The Alexa dye was also included in the ionophoresis electrode, which by virtue of its negative charge, was ejected with the glutamate, allowing visualization of the ionophoresis electrode and the area of glutamate ejection. To quantify responses from different zones of glutamate ionophoresis, averages of at least 30 sweeps were made, aligning on the first rising point of the ionophoretic pulse.

Local perfusion of glutamate transporter blockers. Extracellular solution containing the glutamate transporter blockers DL-threo-beta -benzyloxyaspartate (DL-TBOA, a generous gift from Keiko Shimamoto; Shimamoto et al., 1998) or L-trans-pyrrolidine-2,4-dicarboxylic acid (L-trans-PDC, Tocris Cookson) were applied locally using a pressure application system. Pipettes (2-3 MOmega ) pulled from thin-walled borosilicate filamented glass were used, and the pressure was adjusted to avoid movement artifacts. Using this technique, it was possible to interleave groups of sweeps of evoked EPSCs with those evoked in the presence of blockers, controlling for instability of EPSC amplitude and avoiding the effects of prolonged application of transporter blockers.


    RESULTS
TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

Unitary EPSCs in molecular layer interneurons arise solely from AMPAR activation

To investigate the relative contribution of both AMPA and NMDARs to synaptic transmission in molecular layer interneurons (stellate cells), we have examined spontaneous and evoked EPSCs in nominally Mg2+-free external solution. EPSCs were evoked by low-intensity stimulation (see Materials and Methods) of PFs. To be certain that any NMDAR-mediated component would be detected, EPSCs were recorded at both positive and negative holding potentials. Figure 1A shows single sweeps in which EPSCs were evoked at -60 and +50 mV with low-intensity stimulation. No detectable NMDAR-mediated component was apparent under control conditions at either holding potential.



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  		Figure 1.   Spontaneous EPSCs and those evoked in interneurons by low-intensity stimulation are mediated by AMPA receptors alone. A, Individual sweeps in which EPSCS were successfully evoked by threshold stimulation of the parallel fibers. EPSCs under control conditions (left) and in the presence of 50 µM D-AP-5 (right) are shown at holding potentials of -60 and +50 mV. The stimulus artifact is lost because of the restricted time window shown. B, Overlay of averages of >30 sweeps in both conditions shows that NMDA receptor antagonists have no effect on the EPSC time course. C, Examples of consecutive single spontaneous EPSCs (sEPSCs) occurring in an interneuron recorded at -60 mV in nominally Mg2+-free conditions. The normalized average EPSCs are shown on the far right with the fitted biexponential function indicated by the dotted line. Addition of 50 µM D-AP-5 (bottom row) had no effect on the sEPSC, and there was no significant difference in the fitted average.

To minimize the contribution of asynchronous release to the mean EPSC time course, events with notched rises or multiple peaks were discarded. The averaged currents shown in Figure 1B were generated by aligning EPSCs on their initial rise (10% of full amplitude; mean 10-90% rise time = 0.19 ± 0.01 msec; n = 9). The decay of the averaged EPSCs was rapid and could be fitted with two exponential components, giving a weighted mean time constant (tau w) of 0.82 ± 0.05 msec (n = 9) at -60 mV and 1.24 ± 0.2 msec (n = 4; p = 0.08 paired t test) at +50mV. As is apparent from Figure 1B, the addition of D-AP-5 did not significantly alter the average EPSC decay at either positive or negative potentials (0.83 ± 0.05 msec at -60 mV; 1.27 ± 0.04 msec at +50 mV; p = 0.9). Furthermore, the decay time course of spontaneous EPSCs (tau w = 1.16 ± 0.12 msec at -60 mV, 1.4 ± 0.12 msec at +50mV; n = 5) was not significantly different from EPSCs evoked by low-intensity stimulation. These were also unaffected by D-AP-5, yielding mean weighted decay time constants of 1.16 ± 0.13 msec at -60 mV, and 1.48 ± 0.16 msec at +50 mV (n = 6 cells) (Fig. 1C). Because we found that the EPSCs were abolished by the non-NMDAR antagonist CNQX (10 µM) and by the selective AMPAR antagonist GYKI 53655 (10-25 µM) (Liu and Cull-Candy, 2000), our data indicate that at these synapses the unitary EPSCs were mediated purely by AMPAR activation.

