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PLoS Biol. Nov 2005; 3(11): e354.
Published online Oct 18, 2005. doi:  10.1371/journal.pbio.0030354
PMCID: PMC1255741

Enhanced Odor Discrimination and Impaired Olfactory Memory by Spatially Controlled Switch of AMPA Receptors

Howard Eichenbaum, Academic Editor

Abstract

Genetic perturbations of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionate receptors (AMPARs) are widely used to dissect molecular mechanisms of sensory coding, learning, and memory. In this study, we investigated the role of Ca2+-permeable AMPARs in olfactory behavior. AMPAR modification was obtained by depletion of the GluR-B subunit or expression of unedited GluR-B(Q), both leading to increased Ca2+ permeability of AMPARs. Mice with this functional AMPAR switch, specifically in forebrain, showed enhanced olfactory discrimination and more rapid learning in a go/no-go operant conditioning task. Olfactory memory, however, was dramatically impaired. GluR-B depletion in forebrain was ectopically variable (“mosaic”) among individuals and strongly correlated with decreased olfactory memory in hippocampus and cortex. Accordingly, memory was rescued by transgenic GluR-B expression restricted to piriform cortex and hippocampus, while enhanced odor discrimination was independent of both GluR-B variability and transgenic GluR-B expression. Thus, correlated differences in behavior and levels of GluR-B expression allowed a mechanistic and spatial dissection of olfactory learning, discrimination, and memory capabilities.

Introduction

The sense of smell is of paramount importance for rodents [1], for which rapid odor discrimination and long-lasting olfactory memory permits responses to predator and prey critical for survival. Consequently, the behavioral analyses of olfactory capabilities in rodents are efficient, quantitative, and reproducible [24]. While in the formation and storage of olfactory memory piriform cortex [57], hippocampus [8,9], and olfactory bulb [1012] are all implicated, the cellular correlates for these processes have not been clearly delineated. The contribution of the hippocampus to olfactory memory is presently controversial [2,1318], but is deemed unlikely for simple olfactory discrimination tasks [9,19]. In fact, the most likely candidates for a cellular correlate of olfactory memory appear to be the neuronal connections in the piriform cortex due to the associational connectivity [5] and the expression of several forms of cellular and synaptic plasticity [7,2023].

Concerning odor discrimination itself, cellular mechanisms for this process are often attributed to the inhibitory circuitry of the olfactory bulb ([2430]; reviewed in [3133]). Lateral inhibitory circuits were postulated, in analogy to retina [34,35], to mediate contrast enhancement [24], for which physiological recordings [24,36,37] and modeling data, based on the well-known anatomy [29], provide additional support. Such contrast enhancement may rest in large part on the particular properties of dendrodendritic synapses between the principal output neurons (mitral cells) and local inhibitory neurons (granule cells) of the olfactory bulb. In these distinct synapses, lateral and recurrent inhibition mediated by the gamma-aminobutyric acid-A system may be controlled by the activity of the closely appositioned glutamatergic part, perhaps triggering increased gamma-aminobutyric acid release by Ca2+ influx through glutamate-gated receptor channels ([38]; see also [39]).

Given that neuronal circuits underlying odor discrimination, as well as olfactory memory, rely on properties of fast excitatory neurotransmission mediated by α-amino-3-hydroxy-5-methyl-4-isoxazolepropionate receptors (AMPARs), we sought to alter, by genetic means, the specific functional contribution of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionate (AMPA) channels containing the dominant subunit GluR-B. Of the four AMPAR constituents, GluR-A to D (GluR1 to 4), which form tetrameric channels with different binary subunit combinations, GluR-B is contained in the majority of AMPARs. GluR-B is critically involved in the formation and trafficking of AMPARs, and dominates their ion conductance and gating properties [4046]. Notably, the normally low Ca2+ permeability of AMPA channels in principal neurons is solely mediated by GluR-B, due to a unique arginine residue (R587) in the functionally critical glutamine/arginine (Q/R) site of the pore-forming segment M2 [44,47,48], resulting from RNA editing of GluR-B pre-mRNA ([49]; reviewed in [50]). Hence, either GluR-B deficiency, or the expression of Q/R site-unedited GluR-B with a glutamine residue at the critical channel site, leads to increased Ca2+ permeability of AMPA channels, as amply demonstrated in gene-targeted mice [51,53,58,60]. Thus, the absence of GluR-B, or the expression of GluR-B(Q) in the olfactory bulb, may generate increased inhibition in mitral cells. Moreover, the ablation of GluR-B, but also changes in the extent of Q/R site editing of GluR-B, can alter the strength of excitatory synaptic transmission in the genetically addressed neuronal populations [51,58,60], thus potentially shifting the balance of excitatory and inhibitory transmission in the affected circuits. Similarly, changes in synaptic plasticity due to Ca2+-permeable AMPARs [51,52,60], e.g., in piriform cortex, might alter odor memorization processes. Thus, alterations of AMPAR properties in these brain regions will allow investigation and possibly separation of mechanisms underlying these behavioral traits.

Concerning this intended switch in AMPAR properties, mice lacking all GluR-B, however, show a widespread impairment in behavior, including lethargy, motor coordination problems, and deficits in exploratory activity [51], which preclude detailed behavioral analyses. Similarly, mice expressing (in the entire brain) a substantial part of the GluR-B population in the Q/R site-unedited form become seizure-prone and die prematurely [53]. Some of these problems can be partially overcome by use of spatially and temporally restricted expression systems [5456], in particular the Cre-lox system, with Cre-recombinase expression in defined brain areas of gene-targeted mice carrying GluR-B alleles marked by loxP sites for Cre-mediated recombination [55,57]. Indeed, restricting the expression of Q/R site-unedited GluR-B to forebrain resulted in almost normal lifespan and an only weakly seizure-prone phenotype [58]. Mice with forebrain-specific GluR-B depletion appeared almost completely normal throughout life with no developmental abnormalities, thus permitting a detailed, quantitative investigation of olfactory behavior.

To allow for the mechanistic separation of olfactory learning, discrimination, and memory, we exploited a well-known phenomenon of transgenes, which concerns heterogeneous expression among different founder lines and even among genetically identical individuals of a given line. Although such “mosaic” expression is usually undesired, here we took advantage of it by ablating GluR-B via gene-targeted, floxed GluR-B alleles with the help of a transgenic mouse line with variegated Cre expression in forebrain. By correlating GluR-B levels in olfaction-related brain regions with quantitative behavioral data, we investigated the dependence on GluR-B of olfactory discrimination and memory. Moreover, to delineate the brain areas involved in these distinctive olfactory processes we used transgenic “rescue” of GluR-B ablation, specifically in piriform cortex and hippocampus.

These efforts allowed us to dissect, both spatially and mechanistically, the role of GluR-B-mediated AMPAR properties in selected brain regions in odor learning, discrimination, and memory.

