Excessive reactive oxygen species (ROS) can damage proteins, lipids, and DNA, which result in cell damage and death. The outcomes can be acute, as seen in stroke, or more chronic as observed in age-related diseases such as Parkinson’s disease. Here we investigate the antioxidant ability of a novel synthetic flavonoid, Proxison (7-decyl-3-hydroxy-2-(3,4,5-trihydroxyphenyl)-4-chromenone), using a range of in vitro and in vivo approaches. We show that, while it has radical scavenging ability on par with other flavonoids in a cell-free system, Proxison is orders of magnitude more potent than natural flavonoids at protecting neural cells against oxidative stress and is capable of rescuing damaged cells. The unique combination of a lipophilic hydrocarbon tail with a modified polyphenolic head group promotes efficient cellular uptake and moderate mitochondrial enrichment of Proxison. Importantly, in vivo administration of Proxison demonstrated effective and well tolerated neuroprotection against cell loss in a zebrafish model of dopaminergic neurodegeneration.
Oxidative stress has been implicated in a wide range of age-related conditions, including heart disease, cancer, diabetes and neurodegenerative diseases1,2,3,4. In healthy cells there is a balance between the production of reactive oxygen species (ROS) and their removal by antioxidants, with discrete generation of ROS playing an essential role regulating cell signaling and function5,6. Excessive production of ROS results in oxidative stress causing aberrant cell signaling, damage to cellular components, and subsequent disease. A number of ROS are involved in cellular oxidative stress, including superoxide radicals, hydrogen peroxide and hydroxyl radicals. The chemical reactivity of each of these and their site of production within the cell determines their ability to damage cellular components7,8. Mitochondria produce superoxide radicals and hydrogen peroxide as by-products of oxygen consumption. There are multiple sites of superoxide production in the mitochondrial electron transport chain including NADH-ubiquinone oxidoreductase of complex I, the coenzyme Q pool as well as complexes II and III9,10,11,12,13. Acute increased superoxide production at complex I occurs in stroke through a conserved mechanism14,15. This results in oxidative damage and neuronal cell death by mechanisms that include increased H2O2 release16,17.
Chronic exposure to oxidative stress has been implicated in numerous age-related degenerative conditions, including Parkinson’s disease where age is the most significant risk factor. Post-mortem analysis of Parkinson’s patients brains showed evidence of oxidative damage and mitochondrial complex I dysfunction in the substantia nigra3,18,19,20,21. During earlier stages of Parkinson’s disease, patients also show evidence of mitochondrial dysfunction and oxidative damage in their platelets and plasma22,23. However, it is difficult to determine when in the disease process this damage occurs and how influential it is in disease progression. The use of novel potent antioxidants in combination with refined disease models will be key to definng the role for oxidative stress in disease pathogenesis, and to pinpoint when and where this occurs. If it proves to be an early and pivotal defect, it opens up an exciting new field of potential therapeutic targets for intervention of age-related diseases.
Flavonoids are a large group of polyphenolic antioxidant compounds found in plants that can directly scavenge ROS. Their antioxidant activity is a result of the efficiency by which they can donate hydrogen atoms from their multiple hydroxyl groups to free radicals, a mechanism that is facilitated by the extended conjugation afforded through the π-electron system of the core flavonoid molecular scaffold24,25. The dietary flavonoids, quercetin and myricetin are amongst the most potent24,25,26, although they are poorly absorbed from the diet27,28,29. Furthermore, their physicochemical attributes mitigate against effective uptake and distribution in the cell25. However, cell absorption characteristics and bioactivity can be improved significantly by chemical modification of the parent myricetin compound through attachment of lipophilic alkyl chains of different lengths and by removal of hydroxyl groups that do not contribute to the antioxidant potential. A rational drug design approach, based on structure-activity relationships of natural and modified flavonoid antioxidants led to Proxison (7-decyl-3-hydroxy-2-(3,4,5-trihydroxyphenyl)-4-chromenone) as one of the most promising of these synthetic compounds29. This compound comprises of a straight chain C10 hydrocarbon tail covalently linked to a flavonoid head group similar to myricetin (Fig. 1a). In terms of prevention of lipid peroxidation, Proxison exhibited superior protection when compared to structurally similar compounds30. Recently, Proxison was shown to reduce proliferation of a breast cancer cell line at high concentrations, but its antioxidant functions at physiological concentrations have not been investigated31.
