SIRT1 Activating compounds reduce oxidative stress mediated neuronal loss in viral induced CNS demyelinating disease
© Khan et al.; licensee BioMed Central Ltd. 2014
Received: 29 November 2013
Accepted: 21 December 2013
Published: 2 January 2014
Multiple sclerosis (MS) is characterized by central nervous system inflammation and demyelination, and increasing evidence demonstrates significant neuronal damage also occurs and is associated with permanent functional impairment. Current MS therapies have limited ability to prevent neuronal damage, suggesting additional neuroprotective therapies are needed. Compounds that activate the NAD+-dependent SIRT1 deacetylase prevent neuronal loss in an autoimmune-mediated MS model, but the mechanism of this effect is unknown, and it is unclear whether SIRT1 activating compounds exert similar effects in demyelinating disease induced by other etiologies. We measured neuronal loss in C57BL/6 mice inoculated with a neurotropic strain of mouse hepatitis virus, MHV-A59, that induces an MS-like disease.
Oral treatment with the SIRT1 activating compound SRTAW04 significantly increased SIRT1 activity within optic nerves and prevented neuronal loss during optic neuritis, an inflammatory demyelinating optic nerve lesion that occurs in MS and its animal models. MHV-A59 induced neuronal loss was associated with reactive oxygen species (ROS) accumulation, and SRTAW04 treatment significantly reduced ROS levels while promoting increased expression of enzymes involved in mitochondrial function and reduction of ROS. SRTAW04 exerted similar protective effects in EAE spinal cords, with decreased demyelination.
Results demonstrate that SIRT1 activating compounds prevent neuronal loss in viral-induced demyelinating disease similar to their effects in autoimmune-mediated disease. One mechanism of this neuroprotective effect involves increasing mitochondrial biogenesis with reduction of oxidative stress. SIRT1 activators represent a potential neuroprotective therapy for MS. Understanding common mechanisms of these effects in distinct disease models will help identify targets for more specific therapies.
KeywordsDemyelinating disease Mouse hepatitis virus SIRT1 Neuroprotection Oxidative stress Optic neuropathy
Multiple sclerosis (MS) is an inflammatory demyelinating disease of the central nervous system (CNS) . Significant neuronal damage also occurs in MS, and correlates with permanent neurologic dysfunction [2–6]. Current therapies reduce the inflammatory component of MS, but their ability to prevent neuronal damage is limited [7–10], suggesting additional therapies with neuroprotective benefits are needed.
While evidence suggests MS is an autoimmune disease against CNS myelin, the exact etiology is not known. Other evidence suggests genetic and viral-mediated triggers . Because the etiology is unknown, several MS animal models are used. The most common MS model, experimental autoimmune encephalomyelitis (EAE), is an autoimmune driven CNS demyelinating disease  that also exhibits neuronal damage [13–15]. Another MS model is induced by infection with a neurotropic strain of mouse hepatitis virus (MHV), MHV-A59 [16, 17]. While MHV-A59 induces CNS inflammation and demyelination similar to EAE, the etiology is distinct, involving direct neuronal infection, and the demyelination is not dependant on an intact immune system . Therefore, these models provide unique and contrasting systems for studying potential neuroprotective strategies for MS.
Optic nerve is a frequent site of MS lesions, and optic neuritis is a common presenting sign of MS . Similarly, optic neuritis occurs at high frequency in both EAE and MHV models of MS [20–22]. In addition to optic nerve inflammation, these studies demonstrate significant axonal damage, with loss of retinal ganglion cell (RGC) neurons that comprise the optic nerve also found in EAE optic neuritis, but not examined in the MHV model. RGCs are readily quantified, allowing optic neuritis to serve as a representative lesion for assessing neuronal damage [5, 6, 14, 20, 22].
Activation of SIRT1, an NAD-dependent deacetylase involved in cell stress responses, attenuates neuronal damage in EAE [23–25], although mechanisms mediating this effect are not known. SIRT1 reduces oxidative stress and promotes mitochondrial biogenesis in muscle  and cultures of neuronal cells , and oxidative stress plays a role in neuronal degeneration in MS and EAE [28–30], suggesting SIRT1 activation may prevent neuronal damage by increasing mitochondrial function and reducing oxidative stress.
While mechanisms of neuronal damage in MHV-A59-induced demyelinating disease are not fully understood, oxidative stress is a common mechanism of cellular injury and is likely to occur in MHV-A59 infection. The current studies characterize mechanisms of neuronal loss in viral-induced demyelinating disease, and examine the ability of SIRT1 activating compounds to prevent neuronal loss, reduce oxidative stress, and regulate proteins that promote mitochondrial function.
