GT1b-induced neurotoxicity is mediated by the Akt/GSK-3/tau signaling pathway but not caspase-3 in mesencephalic dopaminergic neurons
- Eun S Chung†1,
- Eugene Bok†1, 2, 3,
- Sunghyang Sohn4,
- Young D Lee5,
- Hyung H Baik1, 2 and
- Byung K Jin1, 2Email author
© Chung et al; licensee BioMed Central Ltd. 2010
Received: 24 December 2009
Accepted: 12 June 2010
Published: 12 June 2010
Gangliosides, sialic acid-containing glycosphingolipids exist in mammalian cell membranes particularly neuronal membranes. The trisialoganglioside (GT1b) is one of the major brain gangliosides and acts as an endogenous regulator in the brain. We previously showed GT1b induces mesencephalic dopaminergic (DA) neuronal death, both in vivo and in vitro. We further investigate the underlying mechanisms of GT1b neurotoxicity.
Consistent with earlier findings, GT1b attenuated the DA neuron number and dopamine uptake level in mesencephalic cultures. Morphological evidence revealed GT1b-induced chromatin condensation and nuclear fragmentation as well as an increased number of TUNEL-positive cells, compared to control cultures. Interestingly, while GT1b enhanced caspase-3 activity, DEVD, a caspase-3 inhibitor, failed to rescue DA neuronal death. Immunoblot analysis revealed that GT1b inactivates Akt through dephosphorylation at both Ser473 and Thr308, subsequent dephosphorylation of GSK-3β, a substrate of Akt, and hyperphosphorylation of tau, downstream of GSK-3β. Moreover, a GSK-3β specific inhibitor, L803-mt, attenuated tau phosphorylation and rescued DA neurons from cell death in mesencephalic cultures.
Our data provide novel evidence that a Akt/GSK-3β/tau-dependent, but not caspase-3 signaling pathway plays a pivotal role in GT1b-mediated neurotoxic actions on mesencephalic DA neurons.
The progressive degeneration of dopaminergic (DA) neurons in the substantia nigra (SN) is a well-known characteristic of Parkinson's disease (PD). In vivo and in vitro models of PD induced by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP), 1-methyl-4-phenylpyridinium (MPP+) or 6-hydroxydopamine (6-OHDA) reveal that apoptosis is the principal mechanism underlying neuronal death [1–4].
The Akt/glycogen synthase kinase (GSK)-3β/caspase-3 signaling pathways are among the essential components regulating apoptosis [5, 6]. Recently, transduction of DA neurons with myristoylated Akt (Myr-Akt), a constitutively active form of Akt prevents 6-OHDA-induced cellular and functional damage of DA neurons , Moreover, increased phospho-Akt levels in LINGO-1 knockout mice provide potent protection of DA neurons in 6-OHDA- or N-methyl-4-phenyl-1,2,3,6-tetrahydropyridine neurotoxicity . Several lines of evidence indicate that GSK-3β mediates DA neuronal death in PD animal models produced by MPTP  or 6-OHDA . In addition, tau, a well-known substrate for GSK-3β [11, 12], mediates DA neuronal death in MPTP-treated mice . Significantly, a number of studies show that caspase-3 contributes to cell death of DA neurons in human PD postmortem brain tissue, animal models of PD, primary cultures of rat mesencephalon, and SN-derived DA cell lines [1, 3, 4, 13].
Gangliosides, sialic acid-containing glycosphingolipids that exist in mammalian cell membranes, are particularly enriched in neuronal membranes . A variety of neurodegenerative disorders are associated with increased ganglioside levels in cerebrospinal fluid (CSF) [15–17]. Furthermore, gangliosides localized to neurofibrillary tangles (senile plaques) in brain tissue of Alzheimer's disease (AD) patients and Betz cells of precentral gyrus in amyotrophic lateral sclerosis patients [18, 19]. These findings support the possibility that under pathological conditions, gangliosides serve as cytotoxic factors in the central nervous system (CNS).