The aim of this study was to examine the antioxidant and cell protective activity of Proxison using in vitro and in vivo model systems. This compound had potent radical scavenging capabilities in a cell-free radical scavenging model and was highly protective in a neuronal cell model of acute oxidative stress. In vivo, Proxison efficiently protected against 6-hydroxydopamine (6-OHDA) induced death of dopaminergic neurons in a zebrafish model. We demonstrate that Proxison is highly cell permeable and shows enrichment in the cytosol, especially to mitochondria, a key characteristic that may be critical for its protective function in neurons. Therefore, Proxison represents a novel class of synthetic antioxidant, which is well tolerated and effective in promoting cell survival in conditions where oxidative stress is the major cause of cell death.
Radical scavenging capabilities of flavonoid antioxidants
To directly compare the scavenging ability of Proxison to the structurally related natural flavonoids, myricetin and quercetin (Fig. 1a), we used the stable free radical galvinoxyl in a cell-free assay. Galvinoxyl has one unpaired electron, which is extensively delocalised throughout the molecule and gives rise to a characteristic electron paramagnetic resonance (EPR) spectrum as a result of the interaction of the electron spin with the nuclear spins of protons in the molecule. All three flavonoids efficiently scavenged galvinoxyl radicals in this chemical model system and mediated a concentration-dependent reduction in EPR signal intensity (Fig. 1b,c). The radical scavenging ability of Proxison was equal to that of myricetin despite having two less hydroxyl groups and increased hydrophobicity, and both compounds were more than twice as potent as quercetin, which has one less hydroxyl group than myricetin on the B-ring (Fig. 1d).
Protection against acute oxidative stress in cells
Next, we compared Proxison to myricetin, quercetin, and other antioxidants for their ability to protect against oxidative stress in a neural cell culture model, SH-SY5Y neuroblastoma cells. These cells were treated with the organic peroxide tert-butyl hydroperoxide (tBHP) to generate peroxyl radicals and cause acute oxidative stress32. Cells exhibited a significant reduction in cell metabolic activity (MTS tetrazolium reduction assay) after 5 h treatment with 200–800 μM tBHP (Supplementary Figure 1). 400 μM tBHP was found to be optimal as it elicited a robust and reproducible stressor effect in this cell-based assay.
Proxison used at 5 and 10 μM significantly prevented the reduction in cell metabolic activity caused by 400 μM tBHP treatment (Fig. 2a). Due to its strong reducing capabilities, concentrations above 50 μM Proxison caused signs of cytotoxicity. Quercetin showed significant protection between 25–100 μM, however, a 10-fold higher concentration was required to exert a level of protection similar to Proxison. In contrast, myricetin showed no appreciable protection against tBHP even at 100 μM. Other antioxidants, including vitamin E, Idebenone (a synthetic derivative of coenzyme Q10) and coenzyme Q10 showed no protection in this assay (Fig. 2a). Furthermore, morphological signs consistent with lipid peroxidation, including membrane blebbing, which were observed by 5 h of tBHP treatment, were rescued by Proxison and high-dose quercetin, but not myricetin (Fig. 2b).
Oxidative stress can also result in cytotoxicity, so we next assessed cell death by the lactate dehydrogenase (LDH) assay. tBHP treatment of SH-SY5Y cells for 16 h caused a significant deterioration of cell membrane integrity resulting in leakage of cytoplasmic LDH into the media. Proxison (5–10 μM) and a high concentration of quercetin (100 μM, but not 25 μM) significantly prevented the cytotoxic effects of tBHP, while myricetin and vitamin E offered no protection (Fig. 2c). Similarly, we further confirmed the cytoprotective capabilities of Proxison with a propidium iodide (PI) exclusion assay (Fig. 2d). Less than 30% of tBHP-treated cells were viable after 16 hours as determined by this assay. However, pre-incubation with Proxison at 10 μM, but not 1 μM, protected against cell death to levels that were not significantly different from non-treated control cells (Fig. 2d).
