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Huntington's disease (HD) is a progressive neurodegenerative disorder caused by a CAG repeat expansion within the huntingtin gene. Mutant huntingtin protein misfolds and accumulates within neurons where it mediates its toxic effects. Promoting mutant huntingtin clearance by activating macroautophagy is one approach for treating Huntington's disease (HD). In this study, we evaluated the mTOR kinase inhibitor and macroautophagy promoting drug everolimus in the R6/2 mouse model of HD.
Everolimus decreased phosphorylation of the mTOR target protein S6 kinase indicating brain penetration. However, everolimus did not activate brain macroautophagy as measured by LC3B Western blot analysis. Everolimus protected against early declines in motor performance; however, we found no evidence for neuroprotection as determined by brain pathology. In muscle but not brain, everolimus significantly decreased soluble mutant huntingtin levels.
Our data suggests that beneficial behavioral effects of everolimus in R6/2 mice result primarily from effects on muscle. Even though everolimus significantly modulated its target brain S6 kinase, this did not decrease mutant huntingtin levels or provide neuroprotection.
Huntington's disease (HD) is a progressive neurodegenerative disorder caused by a glutamine-encoding CAG repeat expansion within the huntingtin gene . Neurodegeneration is most prominent within striatum and neocortex and results in abnormal movements, cognitive decline and psychiatric symptoms. Mutant huntingtin misfolds and accumulates as soluble and insoluble aggregated species primarily in neurons.
Macroautophagy is a lysosomal-dependent process that mediates the turnover of organelles and misfolded proteins that are too large to be degraded by the ubiquitin proteosomal system [2,3]. Steps involve biochemical induction, the sequestering of cytoplasmic fragments into double-membrane bound autophagic vacuoles, subsequent fusion with lysosomes and degradation within autolysosomes . The process involves the coordinated expression and regulation of many core and autophagy-related  as well as lysosomal proteins . There is activation of macroautophagy in HD models [3,7]. Macroautophagy is also involved in the pathogenesis of Parkinson's, Alzheimer's and prion diseases [8-10].
Promoting clearance of mutant huntingtin (mhtt) by induction of macroautophagy is one approach for treating human HD [7,11]. Everolimus (formerly called RAD001) is an inhibitor of mammalian target of rapamycin (mTOR), a protein that is part of an intra-cellular signaling pathway regulating cell metabolism. Everolimus, like rapamycin, inhibits the kinase activity of the raptor-mTOR complex (mTORC1) by binding to the protein FKBP-12, which forms an inhibitory complex with mTOR [12,13]. mTOR kinase is a cytosolic protein that receives inputs from nutrient signaling pathways and is an inhibitor of macroautophagy [14,15]. Everolimus inhibition of mTOR kinase promotes macroautophagy in a number of model systems [16,17]. mTOR-kinase-independent macrophagy inducers have also been identified [9,11] and these may offer an alternative pathway to modulate autophagy. However, the class of mTOR-kinase-inhibiting drugs is well characterized and in clinical use for their anti-neoplastic and anti-solid organ graft rejection effects [18,19]. These compounds would offer advantages of availability and rapid progression into clinical trials if found to have significant beneficial effects in HD models.
The goal of this study was to evaluate the effect of everolimus in the R6/2 transgenic mouse model of HD. These mice express the exon-1 encoded fragment of mutant huntingtin under the control of the huntingtin promoter which results in protein expression in brain and skeletal muscle . We found that everolimus retarded declines in motor improvements. In brain, everolimus inhibited phosphorylation of the mTOR kinase target protein S6 kinase, but did not decrease mutant huntingtin levels, or decrease brain and neuronal atrophy. However, in skeletal muscle everolimus significantly decreased levels of soluble mutant huntingtin protein. While our data demonstrates a beneficial effect of everolimus in R6/2 HD mice, we could not demonstrate neuroprotection.