Results

GluR-B(Q) Expression in the Forebrain Increases Olfactory Learning and Discrimination

To explore the role of fast excitatory neurotransmission carried by GluR-B-containing AMPA channels in olfactory processes, we first analyzed mice that express part of the GluR-B population in a Q/R site-unedited form (Figure 1A; termed “GluR-BΔECS:FB”; see also [58]). These mice carry, in addition to a wild-type GluR-B allele, a gene-targeted GluR-Bneo allele in which the intronic sequence critical for GluR-B pre-mRNA editing at the Q/R site is replaced by a floxed TK-neo gene, which severely reduces splicing of the modified intron and hence attenuates the expression of the GluR-Bneo allele [60]. To unsilence the attenuated GluR-Bneo allele, specifically in the postnatal forebrain, we crossed in the TgCre4 transgene, which encodes Cre-recombinase and is driven by the αCaMKII promoter ([59]; “Camkcre4”). Thus, Cre-recombinase removes in forebrain neurons the intronic TK-neo gene, leading to the active GluR-BΔECS allele for Q/R site-unedited GluR-B(Q) subunits (Figures 1 and S1). As expected [53,60], also in mice expressing postnatally forebrain-specific Q/R site-unedited GluR-B(Q) subunits, Ca2+ permeability through AMPAR was increased and AMPAR currents showed rectification ([58] and unpublished data). GluR-BΔECS:FB mice had, in contrast to mice expressing GluR-B(Q) globally, a prolonged lifespan and no severe developmental alterations. They were however, still seizure-prone [58], and hence behavioral training was restricted to short periods of time.

Figure 1
Odor Learning and Discrimination Is Enhanced in GluR-BΔECS:FB Mice

We trained six GluR-BΔECS:FB mice and six littermate controls on one odor pair in an automated go/no-go olfactory conditioning task [3,61]. In this task, water-deprived mice are trained to distinguish a water-rewarded odor (S+) and an unrewarded odor (S−) by their licking response (Figure 1B). Both GluR-BΔECS:FB and control mice acquired the “simple” task to discriminate between the monomolecular odors amylacetate and ethylbutyrate (percentage correct > 70% after 400 trials). Strikingly, GluR-BΔECS:FB mice showed more rapid learning and enhanced discrimination capabilities (Figure 1C, group effect: F(1,10) = 10.2, p < 0.01). This was confirmed by fitting linear trend lines to the initial part of the learning curve (slope difference: p < 0.05; see Materials and Methods). The training system employed allows for careful monitoring of head positions [3]. For rewarded trials (Figure 1D, green), already weakly trained animals kept their head in the sampling port (large tube in Figure 1B) during the entire 2-s trial, whereas for unrewarded trials the head is retracted quickly (Figure 1D, red). The difference of these two curves (Figure 1E, black) is a very sensitive assay for discrimination performance; the fitted maximum of this curve (Figure 1E, blue) is referred to as the “discrimination index” in the remainder of the paper and is again strongly improved for GluR-BΔECS:FB mice, compared with controls (Figure 1F; group effect: F(1,10) = 11.7, p < 0.01). This was not due to general motor performance, attention, or motivation changes, as both the intertrial interval (group effect: F(1,10) = 0.56, p > 0.4) and the overall licking frequency (group effect: F(1,10) = 0.72, p > 0.4) were unaffected.

Thus, expression of Ca2+-permeable AMPARs in forebrain areas, including the olfactory bulb, resulted in more rapid odor learning and enhanced olfactory discrimination.

GluR-BΔFB Mice Exhibit Increased Olfactory Discrimination Performance

To ascertain if enhanced olfactory learning and odor discrimination may indeed correlate with the increased Ca2+ permeability of AMPA channels in the Q/R site-unedited form, we next analyzed GluR-BΔFB mice, which lack GluR-B in forebrain. This specific ablation was generated by forebrain-selective TgCre4 expression ([59] “Camkcre4”) in gene-targeted GluR-B2lox mice carrying, in both GluR-B alleles, a floxed exon 11 (Figure 2A). The specific GluR-B depletion in GluR-BΔFB mice can be monitored by immunohistochemistry (see below) and immunoblotting. In quantitative immunoblot analyses, we found GluR-B levels reduced to 28 ± 7%, 29 ± 8%, and 52 ± 9% (± SEM; n = 10) in the hippocampus, cortical areas, and olfactory bulb, respectively, relative to GluR-B levels in GluR-B2lox littermate controls. In the absence of GluR-B, the electrophysiological properties of AMPA channels become similar to those with GluR-B/GluR-B(Q) switch [51] showing strong rectification and increased Ca2+ permeability through AMPA channels (unpublished data). However, GluR-B depletion is not lethal and does not produce seizures. In addition, in contrast to the complete GluR-B knockouts, mice with forebrain-specific GluR-B depletion appeared normal throughout life with no developmental abnormalities, or difference in body size and weight in adulthood (wild-type: 31.0 g ± 1.2; GluR-BΔFB: 28.4 ± 0.9; each n = 10). Exploratory activity in an open field task was slightly increased in GluR-BΔFB mice (3,480 cm ± 180, n = 11), compared with wild-type littermates (2,512 cm ± 96, n = 12, p <0.01). Motor coordination measured in an accelerating rotarod was somewhat impaired in the mutant mice (wild-type: 156 s ± 37, n = 6; GluR-BΔFB: 37 s ± 10, n = 6; p < 0.05). Tests in the dark/light box revealed increased anxiety of GluR-BΔFB mice (latency of first exit: wild-type [17 s ± 3], GluR-BΔFB [97 s ± 42], p = 0.047; compartment changes: wild-type [17 s ± 3], GluR-BΔFB [7 ± 2], p < 0.05; time spent in lit compartment: wild-type [103 s ± 10], GluR-BΔFB [59 s ± 19], p = 0.051; each n = 6). Hence, unlike the complete GluR-B knockouts, GluR-BΔFB mice show only very minor changes in general activity and no sign of any major developmental disturbance, thus allowing detailed, quantitative behavioral investigations.

Figure 2
Odor Learning and Discrimination Is Enhanced, but Odor Memory Is Reduced in GluR-BΔFB Mice

If the GluR-B/GluR-B(Q) switch-induced alterations in the Ca2+ permeability of the AMPA channels are linked to enhanced odor discrimination and learning, the depletion of the GluR-B subunit should lead to a similar phenotypic readout. We therefore trained nine GluR-BΔFB mice and nine littermate controls in the same automated associative go/no-go olfactory conditioning task described above. To cover even small phenotypic changes in olfaction, we tested different odor pairs, “simple” monomolecular odors and “difficult” binary mixtures [3]. After habituation, GluR-BΔFB and control mice were trained to discriminate between the “simple” monomolecular odors amylacetate and ethylbutyrate, and subsequently additionally on a “difficult” discrimination task consisting of similar binary mixtures of cineol and eugenol; and finally again on a “simple” discrimination task with the monomolecular odors pelargonic and valeric acid. Similar to GluR-BΔECS:FB, GluR-BΔFB mice also showed enhanced learning and discrimination compared with controls (Figure 2B; group effect: F(1,16) = 6.55; p < 0.05). Increased discrimination performance is expected to show more pronounced effects for closely related odors because of the more challenging “difficult” discrimination task that is closer to the psychophysical limits of the system [3,4]. Consistent with this notion, differences between GluR-BΔFB and control mice were not only larger if the detailed sampling pattern and discrimination index were investigated (Figure 2C and and2D,2D, group effect: F(1,16) = 29.5; p < 10−4), but in particular for the discrimination of binary mixtures with similar composition (group effect: F(1,16) = 27.8; p < 10−4 for the mixture; FAA EB(1,16) = 7.0; p = 0.02, and FPel Val(1,16) = 5.8; p = 0.03 for the “simple” discrimination tasks; 3-way ANOVA: F(6,96) = 2.9; p = 0.01). As activity, measured by the intertrial interval, was not significantly different between genotypes (F(1,16) = 3.1; p = 0.1), and analysis of the lick frequency showed a tendency to reduced motivation of GluR-BΔFB mice in this particular task (F(1,16) = 9.2; p < 0.01), we conclude that depletion of GluR-B in forebrain areas indeed resulted in increased olfactory learning and discrimination performances, rather than motivational alterations. To assess olfaction specificity, we trained ten GluR-BΔFB mice and ten controls in a nonolfactory hippocampus-dependent spatial learning task (elevated Y-maze). Performance in this task was not improved compared with controls (Figure S2); on the contrary, the acquisition of this task was slightly impaired, allowing the conclusion that the enhanced olfactory discrimination performance is likely to be specific to the sense of smell and possibly related to enhanced discrimination capability, rather than a general increase in alertness. Furthermore, enhancement in odor discrimination in both GluR-BΔECS:FB and GluR-BΔFB mice makes it likely that improvement in this task results from the common AMPAR property change mediated by the depletion of GluR-B and the lack of the Q/R site-edited GluR-B subunit, both resulting in Ca2+-permeable AMPARs. Thus, this suggests that increased Ca2+ influx via AMPARs leads to enhanced olfactory learning and discrimination.

