Corrections in Etz Hayim, Various Printings 2nd (2001), 3rd (2002), 4th (2003), 6th (2006), 11th (2013) Element on Page Locale within Element Correction Made Type of problem addressed Inserted letter zayin — replacing « l’mah.ikim » with « l’mah.azikim ». Replaced letter h.et with letter hei. Making room for new Table of Torah ReadingsInserted: «Table of Torah Re
Guybrown.netNitric Oxide Induces Rapid, Calcium-
Dependent Release of Vesicular
Glutamate and ATP From Cultured
ANNA BAL-PRICE,1* ZAHID MONEER,2 AND GUY C. BROWN1
1Department of Biochemistry, University of Cambridge, Cambridge, U.K. 2Department of Pharmacology, University of Cambridge, Cambridge, U.K. KEY WORDS glia; calcium; inflammation; excitotoxicity; neurodegeneration ABSTRACT Nitric oxide (NO; 1 M) or an NO donor (500 M diethylenetriamine-nitricoxide, DETA-NONOate) caused rapid glutamate and ATP release from cultured rat corticalastrocytes. NO-induced glutamate release was prevented by calcium chelators (EGTA orBAPTA-AM) and an inhibitor of vesicular exocytosis (botulinum neurotoxin C, BoTx-C), butnot by a glutamate transport inhibitor, L-trans-pyrrolidine-2,4-dicarboxylate (t-PDC), acyclooxygenase inhibitor (indomethacin), or an inhibitor of soluble guanylate cyclase 1H-[1,2,4]oxadiazolo-[4,3-a]quinoxalin-1-one (ODQ), and was not induced by mitochondrialrespiratory inhibitors (myxothiazol or azide). Similarly to glutamate, NO-induced ATPrelease was also completely blocked by BAPTA-AM and BoTx-C, suggesting again a vesic-ular, calcium-dependent mechanism of release. Addition of DETA-NONOate (500 M) tofura-2–loaded astrocytes induced a rapid, transient increase in intracellular calcium levelsfollowed by a lower, sustained level of calcium entry. The latter was blocked by gadolinium(1 M), an inhibitor of capacitative Ca2ϩ entry. Thus, NO appears to cause rapid exocytosisof vesicular glutamate and ATP from astrocytes by raising intracellular calcium levels.
Astrocytes activated by lipopolysaccharide/endotoxin and interferon-␥ to express inducibleNO synthase (iNOS) maintained substantially higher extracellular glutamate levels thannonactivated cells or activated cells treated with an iNOS inhibitor (1400W), but the rate ofglutamate uptake by these cells was similar. This suggests that NO from inflammatory-activated astrocytes causes release of astrocytic glutamate. NO-induced release of astrocyticglutamate and ATP may be important in physiological or pathological communicationbetween astrocytes and neurons. GLIA 40:312–323, 2002. 2002 Wiley-Liss, Inc.
erative diseases (including multiple sclerosis, AIDS de-mentia, Parkinson’s, Huntington’s, Alzheimer’s, and Physiologically nitric oxide (NO) derived from neu- motor neuron diseases) (Heales et al., 1999; Ignarro, ronal (nNOS) or endothelial (eNOS) NO synthase may 2000; Murphy, 2000). For example, in Alzheimer’s dis- act as an intercellular messenger between neurons, ease, activated microglia and astrocytes expressing astrocytes, and other brain cells (Dinerman et al.,1994; Garthwaite and Boulton, 1995; Prast and Phil- Grant sponsor: the Wellcome Trust; Grant sponsor: Biotechnology and Biolog- ippu, 2001). Pathologically inducible NO synthase ical Sciences Research Council (BBSRC); Grant sponsor: Medical ResearchCouncil (MRC).
(iNOS) may be induced in glia by inflammatory medi- *Correspondence to: Anna Bal-Price, Department of Biochemistry, University ators, and the high level of NO produced may contrib- of Cambridge, Tennis Court Road, Cambridge, CB2 1QW, U.K.
ute to killing neurons in inflammatory, infectious, isch- emic, and neurodegenerative diseases (Loihl and Received 26 March 2002; Accepted 14 June 2002 Murphy, 1998; Bolanos and Almeida, 1999; Knott etal., 2000). NO has been implicated in most neurodegen- iNOS are found in the amyloid plaques surrounded by isolated from cerebral hemispheres were dissociated in dead and dystrophic neurites (Wa et al., 1996; Wallace Hanks’ balanced salt solution (HBSS) containing 0.25% et al., 1997; Lee et al., 1999). ␤-amyloid can induce trypsin (Sigma, Poole, U.K.) and 0.02 mg/ml deoxyri- cultured glia to express iNOS and kill cocultured neu- bonuclease I (Sigma-Aldrich, Steinheim, Germany) rons via NO (Goodwin et al., 1995; Wisniewski et al., and plated at a density of 0.1 ϫ 106 cells/cm2 in 25 or 75 1998) and anti-inflammatory drugs protect against Alz- cm2 culture flasks (Falcon) in DMEM with 10% of fetal heimer’s disease (McGeer and McGeer, 1995; McGeer calf serum. For measurements of [Ca2ϩ] , the cells were grown on coverslips (9 ϫ 22 mm). At confluency (12–14 NO and iNOS-expressing glia can kill neurons in cul- days in vitro, DIV), primary glial cultures were used to ture by excitotoxic mechanisms involving extracellular isolate microglial cells as previously described (Taupe- glutamate (Hewett et al., 1994; Leist et al., 1997; Bal- not et al., 1996). Briefly, mixed glial cells (cultured on Price and Brown, 2001). NO is known to cause rapid the coverslips or in the flasks) were shaken to dislodge glutamate release from neurons (Meffert et al., 1994; microglia that were loosely attached to the astrocytes.