Trisialoganglioside, GT1b, one of the major brain ganglioside [14, 20], possibly acts as an endogenous regulator in the brain. GT1b induces apoptosis in non-neuronal cells, such as thymocytes  and keratinocytes . Moreover, neurotoxic activity of GT1b against DA neurons has been reported in the SN in vivo  and mesencephalic cultures . However, the mechanisms underlying GT1b-induced DA neuronal death are not clarified.
In this study, we demonstrate for the first time that GT1b neurotoxicity is accompanied by inactivation of Akt, activation of GSK-3β and increase in tau phosphorylation in mesencephalic DA neurons, both in vivo and in vitro. Our data further confirm that caspase-3 is not a major effector of DA neuronal death in GT1b neurotoxicity.
Characterization of GT1b-induced neurotoxicity in neuron-enriched mesencephalic cultures
To discriminate between DA and non-DA neurons, mesencephalic cultures were immunostained with a TH antibody specific for DA neurons and electron micrographs obtained. In control cultures, both DA (Figure 2F) and non-DA neurons (Figure 2H) contained intact nuclei with well-preserved cell membranes. In contrast, fragmented nuclei were clearly visible in both DA (Figure 2G) and non-DA neurons (Figure 2I) with a fairly intact cell membrane in GT1b-treated cultures.
GT1b neurotoxicity is independent of caspase-3
Next we examined whether caspase inhibitors block GT1b neurotoxicity. Cultures were treated with a caspase-3-specific inhibitor, DEVD, or a non-specific caspase inhibitor, z-VAD, together with or without GT1b. Surprisingly, neither DEVD nor z-VAD rescued GT1b-induced DA neurotoxicity, as evident from TH-ip neuron counts and level of [3H]dopamine uptake (Figure 3B), although the caspase-3-specific inhibitor (DEVD) significantly attenuated caspase-3 activity (Figure 3A). z-VAD or DEVE only as controls had no effects (Additional file 1E). However, DEVD inhibits not only caspase-3 but also caspase-1 and -2. Thus additional experiments were performed using more specific caspase-3 inhibitor, z-DQMD-FMK . Similar to DEVE, z-DQMD-FMK was unable to prevent GT1b neurotoxicity as evidence by TH immunocytochemistry (Additional file 1).
GT1b promotes inactivation of Akt and subsequent activation of GSK-3β
To assess whether suppression of GSK-3β activity blocks GT1b neurotoxicity, cultures were treated with the GSK-3β-specific inhibitor, L803-mt (20 μM) , together with GT1b for 24 h. L803-mt rescued TH-ip neuron death by 53% in relation to GT1b-treated cultures (Figure 5C). However, L803-mt alone had no effect (data not shown).
GT1b induces tau hyperphosphorylation through GSK-3β activation
Additional Western blot analyses disclosed that 20 μg/ml GT1b significantly upregulated tau phosphorylation in a time-dependent manner (Figure 6J,K). To assess whether suppression of GSK-3β activity affects the tau hyperphosphorylation level, cultures were treated with a GSK-3β specific inhibitor, L803-mt, together with GT1b for 16 h. L803-mt reversed tau hyperphosphorylation by 47%, compared to GT1b-treated cultures (Figure 6L,M).
Increasing evidence has shown that gangliosides enhance cell death in various cell types. For example, GM1 and GT1b produce an increase of cell death in feline thymocytes . GM3 causes apoptosis, decreases BrdUrd incorporation, and up-regulates the cdk inhibitor p27 kip in proliferating astrocytes . Many studies also demonstrate that, GD3 disrupts mitochondria membrane potential [32, 33], induces cell death and activates caspases in HuT78, derived from a human cutaneous T cell lymphoma . Similarly, neurotoxicity of major brain gangliosides, such as GD1a and GD1b against dopaminergic neurons in mesencephalic cultures has been reported . We also found that GT1b was neurotoxic to mesencephalic dopaminergic neurons in vivo and in vitro [23, 24]. This is consistent with our present findings that GT1b neurotoxicity produces DNA cleavage as well as condensation and fragmentation of nuclei, as evident from the TUNEL reaction, Hoechst 33258 nuclear staining and immunoelectron microscopic observations, respectively.