Olfactory Memory Is Significantly Decreased but Highly Variable in GluR-BΔFB Mice

To capture the full extent of the role of Ca2+-permeable AMPARs in olfactory behavior, we next assessed the effects of altered AMPA channels on olfactory memory. To probe olfactory memory in GluR-BΔFB mice, six days after the end of the first training phase for odor discrimination (amylacetate versus ethylbutyrate), the training trials for the third odor pair (pelargonic versus valeric acid) were interleaved with unrewarded trials in which amylacetate or ethylbutyrate were again presented (black bar in Figure 2C). Whereas control mice reliably responded only to the previously rewarded odor (memory of 86 ± 8%, mean ± SD, n = 9, Figure 2E), GluR-BΔFB mice showed reduced olfactory memory (69 ± 16%, n = 9, p < 0.05, Mann-Whitney). Due to the more rapid learning observed in GluR-BΔFB, one could speculate that a decrease in olfactory memory might simply reflect increased extinction. However, extinction levels were low in general, no significant group-trial interaction could be found for the memory trials (2-way ANOVA, F(6,90) = 1.5, p > 0.1), and a restriction of the analysis to early memory trials displayed essentially the same pattern (Figure S3A). Thus, reduced performance in the probe trials is not due to increased extinction but reflects genuine memory impairment. Moreover, because the hippocampus-dependent spatial memory after-task acquisition in the Y-maze was not affected (Figure S2), we conclude that the observed olfactory memory deficit is rather specific for olfaction and does not readily generalize to other modalities.

While the improved odor discrimination and learning behavior showed only little variability, the significantly impaired memory performance observed in GluR-BΔFB mice was highly variable among individual animals compared with control littermates (Figure 2E). This variability in olfactory memory was reflected in the level and extent of Cre-recombinase expression in forebrain of transgenic TgCre4 mice, as visualized by Cre-activity in the Cre-indicator mouse line R26R. We observed that onset and extent of Cre-recombinase expression in different forebrain regions varied among individual TgCre4 mice (Figure 3A), which could also be directly visualized by immunohistochemistry with a Cre-antibody (unpublished data). As this variability persisted after several backcrosses, and Southern blot analysis revealed no differences of transgene integration or number among animals (Figure 3B), it could not be attributed to genetic differences but rather to epigenetic mechanisms.

Figure 3
Variability of Cre Expression of Mouse Line TgCre4

Hence, we hypothesized that the variability in olfactory memory reflected the mosaicism observed in the transgenic TgCre4 line. The evaluation of regional differences in expression pattern of animals with robust and poor olfactory memory could then be applied to identify brain areas responsible for the observed phenotypes.

Olfactory Memory Correlates with Residual GluR-B Protein Expression in GluR-BΔFB Mice

Thus, to examine whether the pronounced variability of olfactory memory in GluR-BΔFB mice (Figure 2E) reflects variability of GluR-B levels in GluR-BΔFB mice, we analyzed the residual amount of GluR-B protein in mice with disparate memory performances (Figure 4A–C). Notably, mice with pronounced memory deficits (memory < 70%) showed essentially no detectable GluR-B protein in hippocampus, amygdala, olfactory bulb, and piriform cortex (n = 2, Figure 4B, and unpublished data), but mice with almost complete memory displayed substantial residual GluR-B levels in all brain areas investigated (n = 2, Figure 4B, and unpublished data).

Figure 4
Olfactory Memory but not Odor Learning/Discrimination Is Correlated with Residual GluR-B Levels in Hippocampus and Forebrain of GluR-BΔFB Mice

To quantify the relation between residual GluR-B protein and olfactory memory, the memory experiment was repeated with nine additional GluR-BΔFB mice and two GluR-B2lox control animals (indicated with shaded symbols in Figure 4A), resulting in the same mean, variability, and range of memory performance (control: 89 ± 10%; GluR-BΔFB: 63 ± 14%). Subsequently, protein was extracted from olfactory bulbs, cortical areas, and hippocampi from each mouse, and GluR-B protein was quantified (Figure 4C). The summarized correlations are depicted in Figure 4D (two animals were used for immunofluorescent analysis that yielded the same results as in the first experiment). Whereas no learning or discrimination-related parameter correlated with residual protein levels (Figure 4D, R2 < 0.3), a strong correlation between memory and GluR-B protein was observed in hippocampus (Figure 4D, R2 = 0.72, p < 0.003, n = 10) and cortical areas (Figure 4D, R2 = 0.62, p < 0.006, n = 10). Only a weakly significant correlation was found in the olfactory bulb (Figure 4D, R2 = 0.48, p = 0.03, n = 10). GluR-A levels were unchanged from wild-type, indicating that compensatory up-regulation of other AMPAR subunits is unlikely (GluR-A levels relative to control: 1.02 ± 0.05, mean ± SEM, n = 10).

In summary, mice with reduced GluR-B levels in forebrain areas showed decreased olfactory memory, which correlated tightly with a reduction in GluR-B levels in the hippocampus and cortical areas. Enhanced odor learning and discrimination, on the other hand, was independent of residual GluR-B levels in the olfactory bulb and other forebrain areas, indicating that moderate GluR-B reductions are sufficient to saturate enhanced odor learning and discrimination. Thus, although both are mediated by alterations in the AMPAR subunit GluR-B, due to the qualitatively different dose-response curves, the phenotypes regarding olfactory memory, and olfactory learning/discrimination must be mechanistically distinct.

Partial Rescue of Olfactory Memory Deficit by Selective Transgenic GluR-B Expression in Hippocampus and Piriform Cortex in GluR-BΔFB Mice

The effect of selective GluR-B depletion in mice indicated that GluR-B-containing AMPARs in the hippocampus, and/or (olfactory) cortex are likely to be important for olfactory memory. The olfactory memory phenotype could be due to depletion of GluR-B in olfactory cortex or hippocampus; enhanced learning and discrimination capabilities might rather be evoked by AMPARs lacking GluR-B in the olfactory bulb.

