WWW.JNEUROSCI.ORG
-
The Journal of Neuroscience
QUICK SEARCH:   [advanced]


     
-


HOME  |   SEARCH  |   ARCHIVE  |   SUBSCRIBE  |   CONTACT  |   HELP
This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Supplemental Movie
Right arrow Submit an eLetter
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (47)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Morikawa, H.
Right arrow Articles by Williams, J. T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Morikawa, H.
Right arrow Articles by Williams, J. T.

 Previous Article  |  Next Article 

The Journal of Neuroscience, January 1, 2003, 23(1):149-157

Two Intracellular Pathways Mediate Metabotropic Glutamate Receptor-Induced Ca2+ Mobilization in Dopamine Neurons

Hitoshi Morikawa1, Kamran Khodakhah2, and John T. Williams1

1 Vollum Institute, Oregon Health and Science University, Portland, Oregon 97201, and 2 Department of Neuroscience, Albert Einstein College of Medicine, Bronx, New York 10461


    ABSTRACT

TOP
ABSTRACT
Introduction
Materials and Methods
Results
Discussion
REFERENCES

Activation of metabotropic glutamate receptors (mGluRs) causes membrane hyperpolarization in midbrain dopamine neurons. This hyperpolarization results from the opening of Ca2+-sensitive K+ channels, which is mediated by the release of Ca2+ from intracellular stores. Neurotransmitter-induced mobilization of Ca2+ is generally ascribed to the action of inositol 1,4,5-triphosphate (IP3) in neurons. Here we show that the mGluR-mediated Ca2+ mobilization in dopamine neurons is caused by two intracellular second messengers: IP3 and cyclic ADP-ribose (cADPR). Focal activation of mGluRs, attained by synaptic release of glutamate or iontophoretic application of aspartate, induced a wave of Ca2+ that spread over a distance of ~50 µm through dendrites and the soma. Simultaneous inhibition of both IP3- and cADPR-dependent pathways with heparin and 8-NH2-cADPR was required to block the mGluR-induced Ca2+ release, indicating a redundancy in the signaling mechanism. Activation of ryanodine receptors was suggested to mediate the cADPR-dependent pathway, because ruthenium red, an antagonist of ryanodine receptors, inhibited the mGluR response only when the cADPR-dependent pathway was isolated by blocking the IP3-dependent pathway with heparin. Finally, the mGluR-mediated hyperpolarization was shown to induce a transient pause in the spontaneous firing of dopamine neurons. These results demonstrate that an excitatory neurotransmitter glutamate uses multiple intracellular pathways to exert an inhibitory control on the excitability of dopamine neurons.

Key words: intracellular Ca2+ signaling; metabotropic glutamate receptors; inositol 1,4,5-triphosphate; cyclic ADP-ribose; inositol 1,4,5-triphosphate receptors; ryanodine receptors; dopamine neurons; firing pattern


    Introduction

TOP
ABSTRACT
Introduction
Materials and Methods
Results
Discussion
REFERENCES

Dopaminergic neurons in the ventral midbrain, i.e., the ventral tegmental area (VTA) and the substantia nigra pars compacta (SNc), are a key component of the endogenous reward circuit. They are transiently activated by the detection, perception, and expectation of rewards, suggesting that they are under the control of highly processed inputs from the cerebral cortex and other brain regions (Schultz, 1998). Repetitive stimulation of glutamatergic inputs evokes a slow IPSP via activation of metabotropic glutamate receptors (mGluRs) in dopamine neurons (Fiorillo and Williams, 1998). Release of Ca2+ from intracellular stores mediates this mGluR-induced hyperpolarization, because the rise in [Ca2+]i will activate small-conductance Ca2+-sensitive K+ channels (SK channels) on the plasma membrane. The resulting prolonged hyperpolarization (~1 sec) is expected to have a significant impact on the firing pattern of dopamine neurons.

It is generally assumed that inositol 1,4,5-triphosphate (IP3) mediates the mobilization of Ca2+ induced by activation of G-protein-linked neurotransmitter receptors in neurons (Berridge, 1998). Recent studies have reported that synaptically released glutamate acting on mGluRs evokes IP3-mediated mobilization of Ca2+ in cerebellar Purkinje neurons and hippocampal pyramidal neurons (Finch and Augustine, 1998; Takechi et al., 1998; Nakamura et al., 1999, 2000). In dopamine neurons, direct application of IP3 into the cytosol has been shown to elicit release of Ca2+ from intracellular stores (Morikawa et al., 2000), consistent with the involvement of IP3 in the mGluR-induced Ca2+ signal.

Cyclic ADP-ribose (cADPR) is another Ca2+-releasing messenger in mammalian systems (Petersen and Cancela, 1999). The Ca2+-mobilizing activity of cADPR was described originally in sea urchin eggs (Lee et al., 1989). Recent studies have shown that it is also involved in the cell surface receptor-mediated Ca2+ signals in pancreatic acinar cells and T-lymphocytes (Cancela et al., 1999; Guse et al., 1999). In the nervous system, cADPR has been found to potentiate Ca2+-induced Ca2+ release via ryanodine receptors and to enhance neurotransmitter release from presynaptic terminals (Hua et al., 1994; Empson and Galione, 1997; Mothet et al., 1998; Brailoiu and Miyamoto, 2000). However, the role of cADPR in mediating neurotransmitter-elicited Ca2+ release has never been demonstrated in neurons.

In this study, the intracellular second messenger cascade mediating the release of Ca2+ after activation of mGluRs in dopamine neurons was investigated using confocal imaging of [Ca2+]i combined with whole-cell recording of the membrane conductance. The results obtained show that both IP3 and cADPR mediate mGluR-induced Ca2+ mobilization.


    Materials and Methods

TOP
ABSTRACT
Introduction
Materials and Methods
Results
Discussion
REFERENCES

Slices and solutions. Horizontal slices (180-220 µm) of the ventral midbrain were prepared from adult Wistar rats (160-220 gm). Slices were cut using a Vibratome (Leica) in an ice-cold physiological saline containing (in mM): 126 NaCl, 2.5 KCl, 1.2 NaH2PO4, 1.2 MgCl2, 2.4 CaCl2, 11 glucose, 21.4 NaHCO3, saturated with 95% O2 and 5% CO2, pH 7.4, 300 mOsm/kg, and then stored in the same solution warmed to 35°C for at least 30 min. For recordings, a single slice was placed in a recording chamber and superfused with the warmed (35°C) physiological saline at 1-2 ml/min. Unless noted otherwise, pipette solutions used for whole-cell and cell-attached recordings contained (in mM): 115 K-methylsulfate, 20 KCl, 1.5 MgCl2, 10 HEPES, 0.1 EGTA, 2 Mg-ATP, 0.2 Na2-GTP, and 10 Na2 phosphocreatine, pH 7.3, 275 mOsm/kg.

