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J Physiol 593.4 (2015) pp 843–856
Dynamic regulation of D-serine release in the vertebrate retina Eric G. Gustafson1 , Eric S. Stevens2 and Robert F. Miller1 1 2
Department of Neuroscience, University of Minnesota Medical School, Minneapolis, MN 55455, USA Oroville Eye Associates Inc., Oroville, CA 95966, USA
Key points
r Activation of NMDA receptors (NMDARs) is essential for encoding visual stimuli into signals
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r r r r
for the brain, although their over-activation can cause cell death. The recruitment of NMDARs is important for encoding light intensity in retinal ganglion cells. D-serine binding is essential for proper activation of NMDARs, although its role in signal processing and the mechanisms that underlie its availability are not well understood. In these light-evoked experiments, the addition of exogenous D-serine had a large effect on low contrast and low intensity NMDAR responses that decreased as the intensity was increased. The degradation of endogenous D-serine decreased the responses more at higher intensities. The results provide compelling evidence favouring a new interpretation of NMDAR recruitment in which light-evoked D-serine release serves an important regulatory control over the recruitment of NMDARs.
Abstract The present study aimed to investigate the functional properties of NMDA receptor coagonist release and to specifically evaluate whether light-evoked release mechanisms contribute to the availability of the coagonist D-serine. Two different methods were involved in our approach: (i) whole-cell recordings from identified retinal ganglion cells in the tiger salamander were used to study light adaptation with positive and negative contrast stimuli over a range of ± 1 log unit against a steady background illumination and (ii) the mechanisms for intensity encoding to a range of light intensities covering 6 log10 units were investigated. This latter study employed extracellular recordings of the proximal negative field potential, pharmacologically manipulated to generate a pure NMDA mediated response. For the adaptation study, we examined the light-evoked responses under control conditions, followed by light stimuli presented in the presence of D-serine, followed by light stimulation in the presence of dichlorokynurenic acid to block the coagonist site of NMDA receptors. For the brightness encoding studies, we examined the action of D-serine on each intensity used and then applied the enzyme D-serine deaminase to remove significant levels of D-serine. These studies provided new insights into the mechanisms that regulate coagonist availability in the vertebrate retina. Our results strongly support the idea that light-evoked coagonist release, a major component of which is D-serine, is needed to provide the full range of coagonist availability for optimal activation of NMDA receptors. (Received 5 September 2014; accepted after revision 29 November 2014; first published online 4 December 2014) Corresponding author E. G. Gustafson: Department of Neuroscience, University of Minnesota Medical School, 6–145 Jackson Hall, 321 Church Street SE, Minneapolis, MN 55455, USA. Email: [email protected] Abbreviations AP7, D,L-2-amino-phosphonoheptanoate; DAAO, D-amino acid oxidase; DCK, dichlorokynurenate; DsdA, D-serine deaminase; GlyT1, glycine transporter type 1; NBQX, 2, 3-dihydroxy-6-nitro-7-sulfamoyl-benzo(F)-quinoxalinedione; NMDAR, NMDAR receptor; PNFP, proximal negative field potential; SR, serine racemase.
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DOI: 10.1113/jphysiol.2014.283432
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Introduction NMDA receptors (NMDARs) are the only glutamate receptors that require a coagonist in addition to glutamate to properly gate the NMDAR ion channel: all other glutamate receptors can be opened by glutamate alone. When the requirement for a coagonist for NMDARs was first discovered, glycine quickly took centre stage as the leading candidate for what turned out to be an obligatory coagonist role (Johnson & Ascher, 1987). Shortly after glycine assumed its new status, studies revealed that other amino acids could substitute for glycine, among which were D-amino acids, including D-serine (Dingledine et al. 1990). Because D-amino acids were not considered to be part of the vertebrate amino acid repertoire, the report that D-serine is found in the brain in relatively high concentrations, especially in brain regions where NMDARs are enriched (Hashimoto et al. 1992), was unexpected. Subsequently, the main synthetic pathway for D-serine was revealed in the form of serine racemase (SR), an enzyme that converts L-serine to D-serine (Wolosker et al. 1999). Initially, SR was identified in astrocytes, although subsequent work revealed that it is also present in neurons, so that the cells responsible for D-serine synthesis and release became and remain an issue of some controversy (Kartvelishvily et al. 2006). More recent insights into the nature of D-serine synthesis have implicated astrocytes as a source of L-serine, whereas D-serine may be synthesized primarily by neurons and then taken up and released by astrocytes (Ehmsen et al. 2013). Whether this recent proposal accounts for D-serine synthesis and release in all regions of the nervous system remains to be explored. It should be added that studies in the retina strongly favour a glial source for the release of the D-serine (Sullivan & Miller, 2010) or at least the component that is evoked by the exogenous application of AMPA + cyclothiazide. Shortly after the discovery of SR in the brain, work in the retina established both the presence of D-serine and its synthesizing enzyme SR (Stevens et al. 2003). Immunolabelling studies localized D-serine and SR to M¨uller cells and astrocytes, although more recent work has also identified retinal ganglion cells as a source of SR (Dun et al. 2008; Kalbaugh et al. 2009). There is evidence that D-serine may be developmentally regulated in the retina (Dun et al. 2008). Physiological studies were carried out in the retina to identify the coagonist preference for NMDA receptors in retinal ganglion cells. This was especially critical because glycine, the competing NMDAR coagonist, subserves inhibition in the retina mediated by a subclass of glycinergic amacrine cells; thus, the inner retina has a cellular source of light-evoked release of glycine that could serve a coagonist function and work reported by Kalbaugh et al. (2009) suggested that this was the case.
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Experiments carried out in the whole retina revealed that the coagonist NMDA receptor sites were not saturated under modest stimulus conditions because exogenous D-serine consistently enhanced NMDAR ionic currents. A powerful D-serine degrading bacterial enzyme, D-serine deaminase (DsdA), was used to significantly reduce D-serine levels, such that the NMDA receptor currents in ganglion cells were almost abolished and reduced to levels very close to those achieved by blocking the NMDA receptors with high levels of competitive antagonists, such as D,L-2-amino-phosphonoheptanoate (AP7) (Gustafson et al. 2007). What emerged from these studies was the idea that D-serine was probably the main and perhaps the only coagonist for NMDA receptors of retinal ganglion cells, at least those activated by light-evoked synaptic pathways. A recent report suggests that non-synaptic NMDA receptors in the retina may utilize glycine as a coagonist (Sullivan & Miller, 2012), an idea that has gained favour based on studies in the brain (Papouin et al. 2012). Additional experiments were carried out to clarify the role of glycine as an NMDAR coagonist. It has been noted that, for D-serine to be effective as a coagonist, glycine, which is present in higher concentrations than D-serine (Reed et al. 2009), must be effectively reduced in concentration by local glycine uptake mechanisms, specifically the Na+ -dependent glycine transporter type 1 (GlyT1) uptake system (Supplisson & Bergman, 1997). When GlyT1 transporters were blocked with N[3-(4 fluorophenyl)-3-(4 -phenylphenoxy)-propyl]sarcosine (Stevens et al. 2010), coagonist NMDAR sites in the retina became fully occupied because external levels of glycine were elevated. Furthermore, mice in which the GlyT1 transporter had been partially knocked out (GlyT1−/+ ) showed full occupancy of NMDA receptor coagonist sites (Reed et al. 2009), supporting the importance of this transport system in reducing local glycine levels, allowing D-serine to serve in this capacity. GlyT1 transporters are richly represented in the inner plexiform of the retina (Jager & Wassle, 1987; Pow & Hendrickson, 1999). The uptake of D-serine in the retina appears to depend on Na+ -dependent ASCT2 transporters (O’Brien et al. 2005; Dun et al. 2007). Although a high affinity, Na+ -independent, Asc-1 transporter has been identified in the brain and may play a role in the release of glycine and D-serine (Rosenberg et al. 2013), its role in the retina has not been established, at least as an uptake transport mechanism, because D-serine uptake in the retina was blocked under Na+ -free conditions, an environmental condition that should not block the uptake of D-serine by the Asc-1 transporter. Additional studies comparing wild-type and serine racemase knockout mice raised the possibility that D-serine release was modulated by light activity (Sullivan & Miller, 2012). The experiments reported in the C 2014 The Authors. The Journal of Physiology C 2014 The Physiological Society
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Retina NMDA receptor coagonist released by light stimulation
present study were undertaken to evaluate the possible light modulation of coagonist release. The fundamental issue addressed in the present study is related to the experimental observation in which exogenous D-serine enhances NMDAR currents (Stevens et al. 2003). This implies that the spatiotemporal distribution of light-evoked glutamate reaches NMDA receptors for which there is no coagonist available for channel gating. How then do the NMDARs find adequate coagonist when light stimulation requires a greater abundance of coagonist during times of enhanced NMDA receptor recruiting? The present study was divided into two components; one of which studied light-adapted contrast sensitivity under (i) control conditions; (ii) elevated D-serine levels by exogenous D-serine application; and (iii) the application of dichlorokynurenate (DCK) used to block NMDA receptors by antagonism towards the coagonist binding site. This study involved whole-cell recordings from retinal ganglion cells that were identified as such in the tiger salamander retina. We also studied a second, related function of the retina, which is the encoding of intensity information using light stimuli that covered a 6 log unit range of intensities against a dark background. This study, which required long duration recordings including pharmacological interventions, was not well suited for whole-cell recordings from retinal ganglion cells. For these experiments, we used extracellular recordings of the proximal negative field potential (PNFP), originally described as the proximal negative response (Burkhardt, 1970). Each of these studies converged to provide evidence that light-evoked coagonist release is required for full activation of the NMDA receptor population found in retinal ganglion cells. Methods Ethical approval