To obtain independent evidence for this spatial and mechanistic dissection of the roles of Ca2+-permeable AMPARs, we expressed by transgenic means N-terminally green fluorescent protein (GFP)-tagged GluR-B specifically in hippocampus and piriform cortex of GluR-BΔFB mice (Figure 5A and and5B).5B). In accordance with the proposed region-dependence, we expected that additional GluR-B subunits in hippocampus and/or piriform cortex improve odor memory but do not alter odor discrimination performance. The mouse line employed for this purpose, termed GluR-BRescue, had the genetic background of GluR-BΔFB mice but additionally carried a bidirectional module for β-galactosidase and GFPGluR-B expression, responsive to the tetracycline-controlled transcriptional transactivator [62]. The transactivator was under the control of a modified αCaMKII-promoter fragment to obtain high expression selectivity (Figure 5A; see also Materials and Methods). The transgenic expression level of GFPGluR-B was 9.72% ± 1.25 (n = 3) in the hippocampus, compared with endogenous GluR-B (Figure 5C and and5D).5D). Analysis of β-galactosidase activity and GFPGluR-B expression in brain sections of GluR-BRescue mice revealed expression in hippocampus and piriform cortex, whereas cortex, amygdala, and striatum only rarely showed any positive cells (Figure 5B). Importantly, both the spatial pattern and intensity of GFPGluR-B expression were constant among all GluR-BRescue mice analyzed (n = 11).

Figure 5
Specific Hippocampus and Piriform Cortex Expression of Transgenic GFPGluR-B

Olfactory memory experiments with GluR-BRescue , and both GluR-BΔFB and GluR-B2lox mice as controls, were performed as described above (indicated with shaded symbols in Figure 6A). Memory was again highly reproducible in both GluR-BΔFB (66 ± 12%; n = 4) and GluR-B2lox (94 ± 2%; n = 3) mice, compared with experiments performed earlier (Figures 2E and and4A).4A). Importantly, olfactory memory in GluR-BRescue mice was intermediate (75 ± 15%, n = 8), below GluR-B2lox control levels, but better than in GluR-BΔFB mice. Assessing memory under extinction-free condition, where each trial was rewarded, confirmed again that the memory deficit was a true memory deficit and not due to increased extinction (Figure S3B). Data from the experiments described in Figures 2 and and44 were combined to allow statistical comparison (Figure 6A and and6B).6B). In summary, GluR-BRescue mice showed both enhanced memory performances compared with GluR-BΔFB (overall ANOVA: F(2,41) = 13.6, p < 10−4; memoryRescue = 75 ± 15%, n = 8; memoryΔFB = 66 ± 14%, n = 22; p < 0.05; Figure 6A), but were still impaired relative to GluR-B2lox controls (memory2lox = 88 ± 8%, n = 14; p < 0.005), consistent with a partial rescue of the memory deficit by circumscribed transgenic GFPGluR-B expression in hippocampus and piriform cortex. Notably, the partial memory is in numerical agreement with the predictions from the protein correlation and the measurement of transgenic protein expression (see predicted memory, blue line, in Figure 6B). In the olfactory memory experiments with GluR-BΔFB animals, olfactory memory linearly depended on GluR-B expression in cortex and hippocampus with a slope of 9.1 ± 2.5% (cortex) and 8.9 ± 2.0% (hippocampus) increase in memory per 10% increase in protein (Figure 4D). A 9.7% increase in GluR-B in these brain regions, as achieved by GluR-BRescue animals (Figure 5), is thus predicted to increase olfactory memory by approximately 9% throughout the heterogeneous population (blue line in Figure 6B). This confirms the role of these brain areas as inferred from the mosaic expression and protein correlation analysis described above (Figure 4). However, odor discrimination (measured by the discrimination index as in Figures 1, ,2,2, and and4D)4D) was as enhanced as in GluR-BΔFB mice (0.79 ± 0.05, mean ± SEM compared with 0.76 ± 0.02, p > 0.7, Figure 6C), and improved relative to GluR-B2lox controls (0.48 ± 0.06; Figure 6C; overall ANOVA: F(2,41) = 17.2, p < 10−5; post hoc Newman Keuls: p < 10−3), as expected if the enhanced discrimination phenotype is due to Ca2+-permeable AMPARs in the olfactory bulb and unaffected by GluR-B expression in piriform cortex or hippocampus.

Figure 6
GluR-B Expression in Hippocampus and Forebrain Partially Rescues the Memory Deficit of GluR-BΔFB Mice

Hence, transgenic GluR-B expression, specifically in the piriform cortex and hippocampus in the GluR-B knockout background, rescues the odor memory deficit but leaves enhanced olfactory discrimination and learning unaltered.

Discussion

Here we present mechanistic and spatial dissections of olfactory discrimination, learning, and memory. We employed gene-targeted and transgenic mice with region-specific expression to demonstrate that a change in GluR-B-mediated properties of AMPA channels in αCaMKII-expressing neurons of mouse forebrain, including olfactory bulb mitral and granule cells, enhances olfactory discrimination and learning but impairs olfactory memory. These pertinent olfactory behaviors were assessed in a go/no-go operant conditioning task, which provides a quantitative, robust, and reproducible behavioral tool [3]. We observed among individual mice a striking variability in olfactory memory performance but not in odor discrimination. This variability could be traced to epigenetic variability in the transgenic expression of Cre-recombinase, which mediated recombination within loxP-flanked segments of gene-targeted alleles for the dominant AMPAR subunit GluR-B, and hence operated the switch in AMPAR properties toward GluR-B ablation and increased Ca2+ permeability. In contrast to variable memory, olfactory discrimination and learning performances appeared already saturated by even moderate extents of Cre expression, and hence moderate changes in AMPAR properties. The subsequent transgene-driven re-introduction of GluR-B, specifically in piriform cortex and hippocampus, reversed the Cre-induced loss of GluR-B and partially rescued the odor memory deficit, but left unaltered the enhanced olfactory discrimination. In a nutshell, we conclude that olfactory discrimination is enhanced by an increase in AMPAR-mediated Ca2+ permeability within the olfactory bulb, whereas olfactory memory becomes impaired upon genetically induced GluR-B ablation in higher brain centers, specifically in piriform cortex.

Olfactory Discrimination Is Increased in Mice with Forebrain-Specific GluR-B Ablation or GluR-B(Q) Expression

Both forebrain-specific GluR-B(Q) expression and GluR-B depletion led to increased olfactory learning and discrimination capabilities. This was rather pronounced for GluR-B(Q)-expressing mice, consistent with the overall stronger phenotypic consequences in comparison to GluR-B depletion, both when forebrain-selective ([58], and this study) or global [53,60].