Whole-cell recording. All recordings were performed in dopamine neurons, which were identified by their large cell bodies (~20 µm), the characteristic pacemaker-like firing (1-5 Hz) observed in the cell-attached mode, and the presence of a large (>200 pA) IH current. Cells were visualized using a 40 or 60× water-immersion objective on an upright microscope (Zeiss) with infrared illumination. Whole-cell pipettes had resistances of 1.5-3 MOmega . Voltage-clamp recordings were made, and the holding potential was routinely set at -55 mV. An Axopatch 1D amplifier (Axon Instruments, Foster City, CA) was used to record the data, which were filtered at 1 kHz, digitized at 5 kHz, and collected on a personal computer using AxoGraph 4 (Axon Instruments).

Cell-attached recording. The firing was monitored with the cell-attached mode, because the spontaneous firing of dopamine neurons was significantly distorted with the whole-cell recording. Usage of low-resistance pipettes (1.5-1.8 MOmega ) together with the formation of a large Omega -shape membrane invagination allowed enough access to the cell interior to monitor the membrane potential with a current-clamp recording.

Ca2+ imaging. Fluorescence imaging was made with the whole-cell recording configuration using a pipette solution containing Oregon Green 488 BAPTA-2 (50 µM). Images were taken at 15 Hz for 3-5 sec using a confocal imaging system (Solamere Technology). Ca2+ signals from selected regions of interest (ROIs) were expressed as fractional change in fluorescence, %Delta F/F = 100 × (F - Fbaseline)/(Fbaseline - Fbackground ). The inclusion of heparin and 8-NH2-cADPR in the pipette did not affect the calcium signal induced by depolarization to 0 mV (200 msec) to cause Ca2+ influx. In this control experiment, the increase in fluorescence was determined at 5 and 15 min after the onset of whole-cell recording, and the 15 min/5 min ratio was 1.3 ± 0.2 (n = 3).

Evoked mGluR-mediated responses. The mGluR-mediated release of Ca2+ is extremely vulnerable to rapid desensitization. Thus, agonists must be applied very rapidly to observe the response. This was achieved either by electrical stimulation of presynaptic fibers or by iontophoresis of aspartate. Synaptic responses were evoked with a bipolar tungsten stimulating electrode (tip separation 50-100 µm), which was placed at 30-100 µm to the recorded cell. A train of 5-10 stimuli were applied at 66 Hz to evoke the mGluR-mediated synaptic response. Iontophoresis was performed with an Axoclamp 2A amplifier (Axon Instruments) (up to 200 nA ejection current, 5-20 nA backing current) using small-tipped pipettes (40-100 MOmega ) containing 1 M aspartate. Iontophoretic pipettes were placed within 5 µm of the soma or dendrites. The direction of the pipette was made at, or close to, right angles to the longitudinal direction of the cell to ensure that aspartate was applied focally to the cell. Experiments were done in the presence of 2,3-dioxo-6-nitro-1,2,3,4- tetrahydrobenzo[f]quinoxaline-7-sulfonamide (NBQX) (5 µM), and the slices were pretreated with (5S,10R)-(+)-5-methyl-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5,10-imine (50-100 µM) to block AMPA- and NMDA-mediated responses. In experiments in which synaptic responses were elicited, picrotoxin (100 µM), CGP 35348 (100 µM), strychnine (1 µM), and eticlopride (100 nM) were further added to block GABAA, GABAB, glycine, and dopamine D2 receptors.

Flash photolysis of caged IP3. Whole-cell recordings were performed with intracellular solutions containing caged IP3 (200 µM). A xenon arc lamp (Cairn Research) was used to produce UV pulses (~1 msec). The capacitance and the voltage of the capacitor supplying current to the flash lamp were set at 4000 µF and 300 V, respectively. This evoked a near-maximal outward current in each cell.

Drugs. Drugs were applied either by extracellular perfusion or intracellular dialysis through the whole-cell pipette. A-methyl-4-carboxyphenylglycine [(S)-MCPG], 7-(hydroxyimino)cyclopropa[b]chromen-1a-carboxylate ethyl ester (CPCCOEt), dihydroxyphenylglycine [(S)-3,5-DHPG], 2-amino-5-phosphonopentanoic acid (D-AP-5), and NBQX were obtained from Tocris Cookson. Thapsigargin and ryanodine were obtained from Calbiochem (LaJolla, CA). Ruthenium red was obtained from Alomone Labs. Caged IP3, 8-NH2-cADPR , and Oregon Green 488 BAPTA-2 were obtained from Molecular Probes (Eugene, OR). CGP 35348 was a gift from Novartis. All other chemicals were obtained from Sigma (St. Louis, MO)/RBI (Natick, MA).

Data analysis. Data are expressed as mean ± SEM. Statistical significance was determined with Student's t test or one-way ANOVA followed by the post hoc Dunnett's test. The difference was considered significant at p < 0.05.


    Results

TOP
ABSTRACT
Introduction
Materials and Methods
Results
Discussion
REFERENCES

mGluR-induced wave of Ca2+

Whole-cell recordings of synaptic responses were made from dopamine neurons in rat midbrain slices. To isolate the mGluR-mediated responses, AMPA, NMDA, GABAA, GABAB, glycine, and dopamine D2 receptors were blocked pharmacologically. [Ca2+]i was monitored by the change in fluorescence of Oregon Green 488 BAPTA-2 (50 µM) loaded into the cell through the whole-cell pipette. A train of 5-10 stimuli (66 Hz) with an extracellular bipolar stimulating electrode (tip separation 50-100 µm) evoked an increase in [Ca2+]i and an outward current (n = 11) (Fig. 1A). These synaptic responses were inhibited by CPCCOEt (50-75 µM; n = 4), an mGluR antagonist. The rise in [Ca2+]i invariably originated in dendrites 10-50 µm away from the soma and propagated bi-directionally as a wave. The Ca2+ wave spread over a distance of 20-50 µm from the origin, reaching the soma in most cases. The speed of wave propagation over the initial 15-20 µm was 111 ± 29 µm/sec (n = 11) (see also Fig. 4C). Frequently, multiple waves were observed either in a same dendrite or in different dendrites and appeared to collide with one another (Fig. 1A), complicating the analysis of wave propagation.



