Estradiol Activates Group I and II Metabotropic Glutamate Receptor Signaling, Leading to Opposing Influences on cAMP Response Element-Binding Protein

Introduction

Estradiol was characterized initially as binding to a single intracellular receptor [estrogen receptor α (ERα)], regulating gene expression through interactions with estrogen response elements (EREs) located within gene promoter regions (Couse and Korach, 1999; Klinge, 2001). With ERα highly expressed in brain regions that control female sexual behavior (Pfaff and Keiner, 1973), it was believed this was the sole mechanism of estrogen action. However, we now know the actions of estradiol in the brain are multifaceted (Pfaff et al., 1994). For instance, a second estrogen receptor (ERβ) has been identified (Kuiper et al., 1996; Tremblay et al., 1997), and ERα and ERβ also influence the expression of genes independent of EREs, through opposing influences on the activator protein-1 (AP-1) class of transcription factor (Gaub et al., 1990; Philips et al., 1993; Umayahara et al., 1994; Paech et al., 1997; Webb et al., 1999).

Further revision of the classical model of estrogen action (i.e., direct influences on gene expression) resulted from observations that estradiol mediates a variety of responses that are initiated at the neuronal membrane surface and occur within seconds to minutes of steroid exposure (McEwen and Alves, 1999). Through unidentified mechanisms, estradiol regulates multiple signaling pathways, including those involving cAMP/protein kinase A (PKA), mitogen-activated protein kinase (MAPK), and phospholipase C (PLC) (Nabekura et al., 1986; Minami et al., 1990; Mobbs et al., 1991; Aronica et al., 1994; Gu et al., 1996; Zhou et al., 1996; Watters et al., 1997; Singh et al., 1999; Toran-Allerand et al., 1999; Qiu et al., 2003; Chaban et al., 2004). These intracellular signaling cascades modulate receptors, channels, other signaling enzymes, and various transcription factors (Weng et al., 1999; Deisseroth et al., 2003; Waltereit and Weller, 2003; Thomas and Huganir, 2004). Thus, although often termed “nongenomic,” these rapid actions of estradiol can also exert long-term effects on neuronal function via changes in gene expression. Not surprisingly, novel actions of estradiol affect synaptic strength and neuronal structure (Gould et al., 1990; Weiland, 1992; Wong and Moss, 1992; Woolley and McEwen, 1992, 1993; Brinton, 1993; Woolley et al., 1997; Foy et al., 1999) and modulate processes including learning and memory, motor control, pain sensitivity, and cognition (McEwen and Alves, 1999).

Interestingly, each of these behaviors is also regulated by the transcription factor cAMP response element-binding protein (CREB) (Lonze and Ginty, 2002). Thus, modulation of CRE-dependent gene expression by estradiol is a candidate for explaining the influence of estrogens on a variety of behaviors. Recent work demonstrating that estradiol triggers CREB phosphorylation (Gu et al., 1996; Zhou et al., 1996; Wade and Dorsa, 2003; Lee et al., 2004) and that dominant-negative CREB inhibits estradiol-induced hippocampal spine formation (Murphy and Segal, 1997) supports this hypothesis. Although a link between estradiol and CREB has been established, the mechanism by which estradiol influences CREB nevertheless remains unclear. Thus, the aims of this study were to characterize the regulation of CREB by estradiol in hippocampal neurons and to identify the underlying cellular mechanisms by which this process occurs. We found estradiol can both increase and decrease CREB activation, with directional changes dependent on the absence or presence of additional neuronal stimuli. Furthermore, estradiol influenced CREB through activation of two distinct signaling pathways, triggered by stimulation of group I and II metabotropic glutamate receptors (mGluRs). Given that mGluRs regulate a variety of intracellular signaling pathways, our data not only describe the means by which estradiol influences CREB function but may also explain the underlying mechanisms by which estradiol rapidly influences a variety of other cellular behaviors.

Materials and Methods

Cell culture. CA3-CA1 Hippocampal pyramidal neurons were cultured from male and female 1- to 2-d-old rat pups as described previously (Mermelstein et al., 2000), using a protocol approved by the Animal Care and Use Committee at the University of Minnesota. Chemicals were obtained from Sigma (St. Louis, MO) unless stated otherwise. After decapitation, the CA3-CA1 region of the hippocampus was isolated (after removal of the dentate gyrus) in ice-cold modified HBSS containing 20% fetal bovine serum (FBS; HyClone, Logan, UT), 4.2 mm NaHCO₃, and 1 mm HEPES, pH 7.35, at 300 mOsm. The tissue was washed, followed by a 5 min digestion in a trypsin solution (type XI; 10 mg/ml) containing 137 mm NaCl, 5 mm KCl, 7 mm Na₂HPO₄, 25 mm HEPES, and 1500 U of DNase, pH 7.2, at 300 mOsm. After an additional wash, the tissue was dissociated, and the cell suspension was pelleted twice to remove contaminants, plated (∼6.4 × 10⁴ viable cells/well) on 10 mm coverslips (treated previously with Matrigel to promote adherence; BD Biosciences, San Jose, CA), and incubated for 15 min at room temperature. Two milliliters of Minimum Essential Media (MEM; Invitrogen, Grand Island, NY) containing 28 mm glucose, 2.4 mm NaHCO₃, 0.0013 mm transferrin (Calbiochem, La Jolla, CA), 2 mm glutamine, 0.0042 mm insulin, 1% B-27 supplement (Invitrogen), and 10% FBS, pH 7.35, at 300 mOsm, were added to each coverslip. Twenty-four hours later, 1 ml of media was replaced with a similar solution containing 4 μm cytosine 1-β-d-arabinofuranoside and 5% FBS. Seventy-two hours later, 1 ml of media was replaced with modified MEM solution containing 5% FBS. Media solutions contained 2 μg/ml gentamicin (Invitrogen) to eliminate bacterial growth. For low-density cultures, ∼4 × 10³ viable cells/well were plated on 10 mm coverslips. Cultures were treated similarly as outlined above, except that on day 6 they were also fed a supplement of glial-conditioned media (Banker and Goslin, 1998).