Mice were treated from 6-8 weeks at 10 and 30 μmol/kg. Plasma and brain everolimus was quantified 4 and 24 hours after the last dose. The analytical method used provided robust measures of everolimus in mouse plasma and brain. Limits of quantification were 1.5 pmol/ml plasma or 7.5 pmol/g brain, respectively. Four hours after the last dose mean plasma everolimus concentrations were 5560 and 10950 pmoles/ml at the 10 and 30 μmol/kg doses, respectively (Figure (Figure1A).1A). Corresponding brain concentrations were 113 and 299 pmoles/g (Figure (Figure1B).1B). Twenty-four hours after dosing mean plasma everolimus concentrations were significantly lower at 580 and 1160 pmoles/ml for the 10 and 30 μmol/kg doses, respectively (Figure (Figure1A).1A). Corresponding mean brain concentrations at 24 hours were 57 and 154 pmoles/g (Figure (Figure1B).1B). Brain everolimus was 2-3% of plasma concentration at 4-hours consistent with plasma contamination. However, at 24 hours it was 12-14% indicating significant brain penetration (Figure (Figure1C)1C) (see discussion). Weight loss is a prominent feature of human and mouse HD. Because pilot tolerability experiments in R6/2 HD mice demonstrated weight loss exceeding 10% with the 30 μmol/kg dose (our working definition of maximum tolerated dose) we tested 10 and 20 μmol/kg doses in subsequent experiments. The use of 20 μmol/kg as a maximum dose is further supported by the finding that it resulted in significantly reduced weight gain from 6 weeks of age as compared to vehicle-treated transgenic mice.
Our pharmacokinetic analysis indicates brain penetration of everolimus. To determine if the concentration in brain is sufficient to inhibit mTOR kinase we undertook a Western blot analysis of S6 kinase, a direct phosphorylation target of mTOR kinase. We chose to evaluate everolimus by dosing on Mondays, Wednesdays and Fridays for two reasons. First, three doses/week were used when testing the rapamycin and everolimus analog CCI-779 in N171-82Q HD mice . Second, in preliminary experiments a single dose of 30 μmol/kg decreased brain S6 kinase phosphorylation for 24 hours (not shown). Mice were dosed from 4-12 weeks and sacrificed 4 hours after the last dose. S6 kinase phosphorylation at the S235-236 epitope was significantly decreased in cortex of R6/2 compared to wild-type mice (Figure (Figure2A).2A). Twenty, but not 10, μmol/kg everolimus resulted in a significant decrease in S235-236 phosphorylation in cortex and striatum (Figure 2A-B). There was no effect of mutant huntingtin expression on phosphorylation of the S240-244 epitope. Twenty, but not 10, μmol/kg everolimus significantly decreased phosphorylation at this epitope (Figure 2C-D). Our pharmacokinetic studies indicated no brain penetration four hours after dosing (Figure (Figure1C).1C). However, Western blot analysis revealed significant effects on S6 kinase phosphorylation four hours after a final dose comprising a total of 8 weeks treatment (Figure (Figure2).2). Together, these data suggest that after prolonged treatment brain effects of the 20 μmol/kg dose last up to 48 hours.
We evaluated the effect of 10 and 20 μmol/kg everolimus on mouse Rota-Rod endurance. Mice were treated from 4 weeks of age. At 6 and 8 weeks of age, 10 μmol/kg everolimus provided significant benefit against the decline in Rota-Rod endurance (Figure (Figure3A).3A). Twenty μmol/kg everolimus provided benefit at 6 weeks only (Figure (Figure3A).3A). Ten μmol/kg everolimus had no effect on body weight, while 20 μmol/kg resulted in a significantly lower, but not progressively declining body weight from 6-weeks (Figure (Figure3B).3B). There was no effect of everolimus on mean survival times (Figure (Figure3C).3C). We sought to determine if the beneficial effect of everolimus is due to a protective effect in brain. R6/2 mice have progressive declines in brain size and increases in mutant huntingtin aggregate burden . Despite the beneficial behavioral effect of everolimus, neither dose was protective against loss of brain mass as measured by brain weight, striatal volume, striatal neuronal cell body volume and nuclear aggregate density (Figure 3D-G). Twenty μmol/kg everolimus resulted in significantly lower brain weight, which is consistent with the lower body weight at this dose (Figure (Figure3D3D).
Upon synthesis, LC3B is cleaved into the cytosolic protein LC3BI. Activation of macroautophagy leads to conversion of LC3BI into LC3BII, a form that associates with autophagosomes . Both normalized LC3BII levels and the LC3BI: LC3BII ratio (conversion) have been used as measures of macroautophagy activation [22,23]. We therefore measured these parameters in brain and muscle of R6/2 HD mice. LC3B I/II ratios were significantly decreased (increased conversion) in striatum, but not cortex, of R6/2 HD mice as compared to control mice (not shown). However, there was no effect of everolimus on normalized LC3BII levels (Figure (Figure4A)4A) or LC3B conversion (not shown) in R6/2 HD brain. In muscle, there was significantly more variability in Western blot results as compared to brain. However, there was a trend towards increased normalized LC3BII levels in muscle of everolimus treated R6/2 mice (global p-value = 0.12; Figure Figure4B4B).