The extrasynaptic spread of glutamate depends critically on temperature (Asztely et al., 1997). Along with a likely increased release probability (Van der Kloot and Molgo, 1994; Hardingham and Larkman 1998), the diffusion coefficient increases slightly with temperature (Hille, 1992). Counterbalancing this, uptake of glutamate by transporters increases strongly with temperature (Wadiche and Kavanaugh, 1998). We examined EPSCs at more physiological temperatures to see if any of these factors could change the contribution of NMDARs. When EPSCs were evoked by low-intensity stimulation at 35°C, the decay times were faster than at room temperature, giving mean weighted decay time constants of 0.61 ± 0.05 msec (n = 5 cells) at -70 mV and 0.86 ± 0.15 msec (n = 3 cells) at +50 mV. Furthermore, the EPSCs remained insensitive to D-AP-5 at positive and negative potentials, confirming the absence of an NMDAR-mediated component to the EPSCs under these conditions.

Recent work has indicated that differences may occur in the synaptic and extrasynaptic distribution of receptors containing the NR2A subunit (Rumbaugh and Vicini, 1999; Tovar and Westbrook, 1999). NR2A-containing receptors can be observed exclusively at synaptic locations during synaptic maturation, whereas extrasynaptic receptors do not contain this subunit. The glycine sensitivity of NMDARs is dependent on receptor subunit composition, with NR1/NR2A receptors requiring a high concentration of glycine to be fully activated (Kutsuwada et al., 1992). One possible explanation for the lack of an NMDAR-mediated component in unitary EPSCs in interneurons might be that the glycine concentration used (10 µM) was insufficient for activation of any NR2A-containing receptors that might be present at PF-interneuron synapses. We compared threshold-evoked EPSCs in the presence of 10 and 50 µM glycine in nominally Mg2+free solution. In five cells tested, no difference was found between EPSCs evoked under the two conditions. An example of this is illustrated in Figure 2.



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  		Figure 2.   An NMDAR-mediated component is not revealed by increased glycine concentration A, Average responses in an interneuron to low-intensity parallel fiber stimulation at 0.5 Hz in the presence of 10 µM (top panel) and 50 µM (bottom panel) glycine at a holding potential of -60 mV. B, Overlay of normalized average EPSCs under the two different glycine concentrations and after addition of D-AP-5 shows that no NMDAR current was revealed when glycine concentration was increased.

NMDARs are present on the dendrites of molecular layer interneurons

There is evidence that spillover of glutamate following bulk activation of PFs can activate NMDARs in molecular layer interneurons (Carter and Regehr, 2000). However, it is not known whether these receptors are located on the dendrites or mainly on the soma and axon. The possibility that at least some NMDARs are present in the axon is supported by the demonstration that direct application of NMDA onto these neurons modulates the release of GABA from their axon terminals (Glitsch and Marty, 1999). To assess whether NMDARs are present on the dendrites of molecular layer interneurons and hence near to synaptic inputs or whether the lack of involvement of NMDARs in the generation of unitary EPSCs reflected their absence from the dendrites, we tested the response of these cells to glutamate applied selectively to different segments of the same neuron (in the presence of 10 µM CNQX). While recording from the soma of interneurons filled with the fluorescent dye Alexa Fluor 594, we mapped NMDAR responses by applying 25 msec ionophoretic pulses of glutamate onto the dendrites, soma, and axon.