Trabace and Kendrick, 2000), which has been attributed Microglia were purified by preplating for 30 min into either to inhibition of mitochondrial respiration followed culture flasks (75 cm2) at the density 0.1 ϫ 106 cells/ by reversal of glutamate uptake (Sequeira et al., 1997; cm2 and then the contaminating cells were removed by McNaught and Brown, 1998; Bal-Price and Brown, 2001), changing the medium. Microglia were maintained in or to a direct action on synaptic vesicle docking/fusion astrocyte-conditioned medium (medium collected from reactions followed by (calcium-independent) vesicular astrocytic cultures after 2 days and spun down) mixed 1:1 v/v with fresh DMEM (containing 10% of fetal calf Astrocytes are now known to have a vesicular pool of serum). The purity of the astrocytic cultures was de- glutamate (and possibly ATP) that is rapidly exocy- termined (after isolation of microglia) in sister cultures tosed in response to agonists that raise intracellular immunocytochemically with OX-42 (microglial marker, calcium (Parpura et al., 1994; Bezzi et al., 1998; Maien- an anti-CR3 complement receptor antibody; Sero- schein et al., 1999; Innocenti et al., 2000; Pasti et al., tec, Oxford, U.K.), anti-GFAP antibody (an astrocytic 2001). The mechanism of calcium-activated exocytosis marker; AutogenBioclear, Calne, U.K.), anti-NeuN of vesicular glutamate appears to be similar in astro- (neuron-specific nuclear protein; Chemicon, Temecula, cytes and neurons (Araque et., 2000; Mazzanti et al., CA), and anti-Ox7 (the cell surface molecule Thy1.1, 2001). During the past few years, it has been shown specifically expressed on fibroblasts; Department of Pa- that by releasing glutamate, astrocytes can modulate thology, University of Oxford). The purity of microglial synaptic transmission and contribute to certain forms cultures was assessed for the presence of microglia and of synaptic plasticity (Mazzanti et al., 2001).
astrocytes only. The cells were fixed in 4% paraformal- NO has been reported to evoke calcium waves in dehyde (Sigma) and then incubated with OX-42 or anti- astrocytes, and endogenous NO may be involve in prop- GFAP (all at 1:200 dilutions) and visualized using bi- agation of such waves (Willmott et al., 2000a, 2000b; otinylated antimouse IgG antibodies (1:200 dilution), Bowman et al., 2001). Calcium waves may propagate avidin-biotin-horseradish peroxidase complex, and dia- between astrocytes via gap junctions or via extracellu- minobenzidine tetrahydrochloride (ABC staining sys- lar mediators and may carry information between as- tem, AutogenBioclear). In the case of Ox-7 and NeuN trocytes (Scemes, 2000). There is evidence that the goat antimouse IgG secondary antibodies were used extracellular propagation of calcium waves between conjugated to tetra-rhodamine isothiocyanate (IgG- astrocytes is also mediated by ATP (Cotrina et al., TRITC) or to fluoroscein isothiocyanate (IgG-FITC), 1998a; James and Butt, 2001). Nanomolar levels of respectively. As a positive control for anti-NeuN immu- ATP can act at various purinergic receptors on astro- nocytochemistry, we used neuronal culture of cerebel- cytes, neurons, microglia, and endothelial cells to in- lar granule cells prepared as described before (Bal- crease intracellular calcium (James and Butt, 2001).
Price and Brown, 2001) and for anti-Thy1.1 fibroblast And increases in intracellular calcium can cause ATP culture prepared from the panning plates after release from neurons and astrocytes (Queiroz et al., Schwann cell purification (Cohen and Wilkin, 1995); 1997). The mechanism of ATP release from astrocytes 99.0% Ϯ 0.8% of the cells in microglial cultures were is unclear, but may, as in neurons, be due to calcium- positive for OX-42, marker for macrophage/microglial induced exocytosis of vesicular ATP. We set out to test cell types (GFAP-positive cells were not present). In whether NO could cause glutamate and ATP release astrocyte cultures, 97%–98% of cells were anti-GFAP– from astrocytes and, if so, by what mechanism.
positive and only 2%–3% cells were OX-42–positive(microglia). Cells anti-NeuN (neuronal marker) or anti-Thy1.1 (fibroblast marker) –positive were not observed, MATERIALS AND METHODS
confirming that neurons or fibroblasts were not present Astrocyte and Microglial Cultures
Microglial cultures were used for the determination Primary, mixed glial cell cultures were prepared of glutamate release 24 h after plating. Cultures of from the cerebral cortex of 7-day-old rats (Wistar) as astrocytes were used between 21 and 28 days. When previously described (Bal et al., 1994). Briefly, cells glutamate release was studied using the fluorometric method, the microglia or astrocytes were gently saccharide from Salmonella typhimurium (LPS; 10 g/ trypsinized (0.1%) for 2–3 min (at 37°C), the cells were ml; Sigma) and interferon-␥ (IFN-␥; 100 units/ml, Sigma) spun down and resuspended in Krebs-Hepes buffer in the presence and absence of an iNOS inhibitor (25 M consisting of 1.5 mM CaCl , 5.6 mM glucose, 10 mM 1400W; Alexis Biochemicals, Lausen, Switzerland) for 18 h. The medium of astrocytes (DMEM with 10% of FCS; level of glutamate 85.3 Ϯ 5.0 M) was changed just before addition of LPS and IFN-␥. After 18 h of exposure toLPS/IFN-␥ (the activation time), the level of glutamate in Measurements of [Ca2؉] in Astrocyte Cultures
the medium was determined by a colorimetric method.
Additionally, to determine the capacity of activated astro- Confluent cultures of astrocytes (21–28 DIV) on cov- cytes to remove glutamate from the medium, 100 M erslips (after shaking off microglia) were incubated glutamate was added to the medium of activated and with 2 M fura-2 AM (Molecular Probe, Leiden, The nonactivated astrocytes, and the level of glutamate in the Netherlands; from a stock of 1 mM in anhydrous medium was measured before and 1, 10, 30 min and 1, 4, DMSO) in PBS supplemented with 1 mg/ml bovine and 24 h after addition of glutamate.
serum albumin (fraction V) and 0.025% w/v PluronicF-127 (to disperse fura-2 AM in solution). After 120min at 20°C in the dark, coverslips were washed three Determination of Glutamate in Culture Media
times with Krebs-Hepes buffer (pH 7.4) containing 1mg/ml BSA and kept in the dark at 20°C for a further Astrocytes for measurements of glutamate release hour. The additional hour was to allow de-esterification were cultured in 25 cm2 culture flasks for 21–28 DIV.
of the acetoxymethyl ester of fura-2.