A detailed analysis of the sampling pattern [3], and in particular the analysis of discrimination tasks that involved “simple” dissimilar monomolecular odor pairs and “difficult” binary mixtures, were necessary to fully capture the characteristics of the olfactory discrimination phenotype for forebrain-specific GluR-B-depleted mice. For closely related binary mixtures, discrimination improvements were largest, consistent with a specific alteration in odor discrimination, rather than a general enhancement of learning capabilities. This is further supported by the notion that no general improvement was observed in other nonolfactory behavioral tasks, e.g., hippocampus-dependent spatial learning tasks such as matching-to-place spatial reference memory tasks (Figure S2). As no Cre expression and activity was observed in the main olfactory sensory neurons at any developmental stage (Figure S4 and unpublished data), olfactory epithelial function was unaltered by the genetic modification. The vomeronasal organ showed very weak Cre expression (unpublished data), but a role of this structure concerning performance in the olfactory discrimination task is unlikely (for review, see [63]). The behavioral phenotype is thus likely to be associated with the processing of olfactory information rather than the detection of odors. Furthermore, increased performance even after long stretches of training and, in particular, increased sampling pattern differences (TB and ATS, unpublished data) supported the notion that GluR-B depletion resulted in enhanced odor discrimination capability. The learning phenotype might thus be a result of this enhanced discrimination capability or reflect additional changes in circuits underlying task acquisition.

Putative Cellular Basis of Enhanced Odor Discrimination and Learning

AMPAR properties were altered specifically in neurons of forebrain areas, most notably olfactory bulb, olfactory cortex, and other cortical areas and hippocampus, leading to enhanced odor discrimination and learning. Interestingly, transgenic expression of GFPGluR-B in GluR-BΔFB mice (genetic “rescue”), specifically in piriform cortex and hippocampus with no detectable expression in the olfactory bulb, did not alter enhanced discrimination and learning capabilities. This is consistent with a primary role of the olfactory bulb in olfactory discrimination and learning. Alternatively, transgenic protein levels might have been too low to alter discrimination and learning capabilities, although memory was clearly affected. This notion will be further tested in mice with piriform cortex-specific GluR-B ablation.

A direct contribution to the phenotype by Ca2+ influx through genetically modified AMPA channels seems to be likely, since mice expressing Q/R site-unedited GluR-B showed even better odor learning and discrimination performance compared with mice with depleted GluR-B. In both mouse models Ca2+ influx through AMPA channels is increased, whereas the effect on the macroscopic AMPA conductance differs. AMPAR currents are reduced in mice not expressing GluR-B [51], possibly due to fewer synaptic AMPA channels and impaired AMPAR trafficking and recycling. In mice expressing the unedited form of GluR-B(Q), macroscopic conductance in whole-cell patches of CA1 pyramidals is increased [60], but excitatory transmission in CA3-to-CA1 cell synapses is somewhat reduced, in spite of a lower threshold for generating a population spike [58], indicating increased synaptic excitability by sustained GluR-B(Q) expression, in line with the seizure-prone phenotype. Yet, both mouse models yield enhanced discrimination and learning capability. The milder phenotype upon GluR-B depletion could be attributed to reduced AMPAR densities at synapses [40,41] and therefore probably to a lesser extent of Ca2+ influx. This is further supported by kainate-induced Co2+ uptake in acute brain slices, revealing considerably higher Co2+ uptake via Ca2+-permeable AMPARs in hippocampal pyramidal neurons of mice expressing GluR-B(Q), than those lacking GluR-B (DRS, RS, and PHS, unpublished data).

Normally, GluR-B-containing AMPARs are prominently localized at the dendrodendritic synapse between mitral and granule cells in the olfactory bulb [64,65]. As Ca2+ influx through glutamate receptors is thought to contribute to lateral and recurrent inhibition ([38] see also [39]), the absence of GluR-B, or the presence of GluR-B(Q) in the olfactory bulb, is likely to result in increased inhibition between the principal neurons in this structure. Notably, the improved olfactory discrimination capabilities were apparent even upon relatively small reductions in GluR-B levels. It will be interesting to see if GluR-B+/neo mice also exhibit enhanced odor discrimination, which is indeed likely given that low levels of GluR-B(Q), and hence a small increase in Ca2+-permeable AMPARs, arise from the attenuated GluR-Bneo allele [60], and, moreover, that GluR-B levels are decreased in these mice due to the single copy of the GluR-B+ allele.

In virtually all models of the olfactory bulb, lateral (and, in fewer models, also recurrent) inhibition plays a dominant role, either in establishing spatiotemporal dynamics [32,6669], or in directly enhancing contrast and therefore simplifying discrimination and learning of similar odorants [24,28,29,36]. Increased inhibition will thus in general improve discriminability, consistent with the behavioral improvements observed with GluR-B(Q) expression, the GluR-B knockout, and the “rescue” mice. A direct test of this link would require the quantitative measurement of inhibition in the intact preparation, a task that might be feasible with further improved in vivo electrophysiological techniques, such as targeted recordings [70,71] or simultaneous pre- and postsynaptic intracellular measurements.

Olfactory Memory Is Reduced in GluR-B Knockout Mice and Improved by GluR-B Expression in Piriform Cortex and Hippocampus

To assess olfactory memory of GluR-BΔFB mice, after six days the mice were probed with unrewarded odor presentations that interleaved a simple discrimination task. Prolonged behavioral tasks such as the assessment of long-term olfactory memory were not performed with the seizure-prone GluR-BΔECS:FB mice. Memory in GluR-BΔFB mice, however, was dramatically impaired. This cannot be attributed to a general, unspecific deficit because, simultaneous to the memory trials, the normal, rewarded discrimination task was performed even better than by controls. Reduced olfactory memory can also not be simply attributed to increased extinction, as no significant trial-group interactions were observed and also, when restricted to the first unrewarded memory trials, a significant impairment was observed (Figure S3A). Additionally, investigating relearning of the first discrimination task revealed a significant correlation with the memory performance, showing a “memory” deficit under extinction-free conditions (Figure S3B). Finally, in other memory-related tasks, such as a hippocampus-dependent spatial reference memory task (Figure S2), mice with GluR-B depletion were not impaired after task acquisition. We therefore conclude that forebrain-specific ablation of GluR-B results in a specific loss of long-term olfactory memory but, at the same time, in enhanced odor discrimination and learning capabilities.

To dissect the discrimination, learning, and memory phenotypes, and ultimately identify potential cellular correlates, we made use of the variegated Cre expression of TgCre4 mice. Therefore, residual GluR-B levels were determined from each mouse that had been tested in the behavioral experiments, and levels were correlated with odor learning, discrimination, and olfactory memory. The significant direct correlation between residual GluR-B levels in hippocampus and cortical areas with olfactory memory suggested hippocampal and/or cortical neurons as putative mediators for odor memorization and/or storage. No measure of discrimination and learning, on the other hand, correlated with residual GluR-B levels; even the smallest reduction in GluR-B levels (about 20%–60%) was sufficient to establish and saturate enhanced odor discrimination capabilities. Together, this allows the conclusion that distinct mechanisms mediate discrimination/learning and memory. This is furthermore consistent with a prominent role of cortical areas or hippocampus in olfactory memory, although GluR-B levels in the olfactory bulb were also weakly correlated with memory performance. Transgenic expression of GFPGluR-B in piriform cortex and hippocampus indeed rescued memory to an extent strikingly consistent with the transgenic protein levels (approximately 10% of wild-type GluR-B), confirming the reliability of the correlation analysis and the sensitivity of the behavioral assay.

In general, the hippocampus is thought to be involved in only those olfactory memory tasks that involve temporal sequence analysis or require other higher cognitive features [2,13,7274]. In particular, extensive lesions to the hippocampal formation in rats do not interfere with long-term olfactory memory in go/no-go successive olfactory discrimination tasks [72], such as the one described. This leaves piriform cortex as the most prominent candidate for the locus of the olfactory memory deficit described, consistent with the prevalent view of piriform cortex as an associational memory structure [75] and learning-associated changes in piriform cortex [7,2023].

