Abstract
Spinocerebellar ataxia 17 (SCA17) is an autosomal-dominant, late-onset neurodegenerative disorder caused by an expanded polyglutamine (polyQ) repeat in the TATA-box-binding protein (TBP). To further investigate this devastating disease, we sought to create a first transgenic rat model for SCA17 that carries a full human cDNA fragment of the TBP gene with 64 CAA/CAG repeats (TBPQ64). In line with previous observations in mouse models for SCA17, TBPQ64 rats show a severe neurological phenotype including ataxia, impairment of postural reflexes, and hyperactivity in early stages followed by reduced activity, loss of body weight, and early death. Neuropathologically, the severe phenotype of SCA17 rats was associated with neuronal loss, particularly in the cerebellum. Degeneration of Purkinje, basket, and stellate cells, changes in the morphology of the dendrites, nuclear TBP-positive immunoreactivity, and axonal torpedos were readily found by light and electron microscopy. While some of these changes are well recapitulated in existing mouse models for SCA17, we provide evidence that some crucial characteristics of SCA17 are better mirrored in TBPQ64 rats. Thus, this SCA17 model represents a valuable tool to pursue experimentation and therapeutic approaches that may be difficult or impossible to perform with SCA17 transgenic mice. We show for the first time positron emission tomography (PET) and diffusion tensor imaging (DTI) data of a SCA animal model that replicate recent PET studies in human SCA17 patients. Our results also confirm that DTI are potentially useful correlates of neuropathological changes in TBPQ64 rats and raise hope that DTI imaging could provide a biomarker for SCA17 patients.
Introduction
The group of polyglutamine diseases contains nine members including spinocerebellar ataxia (SCA) 1, 2, 3, 6, 7, and 17, Huntington disease (HD), dentatorubropallidoluysian atrophy, and spinobulbar muscular atrophy (Zoghbi and Orr, 2000; Riley and Orr, 2006). The proteins involved in these diseases are ubiquitously expressed in the body but cause selective neurodegeneration. Here, we focused on generating an animal of spinocerebellar ataxia type 17, which is an autosomal dominantly inherited, neurodegenerative, late-onset disease caused by a polyglutamine expansion in the TATA-box-binding protein (TBP) (Nakamura et al., 2001). This deadly disease is characterized by ataxia, dystonia, and seizures (Rolfs et al., 2003), as well as dementia, psychiatric and extrapyramidal features, epilepsy, mild sensorimotor axonal neuropathy, and MRI findings of cerebral and cerebellar atrophy (Maltecca et al., 2003). In contrast to most of the other polyQ disease causing proteins, the function of the TBP in the transcription process is well understood (Burley and Roeder, 1996) and potentially allows us to investigate how the mutation alters protein function subsequently leading to neuronal dysfunction in vivo.
Although two transgenic mouse models (Friedman et al., 2007; Chang et al., 2011) and one knock-in mouse model (Huang et al., 2011) already exist, which all mimic several phenotypic characteristics of the disease, mouse models are in general limited for studying certain functional and behavioral measurements (Tecott and Nestler, 2004; Rodriguiz and Wetsel, 2006; Herrmann et al., 2012). Rats, on the other hand, show excellent learning abilities compared to mice and are the species of choice for studying learning and memory in rodents and for pharmacological manipulations (Kujpers, 1999). Their larger brain size also facilitates direct invasive procedures and miniaturized physiological in vivo approaches such as structural and functional imaging of small brain structures (Casteels et al., 2011; Grundmann et al., 2012; Yu-Taeger et al., 2012), electrophysiology (Miller et al., 2010; Ortiz et al., 2012), or stem cell replacement (Rath et al., 2012; Ribeiro et al., 2012). The advantages of the rat prompted us to generate a transgenic rat model for SCA17, which, to our knowledge, is the first transgenic rat model for any inherited spinocerebellar ataxia. In line with previous observations in mouse models for SCA17, our transgenic SCA17 rats (TBPQ64; carrying a full human cDNA fragment of the TBP gene with 64 CAA/CAG repeats) show disease characteristic neuropathology such as neurodegeneration in the cerebellum and the formation of nuclear TBP accumulation as well as a severe neurological phenotype including ataxia, reduced activity, loss of body weight, and early death. Additionally, we were able to perform positron emission tomography (PET) and diffusion tensor imaging (DTI) measurements in vivo in our rat model and detected changes that were unreported in SCA17 patients so far. The accurate replication of the human condition in our TBPQ64 rats, coupled with the possibility to develop in vivo imaging biomarkers, makes this SCA17 rat model highly suited for the assessment of different interventions on the disease phenotype.
Materials and Methods
Generation of transgenic TBPQ64 rats
To generate transgenic SCA17 rats, we used a construct containing a fragment of the murine prion promoter (Prp), an N-terminal myc tag, full-length human TBP cDNA, and a poly-A tail (Fig. 1A).
The human TBP cDNA was amplified from TBP mRNA obtained from genomic DNA and cloned (XhoI/BamHI) into the Bluescript vector pBSSKII+. In this vector, we first cloned a 3.4 kb fragment of the murine prion protein promoter containing 1140 bp of the murine prion protein gene upstream of exon 1, the complete exon 1, intron 1, and the first untranslated 52 bp of exon 2. The promoter fragment was amplified by PCR using the primers phg_Prp_Xba_FP (5′-GCTCTAGAGCCAATCTTGTGTCTGG-3′) and phg_Prp_Bam_RP (5′-CGGGATCCCGGAATGCTTCAGCTCGG-3′). Both primers contain recognition sequences for the restriction enzymes XbaI and BamHI, which were used for the cloning of this fragment into the pBSSKII+ vector. Constructs were additionally tagged N-terminally with an myc tag. The 36 CAG/CAA repeat region was expanded to 38 as well as 64 repeats as described previously (Laccone et al., 1999). The construct was completed with a SV40 polyadenylation signal. After digestion with NeaI and NotI, the inserts were isolated before microinjection in Sprague Dawley oocytes.