Drugs. The drugs used in these studies were as follows: tetrodotoxin (TTX; 1 μm), d(-)-2-amino-5-phosphonopentanoic acid (AP-5; 25 μm; Tocris, Ellisville, MO), nifedipine (5 μm), 17β-estradiol (17βE; 1 nm unless stated otherwise), 4-hydroxy-tamoxifen (1 nm), 7a, 17b-[9[(4,4,5,5,5-pentafluoropentyl)sulfinyl]nonyl]estra-1,3,5(10)-triene-3,17-diol (ICI 182,780) (100 nm; Tocris), 1,4-diamino-2,3-dicyano-1,4-bis[2-aminophenylthio]butadiene (U0126) (10 μm; Calbiochem), 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one (PD98059) (25 μm; Promega, Madison, WI), 1-[6-[[(17b)-3-methoxyestra-1,3,5(10)-trien-17-yl]amino]hexyl]-1H-pyrrole-2,5-dione (U73122) (1 μm), bisindolylmaleimide I (500 nm; Calbiochem), xestospongin C (XC; 1 μm; Sigma), (S)-(+)-a-amino-4-carboxy-2-methylbenzeneacetic acid (LY367385; 100 μm; Tocris), 7-(hydroxyimino) cyclopropa[b]chromen-1a-carboxylate ethyl ester (CPPCCOEt; 50 μm; Tocris), (RS)-3,5-dihydroxyphenylglycine (DHPG; 50 μm; Tocris), (2S)-2-amino-2-[(1S,2S)-2-carboxycycloprop-1-yl]-3-(xanth-9-yl) propanoic acid (LY341495; 100 nm; Tocris), (RS)-a-cyclopropyl-4-phosphonophenylglycine (CPPG; 100 nm; Tocris), (2R,4R)-4-aminopyrrolidine-2,4-dicarboxylate (APDC; 10 μm; Tocris), 4,4′,4″-(4-propyl-[1H]-pyrazole-1,3,5-triyl)trisphenol (PPT; 1 nm; Tocris), 2,3-bis(4-hydroxyphenyl)-propionitrile (DPN; 10 nm; Tocris), 2-methyl-6-(phenylethynyl)pyridine hydrochloride (MPEP; 5 μm; Tocris), pilocarpine (1 μm; Tocris), pertussis toxin (PTX; 500 ng/ml), 8-bromoadenosine-3′,5′-monophosphorothioate, Rp isomer (Rp-8-Br-cAMPs; Rp-cAMPs; 50 μm; Calbiochem), cyclosporin A (CsA; 1 μg/ml), FK506 (200 ng/ml; Calbiochem), and 17β-estradiol, 17-hemisuccinate-BSA (EBSA; 1 nm, Sigma or Steraloids, Newport, RI). As described previously, the EBSA was passed through a 3 kDa cutoff filter (Millipore, Billerica, MA) to remove free estrogens, and the retentate was resuspended immediately before use (Chaban et al., 2004).

Immunocytochemistry. Immunocytochemistry procedures were similar to those described previously (Mermelstein et al., 2001). Cultured neurons [9 d in vitro (d.i.v.)] were preincubated for 3 h in a Tyrode's solution containing 1 μm TTX and 25 μm AP-5, with cells being washed halfway through the preincubation period. Afterward, cells were stimulated for 5 min with estradiol or mock treated. For experiments using 20 mm K⁺, the 3 min depolarization occurred 5 min into the estradiol treatment period, with steroid also present in the high-K⁺ solution. Experiments using the mGluR agonists followed a similar time course. When applicable, inhibitors/antagonists used in this study were applied 30 min before stimulation. Immediately after treatments, cells were fixed for 20 min with ice-cold 4% paraformaldehyde (Electron Microscopy Sciences, Ft. Washington, PA) in PBS containing 4 mm EGTA. After being washed three times in PBS, cells were permeabilized via a 5 min incubation in a 0.1% Triton X-100 (VWR Scientific, West Chester, PA) solution. After an additional three washes, cells were incubated at 37°C for 30 min in a PBS-based block solution containing 1% BSA and 2% goat serum (Jackson ImmunoResearch, West Grove, PA). Coverslips were then incubated at 4°C overnight in a block solution containing a monoclonal antibody directed against serine 133 phosphorylated CREB (pCREB; 1:1000; Upstate Biotechnology, Lake Placid, NY), and, to identify individual cell morphology, a polyclonal antibody targeting microtubule-associated protein 2 (MAP2, 1:1000; Calbiochem). The next morning, cells were washed three times with PBS and incubated for 1 h at 37°C in a block solution containing FITC- and rhodamine RedX-conjugated secondary antibodies for visualization of MAP2 and pCREB, respectively (Jackson ImmunoResearch). After another wash, coverslips were mounted using the antiquenching agent Citifluor (Ted Pella, Redding, CA). Staining for ERα (1:500; Upstate Biotechnology) and ERβ (1:500; Affinity Bioreagents, South San Francisco, CA) was performed similarly, except using α-tubulin (1:2000; Molecular Probes, Eugene, OR) as the cytoskeletal stain, and cells were not stimulated. Acquisition of the nuclear fluorescent intensities for pCREB (n =∼20 cells/group) was performed using a Yokogawa (Tokyo, Japan) spinning-disc confocal system mounted to an Olympus (Tokyo, Japan) IX-70 inverted microscope and attached to a 12-bit digital camera (Hamamatsu Photonics, Hamamatsu City, Japan). Data were quantified using MetaMorph software (version 6.0; Universal Imaging, Downington, PA). Briefly, for each experimental run, there were two coverslips for each treatment group to account for potential inter-coverslip variability. After the confocal settings were first determined using neurons stimulated with 20 mm K⁺ as a guide, they remained constant throughout the experiment. Of note, although not always presented, each experiment contained 20 mm K⁺-treated cells to serve in this capacity. The only exception was for the immunocytochemistry experiments using PTX, in which the PTX plus 20 mm K⁺ group was used as a guide because PTX induced CREB phosphorylation. The coverslip order in which data were acquired was random. For data acquisition, cells were selected randomly (∼10 per coverslide) via MAP2 fluorescence, and a section through the approximate midline of each neuron was captured; the experimenter was blind to pCREB fluorescence. After all of the data were acquired, the experimenter drew a region of interest (ROI) outlining the nucleus of each pyramidal neuron using MAP2 staining. The software program then transferred that ROI to the pCREB image and provided the average fluorescence within each neuron. The data were background subtracted. Each experiment was repeated twice to verify results. Similar procedures were run for estrogen receptor staining, except a nuclear and cytoplasmic ROI was generated using α-tubulin staining as a guide. Because the confocal settings were set at the beginning of each experiment, comparing fluorescent intensities between trials is not appropriate.

Western blot. Cultured neurons (9 d.i.v.) were incubated for 3 h in a Tyrode's solution containing TTX (1 μm) and AP-5 (25 μm), with cells being washed halfway through the preincubation period. Afterward, cells were stimulated for 5 min with estradiol or mock treated. After stimulation, cells were lysed in a radioimmunoprecipitation assay buffer containing 1 mm NaF, 1 mm Na-orthovanadate, and a protease inhibitor mixture (Complete Mini EDTA-free; Roche, Indianapolis, IN). LDS loading buffer and β-mercaptoethanol were added to the lysate (25 and 10% of the total lysate volume, respectively) before the mixture was heated for 5 min to 95°C. Cellular protein was separated on a 4-12% Bis-Tris gel (Invitrogen) and transferred to a nitrocellulose membrane. The membrane was blocked at room temperature for 1 h in a Trisbuffered saline (TBS) solution containing 10% milk and 1% BSA. The membrane was incubated overnight at 4°C with an antibody for either pCREB (1:1000) or the loading control extracellular signal-regulated kinase (ERK; 1:10,000; Upstate Biotechnology), diluted in TBS containing 1% milk, 1% BSA, and 0.1% Tween 20. The next day, the membrane was washed with 0.1% Tween 20-TBS and incubated for 1 h at room temperature with a secondary antibody conjugated to horseradish peroxidase (1:25,000; Pierce, Rockford, IL). After incubation in a chemiluminescent substrate (Super Signal; Pierce), the membrane was exposed to X-Omat XB-1 film (Kodak, Rochester, NY). The experiment was repeated to verify the result.

