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J Neurosci. Author manuscript; available in PMC 2010 September 17.
Published in final edited form as:
PMCID: PMC2843829
EMSID: UKMS29135

Leptin regulates AMPA receptor trafficking via PTEN inhibition

Abstract

The hormone leptin can cross the blood brain barrier and influences numerous brain functions (Harvey, 2007). Indeed, recent studies have demonstrated that leptin regulates activity-dependent synaptic plasticity in the CA1 region of the hippocampus (Shanley et al, 2001; Durakoglugil et al, 2005; Li et al, 2002; Moult et al, 2009). It is well documented that trafficking of AMPA receptors is pivotal for hippocampal synaptic plasticity (Collingridge et al, 2004), but there is limited knowledge of how hormonal systems, like leptin influence this process. In this study we have examined how leptin influences AMPA receptor trafficking and in turn how this impacts on excitatory synaptic function. Here we show that leptin preferentially increases the cell surface expression of GluR1 and the synaptic density of GluR2-lacking AMPA receptors in adult hippocampal slices. The leptin-induced increase in surface GluR1 required NMDA receptor activation and was associated with an increase in cytoplasmic PtdIns(3,4,5)P3 levels. In addition, leptin enhanced phosphorylation of the lipid phosphatase PTEN which inhibits PTEN function and elevates PtdIns(3,4,5)P3 levels. Moreover, inhibition of PTEN mimicked and occluded the effects of leptin on GluR1 trafficking and excitatory synaptic strength. These data indicate that leptin, via a novel pathway involving PTEN inhibition, promotes GluR1 trafficking to hippocampal synapses. This process has important implications for the role of leptin in hippocampal synaptic function in health and disease.

Keywords: leptin, synaptic plasticity, AMPA receptor, PTEN, hippocampus, Glutamate receptor

Introduction

Glutamate is the main excitatory neurotransmitter in the mammalian CNS, and a key feature of neuronal networks is the ability to dynamically alter excitatory synaptic strength. Indeed, hippocampal synaptic plasticity is thought to underlie learning and memory (Bliss and Collingridge, 1993). AMPA receptor trafficking is pivotal for rapid forms of hippocampal synaptic plasticity (Collingridge et al, 2004) such as long-term potentiation (LTP) and long-term depression (LTD). However little is known about how such events are regulated by hormones or altered in pathological states. Recent studies have shown that tumor necrosis factor-α (TNFα) increases AMPA receptor surface expression (Stellwagen and Malenka, 2006), which may contribute to its role in mediating brain damage from pathological insults. Insulin also alters AMPA receptor trafficking and synaptic function (Passafaro et al, 2001; Zhou et al, 2001) and defects in insulin-driven processes are linked to neurodegenerative disorders such as Alzheimer's disease.

AMPA receptor trafficking is dependent on phosphoinositide 3-kinase (PI 3-kinase; Man et al, 2003); an ubiquitous enzyme that promotes phosphorylation of PtdIns(4,5)P2 to generate PtdIns(3,4,5)P3 (Cantley et al, 2002). Thus PI 3-kinase-driven elevations in PtdIns(3,4,5)P3 may contribute to alterations in AMPA receptor trafficking. The tumor suppressor PTEN (phosphatase and tensin homologue deleted on chromosome 10) limits PI 3-kinase-dependent signaling by dephosphorylating PtdIns(3,4,5)P3 into PtdIns(4,5)P2 (Maehama et al, 1998). PTEN contains a tyrosine phosphatase functional domain, exhibiting both protein phosphatase and lipid phosphatase activity in vitro. In most cells, PTEN is constitutively active and influences the basal levels of PtdIns(3,4,5)P3. However inhibition of PTEN activity by reactive oxygen species and phosphorylation leads to modified PI 3-kinase-dependent signaling (Downes et al, 2007). In pancreatic beta cells and a hypothalamic cell line the hormone leptin also promotes phosphorylation of PTEN resulting in inhibition of PTEN activity and an increase in PtdIns(3,4,5)P3 levels (Ning et al, 2006).

Evidence is growing that leptin influences numerous neuronal functions (Harvey, 2007). Leptin regulates energy homeostasis via its hypothalamic actions (Spiegelman and Flier, 2001). Recent studies have implicated leptin in hippocampal synaptic plasticity as leptin-insensitive rodents display impaired LTP and LTD and spatial memory (Li et al, 2002). Administration of leptin into rodent hippocampus improves memory processing (Wayner et al, 2004). Moreover, leptin facilitates LTP (Shanley et al, 2001) and it evokes NMDA-receptor-dependent LTD (Durakoglugil et al, 2005). However it is not known if leptin influences AMPA receptor trafficking and in turn how this impacts on excitatory synaptic function. Here we provide the first compelling evidence that leptin rapidly increases GluR1 surface expression and it promotes an increase in the synaptic expression of GluR2-lacking AMPA receptors in adult hippocampus. The increase in GluR1 trafficking by leptin is associated with an increase in PtdIns(3,4,5)P3 levels. This is accompanied by increased phosphorylation of PTEN; an action resulting in PTEN inactivation and increased PtdIns(3,4,5)P3 levels. Indeed PTEN inhibition mimicked and occluded the effects of leptin on GluR1 trafficking to synapses, indicating the involvement of PTEN inhibition. These findings have important implications for the role of leptin and PTEN in regulating hippocampal synaptic strength.

Experimental Procedures

Hippocampal Cell Culture

Hippocampal cultures were prepared as before (Shanley et al, 2001). Briefly, neonatal Sprague Dawley rats (1-3 days old) were killed by cervical dislocation in accordance with Schedule 1 of UK Animals (Scientific Procedures) Act, 1986. Hippocampi were removed and following washing in HEPES buffered saline comprising (mM): NaCl 135; KCl 5; CaCl2 1; MgCl2 1; HEPES 10; D-glucose 25 at pH 7.4, were treated with protease type X and type XIV (0.5 mg/ml; Sigma) for 25 min at room temperature. Dissociated cells were plated onto sterile dishes (Falcon 3001) treated with poly-L-lysine (20 μgml-1; 1-2 hours). Cultures were maintained in serum replacement medium (SR2; Sigma) in a humidified atmosphere of 5% CO2 and 95% O2 at 37°C for up to 3 weeks.

Transfection protocol

Cells were transfected with PTEN C124S or PTEN G129E in EGFP-C2 or empty vector, EGFP-C2, using lipofectamine 2000 (L2K). L2K was mixed with MEM (ratio of 3μl L2K: 100μl MEM) and the desired plasmid was mixed with Optimem (ratio of 2μg plasmid: 100μl Optimem. After 5 min the diluted L2K and plasmid were mixed and left at room temperature for 20 min. 200 μl L2K+DNA mix was added to each coverslip of neurons (6-10 DIV) in 1 ml of culture media. Cells were returned to the incubator for 1 hr, before washing. Transfected cells were used 24-48 hrs after transfection.