Genotyping
After weaning, transgenic rats were identified by using a transgene-specific PCR protocol. Rat genomic DNA was isolated from rat ear biopsies according to the High Pure PCR Template Preparation Kit protocol (Roche). For the identification of transgenic animals, a PCR protocol with a forward primer from the mouse prion promoter (mTBP_F, 5′-gaaccatttcaaccgagctg-3′) and a reverse primer targeting the hTBP cDNA (mTBP_R, 5′-gtccaatgatgccttatggc-3′) was established. A 189 bp fragment was amplified using the following PCR conditions: 95°C, 30 s for denaturation; 60°C, 30 s for primer annealing; and 72°C, 30 s for elongation, repeated for 35 cycles.
Fragment length analysis
To determine the number of CAG/CAA repeats in the TBP transgene, fragment length analysis of DNA samples was performed. PCRs were performed to amplify a fragment of TBP containing the CAG/CAA repeat by using the following primers: 5′-Cy5-gaccccacagcctattcaga-3′ and 5′-ttgactgctgaacggctgca-3′. The indodicarbocyanine (Cy5)-labeled PCR products were mixed with an internal standard (DNA-Size Standard Kit-600; Beckman Coulter) and separated as well as analyzed on the CEQ8000 Genetic Analysis System (Beckman Coulter).
Plasmid DNA of TBP cDNA containing 13, 38, 64, or 105 CAG repeats was used as a size standard to calculate the number of CAG/CAA repeats.
Animals
Rats were housed in gender- and genotype-matched groups of up to four, according to Federation of European Laboratory Animal Science Associations recommendations (Rehbinder et al., 1996). All rats were kept under a 12 h light/dark cycle with lights on at 2 A.M.; food (Sniff lab chow pellets) and tap water available ad libitum.
For behavioral tests, predominantly male heterozygous and wild-type littermate control rats from litters were used. Two to four rats of randomized genotype were housed together. All rats were tested within the dark phase of a 12 h light/dark cycle. The ataxia score test was conducted in the light cycle, whereas the rotarod, beam walking, and elevated plus maze (EPM) tests were done in dark phase. All research and animal care procedures were approved by the district government (HG9/10, Tübingen, Germany) and performed according to international guidelines for the use of laboratory animals.
Behavioral tests
Before the experiments, animals were handled daily for 2 weeks. Furthermore, animals were weighted weekly. The numbers of animals in the behavioral studies as as follows: TBPQ64 males, n = 12; wild-type males, n = 7; TBPQ64 females, n = 4; wild-type females, n = 8.
Ataxia score test.
This test was established by Guyenet et al. (2010) and facilitates rapid and sensitive quantification of disease severity in rodent models of ataxia. The protocol includes the ledge test, measurement of hindlimb clasping, and assessment of gait abnormalities and severity of kyphosis. For each parameter we used a scale of 0–3 leading to a maximum value of 12 points for all four measurements. Because of the bigger size of rats, the ledge test was performed on a thin beam (width, 1 cm) instead of the cage ledge. The scoring was performed as described (Guyenet et al., 2010).
Rotarod analysis.
This test is widely used to analyze balance capabilities, motor coordination, as well as motor learning of rodents. Seven wild-type animals and 12 transgenic rats were tested at the ages of 1, 3, 5, and 8 months. Rats were trained for 3 d on an accelerating rotarod (Ugo Basile; Biological Research Apparatus). Each training day consisted of four trials, with each trial lasting for 2 min. During the first 30 s, the rod accelerated from 2 to 12 rpm and then operated constantly for 1.5 min at 12 rpm. Rats that fell during this time period were immediately set back on the rod. On the two testing days, only two trials of 5 min duration were performed. Within the first 4 min, the rod accelerated from 4 to 40 rpm and then operated constantly at 4 rpm for the last min. The amount of time that elapsed before the rat fell off the rod was recorded. The mean of all four test runs was taken for analysis.
Beam walking.
With the beam-walking test, motor coordination and balance of rats were assessed by measuring the ability of animals to traverse a series of narrow beams to reach an enclosed safety platform. The test was performed as described previously (Korenova et al., 2009) and consisted of two training and three testing days. On Training Day 1, the animals (7 wild-type, 12 transgenic males) underwent two trials in which they had to traverse a 2 m long beam with a square cross-section of 3 × 3 cm. On Training Day 2, two trials were given, one where they had to traverse the 3 × 3 cm beam, and one trial where a beam with a rectangular cross-section of 4 × 2 cm had to be crossed. On all three testing days, the rats had to cross each beam (3 × 3 cm and 4 × 2 cm in diameter, respectively, and a round beam of 3.5 cm diameter) once. Traversing latency and number of hind-limb slips during test performance were measured and analyzed.
Elevated plus maze.
This well-established test is used to evaluate anxiety in small rodents. It is based on the aversion of rodents to open spaces and height. The setup consists of four elevated arms that built a plus shaped cross. Two opposing arms are open, and the other two arms are enclosed by 40 cm high walls; the width of the arms is 25 cm, and the distance from the floor is 80 cm. The test was performed in the dark phase in a room that was illuminated by a red rope light positioned directly above the maze. The experiment was started by placing the rat on the central platform, with its head facing one of the open arms. The time spent on the open arms during a 5 min period as well as the transitions between the center and the closed arms or the open arm were recorded. After each rat exposure, the maze was carefully cleaned with disinfectant.
