α-Synuclein (α-Syn) is a presynaptic protein [25
] implicated in normal brain function [11
] and in Parkinson’s disease (PD) [32
]. α-Syn functions as a chaperone protein based, in part, on its homology to the 14-3-3 proteins [30
], which bind to and regulate the activity of many cellular proteins. Our laboratory discovered a functional interaction between α-Syn and TH [31
], the major dopamine biosynthetic enzyme that is modulated by 14-3-3. While 14-3-3 is known to bind to and stimulate TH activity [18
], we discovered that α-Syn binding to TH, inhibits its activity by reducing TH phosphorylation [31
], likely acting as a 14-3-3 antagonist to modulate 3,4-dihydroxy-L-phenylalanine (DOPA) generation.
Short term regulation of TH depends on the phosphorylation of seryl residues, Ser19, Ser31, and Ser40, in the TH regulatory domain [5
]. We previously demonstrated significant reduction in TH phosphorylation in dopaminergic cells that overexpress α-Syn [31
]. The serine that regulates 14-3-3 binding to TH is phospho-Ser19 (PSer19), a site that is highly phosphorylated in dopaminergic neurons throughout the brain [36
]. To evaluate the impact of α-Syn on TH in vivo, in the absence of endogenous α-Syn, we obtained ASKO mice [1
] and generated wild type human α-Syn lentivirus using established methodologies [16
]. Herein, we share our novel findings revealing that when α-Syn becomes aggregated, immunoreactivity (ir) for Total-TH appears to be reduced in dopaminergic neurons. However, TH neurons were readily labeled using well-characterized phospho-TH antibodies [15
]. While further analyses are needed to define the mechanism(s) underlying reduced Total-TH-ir as α-Syn becomes aggregated, the data provide the first evidence for an inhibitory role of α-Syn in dopamine synthesis in vivo.
We explored the impact of α-Syn on TH in vivo using male ASKO mice, (strain B6:129X1-Snca, Tm1ROSL/J; Jackson Labs) [1
] weighing 23 – 30g, housed on 12 hr light/dark cycles, with food and water ad libitum. Mice were handled according to NIH guidelines on protocols approved by the University of Pittsburgh Animal Care and Use Committee.
Lentivirus was generated using a vector system modified from human immunodeficiency virus, for transducing non-dividing cells [27
], kindly provided by Prof. Didier Trono (University of Geneva, Switzerland). Plasmids included pCMVΔR8.91 (packaging), pHR’CMVGFP (transfer), and pVSVG (viral envelope). Wild type human α-Syn in pcDNA3.1 (gift of Yong-Jian Liu, University of Pittsburgh) was KpnI/XbaI digested, then inserted in pcDNA3 at KpnI/EcoRV after ligation of KpnI/ApaI (blunt-ended). α-Syn-pcDNA was digested with HinDIII (blunt-ended) and XhoI, and ligated into pHR’CMVGFP. For co-transfections, HEK293T cells were seeded at 9 × 106
cells per 10 cm plate. The next day, media were replaced with OptiMEM (Gibco-Invitrogen, Foster City, CA) followed by triple transfection using Lipofectamine 2000 (Invitrogen). Lentiviral particles were purified from culture media at 72 hr [16
]. Titers ranged from ~ 1 × 108
− 1 × 1010
TU/ml. Transduction efficiency was confirmed in HEK293T cells after 6 - 20 ul of virus in Hexadimethrine bromide (H-9268, Sigma-Aldrich), which yielded a dose dependent increase in α-Syn on immunoblots reacted with α-Syn antibody (610786, BD-Transduction Labs) (not shown). Virus was handled according to EHS and University of Pittsburgh Institutional Biosafety Committee for rDNA Research guidelines.
For in vivo transduction, mice were anesthetized with ketamine, 80 mg/kg, and xylazine, 12 mg/kg (Sigma-Aldrich), prior to bilateral delivery of α-Syn or GFP lentivirus into olfactory bulbs. Coordinates were: ± Bregma (AP +4.28, ML ±0.375, DV −2.75 to −1.75). Mice, immobilized in a stereotaxic frame, received solutions delivered by infusion pump (Stoelting, Wood Dale, IL) as the needle was extracted (1.0 μl per injection, at 0.2μl/min). Mice (N = 33; 22 α-Syn transduced, 4 PBS injected, and 7 GFP transduced) were sacrificed at 3.5, 7, 14, and 21 days by anesthesia overdose. These time points were selected to ensure ample α-Syn transduction in a pool of neurons that turns over. All time points yielded similar results. Brains were extracted, bisected longitudinally, and one hemisphere was post fixed in 4% formaldehyde at 4°C, then cryoprotected in 15–30% sucrose-PBS. The opposite hemisphere was frozen for biochemistry for immunoblots, prepared using established methods [22
], and quantified using Odyssey Infrared Imaging according to the manufacturer (Li-Cor, Lincoln, NB).