We further confirmed the protective capabilites of Proxison with an independent clone of SH-SY5Y cells (Supplementary Movies 1 and 2), and demonstrated that 1 μM Proxison was sufficient to protect these cells from tBHP induced cell death (Supplementary Figure 2). We also compared Proxison, myricetin, and quercetin for their ability to protect a completely different neural cell line, Neuroscreen-1™ (NS-1), from peroxide induced toxicity. Similar to the SH-SY5Y results, a low dose of Proxison (0.5–5 μM) or a high dose of quercetin (25–50 μM) could protect NS-1 cells from tBHP-induced cytotoxicity, while myricetin did not exhibit any protective properties in this cell culture model (Supplementary Figure 3).
Flavonoid antioxidant cellular uptake and intracellular localisation
Given that the antioxidants were similarly potent in the cell-free galvinoxyl assay, the differential protective properties of Proxison, quercetin and myricetin in cells could be due to differences in cellular uptake or subcellular localisation. To investigate the intracellular uptake and localisation of the different flavonoids we took advantage of the endogenous fluorescence characteristics of these molecules33,34. Intrinsic green fluorescence of Proxison, myricetin and quercetin was confirmed using a plate reader with excitation 485 nm and emission 520 nm (Supplementary Figure 4).
Cells were incubated with Proxison (10 μM), quercetin (100 μM), or myricetin (100 μM) for 2 h and washed out before processing for confocal imaging. Whereas quercetin accumulated in nuclei, Proxison was localised to the cytoplasm with some enrichment in filamentous perinuclear structures (Fig. 3a). The subcellular localisation of Proxison was investigated further by staining with the mitochondrial marker, Mitotracker Deep Red. Although Proxison was observed throughout the cytoplasm, the stronger filamentous staining co-localized with Mitotracker Deep Red suggesting some form of enrichment at mitochondria (Fig. 3b). Despite an emission profile similar to quercetin (Supplementary Figure 4), myricetin did not appear to be taken up into cells, as the fluorescence observed in treated cells was similar to the background in control cells (Fig. 3a). Cellular uptake was further investigated by FACS analysis, which showed significant intracellular levels of Proxison and quercetin, whereas myricetin was undetectable (Fig. 3c). This suggests the lack of protective activity of myricetin compared to Proxison and quercetin reflects its inability to enter cells. In summary, Proxison was efficiently taken up by cells and was localised to the cytoplasm with moderate enrichment to mitochondria.
Given that Proxison exhibited some co-localization with a mitochondrial marker, we decided to test its protective capabilities directly against a known mitochondrial antioxidant, MitoQ35. As determined by the LDH release assay, both Proxison and MitoQ at 10 μM significantly protected cells against a high-dose of tBHP (400 μM), and Proxison was at least twice as potent as MitoQ in this acute cytotoxicity assay (Fig. 3d).
Proxison prevents intracellular radical production and downstream effects of oxidative stress
To assess intracellular scavenging potency of Proxison, the ROS biosensor CellROX® Deep Red was used36. Using far-red fluorescence intensity as a read-out of radical production, tBHP was found to significantly increase intracellular ROS in SH-SY5Y cells, and Proxison and quercetin, but not myricetin, were capable of preventing this ROS production (Fig. 4a). Quantification of far-red signals confirmed Proxison and high-dose quercetin effectively blocked the accumulation of tBHP-generated radicals to the level of untreated cells (Fig. 4b).
A major mechanism in the cellular defense against oxidative stress involves activation of the Nrf2-Keap1 antioxidant response signaling pathway35. This requires nuclear localization of a key transcription factor NRF2 to activate a number of antioxidant genes37,38,39. To determine whether Proxison is capable of preventing downstream consequences of tBHP induced oxidative stress we analysed subcellular localisation and action of NRF2. Nuclear NRF2 increased upon tBHP treatment, an effect that was significantly prevented in the presence of Proxison (Fig. 5a,b). To confirm NRF2 was active in the nucleus, we quantified expression of two NRF2-regulated antioxidant response element (ARE) genes, NQO1 and HMOX1. The increased transcription of both ARE genes caused by tBHP treatment was significantly attenuated by Proxison (Fig. 5d). The transcript levels of NRF2 itself were unaffected agreeing with the known post-translational mechanism of action for this transcription factor39.
To determine whether Proxison protects against ROS-induced oxidative damage of nucleic acids, we looked for the presence of 8-hydroxy-2’-deoxyguanosine (8-OHdG) in the cell, a marker of oxidative damage to DNA and RNA. 8-OHdG is a major product of nucleic acid oxidation and its concentrations within a cell act as a read-out of oxidative stress induced damage40. Proxison was able to completely inhibit the accumulation of 8-OHdG marks in cells caused by tBHP treatment (Fig. 5a,c).