The volume of the medium in the culture flasks was For measurements of intracellular free calcium reduced to 2.5 ml just before exposure of astrocytes to ([Ca2ϩ] ) in populations of astrocytes, rectangular 500 M DETA-NONOate or myxothiazol (2 M) for coverslips with confluent fura-2–loaded cells were various intervals of time (5, 30 min or 4 and 24 h). After mounted vertically in a 4.5 ml optical methacrylate this time, the deproteinized medium of cultured astro- cuvette. The cuvette was mounted in a Hitachi F4500 cytes was assessed for levels of glutamate by a colori- spectrofluorimeter with the coverslip at a 30° angle to metric method coupled to glutamate dehydrogenase the excitation light path. Cells were excited by light of producing a formazan end product using a commer- the appropriate wavelengths ( ; 340, 359, and 380 cially available kit (Boehringer Mannheim, Germany).
nm) using a monochromator, and emitted fluorescence In brief, diaphorase, iodonitrotetrazolium chloride ( ) was collected at 0.2-s intervals at 510 nm. After (INT) and conditioned culture medium (after depro- correction for autofluorescence, calibrations of fluores- teinization) were combined (according to the provided protocol) and incubated for 2 min. Then 3.0 U of gluta- formed using look-up tables created from Ca2ϩ stan- mate dehydrogenase solution (GDH) was added, and dard solutions (Molecular Probes). The Krebs-Hepes the absorbance was measured at 492 nm after 15 min (pH 7.4) bathing the cells was changed by perfusion and then every 3 min until the reaction reached steady into the bottom of the cuvette using a peristaltic pump state. A standard curve was constructed by adding while continuously aspirating medium from just above known concentrations of glutamate to culture medium the coverslip. A circulating water bath maintained the in the range between 1 and 50 M. A linear relation- temperature of the perfusate at 37°C. At the perfusion ship between steady-state absorbance and glutamate rate used (17 ml/min), the medium was exchanged with concentration was observed up to 20 M of glutamate.
a half-time of 9.6 Ϯ 0.3 s (n ϭ 3). The latency (i.e., theinterval between switching saline reservoirs and ar-rival of the new media at the cuvette) was 9 s. All Continuous Assay of Glutamate Release
figures have been corrected for this latency. In someexperiments, astrocytes were preincubated with 10 M NO-induced release of glutamate from astrocytes ODQ (Calbiochem, Nottingham, U.K.) for 10 min be- was also assayed by following the conversion of NADP fore applying 500 M DETA-NONOate (diethylenetri- to NADPH using the fluorometric method of Nicholls et amine-nitric oxide adduct, also known as NOC-18; RBI, al. (1987). Changes in NADH fluorescence were used as Sigma). In other experiments, 100 M PTIO (2-phenyl- an indirect indicator of glutamate levels. Confluent 4,4,5,5-tetramethyl-imidazoline-1-oxyl 3-oxide; Sigma), astrocytes (21–28 DIV) were gently tripsinized (0.1%), 10 M verapamil (Calbiochem), or 1 M gadolinium spun down, and resuspended in Krebs-Hepes buffer (2 (Sigma) were perfused together with DETA-NONOate ml with ϳ 4.0 ϫ 106 cells). The astrocytes were equil- ibrated at 37°C in a water bath for ϳ 5 min and thentransferred into a temperature-controlled (37°C) and Activation of Astrocytes in Culture
magnetically stirred cuvette in a Shimadzu model RF15-01 fluorimeter (excitation 340 nm; emission 460 Cultured astrocytes (21–28 DIV, confluent, after shak- nm). After a few minutes (2–3 min), 1 mM NADP and ing off microglia) were activated by exposure to lipopoly- 65 U of L-glutamate dehydrogenase were added. Ap- proximately 2– 4 min later, glutamate release was ini-tiated by addition of 1, 2, or 4 l of NO-saturated waterat 20°C (2 mM). NO-saturated water was prepared bybubbling oxygen-free nitrogen through distilled waterin a glass vial with a rubber seal, then bubbling withNO gas until the water was NO-saturated. Glutamaterelease was calibrated by adding a known amount ofglutamate at the end of each assay. The relationshipbetween glutamate concentration and NADPH fluores-cence was tested by adding 5, 10, or 15 M of glutamateto the assay and was found to be roughly linear overthis range. The amplitude of the NADPH fluorescencereached a plateau after 10 –20 s.
To determine the effects of indomethacin (10 M; Sigma) or 1H-[1,2,4]oxadiazolo-[4,3-a]quinoxalin-1-one(10 M; ODQ; Alexis Biochemicals) on NO-induced glu-tamate release, ODQ or indomethacin was preincu-bated with astrocytes at 37°C in the water bath for 20 Fig. 1. Exposure of rat cortical astrocytes (21–28 DIV) in culture min during the equilibration time. NO-induced gluta- flasks to DETA-NONOate (500 M; n ϭ 6) induced rapid release of mate release was also measured after preincubation glutamate. Values represent means Ϯ SD.
of astrocytes with 25 M 1,2-bis(2-aminophenoxy)-ethane-N,N,NЈ,NЈ,-tetra-acetic acid tetrakis, aceto-xymethyl ester (BAPTA-AM; Sigma) for 30 min, 15 or neurons (Bal-Price and Brown, 2001), cultured rat as- 100 M L-trans-pyrrolidine-2,4-dicarboxylate (t-PDC; trocytes growing in 25 cm2 flasks were exposed to an Sigma) for 1 h, 4 mM EGTA for 1 h, or 1.5 nM botuli- NO donor (500 M DETA-NONOate) and the level of num toxin C (BoTx-C; Calbiochem) for 18 or 24 h in the glutamate was determined by an enzyme-coupled as- incubator (37°C; 95% O and 5% CO ). Results are say in the medium at various times after addition of expressed as the amount (in nmol/106 cells) of gluta- DETA-NONOate. Indeed, DETA-NONOate, even after mate (mean Ϯ SD) for three of more separate experi- short-term incubation (5 min), caused substantial glu- tamate release from cultured astrocytes (extracellularglutamate rose from 0.0 to 6.2 Ϯ 1.7 M; Fig. 1.) How- Measurement of Extracellular ATP Levels
ever, with time, the level of glutamate in the medium ofastrocytes exposed to DETA-NONOate (500 M) de- ATP levels in the medium were determined lumino- creased (after 4 h, 1.85 Ϯ 1.3 M), disappearing com- metrically (Jade luminometer, Labtech International) pletely after 24 h (Fig. 1), possibly due to a lower using an ATP Bioluminescence Assay Kit (Boehringer amount of NO released from DETA-NONOate after Mannheim) according to the provided protocol. Briefly, 24 h, or to downregulation of glutamate release. The astrocytes (after removing the microglia, 21–28 DIV, release of glutamate was caused by NO released from cultured in the flasks 25 cm2) after replacing the DETA-NONOate because it was almost completely DMEM medium with Krebs-Hepes buffer (pH 7.4) were blocked by 100 M PTIO (an NO scavenger) and the exposed to DETA-NONOate (0.5 mM) for 2.5, 5, or 10 residual product (DETA-NONOate kept at room tem- min and samples of the medium were assayed for ATP perature, exposed to light for a few days) did not cause content using the ATP-dependent light emission of the any significant glutamate release from astrocytes (data luciferase-catalyzed oxidation of luciferin. ATP concen- not shown). NO-induced glutamate release from neu- trations were expressed as nM in the medium.