Four-week-old female C57BL/6 (B6) mice were purchased from the Jackson Laboratory (Bar Harbor, ME). Treatment of the animals was reviewed and approved by the Institutional Animal Care and Use Committee at the University of the Pennsylvania, where the mice were maintained and fed ad libitum in an approved animal care facility.
Inoculation and treatment of mice
MHV-free mice were inoculated intracranially with 50% of the half lethal dose of the demyelinating strain MHV-A59 [2000 plaque forming units (pfu)], a related non-demyelinating strain MHV2 (100 pfu) used as a negative control, or isogenic recombinant strains containing a fluorescent tag: RSA59 (20,000 pfu) used as a positive control and RSMHV2 (250 pfu) as negative control. Due to differences in replication and elimination, these doses result in equivalent viral loads in the CNS, and inoculation of each strain was performed as described previously [31, 32]. Mice were monitored daily for mortality and signs of disease [16, 17]. Mock-infected controls were inoculated similarly but with an uninfected cell lysate at a comparable dilution. SRTAW04 (Sirtris, a GSK company, Cambridge, MA) was prepared in PBS containing 0.5% methyl cellulose and 0.1% tween 80. Mice were treated with SRTAW04, 100 mg/kg/mouse/day by oral gavage. The dose was chosen based on previously measured pharmacokinetics of the drug and its ability to activate SIRT1 which has been used previously with maximal effects [27, 33, 34]. Seven day and 30 day treatment groups received SRTAW04 starting from day 1 until sacrifice. To evaluate whether the SRTAW04 target is SIRT1 and its activation, one group of mice received SIRT1 inhibitor EX527 (10 mg/kg/day i.p.) for 30 days . EX527 has the highest inhibitory activity for SIRT1 compared to other analogues and previous studies have shown that EX527 treatment alone does not result in the acetylation of SIRT1/2 target p53 [36, 37]. We have previously shown that SIRT1 inhibitors or conditional deletion of the SIRT1 gene, do not exacerbate RGC loss in optic nerve disease models [24, 38].
RGC labeling and counting
RGCs were labeled and counted as described previously . Briefly, 2.5 μL of 1.25% hydroxystilbamidine (Fluorogold; Molecular Probes, Eugene, OR) in sterile water was injected stereotactically into each superior colliculus through holes drilled in the skull. Mice were killed 7 or 30 days after infection and each eye was removed and fixed in 4% paraformaldehyde. Retinas were isolated, prepared as flattened wholemounts, viewed with a fluorescence microscope (Eclipse E600; Nikon, Tokyo, Japan), and photographed at 20X magnification in 12 standard fields: 1/6, 3/6, and 5/6 of the retinal radius from the center of the retina in each quadrant. RGC numbers shown in each experiment represent the total number of RGCs counted per eye (RGCs/0.74 mm2). RGCs were counted by a masked investigator using image analysis software (Image-Pro Plus 5.0; Media Cybernetics, Silver Spring, MD). Alternatively, to confirm RGC numbers, RGC’s were immunolabelled with antibodies to Brn3a. Retinas were dissected and flat as previously reported . The retinas were washed with PBS, permeabilized in 0.5% TritonX 100 in PBS by freezing them for 15 min at −70°C, rinsed in PBS containing 0.5% Triton, and incubated overnight at 4°C with goat-antiBrn3a antibody (Santa Cruz) diluted 1:100 in blocking buffer (PBS, 2% bovine serum albumin, 2% Triton X 100). The retinas were washed three times in PBS, incubated for 2 hours at room temperature (RT) with anti-goat secondary antibody diluted 1:500 in blocking buffer, washed in PBS and mounted vitreous side up on slides in anti-fading solution. Cells were counted in 12 fields as described above for fluorogold labeled RGCs.