Luciferase-based gene reporter assays. Cultured neurons were transfected 8 d.i.v. with a luciferase-based reporter (1 μg DNA/coverslip) of CRE-dependent transcription (three repeats of the CRE-binding site were incorporated into a minimal promoter expression vector; a gift from K. Heist, Stanford University, Stanford, CA) using a calcium-phosphate method that results in >95% of the transfected cells being neurons (Deisseroth et al., 1998; Weick et al., 2003). To verify that the effects of estradiol could not be attributed to a nonspecific alteration in gene expression or protein synthesis, sister cultures were transfected with a constitutively active luciferase vector (Groth and Mermelstein, 2003). After transfection, cells were placed in serum-free, DMEM (Invitrogen) containing an insulin-transferrin-selenium-A (ITS) supplement (Invitrogen) and 1% B-27 supplement, pH 7.35, at 300 mOsm. The DMEM/ITS/B-27 also contained 2 μg/ml gentamicin to prevent bacterial growth and 1 μm TTX to minimize CRE-dependent transcription triggered by synaptic activity. Twenty-four hours later, one-half of the neurons (n = 10 coverslips) were readministered TTX; the other half (n = 10) received TTX with the addition of 1 nm estradiol. Approximately 16 h after stimulation, cells were lysed and assayed for luciferase expression using a standard luminometer (Monolight 3010; PharMingen, San Diego, CA). Each experiment was replicated to verify the consistency of the results.

Electrophysiology. Miniature EPSCs (mEPSCs) were recorded from cultured hippocampal neurons (9 d.i.v.) at a holding potential of -70 mV using standard voltage-clamp techniques. Neurons were superfused with a room temperature solution containing the following (in mm): 119 NaCl, 2.5 KCl, 1.3 MgSO₄-7 H₂O, 11 glucose, 1 NaH₂PO₄-H₂O, 2.5 CaCl₂-2 H₂O, 26.2 NaHCO₃, 0.001 TTX, and 0.1 picrotoxin, pH 7.35, at 300 mOsm. Warner GC120T-10 (Warner Instruments, Hamden, CT) borosilicate glass electrodes (∼3 MΩ) contained the following (in mm): 117 cesium gluconate, 2.8 NaCl, 20 HEPES, 5 BAPTA, 4 Na₂-ATP, 0.8 Na₃-GTP, 12 phosphocreatine, and 5 tetraethyl-ammonium chloride, pH 7.2, at 285 mOsm. ATP and GTP were obtained from Boehringer Mannheim (Indianapolis, IN); BAPTA was purchased from Calbiochem. Recordings were made using an Axopatch 200B amplifier (Molecular Devices, Foster City CA), controlled by a personal computer running pClamp software (version 8.2). All recordings were filtered at 2 kHz, and the series resistance was not compensated. Experiments with a series resistance >20 MΩ or with a change in input resistance of >20% were discarded. A single recording sweep lasting 500 ms was sampled every 1 s. After acquisition of a stable baseline, cells were stimulated with 1 nm estradiol. Detection criteria included peak amplitudes >5 pA, with fast rise times and slow decay times, and all mEPSCs were confirmed visually. Thirty continuous sweeps were analyzed comparing mEPSC frequency and amplitude before and during estradiol application.

Whole-cell calcium channel currents were measured in cultured hippocampal neurons (9 d.i.v.) as described previously, using 5 mm Ba²⁺ as the charge carrier (Mermelstein et al., 1996, 2000; Weick et al., 2003). To verify the isolation of calcium channel currents, currents were also monitored after the addition of Cd²⁺ (200 μm) to the perfusate. Electrodes (Warner Instruments) were fire-polished with an MF-830 microforge (Narishige, Hempstead, NY). The intracellular recording solution contained the following (in mm): 190 N-methyl-d-glucamine, 40 HEPES, 5 BAPTA, 4 MgCl₂, 12 phosphocreatine, 3 Na₂ATP, and 0.2 Na₃GTP, pH 7.2, at 275 mOsm. The bath solution contained the following (in mm): 140 NaCl, 2 KCl, 23 glucose, 15 HEPES, 1 CaCl₂, 2 MgCl₂, and 0.01 glycine. Drugs (nifedipine, APDC, and DPN) were added to the control external recording solution that contained the following (in mm): 135 NaCl, 20 CsCl, 1 MgCl₂, 10 HEPES, 0.0001 TTX, and 5 BaCl₂. The perfusion system consisted of a convergent single-barrel design that allowed for extracellular solution changes in <1 s. The junction potential (<2 mV) was not compensated. The series resistance was compensated ≥70%. Voltage sweeps were performed once every 5-7 s.

Statistics. Immunocytochemistry experiments were analyzed using ANOVAs (F values) and Fisher's protected least significant difference post hoc tests. Because of the required replication of controls for each immunocytochemistry experiment run and the large number of groups in several experiments, post hoc values are mainly provided for novel comparisons (i.e., not presented in a previous figure) and in which differences can be attributed to a single variable. Luciferase and mEPSC data were analyzed via a Student's t test. p values <0.05 were considered a priori as significant.

Results

Estradiol induces rapid nuclear CREB phosphorylation via MAPK signaling

Estrogens have been reported to rapidly induce CREB phosphorylation in both neurons and cell lines in as little as 15 min, with recent data indicating that steroid effects are mediated via activation of MAPK (Gu et al., 1996; Zhou et al., 1996; Wade and Dorsa, 2003; Lee et al., 2004). Our initial experiments were designed to test whether this signaling pathway was intact within cultured CA3-CA1 hippocampal neurons obtained from 1- to 2-d-old female rat pups. Indeed, a 5 min application of estradiol (1 nm) significantly increased nuclear CREB phosphorylation (hereafter termed CREB phosphorylation). This effect of estradiol was blocked by either of the MAPK/ERK kinase (MEK) inhibitors, PD98059 (25 μm) (Fig. 1A,B) or U0126 (10 μm) (data not shown). Heightened CREB phosphorylation can be caused by an enhancement of protein kinase activity or a reduction in protein phosphate 1 (PP1) activity. Estradiol has been reported to depress calcineurin (CaN) activity (Sharrow et al., 2002; Foster et al., 2003), which may lead to a reduction in PP1 signaling through disinhibition of inhibitor-1 (Bito et al., 1997; Groth et al., 2003). However, estradiol-induced CREB phosphorylation was unaffected after inhibition of CaN with FK506 (200 ng/ml) and CsA (1 μg/ml), indicating this effect of estradiol is primarily routed through activation of MAPK (supplemental Fig. 1, available at www.jneurosci.org as supplemental material).