Proxison protects dopaminergic neurons in a zebrafish model
To determine the ability of Proxison to protect neurons in an intact animal and to detect potential toxic side-effects, we assessed its ability to protect dopaminergic neurons in the brain of zebrafish embryos. The neurotoxic compound 6-hydroxydopamine (6-OHDA) was used to selectively induce death of dopaminergic and noradrenergic neurons in this model, as measured by counts of tyrosine hydroxylase (TH) positive neurons41,42. At 24 hours post fertilisation (hpf), zebrafish embryos were treated with 6-OHDA (250 μM for 24 h) in the absence or presence of the antioxidants Proxison or quercetin. At 48 hpf embryos were fixed and immunostained for TH prior to collection of z-stack images of each embryo head by confocal microscopy (Fig. 6a), and the number of TH positive cells were quantified (Fig. 6b). Embryos treated with 6-OHDA consistently had 30% less TH positive cells than control embryos, while co-incubation with Proxison showed significant protection against 6-OHDA-induced neuronal cell loss (Fig. 6a,b). Quercetin also afforded protection against 6-OHDA induced toxicity, but was less robust than Proxison. None of the treatments reduced survival or perturbed normal development of the embryos, showing that Proxison was not toxic and was well tolerated at the concentrations used that elicited neuroprotective effects in vivo.
Here we characterise the antioxidant profile of a novel synthetic flavonoid, Proxison. Although the intrinsic radical scavenging activity of Proxison is similar to its natural counterparts, it possesses a superior ability to protect against acute oxidative stress in cellular contexts. The lipophilic tail of Proxison enhances its cellular uptake and may improve its stability30. The subcellular localization of Proxison is mostly cytoplasmic with some enrichment at mitochondria, while quercetin localizes to the nucleus. Although myricetin was as potent as Proxison in a cell-free radical scavenging assay, it was poorly taken up by cells, possibly due to its instability at neutral pH or its low lipophilicity43,44. Quercetin was a less potent antioxidant scavenger in the cell-free assay, but it was readily taken up by cells, and it accumulates in the nucleus for, as yet, unknown reasons33. This localization could explain why a 10-fold higher concentration of quercetin is needed to provide a similar level of protection as Proxison, which is cytoplasmic, against tBHP-induced toxicity. The superior potency of Proxison may also be due to the phenoxyl radical (the oxidized form of Proxison) being recycled by intracellular antioxidants, or other reductive pathways, back to Proxison, as occurs for vitamin E45. Flavonoid antioxidants are also capable of chelating transition metal ions such as iron or copper thereby limiting the breakdown of tBHP to its initiating free radical products or inhibiting lipid peroxidation through the Fenton reaction25. Proxison may therefore be able to exert a protective effect by diverse mechanisms beyond the direct scavenging of free radicals by hydrogen atom electron transfer reactions, a model supported by structure-activity studies on a wide range of flavonoids, including myricetin46.
We demonstrated that Proxison scavenges intracellular ROS and prevents downstream oxidative damage to both membranes and nucleic acids. Induction of the NRF2 antioxidant response pathway was significantly dampened by Proxison, but not eliminated. Therefore, Proxison can act in conjunction with other cellular antioxidant responses to acute oxidative stress to promote cell survival. Importantly, the studies in zebrafish embryos showed that Proxison, and to a lesser extent quercetin, is capable of protecting dopaminergic neurons against acute neuronal loss in an intact animal. It is important to demonstrate that this neuronal loss is due to oxidative stress induced by 6-OHDA, and zebrafish models that directly measure oxidative stress in embryos have recently been established47.