The results of such an experiment are depicted in Figure 3. The top panel (Fig. 3A) shows the soma and dendrites of a filled interneuron; the lower panel shows part of the axon at higher magnification. Figure 3B shows the responses obtained when glutamate was applied at the dendritic, somatic, and axonal locations indicated by the arrows in Figure 3A. The largest responses were invariably obtained from the soma, but responses were also readily obtained from the dendrites. No current was recorded when glutamate was ejected onto the axon (n = 4 cells, each axon was tested at multiple locations) or when the ionophoretic pipette was moved ~20 µm above the focal plane of the cell. These experiments indicate that, although not involved in generation of unitary EPSCs, NMDARs are present on the soma and dendrites of molecular layer interneurons. This suggests that they are distant from the sites of glutamate release and therefore are not colocalized with the AMPARs that mediate the unitary EPSC. The lack of response from the axon suggests that any NMDARs present on the axon terminals occur at low density and that the current evoked is too small to be resolved during somatic recording.



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  		Figure 3.   Ionophoretic mapping of NMDAR-mediated responses in a molecular layer interneuron. A, Sagittal view of an interneuron filled with Alexa Fluor 594 during whole-cell patch recording. The dendrites and soma are shown in the top panel, and a section of the axonal arbor is shown in the bottom panel. The locations of glutamate application by ionophoresis are indicated by the arrows. B, Averages of 25 currents recorded in response to 25 msec pulses of glutamate (100 mM in electrode) ejected onto the dendrites, soma, and axon of the illustrated cell. Holding potential was -60 mV, and the antagonists TTX (0.5 µM), picrotoxin (100 µM), and CNQX (10 µM) were present in nominally Mg2+-free solution.

The contribution of NMDARs to EPSCs depends on the number of parallel fibers activated

The AMPAR-mediated EPSCs described above were evoked after the activation of a small number of PFs. Although the duration of the synaptic glutamate transient and the distance over which glutamate travels from its release site are not known, both of these parameters are likely to be increased if release occurs simultaneously at several closely spaced synapses (Otis et al., 1996; Barbour and Häusser, 1997; Rusakov et al., 1999). We therefore next investigated whether activating a greater number of PF axons could influence the type of receptors that contribute to the EPSC.

Figure 4A shows EPSCs produced by activating a progressively larger number of PFs. This was achieved by increasing the stimulus strength from its initial "low intensity" value by 10 V increments. In Figure 4A, the initial low-intensity stimulus (10 V) and the first incremental increase (20 V), evoked an EPSC that was abolished by CNQX. However, it is apparent that at higher stimulus intensities a small, slowly decaying component remained. This residual current was blocked by D-AP-5 (50 µM; data not shown) indicating that it was mediated by NMDARs. Figure 4B shows the relationship between stimulus intensity and the total charge carried by AMPAR and NMDAR channels (five cells). The NMDAR-mediated component was apparent only at stimulus strengths greater than approximately twice the threshold intensity. There was no significant NMDAR-mediated response at the first incremental increase in stimulus strength (charge not significantly different from zero; p = 0.4), showing that synchronous release of glutamate from a larger number of PFs, than was activated using threshold stimulation, was required to activate NMDARs in these cells. Given that NMDARs exhibit a higher apparent affinity for glutamate than do AMPARs, this observation suggests that the NMDARs are distant from release sites and are activated only by pooling of transmitter from multiple active synapses. This idea is supported by the fact that the rise time for the NMDA component was relatively slow (time-to-peak, 40 ± 4.9 msec; n = 9 cells), which may also reflect the lower concentration of glutamate present at the extrasynaptic receptors (Clements and Westbrook, 1991; Haas et al., 1998).



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  		Figure 4.   Increased synaptic activity results in a compound EPSC mediated by both AMPA and NMDA receptors. A, Mean EPSCs (averages of 25-50 sweeps) resulting from parallel fiber stimulation using the different stimulus intensities shown (Vhold = +50 mV). Top traces are controls, and bottom traces are in the presence of 10 µM CNQX (note different calibration), showing the appearance of an NMDA component at 30 V stimulus intensity. B, Summary of charge carried by AMPAR and NMDAR channels with respect to stimulus intensity (n = 4). Values for AMPAR-mediated charge transfer were obtained by subtracting values in CNQX from those in control conditions. T, Threshold low-intensity stimulation.