Estradiol elicited CREB phosphorylation in a dose-dependent manner (Fig. 1C) with an EC₅₀ value of ∼5.5 pm (r = 0.99), indicating a physiologically relevant phenomenon. Of note, because 1 nm was maximally effective in eliciting CREB phosphorylation, this concentration was used for the remainder of the studies. Estradiol-induced CREB phosphorylation occurred rapidly; the time course data were well fitted (r = 0.97) with a single exponential (τ = 29 s) (Fig. 1D). Western blot experiments were performed to verify the immunocytochemistry studies indicating estradiol-induced CREB phosphorylation. As shown in Figure 1E, a 5 min exposure to estradiol elicited an increase in CREB phosphorylation. Because phosphorylation of CREB on serine 133 is necessary but not sufficient for activation of CRE-dependent transcription, we applied estradiol to neuronal cultures transfected with a luciferase-based, CRE reporter construct to monitor changes in CRE-dependent transcription. As shown in Figure 1F, estradiol significantly increased CRE-dependent transcription. Estradiol had no effect on a constitutively active luciferase reporter [control, 967,418 ± 72,834 (mean ± SEM) vs estradiol, 858,751 ± 43,238; p > 0.05]. These results suggest that along with its more defined actions on ERE- and AP-1-based transcription, estrogens may also regulate the expression of genes under control of the CREB family of transcription factors.

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Figure 1.

Estradiol rapidly stimulates MAPK-dependent CREB phosphorylation. A, Example confocal images of cultured CA3-CA1 female hippocampal neurons immunolabeled with MAP2 (green) and pCREB (red). Pyramidal neurons exhibited heightened nuclear staining for pCREB after a 5 min application of estradiol (17βE; 1 nm). No Stim, No stimulation. Scale bar, 20 μm. B, Quantification of the immunolabeling demonstrated that estradiol significantly increased CREB phosphorylation (F = 183.79; ^**p < 0.01). Furthermore, the effect of estradiol was eliminated after inhibition of MEK with PD98059 (PD; 25 μm). C, Estradiol increased CREB phosphorylation in a concentration-dependent manner (F = 14.73; p < 0.05 at 1 pm; p < 0.01 at all other concentrations when compared with control). D, Time course of estradiol-induced CREB phosphorylation. E, Western blot verification of estradiol-induced CREB phosphorylation (∼46 kDa band). ERK was used as the loading control. F, Application of estradiol also increased CRE-dependent transcription (T = 4.42; ^**p < 0.01). Error bars indicate SEM.

The effects of estradiol on CREB phosphorylation are sex specific and occur via a membrane receptor

The previous experiments were performed on hippocampal cultures generated solely from female animals, because many of the characterized actions of estradiol in the brain are sex specific (Arnold and Breedlove, 1985; Williams, 1986). Thus, we next investigated whether the bidirectional effects of estradiol observed in female-derived cultures would also occur in those prepared from male rats. As shown in Figure 3, age-matched cultured hippocampal neurons from male animals did not exhibit either the estradiol-induced increase in MAPK-dependent CREB phosphorylation, or the estradiol-mediated decrease in CREB phosphorylation after activation of L-type calcium channels. As another control, cultures from male rats did not exhibit a change in CRE-dependent transcription after estradiol treatment (control, 17,913 ± 1,934 vs estradiol, 15,511 ± 2,835; p > 0.05). Estradiol was used at 1 nm for comparisons between male- and female-derived cultures. We did not examine whether higher concentrations of steroid would be effective on male-derived tissue.

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Figure 2.

Estradiol attenuates L-type calcium channel-mediated CREB phosphorylation. A, Estradiol alone resulted in an increase (F = 16.97; ^**p < 0.01) in CREB phosphorylation (left 2 bars). However, estradiol treatment in the presence of a 20 mm K⁺ stimulus led to a significant (^**p < 0.01) attenuation of depolarization-induced CREB phosphorylation (middle 2 bars). Pretreatment with the L-type calcium channel blocker nifedipine (NIF; 5 μm) eliminated depolarization-dependent CREB phosphorylation and unmasked estradiol-induced CREB phosphorylation (right 2 bars; ^**p < 0.01). B, Estradiol produced a rightward shift in the cumulative percentile of CREB fluorescence under basal conditions. C, Conversely, estradiol generated a leftward population shift in CREB phosphorylation after a 20 mm K⁺ depolarization. Error bars indicate SEM.

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Figure 3.

The bidirectional effects of estradiol on CREB phosphorylation are sex specific. A, B, Estradiol, in the absence of depolarization, increased (F = 26.82; ^**p < 0.01) CREB phosphorylation and decreased (^**p < 0.01) L-type calcium channel-dependent CREB phosphorylation in neurons derived from female but not male animals. Error bars indicate SEM.

We were also interested in determining the mechanism(s) by which estradiol influenced CREB activation. Because the observed responses were rapid (i.e., seconds to 8 min after steroid application), the classical mechanism of estrogen action appeared unlikely. In support of this hypothesis, both effects of estradiol were mimicked by the membrane-impermeable estrogen analog EBSA (1 nm) (Fig. 4A,B), suggesting that the regulation of CREB phosphorylation occurred via activation of an estrogen receptor localized to the membrane surface. In support of this hypothesis, the mixed estrogen receptor agonist/antagonist 4-hydroxy-tamoxifen (1 nm) acted as an agonist in this paradigm, both increasing and decreasing CREB phosphorylation (Fig. 4C,D). Furthermore, both responses were blocked by the pure estrogen receptor antagonist ICI 182,780 (100 nm) (Fig. 4E).

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Figure 4.

The effects of estradiol occur via action at the plasma membrane, are mimicked by the mixed estrogen receptor agonist/antagonist 4-hydroxy-tamoxifen, and are blocked by the estrogen receptor antagonist ICI 182,780. A, B, The membrane-impermeable estrogen analog EBSA mimicked the bidirectional effects of estradiol on CREB phosphorylation [F = 42.02 and 79.60; ^**p < 0.01 vs basal (A) and 20 mm K⁺ (B)]. C, D, The effect of 4-hydroxy-tamoxifen (4-OH-TMX) also paralleled the effect of estradiol [F = 31.15 and 41.27; ^**p < 0.01 vs basal (C) and 20 mm K⁺ (D)]. E, ICI 182,780 (ICI; 100 nm) eliminated both the estradiol-induced increase in CREB phosphorylation (F = 81.28; ^**p < 0.01 vs 17βE) and the estradiol-induced attenuation of L-type calcium channel-mediated CREB phosphorylation (^**p < 0.01 vs 20 mm K⁺ plus 17βE). Error bars indicate SEM.