Animal maintenance and experimental protocols utilized in the present study were evaluated and approved by the University Institutional Animal Care and Use Committee. Animals
Tiger salamanders (Ambystoma tigrinum) were purchased from a dealer (Charles D. Sullivan Co., Nashville, TN, USA) and maintained in circulated cold-water tanks (4°C) under a 12:12 h room light/dark cycle. Animals were killed by decapitation followed by double pithing. Whole-cell recordings
Two unique retinal preparations from the tiger salamander were utilized for the ganglion cell studies in these
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experiments, including (i) an isolated flatmount retina (Stevens et al. 2003) and (ii) an intact retina-eyecup preparation that was newly developed during the course of these experiments. The flatmount preparation began by removing the cornea and lens and draining the vitreous (Miller & Dacheux, 1976). Next, the internal limiting membrane was removed either mechanically, by removing atomized alumina particles adherent to the surface of the retina with jeweler forceps, or by enzymatic digestion with collagenase and hyaluronidase (120 and 465 units ml–1 ). The retina was then removed from the retinal pigment epithelium using a blunted, fire-polished glass micropipette and placed, ganglion cells up, over a 1 mm hole in the centre of a 13 mm diameter nitrocellulose filter paper (Millipore, Billerica, MA, USA). For the eyecup preparations, we modified previously described procedures (Burkhardt et al. 1989), beginning with enucleation of the eye and the placement of a crystal of dextran conjugated tetramethylrhodamine (10000 MW) onto the severed optic nerve. The eyecup was then half immersed, cornea up, in a 6 mm diameter, 2 mm deep well filled with warmed 4% agarose (Type IX-A) in normal amphibian Ringer solution containing (in mM) 110 NaCl, 2.5 KCl, 1.8 CaCl2 , 1.0 Mg Cl2 , 10 Hepes, 5 D-glucose (pH 7.8). After cooling, the cornea, lens and vitreous were removed, as above, and the internal limiting membrane was treated with collagenase and hyaluronidase (120 and 465 units ml–1 ). The eyecup (in agarose) was then placed in a 15 ml plastic centrifuge tube half filled with normal Ringer solution and secured in a light tight container on ice and bubbled with oxygen for 2–5 h, during which time the dye diffused into the ganglion cell bodies. The eyecups, still in agarose, were removed from the oxygenated Ringer solution, placed on a tissue slicer (Stolting, Chicago, IL, USA) and a vertical cut was made, which removed a side of the eyecup approximately one-quarter to one-third of the diameter of the intact eyecup. This allowed the recording micropipettes to access the retina under a water immersion objective. At this point, the flatmount retina on filter paper and the eyecup in agarose were placed in custom designed chambers for use with water immersion objectives on an BX50WI microscope (Olympus, Tokyo, Japan) and connected to a gravity fed perfusion system at a flow rate of 1–1.5 ml min–1 with cooled (18ºC), oxygenated, normal amphibian Ringer solution. Each preparation had its own custom-built chamber; isolated retinas were transilluminated with infrared light (780 nm) using the microscope’s built-in light source and IR filter. Eyecup preparations were visualized by fluorescence microscopy via the microscope’s fluorescence filter cube. Each preparation was visualized with a CCD camera attached to a small LCD screen or video monitor. For the present study, we did not detect any differences in the results
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between the two preparations, and so the results from both were fused into a single dataset. Whole-cell recordings were obtained from identified ganglion cells. Patch electrodes (5–15 Ms) were pulled using a P-97 Flaming Brown Pipette Puller (Sutter Instruments, Novato, CA, USA) and filled with an intracellular solution containing (in mM): 98 KCH3 SO4 , 3.5 NaCH3 SO4 , 3.0 MgSO4 , 1.0 CaCl2 , 11 EGTA, 5.0 Hepes, 2.0 D-glucose, 1.0 glutathione, 1.0 MgATP, 0.5 NaGTP (pH 7.4). To visualize cells studied in the flatmount preparation, we added 5,6-carboxyfluorescein to the pipette solution. All recorded cells were identified as retinal ganglion cells with an axon clearly present. The pipette was held and manipulated with an MP-285 micromanipulator (Sutter Instruments). Dimpling of the fluorescently labelled ganglion cells in the eyecup preparation indicated the proximity of the pipette to the cell soma; we obtained whole-cell recordings only from ganglion cells that were clearly back labelled with the fluorescent dye. After achieving a high resistance seal onto the cell, the capacitance of the pipette was compensated for by utilizing the automatic circuitry of the Axoclamp 700A amplifier (Molecular Devices, Sunnyvale, CA, USA) or manually with the Dagan 3900 (Dagan Corp., Minneapolis, MN, USA), each configured to record with a 10 kHz low pass Bessel filter at a sampling frequency of 10 kHz. Signals were digitized with a Digidata 1320 and recorded in PClamp 9.0 (Molecular Devices). Breakthrough to the whole-cell recording configuration was achieved using gentle negative pressure to the pipette. The cell was characterized in current clamp mode with input resistance determined by small negative current injections, whereas the light response of the cell was determined by stimulating with a 2 s spot (250 μm) or bar (100 μm) of light centered on the recording electrode (for details of the optical bench, see below). The solution was then switched to the control solution, which consisted of (unless noted otherwise) a nominally magnesium free version of the extracellular Ringer solution containing TTX (0.5 μM) to block action potentials and strychnine (10 μM) to block glycine receptors. Voltage-clamp studies were carried out after adjusting the clamp voltage so that zero current was established (average membrane potential = −64.9 ± 4.8 mV); series resistance was generally compensated by 50% to 95%. Because of the small size of the synaptic currents, the relatively low pipette resistance and the high input resistance of tiger salamander retinal ganglion cells (742.3 ± 183 M), we did not correct for voltage errors associated with uncompensated series resistance. The reported voltages are also not corrected for the liquid junction potential (calculated at 10.1 mV more negative than those reported). All chemical reagants used in the present study were purchased from Sigma Chemical (St Louis, MO, USA), with the
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exception of hyaluronidase and collagenase (Worthington Chemical, Lakewood, NJ, USA), TTX (Alamone Labs, Juresalem, Israel), picrotoxinin (Fluka, Neu-Ulm, Switzerland) and KCH3 SO4 (Pfaltz & Bauer, Westchester, PA); AP7, 5,7-dichlorokynurenic acid (5, 7-DCK) and 2,3-dihydroxy-6-nitro-7-sulfamoyl-benzo-(F)-quinoxalinedione (NBQX) were obtained from Tocris (Ellisville, MO, USA). Light stimulation
Light stimulation was provided by a proprietary computer-controlled LCD projector system using a tungsten-halogen light source (Burkhardt et al. 1998) projected onto the retina through a 20× microscope objective (Olympus, Melville, NY, USA) and focused on the plane of the ganglion cell layer. A Fish-Schurman 6143 heat filter (Fish-Schurman, New Rochelle, NY, USA) and neutral density wedges (Kodak, Rochester, NY, USA) were used to attenuate the full intensity of the lamp to a background intensity of 9 cd m−2 . Unless otherwise indicated, light stimuli were centered on the recording electrode and consisted of a 2 s, 250 μm diameter spot and a 1.0 log unit increase in contrast. Contrast is defined as log10 F/B, where F is the light intensity during the flash and B is the steady background intensity (Fahey & Burkhardt, 2003). The interstimulus interval was 20 s for light stimuli. The diameter and the contrast were varied in a systematic fashion once a whole cell recording condition of stability was established (Fig. 1). In all experiments, three or four data traces were signal averaged for each stimulus condition and voltage-clamp responses were evaluated as the total charge (integrated current) entering the cell during the 2 s light stimulus (ON response) and two seconds following the cessation of the stimulus (OFF response). PNFP
Some of the experiments demanded long-term, stable recordings. To meet this requirement, we used a field potential of the inner retina first described by Burkhardt in the frog and referred to as the proximal negative response (1970). We have studied this response in the tiger salamander and renamed it the PNFP. This response is a reliable index of inner retina excitability and has representation among ganglion and amacrine cells. The PNFP is a very stable, light-evoked index of inner retinal activity and was the obvious choice for this component of the study, particularly because we have been able to generate a large, stable NMDA receptor signals based on pharmacological manipulations (Gustafson et al. 2007). For these experiments, we used a more conventional retina-eyecup preparation, as described previously C 2014 The Authors. The Journal of Physiology C 2014 The Physiological Society
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(Gustafson et al. 2007). Briefly, bevelled glass microelectrodes, with tip resistances or a few megaohms, were filled with Ringer solution and inserted 50 μm into the retina. Responses to a small 110 μm spot of light, centered on the electrode, were measured using an Model 3000 amplifier (A-M Systems, Carlsborg, WA, USA), DigiData 1322 and pCLAMP software (Molecular Devices). A bright spot of varying intensities (reported as a relative value, with log I 6.5 = 250 ft-c or 2700 lux) alternated with a diffuse background of 0.01 ft-c or 0.1 lux. A control cocktail of (in μM) 10 NBQX, 10 strychnine, 50 picrotoxinin and 50 mecamylamine was used to isolate the NMDAR component of the PNR. The peak amplitude of the PNFP was used in the analysis.
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co-linked to pyridoxal phosphate that is essential for normal activity of the enzyme. This enzyme is orders of magnitude more effective than D-amino acid oxidase. DsdA converts D-serine into pyruvate and ammonia; the enzyme almost has no backward reaction. We have analysed this enzyme using capillary electrophoresis methods for D-serine detection. In previous experiments, we tested the sensitivity of DsdA versus D-amino acid oxidase (DAAO) by exposing a 10 μM level of D-serine and glycine to the enzymes. DsdA degraded D-serine below the detection limit of our capillary electrophoresis machine (3.4 nM) by 1 min, whereas DAAO exposure after 8 min left almost 50% of the original concentration (Gustafson et al. 2007). Neither enzyme degraded glycine. Thus, DsdA is a far more powerful enzyme than DAAO for D-serine degradation.
