Wild type human TDP-43 potentiates ALS-linked mutant TDP-43 driven progressive motor and cortical neuron degeneration with pathological features of ALS
Acta Neuropathologica Communications volume 3, Article number: 36 (2015)
Amyotrophic lateral sclerosis (ALS) is a relentlessly progressive neurodegenerative disorder, and cytoplasmic inclusions containing transactive response (TAR) DNA binding protein (TDP-43) are present in ~90 % of cases. Here we report detailed pathology in human TDP-43 transgenic mice that recapitulate key features of TDP-43-linked ALS.
Expression of human wild-type TDP-43 (TDP-43WT) caused no clinical or pathological phenotype, while expression of Q331K mutant (TDP-43Q331K) resulted in a non-lethal age-dependent motor phenotype, accompanied by cytoplasmic TDP-43 aggregation, mild neuronal loss, with astroglial and microglial activation in the motor cortex and spinal cord at 24 months. However, co-expression of WT and Q331K mutant (TDP-43WTxQ331K) resulted in an extremely aggressive motor phenotype with tremor from 3 weeks and progressive hind-limb paralysis necessitating euthanasia by 8–10 weeks of age. Neuronal loss and reactive gliosis was observed in the spinal cord and layer V region of the cortex, with TDP-43, ubiquitin and p62 cytoplasmic inclusions and an increase in insoluble TDP-43. Nuclear clearance of TDP-43 was not observed in TDP-43Q331K mice but was seen in 65 % of aggregate containing spinal cord motor neurons in TDP-43WTxQ331K mice.
We hypothesise that cytoplasmic TDP-43Q331K aggregates facilitate the recruitment of WT protein in compound animals, which dramatically accelerates neurodegeneration and disease progression. The exploration of disease mechanisms in slow and rapid disease models of TDP-43 proteinopathy will help elucidate novel drug targets and provide a more informative platform for preclinical trials.
Amyotrophic lateral sclerosis (ALS) is a relentlessly progressive neurodegenerative disorders characterised by the degeneration of motor neurons in the motor cortex and spinal cord, progressive paralysis and ultimately death due to respiratory failure.
Transactivating response region (TAR) DNA binding protein (TDP-43) has been identified as a major component of neuronal and glial inclusions found in ~95 % of sporadic ALS patients [1, 2]. TDP-43 is predominantly a nuclear protein involved in regulating RNA transcription, splicing, trafficking and microRNA biogenesis . Cortical and motor neurons containing cytoplasmic TDP-43 aggregates often appear to have little or no nuclear TDP-43 [4, 5], implicating a loss of nuclear TDP-43 function in disease pathogenesis, however cytoplasmic aggregation is also toxic and may play a key pathogenic role.
The identification of mutations in the glycine-rich C terminal region of TDP-43 that enhance protein cleavage, aggregation and neurotoxicity confirmed a pathologenic role for TDP-43 mis-accumulation in ALS and FTLD [6, 7, 8]. TDP-43 positive inclusions have also been identified in patients with pathogenic mutations in the genes encoding progranulin (PGRN ), valosin containing protein (VCP ) and Ubiquilin 2 (UBQLN2 ) and the G4C2 hexanucleotide expansion mutation identified in C9ORF72 [12, 13]. The identification of mutations in a structurally and functionally similar nucleic acid binding protein, fused in sarcoma (FUS) [14, 15] supports the hypothesis that defective RNA processing or aberrant assembly of these aggregation prone proteins [16, 17] are mechanistic contributors in the pathogenesis of ALS.
TDP-43 is a 414 amino acid protein, consisting of two RNA recognition motifs (RRM1 and RRM2) [18, 19], a nuclear import and export signal , and a glycine rich region that has been implicated in its protein-protein interactions [16, 17], including those involved in its regulation of RNA splicing [21, 22]. It has been shown to bind to over 6000 pre-mRNAs and over 2000 non-coding RNAs within the central nervous system, affecting the levels of around 600 mRNAs, and regulating the splicing patterns of another 950 [23, 24]. TDP-43 has also been demonstrated to autoregulate its own RNA level [23, 25] at least in part by stimulating the excision of an intron in its 3’ untranslated region (UTR) which initiates its degradation by nonsense mediated RNA decay .
A number of rodent models have been generated to assess the effect of mutation and TDP-43 expression levels in vivo. Disruption or constitutive knockout of the Tardp gene in mice is embryonic lethal [26, 27, 28], while post-natal knockout results in metabolic defects, leading to rapid death . In contrast, heterozygous knockdown results only in a mild impairment in grip strength, with no overt evidence of neurodegeneration , while motor neuron specific knockdown results in age dependent progressive motor dysfunction and motor neuron loss [30, 31]. Studies investigating the effect of overexpression of human wild-type (WT) or disease mutant TDP-43 have demonstrated varying levels of lethality, motor phenotype and pathology [32, 33, 34, 35, 36, 37, 38, 39], with some evidence of a dose-dependent effect  that may be enhanced by the presence of a pathogenic mutation [38, 39]. Some models are also confounded by the presence of phenotypes not identified in patients, such as the existence of a severe gut motility defect [40, 41]. In many cases the pathology observed in rodent models does not convincingly recapitulate many aspects of the human disease.