rons and synaptosomes has been attributed to NO-induced inhibition of respiration (McNaught andBrown, 1998), so we tested whether a specific respira- Statistical Analysis
tory inhibitor would also cause rapid glutamate releasefrom astrocytes as it does with neurons and synapto- Data are expressed as mean Ϯ SD of the means of 2 somes. The release of glutamate was not observed after independent experiments and were analyzed for signif- short-term exposure to 2 M myxothiazol (a specific mitochondrial inhibitor that we have previously shownto inhibit respiration completely at this concentration; extracellular glutamate in control was 0.0 Ϯ 0.0 M Nitric Oxide Donor Induces Glutamate Release
and after addition of 2 M myxothiazol was 0.28 Ϯ From Astrocytes in Culture
0.39, 0.92 Ϯ 0.27, 1.7 Ϯ 2.1 M after 1, 10, and 30 minof exposure, respectively; n ϭ 3). This suggests that To determine whether nitric oxide can stimulate glu- NO-induced rapid release of glutamate from astrocytes tamate release from astrocytes, as it does in the case of is not mediated by inhibition of respiration.
NO Induces Rapid Calcium-Dependent Release
of Vesicular Glutamate From Astrocytes
To study the kinetics and mechanism of NO-induced glutamate release, NO-saturated water was injectedinto a stirred suspension of astrocytes (ϳ 4.0 ϫ 106cells in 2 ml of Krebs-Hepes buffer, pH 7.4, at 37°C)and glutamate release was assayed continuously usinga fluorometric method (Nicholls et al., 1987). Indeed,after addition of NO saturated water (1, 2, or 4 MNO), rapid and dose-dependent release of glutamatefrom astrocytes was observed (Figs. 2A and 3). Gluta-mate release was observed immediately after NO ad-dition and was at least as fast as the response time ofthe method (a few seconds), but stopped after 10 –20 s,presumably because of the rapid decay of NO in suchsolutions (Bal-Price and Brown, 2001). In control ex-periments, in the absence of either L-glutamate dehy-drogenase, NADP, or astrocytes, there were no fluores-cence changes observed when nitric oxide was added.
Glutamate release was mediated by nitric oxide be-cause NO scavenger PTIO (100 M) abolished it almostcompletely (Fig. 3). NO did not induce glutamate re-lease from cultured microglia (Fig. 3) using the sameconditions and the same number of cells, indicatingthat glutamate release is relatively specific to astro-cytes. Interestingly, NO-induced glutamate releasewas completely blocked by the preincubation of astro-cytes with either an extracellular Ca2ϩ chelator 4 mMEGTA (for 1 h; Figs. 2B and 3) or an intracellular Ca2ϩchelator 25 M BAPTA-AM (for 30 min; Figs. 2C and3). Since in the absence of calcium glutamate releasewas not observed, these results indicate that theNO-induced glutamate release from astrocytes wascalcium-dependent.
As there are studies suggesting that Ca2ϩ-dependent glutamate release from astrocytes can occur by a pro-cess resembling neuronal exocytosis, we investigated Fig. 2. Representative fluorescence traces of glutamate release the effect of BoTx-C (1.5 nM), a specific toxin that from rat cortical astrocytes in suspension induced by nitric oxide.
blocks the exocytotic release of neurotransmitters in Without further additions (control), nitric oxide evoked rapid anddose-dependent release of glutamate from cultured astrocytes (21–28 neurons by cleavage of syntaxin (synaptic protein). It DIV; A). Preincubation of astrocytes with either extracellular Ca2ϩ
has been shown that BoTx-C blocks bradykinin-in- chelator 4 mM EGTA for 1 h (B) or an intracellular Ca2ϩ chelator 25
M BAPTA-AM for 30–40 min (C) or 1.5 nM botulinum toxin
duced calcium-dependent glutamate release from as- (BoTx-C) for 24 h (D) blocked completely NO-induced glutamate re-
trocytes (Jeftinija et al., 1997). To determine whether lease from astrocytes. Glutamate release induced by nitric oxide from BoTx-C affects NO-induced glutamate release, astro- astrocytes was not affected by preincubation with an inhibitor of the
glutamate transporter 100 M t-PDC for 1 h (E). For each trace, ϳ 4 ϫ
cytes were incubated with BoTx-C (1.5 nM) for 16 or 106 astrocytes were added to 2 ml of Krebs-Hepes buffer in a fluorim- 24 h before NO addition as prolonged incubation with eter cuvette followed by NADP and glutamate dehydrogenase (GD).
toxin is necessary to inhibit glutamate release from Subsequent additions of 1 M NO, 2 M NO, 4 M NO, and 20 nmol of glutamate were made (indicated by the four arrows).
astrocytes (Bezzi et al., 1998; Pasti et al., 2001). Thisprolonged incubation with BoTx-C (16 –24 h) did notcause any cell death as tested by Hoechst 33342 andpropidium iodide staining to assess whether any apo- nificantly affected by preincubation of astrocytes with ptotic or necrotic cells, respectively, were present. Pre- an inhibitor of the glutamate transporter t-PDC (100 treatment of the astrocytes with BoTx-C for 16 h partly M for 1 h; Figs. 2E and 3), suggesting that glutamate decreased NO-induced glutamate release (data not transporters are not required for NO-induced gluta- shown), but 24-h incubation completely blocked it mate release from cultured astrocytes. However, after (Figs. 2D and 3). This suggests that syntaxin is re- preincubation with t-PDC, NO-induced glutamate re- quired for NO-evoked glutamate release and therefore lease was not significantly dose-dependent. It is possi- the release is probably due to exocytosis of vesicular ble that the prolonged incubation with 100 M t-PDC glutamate. NO-induced glutamate release was not sig- (1 h) may perturb glutamate pools inside and outside Fig. 3. Quantification of glutamate release evoked by 1, 2, or 4 M icant glutamate release was seen in response to 1, 2, or 4 M NO.