DsdA
We initially obtained the bacterial enzyme D-serine deaminase as a gift from Herman Wolosker, who synthesized it (Shleper et al. 2005) using a DsdA clone from the CFT073 Escherichia coli strain. It was shipped in dry ice and stored in a freezer at −80°C and dissolved in physiological Ringer solution just before use. This enzyme is highly specific for D-serine, whereas L-enantiomers are not substrates under normal conditions. D-threonine is a weaker substrate for the enzyme. The enzyme is
Statistical analysis
Electrophysiological data were analysed in Clampfit (Molecular Devices) to total charge; the data were averaged and graphed. Curve fitting and statistics were carried out in Origin, version 9.0 or 9.1 (OriginLab Corp., Northampton, MA, USA). All results are expressed as the mean ± SEM. A paired, one-tailed Student’s t test was used to compare values between treatment groups. P < 0.05 was considered statistically significant.
OFF Center
– 0.03 + ON Center
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Figure 1. Contrast series The two retinal ganglion cells (red traces; OFF-centre cell upper trace, ON-centre cell lower trace) were stimulated with a 2 s light stimulus, 250 µm in diameter at different contrast levels (0.03, 0.07, 0.15, 0.3, 0.5, and 1.0 log unit) against a steady background light of 9 lux. For each magnitude of the contrast displayed, the negative contrast (darker bar) precedes the positive contrast (lighter bar) stimulus. The first 5 s of each stimulus is displayed (of a 20 s interstimulus interval); the positive 1.0 log unit contrast is not shown. Arrows indicate the onset of the first stimulus because this low contrast step is difficult to discern from the background. C 2014 The Authors. The Journal of Physiology C 2014 The Physiological Society
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Table 1. Cell characteristics Preparation
n
Rin (M)
Resting Vm (mV)
Flatmount
53
537.4 ± 198 Range: 257 to 1,256
−63.0 ± 5.3 Range: −53 to −69
Eyecup
43
947.2 ± 205 Range: 498 to 1,738
−66.8 ± 5.9 Range: −58 to −72
Total
96
742.3 ± 183 Range: 257 to 1,738
−64.9 ± 4.8 Range: −53 to −72
Light response ON–OFF: 46 ON: 4 OFF: 3 ON–OFF: 37 ON: 3 OFF: 3 ON–OFF: 83 ON: 7 OFF: 6
Axon visualized∗ 17/24 2/3 3/3 37 3 3 54 5 6
Biophysical properties of cells and method of cell identification: Two different preparations were used in the present study for whole-cell recordings of retinal ganglion cells; 96 ganglion cells comprised the cell population from which whole-cell recording data was obtained; 53 ganglion cell recordings were obtained from the isolated, perfused flatmount retina preparation, whereas 43 cell recordings were obtained from the eyecup preparation. RN : input resistance; Vm : membrane voltage; ∗ For the flatmount experiments, the numerator indicates numbers of axons visualized for ON–OFF, ON, and OFF cells, whereas the denominator indicates the number of experiments where dye was included in the pipette. For the eyecup preparation, all experiments involved recording from cells labelled via the optic nerve backfill.
Results Table 1 summarizes the results obtained with whole-cell recordings from two different salamander retina preparations used during the evolution of our adaptation study focused on retinal ganglion cells. No differences were observed between the results obtained in the two preparations, and so we combined the results for analysis. The input resistance measurements and the average values for the resting membrane potential are indicated. These input resistance values correspond well with those values for the tiger salamander originally reported from the intact retina-eyecup (Coleman & Miller, 1989). Figure 1 illustrates whole-cell recordings from an OFF-center ganglion cell (upper record) and an ON-center ganglion cell (lower record) in response to light stimuli of increasing positive (light bars) and negative contrast (dark bars) against a steady background intensity of 9 lux. The stimulus consisted of a 250 μm diameter light flash of 2 s duration, with an interstimulus interval of 20 s for the responses to recover, of which only the first 5 s are displayed. Under these stimulus conditions, the OFF cell gave a minimal response to the negative contrast beginning with the 0.03 log value and responded to negative contrast levels with excitation at the onset and to positive contrast stimulation with OFF excitation, first evident at the 0.07 contrast level. The ON-cell responded to positive contrast with excitation, as first clearly evident at the 0.07 level, at which time, OFF excitation was also evident. An additional increase in both positive and negative contrast enhanced ganglion cell excitation at the onset of positive contrast stimuli and at the offset for negative contrast stimulation. This stimulation procedure was used in recordings from identified ganglion cells using the LCD panel to provide positive and negative contrast stimuli.
The stimulus protocol described above was used to study the role that D-serine plays in NMDA receptor activity in retinal ganglion cells. Figure 2 illustrates a whole-cell voltage-clamp recording (Vhold −62 mV) from an ON–OFF ganglion cell in response to both positive (Fig. 2A) and negative (Fig. 2B) contrast steps of 1 log10 unit. Each stimulus lasted 2 s as indicated by the bar under each trace. A contrast series of six different values (0.03, 0.07, 0.15, 0.3, 0.5 and 1.0) was applied under control conditions (TTX + strychnine). Control responses (black) were obtained first, followed by an identical contrast series with the application of exogenous D-serine (100 μM; blue trace), after which the contrast series was repeated with DCK added to the bathing medium at 30 μM to block the coagonist site and prevent NMDA receptors from contributing to the response. Based on our recordings in the salamander retina, the IC50 for DCK was 1.5 μM (not shown), such that 30 μM completely blocked light-evoked NMDA receptor contributions to the light response, even at maximal light intensity. Thus, at this concentration of DCK, NMDA receptors were completely blocked, replicating the actions of applying an effective competitive antagonist for the glutamate binding site such as AP7. The expanded traces illustrate the ON and OFF responses evoked at three different contrast steps listed as log10 units at the beginning of each trace. The delay differences in some of the traces reflect the fluctuation in triggering the LCD panel with external triggering procedures. For low contrast values, the enhancement associated with D-serine application is more dominant compared to the actions of DCK but, as the contrast intensity increased, D-serine was less effective in enhancing the response and the actions of DCK were more evident. The blocking action of DCK demonstrates that both C 2014 The Authors. The Journal of Physiology C 2014 The Physiological Society
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NMDA and AMPA receptors were recruited to account for the light response. In the presence of DCK, the light response consists of a relatively pure AMPA receptor contribution.
A
Figure 2C illustrates the relative magnitude differences in the integrated charge (derived by integrating the responses at the onset of the light stimulus for the 2 s duration of the light stimulus) for both positive and
B 250 μm
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Off
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Normalized Control D-Serine DCK
Total Charge (nC)
140 130 120 110 100 90 80 70 –0.8
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0.8
Figure 2. Coagonist sensitivity to D-serine decreases as contrast is enhanced Both positive (A) and negative (B) contrast stimuli were acquired during each experimental run. A, whole-cell voltage-clamp recording (Vhold = −62 mV) of an ON–OFF retinal ganglion cell recorded from an eyecup preparation in response to a 2 s light stimulus (black bar) consisting of a one (1.0) log unit increase in illumination over the background in control Ringer solution (black trace), D-serine (100 µM, blue trace) and DCK (30 µM, red trace). ON and OFF responses to positive contrast steps of 0.07, 0.3 and 1.0 log units are shown below with an expanded timescale. B, same cell as in (A) but showing the results for negative contrast light steps. C, summary data from eight cells plotting the mean ± SEM charge integrated over 2 s for ON responses and 2 s for OFF responses. Control responses were normalized to 100, represented by a horizontal dashed line. D-serine (100 µM, blue dots) and DCK (30 µM, red triangles) to contrast steps of ±0.03, ±0.07, ±0.15, ±0.3, ±0.5 and ±1.0 log unit. ON and OFF responses from each cell were combined for the same intensity level before averaging. C 2014 The Authors. The Journal of Physiology C 2014 The Physiological Society
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negative contrast steps. The application of D-serine and of DCK had similar effects on both the ON and OFF responses of each of the cells recorded; therefore, for each cell, we pooled the ON and OFF responses into a combined cell response. It is this cell response to the pharmacological manipulations that is then averaged and shown in Fig. 2C. The control data were normalized and are represented by the horizontal dashed line at 100%. D-serine (blue circles) enhanced the response especially for low contrast stimuli, whereas the actions of DCK (red triangles) showed a strong NMDA receptor component at each contrast level, albeit with less stimulus-dependent variation (from eight cells, ON and OFF responses combined, n = 14 for each). The D-serine effect at 0.03 contrast was significantly larger than at the 1.0 contrast for both positive and negative steps (P = 0.003 positive contrast, P < 0.001 for negative contrast). Increasing the light stimulation diameter, at the same time as leaving the intensity constant, can also enhance the response of retinal ganglion cells over a wide range of stimulus diameters. We considered whether D-serine enhancement would also influence the light-evoked differences based on diameter, at the same time as keeping the stimulus intensity constant. Figure 3 illustrates a whole cell recording from an ON retinal ganglion cell in which the diameter of the stimulus was changed, whereas the intensity remained fixed at 1.0 log unit above the background. TTX and strychnine continuously bathed the retina to eliminate impulse activity and reduce lateral inhibition. In addition, each cell was clamped at −60 mV, which approximates the reversal potential for chloride, thus eliminating chloride-dependent inhibition. In this example, the diameter of the light stimulus was changed progressively at the same time as keeping the light stimulus intensity constant. We used a discreet series of diameters (50, 100, 250, 600 and 1200 μm) generated on the LCD display with 1 log10 unit increase in contrast against a background of 9 lux. Figure 3A–C illustrates the results that we obtained for three different diameters (50, 250 and 1200 μm) from a sustained ON ganglion cell (current clamp record in 3E), which had a prominent transient inward current, followed by a small, more sustained current. For each diameter of light stimulus, we obtained a control series (black) followed by an identical presentation of stimuli in the presence of 100 μM D-serine (blue) added to the bathing medium, after which DCK perfused the retina and the diameter series was repeated (red traces). Figure 3D shows the normalized control responses (dotted horizontal line at 100), together with the measured integral (2 s) of the current to give total charge. Although these data clearly show that D-serine enhanced the response and DCK reduced the response amplitude, no systematic differences were evident as a function of diameter in terms of a clear trend towards enhancement by D-serine or suppression of the response by DCK. The data