There are currently several published classes of synthetic mitochondrial-targeted antioxidants. The Mito compounds contain a triphenylphosphonium ion (TPP), which has a positive charge that attracts it to the mitochondrial matrix. The TPP ion has been attached to a number of known antioxidants, including vitamin E and coenzyme Q1035,48. MitoQ compounds are taken up into cells and accumulate in mitochondria only when the membrane potential is intact, which may not always be the case in damaged cells35,48,49. MitoQ was tested in a phase II clinical trial for symptomatic Parkinson’s disease patients. However, there was no change in the rate of disease progression50. Currently MitoQ is due to undergo a phase II clinical trial for chronic kidney disease (ClinicalTrials.gov Identifier: NCT02364648). SS peptides are short positively charged peptides that are cell permeable and localise to mitochondria51,52. SS peptide localization is due to their lipophilicity and positive charge and is partially reliant on an intact mitochondrial membrane potential52,53. The lead SS peptide, SS-31 (Bendavia; MTP-131), is protective in rodent models of amyotrophic lateral sclerosis and myocardial infarction54,55. Bendavia is currently in clinical trials for heart failure (ClinicalTrials.gov Identifier: NCT02388464) and genetically confirmed mitochondrial disease (ClinicalTrials.gov Identifier: NCT02805790). The plant-derived antioxidants, plastoquinone and thymoquinone, have also been modified to accumulate in mitochondria56. These mitochondrially-targetted antioxidants show protection in a rat stroke model57. Proxison exhibits some mitochondrial enrichment as a likely consequence of the lipophilicity of a long hydrocarbon tail combined with the unique redox properties of the polyphenolic head group58. However, it is not yet known whether this enrichment is due to the unique properties of mitochondrial lipids or proteins that may have affinity for Proxison, or if the enrichment requires an intact mitochondrial membrane potential.
This novel antioxidant can be applied to investigate oxidative stress in disease models, like α-synucleinopathies and other neurodegeneration models. This would provide insight into disease processes and aid in development of novel treatments. In addition, Proxison could have applications for regenerative medicine where oxidative stress has been implicated in poor cell survival of transplanted cells, with the advantage that the molecule can be pre-loaded into cells prior to transplantation. Proxison could also have applications for conditions, such as stroke or cardiac infarction, in which a temporary, but acute, exposure to oxidative stress is experienced, as well as diseases in which oxidative stress and mitochondrial dysfunction are core features.
Galvinoxyl Electron Paramagnetic Resonance Spectroscopy
Galvinoxyl (182 μM, Sigma) was mixed with 2.5 μM or 5 μM Proxison (7-decyl-3-hydroxy-2-(3,4,5-trihydroxyphenyl)-4-chromenone, Antoxis), myricetin (Sigma) or quercetin (Sigma) in DMSO. Five minutes after addition measurements were taken using the Magnettech Miniscope MS200 EPR machine. Settings: centre field = 3364.05 G; Sweep = 69.59 G; Sweep Time = 20 s; Smooth = 0 s; Steps = 4096; Number of passes = 1 pass; Modulation = 1.5 G; Power = 7 dB; Gain = 1E2. The percentage radical scavenging ability was calculated from the EPR signal intensity with antioxidant relative to the signal intensity of galvinoxyl alone.
The SH-SY5Y cell line was a kind gift from Professor David Porteous (Institute of Genetics and Molecular Medicine, University of Edinburgh). They were cultured at 37 °C in a humidified atmosphere of 5% CO2 in DMEM supplemented with 10% FBS, 2 mM L-glutamine and 1 mM sodium pyruvate (all from Life Technologies). When cells were 70–80% confluent they were passaged using trypsin (Life Technologies). An independent clone of SH-SY5Y cells was kindly provided by Dr Michael J Devine (Institute of Neurology, UCL). The rat Neuroscreen™-1 (NS-1) cells (Thermo Scientific, R04–0001-AP) were cultured in NS-1 medium consisting of RPMI 1640 basal medium (Hyclone, SH30027) supplemented with 10% horse serum (Life Technologies, 26050-088), 5% FBS and 2 mM L-glutamine.
The MTS assay was performed using the Promega CellTiter 96® Aqueous MTS Reagent Powder (Promega) with phenazine methosulphate (PMS; Sigma) as the electron coupler. SH-SY5Y cells were seeded at 1.25 × 105 cells/cm2 in 96-well plates and incubated for 24 hours when either tBHP (Sigma) was added or cells were pre-incubated with antioxidants Proxison, myricetin, quercetin (all from Antoxis), vitamin E (Sigma), Idebenone (Antoxis) or coenzyme Q10 (Sigma) for 30 minutes before tBHP (400 μM) addition. Five hours later phase-contrast images were collected with an Olympus IX51 inverted microscope and the MTS assay was performed, according to manufacturer’s instructions. Briefly, 100 μl of PMS (0.92 mg/ml) was added to 2 ml of MTS (2 mg/ml), and then 20 μl of the MTS/PMS mixture was added to each well of a 96-well plate containing 100 μl of conditioned media. The plate was incubated at 37 °C/5% CO2 for 1 hour when the absorbance at 490 nm was measured using the FLUOstar OMEGA microplate reader (BMG LabTech). The background absorbance from the media incubated with MTS/PMS was subtracted from the well absorbance to give the sample absorbance. The percentage of the sample absorbance relative to control treated cells absorbance gave the % metabolic activity. NS-1 cells were seeded at 3.125 × 104 cells/cm2 on 6 μg/cm2 collagen I coated 96-well plates, and differentiation was initiated the following day medium by replacing medium with a 1 in 10 dilution of NS-1 medium supplemented with 50 ng/ml nerve growth factor β (NGFβ) (Sigma, N2513). On day 3 of differentiation cells were treated with tBHP (200 μM) for 16 hours before an MTS assay was performed as described above.