Estradiol regulates CREB phosphorylation via activation of mGluRs

Unable to distinguish the opposing effects of estradiol using estrogen receptor ligands, we decided on a different strategy. Switching to a “bottom-up” approach, we instead tried to isolate the two signaling pathways by targeting proteins known to influence MAPK. Inhibition of PKC with bisindolylmaleimide (500 nm) or inositol trisphosphate receptors (IP₃Rs) with XC (1 μm) resulted in the attenuation of estradiol-induced CREB phosphorylation (Fig. 5A,B). Coapplication of both drugs eliminated the effect (Fig. 5C). PLC signaling is linked to MAPK activation via both PKC and IP₃R. This particular pathway appeared important for estradiol-induced CREB phosphorylation, because inhibition of PLC with U73122 (1 μm) resulted in the blockade of estradiol-induced CREB phosphorylation (Fig. 5D). Inhibition of the PLC signaling pathway did not affect the influence of estradiol on L-type calcium channel CREB phosphorylation (data not shown).

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Figure 5.

Estradiol-induced CREB phosphorylation is dependent on activation of PLC, PKC, and IP₃R signaling. A, The effect of estradiol was reduced (F = 16.76; ^**p < 0.01) by inhibition of PKC with bisindolylmaleimide (500 nm). B, Similar results (F = 11.37; ^**p < 0.01) were observed after inhibition of IP₃R with XC (1 μm). C, Pretreatment with both bisindolylmaleimide (Bis) and XC eliminated estradiol-induced CREB phosphorylation (F = 25.38; ^**p < 0.01). D, Consistent with estradiol activation of PLC, pretreatment with the inhibitor U73122 (1 μm) significantly (F = 19.89; ^**p < 0.01) attenuated estradiol-induced CREB phosphorylation. Error bars indicate SEM.

PLC, PKC, and IP₃R can be activated by several mechanisms, including Gq G-protein-coupled receptors (GPCRs) (Gutkind, 2000). Kelly and colleagues (Qiu et al., 2003) recently determined that estradiol can stimulate Gq signaling in neurons; this signaling pathway also appears to be present in astrocytes (Chaban et al., 2004). Based on these data, we hypothesized that estradiol may be acting through a previously defined Gq signaling pathway to induce CREB phosphorylation. Group I mGluRs are linked to Gq G-proteins. As shown in Figure 6A, the mGluR1a antagonist LY367385 (100 μm; see Discussion) blocked estradiol-induced CREB phosphorylation without affecting estradiol attenuation of L-type calcium channel-mediated CREB phosphorylation. mGluR1a specificity was verified with a separate antagonist, CPPCCOEt (50 μm) (data not shown). Along with mGluR1a, mGluR5 comprises the Gq-coupled group I mGluRs. Application of the mGluR5 antagonist MPEP (5 μm) (data not shown) had no effect on estradiol signaling to CREB, demonstrating the actions of estradiol within hippocampal neurons are specific to mGluR1a. Additionally, 5 min administration of the group I mGluR agonist DHPG (50 μm) in the presence of MPEP resulted in CREB phosphorylation, similar to estradiol and occluding the effect of the steroid (Fig. 6B). We also applied DHPG (and MPEP) to hippocampal cultures generated from male animals (Fig. 6C). Whereas estradiol had no effect on CREB in male neurons, DHPG significantly increased CREB phosphorylation. These data suggest that the “breakpoint” in the signaling link between estradiol and CREB in cultured neurons from male rats is localized to actions between estradiol and activation of mGluRs (i.e., upstream of mGluRs). Finally, LY367385 had no effect on CREB phosphorylation mediated by the muscarinic agonist pilocarpine (1 μm), indicating application of LY367385 was not globally disrupting Gq signaling (supplemental Fig. 2, available at www.jneurosci.org as supplemental material).

We theorized that estradiol activation of mGluR signaling could either occur by a postsynaptic effect, leading to activation of mGluR1, or by a presynaptic effect, in which estradiol mediated the release of glutamate. To distinguish between these two hypotheses, we first monitored spontaneous glutamatergic activity via whole-cell recordings of hippocampal neurons (n = 9). We hypothesized that if estradiol was inducing neurotransmitter release, the effect would be detected by postsynaptic AMPA receptors. Nevertheless, a 5 min application of estradiol did not evoke measurable glutamate release nor influence mEPSC frequency (Fig. 6D,E) or amplitude (control, 41.5 ± 4.9 pA vs estradiol, 40.4 ± 4.7 pA). In the next experiment, we monitored the effect of estradiol in the absence of extracellular calcium, which eliminates evoked neurotransmitter release. Although there was a reduction in basal pCREB levels, estradiol significantly increased CREB phosphorylation after removal of extracellular calcium (Fig. 6F). In a third experiment, the effects of estradiol were monitored in low-density cultures, reducing the number of cell-cell contacts and extracellular glutamate. Under these conditions, estradiol still elicited CREB phosphorylation (fluorescence intensity: control, 977.0 ± 69.2 vs estradiol, 2179.7 ± 164.4; p < 0.01). In combination, these data strongly suggest that the effects of estradiol are initiated postsynaptically.

Whereas group I mGluRs are coupled to Gq, group II and III mGluRs are coupled to G_i/o G-proteins. G_i/o signaling typically results in inhibition of adenylyl cyclase (AC) (Neves et al., 2002). Previous work has demonstrated that activation of Gs GPCRs results in an enhancement of L-type calcium channel currents, through activation of AC and PKA (Surmeier et al., 1995). PKA-mediated phosphorylation of the L-type calcium channel α_1C subunit at Ser1928 is responsible for increased channel activity (De Jongh et al., 1996; Gao et al., 1997). Thus, activation of G_i/o may result in a decrease in L-type calcium channel phosphorylation and currents, thereby reducing L-type calcium channel-mediated CREB phosphorylation. We hypothesized that similar to its actions on mGluR1a, estradiol can stimulate group II and/or group III mGluRs, ultimately resulting in decreased L-type calcium channel CREB phosphorylation. Consistent with this theory, application of the group II mGluR antagonist LY341495 (100 nm) eliminated the effect of estradiol on L-type calcium channel-mediated CREB phosphorylation (Fig. 7A). Similar results were observed using the group II/III mGluR antagonist CPPG (100 nm) (data not shown). Neither drug blocked estradiol-mediated CREB phosphorylation. Interestingly, inhibition of group II mGluRs with LY341495 exposed estradiol-mediated CREB phosphorylation normally obscured after depolarization.