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reflect the study of eight cells. In summary, the response enhancement in D-serine as well as the response decline in the presence of DCK were both relatively constant over the diameter range used in the present study. We conclude that stimulus intensity rather than stimulus diameter is the most important characteristic of the light stimulation parameters required to change the fraction of NMDA receptors recruited when D-serine was added to the bathing medium. The ganglion cell studies provided a unique insight into how the participation of NMDA receptors might be modified for different contrast stimulation parameters. However, the device used to evoked positive and negative contrast stimuli was limited in its dynamic range and confined to ± 1 log10 units above and below the ambient background light. We next embarked on a different series of experiments to examine a broader range of stimulus intensities, using the PNFP, first described by Burkhardt as the proximal negative response (Burkhardt, 1970). The PNFP is a localized response of the inner retina that reflects activity of third-order retinal neurons and provided us with a stable long-term recording condition such that we could study a broader range of stimulus conditions together with pharmacological modifications. A relatively pure NMDA receptor signal can be revealed with the PNFP via the application of a suitable cocktail of drugs, including NBQX (10 μM), strychinine (10 μM), picrotoxinin (50 μM) and mecamylamine (50 μM) (Gustafson et al. 2007). This cocktail was used throughout the PNFP recordings. Figure 4 illustrates the data obtained from an extensive series of PNFP recordings evaluated across a 6 log unit range of intensities. Figure 4A illustrates recordings made at the indicated log intensities, for the control responses (black) and for those in the presence of 100 μM D-serine (grey); note the gain change between 1.5 log I and that for 3.5 and 6.5 log I. For low intensity light stimulation, D-serine application enhanced the response substantially more than was evident for 3.5 log I, whereas the 6.5 log I stimulus revealed saturation of the coagonist sites in the presence of 100 μM D-serine. Figure 4B graphically illustrates the broad range of stimulus intensities used in our PNFP experiments (cumulative data recorded at each stimulus intensity are presented in Table 2). In this display, control responses were normalized for each intensity (dashed line at 100%), whereas the responses indicated by the filled circles were recorded in D-serine (100 μM) and show the responses compared to the control values. PNFP responses were enhanced by D-serine, although the augmentation depended heavily on the intensity of the light stimulus. Low light intensities showed the biggest enhancement with D-serine application. The trend for D-serine augmentation diminished as the intensity increased until the stimuli above 5.5 log I showed a C 2014 The Authors. The Journal of Physiology C 2014 The Physiological Society
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full saturation of the response, indicating full occupancy of the NMDA receptor coagonist sites or maximum activation of the available pool of NMDA receptors under these stimulus conditions. The open rectangle illustrates the range of stimulus intensities that were achieved by the contrast stimulation method with the LCD panel; in the LCD panel experiments, D-serine elevated the response to values that were typically < 150% of control. Studies of the PNFP, however, allowed us to explore a broader range of stimulus intensities, the lowest of which was enhanced by D-serine to more than 300% of the control. In addition, we obtained several examples under our very lowest stimulus intensity that revealed almost no light response in control Ringer solution but, with the addition of D-serine, a significant response was evident. One such example is shown in Fig. 4C (these data were not included in our totals because no control value was available with which to normalize the data). As the stimulus intensity increased (positive values), the addition
A
of D-serine showed a progressive attenuation in its ability to enhance the PNFP and, at the intensity of 6 log units, the enhancing action of D-serine was eliminated entirely. The fact that D-serine can enhance the response substantially at low light levels argues against the Mg2+ block being the principal mechanism required to account for these responses and, instead, suggests a sufficient release of glutamate that cannot be matched by coagonist, such that the full complement of NMDA receptors for this low intensity range cannot be activated. However, as the intensity of the light increases, the enhancing action of exogenous D-serine diminishes because more coagonist is available, which must be released by light stimulation. The idea that more coagonist is available for high intensity light stimulation poses the obvious question about the species of coagonist that provides this function. The two leading candidates are glycine and D-serine, each of which have been identified in the retina and postulated for coagonist function (Stevens et al. 2003;
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Figure 3. Increasing the stimulus spot diameter does not change the sensitivity to DCK or d-serine Whole-cell voltage-clamp recording (Vhold = −58 mV) of a sustained ON retinal ganglion cell in an eyecup preparation responding to a 50 µm (A), 250 µm (B) and 1200 µm (C) light stimulus 2 s in duration in control Ringer solution (black trace), D-serine (100 µM, blue trace) and DCK (30 µM, red trace). Scale bar under the trace in B applies to traces in A, B and C. D, summary data from eight cells plotting the mean ± SEM charge for responses studied for the range of diameters indicated. Recording in control Ringer solution was standardized to 100% as indicated by the dashed line. D-serine responses (blue dots) and responses recorded in DCK (red triangles). Light stimuli of 50, 100, 250, 600 and 1200 µm diameter were used to generate this data. ON and OFF responses were combined before calculating the mean. E, a current clamp record from an ON ganglion cell, light stimulus is represented by the black line at bottom. C 2014 The Authors. The Journal of Physiology C 2014 The Physiological Society
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Kalbaugh et al. 2009). Figure 5 illustrates an experimental strategy designed to address the question about the identity of the light-evoked coagonist. Figure 5A illustrates single PNFP responses evoked by six different flash intensities, as first observed in the control environment (dark trace) followed by the introduction of D-serine deaminase (DsdA; red trace; 10 μg ml–1 ), which degrades D-serine into pyruvate and NH3 . The DsdA application was followed by exogenous glycine (blue trace; 200 μM). It was necessary to use glycine rather than D-serine because residual enzyme in the retina and perfusion system continued to degrade D-serine. Glycine is not degraded by DsdA (Gustafson et al. 2007). Figure 5B shows the cumulative results of six experiments in which DsdA was added to the bathing media. At the lowest intensities, no effect was seen on the PNFP amplitude. Beginning around the stimulus intensity of 1.5, there is gradual reduction in the PNFP versus control until this reduction plateaus around stimulus 4.5 (reduction of 40%) (Table 2).
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These data suggest a role for D-serine that becomes more pronounced as the intensity of the light stimulus increases. NMDA receptors of the retina play an essential role in expanding the dynamic range of retinal ganglion cell responses in the retina (Diamond & Copenhagen, 1993). To assess the role of D-serine in the light-dependent action, we compared the stimulus–response curves of the PNFP in control Ringer solution versus DsdA containing Ringer solution. Figure 6 illustrates the segregated DsdA (grey circles) and control responses (black squares) from the range of stimulus intensities used in the present study and plotted as V/Vmax . For each curve, we fit a Boltzmann equation to the data (r2 > 0.99 for each fit). Notice that the curve for the DsdA responses reached a maximum at 4.5 log I, an intensity level at which the control still increased in its dynamic range. The truncated dynamic range of the DsdA curve reflects the failure for light-evoked coagonist release to fully compensate and provide sufficient coagonist to activate
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Figure 4. Flash intensity coding revealed through the PNFP illustrates that sensitivity to d-serine decreases as the flash intensity is increased The PNFP was recorded over a range of 6 log units using 2 s flashes of light of increasing intensity; the interflash interval was 25 s. A, initial intensity series under control conditions (black traces) shown for intensities 1.5, 3.5 and 6.5, followed by an identical series in the presence of 100 µM D-serine (grey traces). B, for each intensity, the control was normalized to 100% (dashed line near bottom of the figure), whereas the response in the presence of D-serine is indicated by the filled circles, including the SEM (n = 6). Inset: range over which the adaption experiments explored the contrast sensitivity shown in Fig. 2. C, example of a ‘threshold response’. In the presence of D-serine, a PNFP response was obtained at 0.5 log I when an insignificant response to light was observed under control conditions. C 2014 The Authors. The Journal of Physiology C 2014 The Physiological Society
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Table 2. Effect of D-serine and DsdA on PNFP amplitude D-serine
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SEM
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49.4 11.8 16.5 16.2 11.9 10.9 9.3 9.2 4.0 4.8 5.0 2.66 1.97
0.0012 0.0017 0.007 0.0094 0.015 0.032 0.030 0.030 0.0044 0.028 0.12 0.56 0.62
328.8 171.6 172.8 166.5 143.2 132.2 128.0 127.8 119.4 114.6 109.4 98.33 98.97
% Control SEM 109.7 105.1 94.54 81.12 78.04 72.27 68.04 62.62 60.03 60.49 57.87 58.00 56.65
4.47 9.02 9.51 5.33 2.58 4.33 4.93 5.32 3.16 3.32 3.26 3.47 4.47
P 0.096 0.60 0.59 0.017
J Physiol 593.4 (2015) pp 843–856
Dynamic regulation of D-serine release in the vertebrate retina Eric G. Gustafson1 , Eric S. Stevens2 and Robert F. Miller1 1 2
Department of Neuroscience, University of Minnesota Medical School, Minneapolis, MN 55455, USA Oroville Eye Associates Inc., Oroville, CA 95966, USA
Key points
r Activation of NMDA receptors (NMDARs) is essential for encoding visual stimuli into signals
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r r r r
for the brain, although their over-activation can cause cell death. The recruitment of NMDARs is important for encoding light intensity in retinal ganglion cells. D-serine binding is essential for proper activation of NMDARs, although its role in signal processing and the mechanisms that underlie its availability are not well understood. In these light-evoked experiments, the addition of exogenous D-serine had a large effect on low contrast and low intensity NMDAR responses that decreased as the intensity was increased. The degradation of endogenous D-serine decreased the responses more at higher intensities. The results provide compelling evidence favouring a new interpretation of NMDAR recruitment in which light-evoked D-serine release serves an important regulatory control over the recruitment of NMDARs.