The LDH-Cytotoxicity Assay Kit II (Source Bioscience) was used to quantify cell death due to tBHP treatment. SH-SY5Y cells were pre-incubated with Proxison, myricetin, quercetin, vitamin E, or MitoQ (gift from Prof Mike Murphy) for 30 minutes when 400 μM tBHP was added to the antioxidants for 16 hours. Thirty minutes before the end of tBHP treatment cell lysis buffer was added to the high control wells. At the end of tBHP treatment the 96-well plate was gently mixed to distribute the LDH in the media. The plate was then centrifuged at 600 g for 10 minutes to precipitate cells and debris. 10 μl of media from each well was moved to a new 96-well plate and 100 μl of LDH reaction mix was added to each well. The plate was then incubated at room temperature for 30–60 minutes when absorbance was read using the FLUOstar OMEGA microplate reader. The 650 nm reference absorbance was subtracted from the 450 nm absorbance reading to give the well absorbance. The background absorbance was subtracted from the well absorbance to give the sample absorbance. The sample absorbance was subtracted from control-cultured cells (low control) and divided by the cells that had been lysed (high control) minus the control cells (low control) to give the % cytotoxicity.
The propidium iodide (PI) assay was performed to assess Proxison protection against tBHP-induced toxicity. SH-SY5Y cells were pre-incubated with Proxison (1 or 10 μM) for 30 minutes when 400 μM tBHP was added for 16 hours. Then the media was collected and cells were lifted using trypsin, washed in PBS with 2% FBS and resuspended in 100 μl PBS with 2% FBS. This cell solution was filtered and incubated with PI (1 μg/ml) at room temperature for 10 minutes. Then 300 μl PBS with 2% FBS was added to dilute the cells. Cells were kept on ice until FACS analysis data was collected using the FACS Calibur and post-acquisition analysis was performed using FlowJo X. The unstained sample was used to create gates to determine PI positive cells and the percentage of PI positive and negative cells was calculated.
Live cell imaging of SH-SY5Y cells treated with tBHP (400 μM) in the absence or presence of Proxison (1 μM) was obtained with the Cell-IQ system (CM Technologies) for 5 hours (Supplementary Movies 1 and 2).
Proxison, myricetin and quercetin (1 mM) in DMSO were added to a 96-well plate in triplicate. The intrinsic fluorescence of each compound was measured using a FLUOstar OMEGA microplate reader (BMG LabTech) with excitation 485 nm and emission 520 nm. DMSO background fluorescence was subtracted.
Antioxidant Subcellular Localisation
SH-SY5Y cells were seeded on coverslips and loaded with the following antioxidants for 2 hours; 10 μM Proxison, 100 μM quercetin, 100 μM myricetin or DMSO as a vehicle control. Then cells were fixed in 4% PFA (Sigma) and counterstained with 4′,6-diamidino-2-phenylindole (DAPI; Life Technologies) for 10 minutes. Coverslips were washed in MilliQ water and mounted onto slides using Vectashield (Vector Laboratories, H1000). Images were taken using the 63x objective of the Leica TCS SPE confocal microscope. The 488 nm laser was used to excite the antioxidants and emission was measured between 496–595 nm. To observe Proxison subcellular localization, SH-SY5Y cells on coverslips (as above) were loaded with 100 nM Mitotracker Deep Red (Life Technologies) for 20 minutes before the addition of 10 μM Proxison for 2 hours. The cells were then fixed in 4% PFA and processed as described above. The 635 nm laser was used to excite Mitotracker Deep Red.