Cryomicrotome (Microm HM550, Waldorf, Germany) sections (8 – 30 μm) were thaw-mounted onto slides or collected in −20°C cryoprotectant. Thick sections were processed free-floating. Sections were blocked in 10% goat serum, 5% BSA, 0.1 % glycine, 0.3% Triton-X-100, in 1x PBS, then in three primary antibodies at 4°C for 15 hr, followed by sequential incubations in secondary antibodies, 1 hr at RT. TH antibodies included: (1) chicken polyclonal (TH-S, 1:250, Aves Labs, Tigard, OR) against two peptides in the N- and C-termini but not overlapping TH phosphorylation sites, (2) mouse monoclonal (MAB318, 1:100, Chemicon; Temecula, CA) against TH purified from PC12 cells (epitope is outside the N-terminus); (3) rabbit polyclonal (AB152, 1:100, Chemicon; Temecula, CA) against denatured TH from rat pheochromocytoma, (4) rabbit polyclonal (P40101-0, 1:500, Pel-Freeze, Rogers, AK) against SDS-denatured purified recombinant rat or bovine TH; (5) sheep polyclonal (AB1542, 1:1000, Chemicon) against native TH from rat pheochromocytoma. Other antibodies included phospho-specific TH antibodies: rabbit anti-PSer19 (AB5425, 1:1000, Chemicon), rabbit anti-PSer31 (AB5423, 1:1000, Chemicon), rabbit anti-PSer40 (AB5423, 1:100, Chemicon); or chicken PSer19 and PSer40 TH polyclonal antibodies custom made for us by Aves Labs. GFP transduced neurons were immunolabeled using chicken anti-GFP (AB1690, 1:500, Chemicon). Secondary antibodies included affinity-purified: donkey-anti-goat Alexa-546 (1:700; Invitrogen/Molecular Probes; Foster City, CA), goat-anti-chicken Alexa-488 (1:700; Invitrogen/Molecular Probes), goat-anti-rabbit Alexa-647 (1:700; Invitrogen/Molecular Probes), donkey-anti-sheep Alexa-488 (1:700, Invitrogen/Molecular Probes), or CY3-conjugated goat-anti-chicken (#103-165-155, 1:700, Jackson ImmunoResearch). Nuclei were DAPI stained when mounted on slides using Vectashield Hardset (Vector Labs, Burlingame, CA).
Three-color-laser confocal microscopy (Olympus IX81) for detecting wavelengths from UV for DAPI, to green (Alexa-488), red (Alexa-546 and CY-3), to farred (Alexa-647). Images were captured and data quantified by Fluoview10 (Olympus), with all settings being equal for all conditions. Data from intensity profiles were accumulated in Excel (Microsoft) and evaluated using GraphPad (Instat, San Diego), with statistical significance set at 0.05.
Protein aggregation was measured by proteinase K (PK, Invitrogen) treatment [8
] on thaw-mounted sections that were air dried 20 min at RT, circled with Pap-Pen (Polysciences, Warrington, PA), then rewet in 1 x PBS. Tissues were digested in 2.5μg/ml PK in 0.1 M-Tris-HCL buffer, 0.005 mM EDTA, pH 7.5 for 15–30 min, RT. Sections were then immunostained as described above. For Thioflavin-S we utilized floating sections (30 μm) that were first immunolabled then reacted with 1% aqueous Thioflavin-S (Sigma-Aldrich, St Louis) 30 min RT, followed by ethanol washes. All sections were light protected at 4°C prior to evaluation.
Normal morphology was apparent in α-Syn transduced mouse olfactory bulb as can be appreciated by DAPI staining (). As expected, many periglomerular neurons (, arrows) were dopaminergic as confirmed by Total-TH immunoreactivity (ir) (). Because the lentiviral particles we used are packaged with vesicular stomatitis virus glycoprotein (VSV-G) envelope protein, we anticipated that most olfactory neurons would be transduced. However, to our surprise, α-Syn expression was almost exclusively noted in dopaminergic neurons, seen here at 7 days post-transduction (). The reason for this relatively selective tropism is unknown, however, α-Syn-ir colocalized with TH as noted in this higher magnification image (, arrow). As anticipated, untransduced olfactory bulbs lacked α-Syn-ir ().