Lysosome-associated membrane protein 1 (LAMP1) is primarily a lysosomal protein  that could be a good marker for late steps in the autophagy cascade. We therefore measured LAMP1 protein levels in brain by immunofluorescence and found significant increases in neuronal cell bodies of striatum and cortex of 12-week R6/2 mice (Figure 5A-B). Neuropil LAMP1 staining was not quantified, but also appeared increased in R6/2 mice. Western blot analysis corroborated this finding in striatum, but not cortex. Further, an effect of everolimus on LAMP1 expression in brain was not detected (Figure 5C-D). We evaluated LAMP1 in quadriceps muscle and found that LAMP1 was significantly increased in HD control as compared to wild-type mice. Further, high-dose everolimus significantly decreased LAMP1 close to wild-type levels (Figure 5E-F).
Time-resolved Förster resonance energy transfer (time-resolved FRET) is a recently described technique that can quantify soluble mutant huntingtin (mhtt) levels . We used this method to quantify levels of soluble mhtt in muscle and brain. In agreement with our previous results we found that everolimus had no effect on soluble mutant huntingtin levels in striatum or cortex (Figure (Figure6A).6A). This result was corroborated by Western blot analysis that revealed that monomeric mhtt levels were unaltered in occipital cortex of everolimus treated mice (not shown). However, we found that 20 μmol everolimus decreased soluble mutant huntingtin levels in quadriceps muscle (Figure (Figure6B).6B). We then used the recently described Agarose gel electrophoresis for resolving aggregates (AGERA) biochemical assay to quantify mutant huntingtin aggregates . In agreement with the quantitative pathology data (Figure (Figure3G)3G) there was no effect of everolimus on brain aggregates (see Additional file 1: Figure S1A-B). While everolimus decreased soluble mutant huntingtin levels in muscle of R6/2 mice (Figure (Figure6B),6B), there was no effect of everolimus on aggregated huntingtin as measured by AGERA (see Additional file 1: Figure S1C-D).
R6/2 HD mice have been used extensively in pre-clinical drug trials and numerous compounds, including one that promotes macroautophagy, have shown neuroprotective effects [9,27]. We studied the effect of everolimus, a O-(2-hydroxyethyl) chain substitution of rapamycin  in these mice. We hypothesized that everolimus would decrease mutant huntingtin levels in brain and have neuroprotective effects as measured by decreased brain atrophy. To verify that everolimus could interact with and inhibit its target, brain mTOR kinase, we performed a pharmacokinetic study and also evaluated the phosphorylation state of the mTOR target, S6 kinase. Our results demonstrate that everolimus slowly penetrates brain at doses of 10 and 30 μmol/kg (Figure (Figure1).1). Brain: plasma ratios 4 hours after a final dose were 2-3% which is consistent with plasma contamination (Figure (Figure1C).1C). However, at 24 hours, brain: plasma ratios were 12-14% which is significantly greater than mouse fore-brain vascular volume of ~6% indicating significant brain penetration . Brain everolimus concentrations were in the range 50-180 nM at 24 hours. The IC50 of everolimus in cell proliferation assays is in the sub-nano molar range  which is consistent with the concentrations we found in brain being sufficient to strongly inhibit mTOR kinase. To address this, we used S6 kinase phosphoepitope Western blot analysis. We reduced our high dose from 30 to 20 μmol/kg at this point because of body weight loss following prolonged treatment at the 30 μmol/kg dose. Even though we did not repeat the pharmacokinetic analysis using the 20 μmol/kg dose our Western blot analysis clearly shows decreased S6 kinase phosphorylation at the 20 but not the 10 μmol/kg dose, confirming brain penetration at the higher dose used (Figure (Figure2).2). Decreased S6 kinase phosphorylation in R6/2 HD cortex at the S235-236 epitope, as compared to wild-type mice, is consistent with findings in the N171-82Q HD mouse .