Abstract The present study aimed to investigate the functional properties of NMDA receptor coagonist release and to specifically evaluate whether light-evoked release mechanisms contribute to the availability of the coagonist D-serine. Two different methods were involved in our approach: (i) whole-cell recordings from identified retinal ganglion cells in the tiger salamander were used to study light adaptation with positive and negative contrast stimuli over a range of ± 1 log unit against a steady background illumination and (ii) the mechanisms for intensity encoding to a range of light intensities covering 6 log10 units were investigated. This latter study employed extracellular recordings of the proximal negative field potential, pharmacologically manipulated to generate a pure NMDA mediated response. For the adaptation study, we examined the light-evoked responses under control conditions, followed by light stimuli presented in the presence of D-serine, followed by light stimulation in the presence of dichlorokynurenic acid to block the coagonist site of NMDA receptors. For the brightness encoding studies, we examined the action of D-serine on each intensity used and then applied the enzyme D-serine deaminase to remove significant levels of D-serine. These studies provided new insights into the mechanisms that regulate coagonist availability in the vertebrate retina. Our results strongly support the idea that light-evoked coagonist release, a major component of which is D-serine, is needed to provide the full range of coagonist availability for optimal activation of NMDA receptors. (Received 5 September 2014; accepted after revision 29 November 2014; first published online 4 December 2014) Corresponding author E. G. Gustafson: Department of Neuroscience, University of Minnesota Medical School, 6–145 Jackson Hall, 321 Church Street SE, Minneapolis, MN 55455, USA. Email: [email protected] Abbreviations AP7, D,L-2-amino-phosphonoheptanoate; DAAO, D-amino acid oxidase; DCK, dichlorokynurenate; DsdA, D-serine deaminase; GlyT1, glycine transporter type 1; NBQX, 2, 3-dihydroxy-6-nitro-7-sulfamoyl-benzo(F)-quinoxalinedione; NMDAR, NMDAR receptor; PNFP, proximal negative field potential; SR, serine racemase.
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DOI: 10.1113/jphysiol.2014.283432
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Introduction NMDA receptors (NMDARs) are the only glutamate receptors that require a coagonist in addition to glutamate to properly gate the NMDAR ion channel: all other glutamate receptors can be opened by glutamate alone. When the requirement for a coagonist for NMDARs was first discovered, glycine quickly took centre stage as the leading candidate for what turned out to be an obligatory coagonist role (Johnson & Ascher, 1987). Shortly after glycine assumed its new status, studies revealed that other amino acids could substitute for glycine, among which were D-amino acids, including D-serine (Dingledine et al. 1990). Because D-amino acids were not considered to be part of the vertebrate amino acid repertoire, the report that D-serine is found in the brain in relatively high concentrations, especially in brain regions where NMDARs are enriched (Hashimoto et al. 1992), was unexpected. Subsequently, the main synthetic pathway for D-serine was revealed in the form of serine racemase (SR), an enzyme that converts L-serine to D-serine (Wolosker et al. 1999). Initially, SR was identified in astrocytes, although subsequent work revealed that it is also present in neurons, so that the cells responsible for D-serine synthesis and release became and remain an issue of some controversy (Kartvelishvily et al. 2006). More recent insights into the nature of D-serine synthesis have implicated astrocytes as a source of L-serine, whereas D-serine may be synthesized primarily by neurons and then taken up and released by astrocytes (Ehmsen et al. 2013). Whether this recent proposal accounts for D-serine synthesis and release in all regions of the nervous system remains to be explored. It should be added that studies in the retina strongly favour a glial source for the release of the D-serine (Sullivan & Miller, 2010) or at least the component that is evoked by the exogenous application of AMPA + cyclothiazide. Shortly after the discovery of SR in the brain, work in the retina established both the presence of D-serine and its synthesizing enzyme SR (Stevens et al. 2003). Immunolabelling studies localized D-serine and SR to M¨uller cells and astrocytes, although more recent work has also identified retinal ganglion cells as a source of SR (Dun et al. 2008; Kalbaugh et al. 2009). There is evidence that D-serine may be developmentally regulated in the retina (Dun et al. 2008). Physiological studies were carried out in the retina to identify the coagonist preference for NMDA receptors in retinal ganglion cells. This was especially critical because glycine, the competing NMDAR coagonist, subserves inhibition in the retina mediated by a subclass of glycinergic amacrine cells; thus, the inner retina has a cellular source of light-evoked release of glycine that could serve a coagonist function and work reported by Kalbaugh et al. (2009) suggested that this was the case.
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Experiments carried out in the whole retina revealed that the coagonist NMDA receptor sites were not saturated under modest stimulus conditions because exogenous D-serine consistently enhanced NMDAR ionic currents. A powerful D-serine degrading bacterial enzyme, D-serine deaminase (DsdA), was used to significantly reduce D-serine levels, such that the NMDA receptor currents in ganglion cells were almost abolished and reduced to levels very close to those achieved by blocking the NMDA receptors with high levels of competitive antagonists, such as D,L-2-amino-phosphonoheptanoate (AP7) (Gustafson et al. 2007). What emerged from these studies was the idea that D-serine was probably the main and perhaps the only coagonist for NMDA receptors of retinal ganglion cells, at least those activated by light-evoked synaptic pathways. A recent report suggests that non-synaptic NMDA receptors in the retina may utilize glycine as a coagonist (Sullivan & Miller, 2012), an idea that has gained favour based on studies in the brain (Papouin et al. 2012). Additional experiments were carried out to clarify the role of glycine as an NMDAR coagonist. It has been noted that, for D-serine to be effective as a coagonist, glycine, which is present in higher concentrations than D-serine (Reed et al. 2009), must be effectively reduced in concentration by local glycine uptake mechanisms, specifically the Na+ -dependent glycine transporter type 1 (GlyT1) uptake system (Supplisson & Bergman, 1997). When GlyT1 transporters were blocked with N[3-(4 fluorophenyl)-3-(4 -phenylphenoxy)-propyl]sarcosine (Stevens et al. 2010), coagonist NMDAR sites in the retina became fully occupied because external levels of glycine were elevated. Furthermore, mice in which the GlyT1 transporter had been partially knocked out (GlyT1−/+ ) showed full occupancy of NMDA receptor coagonist sites (Reed et al. 2009), supporting the importance of this transport system in reducing local glycine levels, allowing D-serine to serve in this capacity. GlyT1 transporters are richly represented in the inner plexiform of the retina (Jager & Wassle, 1987; Pow & Hendrickson, 1999). The uptake of D-serine in the retina appears to depend on Na+ -dependent ASCT2 transporters (O’Brien et al. 2005; Dun et al. 2007). Although a high affinity, Na+ -independent, Asc-1 transporter has been identified in the brain and may play a role in the release of glycine and D-serine (Rosenberg et al. 2013), its role in the retina has not been established, at least as an uptake transport mechanism, because D-serine uptake in the retina was blocked under Na+ -free conditions, an environmental condition that should not block the uptake of D-serine by the Asc-1 transporter. Additional studies comparing wild-type and serine racemase knockout mice raised the possibility that D-serine release was modulated by light activity (Sullivan & Miller, 2012). The experiments reported in the C 2014 The Authors. The Journal of Physiology C 2014 The Physiological Society
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Retina NMDA receptor coagonist released by light stimulation
present study were undertaken to evaluate the possible light modulation of coagonist release. The fundamental issue addressed in the present study is related to the experimental observation in which exogenous D-serine enhances NMDAR currents (Stevens et al. 2003). This implies that the spatiotemporal distribution of light-evoked glutamate reaches NMDA receptors for which there is no coagonist available for channel gating. How then do the NMDARs find adequate coagonist when light stimulation requires a greater abundance of coagonist during times of enhanced NMDA receptor recruiting? The present study was divided into two components; one of which studied light-adapted contrast sensitivity under (i) control conditions; (ii) elevated D-serine levels by exogenous D-serine application; and (iii) the application of dichlorokynurenate (DCK) used to block NMDA receptors by antagonism towards the coagonist binding site. This study involved whole-cell recordings from retinal ganglion cells that were identified as such in the tiger salamander retina. We also studied a second, related function of the retina, which is the encoding of intensity information using light stimuli that covered a 6 log unit range of intensities against a dark background. This study, which required long duration recordings including pharmacological interventions, was not well suited for whole-cell recordings from retinal ganglion cells. For these experiments, we used extracellular recordings of the proximal negative field potential (PNFP), originally described as the proximal negative response (Burkhardt, 1970). Each of these studies converged to provide evidence that light-evoked coagonist release is required for full activation of the NMDA receptor population found in retinal ganglion cells. Methods Ethical approval
Animal maintenance and experimental protocols utilized in the present study were evaluated and approved by the University Institutional Animal Care and Use Committee. Animals
Tiger salamanders (Ambystoma tigrinum) were purchased from a dealer (Charles D. Sullivan Co., Nashville, TN, USA) and maintained in circulated cold-water tanks (4°C) under a 12:12 h room light/dark cycle. Animals were killed by decapitation followed by double pithing. Whole-cell recordings