Mice were killed at day 30 post inoculation (p.i.), and were perfused transcardially with PBS followed by PBS containing 4% paraformaldehyde (PFA). Spinal cords or optic nerves were collected, postfixed in 4% PFA overnight and embedded in paraffin. Spinal cord tissues were sectioned at 5 μm and stained with either Luxol Fast Blue (LFB) to detect demyelination or with anti-neurofilament antibodies to detect loss of axons. Areas of demyelination in LFB staining were quantified using a 0–3 point scale as described earlier  0 - no demyelination; 1 - rare foci of demyelination; 2 - a few foci of demyelination; and 3 - large (confluent) areas of demyelination. Two to three sections were examined from each of three spinal cord levels (cervical, thoracic and lumbar) for each mouse. Neurofilament staining was done according to a previously published protocol . Briefly, paraffin embedded sections were dewaxed, rehydrated, and then permeabilized with 0.5% tween-20 in PBS. The sections were blocked with blocking reagent from Vectastain Elite ABC kit and then incubated in the rabbit anti-neurofilament antibody 1:100 (AbCam) at 4°C overnight, washed, and incubated with goat biotinylated anti-rabbit secondary antibody (Invitrogen) for 2 hours at RT. The ABC detection was performed using the Vectastain Elite ABC kit and DAB (diaminobenzidine) substrate kit (both Vector Laboratories, Burlingame, CA) according to manufacturer's instructions. To characterize virus induced inflammation, spinal cords from 7 day p.i. mice were stained with H&E as described previously [21, 32] and scored using an inflammation scale: 0 - no inflammation, 0.5 - few inflammatory cells, 1 - inflammatory cells localized near white matter, 1.5 - small patches of inflammatory cells, 2 - large inflammatory plaques, 3 - diffuse inflammation. Experiments were repeated three times with 3–5 mice in each group. All slides were coded and read in a blinded manner. 30 days p.i. spinal cord sections were also stained with a macrophage/microglial marker anti-Iba1 (Wako, Japan) as described previously . Iba1 stained sections were counterstained with hematoxylin (Vector laboratories). Optic nerve tissues were sectioned as 5 μm longitudinal sections and stained with H&E, LFB and anti-neurofilament antibody using methods described above.
SIRT1 activity assay
SIRT1 activity was determined with a SIRT1 Fluorometric Kit (BIOMOL, Plymouth Meeting, PA) performed according to the manufacturer's instructions. Optic nerves were homogenized in SIRT1 assay buffer, then incubated for 10 min at 37°C to allow degradation of any contaminant NAD+. Protein concentration was determined using a BCA protein assay kit (Thermo Scientific, Rockford, IL). Homogenates (20–30 μg protein/well) were then incubated with 100 μM Fluor de Lys–SIRT1 substrate (Enzo Life Sciences) in the presence or absence of NAD+ to determine NAD+ dependent SIRT1 activity. The reaction was terminated by adding Fluor de Lys Developer (Enzo Life Sciences) and 2 mM nicotinamide after 60 min of incubation at 37°C and fluorescence values were read on a fluorometric plate reader (Wallac Victor2 1420 multi label counter, Perkin Elmer, Waltham, MA) with an excitation wavelength of 360 nm and an emission wavelength of 460 nm. SIRT1 inhibitors nicotinamide (2 mM), suramin (100 μM), and sirtinol (100 μM) were used to confirm the specificity of the reaction.
MitoSOX Red (Invitrogen) superoxide indicator is a fluorogenic dye for selective detection of superoxide, a reactive oxygen species (ROS), in mitochondria. MitoSOX Red reagent is cell permeable and is selectively targeted to the mitochondria, where it is oxidized by superoxide and exhibits red fluorescence. MitoSOX staining was done according to previously published protocols . Briefly, MitoSOX reagent was diluted to a final concentration of 5 μM in PBS and optic nerves were incubated for 30 min at 37°C. After incubation, nerves were washed three times with PBS, fixed with 4% paraformaldehyde for 10 min and mounted in Optimal Cutting Temperature (OCT) compound (Ted Pella, Inc., Redding, CA). 5 μM cross-sections were made, mounted onto glass slides with Mowiol mounting medium, and observed under an Eclipse E600 (Nikon) fluorescence microscope using excitation 510 nm/emission 580 nm, and photographed at 20X magnification. Photographs were taken centered within each optic nerve cross section by a blinded investigator using a standard exposure, and staining was quantified by calculating the optical density using Image J software (nih.gov).