Just as the group I mGluR agonist mimicked the effect of estradiol on stimulating CREB phosphorylation, application of the mGluR2/3 agonist APDC (10 μm) resulted in a significant attenuation of L-type calcium channel-mediated CREB phosphorylation and occluded the effect of estradiol (Fig. 7B). APDC had no effect on basal levels of CREB activation. Application of APDC to hippocampal cultures derived from male animals also significantly decreased depolarization-induced CREB phosphorylation, demonstrating that the lack of an effect of estradiol in these cells is not attributable to deficient mGluR2/3 signaling (Fig. 7C).

Estradiol activation of mGluRs is mediated via surface expression of classical estrogen receptors

It was recently reported that estradiol-induced CREB phosphorylation is eliminated in ERα and ERβ knock-out mice (Abraham et al., 2004). Based on the fact that ERα and ERβ have been identified within the plasma membrane (Razandi et al., 1999, 2004; Watson et al., 1999; Wade et al., 2001) and that CREB signaling is influenced by the estrogen receptor ligands 4-hydroxy-tamoxifen and ICI 182,780, we hypothesized that it is, in fact, these receptors that are directly linked to mGluR activation. To test this hypothesis, we used agonists specific to either ERα (PPT; 1 nm) or ERβ (DPN; 10 nm) (Stauffer et al., 2000). As shown in Figure 8A, PPT application led to a significant increase in CREB phosphorylation, whereas DPN was without effect, indicating that in hippocampal neurons, ERα mediates estradiol-induced CREB phosphorylation. Conversely, both PPT and DPN reduced L-type calcium channel-dependent CREB phosphorylation (Fig. 8B), suggesting that both estrogen receptors are capable of signaling to mGluR2/3.

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Figure 6.

Estradiol-mediated CREB phosphorylation occurs via activation of mGluR1a signaling, independent of glutamate release. A, The mGluR1a antagonist/inverse agonist LY367385 (100 μm) eliminated estradiol-mediated CREB phosphorylation, without affecting estradiol inhibition of depolarization-induced CREB phosphorylation (F = 45.18; ^**p < 0.01 vs 17βE). B, The mGluR1/5 agonist DHPG (50 μm) in the presence of the mGluR5 antagonist MPEP (5 μm) increased CREB phosphorylation in cultures derived from female animals similar to estradiol and occluded the steroid effect (F = 49.98; ^**p < 0.01). C, DHPG (in the presence of MPEP) also resulted in an increase in CREB phosphorylation in cultures derived from male animals (F = 67.87; ^**p < 0.01). D, E, Whole-cell recordings of female hippocampal neurons (n = 9) revealed that estradiol does not evoke glutamate release or alter the frequency of mEPSCs. Calibration: 50 pA, 25 ms. F, Estradiol increased CREB phosphorylation after the removal of extracellular calcium, further supporting the notion that estradiol activation of mGluR1a signaling is independent of presynaptic glutamate release. Error bars indicate SEM.

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Figure 7.

Estradiol attenuates L-type calcium channel-mediated CREB phosphorylation via activation of group II mGluR signaling. A, The group II mGluR antagonist LY341495 (100 nm) eliminated the effect of estradiol on L-type calcium channel-mediated CREB phosphorylation (F = 38.19; ^**p < 0.01 vs 20K⁺ plus LY341495 and 20K⁺ plus 17βE) but had no effect on estradiol-induced CREB phosphorylation. B, The group II mGluR agonist APDC (10 μm) significantly attenuated L-type calcium channel-mediated CREB phosphorylation (F = 126.56) similar to estradiol and also occluded the steroid effect (^**p < 0.01). C, The effect of APDC was also observed in cultures derived from male animals (F = 57.74; ^**p < 0.01). Error bars indicate SEM.

Estradiol and mGluR2/3-mediated diminution of L-type calcium channel currents is routed through G_i/o signaling

As described above, our working hypothesis is that estradiol and mGluR2/3 attenuate L-type calcium channel-mediated CREB phosphorylation in hippocampal neurons via modulation of the calcium channel. Previous work has shown a reduction in L-type calcium channel currents after estradiol administration in both striatal and DRG cells (Mermelstein et al., 1996; Chaban et al., 2003). Furthermore, mixed mGluR agonists reduce L-type calcium channel currents in hippocampal, neocortical, and cerebellar neurons (Sayer et al., 1992; Sahara and Westbrook, 1993; Chavis et al., 1994). Thus, as an initial foray into the signaling pathway by which estradiol and mGluR2/3 reduce L-type calcium channel-mediated CREB phosphorylation, we performed whole-cell recordings of hippocampal neurons. Application of APDC resulted in a decrease in the whole-cell current (Fig. 9A). The actions of APDC were attributable to a reduction in L-type calcium channel activity, because the effect was eliminated in the presence of Nif (Fig. 9B). In this experimental paradigm, APDC was found to reduce the L-type calcium current by 52.6 ± 14.6% (n = 9). Because application of the ERβ agonist DPN only reduced L-type calcium channel-mediated CREB phosphorylation and did not elicit MAPK-dependent CREB phosphorylation (Fig. 8), we next decided to examine the effect of this drug (Fig. 9C). Consistent with our hypothesis, DPN was also found to reduce L-type calcium channel currents by 23.7 ± 9.1% (n = 7).

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Figure 8.

Estradiol activation of mGluR signaling is mediated by classical estrogen receptors located at the membrane surface. A, The ERα-specific agonist PPT (1 nm) led to an increase (F = 22.51; ^**p < 0.01) in CREB phosphorylation, similar to the actions of estradiol. The ERβ-specific agonist DPN (10 nm) was without effect. B, Conversely, both PPT and DPN were equally effective to estradiol in the attenuation of L-type calcium channel-dependent CREB phosphorylation (F = 74.17; ^**p < 0.01). Error bars indicate SEM.

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Figure 9.

Activation of mGluR2/3 and ERβ reduce L-type calcium channel currents. Furthermore, estradiol attenuation of L-type calcium channel-dependent CREB phosphorylation is mediated through G_i/o and PKA. A, Example traces of the whole-cell calcium channel current under control conditions and in the presence of the mGluR2/3 agonist APDC (10 μm). Calibration: 400 pA, 20 ms. B, Plot of the peak current as a function of time. The application of APDC produced a reduction in the whole-cell calcium current. The effect was eliminated in the presence of the L-type calcium channel blocker nifedipine (5 μm), indicating that activation of mGluR2/3 results in a decrease in the L-type calcium channel current. C, Both APDC (n = 9) and the ERβ agonist DPN (10 nm, n = 7) resulted in a decrease in the L-type calcium channel current. D, Estradiol reduction of L-type calcium channel-mediated CREB phosphorylation was eliminated after a 24 h pretreatment with the G_i/o inhibitor PTX (500 ng/ml). E, Inhibition of PKA with Rp-cAMPs (50 μm) also occluded the effect of estradiol on L-type calcium channel-mediated CREB phosphorylation. Neither PTX nor Rp-cAMPs affected estradiol-induced CREB phosphorylation (F = 47.79 and 216.05; ^**p < 0.01 vs baseline). Error bars indicate SEM.