Immunocytochemistry and analysis

Immunocytochemistry was performed on 7-12 day old cultured hippocampal neurons after treatment with vehicle or leptin (50 nM) for 30 min at 21-23 °C. To label surface GluR1 or GluR2, living neurons were incubated with antibodies against N-terminal regions of GluR1 (sheep anti-GluR1; in house antibody against synthetic peptide (RTSDSRDHTRVDWKR) corresponding to 253-267 residues of GluR1; Pickard et al, 2001; 1:100) and GluR2 (mouse anti-GluR2; Zymed; 1:250) at 4°C. Cultures were fixed with 4% paraformaldehyde (10 min) which did not permeabilise cells as assayed by the absence of MAP2 (microtubule-associated protein 2) staining. Surface GluR1 or GluR2 staining was visualized by addition of appropriate Alexa 488- or Cy3- conjugated secondary antibodies (1:250; Stratech Scientific Ltd, UK) for 30 min. No labeling was observed after incubation with secondary antibodies alone. In some studies, cells were permeabilized with 0.1% triton X-100 (5 min) to compare staining relative to synapsin-1 (mouse anti-synapsin-1; 1:250; 30 min; BD Biosciences), PTEN (mouse anti-PTEN; 1:500; 30 min; Cascade Biosciences) or PtdIns(3,4,5)P3 (mouse PtdIns(3,4,5)P3; 1:500; 1 hr; Echelon) labeling. For synaptic colocalisation, surface GluR1 staining was compared to synapsin-1 and percentage of surface GluR1 at synapses was assessed as number of GluR1 positive sites that colocalised with synapsin-1 positive sites.

For global PTEN immunolabeling, neurons were fixed, washed with HBS then permeabilized. Neurons were treated with primary antibody (mouse anti- PTEN; clone 6H2.1; 1:500) for 30 min at room temperature. After washing, neurons were incubated with donkey anti-mouse antibody (1:250; 30 min). In dual labeling studies, the anti-GluR1 antibody (above) was used to assess distribution at somato-dendritic regions or antibody against an N-terminal epitope of CB1 receptor; gift from K Mackie; 1:100; 1 hr; Coutts et al, 2001) to determine PTEN distribution on axons. Living neurons were incubated with either of these antibodies prior to fixation and incubation with a secondary antibody. PTEN distribution was examined after neurons were permeabilized.

For P366-PTEN or P385-PTEN immunostaining, neurons were fixed, permeabilised then incubated with a sheep anti-P366-PTEN antibody (1:500; Maccario et al, 2007) or rabbit anti-P385 PTEN antibody (1:500; Biosource) for 30 min. In dual labeling studies, markers for endosomes (mouse anti-RAB5; 1:500; or rabbit anti-RAB7; 1:500; Sigma), the Golgi apparatus (mouse anti-mannosidase II; 1:1000; Covance), P385 PTEN (rabbit anti-P385 PTEN; 1:500; Biosource) or PtdIns(3,4,5)P3 (above) were used.

Analysis

A confocal imaging system (Zeiss LSM 510) was used for image acquisition. 488nm and 543nm laser lines were used to excite Alexa 488 and Cy3 fluorophores, respectively. Dual labeling images were obtained in multi-tracking mode using a 15s scan speed. Intensity of staining was determined offline using Lasersharp software (Carl Zeiss). Analysis lines (50μm) were drawn along randomly selected dendritic regions (50nm) and mean fluorescence intensity was calculated. Data were obtained from at least 3 randomly selected cells for each condition and all data was obtained from at least three different cultures from different animals. Within a given experiment, all conditions, including illumination intensity and photomultiplier gains, were kept constant. To quantify experimental data obtained from separate days, data were normalized relative to mean fluorescence intensity in control neurons. In a subset of control experiments indicated in the text, both surface and total GluR1 were labeled and changes in surface GluR1 calculated as a function of total GluR1. All data are expressed as means ± s.e.m. and statistical analyses were performed using Student's unpaired t-test for comparison of means, or ANOVA (analysis of variance) for comparisons between multiple groups. P<0.05 was considered significant.

Hippocampal slice preparation and electrophysiology

Hippocampal slices (350 μm) were prepared from 12-16 week old male, Sprague Dawley rats or Zucker lean or fa/fa rats. Animals were killed by cervical dislocation according to UK (Scientific Procedures) legislation. Brains were rapidly removed and placed in ice cold artificial CSF (aCSF; bubbled with 95% O2 and 5% CO2) containing (mM): NaCl 124, KCl 3, NaHCO3 26, NaH2PO4 1.25, CaCl2 2, MgSO4 1, and D-glucose 10. Once prepared, parasaggital slices were allowed to recover at room temperature in oxygenated aCSF for 1h before use. Slices were transferred to a submerged chamber maintained at 30-31°C and perfused with aCSF containing the GABAA receptor antagonist, picrotoxin (50 μM), at a rate of 2-3 mlmin−1. Blind whole-cell recordings from stratum pyramidale of area CA1 were obtained using electrodes (4-7 MΩ) containing (in mM): Cs+ methanesulphonate 130, NaCl 5, CaCl2 1, HEPES 5, EGTA 1, Mg-ATP 5, Na-GTP 0.5, and QX-314 5, pH 7.3. .3. Where 10mM BAPTA was included in the filling solution, EGTA was absent and the concentration of Cs+ methanesulphonate adjusted to maintain osmolarity. Unless otherwise stated cells were voltage clamped at −60 mV. The Schaffer collateral-commissural pathway was stimulated at 0.033H, using a stimulus intensity that evoked a peak amplitude ~ 50% of the maximum. Synaptic currents were low pass filtered at 2kHz and digitally sampled at 10kHz. The mean series resistance for all cells was 23 ± 3 MΩ (n=112).

Data was monitored on line and analysed off-line using the WINltp programme (Anderson and Collingridge, 2007). The degree of potentiation was calculated 40-45 min after addition of leptin or bpV and expressed as a percentage of baseline. The paired pulse ratio (PPR) was calculated as ratio of amplitude of second EPSC to first EPSC. To ensure measurement of second EPSC was not contaminated, the residual component of first EPSC was removed (Moult et al, 2009). The coefficient of variation (CV) was calculated as before (Moult et al, 2009). Briefly, the mean and SD were calculated for EPSC amplitudes recorded during successive 5 min epochs (SDEPSC and meanEPSC). The SD of background noise was calculated for each 5 min epoch using a period immediately before electrical stimulation (SDnoise). The CV for each 5min epoch was calculated as (SDEPSC-SDnoise) / meanEPSC. For calculation of RI, 0.1mM spermine was included in the pipette solution. Cells were depolarized to +40 mV for two min (4 successive stimulations) prior to leptin or bpV application and this was repeated at the peak of their effects. The rectification index (RI) was calculated as the ratio of the initial slopes of the EPSCs: EPSChyperpolarised/ EPSCdepolarized.