View larger version (54K):
[in this window]
[in a new window]
  		Figure 1.   Focal activation of mGluRs induces a wave of Ca2+. A, Extracellular synaptic stimulation induced waves of Ca2+ originating in dendrites. A confocal fluorescence image of a dopamine neuron loaded with Oregon Green 488 BAPTA-2 (50 µM) is shown on the left. Fluorescence changes were measured at the ROIs placed at the origins of waves and 20 µm away from the origins toward the soma. Two Ca2+ waves (Wave 1 and Wave 2) were elicited in opposite dendrites. The IPSC evoked concomitantly is also shown. B, Focal application of aspartate elicited a wave of Ca2+ originating at the application site. A confocal fluorescence image of a dopamine neuron loaded with Oregon Green 488 BAPTA-2 (50 µM) is shown on the left. Aspartate was iontophoresed at the site indicated by the arrow. Fluorescence changes were measured at the ROIs placed every 15 µm starting at the application site. The outward current evoked by aspartate in the same cell is also shown. Aspartate was iontophoresed at the time indicated by arrows. C, The rise in [Ca2+]i and the outward current elicited by aspartate were insensitive to removal of Ca2+ from the extracellular solution for 5 min. The same treatment nearly abolished the rise in [Ca2+]i and the outward current after a depolarization (200 msec) to 0 mV (horizontal bar). D, The aspartate-evoked outward current was abolished by thapsigargin (10 µM). E, The aspartate-evoked outward current is plotted against time after going into the whole-cell mode. Recordings were made with either a control internal solution () or a solution with GDPbeta S (3 mM) (open circle ).

Next, focal application of aspartate was made with iontophoresis (50-200 msec). In these experiments, AMPA- and NMDA-mediated responses were blocked with antagonists. Aspartate iontophoresis also evoked a wave-like increase in [Ca2+]i, which originated at the site of application (supplemental material), that was accompanied with an outward current (n = 15) (Fig. 1B). Both responses were inhibited by the mGluR antagonists MCPG (1 mM; n = 2) and CPCCOEt (50-75 µM; n = 6). Furthermore, both were desensitized by perfusion with a low concentration of DHPG (1 µM; n = 10), an mGluR agonist. Thus, aspartate iontophoresis induced a focal activation of mGluRs to elicit a Ca2+ wave and an outward current.

Aspartate could be applied anywhere on the cell (both the soma and dendrites) to elicit a Ca2+ wave. The aspartate iontophoresis-induced wave traveled over a longer distance (40-80 µm) than the synaptic wave. However, the speed of propagation over the initial 15-20 µm from the origin (121 ± 16 µm/sec; n = 15) was similar to the synaptic wave (p > 0.05) (see Fig. 4C). The magnitude and the rate of the rise in [Ca2+]i, as well as the speed of propagation, decreased significantly as the wave spread away from the origin. In 12 cells in which the wave traveled >45 µm, the propagation speed measured between the origin and 15-20 µm was 123 ± 24 µm/sec. The propagation speed declined to 35 ± 4 µm/sec measured beyond 30 µm from the origin (p < 0.005). Thus, it is suggested that a diffusive process contributes to the overall wave propagation.

The rise in [Ca2+]i and the outward current evoked by aspartate were insensitive to removal of Ca2+ from the extracellular solution (n = 6) (Fig. 1C). Furthermore, the aspartate-evoked outward current was completely abolished by thapsigargin (10 µM; n = 3) (Fig. 1D), which depletes intracellular Ca2+ stores by blocking the endoplasmic reticulum Ca2+-ATPase (Thastrup et al., 1990). Inhibiting the outward current with thapsigargin revealed an aspartate-evoked inward current. It has been shown that this inward current is also mediated by activation of mGluRs but is independent of Ca2+ mobilization (Guatteo et al., 1999). These results indicate that the rise in [Ca2+]i originates from intracellular stores.

The involvement of G-proteins was examined next by applying GDPbeta S (3 mM), a general inhibitor of G-protein function, intracellularly through the whole-cell pipette. The outward current was monitored as readout of [Ca2+]i. In control, the amplitude of the aspartate-induced outward current increased over the first 10 min of recording and stabilized, averaging 169 ± 12 pA at 20 min (n = 32) (Fig. 1E). In contrast, the current gradually declined when GDPbeta S (3 mM) was included in the pipette solution and averaged 75 ± 14 pA (n = 5; p < 0.05 vs control) after 20 min. Furthermore, intracellular application of GTPgamma S (200 µM), which tonically activates G-proteins, completely occluded, or desensitized, the outward current in 1-3 min (n = 5) (data not shown). These results demonstrate that G-proteins are involved in the mGluR-mediated release of Ca2+.

IP3 is not the sole intracellular messenger responsible for the mGluR-mediated release of Ca2+

Application of IP3 directly into the cytosol has been shown to induce release of Ca2+ from intracellular stores and subsequent activation of SK channels in dopamine neurons (Morikawa et al., 2000). Furthermore, it has been shown that the IP3-evoked outward current is desensitized by superfusion of a low concentration of an mGluR agonist (Paladini et al., 2001). Thus, IP3 has been suggested to be the intracellular messenger responsible for the mGluR-mediated release of Ca2+. To directly test this idea, heparin, a competitive antagonist of IP3 receptors (Ghosh et al., 1988), was used. The effect of heparin on the outward current evoked by flash photolysis of caged IP3 (200 µM) loaded into the cytosol was examined first. Photolytic release of IP3 produced a transient outward current, as reported previously (Morikawa et al., 2000). The peak amplitude of the IP3-evoked current reached a plateau in 10-20 min after the onset of recording (228 ± 34 pA; n = 6) (Fig. 2A). Inclusion of heparin (1 mg/ml) in the internal solution completely blocked the IP3-evoked current within 10 min after breaking in (3 ± 2 pA; n = 6; p < 0.0001 vs control), indicating that heparin is an effective antagonist of IP3 receptors in dopamine neurons. In contrast, intracellular dialysis of heparin (1 mg/ml) failed to significantly affect the aspartate-induced current (136 ± 17 pA; n = 10; p > 0.05 vs control) (Fig. 2B). These results strongly suggest that an intracellular messenger besides IP3 causes Ca2+ mobilization after mGluR activation.



View larger version (27K):
[in this window]
[in a new window]
  		Figure 2.   IP3 receptors do not entirely mediate the mGluR-induced outward current. A, B, The outward current evoked by flash photolysis of caged IP3 (200 µM) (A) or iontophoretic application of aspartate (B) is plotted against time after going into the whole-cell mode. Recordings were made with either a control internal solution () or a solution with heparin (1 mg/ml) (open circle ). Representative traces of IP3-evoked currents are shown as an inset in A. C, Previous iontophoresis of aspartate completely desensitized the outward current evoked by flash photolysis of caged IP3 (200 µM) (left traces). The interval between aspartate iontophoresis and photolytic release of IP3 was 5 sec. In the same cell, previous iontophoresis of aspartate failed to completely desensitize the outward current elicited by a second application of aspartate 5 sec later (right traces). The black traces [Pre-Asp (-)] are from recordings in which the first application of aspartate was omitted, whereas the red traces [Pre-Asp (+)] are from recordings in which the aspartate iontophoresis preceded the photolytic release of IP3 (left trace) or the second aspartate iontophoresis (right trace). D, Previous photolytic release of IP3 failed to completely desensitize the outward current induced by aspartate 2 sec later. Aspartate iontophoresis and flash photolysis of caged IP3 were made at the times indicated by arrows. Photolytic release of IP3 was omitted in the black trace [Pre-IP3 (-)], whereas it was made 2 sec before aspartate iontophoresis in the red trace [Pre-IP3 (+)].