The following parameters were calculated for a total trial duration (TT) of 300 s: duration of stay in closed arms [closed time (CLT)], percentage share of CLT in total arms-stay duration (%CLT; CLT × 100/TT), duration of stay in open arms [open time (OT)], percentage share of OT in total arm-stay duration (%OT; OT × 100/TT), duration of stay in the neutral zone [neutral time (NT)], and percentage share of NT in total arm-stay duration (%NT; NT × 100/TT).
PhenoMaster system.
The TSE PhenoMaster system (http://www.tse-systems.com/products/behavior/phenomaster/index.htm) is an automated cage system that allows behavioral and metabolic monitoring, e.g., activity, food and water consumption, as well as calorimetric measurements. The system consists of a combination of sensitive feeding and drinking sensors for automated online measurements. Values for cumulative amounts of feeding and drinking were given by the system, and these were used to compare iterative food and water intake. The calorimetric system is an open-circuit system that determines O2 consumption, CO2 production, and respiratory exchange rate. To investigate locomotor activity, a photobeam-based activity monitoring system detects and records the number and duration of every total, fine, and ambulatory movement including rearing (Urbach et al., 2010).
In detail, rats were singly housed in a home cage equipped with the technical requirements to individually monitor one rat per cage at a time. The system was set up to measure up to 12 animals in parallel with high resolution for food and water consumption, calorimetric parameters, and activity. This allowed the measurement of fine and ambulatory movement as well as rearing behavior. Results for locomotor activity are given as number of counts, and all measurements were monitored using PhenoMaster software, version V1.9.20-06/2007 (TSE Systems).
Further analysis binned the exploratory phase in the first 20 min for the purpose of isolating animal activity before adaptation to the new environment. From these we calculated periphery to center ambulation ratio.
Animals (nine wild-type vs nine heterozygous males) were tested every second month for 72 h starting at the age of 3 and ending at 9 months.
Immunohistochemistry
Light microscopy on paraffin sections.
Immunohistochemistry was performed as described previously (Boy et al., 2009). Transgenic and wild-type rats of both sex were investigated at the ages of 3 and 10 months. Antibodies were used at the following dilutions: 1C2 (clone 5TF1-1C2; Millipore), 1:5000; anti-β-III tubulin (clone TuJ-1, MAB1195; R&D Systems), 1:1000; and anti-myc (SA-294, clone 9E10; Biomol), 1:350.
Paraffin sections from human brains were treated like described previously (Koeppen et al., 2011). Sections were incubated in citrate buffer (0.01 m, pH 6.0) for 20 min at 90°C and stained with 1C2 (Millipore Bioscience Research Reagents), α-TBP (clone 1TBP18, 70102; QED Bioscience), and anti-β-III tubulin (clone TuJ-1, MAB1195; R&D Systems), respectively.
Light and electron microscopy on epoxide embedded vibratome sections.
Male TBPQ64 and wild-type littermates, 9 months of age, were transcardially perfused with 4% PFA, embedded into 2% agarose, and cut into series of 50 μm vibratome slices from blocks containing the striatum and cerebellum. Every fifth section was taken either for light- and electron-microscopical TBP (1:5000) or calbindin D28 immunohistochemistry (1:10,000; No. 300, monoclonal; Swant) according to an avidin-biotin-peroxidase complex protocol as described previously (Petrasch-Parwez et al., 2007). For semithin and ultrathin section analysis, immunostained vibratome slices were postfixed with 2% osmium tetroxide in 0.1 m phosphate buffer, dehydrated, and flat-embedded in Araldite (Serva). Alternating semithin (0.8 μm) and ultrathin (100nm) section series were cut with a Leica Ultracut UCT microtome. Every second semithin section was slightly counterstained with 1% toluidine blue, and ultrathin sections were contrasted with 5% aqueous uranyl acetate followed by lead citrate.
Western blot analysis
Preparation of samples was performed as described previously (Boy et al., 2009). The 1C2 antibody (clone 5TF1-1C2; Millipore) was used at a concentration of 1:4000.
Secondary antibody anti-mouse HRP (NXA931; GE Healthcare) was diluted 1:2500.
PET analysis
For the PET experiments, female transgenic TBPQ64 (n = 6) and control rats (n = 6) were imaged using an Inveon dedicated small-animal PET scanner (Siemens Preclinical Solutions), yielding a spatial resolution of about 1.3 mm in the reconstructed image. Rats were lightly restrained and injected with 29.6 MBq [11C]raclopride via a lateral tail vein. A 60 min dynamic PET scan was obtained immediately after tracer injection followed by a 15 min attenuation correction. During imaging, the animals were anesthetized with a mixture of 1.5% isoflurane and 100% oxygen. The animals were centered in the field of view of the PET scanner. Anesthesia was monitored by measuring respiratory frequency, and the body temperature was kept at 37°C by a heating pad underneath the animal. PET data were acquired in list mode, graphed in time frames of 4 × 60 s, 4 × 120 s, 8 × 300 s, and 2 × 450 s, and reconstructed using filtered backprojection algorithm with a matrix size of 256 × 256 and a zoom factor of two. Image files were analyzed using PMOD and AsiPro software (Siemens Preclinical Solutions). The PMOD image fusion software allowed linear transformation and rotation to overlay PET and MR template images. The PET/MR fusioned images were used to calculate specific regions of interest in different brain areas with reference to the stereotactic brain atlas of Franklin and Paxinos (2001). With the PMOD software we also analyzed the [11C]raclopride uptake in various brain areas including cerebellum, orbitofrontal cortex (OFC), and striatum. As a reference region, the cerebellum was chosen to correlate the unspecific uptake with the tracer uptake in the striatum and the OFC.