GT1b neurotoxicity is not mediated by caspase-3
Nuclear DNA damage occurs due to activation of caspase-3, which appears to be a major effector of DA neuronal cell death in human PD patients , animal models of PD , and MPP+-treated rat mesencephalic cultures  and SN-derived DA cell lines . Regarding this, our data indicated that GT1b-induced nuclear DNA damage was accompanied by caspase-3 activation, which was effectively suppressed by the specific inhibitor, DEVD (Figure 3A). However, the caspase-3 inhibitor, DEVD, and the non-specific caspase inhibitor, Z-VAD, were unable to block GT1b-induced neurotoxicity, as confirmed from the number of TH-ip neurons and level of [3H]dopamine uptake in mesencephalic cultures (Figure 3B). These results carefully suggest that under our experimental conditions, caspase-3 may not be a major effector of GT1b-induced DA neuronal cell death. This hypothesis is supported by recent findings that inhibition of caspases, including caspase-3, does not always prevent neuronal death in MPP+-treated cerebellar granule neurons , proteasome inhibitor-mediated death of HT4 cells (hippocampal cell line) , and global ischemia-induced hippocampal neurodegeneration . Moreover, a wide range of caspase inhibitors, including DEVD, had no effects on cytotoxicity induced by another major brain ganglioside, GD3, in rat hepatocytes  and HuT78, a cell line derived from a human cutaneous T cell lymphomas .
The Akt/GSK-3β/tau signaling pathway is implicated in GT1b neurotoxicity
Akt, a serine/threonine protein kinase, is significantly associated with neuronal survival/degeneration [5, 26]. In particular, decreased Akt signaling is associated with neurodegeneration in the brains of MPTP [40, 41] or 6-OHDA-induced Parkinsonism  and Drosophila models of PD . Moreover, several studies demonstrate that transduction of DA neurons with myristoylated Akt (Myr-Akt),  and increasing phospho-Akt in LINGO-1 knockout mice  provide potent protection against 6-OHDA- or MPP+-induced cellular and functional damage of DA neurons, respectively, consistent with our present observation that GT1b neurotoxicity is associated with dephosphorylation/inactivation of Akt. The result is further supported by previous findings that GT1b-induced apoptosis is mediated by decreased phosphorylation of Akt in keratinocyte-derived SCC12 cells , and GT1b depletion increases cell survival through Akt activation .
Akt contains two regulatory phosphorylation sites, Thr308 and Ser473. While phosphorylation at both sites is dependent on phosphoinositide 3-OH kinase (PI3K), the mechanism of Ser473 phosphorylation remains controversial. In this regard, there is evidence suggesting that the Ser473 site is autophosphorylated [45, 46] or phosphorylated by distinct serine kinase, including the integrin-linked kinase (ILK) [27, 47]. In SSC12 cells, GT1b-induced cell death is mediated by inhibiting phosphorylation of Akt at Ser473, but not Thr308, through inactivation of ILK that does not require PI3K [22, 44]. Data from the present study show that GT1b neurotoxicity is accompanied by Akt dephosphorylation at both Ser473 and Thr308. Therefore, it is likely that in mesencephalic cultures, ILK or PI3K signaling or both participate in GT1b neurotoxicity. However, we did not provide direct evidence of whether GT1b neurotoxicity is mediated by ILK or PI3K signaling or both.
The anti-apoptotic function of Akt involves phosphorylation/inactivation of its downstream substrate, GSK-3β. Inactivation of Akt triggers GSK-3β activity through decreasing phosphorylation, which plays a key role in neuronal loss occurring in neurodegenerative diseases, such as PD [9, 48] and AD . Two PD mimetics, 6-OHDA and MPP+, induce GSK-3β-dependent neurodegeneration in cell types, including SH-ST5Y, PC12, and cerebellar granule neurons [10, 28], suggesting that GSK-3β is a key mediator of neuronal death. Our results show that in mesencephalic cultures, GT1b induces dephosphorylation of GSK-3β, indicative of GSK-3β β involvement. This finding is further supported by TH immunocytochemistry data showing that blockage of GSK-3β activation by the inhibitor, L803-mt, leads to reduced GT1b neurotoxicity.