Facilitation of glutamate release from a small number of parallel fibers can activate NMDARs

Although dendritic NMDARs in these interneurons can be activated by glutamate released by large numbers of PFs, in principle, if release was facilitated, these receptors should also be activated during stimulation of a small number of fibers. To address this issue we examined the effect of trains of stimuli, which have been shown to enhance glutamate release without recruiting additional PFs (Kreitzer and Regehr, 2000). Specifically, we investigated the frequency dependence of NMDAR activation by using suprathreshold stimulation intensities, which were just sufficient to avoid failures of the fast AMPAR-mediated EPSCs.

After the addition of 10 µM CNQX, we applied bursts of four stimuli (0.5-100 Hz) to PFs. As shown in Figure 5A, an NMDAR-mediated component was activated at stimulus frequencies of >= 6.25 Hz. The size of this current varied considerably from cell to cell, particularly at longer interstimulus intervals when its amplitude was difficult to quantify. We therefore integrated the average current to obtain the charge transfer. Figure 5A shows typical examples of these current integrals (smooth line) at the frequencies tested, overlaid with the averaged currents in which four stimulus artifacts indicate the timing of the stimuli. The mean charge transfer from seven cells is summarized in Figure 5B. Values have been normalized to those obtained at 100 Hz. The NMDAR charge transfer increased steeply in the lower frequency range and had still not reached a plateau at 100 Hz stimulation. These experiments indicate that a modest increase in action potential firing frequency, arising within a small number of fibers, is sufficient to change the synaptic response from AMPAR-only to one mediated both by AMPARs and NMDARs at these synapses.



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  		Figure 5.   Frequency dependence of NMDA receptor-mediated EPSCs. A, Trains of four parallel fiber stimuli evoked CNQX-insensitive currents in interneurons voltage clamped at +50 mV, which increased in amplitude with increasing frequency of stimulation. The current integral (smooth line) is superimposed on the mean synaptic currents (averages of 25-30 sweeps). B, Charge transfer normalized to that obtained at 100 Hz is represented with respect to stimulation frequency for seven cells. Error bars indicate SEM.

The influence of glutamate transporters on NMDAR contribution to EPSCs

Inhibitors of glutamate transporters have been shown previously to have little effect on the time course of the non-NMDAR-mediated EPSC in molecular layer interneurons (Barbour et al., 1994). However, if the NMDAR-mediated EPSC that we observed was generated by receptors located distant from release sites, it would be expected to be enhanced in the presence of glutamate uptake blockers. We therefore examined this possibility. In the absence of synaptic stimulation, application of the transporter blocker L-trans-pyrrolidine-2,4-dicarboxylic acid (L-trans-PDC; 100 µM) reduced the amplitude of spontaneous synaptic currents and generated a large inward current accompanied by a noise increase. This suggested an accumulation of glutamate in the extracellular space, likely not only because of block of uptake but also because of glutamate release by heteroexchange triggered by the transport of L-trans-PDC (Griffiths et al., 1994; Volterra et al., 1996; Koch et al., 1999). It was therefore not possible to interpret the data obtained in the presence of this transporter blocker.

We next turned to the selective glutamate transporter blocker DL-TBOA (50 µM), which is neither transported nor causes heteroexchange of glutamate (Shimamoto et al., 1998; Waagepetersen et al., 2001). In addition, we made these recordings at positive holding potentials in the presence of 1 mM Mg2+. This was to minimize the actions of untransported glutamate on NMDARs in other neurons in the slice. Figure 6 illustrates average data from a cell in which EPSCs were evoked at 0.5 Hz (Fig. 6A) and 50Hz (Fig. 6B) at increasing stimulus intensities (V1-V3). DL-TBOA was applied locally from a perfusion pipette. The top traces in Figure 6, A and B, illustrate the effect of DL-TBOA on EPSCs in the absence of glutamate receptor antagonists; the bottom traces show its effect on the NMDAR component (in the presence of 5 µM CNQX). From the data in the left-hand panels of Figure 6A, it is apparent that DL-TBOA had little effect on EPSCs evoked by low-intensity, low-frequency stimuli. However, when a greater number of PFs were activated at low frequency (V2 and V3), DL-TBOA prolonged the EPSCs. When bursts of stimuli were used to facilitate release (Fig. 6B), DL-TBOA had a small effect when the stimulus intensity was low (V1), but this effect was greatly enhanced with increasing stimulus strength. The dramatic effect of DL-TBOA on the NMDAR-mediated component is more clearly seen in the presence of CNQX (Fig. 6B, bottom traces).