Previous reports have established that micromolar concentrations of estradiol can directly inhibit L-type calcium channels (Kurata et al., 2001). In the final set of experiments, the effect of estradiol on CREB phosphorylation was examined in the presence of the G_i/o inhibitor PTX and the PKA inhibitor Rp-cAMPs to verify the actions of estradiol in our preparation were mediated through an intracellular signaling pathway. Although overnight treatment with PTX (500 ng/ml) was found to increase basal levels of CREB phosphorylation (data not shown), significant increases in CREB phosphorylation were still observed after application of either estradiol or depolarization with 20 mm K⁺. However, the reduction in L-type calcium channel-mediated CREB phosphorylation by estradiol was eliminated (Fig. 9D). Furthermore, a 3 h preincubation of the PKA inhibitor Rp-cAMPs (50 μm) occluded estradiol attenuation of L-type calcium channel-mediated CREB phosphorylation (Fig. 9E). After application of both PTX and Rp-cAMPs, estradiol tended to enhance 20 mm K⁺ CREB phosphorylation, although the effects never reached significance. In the last series of experiments, PTX eliminated the APDC-induced reduction in CREB phosphorylation (supplemental Fig. 3A, available at www.jneurosci.org as supplemental material). Moreover, Rp-cAMPs occluded the effect of APDC (supplemental Fig. 3B, available at www.jneurosci.org as supplemental material). These experiments confirm that both estradiol and mGluR2/3 stimulation reduce L-type calcium channel-dependent CREB phosphorylation through G_i/o and AC/PKA signaling.

Discussion

Previous research has determined that estradiol will induce CREB phosphorylation via activation of MAPK. We have expanded on these studies, uncovering that in hippocampal neurons, estradiol has bidirectional influences on CREB phosphorylation, initiated through activation of membrane-localized estrogen receptors. We hypothesize that estradiol binds to membrane-associated estrogen receptors, leading to activation of both group I and II mGluR signaling in a glutamate-independent manner. mGluR1a stimulation through activation of ERα leads to PLC, MAPK, and IP₃R signaling, resulting in CREB phosphorylation. Concurrently, activation of mGluR2 and/or mGluR3 via ERα or ERβ leads to diminished cAMP concentrations and a reduction in PKA activity, ultimately resulting in dephosphorylation of L-type calcium channels and a reduction in L-type calcium channel-mediated CREB phosphorylation (Fig. 10). Of note, without specific mGluR2 or mGluR3 agonists/antagonists, we were unable to definitively determine whether this effect was mediated by both or just one of these receptors, although within hippocampal pyramidal neurons, mGluR2 expression appears predominant (Ohishi et al., 1993a,b). The actions of estradiol on mGluR signaling were found to be sex specific and occurred with physiological concentrations of hormone. Collectively, these results not only clarify the actions of estradiol on CREB signaling but may also provide insight into the major signaling mechanisms by which estrogens rapidly affect brain function through processes initiated at the membrane surface.

Regulation of CREB is believed to play a principal role in hippocampal learning and memory (Silva et al., 1998; Lonze and Ginty, 2002; Balschun et al., 2003). Previous work describing estradiol-mediated CREB phosphorylation outlined a potential mechanism by which estrogens could augment gene expression and, presumably, performance on learning and memory tasks. In fact, the effects of estradiol on these behaviors have been examined in great detail. Yet, these studies have provided inconsistent results, with some groups suggesting that estrogens enhance performance on hippocampal-dependent learning and memory tasks, whereas others report no effect or even cognitive deficits (Dohanich, 2002). The demonstration that estradiol exerts bidirectional effects on CREB phosphorylation may be one cause for these conflicting reports, because estradiol will either promote or attenuate CREB signaling reliant on the magnitude of concurrent excitatory inputs.

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Figure 10.

Proposed mechanism by which estradiol produces bidirectional effects on CREB phosphorylation. Via interactions with classical estrogen receptors localized at the neuronal membrane, estradiol activates both group I and group II mGluR signaling. In one case, estradiol stimulation of mGluR1a leads to PLC/MAPK-induced CREB phosphorylation. Concurrently, activation of group II mGluR signaling decreases L-type calcium channel-dependent CREB phosphorylation through G_i/o inhibition of AC and PKA. The shaded arrows indicate decreased activity. CaM, Calmodulin; RSK, p90 ribosomal protein S6 kinase; CaMKIV, calmodulin-dependent protein kinase IV.

CREB is a stimulus-induced transcription factor that, although frequently studied in the context of hippocampal learning and memory, acts throughout the nervous system to regulate various behaviors (Lonze and Ginty, 2002). For instance, in areas such as the nucleus accumbens and DRG of the spinal cord, CREB regulates properties related to addiction and chronic pain (Blendy and Maldonado, 1998; Berke and Hyman, 2000; Nestler, 2001; Ji et al., 2003). Other examples of CREB-dependent cellular processes include neuronal survival, proliferation, and differentiation (Rudolph et al., 1998; Lonze et al., 2002; Redmond et al., 2002). Intriguingly, considerable overlap exists between behaviors and processes reliant on CREB and those that are influenced by estradiol (Lee and McEwen, 2001; Aloisi, 2003; Carroll et al., 2004; Hu et al., 2004). Thus, the present study may provide insight into a functional means by which estradiol, by acting through CREB, extensively modulates nervous system function.

Although rapid actions of estradiol have been studied for >20 years (Szego and Pietras, 1981), the underlying mechanisms by which they occur have remained elusive (McEwen, 2002). Although a membrane-specific estrogen receptor has been identified recently (ER-X), this protein seems only to be expressed during development or after neuronal injury (Toran-Allerand et al., 2002; Toran-Allerand, 2004). Because ER-X is unable to account for many of the actions of estradiol within adult tissue, two major theories suggesting the mechanism by which estrogens rapidly influence cell function have continued to endure. The first hypothesis is that classical estrogen receptors can have rapid effects on neuronal excitability. Consistent with this hypothesis, ERα and ERβ are found within neuronal membranes where they appear capable of influencing cell signaling (Razandi et al., 1999; Watson et al., 1999; Belcher and Zsarnovszky, 2001; Wade et al., 2001; Levin, 2002). Alternatively, because many of the novel effects of estradiol are sensitive to modulation of G-proteins, the opposing hypothesis suggests estradiol activates GPCRs (Kelly and Wagner, 1999; Kelly et al., 1999). Our results suggest a parsimonious explanation, incorporating major aspects from each of the previous theories. That is, estradiol acts with classical estrogen receptors localized to the neuronal membrane, which in turn stimulate several different classes of mGluRs, modulating cell function through activation of G-proteins.