Tau is one of the major microtubule-associated proteins identified in neurons. Hyperphosphorylation of tau inhibits its binding to microtubules, leading to neuronal death [49–51] and is mediated by several protein kinases, including GSK-3β . Our Western blot and double immunostaining data show that in parallel with increased GSK-3β activity, GT1b induces tau hyperphosphorylation in mesencephalic DA neurons in vivo and in vitro. In addition, L803-mt, a GSK-3β inhibitor, attenuates tau phosphorylation, suggesting that GT1b neurotoxicity is mediated by the GSK-3β/tau signaling pathway.
In the present study, we show that GT1b neurotoxicity is associated with inhibition of Akt, resultant activation of GSK-3β and increasing cleavaged tau as well as phosphorylation in mesencephalic neurons including DA neuron. Interestingly, while GT1b activates caspase-3, a key molecule of DA neuronal death, inhibition of caspase-3 fails to rescue DA neurons. Our data collectively suggest that GT1b neurotoxicity is associated with Akt/GSK-3β/tau, but not with caspase-3.
Materials were purchased from the following companies: mouse anti-tyrosine hydroxylase (TH; Pel-Freez, Rogers, AR, USA), rabbit anti-tyrosine hydroxylase (TH; Pel-Freez), mouse anti-neuron specific nuclear protein (NeuN; Chemicon, Temecula, CA, USA), rabbit anti-GABA and mouse anti-actin (Sigma, St. Louis, MO, USA), rabbit anti-phospho-Akt (Ser473), rabbit anti-phospho-Akt (Thr308), rabbit anti-phospho-GSK-3β (Ser9), rabbit anti-Akt and rabbit anti-GSK-3β (Cell Signaling Technology, MA, USA), mouse anti-AT8 (phospho-tau (Ser202), INOGENETICS, Gent, Belgium), biotinylated secondary antibody and ABC kit (Vector Laboratory, Burlington, CA, USA), FITC-conjugated anti-mouse IgG and Texas Red-conjugated anti-rabbit IgG (Molecular Probes, OR, USA). GT1b (Matreya, Pleasant Gap, PA), DEVD-FMK (Biochemicals, San Diago, CA), z-DQMD-FMK (Tocris Elliscille, MO), z-VAD (R&D systems Minneapolis, MN), L803-mts (Calbiochem, San Diego, CA, USA), tritiated dopamine ([3H]dopamine; Amersham, Oakville, ON, USA), Apotag fluorescein in situ detection kit (Chemicon), Hoechst 33258 (Molecular Probes), ApoAlert Caspase Fluorescent Assay Kits (CLONTECH Laboratories, Palo Alto, CA, USA), Akt kinase Assay Kit (Cell Signaling Technology).
Neuron-enriched mesencephalic cultures were prepared as previously described with some modifications . In brief, cells from the ventral mesencephalons of embryonic day 14 Sprague-Dawley rats were seeded on 12 mm round aclar plastic coverslips or culture plates pre-coated with 100 μg/ml poly-D-lysine (Sigma) and 4 μg/ml laminin (Upstate Biotech, NY, USA) at a density 1.25~2 × 105 cells/cm2. The cultures were incubated in a humidified incubator at 37°C, 5% CO2 for 24 h. To suppress the proliferation of glial cells, on the second day in vitro (DIV2), the media were replaced with a chemically defined serum-free media (DM) composed of Ham's nutrient mixture F12/DMEM and supplemented with ITS (insulin, transferrin and sodium selenite; Sigma), glucose, L-glutamine and penicillin/streptomycin (P/S). On DIV 4, cultures were treated with various concentrations of GT1b in DM without ITS. As described previously, the cell composition included ~5% astrocytes and less than 1% microglia which were glial fibrillary acidic protein (GFAP; Sigma) immunopositive (ip) and CD11b (OX-42, Serotec, Oxford, UK)-ip cells, respectively. The remaining cells were presumed to be neurons, 4.5~6% and 9.5~11% of which were tyrosine hydroxylase-ip (TH-ip) and gamma amino butyric acid (GABA, ; Sigma)-ip neurons, respectively .