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  		Figure 6.   Effect of glutamate transporter blockade on interneuron EPSCs. A, Average EPSCs evoked at 0.5 Hz at three increasing stimulus intensities. Superimposed thin and thick traces are averaged data in the absence and presence of 50 µM DL-TBOA, respectively. Top traces show the effect of DL-TBOA under control conditions, and bottom traces show the effect on the NMDAR-mediated component isolated in 20 µM CNQX. B, Responses of the same cell as in A to 50 Hz trains of parallel fiber stimuli. DL-TBOA application prolonged the compound EPSC train at all stimulus intensities and, in this cell, enabled activation of an NMDA component that was previously absent at V1. Stimulus artifacts have been blanked, and stimulus timing is marked by the filled triangles.

The remaining experiments on the effect of DL-TBOA on the NMDAR-mediated component of the EPSC were performed in the presence of CNQX. The results are summarized in Figure 7. The magnitude of the effect of DL-TBOA was clearly dependent on the initial NMDAR-mediated charge transfer with both 0.5 and 50 Hz stimulation (Fig. 7A,B). This is consistent with the idea that the effect of DL-TBOA depended on the quantity of glutamate released. Hence, the larger the initial charge, the greater its increase in the presence of DL-TBOA. As shown in Figure 7C, the time taken for the NMDA current to reach its peak (measured from the beginning of the 50 Hz train) depended on stimulus intensity and was prolonged by blockade of glutamate transport.



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  		Figure 7.   The effect of inhibition of glutamate transporters is correlated with the amount of glutamate released. A, The relationship between initial NMDAR-mediated charge resulting from a single stimulus at 0.5 Hz for different stimulation intensities. Each data point represents one stimulation intensity for each of the seven cells included. Correlation coefficients (R) and degree of significance (p) were obtained using nonparametric tests (KS). B, Same as A, but for 50 Hz trains. C, The effect of stimulus intensity on the time taken for NMDAR-mediated current resulting from 50 Hz trains to reach peak amplitude.


    DISCUSSION
TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

We have identified a synapse in molecular layer interneurons, at which unitary EPSCs are mediated by AMPA receptors alone, despite the observation that these cells express functional NMDARs. These NMDARs are activated by synaptically released glutamate only under conditions of intense activity. Our findings reveal a switch in functional behavior of the synapse that is regulated by the level of presynaptic activity: unitary EPSCs are mediated purely by AMPARs, whereas compound EPSCs are mediated by both AMPAR and NMDARs. Transporters regulate the extent of NMDAR activation, but only under conditions of dense PF activity. These findings identify, for the first time, a synapse in which the type of ionotropic glutamate receptor activated depends on the amount of synaptic activity.

Activity dependence of glutamate receptor contribution to EPSCs

We find that activation of a small number of PF synapses on molecular layer interneurons (such as during spontaneous synaptic release of glutamate) generates EPSCs mediated purely by AMPARs. The decay time course of these EPSCs is fast and is consistent with the deactivation time constant of AMPARs measured in outside out patches from these neurons (Barbour et al., 1994). Stimulation of larger numbers of fibers increases the EPSC amplitude and recruits an NMDAR-mediated current to the synaptic response. Because our experiments show that NMDARs are present in the dendrites of these neurons, it is likely that these receptors are involved in generating this current.