Continuous activation of mGluRs desensitizes both mGluR- and IP3-induced responses (Paladini et al., 2001). To gain further insight into the intracellular mechanism involved, the interaction of the mGluR-mediated and the IP3-evoked responses was investigated by sequentially applying aspartate with iontophoresis and IP3 with flash photolysis of caged IP3 (200 µM). In the cell shown in Figure 2C, the outward current produced by photolytic release of IP3 was completely desensitized when aspartate was applied 5 sec before; however, aspartate still evoked a considerable outward current at 5 sec after aspartate iontophoresis in the same cell. The same observation was made in two other cells. Furthermore, photolytic release of IP3 2-5 sec before aspartate iontophoresis failed to completely desensitize the aspartate-elicited current in four cells tested (Fig. 2D). These results are consistent with the idea that the mGluR-mediated response involves an IP3-independent mechanism.

Both IP3 and cADPR pathways mediate the mGluR-induced release of Ca2+

To search for an alternative intracellular mechanism, 8-NH2-cADPR, a specific cADPR antagonist (Walseth and Lee, 1993), was used. The effects of heparin and 8-NH2-cADPR were tested on mGluR IPSCs. Recordings were first made with a pipette containing a control internal solution to obtain a control IPSC amplitude (Fig. 3A). In this way, the stimulus intensity was optimized in each cell. After the first pipette was removed from the cell, a second pipette containing a control internal solution or a solution with heparin (1 mg/ml) alone, 8-NH2-cADPR (50 µM) alone, or both heparin and 8-NH2-cADPR was patched onto the same cell, and IPSCs were evoked with the same stimulus intensity. The amplitude of the IPSC in the first recording (~10 min after the onset; IPSC1) was used to normalize the IPSC amplitude obtained with the second pipette (IPSC2). The normalized IPSC amplitude (IPSC2/IPSC1) measured 20 min after the onset of the second recording was similar when the second pipette contained the control solution, heparin alone, or 8-NH2-cADPR alone (Fig. 3B). The IPSP was significantly smaller only in the presence of both heparin and 8-NH2-cADPR (0.11 ± 0.04, n = 4, vs 1.47 ± 0.18 with control solution, n = 3; p < 0.001) (Fig. 3A,B).



View larger version (20K):
[in this window]
[in a new window]
  		Figure 3.   Simultaneous blockade of IP3- and cADPR-induced signaling inhibits mGluR IPSCs. A, Intracellular dialysis of both heparin (1 mg/ml) and 8-NH2-cADPR (50 µM) nearly abolished mGluR IPSCs. The cell was first recorded with a control internal solution to obtain a control IPSC amplitude (IPSC1) at ~10 min after the onset of recording. The same cell was subsequently patched with a pipette containing a control solution or a solution with both heparin and 8-NH2-cADPR. IPSCs were recorded by applying the same train of stimuli used for the first patch (IPSC2) and plotted after they were normalized by the IPSC1. Representative traces are shown above. B, The normalized IPSC amplitudes at 20 min of recording are shown for the second patch with a control solution or a solution containing heparin (1 mg/ml) alone, 8-NH2-cADPR (50 µM) alone, or both heparin and 8-NH2-cADPR.

The effect of 8-NH2-cADPR was also examined on the aspartate-evoked responses. Intracellular dialysis of 8-NH2-cADPR (50 µM) alone had no significant effect on the aspartate-evoked current (136 ± 19 pA, n = 22, p > 0.05 vs control) (Fig. 4A). However, inclusion of heparin (1 mg/ml) together with 8-NH2-cADPR (50 µM) in the pipette abolished the aspartate-evoked outward current and turned it into inward in 8 of 11 cells tested. On average, the current amplitude in the presence of both heparin and 8-NH2-cADPR was -14 ± 12 pA (inward; n = 11, p < 0.001 vs control) at 20 min. The effects of heparin and 8-NH2-cADPR were also tested on the rise in [Ca2+]i produced by aspartate. Here, the rise in [Ca2+]i at the soma was first measured with a control solution containing Oregon Green 488 BAPTA-2 (50 µM) (Fig. 4B). Then, the pipette was withdrawn, and a second pipette containing both heparin (1 mg/ml) and 8-NH2-cADPR (50 µM) together with Oregon Green 488 BAPTA-2 was used to make a second whole-cell recording from the same cell. In the second recording, the rise in [Ca2+]i was reduced to <10% of control after 15-20 min in all three cells tested. When the second pipette contained only the calcium indicator, the rise in [Ca2+]i was not significantly different from the first recording (second/first = 1.0 ± 0.2; n = 4). Aspartate elicited a Ca2+ wave in the presence of either heparin or 8-NH2-cADPR alone that had a propagation velocity that was not significantly different from the wave with a control solution (Fig. 4C).



View larger version (20K):
[in this window]
[in a new window]
  		Figure 4.   Simultaneous blockade of IP3- and cADPR-induced signaling inhibits mGluR-mediated responses. A, The aspartate-induced outward current is plotted versus time after going into the whole-cell mode. Recordings were made with a pipette containing a control internal solution (), 8-NH2-cADPR (50 µM) (open circle ), or both heparin (1 mg/ml) and 8-NH2-cADPR (50 µM) (). B, Traces of the rise in [Ca2+]i and the outward current evoked by aspartate iontophoresis. Recordings on the left were done with control internal solution containing Oregon Green 488 BAPTA-2 (50 µM). The traces on the right were from a second recording in the same cell using a pipette containing both heparin (1 mg/ml) and 8-NH2-cADPR (50 µM) in addition to Oregon Green 488 BAPTA-2. C, A bar graph showing the speed of propagation at the initial 15-20 µm from the origin for the Ca2+ waves induced by synaptic stimulation and aspartate iontophoresis. For aspartate iontophoresis, the speed is shown for the recordings with a control internal solution and a solution with either heparin (1 mg/ml) alone or 8-NH2-cADPR (50 µM) alone.

Taken together, these results demonstrate that the mGluR-mediated Ca2+ mobilization involves two pathways mediated by IP3 and cADPR in a redundant manner.