As previously described [24, 35], paraformaldehyde-fixed cells were immunostained with following cell type specific antibodies; mouse-neuron specific nuclear protein (NeuN, 1:300) for general neurons, mouse-TH (1:7500) for DA neurons or rabbit-GABA (1:2000) for GABAergic neurons. Cultures were incubated with a primary antibody for overnight at room temperature (RT) and subsequently incubated with an appropriated biotinylated secondary antibody. Immunostaining was visualized by the ABC method followed by color development with diaminobenzidine (DAB; Sigma), and analysed under a bright-field microscope (Olympus, Tokyo, Japan).
Measurement of Dopamine Uptake
The measurement of dopamine uptake was performed as our described previously [24, 35]. Briefly, cultures were washed twice with the incubation solution (HBSS containing 10 mM HEPES, 0.6% glucose, 0.2 mM pargyline, and 0.01% ascorbic acid, pH 7.4), and then incubated at 37°C for 20 min in incubation solution with a final concentration of 83.3 nM tritiated dopamine ([3H]dopamine, 444 GBq/mmol). Blank values were obtained by incubating cultures at 0°C. The reaction was terminated by removal of the solution followed by three rapid washes with ice-cold incubation solution. The cultures were then lysed with lysis buffer (0.2 M NaOH containing 0.2% Triton X-100) and transferred to scintillation vials for counting.
The TUNEL assay was performed using the Apotag fluorescein in situ detection kit that detects the 3'-OH region of cleaved DNA. Briefly, cultures were exposed to GT1b 20 μg/ml for indicated time points. And then cultures were fixed with 4% paraformaldehyde in PB for 15 min at RT. Subsequently, cultures were incubated with a mixture of terminal deoxynucleotidyl transferase and reaction buffer containing FITC fluorescein conjugated-digoxigenin-dUTP in a humidified chamber for 1 h at 37°C, and washed in washing buffer for 10 min. Finally, cultures were counterstained with 1 μg/ml Hoechst 33258 at RT for 10 min, and viewed using an Olympus IX71 confocal laser scanning microscope (Olympus, Tokyo, Japan).
Mesencephalic cultures were fixed using Karnovsky's fixative solution (2% paraformaldehyde, 2% glutaraldehyde, 0.5% calcium chloride in cacodylate buffer, pH 7.2) for 30 min and then immunostained with mouse-TH antibody. Subsequently, cultures were incubated with a biotinylated anti-mouse IgG. Immunostaining was visualized by the ABC method followed by color development with DAB. Immunostained cultures were processed for an electron microscope. In brief, cultures were washed with cacodylate buffer, dehydrated in a series of graded ethanol, and then embedded in epon mixture. Ultrathin sections were cut using on Reichert Jung Ultracut S (Leica, Markham, Ontario, Canada) and mounted on grids, stained with uranyl acetate and lead citrate, and analyzed under a Zeiss EM 902 A electron microscope (Carl Zeiss, German).
Measurement of caspase activities
Caspase activity was determined using the ApoAlert Caspase Fluorescent Assay Kits in mesencephalic cultures. Briefly, cultures were treated with 20 μg/ml GT1b for indicated time points. And then the harvested lysate was centrifuged for 20 min at 14,000g and the supernatant (10 μg/ml) were incubated at 37°C in a reaction buffer adding 10 mM DTT with the fluorogenic substrate DEVD-AFC, and the emitted fluorescence was measured in a Spectrometer-Luminescene (Perkin Elmer, Norwalk, CT, USA).
Akt kinase activation
For Akt kinase assay, cultures were washed with ice-cold phosphate-buffered saline (PBS), lysed with cell lysis buffer (20 mM Tris-HCL, pH 7.5, 150 mM NaCl, 1 mM EDTA, 1 mM EGTA, 1% Triton X-100, 2.5 mM sodium pyrophosphate, 1 mM β-glycerophosphate, 1 mM Na3VO4, 1 μg/ml leupeptin; Cell Signaling Technology) adding 1 mM phenylmethylsulfonyl fluoride (PMSF). Equivalent amounts of Akt were immunoprecipitated by rabbit-Akt antibody prebound to protein A-agarose beads, and kinase assays were carried out according to the manufacturer's instruction manual of the Akt kinase Assay Kit (Cell Signaling Technology). GSK-3α/β fusion protein was used as the substrate for Akt. Immunoprecipitated Akt and phosphorylated GSK-3α/β were measured by Western blotting using Akt antibody and phospho-GSK-3α/β (Ser 21/9) antibody, respectively.