Two unique retinal preparations from the tiger salamander were utilized for the ganglion cell studies in these
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experiments, including (i) an isolated flatmount retina (Stevens et al. 2003) and (ii) an intact retina-eyecup preparation that was newly developed during the course of these experiments. The flatmount preparation began by removing the cornea and lens and draining the vitreous (Miller & Dacheux, 1976). Next, the internal limiting membrane was removed either mechanically, by removing atomized alumina particles adherent to the surface of the retina with jeweler forceps, or by enzymatic digestion with collagenase and hyaluronidase (120 and 465 units ml–1 ). The retina was then removed from the retinal pigment epithelium using a blunted, fire-polished glass micropipette and placed, ganglion cells up, over a 1 mm hole in the centre of a 13 mm diameter nitrocellulose filter paper (Millipore, Billerica, MA, USA). For the eyecup preparations, we modified previously described procedures (Burkhardt et al. 1989), beginning with enucleation of the eye and the placement of a crystal of dextran conjugated tetramethylrhodamine (10000 MW) onto the severed optic nerve. The eyecup was then half immersed, cornea up, in a 6 mm diameter, 2 mm deep well filled with warmed 4% agarose (Type IX-A) in normal amphibian Ringer solution containing (in mM) 110 NaCl, 2.5 KCl, 1.8 CaCl2 , 1.0 Mg Cl2 , 10 Hepes, 5 D-glucose (pH 7.8). After cooling, the cornea, lens and vitreous were removed, as above, and the internal limiting membrane was treated with collagenase and hyaluronidase (120 and 465 units ml–1 ). The eyecup (in agarose) was then placed in a 15 ml plastic centrifuge tube half filled with normal Ringer solution and secured in a light tight container on ice and bubbled with oxygen for 2–5 h, during which time the dye diffused into the ganglion cell bodies. The eyecups, still in agarose, were removed from the oxygenated Ringer solution, placed on a tissue slicer (Stolting, Chicago, IL, USA) and a vertical cut was made, which removed a side of the eyecup approximately one-quarter to one-third of the diameter of the intact eyecup. This allowed the recording micropipettes to access the retina under a water immersion objective. At this point, the flatmount retina on filter paper and the eyecup in agarose were placed in custom designed chambers for use with water immersion objectives on an BX50WI microscope (Olympus, Tokyo, Japan) and connected to a gravity fed perfusion system at a flow rate of 1–1.5 ml min–1 with cooled (18ºC), oxygenated, normal amphibian Ringer solution. Each preparation had its own custom-built chamber; isolated retinas were transilluminated with infrared light (780 nm) using the microscope’s built-in light source and IR filter. Eyecup preparations were visualized by fluorescence microscopy via the microscope’s fluorescence filter cube. Each preparation was visualized with a CCD camera attached to a small LCD screen or video monitor. For the present study, we did not detect any differences in the results
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between the two preparations, and so the results from both were fused into a single dataset. Whole-cell recordings were obtained from identified ganglion cells. Patch electrodes (5–15 Ms) were pulled using a P-97 Flaming Brown Pipette Puller (Sutter Instruments, Novato, CA, USA) and filled with an intracellular solution containing (in mM): 98 KCH3 SO4 , 3.5 NaCH3 SO4 , 3.0 MgSO4 , 1.0 CaCl2 , 11 EGTA, 5.0 Hepes, 2.0 D-glucose, 1.0 glutathione, 1.0 MgATP, 0.5 NaGTP (pH 7.4). To visualize cells studied in the flatmount preparation, we added 5,6-carboxyfluorescein to the pipette solution. All recorded cells were identified as retinal ganglion cells with an axon clearly present. The pipette was held and manipulated with an MP-285 micromanipulator (Sutter Instruments). Dimpling of the fluorescently labelled ganglion cells in the eyecup preparation indicated the proximity of the pipette to the cell soma; we obtained whole-cell recordings only from ganglion cells that were clearly back labelled with the fluorescent dye. After achieving a high resistance seal onto the cell, the capacitance of the pipette was compensated for by utilizing the automatic circuitry of the Axoclamp 700A amplifier (Molecular Devices, Sunnyvale, CA, USA) or manually with the Dagan 3900 (Dagan Corp., Minneapolis, MN, USA), each configured to record with a 10 kHz low pass Bessel filter at a sampling frequency of 10 kHz. Signals were digitized with a Digidata 1320 and recorded in PClamp 9.0 (Molecular Devices). Breakthrough to the whole-cell recording configuration was achieved using gentle negative pressure to the pipette. The cell was characterized in current clamp mode with input resistance determined by small negative current injections, whereas the light response of the cell was determined by stimulating with a 2 s spot (250 μm) or bar (100 μm) of light centered on the recording electrode (for details of the optical bench, see below). The solution was then switched to the control solution, which consisted of (unless noted otherwise) a nominally magnesium free version of the extracellular Ringer solution containing TTX (0.5 μM) to block action potentials and strychnine (10 μM) to block glycine receptors. Voltage-clamp studies were carried out after adjusting the clamp voltage so that zero current was established (average membrane potential = −64.9 ± 4.8 mV); series resistance was generally compensated by 50% to 95%. Because of the small size of the synaptic currents, the relatively low pipette resistance and the high input resistance of tiger salamander retinal ganglion cells (742.3 ± 183 M), we did not correct for voltage errors associated with uncompensated series resistance. The reported voltages are also not corrected for the liquid junction potential (calculated at 10.1 mV more negative than those reported). All chemical reagants used in the present study were purchased from Sigma Chemical (St Louis, MO, USA), with the
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exception of hyaluronidase and collagenase (Worthington Chemical, Lakewood, NJ, USA), TTX (Alamone Labs, Juresalem, Israel), picrotoxinin (Fluka, Neu-Ulm, Switzerland) and KCH3 SO4 (Pfaltz & Bauer, Westchester, PA); AP7, 5,7-dichlorokynurenic acid (5, 7-DCK) and 2,3-dihydroxy-6-nitro-7-sulfamoyl-benzo-(F)-quinoxalinedione (NBQX) were obtained from Tocris (Ellisville, MO, USA). Light stimulation
Light stimulation was provided by a proprietary computer-controlled LCD projector system using a tungsten-halogen light source (Burkhardt et al. 1998) projected onto the retina through a 20× microscope objective (Olympus, Melville, NY, USA) and focused on the plane of the ganglion cell layer. A Fish-Schurman 6143 heat filter (Fish-Schurman, New Rochelle, NY, USA) and neutral density wedges (Kodak, Rochester, NY, USA) were used to attenuate the full intensity of the lamp to a background intensity of 9 cd m−2 . Unless otherwise indicated, light stimuli were centered on the recording electrode and consisted of a 2 s, 250 μm diameter spot and a 1.0 log unit increase in contrast. Contrast is defined as log10 F/B, where F is the light intensity during the flash and B is the steady background intensity (Fahey & Burkhardt, 2003). The interstimulus interval was 20 s for light stimuli. The diameter and the contrast were varied in a systematic fashion once a whole cell recording condition of stability was established (Fig. 1). In all experiments, three or four data traces were signal averaged for each stimulus condition and voltage-clamp responses were evaluated as the total charge (integrated current) entering the cell during the 2 s light stimulus (ON response) and two seconds following the cessation of the stimulus (OFF response). PNFP
Some of the experiments demanded long-term, stable recordings. To meet this requirement, we used a field potential of the inner retina first described by Burkhardt in the frog and referred to as the proximal negative response (1970). We have studied this response in the tiger salamander and renamed it the PNFP. This response is a reliable index of inner retina excitability and has representation among ganglion and amacrine cells. The PNFP is a very stable, light-evoked index of inner retinal activity and was the obvious choice for this component of the study, particularly because we have been able to generate a large, stable NMDA receptor signals based on pharmacological manipulations (Gustafson et al. 2007). For these experiments, we used a more conventional retina-eyecup preparation, as described previously C 2014 The Authors. The Journal of Physiology C 2014 The Physiological Society
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(Gustafson et al. 2007). Briefly, bevelled glass microelectrodes, with tip resistances or a few megaohms, were filled with Ringer solution and inserted 50 μm into the retina. Responses to a small 110 μm spot of light, centered on the electrode, were measured using an Model 3000 amplifier (A-M Systems, Carlsborg, WA, USA), DigiData 1322 and pCLAMP software (Molecular Devices). A bright spot of varying intensities (reported as a relative value, with log I 6.5 = 250 ft-c or 2700 lux) alternated with a diffuse background of 0.01 ft-c or 0.1 lux. A control cocktail of (in μM) 10 NBQX, 10 strychnine, 50 picrotoxinin and 50 mecamylamine was used to isolate the NMDAR component of the PNR. The peak amplitude of the PNFP was used in the analysis.
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co-linked to pyridoxal phosphate that is essential for normal activity of the enzyme. This enzyme is orders of magnitude more effective than D-amino acid oxidase. DsdA converts D-serine into pyruvate and ammonia; the enzyme almost has no backward reaction. We have analysed this enzyme using capillary electrophoresis methods for D-serine detection. In previous experiments, we tested the sensitivity of DsdA versus D-amino acid oxidase (DAAO) by exposing a 10 μM level of D-serine and glycine to the enzymes. DsdA degraded D-serine below the detection limit of our capillary electrophoresis machine (3.4 nM) by 1 min, whereas DAAO exposure after 8 min left almost 50% of the original concentration (Gustafson et al. 2007). Neither enzyme degraded glycine. Thus, DsdA is a far more powerful enzyme than DAAO for D-serine degradation.