Whole-cell recordings from hippocampal cultures

Whole-cell recordings from pyramidal neurons were obtained as previously detailed. Cells were voltage clamped at −60 mV using the same intracellular solutions used for recording from hippocampal slices. Cells were perfused continuously with HEPES-buffered saline (HBS) of the following composition (in mM): 119 NaCl, 5 KCl, 2 CaCl2, 2 MgCl2, 25 HEPES, 33 D-glucose, 0.005 tetrodotoxin citrate, 0.1 picrotoxin, and 0.001 glycine, pH 7.4, at a rate of 2–3 mlmin−1. Leptin was applied by addition to the HBS perfusate. Data were filtered at 2 kHz and digitized at 10 kHz. Continuous recording of miniature EPSCs (mEPSCs) was made using the WinLTP program (Anderson and Collingridge, 2007). mEPSC detection was performed using MiniAnalysis software (Synaptosoft). Events were detected by setting the threshold value for detection at three times the level of the root mean square noise, followed by visual confirmation of mEPSC detection. For construction of cumulative probability plots, 400 successive events were used from the period immediately preceding application of leptin and from the period before 20 min after commencing washout of leptin. For pooled cumulative probability plots, data were normalized to the median value in the pre-leptin period.

Western blotting for P366 experiments

Samples were processed for western blotting as previously described (Maccario et al., 2007). Briefly, after exposure of slices to either leptin or control media, slices were homogenized in ice cold lysis buffer consisting of 25mM HEPES, 150mM NaCl, 1% Triton X-100, 0.1% 2 mercaptoethanol, 1mM EDTA, 1mM EGTA, 10 mM β glycerophosphatase, 50 mM sodium fluoride, 10μg/ml leupeptin, 100 μM PMSF and 1mM benzamidine. Proteins were separated by PAGE using pre-cast 4-12% gradient gels and blotted onto PVDF membranes (Polyscreen: NEN/PerkinElmer). Immunoprecipitation of PTEN used the A2B1 monoclonal anibody (Santa Cruz Biotechnology), pre-conjugated with agarose beads. Immunopresipitation of P366 PTEN used the phospho-specific antibody against PTEN phosphor-Thr366 synthesized by Dr Graham Bloomberg (Molecular Recognition Centre, University of Bristol, Bristol, UK). Quantification was made using AIDA image analysis software. Each experiment was done in triplicate and data was normalized to control values within each experiment and then expressed as mean percentage of normalized control ± standard error of mean.

Cell surface protein biotinylation in hippocampal slices

Hippocampal slices (350 μm) obtained from Sprague Dawley rats of 3-4 weeks old and 13-16 weeks old and Zucker lean and fa/fa rats (13-16 week old) were used (Thomas-Crusells et al, 2003). Zucker fa/fa rats contain a mutation (fa mutation) in the extracellular region of the leptin receptor, resulting in resistance to exogenous administration of leptin. Slices (three slices per condition) were incubated for 15 min at 37°C in aCSF (control condition), or 25 nM leptin and 50 μM picrotoxin in aCSF, under continuous gasification with 95% O2 and 5% CO2. Slices were transferred to aCSF solution containing 0.3mg/ml NHS-SS-Biotin (Pierce) and kept on ice with agitation for 45 min. Slices were then incubated in aCSF with 1μM Lysine to block all reactive NHS-SS-Biotin in excess. Slices were then collected in 500μl of lysis buffer (1% Triton X-100, 0.1% SDS, 1mM EDTA, 50mM NaCl, 20mM Tris, pH 7.5, supplemented with 1 mM DTT and a cocktail of proteases inhibitors −0.1mM PMSF; 1μg/ml chymostatin, 1μg/ml leupeptin, 1μg/ml antipain, 1μg/ml pepstatin) and sonicated on ice for 30 s. To discard extra debris, homogenates were centrifuged for 5 min at 4°C at 13000 rpm and supernatants collected. Protein concentration was quantified by the BCA method (Pierce) and the same amount of protein (500-750μg) was used in all experimental conditions. To precipitate biotinylated proteins, 40μl of Ultra-link immobilized neutravidin plus beads were added to samples for 2h at 4°C, under constant agitation. Non-biotinylated proteins were removed by centrifugation at 2500×g for 2 min and beads were washed three times with lysis buffer. Biotinylated proteins were eluted with denaturing buffer at 95°C for 5 min. Samples were processed for Western blotting analysis with the sheep anti-GluR1 antibody (1:750) or rabbit anti-GluR2 antibody (1:600). Alkaline phosphatase-conjugated secondary antibodies were used and alkaline phosphatase activity was visualized by enhanced chemifluorescence (ECF) on Storm 860 Gel and Blot Imaging System (Amersham Biosciences). Scanned digital images were quantified using ImageQuant 5 software (Amersham Biosciences). Results are presented as means ± SEM of number of experiments carried out in different preparations. Statistical significance was determined by the Students t-test (* P<0.05).

Materials

Recombinant human leptin (R and D Systems Europe Ltd, Abingdon, UK) was used in all experiments. LY294002, wortmannin, bisperoxovanadium (Calbiochem, La Jolla, USA) and D-AP5 (Tocris Cookson, Baldwin, MO, USA) were all obtained commercially.

Statistical Analyses

All data are expressed as means ± s.e.m. and statistical analyses were performed using Paired t-test (two-tailed; 95% confidence interval) for comparison of means or two-way ANOVA (analysis of variance) with Tukey's post hoc test for comparisons between multiple groups (unless otherwise stated). P<0.05 was considered significant.

Results

Leptin differentially regulates the surface expression of GluR1 and GluR2

To determine if leptin alters the density of AMPA receptors, the cell-surface expression of AMPA receptors was assayed using an N-terminal antibody against GluR1 on living hippocampal neurons (Fig 1A&B). Leptin (50nM; 30min) induced a robust increase (154 ± 4.9% of untreated cultures; n=78; P<0.01) in GluR1 surface expression. This effect was due to leptin as application of the inactive boiled peptide failed to alter GluR1 surface staining (103 ± 1.2 % of control; n=9; P>0.05).

Figure 1
Leptin increases the surface expression of AMPA receptors

In hippocampal pyramidal cells, endogenous AMPA receptors consist of GluR1 and GluR2 subunits. To examine if leptin influenced GluR2 surface expression, dual labeling approaches were used to compare the effects of leptin on GluR1 versus GluR2. Leptin (1-50nM; 30min) produced a concentration-dependent increase in GluR1 surface staining (Fig 1B). Thus 1nM leptin increased surface GluR1 staining to 115 ± 5.1% of control (n=27; P<0.05) whereas 50 nM leptin resulted in an increase to 144 ± 5.7 % (n=34; P<0.01). In contrast, leptin was less potent at altering GluR2 surface expression (Fig 1B). At 1nM (106 ± 3.6% of control; n=27; P>0.05) and 10nM (109 ± 4.0%; n=29; P>0.05), leptin failed to evoke a significant change in surface GluR2 staining, however at higher concentrations, leptin increased GluR2 staining to 121 ± 5.4% of control (n=37; P<0.01).