NO from control astrocytes (nontreated; n ϭ 24) or preincubated with Glutamate levels were measured using a continuous fluorometric either 25 M BAPTA-AM (for 30 – 40 min; n ϭ 9), 4 mM EGTA (for 1 h; assay. Results are expressed as the amount of glutamate released in n ϭ 9), 100 M t-PDC (for 1 h; n ϭ 6), 1.5 nM botulinum toxin-C nmol/106 cells means Ϯ SD. Levels that are statistically significantly (BoTx-C; for 24 h; n ϭ 6), 10 M ODQ (for 20 min; n ϭ 6), 10 M different from control astrocytes treated with 1, 2, or 4 M NO (first indomethacin (INDO; for 20 min; n ϭ 6), or 100 M PTIO (n ϭ 6).
columns) are marked *P Ͻ 0.05, **P Ͻ 0.01, and ***P Ͻ 0.001.
Alternatively, the same number of microglia was added but no signif- the cells, but it is clear that the inhibitor does not blockNO-induced glutamate release.
To provide further insights into the mechanism of NO-induced glutamate release, astrocytes were alsopreincubated with 10 M ODQ (inhibitor of solubleguanylate cyclase) to test whether guanylate cyclase isinvolved. However, ODQ did not block NO-induced glu-tamate release from astrocytes, suggesting that guan-ylate cyclase is not involved (Fig. 3).
It has been reported that glutamate release from astrocytes can be blocked by indomethacin, a cycloox-ygenase inhibitor (Bezzi and Volterra, 2001). However,in our studies, preincubation of astrocytes with indo-methacin (10 M) had no effect (Fig. 3), suggesting thatgeneration of prostaglandins is not involved in NO- Fig. 4. Time course of 500 M DETA-NONOate–induced ATP re- induced glutamate release from astrocytes. Indometh- lease from ϳ 1.0 ϫ 106 of rat cortical astrocytes (21–28 DIV) prein- acin, ODQ, or BoTx-C did not affect the glutamate cubated with either PTIO (100 M; n ϭ 6), 25 M BAPTA-AM (n ϭ 6), 1.5 nM botulinum toxin-C (BoTx-C; n ϭ 6), or without additional assays on their own and did not cause any cell death treatment (n ϭ 9). ATP levels were determined luminometrically.
after the preincubation time as estimated by trypan Results are expressed as concentration (nM in the medium) means Ϯ SD. *P Ͻ 0.05, **P Ͻ 0.01, and ***P Ͻ 0.001 statistical significance of difference from ATP release after the same time of DETA-NONOate Release of glutamate was not observed after addition treatment, but with no other additions (black bars).
of 2 mM azide (an inhibitor of cytochrome oxidase; datanot shown), suggesting again that NO-induced rapidrelease of glutamate from astrocytes was not mediated Krebs-Hepes buffer (pH 7.4). Indeed, DETA-NONOate caused a rapid increase of extracelluar ATP and after10 min was about 10-fold higher (5.8 Ϯ 0.7 nM) thanthe basal level (0.5 Ϯ 0.4 nM; Fig. 4). The ATP release NO Induces Rapid Calcium-Dependent Release
was caused by nitric oxide since 100 M PTIO (NO of Vesicular ATP From Astrocytes
scavenger) prevented it almost completely (Fig. 4).
Similarly to NO-mediated glutamate release, ATP To test whether nitric oxide could also stimulate release was also entirely calcium-dependent since release of ATP, as it does in the case of glutamate, 30-min preincubation of cultured astrocytes with cultured rat astrocytes (after shaking off microglia) BAPTA-AM (25 M) completely blocked the ATP re- were exposed to 500 M DETA-NONOate for 2.5, 5, lease (Fig. 4). Since these results suggested that the and 10 min and the level of ATP was measured in vesicular mechanisms could be involved in NO-medi- ated ATP release, the astrocytes were exposed to by voltage-sensitive Ca2ϩ channels. To study further BoTx-C (1.5 nM). Prolonged treatment with BoTx-C the mechanisms of NO-induced [Ca2ϩ] increase, the (24 –28 h) before exposure to DETA-NONOate (0.5 astrocytes were preincubated for 10 min with 10 M mM) blocked NO-induced ATP release (Fig. 4). These ODQ (guanylate cyclase inhibitor) before DETA- results indicate that NO-induced ATP release from NONOate application to determine whether NO-in- cultured astrocytes was mediated by calcium-depen- duced calcium entry into the cells could be mediated by dent vesicular release, as in the case of NO-induced the cGMP pathway. However, preincubation of astro- glutamate release. Exposure of astrocytic culture to cytes with ODQ did not have any influence on NO- DETA-NONOate (500 M) for 2.5, 5.0, or 10 min, induced increase of [Ca2ϩ] (Figs. 5D and 6), indicating BoTx-C (1.5 nM) for 28 h, or BAPTA (25 M) for 30 min that the NO-mediated Ca2ϩ entry is cGMP-indepen- did not cause any cell death as determined by pro- pidium iodide and Hoechst 33342 staining.