DsdA
We initially obtained the bacterial enzyme D-serine deaminase as a gift from Herman Wolosker, who synthesized it (Shleper et al. 2005) using a DsdA clone from the CFT073 Escherichia coli strain. It was shipped in dry ice and stored in a freezer at −80°C and dissolved in physiological Ringer solution just before use. This enzyme is highly specific for D-serine, whereas L-enantiomers are not substrates under normal conditions. D-threonine is a weaker substrate for the enzyme. The enzyme is
Statistical analysis
Electrophysiological data were analysed in Clampfit (Molecular Devices) to total charge; the data were averaged and graphed. Curve fitting and statistics were carried out in Origin, version 9.0 or 9.1 (OriginLab Corp., Northampton, MA, USA). All results are expressed as the mean ± SEM. A paired, one-tailed Student’s t test was used to compare values between treatment groups. P < 0.05 was considered statistically significant.
OFF Center
– 0.03 + ON Center
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– 0.15 +
250 μm
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+
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Figure 1. Contrast series The two retinal ganglion cells (red traces; OFF-centre cell upper trace, ON-centre cell lower trace) were stimulated with a 2 s light stimulus, 250 µm in diameter at different contrast levels (0.03, 0.07, 0.15, 0.3, 0.5, and 1.0 log unit) against a steady background light of 9 lux. For each magnitude of the contrast displayed, the negative contrast (darker bar) precedes the positive contrast (lighter bar) stimulus. The first 5 s of each stimulus is displayed (of a 20 s interstimulus interval); the positive 1.0 log unit contrast is not shown. Arrows indicate the onset of the first stimulus because this low contrast step is difficult to discern from the background. C 2014 The Authors. The Journal of Physiology C 2014 The Physiological Society
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Table 1. Cell characteristics Preparation
n
Rin (M)
Resting Vm (mV)
Flatmount
53
537.4 ± 198 Range: 257 to 1,256
−63.0 ± 5.3 Range: −53 to −69
Eyecup
43
947.2 ± 205 Range: 498 to 1,738
−66.8 ± 5.9 Range: −58 to −72
Total
96
742.3 ± 183 Range: 257 to 1,738
−64.9 ± 4.8 Range: −53 to −72
Light response ON–OFF: 46 ON: 4 OFF: 3 ON–OFF: 37 ON: 3 OFF: 3 ON–OFF: 83 ON: 7 OFF: 6
Axon visualized∗ 17/24 2/3 3/3 37 3 3 54 5 6
Biophysical properties of cells and method of cell identification: Two different preparations were used in the present study for whole-cell recordings of retinal ganglion cells; 96 ganglion cells comprised the cell population from which whole-cell recording data was obtained; 53 ganglion cell recordings were obtained from the isolated, perfused flatmount retina preparation, whereas 43 cell recordings were obtained from the eyecup preparation. RN : input resistance; Vm : membrane voltage; ∗ For the flatmount experiments, the numerator indicates numbers of axons visualized for ON–OFF, ON, and OFF cells, whereas the denominator indicates the number of experiments where dye was included in the pipette. For the eyecup preparation, all experiments involved recording from cells labelled via the optic nerve backfill.
Results Table 1 summarizes the results obtained with whole-cell recordings from two different salamander retina preparations used during the evolution of our adaptation study focused on retinal ganglion cells. No differences were observed between the results obtained in the two preparations, and so we combined the results for analysis. The input resistance measurements and the average values for the resting membrane potential are indicated. These input resistance values correspond well with those values for the tiger salamander originally reported from the intact retina-eyecup (Coleman & Miller, 1989). Figure 1 illustrates whole-cell recordings from an OFF-center ganglion cell (upper record) and an ON-center ganglion cell (lower record) in response to light stimuli of increasing positive (light bars) and negative contrast (dark bars) against a steady background intensity of 9 lux. The stimulus consisted of a 250 μm diameter light flash of 2 s duration, with an interstimulus interval of 20 s for the responses to recover, of which only the first 5 s are displayed. Under these stimulus conditions, the OFF cell gave a minimal response to the negative contrast beginning with the 0.03 log value and responded to negative contrast levels with excitation at the onset and to positive contrast stimulation with OFF excitation, first evident at the 0.07 contrast level. The ON-cell responded to positive contrast with excitation, as first clearly evident at the 0.07 level, at which time, OFF excitation was also evident. An additional increase in both positive and negative contrast enhanced ganglion cell excitation at the onset of positive contrast stimuli and at the offset for negative contrast stimulation. This stimulation procedure was used in recordings from identified ganglion cells using the LCD panel to provide positive and negative contrast stimuli.
The stimulus protocol described above was used to study the role that D-serine plays in NMDA receptor activity in retinal ganglion cells. Figure 2 illustrates a whole-cell voltage-clamp recording (Vhold −62 mV) from an ON–OFF ganglion cell in response to both positive (Fig. 2A) and negative (Fig. 2B) contrast steps of 1 log10 unit. Each stimulus lasted 2 s as indicated by the bar under each trace. A contrast series of six different values (0.03, 0.07, 0.15, 0.3, 0.5 and 1.0) was applied under control conditions (TTX + strychnine). Control responses (black) were obtained first, followed by an identical contrast series with the application of exogenous D-serine (100 μM; blue trace), after which the contrast series was repeated with DCK added to the bathing medium at 30 μM to block the coagonist site and prevent NMDA receptors from contributing to the response. Based on our recordings in the salamander retina, the IC50 for DCK was 1.5 μM (not shown), such that 30 μM completely blocked light-evoked NMDA receptor contributions to the light response, even at maximal light intensity. Thus, at this concentration of DCK, NMDA receptors were completely blocked, replicating the actions of applying an effective competitive antagonist for the glutamate binding site such as AP7. The expanded traces illustrate the ON and OFF responses evoked at three different contrast steps listed as log10 units at the beginning of each trace. The delay differences in some of the traces reflect the fluctuation in triggering the LCD panel with external triggering procedures. For low contrast values, the enhancement associated with D-serine application is more dominant compared to the actions of DCK but, as the contrast intensity increased, D-serine was less effective in enhancing the response and the actions of DCK were more evident. The blocking action of DCK demonstrates that both C 2014 The Authors. The Journal of Physiology C 2014 The Physiological Society
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NMDA and AMPA receptors were recruited to account for the light response. In the presence of DCK, the light response consists of a relatively pure AMPA receptor contribution.
A
Figure 2C illustrates the relative magnitude differences in the integrated charge (derived by integrating the responses at the onset of the light stimulus for the 2 s duration of the light stimulus) for both positive and
B 250 μm
250 µm 1.0
1.0 Control D-Serine DCK
On
Off
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.07
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200 pA 1.0
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C
Normalized Control D-Serine DCK
Total Charge (nC)
140 130 120 110 100 90 80 70 –0.8
–0.4 0.0 0.4 Log10 Stimulus Contrast
0.8
Figure 2. Coagonist sensitivity to D-serine decreases as contrast is enhanced Both positive (A) and negative (B) contrast stimuli were acquired during each experimental run. A, whole-cell voltage-clamp recording (Vhold = −62 mV) of an ON–OFF retinal ganglion cell recorded from an eyecup preparation in response to a 2 s light stimulus (black bar) consisting of a one (1.0) log unit increase in illumination over the background in control Ringer solution (black trace), D-serine (100 µM, blue trace) and DCK (30 µM, red trace). ON and OFF responses to positive contrast steps of 0.07, 0.3 and 1.0 log units are shown below with an expanded timescale. B, same cell as in (A) but showing the results for negative contrast light steps. C, summary data from eight cells plotting the mean ± SEM charge integrated over 2 s for ON responses and 2 s for OFF responses. Control responses were normalized to 100, represented by a horizontal dashed line. D-serine (100 µM, blue dots) and DCK (30 µM, red triangles) to contrast steps of ±0.03, ±0.07, ±0.15, ±0.3, ±0.5 and ±1.0 log unit. ON and OFF responses from each cell were combined for the same intensity level before averaging. C 2014 The Authors. The Journal of Physiology C 2014 The Physiological Society
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negative contrast steps. The application of D-serine and of DCK had similar effects on both the ON and OFF responses of each of the cells recorded; therefore, for each cell, we pooled the ON and OFF responses into a combined cell response. It is this cell response to the pharmacological manipulations that is then averaged and shown in Fig. 2C. The control data were normalized and are represented by the horizontal dashed line at 100%. D-serine (blue circles) enhanced the response especially for low contrast stimuli, whereas the actions of DCK (red triangles) showed a strong NMDA receptor component at each contrast level, albeit with less stimulus-dependent variation (from eight cells, ON and OFF responses combined, n = 14 for each). The D-serine effect at 0.03 contrast was significantly larger than at the 1.0 contrast for both positive and negative steps (P = 0.003 positive contrast, P < 0.001 for negative contrast). Increasing the light stimulation diameter, at the same time as leaving the intensity constant, can also enhance the response of retinal ganglion cells over a wide range of stimulus diameters. We considered whether D-serine enhancement would also influence the light-evoked differences based on diameter, at the same time as keeping the stimulus intensity constant. Figure 3 illustrates a whole cell recording from an ON retinal ganglion cell in which the diameter of the stimulus was changed, whereas the intensity remained fixed at 1.0 log unit above the background. TTX and strychnine continuously bathed the retina to eliminate impulse activity and reduce lateral inhibition. In addition, each cell was clamped at −60 mV, which approximates the reversal potential for chloride, thus eliminating chloride-dependent inhibition. In this example, the diameter of the light stimulus was changed progressively at the same time as keeping the light stimulus intensity constant. We used a discreet series of diameters (50, 100, 250, 600 and 1200 μm) generated on the LCD display with 1 log10 unit increase in contrast against a background of 9 lux. Figure 3A–C illustrates the results that we obtained for three different diameters (50, 250 and 1200 μm) from a sustained ON ganglion cell (current clamp record in 3E), which had a prominent transient inward current, followed by a small, more sustained current. For each diameter of light stimulus, we obtained a control series (black) followed by an identical presentation of stimuli in the presence of 100 μM D-serine (blue) added to the bathing medium, after which DCK perfused the retina and the diameter series was repeated (red traces). Figure 3D shows the normalized control responses (dotted horizontal line at 100), together with the measured integral (2 s) of the current to give total charge. Although these data clearly show that D-serine enhanced the response and DCK reduced the response amplitude, no systematic differences were evident as a function of diameter in terms of a clear trend towards enhancement by D-serine or suppression of the response by DCK. The data