DTI measurements
Male transgenic rats as well as wild-type littermates were measured using DTI at 10 months (n = 6 for TBPQ64; n = 3 for WT) and 5 months of age (n = 3 for TBPQ64; n = 3 for WT). The images were produced using a Clinscan 7T MR scanner (Bruker BioSpin and Siemens Medical Solutions) and a four-channel rat brain surface coil. Rats were anesthetized using isoflurane with an induction of 2.5% and maintenance at 1.5%. Temperature and breathing rate were monitored throughout the studies, with a constant temperature at 37 ± 0.5°C. The measurements lasted ∼60 min. Diffusion tensor images were acquired using an echo planar imaging with 256 directions [b = 0; 1000 s/mm2; field of view (FOV), 54 × 21 mm; matrix, 128 × 52 mm; 26 1 mm slices; TE, 60 ms; TR, 5500 ms]. An anatomical T2-weighted image was also produced (matrix, 256 × 161 mm; FOV, 35 × 57 mm; TR, 3000 ms; TE, 205 ms; slice thickness, 0.22 mm). Fractional anisotropy (FA), radial diffusivity, diffusion weighted images, and apparent diffusion coefficient (ADC) maps were generated using DTI Studio software. PMOD software was used for the coregistration of the maps to the anatomical image, where a region of interest approach was implemented on the different parts of the striatum [dorsomedial (DMS) and ventral (ACB), substantia nigra (SN), and external capsule] using the following Paxinos coordinates: DMS, AP, −0.4 mm; ML, ±2.6 mm; DV, −5.0 mm; ACB, AP, +3.4 mm; ML, ±1.9 mm; DV, 5.3 mm; SN, AP, −4.8 mm; ML, ±2.0 mm; DV, −8.5 mm.
Statistical analysis
Data were analyzed by using GraphPad Prism 5. All results are shown as mean ± SEM. Results were regarded as significant with a p value <0.05.
Student's t test (for the EPM analysis) and two-way ANOVA for repeated measurements with a Bonferroni posttest were performed. We analyzed the interaction between age and genotype for all the other behavioral tests as well as for the weight measurement.
Results
Generation and first characterization of SCA17 rats
To generate SCA17 rats, we used a cDNA encoding human full-length TBP with a poly-glutamine stretch of 64 CAG/CAA repeats under the control of the murine prion promoter (Prp-TBPQ64) (Fig. 1A). This promoter was used previously to drive expression of mutant ataxin-3 in a SCA3 transgenic mouse model with a cerebellar phenotype (Bichelmeier et al., 2007). After injecting the transgenic construct into fertilized Sprague Dawley oocytes, we received 64 pups. Ten of these 64 animals carried the transgene as determined by PCR. However, three potential founders died prematurely without any offspring, and two animals did not transmit the transgene to their offspring. Therefore, only in the remaining five lines the expression pattern of mutant TBP (mTBP) was analyzed by Western blot analysis. mTBP was detected in the cerebellum of all analyzed lines, with line 8.4 showing the highest expression level (Fig. 1D). Based on this, we chose line 8.4 for further characterization. Western blot analyses showed that these animals express mutant TBP predominantly in the cerebellum, with moderate levels of mTBP in the olfactory bulb and cortex, whereas the hypothalamus, brain stem, and striatum displayed only very low levels of mTBP (Fig. 1B,C), respectively. To verify the conservation of the CAG/CAA repeat in the mutant TBP cDNA of TBPQ64 rats, we analyzed the PCR fragment length of DNA samples from transgenic rats. We found that the CAG/CAA repeat is stable for at least three generations (data not shown), which is in line with observations in SCA17 patients (Tomiuk et al., 2007). Additionally, using the same construct only with 38 CAG/CAA repeats, transgenic rats bearing human TBP with a normal polyglutamine tract were generated. While 2 lines of TBPQ38 rats were established, these rats did not showing any phenotypic abnormalities during their normal life span and were indistinguishable from the wild-type littermates (data not shown). This is expected as it has been shown for mice carrying TBP with a normal polyQ tract of 13 (Friedman et al., 2007). Therefore, here we show only data on TBPQ64 rats and their wild-type littermates.
Decreased body weight and a severe neurological phenotype in SCA17 rats
At birth and for the first 3 months of age, TBPQ64 rats appeared normal compared to their wild-type littermates. However, starting at 4 months of age, transgenic male rats had a significantly lower body weight than age-matched controls (Fig. 2A). This significant decrease of body weight was also observed in female TBPQ64 rats. Notably, TBPQ64 rats not only failed to gain weight after 5 months of age, but also showed a loss of body weight thereafter. On the other hand, wild-type animals continued to gain weight as expected. At the age of 8 months, TBPQ64 rats were highly phenotypic and easily distinguishable from control animals: they were cachectic, substantially smaller in body size when compared to wild types (Fig. 2B), and exhibited a hunched posture (kyphosis), poor grooming (Fig. 2F), and tremor. When suspended by the tail, these rats showed abnormal postures comparable to clasping (Fig. 2D), whereas wild-type animals demonstrated normal escape reflexes with hindlimbs spread widely (Fig. 2C). At the age of 10 months, transgenic male TBPQ64 rats weighed, on average, 35% less than age-matched control animals even though they were additionally fed with mashed food pellets. Because of the poor health status of TBPQ64 rats at this end stage, and according to our animal health regulations, we had to kill all TBPQ64 rats after 10 months of age. Therefore, an analysis of lifespan was not possible, but considering the severe phenotype observed, it can be assumed that TBPQ64 rats have a decreased survival.