Potential Mechanisms of Specific Olfactory Memory Impairment

What could be the cellular basis of the long-term memory deficit brought about by lack of GluR-B-containing AMPARs? For complete GluR-B knockouts, increased long-term plasticity (LTP) was reported in hippocampal field recordings [51]. In addition, in hippocampal and amygdala pathways lacking GluR-B, an AMPAR-dependent, N-methyl-D-aspartate (NMDA) receptor-independent form of LTP can be readily induced [51,52]. Mechanistically, this is likely to be due to Ca2+ influx through GluR-B-less AMPA channels leading to non-hebbian forms of plasticity. However, hebbian dependence on simultaneous pre- and postsynaptic activity is often a critical feature for memory storage (reviewed in e.g. [76]); hence, a non-hebbian form of plasticity should result in impaired memorization.

Surprisingly, in GluR-BΔFB mice no LTP changes could be observed in field measurements in the hippocampus, nor could NMDA-independent LTP be induced in hippocampal synapses between Schaffer collaterals and CA1 pyramidal cells in presence of the NMDA antagonist APV (K. Jensen, O. Hvalby, personal communication). However, in other brain areas that are potentially important for the processing of olfactory information, such as piriform cortex or olfactory bulb, LTP measurements have not yet been performed; synapses of these pathways may be regulated differently than hippocampal CA3/CA1 synapses.

Additionally, by changing the Ca2+ permeability of AMPARs, Ca2+ signaling via AMPA and colocalized NMDA channels might be disturbed, thereby impairing memory formation. Other forms of plasticity [77,78] induced by Ca2+-permeable AMPARs might play a prevalent role in olfactory memory. Alternatively, long-term stabilization might involve GluR-B phosphorylation similar to cerebellar long-term depression [79] and thus be selectively impaired by GluR-B depletion. Physiological experiments to assess these hypotheses will ideally make use of even more restricted genetic modifications with completely undisturbed input structures. One possibility would be Cre-mediated GluR-B depletion and GluR-B(Q) expression in piriform cortex as suggested above.

Correlating Quantitative Behavior and Mosaic Gene Expression for Dissecting Phenotypes

A critical step in discerning the discrimination and learning phenotypes from the memory phenotype was the observation of increased variability in the memory of the GluR-B knockout animals and, subsequently, the individual analyses of protein expression levels. We made use of the epigenetic variability in GluR-B excision that could be correlated to the variability in memory but showed no correlation to variability in discrimination.

The analysis of quantitative trait loci (for review, see [80]), or classically correlating different behavioral phenotypes within a truly wild-type population [8184], also attempts to find common or distinct genetic origins of different behavioral traits. These attempts undoubtedly contribute significantly to unraveling the molecular basis of behavior. Due to subtle and multigenic differences between different strains of rodents or different individuals in a wild-type population, however, they suffer from a rather low “signal-to-noise” ratio. Differences in individual genes are rather small compared with the vast number of genes involved. As a result, purely correlating behavioral traits within a wild-type population usually remains rather descriptive, whereas quantitative trait loci analysis is capable of revealing multigenic basis of behavioral traits but usually lacks the power to identify the individual genes themselves.

Herein, we described a way to enhance the signal-to-noise ratio by making use of the mosaic expression often associated with transgenic approaches: combining the advantages of “classical” genetic manipulation—namely, that the target of the manipulation is well defined—with the possibility to analyze variability, might also in future provide novel ways to define molecular and cellular correlates of complex behavioral traits.

In this study, we combined genetically induced manipulation of the AMPAR composition with quantitative behavioral and molecular analyses. We could thus provide evidence for opposing roles of specific GluR-B manipulation and increased Ca2+ influx via AMPARs in olfactory discrimination/learning, and memory, potentially in the olfactory bulb and piriform cortex, respectively. To achieve this, we made use of the epigenetic variability in the extent of GluR-B ablation, which correlated with the variability in odor memory, but not in discrimination and learning; this finding was subsequently confirmed in GluR-B rescue mice with piriform cortex-specific transgenic expression of GluR-B. Extending these principles of combining quantitative behavioral analyses with minimal and dosed genetic interference, together with further physiological analyses, will ultimately pinpoint the neural circuitries underlying related, but distinct, behavioral traits in olfactory and other systems.

Materials and Methods

Mouse lines

The R26R line [85] was employed as Cre indicator. GluR-BΔECS:FB mice were of mixed C57Bl/6 and NMRI genetic background and generated from TgCre4 (“Camkcre4” in [59]) and GluR-B+/neo [60] mice. GluR-B+/neo mice carry a wild-type GluR-B allele and a gene-targeted GluR-B allele in which the intron 11 sequence critical for Q/R site editing is replaced by a TK-neo gene flanked by loxP sites (“floxed”). GluR-B2lox mice [86] carry gene-targeted GluR-B alleles in which exon 11 is floxed. GluR-BΔFB mice were of C57Bl/6 genetic background and generated from TgCre4 and GluR-B2lox mice. TgCN12-itTA mice were generated as described for TgCN10-itTA mice (see Materials and Methods in [58]), and represent another founder line obtained from the same pronucleus injection, with more widespread forebrain expression. For exogeneous expression of GFPGluR-B, the mouse line TgOCN1 was generated: an AseI fragment of plasmid pnlacZ/GFPGluR-B was injected into the pronucleus of oocytes obtained from DBA1/C57Bl/6 F1 hybrids. Positive founders were backcrossed into C57Bl/6 for further analysis. Plasmid pnlacZ/GFPGluR-B was constructed from pnlacZ/GFPGluR-A [87] by replacing GluR-A cDNA with the rat cDNA for GluR-B. Transgenic GFPGluR-B protein levels were measured in hippocampus of TgOCN1 mice also carrying a transgene for forebrain-specific homogeneous tTA expression [88].

Experimental groups

Mice heterozygous for TgCre4 and heterozygous for the TK-neo cassette in the GluR-B allele (GluR-BΔECS:FB) or homozygous for the floxed GluR-B (GluR-BΔFB) were used in the experiments. The “rescue” mice (GluR-BRescue) were positive for TgCre4, homozygous for the floxed GluR-B gene, and positive for the tet-sensitive responder transgene TgOCN1 and for the itTA expressing activator transgene TgCN12-itTA.

Control groups

Littermate controls were used in all experiments. GluR-B+/+ mice were used as controls in the task described in Figure 1. GluR-B+/2lox and GluR-B2lox/2lox (both negative for TgCre4) mice were used as controls in experiments described in Figures 2, ,4,4, and and6.6. For the GluR-BRescue experiments (Figure 6), controls positive for either TgCN12-itTA or TgOCN1 in a GluR-B+/2lox and GluR-B2lox/2lox (both negative for TgCre4) background were used.

Genotyping

Mice were selected by PCR of mouse-tail DNA with specific primers as described below. Indicated are the sequences and the approximate length of the amplified DNA fragments. TgCre4: rspCre1 (5′- ACCAGGTTCGTTCACTCATGG-3′) and rspCre2 (5′- AGGCTAAGTGCCTTCTCTACAC-3′), 200 basepairs (bp).