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reflect the study of eight cells. In summary, the response enhancement in D-serine as well as the response decline in the presence of DCK were both relatively constant over the diameter range used in the present study. We conclude that stimulus intensity rather than stimulus diameter is the most important characteristic of the light stimulation parameters required to change the fraction of NMDA receptors recruited when D-serine was added to the bathing medium. The ganglion cell studies provided a unique insight into how the participation of NMDA receptors might be modified for different contrast stimulation parameters. However, the device used to evoked positive and negative contrast stimuli was limited in its dynamic range and confined to ± 1 log10 units above and below the ambient background light. We next embarked on a different series of experiments to examine a broader range of stimulus intensities, using the PNFP, first described by Burkhardt as the proximal negative response (Burkhardt, 1970). The PNFP is a localized response of the inner retina that reflects activity of third-order retinal neurons and provided us with a stable long-term recording condition such that we could study a broader range of stimulus conditions together with pharmacological modifications. A relatively pure NMDA receptor signal can be revealed with the PNFP via the application of a suitable cocktail of drugs, including NBQX (10 μM), strychinine (10 μM), picrotoxinin (50 μM) and mecamylamine (50 μM) (Gustafson et al. 2007). This cocktail was used throughout the PNFP recordings. Figure 4 illustrates the data obtained from an extensive series of PNFP recordings evaluated across a 6 log unit range of intensities. Figure 4A illustrates recordings made at the indicated log intensities, for the control responses (black) and for those in the presence of 100 μM D-serine (grey); note the gain change between 1.5 log I and that for 3.5 and 6.5 log I. For low intensity light stimulation, D-serine application enhanced the response substantially more than was evident for 3.5 log I, whereas the 6.5 log I stimulus revealed saturation of the coagonist sites in the presence of 100 μM D-serine. Figure 4B graphically illustrates the broad range of stimulus intensities used in our PNFP experiments (cumulative data recorded at each stimulus intensity are presented in Table 2). In this display, control responses were normalized for each intensity (dashed line at 100%), whereas the responses indicated by the filled circles were recorded in D-serine (100 μM) and show the responses compared to the control values. PNFP responses were enhanced by D-serine, although the augmentation depended heavily on the intensity of the light stimulus. Low light intensities showed the biggest enhancement with D-serine application. The trend for D-serine augmentation diminished as the intensity increased until the stimuli above 5.5 log I showed a C 2014 The Authors. The Journal of Physiology C 2014 The Physiological Society
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full saturation of the response, indicating full occupancy of the NMDA receptor coagonist sites or maximum activation of the available pool of NMDA receptors under these stimulus conditions. The open rectangle illustrates the range of stimulus intensities that were achieved by the contrast stimulation method with the LCD panel; in the LCD panel experiments, D-serine elevated the response to values that were typically < 150% of control. Studies of the PNFP, however, allowed us to explore a broader range of stimulus intensities, the lowest of which was enhanced by D-serine to more than 300% of the control. In addition, we obtained several examples under our very lowest stimulus intensity that revealed almost no light response in control Ringer solution but, with the addition of D-serine, a significant response was evident. One such example is shown in Fig. 4C (these data were not included in our totals because no control value was available with which to normalize the data). As the stimulus intensity increased (positive values), the addition
A
of D-serine showed a progressive attenuation in its ability to enhance the PNFP and, at the intensity of 6 log units, the enhancing action of D-serine was eliminated entirely. The fact that D-serine can enhance the response substantially at low light levels argues against the Mg2+ block being the principal mechanism required to account for these responses and, instead, suggests a sufficient release of glutamate that cannot be matched by coagonist, such that the full complement of NMDA receptors for this low intensity range cannot be activated. However, as the intensity of the light increases, the enhancing action of exogenous D-serine diminishes because more coagonist is available, which must be released by light stimulation. The idea that more coagonist is available for high intensity light stimulation poses the obvious question about the species of coagonist that provides this function. The two leading candidates are glycine and D-serine, each of which have been identified in the retina and postulated for coagonist function (Stevens et al. 2003;
C
B 50 μm
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E
D-serine DCK
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100 90 80 70 60 0
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400 600 800 1000 Stimulus Diameter (mM)
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Figure 3. Increasing the stimulus spot diameter does not change the sensitivity to DCK or d-serine Whole-cell voltage-clamp recording (Vhold = −58 mV) of a sustained ON retinal ganglion cell in an eyecup preparation responding to a 50 µm (A), 250 µm (B) and 1200 µm (C) light stimulus 2 s in duration in control Ringer solution (black trace), D-serine (100 µM, blue trace) and DCK (30 µM, red trace). Scale bar under the trace in B applies to traces in A, B and C. D, summary data from eight cells plotting the mean ± SEM charge for responses studied for the range of diameters indicated. Recording in control Ringer solution was standardized to 100% as indicated by the dashed line. D-serine responses (blue dots) and responses recorded in DCK (red triangles). Light stimuli of 50, 100, 250, 600 and 1200 µm diameter were used to generate this data. ON and OFF responses were combined before calculating the mean. E, a current clamp record from an ON ganglion cell, light stimulus is represented by the black line at bottom. C 2014 The Authors. The Journal of Physiology C 2014 The Physiological Society
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Kalbaugh et al. 2009). Figure 5 illustrates an experimental strategy designed to address the question about the identity of the light-evoked coagonist. Figure 5A illustrates single PNFP responses evoked by six different flash intensities, as first observed in the control environment (dark trace) followed by the introduction of D-serine deaminase (DsdA; red trace; 10 μg ml–1 ), which degrades D-serine into pyruvate and NH3 . The DsdA application was followed by exogenous glycine (blue trace; 200 μM). It was necessary to use glycine rather than D-serine because residual enzyme in the retina and perfusion system continued to degrade D-serine. Glycine is not degraded by DsdA (Gustafson et al. 2007). Figure 5B shows the cumulative results of six experiments in which DsdA was added to the bathing media. At the lowest intensities, no effect was seen on the PNFP amplitude. Beginning around the stimulus intensity of 1.5, there is gradual reduction in the PNFP versus control until this reduction plateaus around stimulus 4.5 (reduction of 40%) (Table 2).
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These data suggest a role for D-serine that becomes more pronounced as the intensity of the light stimulus increases. NMDA receptors of the retina play an essential role in expanding the dynamic range of retinal ganglion cell responses in the retina (Diamond & Copenhagen, 1993). To assess the role of D-serine in the light-dependent action, we compared the stimulus–response curves of the PNFP in control Ringer solution versus DsdA containing Ringer solution. Figure 6 illustrates the segregated DsdA (grey circles) and control responses (black squares) from the range of stimulus intensities used in the present study and plotted as V/Vmax . For each curve, we fit a Boltzmann equation to the data (r2 > 0.99 for each fit). Notice that the curve for the DsdA responses reached a maximum at 4.5 log I, an intensity level at which the control still increased in its dynamic range. The truncated dynamic range of the DsdA curve reflects the failure for light-evoked coagonist release to fully compensate and provide sufficient coagonist to activate
A Control D-serine
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C D-serine enhanced (% Control)
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3.5 Log Stimulus Intensity
6.0
Figure 4. Flash intensity coding revealed through the PNFP illustrates that sensitivity to d-serine decreases as the flash intensity is increased The PNFP was recorded over a range of 6 log units using 2 s flashes of light of increasing intensity; the interflash interval was 25 s. A, initial intensity series under control conditions (black traces) shown for intensities 1.5, 3.5 and 6.5, followed by an identical series in the presence of 100 µM D-serine (grey traces). B, for each intensity, the control was normalized to 100% (dashed line near bottom of the figure), whereas the response in the presence of D-serine is indicated by the filled circles, including the SEM (n = 6). Inset: range over which the adaption experiments explored the contrast sensitivity shown in Fig. 2. C, example of a ‘threshold response’. In the presence of D-serine, a PNFP response was obtained at 0.5 log I when an insignificant response to light was observed under control conditions. C 2014 The Authors. The Journal of Physiology C 2014 The Physiological Society
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Table 2. Effect of D-serine and DsdA on PNFP amplitude D-serine
DsdA
Stimulus intensity % Control
SEM
P
0.5 1 1.5 2 2.5 3 3.5 4 4.5 5 5.5 6 6.5
49.4 11.8 16.5 16.2 11.9 10.9 9.3 9.2 4.0 4.8 5.0 2.66 1.97
0.0012 0.0017 0.007 0.0094 0.015 0.032 0.030 0.030 0.0044 0.028 0.12 0.56 0.62
328.8 171.6 172.8 166.5 143.2 132.2 128.0 127.8 119.4 114.6 109.4 98.33 98.97
% Control SEM 109.7 105.1 94.54 81.12 78.04 72.27 68.04 62.62 60.03 60.49 57.87 58.00 56.65
4.47 9.02 9.51 5.33 2.58 4.33 4.93 5.32 3.16 3.32 3.26 3.47 4.47
P 0.096 0.60 0.59 0.017