Leptin increases the density of GluR1 subunits at hippocampal synapses

As the circulating leptin levels are in the low nanomolar range (Caro et al, 1996), the GluR1 subunit is likely to be the main target for leptin under physiological conditions. As the surface expression of receptors is a balance between exocytotic and endocytotic mechanisms, the increase in surface GluR1 expression by leptin could be due to alterations in either process. To determine if leptin alters GluR1 exocytosis, we examined the effects of two inhibitors namely NEM, a broad spectrum inhibitor of N-ethylmaleimide-sensitive fusion protein (NSF) and brefeldin A (Fig 1C). Application of NEM (5mM; 40min; n=27) or brefeldin A (5μM; 40min; n=27) had no significant effect on GluR1 surface expression per se. However, prior exposure to either agent attenuated the effects of leptin as the increase in GluR1 surface staining induced by leptin (to 141 ± 4%; n=27) was reduced to 104 ± 6% of control (n=27; P>0.05) and 113 ± 5% of control (n=27; P>0.05) in the presence of NEM or brefeldin A, respectively. These data indicate that leptin increases GluR1 surface density by promoting GluR1 exocytosis.

The strength of excitatory synaptic transmission is dependent on the density of AMPA receptors expressed at synapses. To assess if leptin influences the synaptic localization of GluR1, we compared the distribution of surface GluR1 relative to synapses (anti-synapsin-1 antibody) using immunocytochemistry and the percentage colocalization was evaluated. In accordance with our previous findings (O'Malley et al, 2007), leptin increased synapsin-1 staining to 113.4 ± 4% of control (n=21; P<0.05). Moreover leptin increased surface GluR1 that colocalized with synapsin-1 staining from 33.7 ± 2.6% to 48.9 ± 3.1% (n=21; P<0.05; Fig 1D). These data indicate that leptin promotes the synaptic expression of GluR1.

In order to determine directly how the immunocytochemical findings from hippocampal cultures relate to excitatory synaptic transmission, we assessed initially at what stage of development the effects of leptin on acute hippocampal slices mirrored those observed effects in culture. Thus in parallel studies, we examined the effects of leptin on AMPA receptor expression in hippocampal slices using cell-surface biotinylation assays. Exposure of adult slices (13-16 weeks old) to leptin (25nM; 15min) increased GluR1 (129 ± 9.5% of control; n=6; P<0.05), but not GluR2 (104 ± 7.9% of control; n=6; P>0.05) surface expression. Application of leptin (25nM; 15min) to younger slices (3-4 weeks old) had no effect on GluR1 (94 ± 12% of control; n=3; P>0.05) or GluR2 (88 ± 21% of control; n=3; P>0.05) surface expression (Fig 1Ei & Eii). It is well documented that Zucker fa/fa rats contain a mutation in the leptin receptor that renders them leptin-insensitive. Thus, to determine if leptin receptor activation was required, we also examined the effects of leptin on GluR1 and GluR2 expression in hippocampal slices from adult Zucker fa/fa or lean rats using cell surface biotinylation assays. In agreement with results from adult (13-16 week old) rats, exposure of slices from Zucker lean rats to leptin (25 nM, 15 mins) increased GluR1 (128 ± 13%, n=9/3; P < 0.05), but not GluR2 (94 ± 14%, n=9/3; P>0.05) surface expression. In contrast exposure of slices from fa/fa rats to leptin had no effect on either GluR1 (91 ± 15%, n=9/3; P > 0.05) or GluR2 (107 ± 15%, n=9/3; P>0.05) surface expression (Fig 1Fi & Fii). Thus these data indicate that leptin receptor activation is required for the increase in GluR1 surface expression.

To determine the consequences for hippocampal synaptic function, the effects of leptin on excitatory postsynaptic currents (EPSCs) were examined in adult (13-16 week old) slices. Application of 25nM leptin (15min) produced a robust enhancement of EPSCs to 197 ± 10% (n=6; P<0.001) of baseline (Fig 2A&B), that was maintained for the duration of recordings (up to 90min). Changes in paired pulse ratio (PPR) or the coefficient of variation (CV) classically reflect alterations in release probability (Pr). To identify the locus of this effect of leptin we analyzed PPR and CV in the above experiments, by delivering two pulses at an interval of 50ms. The leptin increase in EPSC amplitude was not accompanied by any significant change in PPR (n=6; P>0.05; Fig 2C) or CV (n=6; P>0.05; Fig 2D), indicating the likely involvement of a postsynaptic expression mechanism rather than altered Pr. The effects of leptin were also examined in slices from leptin-insensitive rats (Zucker fa/fa) and in lean animals (12-16 week old). Leptin (25nM) increased EPSC amplitude to 190 ± 14% of control (n=6; P<0.05) in Zucker lean animals, but it had no significant effect on EPSCs (102 ± 6% of control) in fa/fa animals (n=6; P>0.05; Fig 2E), indicating that leptin receptor activation was required for the effects of leptin.

Figure 2
Leptin increases the synaptic density of GluR2-lacking AMPA receptors

GluR2-lacking AMPA receptors are Ca2+-permeable and display pronounced inward rectification (Koh et al, 1995) that is due to high affinity voltage-dependent block of the channel by endogenous polyamines at positive membrane potentials. To determine if leptin alters the GluR2 content of synaptic AMPA receptors, the rectification properties of EPSCs were monitored during whole cell recordings with spermine-containing pipettes, as described previously (Moult et al, 2009). Application of leptin (25nM; 15min) increased EPSC amplitude to 186 ± 10 % of control (n=6) and this was accompanied by an increase in rectification index (RI) from 1.3 ± 0.2 to 2.2 ± 0.3 (n=6; P<0.05; Fig 2F,G&H). In interleaved control experiments, no significant change in RI was detected using spermine-lacking pipettes (n=6; P>0.05; Fig 2G&H). Application of philanthotoxin (1μM), a selective inhibitor of GluR2-lacking AMPA receptors blocked the inserted receptors resulting in a decrease in synaptic transmission (from 212 ± 12% of control) to 110 ± 12% (n=6; P<0.05; Fig 2I). These data are consistent with leptin increasing the density of GluR2-lacking AMPA receptors at hippocampal synapses.

Our data indicate that leptin increases GluR1 surface expression by promoting GluR1 exocytosis. Thus, we examined if the increase in synaptic strength induced by leptin involved increased GluR1 exocytosis, by inclusion of inhibitors of exocytosis in the pipette (Fig 2J). Both NEM (5mM) and brefeldin A (5μM) attenuated the potentiation caused by leptin (105 ± 8%; n=6; P>0.05 and 112 ± 8%; n=6; P>0.05, respectively). The effects of bafilomycin (1μM), an inhibitor of endocytosis were also examined. In neurons dialysed with bafilomycin, leptin resulted in a 166 ± 7% increase in EPSC amplitude (n=6; P<0.01); an effect not significantly different from control (P>0.05). These data are consistent with leptin increasing synaptic strength via promoting GluR1 exocytosis.