α-Syn is co-expressed with Total-TH in periglomerular olfactory neurons of lentivirus transduced α-Syn knockout mice
Previously, we noted that α-Syn acts to inhibit TH phosphorylation and dopamine synthesis in vitro [31
]. Under normal conditions, functional α-Syn and TH are soluble proteins, but both accumulate in Lewy bodies [20
]. We have long hypothesized that TH phosphorylation levels will increase when α-Syn aggregates [32
]. To begin evaluating this possibility, we triple immunolabeled ASKO olfactory bulbs at 3.5 – 21 days post-transduction with antibodies for α-Syn, Total-TH, or TH phosphorylated at Ser19, Ser31, or Ser40. Because our data were nearly identical for all three phospho-Ser-specific-TH antibodies, we present only the PSer19 results herein. At 3.5 days after PBS injection olfactory bulbs had overlapped Total-TH and TH PSer19 signals and no α-Syn-ir, as expected (). In ASKO mice transduced with wild type human α-Syn there was extensive overlap of α-Syn-ir with Total-TH-ir (). However, cells having stronger α-Syn-ir showed reduced Total-TH-ir (, cells at arrowheads), although their dopaminergic phenotype was confirmed by PSer19 staining (). When we quantified signal intensities for cells 1, 2, and 3 in , we noted a significant inverse correlation between Total-TH-ir and α-Syn-ir and a positive correlation between α-Syn-ir and TH PSer19-ir () (N = 85 cells, P < 0.0001). In contrast, GFP transduction did not reduce Total-TH-ir or increase PSer19-ir, as can be appreciated in the merged image where GFP-transduced dopaminergic neurons appear yellow (). Total-TH levels were equivalent on tissue homogenate immunoblots from α-Syn- and GFP-transduced mice at 3.5 and 7 days (), although PSer19 levels were significantly higher in α-Syn transduced tissues compared to GFP-transduced controls (, ANOVA, P < 0.02).
α-Syn transduction, but not GFP transduction, reduces Total-TH immunoreactivity in dopaminergic neurons
We verified that α-Syn aggregation was associated with reduced Total-TH-ir, using proteinase K (PK) and Thioflavin-S labeling of tissue sections from α-Syn- and GFP-transduced tissues at 3.5 and 21 days post-transduction using well-established methods [2
]. After PK, tissues triple-labeled for α-Syn, PSer19, and Total-TH revealed that PK-resistant α-Syn colocalized with PSer19-ir, however, Total-TH labeling was absent () as verified by Fluoview analysis (N = 50, t = 41.75, P < 0.0001), suggesting that Total-TH was soluble and digested away. Triple labeling for Thioflavin-S, α-Syn, and Total-TH at 14 days post-transduction revealed coincident α-Syn and Thioflavin-S staining confirming aggregation in cells with reduced, but perceptible, Total-TH-ir (, at arrowhead). Untransduced neurons, at the border of the injection site, maintained robust Total-TH-ir (, at arrows) much like labeling noted in cells of . Similar findings were noted at all time points. Importantly, GFP aggregation sometimes occurred as confirmed by Thioflavin-S staining; however Total-TH-ir was not reduced nor was PSer19-ir increased under those conditions (not shown). This suggests that α-Syn aggregation may have unique effects on TH phosphorylation and the reduction in Total-TH-ir.
α-Syn aggregation, confirmed by proteinase K or Thioflavin-S labeling, correlates with TH PSer19 immunoreactivity
α-Syn has a tendency to aggregate both in vitro [3
] and in vivo [7
]. Furthermore, α-Syn levels increase with age in nigral dopaminergic neurons [8
], and toxins can further increase α-Syn levels which may enhance aggregation [24
]. The presence of extra copies of the α-Syn gene can induce pathology in rare PD families [7
]. Our previous data show that α-Syn inhibits TH phosphorylation and activity [31
], likely working in counterpoint to 14-3-3 to modulate DA synthesis. Because phosphorylation of TH Ser19 potentiates Ser40 phosphorylation [4
], leading to increased DA synthesis [34
], our finding of high levels of phosphorylated TH in neurons bearing α-Syn aggregates () suggests that TH activity and DA synthesis may be increased in the cells [32
]. Because our earlier work revealed that α-Syn also inhibits aromatic amino acid decarboxylase (AADC), the enzyme that converts DOPA to dopamine [39
], unbridled DA synthesis may occur as soluble α-Syn levels drop below an acceptable threshold, although this awaits confirmation.
Cumulatively, our findings suggest that increasing α-Syn to levels that promote its aggregation may have the capacity to overactivate TH and AADC, which may ultimately contribute to nigral cell loss over time [32
]. Our findings further suggest that immunostaining of Total-TH may underestimate dopaminergic loss in cells with insoluble α-Syn, as noted using five different Total-TH antibodies. In contrast, cells were strongly labeled for TH PSer19, not only pointing to important effects of α-Syn on TH regulation, but also providing a novel tool for confirming dopaminergic phenotypes. Additionally, our findings reveal the usefulness of lentiviral α-Syn transduction of ASKO mice as a model system in which to further elucidate the impact of α-Syn on TH regulation, dopamine synthesis, and cell viability.