Intracellular Antioxidant Fluorescence (FACS)
SH-SY5Y cells were treated as above for antioxidant localisation but 2 hours after antioxidant addition cells were lifted using trypsin, washed in PBS with 2% FBS and resuspended in 100 μl PBS with 2% FBS. The cell solution was then filtered and cells were incubated with PI (1 μg/ml) on ice. 300 μl PBS with 2% FBS was added. Cells were kept on ice until fluorescence was analysed using the FACS Calibur. Post-acquisition analysis using FlowJo X was used to exclude PI positive cells and to graph the cells positive for green (FL-1) fluorescence. Mean green fluorescence was calculated with FlowJo X.
CellROX® Deep Red Assay
SH-SY5Y cells were seeded at 6.25 × 104 cells/cm2 on 13 mm coverslips. 24 hours later cells were incubated with 10 μM CellROX® Deep Red (Life Technologies) and 2.8 μg/ml Hoechst 33342 (Fluka) for 30 minutes. CellROX® and Hoechst 33342 were removed and cells were washed three times with complete medium. Proxison (10 μM) or DMSO vehicle was added for 30 minutes, and then 400 μM tBHP was added. One hour after tBHP addition, the coverslips were placed into an Attofluor® Cell Chamber (Life Technologies) holder and washed with Hank’s balanced salt solution (HBSS) with calcium and magnesium. Images were taken on the Zeiss Observer of phase contrast, CellROX® Deep Red and Hoechst 33342 fluorescence. Random areas (n = 5–6) of each coverslip were imaged. Post-acquisition analysis was performed using Volocity. A small area around each apparent cell nuclei was selected in all images and the mean fluorescence in arbitrary units (au) in these areas was calculated. The mean and standard error of mean (SEM) was calculated (n = 4).
Immunocytochemistry and quantification
SH-SY5Y cells were seeded at 1.25 × 105 cells/cm2 on coverslips and incubated for 24 hours prior to addition of Proxison or vehicle (DMSO) for 30 minutes. Then 400 μM tBHP was added for 4.5 hours when cells were fixed with 4% PFA for 20 minutes and washed three times with PBS. Immunocytochemistry was performed by the addition of blocking buffer (0.1% Triton X-100 or 0.3% Triton-X100 for nuclear staining, 2% goat serum, PBS) for 30 minutes. Primary antibodies rabbit IgG NRF2 (1:800, C-20, Santa Cruz), mouse IgG2b 8-OHdG (1:1000, 15A3, abcam) in blocking buffer were added to cells for 16 hours at 4 °C, when they were washed 3 times in PBS with 0.1% Triton X-100. Secondary antibodies (Life Technologies) in blocking buffer were incubated with cells for 2 hours at room temperature in the dark, when they were washed 3 times in PBS with 0.1% Triton X-100. DAPI (10–50 μg/ml, Life Technologies) in PBS was added for 10 minutes. Cells were imaged using Leica TCS SPE confocal microscope. NRF2 images were quantified using ImageJ. The z-stack images were flattened and a mask was created using the DAPI channel. This mask was then used to calculate the nuclear red fluorescence intensity. The mean fluorescence from each image (2–4 images) and from each coverslip was calculated. The 8-OHdG images were quantified using ImageJ. The z-stack images were flattened and a mask was created using the DAPI channel, this mask included the nuclei and the area surrounding the nuclei by reducing the threshold. This mask was then used to calculate the nuclear green fluorescence intensity. The mean fluorescence from each image was calculated with ImageJ.