Leptin increases surface GluR1 expression via an NMDA receptor-dependent process

NMDA receptor activation is required for LTP induction (Collingridge et al, 1983) and the membrane insertion of AMPA receptors during LTP (Man et al, 2003). To verify if the effects of leptin involved NMDA receptors, the effects of the competitive NMDA receptor antagonist, D-AP5 were assessed. D-AP5 (50μM; 30 min) had no effect on surface GluR1 staining (96.1 ± 3.5 % of control; n=37; P<0.05) per se. However the leptin increase in GluR1 surface staining (141 ± 7.7%; n=37) was reduced to 109 ± 3.8% of control (n=37; P>0.05) in D-AP5 (Fig 3A&B). The ability of leptin to increase synaptic strength was attenuated in the presence of D-AP5 such that leptin increased synaptic transmission to only 103 ± 9% of baseline (n=6; P>0.05); an effect significantly different to interleaved control experiments (n=6; P<0.05; Fig 3C&D). We also evaluated if leptin altered the magnitude of NMDA receptor-mediated EPSCs as leptin enhances pharmacologically isolated NMDA EPSCs in juvenile hippocampus (Shanley et al, 2001). Similarly in adult hippocampus leptin (25nM) increased the amplitude of NMDA EPSCs (175 ± 9% of control; n=5; P<0.05): an effect that readily reversed on leptin washout. The leptin-induced increase in EPSCs was associated with a significant increase in the NMDA receptor-mediated component of the EPSC (amplitude of EPSC at +40mV, at 60ms latency) to 131 ± 11% of control (n=6; P<0.05), but no change in the AMPA component (initial slope of EPSC at +40mV) was detected (102 ± 5%; n=6; P>0.05). This small increase in NMDA receptor current is likely to be sufficient for the NMDA receptor-dependent enhancement of synaptic strength by leptin. However, in order to show conclusively that synaptic activation of NMDA receptors was required a two pathway experiment was performed such that during leptin application stimulation was stopped in the test pathway but maintained in the control pathway. Under these conditions, leptin failed to significantly increase synaptic transmission in the test pathway (109 ± 10%; n=5; P>0.05) whereas leptin markedly increased EPSCs in the control path (188 ± 14%; n=5; P<0.001; Fig 3E). These data indicate that leptin increases the density of functional AMPA receptors at hippocampal synapses via a process requiring the synaptic activation of NMDA receptors.

Figure 3
Leptin increases surface GluR1 expression via an NMDA receptor-dependent process

It is well established that NMDA receptors are highly permeable to Ca2+ and that Ca2+ influx via NMDA receptors is pivotal for various forms of activity-dependent changes in synaptic efficacy (Nicoll and Malenka, 1999). Thus, as the leptin-driven increase in synaptic strength requires the synaptic activation of NMDA receptors, we examined if Ca2+ influx via NMDA receptors was also required for this effect. In this series of experiments, whole cell recordings were made using recording pipettes containing the Ca2+ chelator, BAPTA (10mM). Following at least 30 min dialysis with the BAPTA-containing solution, application of leptin failed to significantly alter synaptic transmission (107 ± 14% of baseline; n=4; P>0.05), indicating that an increase in intracellular Ca2+ is required for the leptin-dependent facilitation of synaptic transmission.

Leptin-induced increase in surface GluR1 is correlated with an increase in PtdIns(3,4,5)P3 levels

PI 3-kinase is a key element of neuronal leptin receptor-driven signaling (Harvey, 2007), and it is required for AMPA receptor insertion during LTP (Man et al, 2003). As PI 3-kinase phosphorylates PtdIns(4,5)P2 into PtdIns(3,4,5)P3, the increase in surface GluR1 may be due to enhanced PtdIns(3,4,5)P3 levels. To address this, dual labeling was used to simultaneously compare surface GluR1 staining and the intracellular levels of PtdIns(3,4,5)P3 in cultures. Leptin (25nM; 30 min) increased surface GluR1 staining (163 ± 9.1% of control; n=30; P<0.001) with a parallel increase in PtdIns(3,4,5)P3 staining (173 ± 8.3% of control; n=30; P<0.001; Fig 4A&B). Shorter duration applications of leptin (5min) increased PtdIns(3,4,5)P3 staining (147 ± 8.3% of control; n=25; P<0.001) with no significant alteration in surface GluR1 staining (106 ± 5.1% of control; n=25; P>0.05), suggesting that leptin increases PtdIns(3,4,5)P3 levels which in turn drives the alterations in GluR1 trafficking.

Figure 4
Leptin increases surface GluR1 via a PI 3-kinase-dependent increase in PtdIns(3,4,5)P3 levels

We further characterized the connection between surface GluR1 expression and PI 3-kinase/PtdIns(3,4,5)P3 using the well characterized PI 3-kinase inhibitors wortmannin and LY294002, since processes dependent on class I PI 3-kinase-generated PtdIns(3,4,5)P3 are sensitive to these inhibitors. Blockade of PI 3-kinase activity with wortmannin (10nM; 30min) or LY294002 (10μM; 30min) had no effect on surface GluR1 or PtdIns(3,4,5)P3 levels (Fig 4C). However, wortmannin reduced the leptin driven increase in GluR1 surface staining to 107 ± 4.5 % (n=33; P>0.05), compared to 146 ± 5.3% (n=33; P<0.001) in control. The leptin-induced increase in PtdIns(3,4,5)P3 levels was also reduced from 152 ± 8.2% in control (n=30; P<0.01) to 109 ± 6.9% (n=30; P<0.01) in wortmannin. Exposure to LY294002 also attenuated leptin's effects such that the increase in surface GluR1 staining by leptin was reduced from 138 ± 5.2% to 106 ± 4.4% (n=29; P>0.05), whereas the leptin-induced increase in PtdIns(3,4,5)P3 staining was reduced from 147 ± 5.6% (n=35; P<0.01) to 109 ± 7.1% (n=35; P<0.05) in the presence of LY294002. In parallel studies the ability of leptin to enhance excitatory synaptic strength was prevented by prior exposure to either LY294002 (n=6; Fig 4D) or wortmannin (n=6). LY294002 also prevented any significant leptin-driven changes in AMPA receptor rectification (1.38 ± 0.14 to 1.43 ± 0.20; n=6; P>0.05). These data indicate that a PI 3-kinase-dependent process underlies the leptin-driven increase in GluR1 surface expression and PtdIns(3,4,5)P3 levels.

PTEN and phosphorylated PTEN are localised to distinct subcellular compartments in hippocampal neurons

Although our data suggests that leptin increases surface GluR1 expression, via a PI 3-kinase-dependent increase in PtdIns(3,4,5)P3, the possibility that leptin uses an alternative mechanism to raise intracellular PtdIns(3,4,5)P3 levels cannot be excluded. It is known that the PtdIns(3,4,5)P3 levels are also regulated by PTEN. Although PTEN plays an important role in the CNS, there is limited information about its cellular distribution in neurons. Thus, initially the functional localization of PTEN was assessed in cultured hippocampal neurons immunocytochemically. PTEN labeling was present on principle neurons in hippocampal cultures. Comparison of PTEN immunoreactivity with surface cannabinoid CB1 receptor labeling, an axonal marker (Coutts et al, 2001) and surface GluR1 staining which is restricted to somato-dendritic regions, demonstrated high levels of PTEN expression within these neuronal compartments (Fig 5A). Dual labeling with an antibody against synapsin-1 also revealed clusters of PTEN labeling associated with synapses (not shown).