Despite demonstrating penetration of everolimus into brain and modulation of its target, we were unable to demonstrate any protective effects in R6/2 HD mouse brain as determined by a detailed quantitative neuropathology study (Figure 3D-G) and using three independent methods to quantify mutant huntingtin levels (Figures (Figures3G,3G, ,6,6, see also Additional file 1: Figure S1) all at 12 weeks of age. Our body weight data (Figure (Figure3B)3B) demonstrate that the high (20 μmol/kg) dose we used in our efficacy study was the maximum tolerated dose using our working definition of a 10% loss of body weight over the study period. As brain weights were slightly but significantly lower in the 20 μmol/kg versus placebo group (Figure (Figure3D),3D), this further suggests that doses higher than that used would not have shown beneficial effects. The three times a week dosing paradigm that we used has been reported previously for the closely related rapamycin analog CCI-779 in a study in N171-82Q HD mice . The suitability of this dosing frequency is also supported by our own data in which mice sacrificed four hours after the last dose of an eight week dosing study had decreased brain S6 kinase phosphorylation (Figure (Figure2)2) even though everolimus did not enter brain 4 hours after a final dose in the pharmokinetic study (Figure (Figure1).1). This suggests that with repeated, three times a week, dosing everolimus has a prolonged effect on S6 kinase phosphorylation. Taken together, our results suggest that failure to find a neuroprotective effect of everolimus in R6/2 HD mice was not due to insufficient inhibition of brain mTOR kinase activity.
Muscle is a target of mutant huntingtin in mouse and human HD [31,32]. We found that everolimus demonstrated an early protective effect on Rota-rod performance that was stronger for the low (10 μmol/kg) dose group (Figure (Figure3A).3A). As there was no effect of this low dose on brain S6 kinase phosphorylation (Figure (Figure2)2) we reasoned that a beneficial effect of everolimus in muscle could explain why the 10 μmol/kg group performed better than the 20 μmol/kg group on Rota-Rod analysis. We did not measure S6 kinase phosphorylation in muscle. However, both mTOR and S6 kinase are expressed in muscle . Given the sub-nanomolar IC50 of everolimus for mTOR kinase and expected high penetration of everolimus into muscle, we would expect strong suppression of S6 kinase phosphorylation. Instead, we measured mutant huntingtin levels in everolimus treated R6/2 mice at 12 weeks by FRET. We found significantly decreased soluble mutant huntingtin at the high dose and a trend towards decreased levels at the low dose (Figure (Figure6).6). There was no effect on aggregated huntingtin levels (see Additional file 1: Figure S1 C-D). Better Rota-rod performance in the low dose group (Figure (Figure3A)3A) could be related to the high dose having both beneficial and toxic effects (Figure (Figure3B).3B). Therefore, our data are consistent with Rota-Rod effects of everolimus being, at least in part, due to beneficial effects in skeletal muscle. We cannot rule out the possibility of a transient suppression of mutant huntingtin levels in brain occurring in the 6-8 week period contributing to behavioral benefits. However, as several compounds demonstrate prolonged protective activity in R6/2 brain , including one that promotes autophagy [9,27], this would suggest that even if everolimus decreased brain mutant huntingtin levels transiently that mTOR kinase inhibition is not as effective as modulation of other therapeutic targets in R6/2 mice.
LAMP1 is a type I transmembrane glycoprotein and a marker of lysosomes and autolysosomes , organelles critical for downstream steps of the autophagy cascade. While not a core macroautophagy protein, LAMP1 is a lysosome marker and therefore should reflect activity within the terminal clearance steps of the autophagic cascade. We evaluated LAMP1 in our study to determine if levels are increased in R6/2 HD mice and to determine the effect of everolimus. As expected, we found that LAMP1 protein levels were increased in muscle and brain (Figure (Figure5)5) of R6/2 as compared to wild-type mice. Everolimus had a significant effect on LAMP1 in muscle, but not brain. In muscle, high dose everolimus decreased LAMP1 towards wild-type levels and there was a trend towards a decrease with the low dose (Figure 5E-F). This result was unexpected and the reasons are not clear. We speculate that everolimus may promote clearance of autolysosomes. Further studies are clearly needed to better understand the mechanism(s) by which everolimus decreases mutant huntingtin and LAMP1 levels in muscle.