Ryanodine receptors mediate the cADPR pathway

cADPR is known to act on ryanodine receptors (Galione et al., 1991; Meszaros et al., 1993). To examine the involvement of ryanodine receptors in the cADPR-dependent pathway, ruthenium red, an antagonist of ryanodine receptors (Smith et al., 1988), was tested. Intracellular dialysis of ruthenium red (50 µM) alone had no significant effect on the aspartate-evoked current (123 ± 11 pA, n = 6, p > 0.05 vs control) (Fig. 5A). However, when the IP3-dependent pathway was blocked with heparin (1 mg/ml), intracellular ruthenium red significantly suppressed the aspartate-evoked current (59 ± 12 pA, n = 8, p < 0.001 vs control). The small outward current remaining in the presence of both heparin and ruthenium red may be caused by an incomplete blockade of ryanodine receptors by ruthenium red. These results show that the cADPR pathway is dependent on the activation of ryanodine receptors.



View larger version (22K):
[in this window]
[in a new window]
  		Figure 5.   Ryanodine receptors mediate the cADPR pathway. A, The aspartate-evoked outward current is plotted versus time after the onset of recording. Recordings were made with a pipette containing a control internal solution (), ruthenium red (50 µM) (open circle ), or both heparin (1 mg/ml) and ruthenium red (50 µM) (). B, A summary time graph showing the effect of ryanodine (10 µM) on the aspartate-evoked outward current. Recordings were done with a control internal solution () or a solution with heparin (1 mg/ml) (open circle ). Ryanodine was perfused for 20 min at the time indicated by the bar. The data are shown after the amplitude of the aspartate-induced current had reached a steady state (15-20 min after the onset of whole-cell recording). Current amplitude was normalized to the mean amplitude over a 5 min period before ryanodine application. Representative traces before and after ryanodine application are shown above. C, A summary bar graph showing the effect of ryanodine (10 µM) on the aspartate-induced current recorded with a control internal solution and a solution with either heparin (1 mg/ml) or 8-NH2-cADPR (50 µM). The hatched bar shows the effect of ryanodine (20 µM) on the current with a control internal solution. **p < 0.01.

To further confirm the involvement of ryanodine receptors, the effect of ryanodine was examined next. Ryanodine locks the ryanodine receptor channel in a subconductance open state (Rousseau et al., 1987). Thus, ryanodine blocks the ryanodine receptor-dependent Ca2+ signal in two ways by (1) preventing the full activation of ryanodine receptors and (2) gradually depleting the stores expressing ryanodine receptors, whereas the IP3-induced Ca2+ release will be inhibited by ryanodine only via the second mechanism, i.e., store depletion, if the IP3-sensitive stores coexpress ryanodine receptors (Khodakhah and Armstrong, 1997; Morikawa et al., 2000). Therefore, the ryanodine receptor-mediated Ca2+ signal is expected to be more sensitive to ryanodine, because ryanodine can more directly block it even before store depletion. Bath perfusion of ryanodine (10 µM) for 20 min reduced the aspartate-evoked current by 44 ± 6% (n = 12) (Fig. 5B,C). When the IP3-dependent pathway was blocked with heparin (1 mg/ml), the rate of ryanodine block was accelerated, and ryanodine nearly abolished the aspartate-induced current after 20 min (99 ± 12% inhibition, n = 5, p < 0.001 vs control). On the other hand, when the cADPR-dependent pathway was blocked with 8-NH2-cADPR (50 µM), ryanodine produced an inhibition of the aspartate-evoked current comparable with that of the control current (42 ± 7% inhibition, n = 5, p > 0.05 vs control). Hence, the cADPR-dependent pathway was significantly more sensitive to the ryanodine blockade than the IP3-dependent pathway (p < 0.001), which is consistent with the involvement of ryanodine receptors in the cADPR-dependent pathway. Increasing the concentration of ryanodine to 20 µM completely blocked the control aspartate-induced current in 20 min (108 ± 19% inhibition; n = 4) (Fig. 5C). The accelerated blockade achieved by the higher concentration of ryanodine (20 µM) was most likely caused by the accelerated depletion of IP3-sensitive stores coexpressing ryanodine receptors. In this series of experiments, the calculated inhibition of the outward current is likely to be a slight overestimate of the true value, because the outward current is riding on top of an inward current.

mGluR-mediated hyperpolarization induces a pause of firing

The effect of extracellular synaptic stimulation or aspartate iontophoresis on the firing was examined next. These experiments were done in the absence of AMPA and NMDA antagonists. In the case of synaptic stimulation, GABAA, GABAB, glycine, and dopamine D2 receptors were blocked with respective antagonists. The firing was monitored with a cell-attached configuration. Dopamine neurons displayed a spontaneous pacemaker-type firing with a firing frequency of 1-5 Hz, as reported previously (Fig. 6) (Grace and Onn, 1989). Repetitive extracellular stimulation (8-10 stimuli at 66 Hz) induced a pause of firing lasting 1-2 sec in all five cells tested. A burst of firing lasting ~200 msec with a firing frequency of ~20 Hz preceded the pause in two of five cells. Iontophoretic application of aspartate (50-200 msec) invariably induced a burst firing (10-20 Hz for 200-500 msec) followed by a pause lasting 0.5-5 sec (n = 10). Perfusion of MCPG (1 mM), an mGluR antagonist, dramatically attenuated the pause (n = 2 for synaptic stimulation, n = 3 for iontophoresis). Furthermore, perfusion with a low concentration of DHPG (1 µM), an mGluR agonist, also reversibly inhibited the pause (n = 3 for synaptic stimulation, n = 5 for iontophoresis) by desensitizing the mGluR-mediated hyperpolarization. On the other hand, bath application of AP-5 (50 µM), an NMDA antagonist, reversibly inhibited the burst without affecting the pause (n = 2 for synaptic stimulation, n = 5 for iontophoresis). Therefore, synaptic release of glutamate, as well as aspartate iontophoresis, evoked an NMDA receptor-dependent burst followed by a pause caused by the mGluR-mediated hyperpolarization.



View larger version (28K):
[in this window]
[in a new window]
  		Figure 6.   mGluR-mediated hyperpolarization induces a pause after burst firing. The firing pattern of a dopamine neuron is shown in the control condition, in the presence of MCPG (1 mM), and in the presence of AP-5 (50 µM). Repetitive synaptic stimulation (8 stimuli at 66 Hz; left traces) or aspartate iontophoresis (200 msec; right traces) were made at the times indicated by bars.


    Discussion

TOP
ABSTRACT
Introduction
Materials and Methods
Results
Discussion
REFERENCES

This study demonstrates that mGluRs can release Ca2+ in dopamine neurons through the activation of both IP3 and ryanodine receptors. The activation of either receptor alone is sufficient to cause the release of Ca2+. IP3 and cADPR most likely mediate the activation of IP3 and ryanodine receptors, respectively (Fig. 7). This is in accord with previous reports showing that the fertilization-induced Ca2+ wave in sea urchin eggs is mediated by a redundant mechanism involving both IP3 and cADPR (Galione et al., 1993; Lee et al., 1993). Finally, mGluR-induced hyperpolarization resulting from the rise in [Ca2+]i is shown to mediate the pause of firing that acts to curtail the burst firing caused by NMDA receptor activation. This observation would provide a cellular mechanism responsible for the burst-pause type of firing observed in vivo.