Figure 5
Cellular distribution of PTEN in hippocampal neurons

As the phosphorylation status of PTEN is important for its function, the distribution of PTEN when phosphorylated on one key site, threonine 366 (P366-PTEN) was compared. In contrast to PTEN distribution, the phosphorylated form of PTEN exhibited a very distinct cellular distribution such that labeling was restricted to specific sub-membrane cytoplasmic regions within somata and dendrites. Dual labeling studies demonstrated that when phosphorylated, PTEN localised to the golgi apparatus as P366-PTEN labeling directly correlated with the golgi marker, mannosidase II, but to a much lesser extent with the endosomal markers, Rab7 (20 ± 5% co-localisation; n=6; Fig 5B) or Rab5 (17 ± 4% colocalisation; n=4). Thus these data suggest that phosphorylation of PTEN significantly alters the subcellular localization of PTEN such that it is limited to the golgi apparatus.

Leptin promotes PTEN inactivation in hippocampal neurons

One way of modulating PTEN function is by phosphorylation, which results in inactivation of this phosphatase (Downes et al, 2007). Recent studies have implicated increased phosphorylation and inhibition of PTEN in leptin receptor coupling to KATP channels (Ning et al, 2006; Plum et al, 2006). Thus, we examined the effects of leptin on P366-PTEN labeling in hippocampal neurons. Leptin produced an increase in P366-PTEN labeling to 123 ± 5.2 % of control (n=34; P<0.01) whereas the levels of PTEN protein were unaffected by leptin (104 ± 3.6% of control; n=35; P>0.05; Fig 6A&B).

Figure 6
The leptin-driven increase in PtdIns(3,4,5)P3 levels is associated with increased phosphorylation of PTEN

In parallel biochemical studies, the effects of leptin exposure on total PTEN and P366-PTEN were examined in hippocampal slices from both Zucker fa/fa and lean adult rats. Exposure to leptin (25 nM; 15 min) resulted in a modest increase in P366 PTEN levels in slices from Zucker lean rats (263 ± 73%, n=6; Fig 6C), with no change in total PTEN levels. In contrast, leptin had no effect on P366-PTEN or total PTEN levels in slices from Zucker fa/fa rats. These data are consistent with leptin increasing phosphorylation of PTEN via activation of the leptin receptor.

As phosphorylation of PTEN promotes its inactivation with a resultant increase in PtdIns(3,4,5)P3, we compared the levels of PtdIns(3,4,5)P3 and P366-PTEN. Leptin increased P366-PTEN staining to 131 ± 4.2% of control (n=27; P<0.05) with a concomitant increase in PtdIns(3,4,5)P3 labeling to 140 ± 4.9% of control (n=27; P<0.05). This suggests that leptin increases PtdIns(3,4,5)P3 levels at least in part via PTEN phosphorylation and hence inhibition of PTEN activity.

As PTEN is phosphorylated by the protein kinase, CK2 (Torres and Pulido, 2001), and CK2 activity is increased following NMDA receptor activation (Charriaut-Marlangue et al, 1991), we examined the effects of a selective CK2 inhibitor, 2-dimethyl-amino-4,5,6,7-tetrabromobenzimadazole (DMAT; Pagano et al, 2004). Exposure to DMAT (10μM) prevented the leptin-driven increase in P366-PTEN (100 ± 4%; n=27; P>0.05; Fig 6D) and surface GluR1 staining (105 ± 10%; n=27; P>0.05; Fig 6D). Leptin also failed to increase excitatory synaptic strength (110 ± 12% of control; n=5; P>0.05) in DMAT-treated slices compared to control slices (198 ± 15% of control; n=3; Fig 6E). These data indicate that CK2 underlies phosphorylation of PTEN and subsequent alterations in glutamate receptor trafficking and synaptic strength by leptin.

Inhibition of PTEN mimics and occludes the effects of leptin

Our data suggest that leptin promotes increases in PtdIns(3,4,5)P3 and surface GluR1 levels via PTEN inhibition. Consequently, to explore the role of PTEN further, we examined the effects of two dominant-negative PTEN mutants on surface GluR1 staining. Cultured hippocampal neurons were transfected with either one of the PTEN mutants (PTEN C124S or PTEN G129E) or the empty vector (EGFP-C2). Cells transfected with either PTEN C124S or PTEN G129E showed a significant increase in surface GluR1 labeling relative to control cells transfected with the empty vector (120.2 ± 4%, P<0.01 and 122.7 ± 3%, P < 0.001 relative to control respectively; n=27 for each; Fig 7A&B). Leptin failed to increase surface GluR1 staining in cells transfected with PTEN C124S or PTEN G129E (106.1 ± 4%, P>0.05 and 104.3 ± 3%, P>0.05 relative to control respectively; n=27 for each; Fig 7Bii). Conversely, leptin increased surface GluR1 expression in neighboring non-transfected cells (130.7 ± 2%, P<0.001 relative to control; n=81). These data support the idea that PTEN inhibition increases GluR1 surface expression and that leptin increases surface GluR1 via inhibition of PTEN.

Figure 7
Inhibition of PTEN increases surface expression of GluR1 and occludes the effects of leptin

We also examined the impact of PTEN inhibition on the properties of mEPSCs in primary hippocampal neurons. Cells were transfected with either of two dominant negative PTEN constructs, G129E or C124S, and the amplitude and frequency of mEPSCs were compared to neighbouring non-transfected control cells. Application of leptin (25 nM; 15 min) resulted in a persistent increase in the amplitude of mEPSCs (amplitude, 141±10% of baseline 20 min after leptin washout, n=6, P<0.01; Fig 7C) with no significant change in mEPSC frequency. This effect of leptin was completely reversed (to 106±21% of baseline; n=3) by addition of the selective antagonist for GluR2-lacking AMPA receptors, philanthotoxin. In contrast, application of leptin to cells transfected with either dominant negative PTEN construct, G129E or C124S failed to alter mEPSC amplitude (108±12% and 104±8% of baseline 20 min after leptin, respectively. n=4; P>0.05 for each; Fig 7Ci). Furthermore, cells transfected with either G129E or C124S showed significantly higher mean basal mEPSC amplitudes (139 ± 12% and 132 ± 13% of control; Fig 7Cii&iii) with no significant change in mEPSC frequency. In addition, application of philanthotoxin reduced the mean amplitude of mEPSCs recorded from cells transfected with either G129E or C124S to that similar to neighbouring control cells (amplitude, 103±20% and 103±20% of control; n=4 for each) whilst having no effect on basal transmission of neighbouring control cells (Fig 7Cii). Thus these data indicate that PTEN inhibition selectively increases functional expression of GluR1 at hippocampal synapses, and that the ability of leptin to deliver GluR1 subunits to synapses is blocked following inhibition of PTEN.

As low concentrations of the phosphatase inhibitor, bisperoxovanadium (bpV) has been shown to specifically inhibit PTEN (Schmid et al, 2004), the effects of pharmacological inhibition of PTEN with bpV were also assessed. To determine the functional effects of PTEN inhibition, the effects of bpV on evoked EPSCs were examined. Application of 100 nM bpV produced a robust potentiation of EPSCs to 128 ± 8% of baseline (n=6; P<0.001; Fig 8A&B), that was not accompanied by any significant change in PPR (n=6; P>0.05; Fig 8C) or CV (n=6; P>0.05; Fig 8D), indicating the involvement of a postsynaptic change. To determine if bpV alters the GluR2 content of synaptic AMPA receptors, the RI of evoked EPSCs were monitored. Application of bpV (100nM) increased EPSC amplitude to 143 ± 12 % of control (n=6) with a concomitant increase in the RI from 1.3 ± 0.1 to 2.0 ± 0.1 (n=6; P<0.05; Fig 8E, F&G). There was no significant change in RI during interleaved experiments with no spermine in the recording pipette (n=6; Fig 8F&G).