CCI-779 is a rapamycin dihydoxymethyl propionic acid ester  that has been shown to demonstrate behavioral benefits and decrease aggregate density in N171-82Q HD mice . Our results using everolimus, a related rapamycin derivative in the R6/2 HD model demonstrate a different effect. While our data confirms entry of everolimus into brain, as measured by direct chemical analysis and S6 kinase phosphorylation levels, we could not demonstrate decreased neurodegeneration or brain mutant huntingtin levels. The difference between our findings and that of Ravikumar et al (2004) could be for a number of reasons. R6/2 HD mice have a more aggressive phenotype than the N171-82Q HD mice used in the CCI-779 study [21,35]. Factors such as longer polyglutamine expansion in R6/2 compared to N171-82Q mice could also be important.
Our findings suggest that mTOR kinase inhibition in R6/2 HD mice using everolimus has, at most, a minimal effect on disease progression in brain. Everolimus effectively modulated brain S6 kinase, which is upstream of macroautophagy induction, but had no effect on mutant huntingtin levels. Everolimus did decrease soluble mutant huntingtin levels in muscle. While the exact mechanisms by which this occurs were not fully established, our data indicates that a beneficial effect of everolimus in muscle is a likely mechanism for the protective behavioral effects observed in our HD mice. Given the discrepancy between our findings using everolimus in R6/2 mice and Ravikumar et al  using CCI-779 in N171-82Q mice, side-by-side testing of these molecules in both R6/2 and N171-82Q mice, and perhaps as well in a full-length huntingtin mouse model, would provide additional insight into the value of this class of molecule as a treatment for HD.
R6/2 mice were maintained by crossing R6/2 males (available from The Jackson Laboratory, Bar Harbor, ME) with C57BL/6 X CBA F1 females. Tail tips were obtained at 14 days. Tail DNA CAG expansion sizes of male breeder mice were in the range 120-130, as determined by Laragen Inc. Mice were weaned at 22 days, and assigned to treatment groups 1-2 days later. Systematic assignment to treatment groups was used to minimize the effects of body weight variability, litter and paternal effects. Everolimus was prepared as described . Mice were female and were dosed by gavage on Mondays, Wednesdays and Fridays (see discussion). Body weights were measured weekly and used to adjust doses.
One-hundred μl plasma was extracted three times in 500 μl ethyl acetate. Extracts were dried under a stream of nitrogen before re-dissolving in 100 μl acetonitrile. Brains were weighed then homogenized in water (1:5 w/v) using an Ultra-Turrax® Mod T8 for 30 seconds. Two 100 μl aliquots of each homogenate were extracted thrice with 500 μl ethyl acetate, then processed as for plasma. Calibration standards were prepared by supplementing 100 μl of mouse plasma (from untreated animals) with everolimus and the analysis quality monitored by routine use of an external standard. For HPLC separation, a Nucleosil CC-125/2 C4 reversed phase column (Macherey & Nagel, Oensingen, Switzerland) under isocratic conditions using 60% acetonitrile and 0.05% formic acid in H2O (v/v) with a column temperature of 40°C was used. The flow rate was 0.35 ml/minute and sample injection volume was 10 μl. Retention times were 1.6 and 2.2 minutes for everolimus and NVP-BDF461, respectively. Column efflux was introduced directly into the ion source of a Micromass Platform II LC detector (single quadrupole). The MS conditions were as follows: ionization APCI negative polarity, corona voltage set to 3.2 kV, fragmentor voltage (cone) 50 V, source temperature 350°C. Quantitative analysis was performed by selected ion recording over the de-protonated molecular ion [M+H-] of everolimus (m/z 956.8 ± 0.5). Peaks were integrated using MassLynx (Micromass). Two independent extractions were analyzed per animal. Standard curves were prepared by spiking plasma and brain homogenates originating from untreated animals with five concentrations of everolimus as external standard. A second set of standards in acetonitrile was directly analyzed to estimate extraction yield. A linear calibration was calculated for each analytical batch from the ratio between calibrant and internal standard and the calibrant in spiked plasma or brain samples. Regression was performed using Origin® software. Unknown concentrations were calculated from the calibration parameters obtained with extracted samples containing internal standard.