View larger version (24K):
[in this window]
[in a new window]
  		Figure 7.   Proposed intracellular signaling cascade mediating the mGluR-induced Ca2+ mobilization. Activation of mGluRs leads to dual activation of phospholipase C (PLC) and ADP-ribosyl cyclase (ADPRC). PLC catalyzes the production of IP3, whereas ADPRC catalyzes the production of cADPR. IP3 and cADPR induce release of Ca2+ via IP3 receptors (IP3R) and ryanodine receptors (RyR), respectively. IP3Rs and RyRs are coexpressed on a common Ca2+ pool.

A wave of Ca2+

In the present study, both synaptic release of glutamate and focal application of aspartate evoked a wave of Ca2+. Repetitive stimulation of glutamatergic fibers was necessary to elicit a Ca2+ wave, suggesting that extrasynaptic spillover of glutamate may mediate the activation of postsynaptic mGluRs (Brasnjo and Otis, 2001). In line with this, group I mGluRs have been located at extrasynaptic sites in the SNc (Hubert et al., 2001). The aspartate-induced wave initiated at the application site regardless of the placement of the iontophoretic pipette, indicating that the machinery necessary for the mGluR-mediated Ca2+ mobilization is present throughout the cell. On the other hand, the origin of the synaptic wave was invariably located in dendrites. Glutamatergic synapses are widely distributed in dopamine neurons, on both the soma and dendrites (Smith et al., 1996). Multiple glutamatergic fibers synapsing on both the soma and dendrites were most likely stimulated in the present study, because the bipolar stimulating electrode used had a wide tip separation (50-100 µm). Therefore, it is possible that only the synapses on dendrites are associated with sufficient levels of perisynaptic mGluRs to induce the release of Ca2+. Indeed, mGluRs are expressed more densely in dendrites than in the soma in dopamine neurons (Kosinski et al., 1998).

The mGluR-induced Ca2+ signal has different spatiotemporal profiles in different neurons (Finch and Augustine, 1998; Takechi et al., 1998; Nakamura et al., 1999, 2000). In this study, the velocity and amplitude of the wave tended to decline as it spread away from the origin, suggesting that diffusion of intracellular messengers, in concert with a regenerative process, may contribute to the overall wave propagation. The propagation of the wave front of the aspartate-induced wave could be well fitted to a diffusion equation (distance = (6Dt)1/2, where D is the diffusion coefficient), which gave an average diffusion coefficient of 378 ± 35 µm2/sec (n = 15). This is in good agreement with the known diffusion coefficient of IP3 (283 µm2/sec) measured in Xenopus oocytes (Allbritton et al., 1992). To our knowledge, the diffusion coefficient of cADPR has not been reported. The speed of wave propagation was not affected when either the IP3- or the cADPR-mediated release was isolated (Fig. 4C), suggesting that their diffusion rates may be in the similar range.

Intracellular signaling cascade

Experiments with GDPbeta S and GTPgamma S confirmed the involvement of G-proteins. It is well established that the Gq family of G-proteins couples various neurotransmitter receptors, including group I mGluRs expressed in dopamine neurons, to the phospholipase C-IP3 cascade (Hepler and Gilman, 1992). The synthesis of cADPR is catalyzed by the enzyme ADP-ribosyl cyclase; however, it is not known what subtype of G-proteins activates this enzyme. Recent evidence suggests that cell surface receptors can stimulate ADP-ribosyl cyclase activity in various mammalian cells (Cancela, 2001; Lee, 2001). In particular, the involvement of G-proteins was suggested in the cases of muscarinic receptor- and beta -adrenergic receptor-mediated stimulation of ADP-ribosyl cyclase in NG108-15 cells and cardiac myocytes, respectively (Higashida et al., 1997, 1999).

In neurons, IP3 acting on IP3 receptors is thought to be solely responsible for the Ca2+ mobilization after activation of mGluRs and other G-protein-coupled receptors (Finch and Augustine, 1998; Takechi et al., 1998; Nakamura et al., 1999, 2000; Power and Sah, 2002). Previous studies in cultured cerebellar granule neurons have proposed that ryanodine receptor-mediated Ca2+ mobilization acts to amplify the IP3-induced Ca2+ signal via Ca2+-induced Ca2+ release (Irving et al., 1992; Simpson et al., 1995, 1996). This proposal was based mainly on the inhibitory effect of ryanodine on mGluR- and muscarinic acetylcholine receptor-mediated Ca2+ signals, which were known to involve IP3-dependent Ca2+ mobilization. However, ryanodine, which locks ryanodine receptor channels in an open state, may have caused depletion of IP3-sensitive stores if those stores coexpressed ryanodine receptors (Khodakhah and Armstrong, 1997; Morikawa et al., 2000).

mGluR-mediated hyperpolarization and firing pattern

Dopamine neurons display a spectrum of activity ranging from pacemaker-like firing to burst firing in vivo. The burst firing is often followed by a pause of activity (Overton and Clark, 1997; Kitai et al., 1999). In contrast, they fire in a uniform pacemaker mode in a slice preparation, which is assumed to result from the loss of active synaptic inputs. In the present study, stimulation of glutamatergic fibers, as well as focal application of aspartate, reproduced the burst-pause pattern observed in vivo. A large body of evidence has implicated the glutamatergic inputs as the trigger for the burst, mainly by activating NMDA receptors (Overton and Clark, 1997; Kitai et al., 1999). In line with this, the burst was blocked by an NMDA receptor antagonist. In contrast, very few studies have addressed the mechanism of the pause, which has been explained mainly as a rebound phenomenon of the burst itself (Shepard and Bunney, 1991; Johnson et al., 1992). Our data show that the mGluR-induced hyperpolarization can mediate the pause independent of the burst.

Studies in monkeys have shown that burst firing of dopamine neurons is elicited by explicit reward-predicting stimuli. However, the pause of activity after the burst is promoted by presentation of stimuli that resemble, but are different from, these reward-predicting stimuli or some novel stimuli that are not necessarily related to rewards (Schultz, 1998). These data suggest that the pause by itself is caused by highly processed afferent inputs, rather than a rebound phenomenon of the burst. The present study proposes that a redundant mechanism activated by glutamatergic inputs ensures precise control of the firing pattern of dopamine neurons.


    FOOTNOTES

Received July 23, 2002; revised Sept. 16, 2002; accepted Oct. 22, 2002.