Nitric Oxide Released From
Nitric Oxide Induces a Rapid Biphasic Increase
LPS/IFN-␥–Activated Astrocytes Causes High
in Intracellular Calcium ([Ca2؉] )
Extracellular Glutamate Levels But Has Little
Effect on Glutamate Uptake
To determine whether NO increased intracellular calcium, astrocytes cultured on coverslips loaded with Since exogenously added NO caused rapid glutamate fura-2 were perfused with DETA-NONOate (500 M) release, we tested whether endogenously produced NO and intracellular calcium levels were monitored. The from cytokine-activated astrocytes could elevate extra- mean resting [Ca2ϩ] in astrocytes was 38.5 Ϯ 15.3 nM (n ϭ 15; Fig. 6). Application of 500 M DETA-NONO- Astrocytes (21–28 DIV, confluent) were exposed for ate resulted in a rapid, transient (1–3 min) increase in 18 h to LPS and IFN-␥, which leads to high levels of NO [Ca2ϩ] (to 141.2 Ϯ 17.8 nM; Figs. 5 and 6) followed by production from iNOS (Bal-Price and Price, 2001) in return to a lower, but still elevated, level of calcium the presence or absence of an iNOS inhibitor 1400W (63.1 Ϯ 8.3 nM) sustained for at least 10 min (Figs. 5 (25 M). After 18 h of activation, glutamate levels in and 6). The observed increase in [Ca2ϩ] in astrocytes the medium were measured using a colorimetric was indeed induced by NO and was completely and method and compared with nonactivated astrocytes. In rapidly reversible; after addition of 100 M PTIO (NO the case of activated astrocytes, high levels of gluta- scavenger), the level of [Ca2ϩ] dropped to the level mate were present in the medium (7.38 Ϯ 1.6 M) after observed before DETA-NONOate application (Figs. 5A 18 h of activation as compared with very low level of glutamate in the medium of control astrocytes (0.43 Ϯ To test whether the nitric oxide-induced [Ca2ϩ] rise 0.06 M; Fig. 7). In the presence of the iNOS inhibitor resulted from calcium influx across the plasma mem- (25 M 1400W), glutamate was still present in the brane or mobilization from intracellular stores, calcium medium but at a lower level (3.72 Ϯ 0.6 M). These was removed from Krebs-Hepes buffer prior to DETA- results are compatible with NO from activated astro- NONOate application. In this case, only a transient cytes inducing glutamate release. However, the same increase in [Ca2ϩ] was observed after DETA-NONOate result could be caused by a decreased capacity of acti- application (Fig. 5E), suggesting that extracellular cal- vated astrocytes for glutamate uptake.
cium was required for the generation and maintenance To determine whether nitric oxide produced by the of the sustained [Ca2ϩ] plateau observed during con- proinflammatory cytokine-activated astrocytes could tinued presence of extracellular calcium. The specific attenuate astrocytic capacity for glutamate uptake, inhibitor of capacitative calcium entry (CCE) 1 M 100 M exogenous glutamate from stock solution was gadolinum (Moneer and Taylor, 2002) immediately added to the astrocytes after 18 h of activation in the blocked the increase in [Ca2ϩ] observed after DETA- presence and absence of iNOS inhibitor (25 M NONOate application (Fig. 5B). These results suggest 1400W), and then samples of the medium were taken that the biphasic [Ca2ϩ] increase induced by nitric at various intervals of time (1, 10, 30 min or 1, 4, and oxide could be separated into two components: an ini- 24 h) and glutamate content was measured. In the tial transient component that is due to calcium mobi- control cultures, glutamate concentrations showed a lization from intracellular stores and a plateau compo- rapid initial decline; within 30 min glutamate concen- trations dropped to 6.7 Ϯ 1.46 M (Fig. 7) and after 1 h Since several studies have described the expression reached values below 1 M. These data show that of voltage-activated calcium channels in astrocytes, we control astrocytes were capable of taking up glutamate tested whether nitric oxide-induced Ca2ϩ entry could rapidly and efficiently. LPS/IFN-␥–activated astro- be partially mediated by voltage-gated Ca2ϩ channels.
cytes removed glutamate from the medium at a similar However, 10 M verapamil (blocker of L-type Ca2ϩ rate to nonactivated (or 1400W-treated) astrocytes.
channels) did not affect the [Ca2ϩ] plateau induced by However, the level of glutamate in the medium of ac- DETA-NONOate (Figs. 5C and 6), suggesting that NO- tivated astrocytes was always higher than in the con- induced Ca2ϩ entry into astrocytes was not mediated trol culture at each time point both before and after glutamate addition (Fig. 7). After 24 h, glutamate was a steady-state level lower than in the absence of 1400W still present in the medium of activated astrocytes (but higher than in nonactivated astrocytes).
(7.8 Ϯ 1.5 M) at concentration similar to that prior the These results suggest that the elevated extracellular addition of 100 M glutamate. In the presence of the glutamate level maintained by activated astrocytes is iNOS inhibitor (1400W), glutamate uptake was again due to increased glutamate release, with little or no similar, but after 24 h the glutamate level returned to DISCUSSION
It has previously been shown that NO can cause acute glutamate release from neurons or synaptosoms(Sequeira et al., 1997; McNaught and Brown, 1998;Bal-Price and Brown, 2001), and we have attributedthis to NO inhibition of mitochondrial respiration caus-ing a fall in ATP, inhibition of the sodium pump, andreversal of the glutamate transporter. Evidence for thismechanism was that the time, oxygen, and NO depen-dence of glutamate release and respiratory inhibitionwere similar, glutamate release was calcium-indepen-dent, and specific respiratory inhibitors caused a sim-ilar fall in ATP and glutamate release (McNaught andBrown, 1998; Bal-Price and Brown, 2001). Sequeira etal. (1997) found a similar calcium-independent gluta-mate release from synaptosomes induced by NO, asso-ciated with a decrease in ATP/ADP ratio and inhibitedby t-PDC (an inhibitor of the glutamate transporter).
In contrast, we find here that NO-induced glutamaterelease from astrocytes is completely calcium-depen-dent and is not replicated by respiratory inhibitors.
The reason NO does not cause energy depletion-in-duced glutamate release from astrocytes is probablybecause although it inhibits astrocytic respiration(Brown et al., 1995), it does not cause a fall in astrocyticATP (Bal-Price and Brown, 2001), presumably becauseof the relatively high glycolytic capacity of astrocytes(Pauwels et al., 1985; Peuchen et al., 1997). Our findingthat t-PDC did not have any significant effect on NO-induced glutamate release from astrocytes confirmsthat this release is not mediated by reversal of theglutamate transporter.