Motor deficits and increased anxiety in SCA17 rats
To assess progression of disease severity in TBPQ64 rats over time, we first repeatedly applied a modified ataxia score test (Guyenet et al., 2010), which has been successfully used in mouse models of cerebellar ataxia type 7. As expected, with increasing age the ataxia score increased significantly in SCA17 rats, reflecting a progression of symptoms (Fig. 3A; genotype by age, F(4,68) = 19.96, p < 0.0001; genotype, F(1,68) = 40.55, p < 0.0001). Already at the age of 5 weeks, TBPQ64 animals had a higher ataxia score than control animals; however, this difference became significant starting from the age of 5 months (Fig. 3A). Notably, during testing we observed that phenotypic TBPQ64 rats were not able to descend properly from a small beam into their home cage, but rather “fell” onto their head into the cage. To further analyze this apparent motor coordination and balance impairment, we performed rotarod and the beam-walking tests. Repeated-measures ANOVA revealed a significant main effect of genotype (F(1,51) = 5.53, p = 0.031). Unexpectedly, by subsequent post hoc analysis with Bonferroni tests, we found no significant differences in the latency to fall between TBPQ64 and wild-type animals until the age of 8 months regarding the single time points (Fig. 3B). However, in the beam-walking test, transgenic animals showed significant difficulties in traversing the beams of different shapes and width (square beam with 3 cm cross section, genotype by age, F(3,51) = 4.15, p < 0.01; genotype, F(1,51) = 48.99, p < 0.0001; round beam with 3.5 cm diameter, genotype by age, F(3,51) = 11.36, p < 0.0001; genotype, F(1,51) = 34.66, p < 0.0001). TBPQ64 rats slipped more often when traversing the beams compared to age-matched control animals (Fig. 3C,D). Interestingly, there was no significant difference in the latency to traverse the various beams between both genotypes (data not shown). It should be noted that because of the severe phenotype at the age of 10 months, we could not perform these motor tests at this age.
Since psychiatric symptoms and behavioral symptoms are present in SCA17 patients, we assessed anxiety in the EPM test, which has been validated behaviorally and pharmacologically extensively (Pellow et al., 1985; Huang et al., 2012). Already at the age of 4 months, significant differences were found between TBPQ64 rats and their wild-type littermates (Fig. 4). Transgenic animals spent significantly less time on the open arms as well as significantly more time in the central zone than wild-type littermates, indicating that TBPQ64 rats have an increased anxiety (Fig. 4A). There were no differences in general activity between SCA17 rats and wild-type rats in the EPM test, as no significant differences in the total number of transitions into the various arms were observed (Fig. 4B). However, TBPQ64 rats showed significantly less transitions into the open arms (data not shown) and spent more time in the center area (neutral zone; Fig. 4A), supporting the notion that TBPQ64 rats are more anxious than wild-type littermates to enter the open arms. Furthermore, it was apparent that TBPQ64 rats had problems with keeping the balance as 20% of the transgenic animals fell from the open arms of the EPM, while this did not occur in the control group.
To provide further support of increased anxiety-related behavior in SCA17 rats, we analyzed the adaptation period (the first 20 min) in the PhenoMaster system, which is the time the animals need to adapt to the system or the new environment. The periphery to center ambulation ratio measurement is similar to the open-field test for anxiety in a novel environment. At the ages of 3 and 5 months, TBPQ64 rats and their wild-type littermates displayed the same ratio of peripheral to central activity (Fig. 4C). But starting at 7 months, TBPQ64 rats showed a higher ratio of periphery to center ambulation than controls, which reached significance at 9 months of age (Fig. 4C). This indicates an increased anxiety-like behavior in TBPQ64 rats and supports our findings in the EPM test. Regarding the total ambulatory activity in the adaptation period, we did not find significant differences (Fig. 4D).
Decreased activity in SCA17 rats
As SCA17 rats appeared to be less active, we evaluated the activity of TBPQ64 rats and their wild-type littermates in the PhenoMaster system that supplies quantitative measures. Animals were tested at 3, 5, 7, and 9 months of age. They were housed singly for 72 h in a home cage while rearing behavior and the total ambulatory activity was monitored continuously during these 72 h. Both transgenic and wild-type rats showed a pronounced dark/light cycle in their behavioral activities, with their main activity taking place during the dark phases. Exemplarily, data of the activity pattern are shown for 3 and 9 months of age, respectively (Fig. 5A,B). We observed a decreased rearing behavior in 9-month-old transgenic animals when compared to controls of the same age and to 3-month-old TBPQ64 rats (Fig. 5A). Furthermore, 3-month-old TBPQ64 rats showed an increased total ambulatory activity in comparison to their wild-type littermates and to 9-month-old transgenic rats. The latter were less active than both age-matched controls and 3-month-old transgenic rats (Fig. 5B).