What underlies this activity-dependent difference in NMDAR involvement in synaptic transmission? Because NMDARs have a high apparent affinity for glutamate when compared with AMPARs (Lester et al., 1990; Clements and Westbrook, 1991), their activation would be expected to accompany the AMPAR-EPSC if both receptor types were present in the PSD (Clements et al., 1992; Holmes, 1995; Diamond, 2001). The most likely explanation for the lack of NMDAR contribution to the unitary response, is that, although AMPARs are present in the PSD (as indicated by the rapid AMPAR EPSC rise time; 0.19 ± 0.01 msec n = 9 10-90%), NMDA receptors are located outside the postsynaptic specialization and activated only after increased transmitter release.

Immunocytochemical techniques using nondiffusible markers (such as gold particles) have been used to examine synaptic localization of neurotransmitter receptors in electron microscopic sections of tissue from different brain regions. To date, no detailed comparison of AMPA and NMDAR localization has been made in the molecular layer of cerebellum. In particular, immunoreactivity for NMDARs at PF-interneuron synapses has not been described. Although immunocytochemical (Takumi et al., 1999; Racca et al., 2000) and functional approaches (Wu et al., 1996; Isaac et al., 1997; Li and Zhuo, 1998; Rumpel et al., 1998) have identified synapses in various brain regions that contain only NMDARs, most central synaptic currents are mediated both by AMPARs and NMDARs, when both are present in the cell. Indeed, available evidence suggests that the majority of AMPAR and NMDARs are concentrated in the PSD with a steep decline in concentration at the edges of the postsynaptic specialization. In contrast, our data suggest that at PF-interneuron synapses, NMDARs are not targeted to the PSD and are expressed only in the extrasynaptic membrane.

The dendrites of molecular layer interneurons are mostly aspiny, and the majority of excitatory synapses are made onto smooth dendritic membrane (Palay and Chan-Palay, 1974). In addition, glial processes are rarely observed in close proximity to these synapses (Chaudhry et al., 1995), and so diffusion out of the synaptic cleft will be less restricted in comparison with synapses made onto spines. When glutamate is released from few (one or two) synapses, the glutamate transient is likely to be short-lived, because glutamate diffuses quickly away from the release site and is diluted in the extracellular space. Under these conditions, the transmitter concentration outside the synaptic cleft is unlikely to be sufficient to activate extrasynaptic receptors. The fast decay kinetics of the pure AMPAR EPSC that we observe when few fibers are activated suggests that this is the case at PF synapses on interneurons. With dense activity of parallel fibers, glutamate may accumulate to activate extrasynaptic NMDARs, because the free diffusion between synapses would be expected to allow spillover of transmitter from adjacent boutons. In this context we use "spillover" to refer to glutamate diffusion to extrasynaptic receptors and not necessarily to receptors at neighboring synapses. Our experiments demonstrate with, stimulus trains, that frequency-dependent facilitation of glutamate release enhances this effect.

Another possible explanation of our findings may be that some PF synapses onto interneurons do contain NMDARs but that these synapses have a very low release probability (Pr) and generate EPSCs only under conditions when Pr is enhanced, such as during high-frequency activation. This possibility is difficult to address directly, because manipulations to increase Pr also greatly reduce the likelihood of evoking EPSCs from just a small number of synapses. However, we found that an increase in temperature, another condition that is expected to increase Pr (Van der Kloot and Molgo, 1994; Hardingham and Larkman 1998), did not reveal a population of synapses at which an NMDAR component contributed to EPSCs evoked by low-intensity stimulation. It is also not possible to entirely rule out that some PF synapses on interneurons may contain NMDARs, although we did not detect them in this study. If this is the case, they may contribute to the NMDAR-mediated component observed during high-intensity or high-frequency stimulus protocols. However, it is unlikely that they would be solely responsible for the NMDAR component, because such synapses are likely to be few in number, in comparison with the AMPAR-only synapses.

The role of glutamate transporters in NMDA receptor activation

We find that, during low-intensity stimulation at low frequency, block of glutamate transport does not induce an NMDAR involvement in the EPSC. However, it does increase the NMDAR-mediated charge transfer when glutamate release is enhanced, either by activation of more synapses or by facilitation by high-frequency bursts. This is likely to be a consequence of two factors. First, as discussed above, the spatial profile of glutamate will be different under the two conditions, with greater activity producing a much wider spread of glutamate. Second, if glutamate transporters are located distant from the synapse, uptake will be effective only when the glutamate transient spreads far enough to reach them.