In the case of neurons, it has been proposed that NO causes glutamate release by directly modifying the exo-cytotic machinery of synaptic vesicles. This was basedon the finding that neuronal glutamate release inducedby NO was calcium-independent but inhibited by butu- Fig. 5. Representative traces of NO-induced increase in intracellu- lar calcium [Ca2ϩ] in astrocytes after perfusion with 500 M DETA- NONOate. The increase was caused by NO released from DETA-NONOate because 100 M PTIO (NO scavenger) completely reversed the increase (A). The sustained component of Ca2ϩ entry was also
inhibited by the inhibitor of capacitative calcium entry, 1 M gado-
linium (Gd3ϩ; B), but was unaffected by the L-type Ca2ϩ channel
inhibitor, 10 M verapamil (C) or by the soluble guanylate cyclase
inhibitor, 10 M ODQ (D). The sustained level of [Ca2ϩ] induced by
DETA-NONOate (500 M) was abolished by removal of extracellular Ca2ϩ, whereas the initial mobilization was unaffected (E). The mea-
surements of [Ca2ϩ] were performed in fura-2–loaded astrocytes us-
ing one coverslip (ϳ 0.15 ϫ 106 cells). Bars represent the time of perfusion with the indicated substances. DETA-NONOate (500 M) was used in all the above experiments.
nisms are not relevant in astrocytes, at least in ourconditions.
Astrocytes have a glutamate release mechanism sim- ilar to that of neurons, mediated by exocytosis of vesi-cles loaded with glutamate (Araque et al., 2000; Bezziand Volterra, 2001). This exocytosis is triggered byincreased cytosolic calcium (often in the form of cal-cium waves) (Bezzi et al., 1998; Araque et al., 2000)and is inhibited by botulinum neurotoxin C or B (Jeft-inja et al., 1997; Araque et al., 2000). As we found thatNO-induced glutamate and ATP release from astro-cytes BoTx-C, it seems likely that this release is mediated byvesicular exocytosis.
It has previously been shown that NO induces acute increases of cytosolic calcium (and calcium waves) inastrocytes, possibly via activation of soluble guanylate Fig. 6. Quantification of the increase in intracellular calcium in- cyclase (Willmott et al., 2000a). In our present studies, duced by DETA-NONOate (500 M) in cultured rat astrocytes in the absence (n ϭ 24) or presence of 100 M PTIO (n ϭ 3), 10 M ODQ (n ϭ we show that the application of DETA-NONOate to 6), 10 M verapamil (n ϭ 3), 1 M gadolinium (Gd3ϩ) (n ϭ 3), or in the fura-2–loaded astrocytes caused a very rapid increase absence of extracellular Ca2ϩ (n ϭ 3). Values represent means Ϯ SD.
of [Ca2ϩ] , but this was not blocked by ODQ (a soluble **P Ͻ 0.01 from calcium concentration in astrocytes exposed to DETA-NONOate (500 M) alone for 11 min in Krebs-Hepes buffer guanylate cyclase inhibitor), suggesting that soluble guanylate cyclase was not involved. The discrepancybetween our studies and the results described by Will-mot et al. (2000a) is possibly due to the fact that intheir studies LY83583 was used to block guanylatecyclase activity, but this compound is known also toinactivate nitric oxide (Barbier and Lefebvre, 1992), incontrast to ODQ, which does not affect NO levels.
cGMP-independent mechanisms of NO-induced in-crease in [Ca2ϩ] were also shown in C6 glioma (Bow- man et al., 2001) and Bergmann glial cells (Matyash etal., 2001).
Since gadolinum returned the [Ca2ϩ] from the pla- teau level to the basal level, these results suggest thatCa2ϩ entry occurs through CCE mechanism in astro-cytes. However, gadolinum can also inhibit L- and N-type voltage-dependent calcium channels that areexpressed on some astrocytes (Sontheimer, 1994;Agrawal et al., 2000). Ca2ϩ entry across the plasmamembrane was not mediated by L-type voltage-sensi-tive Ca2ϩ channels because verapamil did not affect Fig. 7. Extracellular glutamate levels before and after addition of [Ca2ϩ] levels but we cannot rule out that N-type chan- 100 M glutamate to the medium of nonactivated (control) and LPS/ IFN-␥–activated astrocytes in the presence or absence of iNOS inhib- nels contribute to calcium entry. As in other nonexcit- itor 1400W (25 M; n ϭ 3). Samples of media were taken at the points able cells exposed to agents mobilizing calcium from indicated and the glutamate content was determined. Note that the endoplasmic reticulum (Matsumoto et al., 1986; Kot- levels of glutamate in the medium of astrocytes prior to glutamateadditions were 0.43 Ϯ 0.06 M (control, nonactivated), 7.38 Ϯ 1.6 M likoff et al., 1987), the initial component of the biphasic (activated in the absence of 1400W; P Ͻ 0.001 from control), and [Ca2ϩ] increase observed after application of DETA- 3.72 Ϯ 0.6 M (activated in the presence of 1400W; P Ͻ 0.01 from NONOate was insensitive to the removal of extracellu- activated without 1400W). Twenty-four hours after glutamate addi-tion (100 M), the levels of glutamate were 0.0 M in control culture, lar Ca2ϩ, indicating that it was due to mobilization of 7.8 Ϯ 1.5 M in the medium of activated astrocytes without 1400W Ca2ϩ from intracellular stores. Depletion of intracellu- (P Ͻ 0.001 from control culture), and 2.58 Ϯ 0.8 M in activated astrocyte with 1400W (P Ͻ 0.05 from activated astrocytes without lar Ca2ϩ could provide a sufficient signal for activation 1400W). Values represent means Ϯ SD.
of Ca2ϩ entry through the plasma membrane as extra-cellular Ca2ϩ is required for the generation and main-tenance of the sustained [Ca2ϩ] plateau during pro- linum neurotoxins A, C, and F and associated with longed application of DETA-NONOate. The NO- covalent modifications of vesicle proteins (Meffert et induced glutamate release from astrocytes found here al., 1996). However, our finding that NO-induced glu- was fast—faster than the response time of the contin- tamate (and ATP) release in astrocytes is completely uous assay (Fig. 2)—and terminated when the added calcium-dependent suggests that such direct mecha- NO was likely to have disappeared from the medium, so further NO addition caused more glutamate release.