Western blot analysis
Optic nerves or retinas in RIPA buffer (150 mM NaCl, 1% NP-40, 0.5% desoxycholic acid, 0.1% SDS and 50 mM Tris, pH 8) were ultrasonicated on ice 5 times for 5 sec each at 10-sec intervals to obtain total protein extracts. Cell lysates were then centrifuged at 14,000 g for 10 min at 4°C, and the protein concentration of the supernatant was determined using a BCA protein assay kit (Thermo Scientific). Sodium dodecyl sulfate polyacrylamide gel electrophoresis was performed on 10% polyacrylamide gels, with 20 μg of protein per lane, and then transferred to nitrocellulose High bound ECL membranes (GE Healthcare Biosciences, Pittsburgh, PA). The membrane was blocked with Odyssey Blocking Buffer (Licor Biotechnology, Lincoln, NE) for 1 hr at RT and probed with rabbit polyclonal antibodies against SIRT1 (1:1500) (Abcam, Cambridge, MA), SOD2 (1:1000) (GeneTex, Irvine, CA) and PGC-1α (1:1000) (Novus Biologicals, Littleton, CO) and mouse monoclonal antibodies against succinate dehydrogenase B (SDHb) (1:1000) (Abcam) overnight at 4°C. After being washed three times using PBS, the membranes were incubated with IRDye® 800CW goat anti-rabbit IgG or IRDye® 600 goat anti-mouse IgG (Licor) as secondary antibodies at a dilution of 1:5000 for 1 hr at RT. After being washed a further three times with PBS, fluorescence was visualized using Odyssey infrared imaging system (Licor). For normalization of signals, blotted membranes were stained for β-actin (Sigma). The intensity of each band was determined using Image J software (nih.gov).
Data are expressed as means ± SEM. Differences in RGC numbers, SIRT1 activity, and protein expression were assessed using one-way ANOVA followed by Student Neuman–Keuls post-hoc test. Statistical differences were considered significant at P < 0.05.
MHV-A59 infection induces optic nerve inflammation and neuronal loss
SRTAW04 treatment increases SIRT1 activity in optic nerves
We next examined SIRT1 activity in the optic nerves of MHV-A59 infected mice after 30 days of SRTAW04 treatment. 4 week old mice were infected with MHV-A59 and were treated with SRTAW04 starting from day 1 with 100 mg/kg/day for 30 days. On the 30th day mice were sacrificed 1 hr after SRTAW04 treatment and protein was extracted from optic nerves for SIRT1 activity assay. Optic nerves of MHV-A59 mice treated with SRTAW04 showed a significant increase in SIRT1 activity compared to control and untreated MHV-A59 infected mice (Figure 2b). Interestingly, untreated MHV-A59 infected mouse optic nerves also showed a smaller but significant increase compared to control, possibly as a natural defense mechanism. We also examined levels of SIRT1 in retinas and optic nerves of mice after 7 or 30 days with or without treatment by SRTAW04. SIRT1 protein expression levels measured by Western blotting showed no significant differences between any treatment groups in day 30 optic nerves (Figure 2c), with similar lack of change in day 7 optic nerves and in retinas at either time point (data not shown).
SRTAW04 treatment prevents neuronal loss in MHV-A59 infected mice
Effects of SRTAW04 on neuronal loss in the optic nerve
SRTAW04 treatment reduces accumulation of ROS in MHV-A59 infected optic nerves
Effects of SRTAW04 on expression of markers of mitochondrial and anti-oxidant function
Effects of SRTAW04 on demyelination in the spinal cord
Effects of SRTAW04 on inflammation in the spinal cord
Results confirm that infection with demylinating strains MHV-A59 and RSA59 induce optic neuritis in this model of MS, and for the first time demonstrate significant RGC loss occurs in this model as well. SIRT1 activating compound SRTAW04 significantly attenuates neuronal loss induced by MHV-A59 and RSA59 infection. Similar neuroprotective effects mediated by several SIRT1 activators were previously demonstrated in two different EAE models of MS, relapsing/remitting EAE in SJL/J mice [23, 24] and chronic EAE in C57BL/6 mice , but the mechanism of these effects was not assessed beyond the role of activating SIRT1. The current results suggest SIRT1 activators can work by promoting mitochondrial function and reducing the accumulation of ROS. While such oxidative stress has been demonstrated previously in EAE [28, 30], it was not clear whether similar mechanisms would be found in the MHV induced demyelinating disease. While we found that SIRT1 activation is associated with reduced accumulation of ROS in optic nerves, one limitation of this study that will be addressed in future studies is that a causal relation of this effect has not been confirmed using ROS inhibitors as positive controls.
Interestingly, pathogenesis of neuronal injury begins with different triggers in EAE optic neuritis as compared to MHV optic neuritis, despite similar gross levels of inflammation. Axonal injury and loss of neurons in relapsing/remitting EAE occurs secondary to inflammation [47, 48], predominantly mediated by effector T cells, whereas neurotropic strains of MHV can directly infect neurons leading to direct injury, and leading to myelin stripping by activated microglia/macrophages . MHV induced disease also occurs even in the absence of lymphocytes . The ability of SIRT1 activators to prevent neuronal loss in both models therefore suggests they modulate a common mechanism of neurodegeneration downstream of the initial mechanisms of injury. SIRT1 activators appear to work by increasing expression of proteins involved in mitochondrial biogenesis and reduction of ROS, and indicate these are important targets for neuroprotective therapies. Consistent with this, SIRT1 activators were found to have similar neuroprotective effects in a model of traumatic optic nerve injury .