When analyzing the activity pattern, it was evident that differences between TBPQ64 rats and wild-type rats were pronounced in the dark cycle, the animals' active phase, so that subsequent analyses of all time points tested are restricted to the dark phase. Rearing behavior decreased in TBPQ64 rats with age (genotype by age, F(3,280) = 19.93, p < 0.0001; genotype, F(1,280) = 33.70, p < 0.0001), mirroring progression of symptoms. We found no differences between both genotypes at 3 and 5 months, but detected a significant decrease of rearing in 7- and 9-month-old TBPQ64 rats (Fig. 5C) compared to controls. Interestingly, ambulatory activity showed a biphasic profile as transgenic rats at the ages of 3 and 5 months were more active than control animals, whereas at 9 months of age the total ambulatory activity was significantly decreased in TBPQ64 rats compared to wild-type rats (Fig. 5D; genotype by age, F(3,280) = 9.349, p < 0.0001; genotype, F(1,280) = 48.42, p < 0.0001).
Moreover, we analyzed the feeding and drinking behavior of these rats (Fig. 5E–H). Graphs in Figure 5, E and G, shows absolute values, but as transgenic animals display such a low body weight at later stages, we also normalized the consumed food and liquid to the body weight of the animals (grams of food consumed per kilogram of body weight, or milliliter of liquid consumed per kilogram of body weight) in Figure 5, F and H. Despite their lower body weight, TBPQ64 rats had similar total food intake and water consumption until 7 months of age. Only at 9 months of age, when TBPQ64 rats are severely affected, was food intake significantly reduced in TBPQ64 rats compared to controls (Fig. 5E). When normalizing the food intake and water consumption to the body weight, we detected a significantly higher food intake at the ages of 3, 5, and 7 months in transgenic rats; at 9 months of age this increase in food intake did not reach significance (Fig. 5F; genotype by age, F(3,48) = 0.1154, not significant; genotype, F(1,48) = 27.48, p < 0.0001). Water consumption was also increased in transgenic rats (genotype, F(1,48) = 9.768, p < 0.01), but the values reached significance only for the 3-month-old animals when applying the post hoc tests (Fig. 5H; genotype by age, F(3,48) = 0.5727, not significant).
Immunohistochemistry and neurodegeneration in the cerebellum of SCA17 rats and human SCA17 brain
At the ages of 3 and 10 months, we investigated the cerebellar cortex by TuJ immunohistochemistry (Fig. 6A–D) and analyzed cellular and subcellular localization of TBP in TBPQ64 rats (Figs. 6E–H, 7A–I), where it is most predominantly expressed (Fig. 1B,C).
TuJ-1 staining lacked in the stellate and basket cells among the dendrites of degenerating Purkinje cells (PCs) in both young and 10-month-old TBPQ64 rats (Fig. 6B,D), whereas wild-type animals showed normal branching of the PC dendrites (slightly varying according to the tilt of section) and regular staining of interneurons in the molecular layer (Fig. 6A,C). Strong TBP immunoreactivity was detected mainly in the granule cell layer and the interneurons of the molecular layer, and less expressed in the Purkinje cell nuclei of TBPQ64 rats (Fig. 6F,H). Some unspecific staining was also observed in age-matched wild-type rats (Fig. 6E,G). Staining with a myc antibody showed a similar distribution of myc-tagged mutant TBP (Fig. 6J) as observed with the 1C2 antibody (Fig. 6F,H), whereas the wild types displayed only very faint endogenous myc protein (Fig. 6I). Some of the abnormalities observed in the transgenic rats resembled the cerebellar lesions of a patient with SCA17. Immunostaining with TuJ-1 revealed severe loss of Purkinje cells and tortuosity of the remaining dendrites (Fig. 6M,N). Basket and stellate neurons in the molecular layer (Fig. 6L) lacked TuJ-1 immunoreactivity when compared with a healthy control (Fig. 6K). As already observed in the transgenic rat, TBP reaction product occurs in numerous interneurons of the molecular layer (Fig. 6O,P), a subset of granule cells but only in very few Purkinje cell nuclei (Fig. 6P, inset).
Electron microscopy confirms neurodegeneration and nuclear TBP immunoreactivity in the cerebellum of SCA17 rats
Semithin and ultrathin sections showed specific nuclear TBP immunoreactivity in a subpopulation of granule cells, in numerous stellate, and some Purkinje cells in heterozygous TBPQ64 rat cerebellar cortex (Fig. 7). Immunopositive granule cells were often localized in groups between unstained cells. The nuclear TBP reactivity was varying in expression (Fig. 7A,B,H); several positive granule cell nuclei exhibited dysmorphic features (Fig. 7H). Some Purkinje cells showed tiny immunopositive intranuclear spots (Fig. 7A), clearly detected by electron microscopy (Fig. 7D).
Dark Purkinje cells were frequently observed (Fig. 7A) when compared with the cerebellar cortex of wild-type littermates (Fig. 7C), indicating Purkinje cell degeneration. The shrunken dark cytoplasm was often surrounded by degenerated basket fibers as detected electron microscopically (Fig. 7E). Dark Purkinje cell dendrites with irregular contours were also abundant in the molecular layer (Fig. 7A,F) confirming the distorted dendrites observed light microscopically (Fig. 6D). TBP-immunopositive nuclei of stellate cells (Fig. 7B,G) also reflected the results in the TBPQ64 rats (Fig. 6F,H) and human SCA17 brains (Fig. 6O,P). In the granule cell layer, numerous degenerated structures with dense lysosomal inclusions were observed, often associated with the glomerula (Fig. 7I).
Calbindin immunoreactivity was found to be reduced in Purkinje cell somata of TBPQ64 rats (Fig. 7J) when compared with wild-type littermates (Fig. 7L). The dendritic trees appeared distorted, also confirming the observations by the TuJ-1 antibody (Fig. 6B,D). Electron microscopically, calbindin-immunopositive Purkinje cell dendrites and spines were detected in the molecular layer neighbored to strongly degenerated dark dendrites lacking immunoreactivity (Fig. 7K).