GluR-Bneo: MH60 (5′- CACTCACAGCAATGAAGCAGGAC-3′), MH53a (5′- GAATGTTGATCATGTGTTTCCCTG-3′), and MH117 (5′- GTTCGAATTCGCCAATGACAAGACG-3′), wild-type: 500 bp and mutant: 400 bp.

GluR-B2lox: VM12 (5′- GCGTAAGCCTGTGA AATACCTG-3′) and VM10 (5′- GTTGTCTAACAAGTTGTTGACC-3′), wild-type: 250 bp and mutant: 350 bp.

TgOCN1: VM4 (5′- CTCCCAGACAACCATTACCTGTCC-3′) and GluR-B882BST (5′- CGAAGTATACTTAATTGTCGCTGTGTG-3′), 600 bp.

TgCN12-itTA: htTA1 (5′- AGAGCAAAGTCATCAACTCTG-3′) and htTA2 (5′- GTGAGAGCCAGACTCACATTTCA-3′), 1,000 bp.

Southern blot analysis

Genomic DNA from mouse-tail/liver was digested with restriction enzyme BglII (NEB), and the Southern blot was done with a 320-bp probe (“integ”) obtained by PCR detecting the αCaMKII promoter.

Histochemistry

Histochemistry was performed as described previously [89], with the following exceptions: Coronal 70- to 100-μm vibratome slices were used for immunohistochemistry with GluR-B (1:60, polyclonal; Chemicon, Temecula, California, United States), GFP (1:8,000, polyclonal; MobiTech, Göttingen, Germany), and Cre (1:8,000, polyclonal; BAbCO, Berkeley, California, United States) primary antibodies, and FITC-coupled (1:200; Dianova, Hamburg, Germany) and peroxidase-coupled (1:600; Vector, Burlingame, California, United States) secondary goat anti-rabbit antibodies.

The main olfactory epithelium was obtained via cryostat sectioning, and immunohistochemistry was performed (primary antibody Cre, 1:5,000, polyclonal; BAbCO). X-gal staining was performed as described [89].

Immunoblot analysis

Mouse brains were removed, and the hippocampus, olfactory bulb, and remaining forebrain areas were isolated. Total protein was prepared, and immunoblots were performed as described [87]. Antibodies used were against GluR-B (1:800, monoclonal; Chemicon), β-actin (1:40,000, monoclonal; Sigma, St. Louis, Missouri, United States) as an internal standard, and secondary goat anti-rabbit and goat anti-mouse antibodies (Vector, 1:15,000). Immunoreactivity was detected with ECLplus (Amersham, Little Chalfont, United Kingdom), and immunoblots were scanned and quantitatively analyzed with ImageJ.

Behavioral analysis: Subjects

All mice were four to six weeks old at the beginning of the experiments. Subjects were maintained on a 12-h light-dark cycle in isolated cages in a temperature and humidity-controlled animal facility. All behavioral training was conducted during daytime. During the training period, animals were kept on free food but on a water-restriction schedule designed to keep them at > 85% of their free food body weight. Continuous water restriction was never longer than 12 h. All animal care and procedures were in accordance with the animal ethics guidelines of the Max-Planck Society.

Apparatus

All olfactory discrimination experiments were performed using three modified eight- channel olfactometers ([61], Knosys, Bethesda, Maryland, United States of America) operated by custom-written software in Igor (Wave Metrics, Lake Oswego, Oregon, United States of America) on Pentium I, II, and III PCs running Microsoft Windows 98. Great care was taken to counterbalance groups between setups. In brief, animals were presented with odor from one out of eight possible odor channels and rewarded with a 2- to 4-μl drop of water in a combined odor/reward port (Figure 1B), ensuring tight association of the water-reward with a presented odorant. Head insertion into the port was monitored by an IR beam and photodiode (Figure 1B). Odors used were n-amyl acetate, ethyl butyrate, pelargonic acid, valeric acid, and binary mixtures of cineol and eugenol. If not otherwise noted, odors were diluted to 1% in mineral oil (Fluka Chemie, Steinheim, Germany) and further diluted by airflow to a final concentration of approximately 0.15%. All dilutions in the text refer to the dilution in mineral oil. All chemicals were obtained from Fluka Chemie.

Task habituation training

Beginning 1–3 d after the start of the water restriction schedule, animals were trained using standard operant-conditioning procedures [3]. In a first pretraining step, each lick at the water delivery tube was rewarded. After 20 licks, a second stage was entered in which head insertion initiated a 2-s “odor” presentation during which a lick was rewarded. The “odorant” used in the pretraining was the carrier medium mineral oil. All animals learned this task within one day (2–3 sessions 30 min each).

Structure of an individual trial

The mouse initiates each trial by breaking a light barrier at the opening of the sampling port (see also [3]). This opens one of eight odor valves, and a diversion valve that diverts all air flow away from the animal for typically 500 ms. After the release of the diversion valve, the odor is accessible to the animal for 2,000 ms. If it continuously licks at the lick port during this time (once in at least three out of four 500-ms bins), it can receive a 2- to 4-μl water reward after the end of the 2,000-ms period. If the animal does not continuously lick, or if the presented odor was a designated nonrewarded odor, neither a reward is given nor any sort of punishment, to minimize stress for the animal. Trials are counted as correct if the animal licks continuously upon presentation of a rewarded odor or does not lick continuously with a nonrewarded odor. A second trial cannot be initiated unless an intertrial interval of at least 5 s has passed. This interval is sufficiently long so that animals typically retract quickly after the end of the trial. Odors are presented in a pseudo-randomized scheme (no more than two successive presentations of the same odor, equal numbers within each 20-trial block). No intrinsic preference toward any of the odors was observed but controlled for by counterbalancing.

A total of 100–300 trials were performed each day, separated into 30- to 40-min stretches to ensure maximal motivation despite the mild water restriction scheme. Additionally, motivation was controlled by monitoring intertrial intervals and the response frequency [3].

Measurement of performance

The simplest measure of performance is the fraction of trials in which the animal responds correctly—that is, responds with licking to the presentation of the S+ odor and does not lick with presentation of the S− odor.

It was shown previously, however, that the detailed sampling pattern is a more sensitive measure of discrimination performance [3]. To avoid long (> 3-week) training periods, we chose not to measure discrimination times [3] but to analyze the average sampling behavior in total. Upon presentation of a rewarded odor, the animal usually continuously breaks the beam, whereas upon presentation of an unrewarded odor the head is quickly retracted. The difference in response to the rewarded and unrewarded odor is approximately sigmoidal (Figures 1D, D,1E,1E, and and2D)2D) and yields a sensitive measure of the discrimination performance. From this difference or from a sigmoidal fit to the difference (Figure 1E), several measures of discrimination can be determined: the average difference, peak, or maximum, time of half maximum, and slope of the fitted sigmoid. Whereas for small trial numbers (< 200) the slope often is not well constrained, any of the other parameters yielded essentially the same results. The discrimination index plotted in Figures 1F, F,2C,2C, C,4D,4D, and and6C6C refers to the fitted maximum, generally ranging from zero to one, one indicating the best discrimination. Identical results were obtained with other measures of discrimination, such as the average sampling difference.