SH-SY5Y cells were loaded with Proxison or DMSO as a control for 30 minutes before 400 μM tBHP was added for 4.5 hours when cells were lifted with trypsin and pelleted. RNA extraction was performed using the Epicentre MasterPure™ Complete DNA and RNA Purification Kit (Epicentre, MC85200), according to manufacturer’s instructions. RNA concentration was quantified using a Nanodrop spectrophotometer. Total RNA (1 μg) was used for cDNA synthesis. RNase-free water was added to the RNA to give a 10 μl sample. The samples were incubated with 1 μl dNTP mix (10 mM Life Technologies) and 1 μl random primers (50 ng/μl, Thermo Fisher) at 65 °C for 5 minutes and then chilled on ice. After brief centrifugation, 4 μl 5x First strand buffer (Life Technologies), 2 μl 0.1 M DTT (Life Technologies) and 1 μl RNAse OUT (40 units/μl, Life Technologies) were added. The contents was incubated at 37 °C for 2 minutes. Then 1 μl M-MLV reverse transcriptase (200 units/μl, Life Technologies) or 1 μl RNase-free water for the negative reverse transcriptase sample was added. This was mixed and incubated at room temperature for 10 minutes when it was moved to 37 °C for 60 minutes. The reaction was inactivated by incubation at 90 °C for 10 minutes. The cDNA mix was placed on ice and 80 μl RNase-free water was added. qPCR was performed using the Roche LightCycler® 480 System with the Universal Probe Library (UPL) (Roche). The Roche UPL Assay design centre was used to design intron-spanning primers with a specific UPL probe for each gene (TBP F-gaacatcatggatcagaacaaca R-atagggattccgggagtcat Probe 87; NRF2 F-acacggtccacagctcatc R-tgcctccaaagtatgtcaatca Probe 18; HMOX1 F-cagtcaggcagagggtgatag R-agctcctgcaactcctcaaa Probe 42; NQO1 F-acgctgccatgtatgacaaa R-ggatcccttgcagagagtaca Probe 9). Reactions (10 μl) containing primers, UPL Probe, LightCycle® 480 Probes Master mix (Roche) and PCR water were performed in 386-well plates as described in the manufacturer’s instructions. The results were normalized to RNA levels of TATA-binding protein (TBP).
Treatment of zebrafish embryos with 6-hydroxydopamine (6-OHDA) and neuroprotective compounds
All zebrafish were maintained under Home Office Project Licence No.: 60/4196 and all experiments were performed in accordance with the relevant guidelines and regulations, and approved by the Animal Welfare and Ethical Review Body of the University of Edinburgh. The Wik wild-type strain of zebrafish was used for this study, and they were maintained in standard conditions59. Clutches of embryos were obtained from single pair matings to ensure all embryos were at the same developmental stage across treatments. At 24 hours post fertilisation (hpf) embryos were split into groups of 24–30 embryos and treated with 250 µM 6-OHDA (162957, Sigma) or 250 µM 6-OHDA + 10 µM Proxison or quercetin in 3 ml embryo medium for 24 hours (water for control). At 48 hpf embryos were fixed in 4% paraformaldehyde in PBS for 45 min. Samples were then blocked (2% bovine serum in 0.1% PBS-triton) for 1 h at room temperature. A mouse monoclonal anti-TH antibody (1:1000 diluted in blocking buffer, MAB318, Millipore) was used as the primary antibody and incubated with the samples overnight at 4 °C. The next day samples were washed in 0.1% PBS-T, followed by incubation with a secondary antibody Cy3 donkey α-mouse IgG (1:200 diluted in blocking buffer, 715165150, Jackson Immuno) overnight at 4 °C. Samples were then washed and mounted in 70% glycerol in PBS. Embryos were imaged by confocal microscopy (LSM710, Zeiss, Oberkochen, Germany), and Z-stacks were taken through the head ensuring all cells could be quantified. Cell counts were performed using ImageJ. The observer was blinded for all quantifications of confocal images.
Statistical Analysis and Raw Data
Statistical Analysis was performed in Minitab using the Analysis of Variance (ANOVA) statistical test with a Tukey’s post-hoc test. Raw data used to generate all graphs can be found at LabArchives DOI 10.6070/H44X55WM.
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This work was funded by a Scottish Universities Life Sciences Alliance (SULSA) BioSkape Industry PhD studentship to NJD and Antoxis Limited as the industrial sponsor. TK was funded by a Parkinson’s UK Senior Research Fellowship (F-0902) and an MRC grant (MR/J012831/1). JEL was funded by a Royal Society University Fellowship and grant (RF 120645). MRM was funded by a British Heart Foundation Special Project Grant (SP/15/8/31575). NOD was funded by an MRC PhD studentship. TB and CGB were funded by a BBSRC project grant (BB/M003892/1). We thank Prof Mike Murphy (MRC Mitochondrial Biology Unit, Cambridge) for the generous gift of MitoQ compound. We are grateful to Dr Pleasantine Mill and Dr Ammar Natalwala for critical comments on the manuscript. We thank Dr Judith Sleeman for use of cell culture facilities at St Andrew’s University.
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