PET and DTI imaging in SCA17 rats
Dynamic PET scans showed a specific uptake of the D2 receptor antagonist [11C]raclopride in the striatum of wild-type and transgenic rats at 10 months of age (Fig. 8A,B, black circles). This effect did not occur in the cerebellum or the OFC. Interestingly, there is only a trend toward significance in the striatal TACs between wild-type and transgenic rats (p = 0.061). Also, the binding potential, while indicating a difference between transgenic and wild-type rats, did not reach significance (Fig. 8C). Because of the increased perfusion in the cerebellum in the first 15 min in transgenic compared to wild-type rats, we acquired ADC maps of these rats (Fig. 9). We observed that the cerebellar diffusion in SCA17 rats is significantly higher than in wild-type controls (p < 0.001). This strong effect only occurs in the cerebellum, while in dorsal striatum only a small trend toward significance could be shown (p = 0.067; Fig. 9D).
FA comparisons of the SCA17 and wild-type groups showed a clear tendency for lower FA values in the external capsule in the transgenic group, reaching statistical significance (p = 0.032; Fig. 9C). No significant difference in the dorsal striatum or the SN was observed (p > 0.3, not significant).
To investigate whether these changes in diffusion tension imaging occurred at an earlier age, we also examined a separate cohort of rats at the age of 5 months. However, at this age no significant differences in FA and ADC values in any of the investigated brain regions were found between TBPQ64 rats and wild-type rats (Fig. 9A,B).
Discussion
We generated and characterized the first transgenic rat model for spinocerebellar ataxia type 17. TBPQ64 rats showed characteristic phenotypic abnormalities and neuropathological changes similar to findings in human SCA17 patients. While some of these changes are well recapitulated in existing mouse models for SCA17, we provide evidence that crucial characteristics of SCA17 are better mirrored in our transgenic rats and that they represent a valuable tool to pursue experimentation and therapeutic approaches, currently difficult or impossible to perform with existing SCA17 transgenic mice.
A progressive loss of body weight was observed starting at 5 months of age leading to severe cachexia, so that all transgenic rats had to be killed after 10 months of age. This striking body weight loss is in line with findings in a transgenic mouse model for SCA17, although a peculiar increase of body weight preceded weight loss in these transgenic mice (Friedman et al., 2007). For another transgenic mouse model of SCA17 with a severe phenotype, no changes in body weight were described (Chang et al., 2011). In this regard, our transgenic rat model resembles more closely the human condition (Koide et al., 1999; Zühlke et al., 2001; Rolfs et al., 2003; Mariotti et al., 2007), e.g., reduced body weight (Koide et al., 1999). A similar body weight phenotype was observed in the only existing knock-in mouse model for SCA17 (Huang et al., 2011). However, as with other knock-in models of polyQ diseases (Wheeler et al., 2000; Lin et al., 2001; Menalled et al., 2002), these have a milder phenotype and do not die prematurely. This milder phenotype would require the use of large numbers of animals and a longer period of testing to determine a significant effect of an intervention, possibly decreasing the feasibility of such studies.
We also demonstrated that weight loss cannot be contributed to a lower food intake in TBPQ64 rats (Fig. 5E). In fact, when normalizing to the body weight, TBPQ64 rats even had a significantly higher food intake (Fig. 5F), indicating that increased metabolism might underlie the weight loss. Comparable observations have been made in HD mice where it was shown that weight loss in R6/2 mice is associated with elevated oxygen consumption and abnormalities in several weight-regulation factors (van der Burg et al., 2008) as well as mitochondrial dysfunction and impaired energy metabolism (Grünewald and Beal, 1999; Weydt et al., 2006). Further studies will be required to investigate whether the weight loss in SCA17 and HD are based on the same pathomechanisms.
Interestingly, besides severe ataxia and motor coordination problems (Fig. 3), we observed a biphasic activity profile in SCA17 rats with hyperkinesia in early stages of the disease progressing to bradykinesia at later stages (Fig. 5D). This is in agreement with findings in HD rodent models (Slow et al., 2003; André et al., 2011) and has been argued to reflect hyperkinetic symptoms such as chorea, and bradykinetic symptoms (e.g., dystonia or rigidity) at different stages of the disease (Slow et al., 2003). The prodromal hyperactive phase has not been described in the SCA17 mouse models so far (Chang et al., 2011; Huang et al., 2011), which might be due to the higher CAG repeat sizes in these models compared to our TBPQ64 rats. Higher CAG repeat sizes correlate with an earlier onset of disease and an increased severity of symptoms resulting in a different phenotype (Fujigasaki et al., 2001; Nakamura et al., 2001; Zühlke et al., 2001; Rolfs et al., 2003). In HD, for example, repeat sizes of >60 CAGs will lead to juvenile HD with bradykinesia and dystonia as predominant motor symptoms rather than chorea (Siesling et al., 1997; Squitieri et al., 2006; Quarrell et al., 2009). Animal models such as our TBPQ64 rats, which exhibit a biphasic activity profile, will be of great value to investigate the contribution of the indirect pathway to the development of hyperkinetic symptoms such as chorea as it has been shown in an HD patient (Starr et al., 2008), and to test therapeutics targeted to this pathway. Furthermore, the larger size of rats facilitates greatly the use of in vivo electrophysiology, which will be essential to understand how the neuronal circuitry is affected and how compounds such as phospodiesterase 10 inhibitors could restore the function of indirect pathway neurons not only in HD but also in SCA17 (Threlfell et al., 2009; Beaumont, 2012).