Antibodies used were: mutant huntingtin (MAB5492-Chemicon), actin (AC40-Sigma), LC3B (Novus Biologicals) and LAMP1 (BioLegend). Total S6 (54D2) and phosphor-S6 protein (serines 235/236 and 240/244) antibodies (Cell Signaling). Primary antibodies were used at 1:2000, except for AC40 (1:4000). For mutant huntingtin analysis, dissected brain regions were homogenized in 20 volumes of 20 mM TRIS (pH 7.2), 150 mM sodium chloride, 1 mM EDTA, 1 mM DTT and HALT protease inhibitor cocktail (Pierce) using a Pellet pestle® (Kontes). Samples were cleared at 18000 g for 15 minutes at 4°C. Thirty μg protein was resolved by SDS-PAGE and transferred to PVDF. Membranes were blocked in 5% milk powder in TRIS-buffered saline containing 1% Tween-20 (TBST) and then probed with primary antibody overnight in blocking buffer at 4°C. After washing and incubation in HRP-conjugated secondary antibody membranes were developed using Western Lightening™ chemiluminescent reagent plus (Perkin-Elmer). For analyses of all other proteins, the procedure was identical to that described above except for the homogenization buffer; this comprised 25 mM HEPES (pH 7.4), 75 mM sodium chloride, 12.5 mM β-glycerophosphate, 12.5 mM sodium fluoride, 2.5 mM EGTA, 0.5 mM EDTA, 7.5 mM sodium pyrophosphate, 2 mM sodium vanadate, 0.1% Nonidet-P40 and HALT protease inhibitor. For muscle analysis, the same procedures were used except that tissues were homogenized using a Tissuemiser® (Fisher). For brain, actin was used to normalize Western blots. For muscle, we used parallel run coomassie gels because we do not have a validated housekeeping gene for R6/2 muscle and because actin mRNA is down regulated in this tissue .
Rota-Rod endurance was assessed using an accelerating Rota-rod (Stoelting). The rod speed accelerated from 4.5-45 rpm at a constant rate. Measurements were first taken prior to dosing at 3.5 weeks, then at every 2 weeks of age. For each time point, mice were evaluated on four consecutive days. Day 1 was a training day. On days 2-4 accelerating Rota-rod endurance was evaluated once/day up to a maximum of 15 minutes and endurance times recorded. The average of three trials was used for statistical analysis.
At 12 weeks of age, mice were deeply anesthetized with a tribromoethanol-based anesthetic. They were then perfused with freshly prepared room temperature 2% paraformaldehyde in 0.1 M phosphate buffer (pH 7.4) for 15 minutes at a flow rate of 12 mls/minute. Perfused mice were stored at 4°C for 2 hours prior to brain removal. Brains were post-fixed in the same fixative overnight at 4°C prior to cryoprotection for 3 days in 10% glycerol, 2% DMSO and 0.1 M phosphate buffer. The entire striatum was sectioned coronally at 50 μm and every eighth section was mounted and stained for Nissl substance using the thionin method.
Fifty-μm sections at the level of the anterior commissure were used for immunohistochemical (IHC) staining for mutant huntingtin aggregates and LAMP1 immunofluorescence (IF). For IHC, we used a 1:2000 dilution of EM48 antibody incubated with floating sections in PBS containing 0.5% Tween-20 for 48 hours to aid penetrance. After washing, sections were incubated in a biotinylated anti-rabbit antibody overnight. Reactivity was developed using the Vectastain ABC kit (Vector Laboratories). Sections were mounted in aqueous medium (Fluoromount G, Southern Biotech) to prevent z-axis shrinkage. For IF, sections were incubated in 1:100 anti-LAMP1 (BioLegend) in PBS containing 0.1% Tween-20 and 10% normal goat serum for 48 hours. Sections were washed three times in PBS, then incubated in AlexaFluor-488 labeled anti-rat antibody (Invitrogen) for 4-hours at 25°C. After washing in PBS, sections were stained with the nucleic acid stain ethidium dimer at 5 μM for 2 hours in the dark. Sections were washed in PBS before mounting. Three-layered z-stack images were collected using a Leica TCS SL confocal microscope. Neurons were identified within the central stack using ethidium dimer signal that delineates nuclei and cytosol. LAMP1 signal was quantified by outlining neuronal cell body outlines and quantifying fluorescence using Metamorph software (Molecular Devices).
The methodologies used were exactly the same as we have fully described previously .