This work was supported by National Institutes of Health Grant DA04523. We thank Olivier Manzoni for comments on this manuscript.

Correspondence should be addressed to John T. Williams, Vollum Institute, Oregon Health and Science University, Portland, OR 97201. E-mail: williamj{at}ohsu.edu.

H. Morikawa's present address: Waggoner Center for Alcohol and Addiction Research, University of Texas, 2500 Speedway, MBB 1.150A, Austin, TX 78712.


    References

TOP
ABSTRACT
Introduction
Materials and Methods
Results
Discussion
REFERENCES

  • Allbritton NL, Meyer T, Stryer L (1992) Range of messenger action of calcium ion and inositol 1,4,5-trisphosphate. Science 258:1812-1815[Abstract/Free Full Text].
  • Berridge MJ (1998) Neuronal calcium signaling. Neuron 21:13-26[ISI][Medline].
  • Brailoiu E, Miyamoto MD (2000) Inositol trisphosphate and cyclic adenosine diphosphate-ribose increase quantal transmitter release at frog motor nerve terminals: possible involvement of smooth endoplasmic reticulum. Neuroscience 95:927-931[Medline].
  • Brasnjo G, Otis TS (2001) Neuronal glutamate transporters control activation of postsynaptic metabotropic glutamate receptors and influence cerebellar long-term depression. Neuron 31:607-616[ISI][Medline].
  • Cancela JM (2001) Specific Ca2+ signaling evoked by cholecystokinin and acetylcholine: the roles of NAADP, cADPr, and IP3. Annu Rev Physiol 63:99-117[ISI][Medline].
  • Cancela JM, Churchill GC, Galione A (1999) Coordination of agonist-induced Ca2+-signalling patterns by NAADP in pancreatic acinar cells. Nature 398:74-76[Medline].
  • Empson RM, Galione A (1997) Cyclic ADP-ribose enhances coupling between voltage-gated Ca2+ entry and intracellular Ca2+ release. J Biol Chem 272:20967-20970[Abstract/Free Full Text].
  • Finch EA, Augustine GJ (1998) Local calcium signalling by inositol-1,4,5-triphosphate in Purkinje cell dendrites. Nature 396:753-756[Medline].
  • Fiorillo CD, Williams JT (1998) Glutamate mediates an inhibitory postsynaptic potential in dopamine neurons. Nature 394:78-82[Medline].
  • Galione A, Lee HC, Busa WB (1991) Ca2+-induced Ca2+ release in sea urchin egg homogenates and its modulation by cyclic ADP-ribose. Science 253:1143-1146[Abstract/Free Full Text].
  • Galione A, McDougall A, Busa WB, Willmott N, Gillot I, Whitaker M (1993) Redundant mechanism of calcium-induced calcium release underlying calcium waves during fertilization of sea urchin eggs. Science 261:348-352[Abstract/Free Full Text].
  • Ghosh TK, Eis PS, Mullaney JM, Ebert CL, Gill DL (1988) Competitive, reversible, and potent antagonism of inositol 1,4,5-triphosphate-activated calcium release by heparin. J Biol Chem 263:11075-11079[Abstract/Free Full Text].
  • Grace AA, Onn SP (1989) Morphology and electrophysiological properties of immunocytochemically identified rat dopamine neurons recorded in vitro. J Neurosci 9:3463-3481[Abstract].
  • Guatteo E, Mercuri NB, Bernardi G, Knopfel T (1999) Group I metabotropic glutamate receptors mediate an inward current in rat substantia nigra dopamine neurons that is independent from calcium mobilization. J Neurophysiol 82:1974-1981[Abstract/Free Full Text].
  • Guse AH, da Silva CP, Berg I, Skapenko AL, Weber K, Heyer P, Hohenegger M, Ashamu GA, Schulze-Koops H, Potter BV, Mayr GW (1999) Regulation of calcium signalling in T lymphocytes by the second messenger cyclic ADP-ribose. Nature 398:70-73[Medline].
  • Hepler JR, Gilman AG (1992) G proteins. Trends Biochem Sci 17:383-387[ISI][Medline].
  • Higashida H, Yokoyama S, Hashii M, Taketo M, Higashida M, Takayasu T, Ohshima T, Takasawa S, Okamoto H, Noda M (1997) Muscarinic receptor-mediated dual regulation of ADP-ribosyl cyclase in NG108-15 neuronal cell membranes. J Biol Chem 272:31272-31277[Abstract/Free Full Text].
  • Higashida H, Egorova A, Higashida C, Zhong ZG, Yokoyama S, Noda M, Zhang JS (1999) Sympathetic potentiation of cyclic ADP-ribose formation in rat cardiac myocytes. J Biol Chem 274:33348-33354[Abstract/Free Full Text].
  • Hua SY, Tokimasa T, Takasawa S, Furuya Y, Nohmi M, Okamoto H, Kuba K (1994) Cyclic ADP-ribose modulates Ca2+ release channels for activation by physiological Ca2+ entry in bullfrog sympathetic neurons. Neuron 12:1073-1079[ISI][Medline].
  • Hubert GW, Paquet M, Smith Y (2001) Differential subcellular localization of mGluR1a and mGluR5 in the rat and monkey substantia nigra. J Neurosci 21:1838-1847[Abstract/Free Full Text].
  • Irving AJ, Collingridge GL, Schofield JG (1992) Interactions between Ca2+ mobilizing mechanisms in cultured rat cerebellar granule cells. J Physiol (Lond) 456:667-680[Abstract/Free Full Text].
  • Johnson SW, Seutin V, North RA (1992) Burst firing in dopamine neurons induced by N-methyl-D-aspartate: role of electrogenic sodium pump. Science 258:665-667[Abstract/Free Full Text].
  • Khodakhah K, Armstrong CM (1997) Inositol trisphosphate and ryanodine receptors share a common functional Ca2+ pool in cerebellar Purkinje neurons. Biophys J 73:3349-3357[Abstract/Free Full Text].
  • Kitai ST, Shepard PD, Callaway JC, Scroggs R (1999) Afferent modulation of dopamine neuron firing patterns. Curr Opin Neurobiol 9:690-697[ISI][Medline].
  • Kosinski CM, Standaert DG, Testa CM, Penney Jr JB, Young AB (1998) Expression of metabotropic glutamate receptor 1 isoforms in the substantia nigra pars compacta of the rat. Neuroscience 86:783-798[ISI][Medline].
  • Lee HC (2001) Physiological functions of cyclic ADP-ribose and NAADP as calcium messengers. Annu Rev Pharmacol Toxicol 41:317-345[ISI][Medline].
  • Lee HC, Walseth TF, Bratt GT, Hayes RN, Clapper DL (1989) Structural determination of a cyclic metabolite of NAD+ with intracellular Ca2+ mobilizing activity. J Biol Chem 264:1608-1615[Abstract/Free Full Text].
  • Lee HC, Aarhus R, Walseth TF (1993) Calcium mobilization by dual receptors during fertilization of sea urchin eggs. Science 261:352-355[Abstract/Free Full Text].
  • Meszaros LG, Bak J, Chu A (1993) Cyclic ADP-ribose as an endogenous regulator of the non-skeletal type ryanodine receptor Ca2+ channel. Nature 364:76-79[Medline].
  • Morikawa H, Imani F, Khodakhah K, Williams JT (2000) Inositol 1,4,5-triphosphate-evoked responses in midbrain dopamine neurons. J Neurosci 20:RC103(1-5).
  • Mothet JP, Fossier P, Meunier FM, Stinnakre J, Tauc L, Baux G (1998) Cyclic ADP-ribose and calcium-induced calcium release regulate neurotransmitter release at a cholinergic synapse of Aplysia. J Physiol (Lond) 507:405-414[Abstract/Free Full Text].
  • Nakamura T, Barbara JG, Nakamura K, Ross WN (1999) Synergistic release of Ca2+ from IP3-sensitive stores evoked by synaptic activation of mGluRs paired with backpropagating action potentials. Neuron 24:727-737[ISI][Medline].
  • Nakamura T, Nakamura K, Lasser-Ross N, Barbara JG, Sandler VM, Ross WN (2000) Inositol 1,4,5-trisphosphate (IP3)-mediated Ca2+ release evoked by metabotropic agonists and backpropagating action potentials in hippocampal CA1 pyramidal neurons. J Neurosci 20:8365-8376[Abstract/Free Full Text].
  • Overton PG, Clark D (1997) Burst firing in midbrain dopamine neurons. Brain Res Rev 25:312-334[Medline].
  • Paladini CA, Fiorillo CD, Morikawa H, Williams JT (2001) Amphetamine selectively blocks glutamate transmission in dopamine neurons. Nat Neurosci 4:275-281[ISI][Medline].
  • Petersen OH, Cancela JM (1999) New Ca2+-releasing messengers: are they important in the nervous system? Trends Neurosci 22:488-495[Medline].
  • Power JM, Sah P (2002) Nuclear calcium signaling evoked by cholinergic stimulation in hippocampal CA1 pyramidal neurons. J Neurosci 22:3454-3462[Abstract/Free Full Text].
  • Rousseau E, Smith JS, Meissner G (1987) Ryanodine modifies conductance and gating behavior of single Ca2+ release channel. Am J Physiol 253:C364-C368[Abstract/Free Full Text].
  • Schultz W (1998) Predictive reward signal of dopamine neurons. J Neurophysiol 80:1-27[Abstract/Free Full Text].
  • Shepard PD, Bunney BS (1991) Repetitive firing properties of putative dopamine-containing neurons in vitro: regulation by an apamin-sensitive Ca2+-activated K+ conductance. Exp Brain Res 86:141-150[ISI][Medline].
  • Simpson PB, Challiss RA, Nahorski SR (1995) Neuronal Ca2+ stores: activation and function. Trends Neurosci 18:299-306[ISI][Medline].
  • Simpson PB, Nahorski SR, Challiss RA (1996) Agonist-evoked Ca2+ mobilization from stores expressing inositol 1,4,5-trisphosphate receptors and ryanodine receptors in cerebellar granule neurones. J Neurochem 67:364-373[ISI][Medline].
  • Smith JS, Imagawa T, Ma J, Fill M, Campbell KP, Coronado R (1988) Purified ryanodine receptor from rabbit skeletal muscle is the calcium-release channel of sarcoplasmic reticulum. J Gen Physiol 92:1-26[Abstract/Free Full Text].
  • Smith Y, Charara A, Parent A (1996) Synaptic innervation of midbrain dopaminergic neurons by glutamate-enriched terminals in the squirrel monkey. J Comp Neurol 364:231-253[ISI][Medline].
  • Takechi H, Eilers J, Konnerth A (1998) A new class of synaptic response involving calcium release in dendritic spines. Nature 396:757-760[Medline].
  • Thastrup O, Cullen PJ, Drobak BK, Hanley MR, Dawson AP (1990) Thapsigargin, a tumor promoter, discharges intracellular Ca2+ stores by specific inhibition of the endoplasmic reticulum Ca2+-ATPase. Proc Natl Acad Sci USA 87:2466-2470[Abstract/Free Full Text].
  • Walseth TF, Lee HC (1993) Synthesis and characterization of antagonists of cyclic-ADP-ribose-induced Ca2+ release. Biochem Biophys Acta 1178:235-242[Medline].