mate release but we have not studied whether the This suggests that the effect was mediated by NO it- NO-induced ATP release potentiates glutamate release self, rather than one of its derivatives (peroxynitrite, or vice versa, as has been suggested in other studies NO , N O , or S-nitrosothiols), as it would take time for (Queiroz et al., 1999). However, the NO-induced in- these derivatives to be produced from NO. Virtually all crease in extracellular ATP observed in our studies is rapid, reversible effects of NO are mediated by NO rather low (5.8 Ϯ 0.7 nM), and whether it could play a binding to hemeproteins, such as soluble guanylate significant role in intercellular signaling needs further cyclase or cytochrome oxidase (Xu et al., 1998; Eu et al., 2000). However, neither of these hemeproteins appears Physiologically, in the brain NO is mainly produced to mediate the NO-induced glutamate release from as- by nNOS in subpopulation of neurons, and this nNOS trocytes as release was not prevented by an inhibitor of is transiently activated by calcium elevations during soluble guanylate cyclase (ODQ) and release was not neuronal activity (Vincent, 1994; Baader and Schilling, induced by an inhibitor of cytochrome oxidase (azide).
1996; Baltrons et al., 1997). This suggests the possibil- Willmott et al. (2000a) found that NO-induced calcium ity that NO released from active neurons may cause waves in astrocytes were eliminated by high concen- calcium waves in and glutamate (and ATP) release trations of ryanodine, suggesting that NO activates from surrounding astrocytes, and thus might be in- ryanodine receptor-mediated calcium release from en- volved in neuronal-astrocytic communication and could doplasmic reticulum. NO can elevate calcium in heart particularly affect synaptic transmission as astrocytes and skeletal muscle by S-nitrosating or oxidizing ryan- and their processes surround synapses (Parpura et al., odine receptors (Eu et al., 2000). This has not been 1994; Bezi and Volterra, 2001). eNOS is expressed in reported in astrocytes, but as astrocytes express the R3 some astrocytes and has been suggested to be involved isoform of ryanodine receptors (Matyash et. al, 2002), a in initiation and propagation of calcium waves (Will- possible mechanism by which NO elevates calcium in mott et al., 2000b), and thus potentially astrocytic astrocytes is by S-nitrosating or promoting thiol oxida- eNOS might regulate glutamate and ATP release from tion of the ryanodine receptor to cause release from the astrocytes. Whether neurons or astrocytes locally re- lease sufficient NO to cause significant glutamate or The mechanisms by which ATP is released from as- ATP release from astrocytes is unclear, but levels of trocytes are still unclear. In our present studies, NO- NO up to 100 nM have been measured by electrode in induced ATP release was entirely calcium-dependent brain slices induced by electrical stimulation (Shibuki and blocked by BoTx-C, suggesting vesicular exocyto- and Kimura, 1997), up to 1 M NO released from sis. Indeed, ATP has been identified as a storage com- cultured aortic endothelial cells induced by bradykinin ponent of astrocytic vesicles released from cultured (Clementi et al., 1999), and up to 1– 4 M has been astrocytes (Maienschein et al., 1999) by receptor-medi- measured in rat brain in vivo during ischemia and ated mechanisms (Queiroz et al., 1997). Calcium-de- reperfusion (Malinski et al., 1993). The NO released pendent ATP release from astrocytes was also reported during ischemia or reperfusion might trigger extensive in response to excitatory amino acids like N-methyl-D- glutamate release from astrocytes, which could contrib- aspartate (NMDA) and kainite (Queiroz et al., 1999).
ute to the known pathological glutamate release in However, other mechanisms of ATP release have been these conditions (Szatkowski and Attwell, 1994; Rossi reported, for example, through connection hemi- channels (Cotrina et al., 1998b; Stout et al., 2002) or In a wide range of brain pathologies, astrocytes and calcium-independent mechanism after stimulation of microglia become activated by inflammatory mediators alpha-amino-3-hydroxy-5-methylisoxazole-4-propio to express iNOS (Wisniewski et al., 1998; Murphy, (ATP) receptors (Queiroz et al., 1999).
2000). In culture, activated glia can kill cocultured Recently, it has been shown that ATP released from neurons by NO and excitotoxic mechanisms (Chao, astrocytes mediates increases in cytosolic calcium and 1996; Kingham et al., 1999; Bal-Price and Brown, propagation of calcium waves in glia (Cotrina et al., 2001). Such activated astrocytes and microglia contin- 1998a; James and Butt, 2001). ATP-dependent calcium uously produce an extracellular NO level of about 1 M signaling in astrocytes is mediated by metabotropic (Brown et al., 1995; Bal-Price and Brown, 2001), suffi- purinergic P2Y receptors (coupled to calcium release cient to cause substantial glutamate release from as- from internal stores) (Guthrie et al., 1999; Fam et al., trocytes according to our results here. And indeed we 2000). ATP apparently also mediates calcium signaling have shown here that activated astrocytes maintain a between astrocytes and microglia through P2X puri- substantially higher extracellular glutamate level, nergic receptor located on microglia (Verderio and Mat- which appears to be due to enhanced glutamate release teoli, 2001). ATP-mediated increase in intracellular rather than reduced uptake. It has previously been calcium was also observed after the mechanical stimu- reported (Ye and Sontheimer, 1998) that uptake of lation of astrocytes in culture (Stout et al., 2002). In- glutamate into astrocytes is inhibited by NO or inflam- terestingly, ATP can also cause a dose-dependent re- matory activation; however, the level of inhibition re- lease of glutamate and aspartate from cultured rat ported was relatively small (about 30%), such that it astrocytes (Jeremic et al., 2001). In the present studies, would be unlikely to contribute substantially to an we have shown that NO induced both ATP and gluta- elevated extracellular glutamate level. We found no obvious inhibition of glutamate uptake by activated Dinerman JL, Dawson TM, Schell MJ, Snowman A, Snyder SH. 1994.
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3400-A O ld M ilton Pkw y, Suite 360, A lpharetta G A 30005 770-475-0077 What are bio-identical hormones? The ovaries, testicles and the adrenal glands manufacture a series of hormones all derived from cholesterol. These are called the steroid hormones. Since the early 1960s, chemists have been able to synthesize all of these molecules starting either from cholesterol or from plant stero