Unlike the other spinocerebellar ataxias, SCA17 is not only characterized by progressive cerebellar ataxia, but also a broad spectrum of other neuropsychiatric signs (Zühlke et al., 2001; Mariotti et al., 2007). Mouse models are in general limited for studying these functional and behavioral measurements (Tecott and Nestler, 2004; Rodriguiz and Wetsel, 2006), especially since most standard test designs were originally developed and validated for rats. Whether they can be transferred to mice by mere downsizing of the test systems is unclear. Therefore, TBPQ64 rats are a valuable resource to study nonmotor abnormalities in SCA17. Indeed, we demonstrated increased anxiety-like behavior for the first time in a rodent model of SCA17 paralleling the human condition (Zühlke et al., 2001; Mariotti et al., 2007). This is especially interesting as several anxiolytic drugs are available, which have been validated in rats using the elevated plus maze for more than two decades (reviewed in File, 1990). Whether cognitive changes are also present in TBPQ64 rats has not been evaluated in the current study but testing will be readily feasible in this rat model in future studies.
Neuropathologically, the severe phenotype of SCA17 rats was associated with neuronal loss, particularly in the cerebellum. Degeneration of Purkinje cells, basket cells, and stellate neurons; changes and degenerations in the morphology of the Purkinje cell dendrites; axonal torpedos; and TBP-positive immunoreactivity of stellate and basket cells in the molecular layer were readily found by light and electron microscopy (Fig. 6; 7), consistent with findings in human SCA17 patients (Fig. 6) (Rolfs et al., 2003). Interestingly, we also observed numerous TBP-positive granule cells adjacent to immunonegative cells, which was not found to this extent in the human SCA17 patients investigated here. However, there is a report of nuclear TBP reactivity in granule cell nuclei in SCA17 human patients (Fujigasaki et al., 2001). The abundant expression of mutant TBP in granule cells of the TBPQ64 rat may be due to the prion promoter construct that we used and in agreement with the known expression pattern of the transgene expression driven by this promoter (Borchelt et al., 1996; Schilling et al., 1999a,b; Garden et al., 2002). Together, the neuropathological changes detected in the TBPQ64 rats recapitulate many characteristics of human SCA17 and extend findings in SCA17 mouse models (Friedman et al., 2007; Chang et al., 2011; Huang et al., 2011), especially in regard to changes in dendrite morphology.
To take advantage of the larger brain size of rats compared to mice, we performed in vivo PET and DTI imaging to detect a potential biomarker for SCA17. Previous PET data with the dopamine 2 receptor antagonist raclopride in SCA17 patients showed loss of postsynaptic D2 receptors in the caudate nucleus (Brockmann et al., 2012). In our TBPQ64 rats, a decreased binding potential of the D2 receptor antagonist [11C]raclopride was found in the caudate–putamen, consistent with the human data, although this difference did not reach significance. This may be due to the low expression of mutant TBP in this brain region in the SCA17 rats, and maybe attributed to the use of the Prp promoter to drive transgene expression.
Since the D2 receptor is expressed only at low levels in the cerebellum (Farde et al., 1985), the most affected brain region in the TBPQ64 rats, we applied DTI, which allows the observation of gray and white matter changes over time. In HD patients, DTI has also been shown to allow detection of altered tissue integrity in both preclinical and clinical stages of HD (Mascalchi et al., 2004; Reading et al., 2005; Rosas et al., 2006, 2010; Seppi et al., 2006; Bohanna et al., 2008; Klöppel et al., 2008; Douaud et al., 2009; Della Nave et al., 2010; Mandelli et al., 2010; Sritharan et al., 2010). DTI has also been successfully applied in an inducible rat model of HD (Van Camp et al., 2012) and in one of the transgenic rat models of HD (Antonsen et al., 2012; Blockx et al., 2012), as well as in other rodent disease models (Song et al., 2004; Boska et al., 2007; Lope-Piedrafita et al., 2008; Van Camp et al., 2009; Grundmann et al., 2012). DTI thus appears as a promising tool for monitoring neuropathology in transgenic SCA17 rats. In the TBPQ64 rats we detected a significant increase in cerebellar diffusion (higher ADC values) indicating cell death, which is in good agreement with our neuropathological findings (loss of basket and stellate neurons in the molecular layer, dark cell degeneration of PCs). Furthermore, we found a significant decrease of FA values in the external capsule, although no significant difference in the dorsal striatum, the ventral striatum, or the substantia nigra could be observed. The significantly lower FA value in the external capsule could hint to a degeneration of the fiber bundles that project to the dopaminergic neurons of the striatum. Consistent with this we had observed fiber degeneration in the striatum of some SCA17 rats (data not shown). Our results confirm that DTI measures are potentially useful correlates of neuropathological changes in these transgenic rats and raise hope that DTI imaging could provide a biomarker for SCA17 patients, which has not been pursued so far.
Footnotes
This work was supported by the RATstream Project (European Union Contract LSHM-03784). We are grateful for excellent technical assistance of Marlen Löbbecke-Schumacher, Hans-Werner Habbes, Celina Tomczak, and Therese Stanek.
- Correspondence should be addressed to Dr. Huu Phuc Nguyen, Institute of Medical Genetics and Applied Genomics, University of Tübingen, Calwerstrasse 7, 72076 Tübingen, Germany. hoa.nguyen{at}med.uni-tuebingen.de