Resveratrol, a naturally-occurring polyphenolic compound, is the most studied SIRT1 activator . A role for resveratrol and SIRT1 in neuroprotection has been suggested in other neurodegenerative processes besides demyelinating disease, including models of Alzheimer’s disease [51, 52], amyotrophic lateral sclerosis , and axotomized dorsal root ganglion cells . However, resveratrol also modulates a variety of cellular signaling pathways independent of its ability to activate SIRT1, exerting a number of potentially beneficial effects including anti-carcinogenic properties, anti-inflammatory effects by inhibiting pro-inflammatory mediators and/or activated immune cells, and inhibition of inducible nitric oxide synthase and cycooxygenase-2 [53, 54]. For the current studies, we used the SIRT1 activator SRTAW04 to avoid activating other pathways affected by resveratrol. In addition, compounds like SRTAW04 that activate SIRT1 by distinct mechanisms from resveratrol exert similar SIRT1 activation levels at concentrations an order of magnitude lower than resveratrol , and have shown good safety profiles in early phase clinical trials. In addition, we have shown previously that SRTAW04 itself prevents oxidative stress-induced loss of neurons in vitro .
Specific targets of the SIRT1 deacetylase that mediate observed changes in expression of mitochondrial enzymes require further study. SIRT1 was originally identified as a histone deacetylase [55, 56], leading to large changes in overall gene expression, but SIRT1 also has been found to deacetylate a number of other protein targets [57, 58], including transcription factors that may directly affect expression of specific genes. In addition, post-translational modifications of mitochondrial enzymes may further promote mitochondrial biogenesis, as SIRT1-mediated deacetylation of PGC1-α has been shown to do in muscle cells . Results here show that transient increases in SIRT1 activity following administration of SRTAW04 were capable of providing long-term neuroprotective effects in MHV-A59 infected mice, suggesting that deacetylation of SIRT1 substrates may persist beyond the timing of acute SIRT1 activation.
The current studies show SRTAW04 exerts neuroprotective effects without suppressing gross levels of inflammation assessed by H&E staining, and confirmed by staining with macrophage/microglial markers. Unlike EAE models of MS mediated by T cells, in this virus induced model of MS inflammation consists almost exclusively of macrophages, as demonstrated in prior studies [18, 21, 42]. It is interesting that SIRT1 activation fails to block the migration of macrophages into the CNS, as prior studies have shown that SIRT1 activation can block the accumulation of macrophages in peripheral tissues , although even outside the CNS this effect appears to be tissue specific.
Evidence suggests neurologic dysfunction in MS occurs as a result of axonal degeneration [60, 61], which may be dependent on or occur independently of chronic demyelination . Our results show that SIRT1 activation can preserve RGCs and reduce axonal loss following infection with MHV. SRTAW04 treated mice that also received the SIRT1 inhibitor EX527 did not show a significant reduction in axonal loss or preserve RGCs, suggesting that the neuroprotective effect of SRTAW04 is mediated by SIRT1 activation. Furthermore, SIRT1 activation with SRTAW04 prevented myelin loss following MHV infection. These findings are consistent with a recent study  showing that mice overexpressing SIRT1 in neurons have reduced axonal loss and demyelination in the EAE model of MS. Together, results suggest SIRT1 promotes neuronal survival and prevents demyelination in CNS demyelinating diseases.
SIRT1 activating compounds represent potential new neuroprotective agents for demyelinating diseases. Results suggest SIRT1 activators can modulate oxidative stress, a common mechanism of neuronal injury, and begin to identify mechanisms that can be targeted for development of more specific neuroprotective therapies.
This work was supported by NIH grant EY015014, Research to Prevent Blindness, and the F. M. Kirby Foundation to KSS, and Research Grant BT/PR14260/MED/30/437/2010 from Dept. of Biotechnology (DBT), India, IISER-K start up Fund and Research Grant RG3774A2/1 from the National Multiple Sclerosis Society, to JDS. We thank Sirtris, a GSK company, for kindly providing the SRTAW04 compound. The authors declare no competing financial interests.
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