The lack of glial processes around excitatory synapses onto cerebellar interneurons (Chaudhry et al., 1995) not only implies that the diffusional path between synapses is clear, but also that the distance from the site of glutamate release to the nearest glial glutamate transporters (GLT1 and GLAST) is long. Immunogold labeling of GLT1 and GLAST has shown that these transporters are located more distant from PF-interneuron synapses compared with PF-Purkinje cell synapses and, in addition, that they are present at lower densities (Chaudhry et al., 1995). Although there is some evidence that the neuronal transporter EAAC1 may be present in molecular layer interneurons (Furuta et al., 1997), it is not known whether this transporter is localized perisynaptically in these cells. Because transporter blockers did not affect EPSCs arising from a small number of active parallel fibers, it is probable that any neuronal glutamate transporters present are not optimally located to regulate NMDAR involvement under conditions when release is low. This result also rules out the possibility that NMDARs are perisynaptic and that synaptic glutamate transporters prevent their activation during single fiber EPSCs.

Functional implications for excitation of molecular layer interneurons

Parallel fibers (granule cell axons), are densely packed in the molecular layer of the cerebellum. Little is known about patterns of activity in vivo from the granule cells onto their targets (interneurons and Purkinje cells). Specifically, it is not known whether coincident excitatory inputs converge onto a localized area of dendrite or if they are distributed across different, distinct dendritic areas. According to our findings, the number and spatial distribution of active fibers will determine whether or not NMDARs are activated in vivo. Although dense parallel fiber activity (when many adjacent fibers are activated), will result in NMDAR activation in interneurons, it is probable that an equivalent number of sparsely distributed but coincident inputs might generate purely AMPAR-mediated EPSCs. In effect this means that the same number of active inputs can drive two different kinds of postsynaptic response, depending on the way in which they are organized.

Molecular layer interneurons spontaneously fire action potentials in vivo (Armstrong and Rawson, 1979) and in slice preparations. This provides a continuous but irregular barrage of inhibitory input to both Purkinje cells and other interneurons, which modulates integration of postsynaptic potentials (Häusser and Clark, 1997). In addition, synaptically driven action potentials in interneurons are thought to provide specifically targeted inhibitory inputs that shape the response of Purkinje cells to excitation (Eccles et al., 1967). The presence of AMPAR-only synapses that generate EPSCs of relatively fast kinetics will allow temporally precise coupling of single EPSCs to action potentials and thus enable accurately timed inhibitory output. This behavior would be consistent with emerging principles of interneuron function (Geiger et al., 1997).

We have found previously that AMPARs at PF-interneuron synapses can be Ca2+-permeable when parallel fibers are stimulated at low frequency (Liu and Cull-Candy, 2000). Little is known about the characteristics of calcium transients resulting from synaptic activation of calcium-permeable AMPARs or from slower NMDAR-mediated currents resulting from spillover of transmitter onto extrasynaptic sites. It will be interesting to discover whether the calcium signals resulting from these two routes of calcium entry are quantitatively different. It may be that a spatial separation of calcium-permeable AMPARs and NMDARs in some neuronal dendrites can provide for two distinct types of calcium signal in response to synaptic input.


    FOOTNOTES

Received Dec. 19, 2001; revised March 22, 2002; accepted March 22, 2002.

This work was supported by The Wellcome Trust. We are grateful to Keiko Shimamoto (Suntory Institute for Bioorganic Research) for the generous gift of TBOA. We thank Steven Brickley, Mark Farrant, Michael Häusser, and Arnd Roth for helpful comments on this manuscript.

Correspondence should be addressed to S. G. Cull-Candy, Department of Pharmacology, University College London, Gower Street, London WC1E 6BT, UK. E-mail: s.cull-candy{at}ucl.ac.uk or b.clark{at}ucl.ac.uk.


    REFERENCES
TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
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