An appealing feature to this revised model is that mGluR signaling can account for the ability of estradiol to regulate a diverse array of intracellular signaling cascades. These estrogen-sensitive pathways include PKA, MAPK, phosphoinositide 3-kinase, protein kinase B, PLC, and IP₃ (Nabekura et al., 1986; Minami et al., 1990; Mobbs et al., 1991; Aronica et al., 1994; Gu et al., 1996; Zhou et al., 1996; Watters et al., 1997; Wiebe, 1997; Marino et al., 1998; Singh et al., 1999; Cardona-Gomez et al., 2002; Qiu et al., 2003). With promiscuous but also differential expression of mGluRs throughout the brain (Shigemoto et al., 1992; Ohishi et al., 1993a), activation of surface-expressed estrogen receptors can potentially have varied responses in nervous system tissue. Thus, our results may also impact other studies regarding nonclassical mechanisms of estrogen action. Of note, we focused on the major signaling pathways activated by group I and II mGluRs. Yet, there are mechanisms by which cross talk may occur between mGluR signaling. For example, activation of mGluR1a can affect L-type calcium channels (Sayer, 1998), possibly through IP₃R (Lester and Jahr, 1990). Thus, estradiol regulation of intracellular signaling is most likely an assorted integration of numerous signaling pathways.

Because estradiol triggered CREB phosphorylation in the absence of depolarization, it was initially surprising that a significant attenuation of CREB signaling was observed after 20 mm K⁺ depolarization. Stated another way, why did the competing process of MAPK activation not obscure estradiol inhibition of L-type calcium channel-dependent CREB phosphorylation? The answer most likely is a result of depolarization-induced activation of CaN and PP1, which act in concert to counteract CREB phosphorylation (Bito et al., 1996, 1997). By attenuating calmodulin-dependent protein kinase IV-dependent CREB phosphorylation, estradiol may have unmasked depolarization-induced activation of CaN and PP1, resulting in decreased CREB activation.

A recent study using estrogen receptor knock-out mice demonstrated that expression of ERα and ERβ is necessary for estradiol-induced CREB phosphorylation (Abraham et al., 2004). Although these results strongly suggested a direct effect of estrogen receptors on CREB activation, they did not rule out the possibility that classical estrogen receptors are responsible for the expression of another estrogen-sensitive protein that directly initiates CREB phosphorylation. Our results help support the hypothesis that classical estrogen receptors, without activation of gene expression, can regulate CREB functioning.

One avenue of future research will be to pursue the additional discovery and quantification of classical estrogen receptors on the membrane surface. Consistent with previous reports (Su et al., 2001; Prange-Kiel et al., 2003), we readily observed expression of ERα and ERβ within the cytosol and nucleus of cultured hippocampal neurons (supplemental Fig. 4, available at www.jneurosci.org as supplemental material). Interestingly, ERα and ERβ expression was comparable between cultures derived from male versus female animals, consistent with previous reports (Weiland et al., 1997; Kalita et al., 2005) and highlighting the mystery surrounding the sexually dimorphic actions of estradiol. Detection of membrane estrogen receptors has proven to be substantially more difficult using conventional methods, although several recent reports have begun to identify localization of ERα and ERβ within the plasma membrane (Razandi et al., 1999; Watson et al., 1999; Wade et al., 2001). However, these results are still somewhat controversial, and membrane expression is not readily quantifiable (McEwen and Alves, 1999; Toran-Allerand, 2004). Hopefully, future studies will allow correlations between the expression of membrane estrogen receptors and physiological responses to the steroid hormone. Related, with the development of estrogen receptor-specific ligands, functional effects of these presumptive membrane receptors are just now being characterized, possibly leading to increased acceptance that detection of ERα and ERβ on the membrane surface is of physiological relevance.

Future research will also need to determine how membrane-localized ERα and ERβ stimulate mGluR signaling. The protein structure of classical estrogen receptors (ligand-binding domain, DNA-binding domain, etc.) does not lend itself to many clues regarding this process. However, in non-neuronal cells, estrogen receptors have been found to interact and activate the epidermal growth factor receptor and insulin-like growth factor-1 receptor (Kahlert et al., 2000; Razandi et al., 2003). These interactions between estrogen receptors and surface receptors appear to occur within caveolae (Wyckoff et al., 2001; Razandi et al., 2002). Interestingly, mGluRs are also concentrated within caveolae (Burgueno et al., 2003, 2004). Thus, through a similar process, estrogen receptors may activate mGluR signaling via direct protein-protein interactions. Experiments are under-way to test this hypothesis. These studies may also clarify whether one or both group II mGluRs are activated after estradiol treatment.

Three lines of evidence (mEPSC analysis and estradiol-induced CREB phosphorylation in both zero external calcium and in low-density cultures) suggest estradiol activates mGluRs via a postsynaptic mechanism. Thus, our working hypothesis is that estradiol binds to membrane-localized estrogen receptors, leading to activation of mGluRs. However, this raises an important issue regarding the ability of mGluR antagonists to eliminate estradiol-induced responses. Because antagonists are classically defined as preventing the binding of agonist, and not altering rates of transition between inactive and active states, why do these drugs block estradiol responses? Most likely, the answer is attributable to the fact that many GPCR antagonists also have the ability to dampen the activity of their targeted receptor (Lefkowitz et al., 1993; Milligan et al., 1995) and thus act as inverse agonists (Chen et al., 2000). Only modest work has been done to examine inverse agonist properties of antagonists, although there is some recent evidence implicating LY367385 (Pula et al., 2004). Notably, studies examining inverse agonists typically measure changes in basal rates of activity, and thus stimulus-induced activation may not be equally affected. Nevertheless, it is suggestive that estradiol-induced changes in CREB phosphorylation are blocked by the mGluR “antagonists” because of the capability of these drugs to generate hindrance in the transition of the receptor to an active confirmation.

Another area that will require additional research is determining the cause for the observed sex differences in response to estradiol. Given that postnatal animals were used in the present study, the testosterone surge in male animals occurring at birth may have affected estrogen sensitivity. Future use of prenatal animals, castration of newborn male pups, and injection of female pups with testosterone may determine whether the masculinization and defeminization of male animals at birth is responsible for this outcome, or whether an earlier developmental component is responsible. Other avenues of future research will include the use of knock-out mice (mGluR and estrogen receptor) in our paradigm to determine the overall significance of estradiol regulation of CREB activity, and to more fully characterize estradiol and mGluR2/3 inhibition of L-type calcium channel-mediated CREB phosphorylation.

In conclusion, we provide evidence that estradiol can trigger mGluR signaling through activation of classical estrogen receptors located at the plasma membrane. This previously undefined mechanism of estrogen action results in the stimulation of numerous intracellular signaling pathways, which may lead to both rapid and enduring changes in cell function. These novel estrogen actions most likely work synergistically with previously defined estrogen receptor responses to influence a diverse array of brain functions.