Soluble mutant huntingtin was quantified by time-resolved FRET as described . In brief, muscle samples were homogenized in 20 volumes of PBS containing 0.4% (v/v) Triton-X100 and protease inhibitor using a Precellys®24 (Bertin technologies) for 2 × 30 seconds at 5000 rpm. Homogenates were cleared at 3000 rpm for 10 minutes at 4°C. The supernatant was transferred into a fresh tube and total protein was measured using the BCA-Protein detection kit (Perbio, Cramlington, UK). Brain samples were homogenized in 25 mM HEPES (pH 7.4), 75 mM sodium chloride, 12.5 mM beta-glycerophosphate, 12.5 mM sodium fluoride, 2.5 mM EGTA, 0.5 mM EDTA, 7.5 mM sodium pyrophosphate, 2 mM sodium vanadate, 1 mM dithiothreitol, 0.1% nonidet p40, and 0.1% HALT protease inhibitor. The amount of homogenate needed to reach levels in the linear range of time-resolved FRET detection was determined and resulted in 2 μl of homogenate for brain samples (~12 μg protein/well), and 5 μl of homogenate for muscle samples (~17 μg protein/well). Brain or muscle homogenates were mixed with an antibody solution (5 μl) composed of 2B7-Europium-Cryptate (1 ng) and MW1-d2 (10 ng) dissolved in NaH2PO4 (50 mM, pH 7.4), NaF (400 mM), BSA (0.1% w/v), and Tween 20, (0.05% v/v) in a low-volume 384-well plate and incubated at 4 degrees centigrade overnight. The final volume was 15 μl. Time-resolved FRET with excitation at 320 nm and emission at 620 and 665 nm was measured using an Envision fluorimeter (Perkin-Elmer). Time-resolved FRET signals are given as the 665/620 nm ratio. Background levels (wild-type) were deducted and values normalized for protein concentration. Results are expressed as a percentage of vehicle treated animals. Aggregated huntingtin was quantified using the recently described agarose gel electrophoresis for resolving aggregates (AGERA) method . Briefly, mouse brain samples were homogenized in 10 volumes (w/v) tris-saline (100 mM Tris, pH 7.4, 150 mM NaCl) and Complete Protease Inhibitor (Roche Diagnostics) by 10 ultrasound pulses with a Branson sonifier and stored at −80°C. For 1.7% agarose gels, 1.7 g agarose (Biorad, #161-3101) was dissolved in 100 mL 375 mmol/L Tris-HCl, pH 8.8 and brought to boiling in a microwave oven. After melting, SDS was added to a final concentration of 0.1% (w/v). Gels were poured on short Biorad DNA Sub Cell™ trays. Samples were diluted 1: 1 into non-reducing Laemmli sample buffer (150 mmol/L Tris-HCl pH 6.8, 33% glycerol, 1.2% SDS and bromophenol blue) and incubated for 20 minutes at 95°C. Two-hundred μg of protein was loaded per AGERA lane. After loading, gels were run in Laemmli running buffer (192 mmol/L glycine, 25 mmol/L Tris-base, 0.1% (w/v) SDS) at 100 V, 2 A until the bromophenol blue running front reached the bottom of the gel. Semi-dry electroblotter model B (Ancos, Højby, Denmark) was used to blot the gels on PDVF membranes (Millipore) at 200 mA for 1 hour. Membranes were then developed using MW8 mouse monoclonal antibodies (3 μg/ml), and aggregate quantification performed by densitometry analysis.
All data was analyzed using SAS version 9.1 software (Cary, NC). Rota-rod and body weight data was analyzed using a mixed-model method that included age by treatment interaction effects. Slice functions and t-tests were used to determine significant differences. All other data was analyzed by one-way analysis of variance (ANOVA) using a generalized-linear model procedure followed by pair-wise comparisons. All p-values < 0.05 were considered significant.
PP, DB, CB, DH and SF are employed by Novartis Institutes for Biomedical Research, Basel, Switzerland.
JF, TC and VC carried out the protein expression and stereology studies. KD and JK carried out the behavioral experiments and maintained the mice. DH and CB carried out the pharmacokinetic analysis. DB and SF completed the quantification of aggregated and soluble mutant huntingtin. JF, PP, MF and SH designed the experiments and wrote the paper with assistance from all other authors. All authors read and approved the final manuscript.
Everolimus treatment has no effect on aggregated mutant huntingtin levels in R6/2 brain and muscle. Mutant huntingtin aggregates were quantified using the AGERA assay in brain and muscle at 12-weeks after 8-weeks of treatment. There is no effect of everolimus on aggregated mutant huntingtin levels in brain (A-B) or muscle (C-D) of R6/2 HD mice. Representative gels (A, C) and quantification (B, D). Bars represent means ± SEM. n = 10-12
This work was supported by the BeatHD Collaborative grant from the Novartis Institutes for BioMedical Research (NIBR).