Figure 8
The effects of leptin are mimicked and occluded by inhibition of PTEN by bpV

In addition, application of bpV (50nM; 30min) increased surface GluR1 expression to 148 ± 5.8% of control (n=46; P<0.01; Fig 8H&I). BpV also altered the synaptic density of GluR1-containing AMPA receptors as co-localisation between GluR1 and synapsin-1 positive sites was significantly enhanced from 31.8 ± 2.6% to 43.2 ± 3.9% (n=36; P<0.05); effects not significantly different (P>0.05) to those of leptin (49.2 ± 6.0% colocalisation; n=27; P<0.01) in paired experiments. These data indicate that PTEN inhibition promotes an increase in the synaptic density of GluR1-containing AMPA receptors.

As PTEN inhibition results in increased PtdIns(3,4,5)P3 levels, we examined if the increase in surface GluR1 labeling was associated with increased PtdIns(3,4,5)P3 levels. Treatment with bpV increased surface GluR1 labeling (146 ± 5.0% of control; n=38; P<0.01) and PtdIns(3,4,5)P3 staining (154 ± 6.2% of control; n=38; P<0.05; Fig 8H&I). These effects of bpV were not significantly different to leptin as leptin resulted in increases to 152 ± 6.9% (n=29; P<0.01: P>0.05 compared to bpV) and 159 ± 5.8% (n=29; P<0.01: P>0.05 compared to bpV) in GluR1 and PtdIns(3,4,5)P3 labelling, respectively. These data indicate that the effects of leptin are mimicked by PTEN inhibition. As leptin increases the synaptic density of GluR1 via PTEN inhibition, we determined if PTEN inhibition altered the effects of leptin on GluR1 and PtdIns(3,4,5)P3 labeling. Treatment of hippocampal neurons with bpV occluded the effects of leptin such that GluR1 staining was 155 ± 7.1% of control (n=32; P<0.01) whereas PtdIns(3,4,5)P3 labeling was 161 ± 6.2% of control (n=32; P<0.001), in the combined presence of bpV and leptin (Fig 8I). Exposure of hippocampal slices to leptin also occluded the effects of bpV such that leptin increased EPSC amplitude to 208 ± 10% of baseline (n=6) but subsequent application of bpV caused no significant change in EPSC amplitude (n=6; P>0.05). These data indicate that leptin increases the synaptic density of GluR1 via inhibition of PTEN as bpV not only mimicked but also occluded the effects of leptin.

Discussion

Evidence is growing that leptin has widespread actions in the CNS. Several studies have implicated leptin in activity-dependent synaptic plasticity and hippocampal dependent learning and memory (Harvey, 2007). AMPA receptor trafficking plays a pivotal role in regulating excitatory synaptic strength and numerous growth factors and hormones modulate this process (Poo, 2001). In this study we provide compelling evidence that leptin regulates AMPA receptor trafficking in hippocampal neurons. Leptin preferentially increased the density of GluR1, as opposed to, GluR2 subunits as leptin was around 50 fold more potent at increasing GluR1 surface expression in hippocampal cultures. Leptin also increased GluR1 but not GluR2 surface expression in adult hippocampal slices. Furthermore, leptin increased the synaptic density of GluR1 subunits suggesting that leptin promotes delivery of GluR1-containing AMPA receptors to synapses. Indeed leptin enhanced the density of polyamine-sensitive EPSCs indicating that leptin upregulates the synaptic expression of GluR2-lacking AMPA receptors. The differential effects of leptin on GluR1 versus GluR2 subunits displays parallels to the effects of BDNF and TNF-α on these subunits (Stellwagen and Malenka, 2006; Caldeira et al, 2007). Our findings also support the notion that distinct cellular mechanisms regulate the delivery of GluR1 and GluR2 to synapses (Passafaro et al, 2001; Shi et al, 2001). Our data demonstrate that blockade of exocytosis, but not endocytosis attenuated the effects of leptin on surface GluR1 expression and synaptic transmission, indicating that leptin influences the synaptic density of AMPA receptors by promoting GluR1 exocytosis.

In contrast to the transient synaptic depression elicited by leptin in juvenile hippocampus (Shanley et al, 2001; Xu et al, 2008), leptin produced a persistent increase in excitatory synaptic strength in adult, suggesting that the effects of leptin on synaptic strength are developmentally regulated. However, leptin also transiently depresses excitatory synaptic transmission in 6-8 week mouse hippocampus (Xu et al, 2008), suggesting that modulation of excitatory synaptic transmission by leptin in adult hippocampus is age-dependent, or alternatively species-dependent differences underlie the differential effects of leptin on synaptic transmission. We have shown that NMDA receptor activation is required for facilitation of hippocampal LTP and LTD induced by leptin (Shanley et al, 2001; Durakoglugil et al, 2005). Leptin-driven dendritic morphogenesis requires the synaptic activation of NMDA receptors (O'Malley et al, 2007). NMDA receptor activation also mediates delivery of GluR1 subunits to hippocampal synapses by leptin as leptin-dependent increases in surface GluR1 expression and EPSC amplitude were reduced by D-AP5. Moreover, the increase in synaptic strength by leptin was associated with an increase in NMDA receptor-mediated synaptic currents, and synaptic activation of NMDA receptors was required for the effects of leptin as leptin failed to increase synaptic transmission when stimulation was stopped. Similarly, the synaptic delivery of GluR1-containing AMPA receptors induced by tetanic stimulation or chemical induction of LTP requires synaptic activation of NMDA receptors (Passafaro et al, 2001; Man et al, 2003; Shi et al, 2001).

How the synaptic activation of NMDA receptors contributes to facilitation of synaptic transmission by leptin is not entirely clear. However, influx of Ca2+ via NMDA receptors is likely to play a significant role as chelation of Ca2+ ions with BAPTA blocked the effects of leptin, and we have shown previously that leptin has no effect on intracellular Ca2+ levels (Shanley et al, 2001). Recent studies indicate that CK2 is a downstream target of NMDA receptors (Chung et al, 2004), and Ca2+-dependent increases in CK2 activity have also been reported following NMDA receptor-dependent LTP (Charriaut-Marlangue et al, 1991). Moreover, PTEN is phosphorylated by CK2 (Torres and Pulido, 2001) and our data indicate that CK2 activation is required for leptin driven increases in GluR1 surface expression and synaptic transmission. Thus it is feasible that leptin, via enhancing NMDA receptor activation, promotes an increase in CK2 activity, which in turn results in phosphorylation and subsequent inhibition of PTEN.