Western blot analysis
Cultures were washed with ice-cold PBS, lysed with cell lysis buffer adding 1 mM PMSF and protease inhibitor mixture (Sigma). Equal amounts of protein (50 μg) were mixed with loading buffer (0.125 M Tris-HCl, pH 6.8, 20% glycerol, 4% SDS, 10% mercaptoethanol, and 0.002% bromophenol blue), boiled for 5 min, and separated by SDS-PAGE. After electrophoresis, proteins were transferred to polyvinylidene difluoride (PVDF) membranes (Millipore, Bedford, MA, USA) using an electrophoretic transfer system (Bio-Rad, Hercules, CA, USA). The membranes were then incubated for overnight at 4°C with one of the following the specific primary antibodies: rabbit-phospho-Akt (Ser473), rabbit-phospho-Akt (Thr308), rabbit-phospho-GSK-3β (Ser9), and mouse-AT8 phospho-tau (Ser202). After washing, the membranes were incubated with HRP-conjugated secondary antibodies (1:2000; Amersham Biosciences) for 1 h at RT. Finally, the blots were developed with enhanced chemiluminescence detection reagents. The blots were reprobed with antibodies against rabbit-Akt, rabbit-GSK-3β r mouse-actin (1:10000). For semiquantitative analyses, the densities of bands on immunoblots were measured with the Computer Imaging Device and accompanying software (Fujifilm, Tokyo, Japan).
Infusion of GT1b and tissue preparation
For infusion of GT1b in the SN, female SD rats (230~250g) were anesthetized with an injection of chloral hydrate [360 mg/kg, intraperitoneal (i.p.) injection], positioned in a stereotaxic apparatus (Kopf Instrument, Tujunga, CA, USA). Each rat received a unilateral administration of GT1b into the right SN [anteroposterior (AP) 5.3 mm, mediolateral (ML) 2.3 mm, dorsoventral (DV) 7.6 mm from bregma], according to the atlas of Paxinos and Watson (1998). All injections were made using a Hamilton syringe equipped with a 30S-gauge beveled needle and attached to a syringe pump (KDScientific, MA, USA). Infusions were made at a rate of 0.2 μl/min for GT1b (60 μg in 3 μl distilled water). Animals were transcardially perfused with saline solution containing 0.5% sodium nitrate and heparin (10 U/ml) and fixed with 4% paraformaldehyde dissolved in 0.1 M PB. Brains were removed from the cranium, post-fixed for 1 h, washed in 0.1 M PB and immersed in 30% sucrose solution until they sank. Tissues were sectioned at a thickness of 35 μm using a sliding microtome. Every sixth serial section was selected and processed for immunohistochemical staining.
For immunofluorescence double labeling, cultures or tissue sections were incubated in a combination of mouse-AT8 antibody and rabbit-TH antibody. The next day, cultures or tissue sections were rinsed and incubated with FITC-conjugated anti-mouse IgG (1:200) and Texas Red-conjugated anti-rabbit IgG (1:200) for 1 h at RT. Stained cells were viewed using an Olympus IX71 confocal laser-scanning microscope (Olympus).
All data are represented as the means ± SEM. The statistical significance of differences was assessed using analysis of variance (ANOVA), followed by Student-Newman-Keuls analyses or Student's two-tailed t-test (SPSS for windows: Standard Version). Statistical significance was defined as p < 0.05 for all analyses.
amyotrophic lateral sclerosis
day in vitro
glial fibrillary acidic protein
glycogen synthase kinase 3
transferase-mediated fluorescein-dUTP nick-end labeling.
This research was supported by the KOSEF grant funded by the Korea government (R11-2008-036-01001-0) and the Kyung Hee University Post-Doctoral Research Fund in 2008 (KHU-20080277).
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