Copyright © 2003 Society for Neuroscience  0270-6474/03/231149-09$05.00/0


This article has been cited by other articles:


Home page
 J. Neurosci.Home page
J. M. Power and P. Sah
Competition between Calcium-Activated K+ Channels Determines Cholinergic Action on Firing Properties of Basolateral Amygdala Projection Neurons
J. Neurosci., March 19, 2008; 28(12): 3209 - 3220.
[Abstract] [Full Text] [PDF]

Home page
 J. Neurosci.Home page
B. Pan, C. J. Hillard, and Q.-s. Liu
Endocannabinoid Signaling Mediates Cocaine-Induced Inhibitory Synaptic Plasticity in Midbrain Dopamine Neurons
J. Neurosci., February 6, 2008; 28(6): 1385 - 1397.
[Abstract] [Full Text] [PDF]

Home page
 Cereb CortexHome page
A. M. Hagenston, J. S. Fitzpatrick, and M. F. Yeckel
MGluR-Mediated Calcium Waves that Invade the Soma Regulate Firing in Layer V Medial Prefrontal Cortical Pyramidal Neurons
Cereb Cortex, February 1, 2008; 18(2): 407 - 423.
[Abstract] [Full Text] [PDF]

Home page
 J. Physiol.Home page
M. Hong and W. N. Ross
Priming of intracellular calcium stores in rat CA1 pyramidal neurons
J. Physiol., October 1, 2007; 584(1): 75 - 87.
[Abstract] [Full Text] [PDF]

Home page
 J. Physiol.Home page
J. M. Power and P. Sah
Distribution of IP3-mediated calcium responses and their role in nuclear signalling in rat basolateral amygdala neurons
J. Physiol., May 1, 2007; 580(3): 835 - 857.
[Abstract] [Full Text] [PDF]

Home page
 J. Neurosci.Home page
G. Cui, B. E. Bernier, M. T. Harnett, and H. Morikawa
Differential Regulation of Action Potential- and Metabotropic Glutamate Receptor-Induced Ca2+ Signals by Inositol 1,4,5-Trisphosphate in Dopaminergic Neurons
J. Neurosci., April 25, 2007; 27(17): 4776 - 4785.
[Abstract] [Full Text] [PDF]