Our data indicate that the effects of leptin on GluR1 trafficking involve an increase in PtdIns(3,4,5)P3 levels secondary to PTEN inhibition as the effects of leptin on surface GluR1 staining were associated with increased PtdIns(3,4,5)P3 levels and elevations in PtdIns(3,4,5)P3 levels occurred prior to altered GluR1 trafficking. In agreement with previous studies (Man et al, 2003), inhibitors of PI 3-kinase attenuated the effects of leptin on surface GluR1 and PtdIns(3,4,5)P3 levels, consistent with PI 3-kinase-dependent signaling underlying these effects. However, our studies indicate that leptin trafficking of GluR1 to synapses is mediated by a novel mechanism involving PTEN inhibition. Leptin increased phosphorylation of PTEN; an effect associated with an increase in PtdIns(3,4,5)P3 levels. Moreover, inhibition of PTEN mimicked and occluded leptin-induced trafficking of GluR1 to hippocampal synapses and facilitation of excitatory synaptic transmission. The role of PTEN inhibition in hippocampal leptin-driven signaling displays parallels to the role of PTEN in the activation of hypothalamic KATP channels by leptin (Ning et al, 2006; Plum et al, 2006). Indeed, genetic inactivation of hypothalamic PTEN elevates PtdIns(3,4,5)P3-dependent signaling which is pivotal for KATP channel activation by leptin (Plum et al, 2006).

In most cells PTEN is constitutively active and thereby influences the basal levels of PtdIns(3,4,5)P3. Transgenic mouse studies indicate that regulation of PTEN occurs primarily via its inhibition or reduced cellular expression which in turn enhances PI 3-kinase-dependent signaling. Our studies show that leptin regulates PTEN by increasing its phosphorylation which is likely to result in inhibition of its phosphatase activity. Our data also indicate that the cellular distribution of PTEN was altered following phosphorylation as the phosphorylated form of PTEN localized to the Golgi apparatus. In agreement with these findings, studies in non-neuronal cells have shown that phosphorylation of PTEN alters its subcellular localization (Leslie et al, 2008). As PTEN needs to associate with the plasma membrane for its constitutive activity, it is likely that translocation of PTEN to the golgi apparatus limits its ability to antagonize PI 3-kinase-dependent signaling. However, it is not clear if PTEN redistribution to the Golgi directly influences AMPA receptor trafficking and excitatory synaptic function. During exocytosis, membrane proteins can be delivered directly from the trans-Golgi network to the plasma membrane. The trans-Golgi network also regulates the synaptic delivery of GluR1-containing AMPA receptors during synaptic plasticity (Gerges et al, 2004). Thus, specific targeting of inactive, phosphorylated PTEN to the Golgi may result in highly localized elevations in PtdIns(3,4,5)P3 levels close to this subcellular compartment. However, it is not clear how elevations in PtdIns(3,4,5)P3 levels influence delivery of AMPA receptors to synapses. As PtdIns(3,4,5)P3 modifies the activity of numerous signaling molecules, including phosphoinositide-dependent kinases and guanine nucleotide exchange factors (GEFs; Cantley, 2002), one or more of these downstream targets may play a role in this process. One potential target for PtdIns(3,4,5)P3 is Akt, a kinase that promotes phosphorylation and inhibition of glycogen synthase kinase-3 (GSK-3). Indeed, nerve growth factor phosphorylates and inactivates PTEN, leading to GSK-3β inhibition and axonal outgrowth (Arevalo et al, 2006). GSK-3β is also implicated in AMPA receptor trafficking, as AMPA receptor insertion following chemical induction of hippocampal LTP is associated with increased PI 3-kinase/Akt-driven inhibition of GSK-3β (Peineau et al, 2007). Alterations in PtdIns(3,4,5)P3 levels may promote structural rearrangement of the actin cytoskeleton which in turn influences the synaptic density of AMPA receptors (Zhou et al, 2001). Indeed, GEFs control the activity and function of Rho GTPases, a family of proteins that regulate the actin cytoskeleton. Moreover, one particular GEF, kalirin-7 associates with and controls the synaptic expression of GluR1-containing AMPA receptors (Xie et al, 2007).

Most evidence points to altering the phosphorylation status of PTEN as the main mechanism for regulating PTEN function. Changes in PTEN phosphorylation not only regulates its activity, but also influences its association with PDZ domains from other regulatory molecules, including the scaffolding proteins MAGI-2 and synapse-associated protein-97 (SAP97; Valiente et al, 2005; Vazquez et al, 2001). As SAP97 is a membrane associated guanylate kinase (MAGUK) that regulates the insertion and synaptic localization of GluR1-containing AMPA receptors (Rumbaugh et al, 2003), leptin, by promoting PTEN phosphorylation may alter PTEN/SAP-97 interactions which influences GluR1 trafficking. MAGI-2 is also linked to AMPA receptor trafficking as it interacts with TARPS (transmembrane AMPA receptor regulating proteins) and it links TARP/AMPA receptor complexes to other postsynaptic molecules (Deng et al, 2006). MAGI-2 binding to PTEN enhances PTEN-dependent suppression of PI 3-kinase/Akt activation (Wu et al, 2000) whereas PTEN phosphorylation causes a conformational change that reduces MAGI-2 binding to PTEN (Valiente et al, 2005). Thus, our data are consistent with leptin promoting PTEN phosphorylation which would reduce MAGI-2/PTEN interactions and thereby enhance PI 3-kinase/Akt signaling and AMPA receptor trafficking.

Leptin is a circulating hormone that is transported to most brain regions via transport across the blood brain barrier. Leptin mRNA and protein have been detected in several brain regions, including the hippocampus (Morash et al, 1999) and recent studies have shown leptin production by the brain (Eikelis et al, 2006). Thus the concentration of leptin reaching hippocampal synapses is likely to be derived from that released locally as well as from peripheral sources. Several studies indicate that leptin markedly influences the cellular events underlying hippocampal-dependent learning and memory (Harvey, 2007). Indeed leptin facilitates hippocampal LTP via enhancing NMDA receptor function and it promotes rapid changes in hippocampal dendritic morphology and synaptic density. The ability of leptin to rapidly alter the synaptic density of GluR1-containing AMPA receptors provides additional evidence in support of a role for leptin in regulating hippocampal synaptic plasticity.

Evidence is accumulating that cognitive deficits occur in leptin-insensitive rodents (Li et al, 2002) and are associated with obesity-related diseases like type II diabetes. Recent studies have linked altered leptin levels to neurodegenerative disorders as patients with Alzheimer's disease display attenuated leptin levels (Power et al, 2001). Studies in transgenic mice overexpressing amyloid β indicate that leptin significantly reduces amyloid β levels. As obesity and related disorders are thought to be a consequence of blood brain barrier resistance to leptin, resistance to this hormone may contribute to cognitive deficits in diabetics and in neurodegenerative disorders. Thus, the ability of leptin to promote changes in the efficacy of excitatory synaptic transmission via rapid trafficking of AMPA receptor may be crucial for its role not only in normal CNS function but also in neurological disorders associated with leptin resistance or insensitivity.

Acknowledgements

This work is supported by the Wellcome Trust (075821), Medical Research Scotland and The Royal Society. We would also like to thank Karen-Ann Bollan and Hemanth Tummala for their valuable help with the biotinylation studies.

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