Structure of training

After habituation, mice were trained to discriminate 1% amylacetate from 1% ethylbutyrate for 500 trials. During the last 100 trials, the S+ odor was rewarded in only 50% of the cases to increase the resistance to extinction of the acquired memory. These trials were excluded for the statistical analysis of the learning curves. Inclusion did not alter the result of the ANOVA; however, linear fitting of the learning curve was not appropriate anymore as partial saturation of learning performance had already occurred. Subsequently, animals were trained for 500 trials on the “difficult” discrimination task [3] between the binary mixtures 0.6% eugenol/0.4% cineol and 0.4% eugenol/0.6% cineol. To allow comparison, the last 100 trials were altered as for the “simple” discrimination task above. After two days of rest, animals were finally trained on the “simple” discrimination task between 1% pelargonic acid and 1% valeric acid for another 600 trials.

In all experiments, counterbalancing between both odors and setups was ensured within and between genetic groups, or results were compared with counterbalanced subgroups, which in every case yielded identical results. During the entire course of the experiment, the person handling the animals and operating the olfactometers was blind to the genotype of the mice.

Memory measurement

To assess memory, after 280 trials of training to discriminate between pelargonic acid and valeric acid, memory trials were interleaved for 120 trials; that is, within each block of 20 trials two unrewarded amylacetate and two unrewarded ethylbutyrate trials were included. Memory scores are given as the fraction of those unrewarded trials that were responded to “correctly” (licking response to the odor that was rewarded in the initial training session [S+], no response to the odor that was not rewarded initially [S−]). Due to the epileptic phenotype and the slightly increased mortality [58], GluRBΔECS:FB mice were trained only for the initial period of 400 trials.

Statistics

Learning curves for both correct performance (“percentage correct”) and the discrimination performance were analyzed by repeated measure ANOVA. Additionally, learning curves were assessed by linearly fitting of trend lines to the data with fixed offsets, leaving the slope as the only variable. In general, binning was 100 trials per block. To allow for the investigation of group/block interactions, the repeated measure ANOVA binning was reduced to 20 trials per block. To compare memory performance in the GluR-BRescue (n = 8) and GluR-BΔFB (n = 22) mice, due to the high variability, a bootstrap approach was employed. Subpopulations of eight animals were selected from the population of 22 GluR-BΔFB mice, and mean memory was determined. In only 343 out of 20,000 subpopulations, mean memory exceeded the mean GluR-BRescue memory of 74.99%, resulting in a p value of p = 343/20,000 = 0.017.

Supporting Information

Figure S1

Forebrain-Specific Gene Manipulation:

(A) Schematic diagrams depicting Cre under the αCaMKII promoter control [59] and Cre-dependent expression of β-galactosidase (LacZ) by the R26R indicator mouse [85].

(B) Coronal forebrain sections (left) and sagittal brainstem/cerebellum sections of mice at P42 positive for TgCre4 and R26R Cre-indicator. Cre expression visualized by enzymatic β-galactosidase activity (blue, X-gal, counterstain by eosin) of R26R and by anti-Cre immunostainings (brown, DAB [diaminobenzadine]) was restricted to forebrain regions. Scale bars: 1 mm. A, amygdala; Ce, Cerebellum; Cx, cortex; H, hippocampus; Me, medulla oblongata.

(C) Olfactory bulb sections of the same mouse to visualize Cre expression by Cre immunoreactivity (left, DAB) and by enzymatic β-galactosidase activity (right, X-gal, counterstain by eosin) in granule cells (GC) and mitral cells (MC) as indicated by arrows. Scale bars: 400 μm (upper panel), 50 μm (lower panel).

(3.4 MB TIF).

Figure S2

Performance of GluR-BΔFB (n = 10) and Littermate Control (n = 10) Mice in a Spatial Reference Task on the Elevated Y-Maze:

Details of the methodology are described in [90]. * indicates p < 0.05.

(126 KB TIF).

Figure S3

Memory Deficit Is Not Due to Increased Extinction:

(A) Memory performance as a function of time for the experiment described in Figure 2E (nine GluR-BΔFB and nine GluR-B2lox control animals). Only four unrewarded “memory +” trials are binned for each data point. Memory of GluR-BΔFB animals was significantly reduced (F(1,33) = 17; p < 0.001). Whereas a weak overall time effect could be observed (F(2,66) = 3.6; p = 0.03), there was no genotype-time interaction effect (F(2,66) = 0.67; p = 0.5), indicating that there is no differential effect of putative extinction on memory performance. * indicates p-values for a Mann-Whitney U test (* < 0.05, ** < 0.01).

(B) After the memory experiments from Figure 6A, the last set of animals (eight GluR-BRescue, four GluR-BΔFB, and three controls) was further trained on AA versus EB for 900 trials one week after the memory experiment. Subsequently, training continued on AA/EB mixtures for 1,200 trials. Finally, the animals were retrained on AA and EB for 100 trials. Relearning performance during the last retraining task is highly correlated to the original memory performance (R2 = 0.46, p = 0.006, n = 15).

(264 KB TIF).

Figure S4

Absence of Cre Expression in the Main Olfactory Epithelium of TgCre4 Mice:

(A) Overview of the main olfactory epithelium. (B) Higher magnification of (A) showing all cells with propidium iodide (red) and absence of Cre-positive cells (green, anti-Cre). (C) Positive control showing granule cells of the dentate gyrus stained for nuclear Cre (green) from the same mouse.

(3.7 MB TIF).

Acknowledgments

The authors want to thank Troy Margrie and Bert Sakmann for support, encouragement, and discussion; Onyeka Nobuka for help with the construct OCN; Mark Mayford for the αCaMKII promoter; Bettina Suchanek for the NR2C silencer; Annette Herold, Juliana Kling, and Christiane Zacher for experimental and technical supports; Nixon Abraham for assistance with some behavioral experiments; and David Bannerman, Thomas Kuner, and Pavel Osten for critically reading early versions of the manuscript. This work was supported by a Deutsche Forschungsgemeinschaft grant (SFB 636) to RS, the Heidelberger Akademie der Wissenschaften, the Boeringer Ingelheim Fonds, and the Leopoldina Akademie der Wissenschaften to ATS, the BMBF, and the MPG.

Competing interests. The authors have declared that no competing interests exist.

Abbreviations

AMPA
α-amino-3-hydroxy-5-methyl-4-isoxazolepropionate
AMPAR
α-amino-3-hydroxy-5-methyl-4-isoxazolepropionate receptor
bp
basepair
GFP
green fluorescent protein
LTP
long-term plasticity
NMDA
N-methyl-D-aspartate
Q
glutamine
R
arginine

Footnotes

Author contributions. DRS and ATS conceived and designed most of the experiments. The manuscript was written by DRS, PHS, RS, and ATS. Mouse lines were conceived and designed by DRS, PHS, RS (GluR-BΔFB, GluR-BΔECS:FB); DRS, PHS, RS, ATS (GluR-BRescue); JK, PHS, RS (TgCN12-itTA); and VM, PHS, RS (GluR-B2lox, TgOCN1). Olfactory behavioral experiments were done by TB and ATS; AM performed the GFPGluR-B Western blots; immunohistochemical experiments and other Western blots as well as the nonolfactory behavioral experiments were performed by DRS.

¤ Current address: Department of Physiology, University College London, London, United Kingdom

Citation: Shimshek DR, Bus T, Kim J, Mihaljevic A, Mack V, et al. (2005) Enhanced odor discrimination and impaired olfactory memory by spatially controlled switch of AMPA receptors. PLoS Biol 3(11): e354.

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