Here we report the physical, pathological and biochemical characterisation of mice transgenic for human wild-type (WT) and ALS-linked Q331K mutant TDP-43. Mice overexpressing human TDP-43WT develop no overt physical or pathological phenotype, while those overexpressing mutant human TDP-43Q331K develop an age-dependent mild motor and pathological phenotype. Mice co-expressing TDP-43WT and TDP-43Q331K mutant TDP-43 develop marked tremor at 3 weeks and rapidly progressive paralysis requiring euthanasia by 8–10 weeks. Pathologically, TDP-43WTxQ331K mice demonstrate major neuronal loss, robust astroglial reactivity, increased cytoplasmic TDP-43 accumulation and detergent resistant TDP-43. We propose that mislocalisation and aggregation of the mutant protein seeds the rapid recruitment of wild-type TDP-43 that greatly accelerates the disease processes.
Materials and methods
All experiments were performed under the terms of the UK Animals (Scientific Procedures) Act 1986, and were approved by the Kings College, London ethics review panel.
Generation of transgenic animals
Construction of transgenic mice expressing TDP-43WT (line 96) or TDP-43Q331K (line 31) has been previously described (see Additional file 1: Figure S1 in reference ). Briefly, cDNAs containing N-terminal myc-tagged full length wild-type or Q331K mutant TDP-43 were amplified by PCR to insert flanking SalI digestion sites. The resulting products were digested by SalI and cloned into the XhoI insertion site of the MoPrP. XhoI vector (ATCC #JHU-2). The resultant MoPrP. XhoI-mychuTDP-43 construct was then digested upstream of the minimal PrP promoter and downstream of the final PrP exon 3 using BamHI and NotI and subcloned into a shuttle vector containing loxP flanking sites (see Fig. 1a in reference ). The final construct was then linearized using XhoI, injected into the pro-nuclei of fertilized C57Bl6/C3H hybrid eggs and implanted into pseudopregnant female mice. After obtaining multiple founder mice, lines displaying comparable levels of mutant or wild-type transgene accumulation were selected and backcrossed to C57Bl6 to establish the lines detailed in this paper. The mice used for analysis were backcrossed to C57Bl6 for a minimum of four generations. All mice were maintained on a C57B6/J background, and compound hemizygous animals were generated by crossing hemizygous TDP-43WT animals with TDP-43Q331K mutant expressing animals (TDP-43WTxQ331K). Mice from the single hemizygous lines were identified using PCR with primers 5’- GGATGAGCTGCGGGAGTTCT and 3’- GTCAACCCCATACTACCCGT. Animals from the compound hemizygous lines were identified with direct sequencing using the primers 5’- ATGACTGAGGATGAGCTGCG and 3’- GGATGCTGATCCCCAACCAA.
Evaluation of motor function and health
From 3 weeks of age, mice were regularly weighed and general health status was recorded. Animals showing signs of hind-limb paralysis were monitored daily, and disease end stage and death was defined as the time when animals could no longer obtain food or water, or had lost 25 % of their body weight, at which point they were euthanized.
Motor strength and coordination were evaluated on the rotarod (Columbus Instruments) at multiple ages (5 weeks, 3, 6, 12, 18 24 months), using a 5 min accelerating protocol starting at 2 rpm, and rising to 30 rpm throughout the 5 min testing period. Mice were tested on multiple occasions, and all animals received an initial training session of 2 min at 2 rpm to acclimatise them to the equipment.
Data from 5 week old TDP-43WTxQ331K mice and their littermates were assessed statistically by one-way analysis of variance (ANOVA) followed by the Tukey test. All other data were assessed statistically by two-way ANOVA followed by the post-hoc Holm-Sidak test.
Histology and immunohistochemistry
Eight week old, end stage TDP-43WTxQ331K mice, and 24 month old single hemizygous mice and their respective age-matched littermates were anaesthetised and transcardially perfused with PBS followed by 4 % paraformaldehyde (PFA) in phosphate buffer. Brain, spinal cord and gastrocnemius muscles were postfixed in 4 % PFA in 15 % sucrose for 5 h, cryoprotected in 30 % sucrose for 24 h and cut into 30 μm (brain and cord) or 40 μm (muscle) sections on a cryostat.
For immunohistochemistry, the following antibodies were used: rabbit anti-TDP-43 (1:500, Proteintech), rabbit anti-mouse TDP-43 (0.1 μg/ml, a gift from Prof. Virginia Lee (Igaz et al. 2011)), rabbit anti-ubiquitin (1:1000, DAKO), rat anti-myc (1:1000, Serotec), rabbit anti-GFAP (1:4000, DAKO), mouse anti-CD68 (1:2000, Serotec), rabbit anti-p62 (sequestosome 1) (1:10,000; Abcam). For bright field imaging, sections were washed and incubated with the appropriate biotinylated secondary antibody (1:1000, Vector), and then with an ABC kit (Vector). Sections were imaged using a Zeiss light microscope and Axiovision software. For fluorescence imaging, sections were incubated with rat anti-myc (1:200) and either rabbit anti-ubiquitin (1:200) or rabbit anti-p62 (1:5000), sections were washed and incubated with goat anti-rat Alexa Fluor 488 and goat anti-rabbit AlexaFluor 568 (Invitrogen), and imaged using a Leica confocal microscope and LAS-AF software.
For motor neuron counts, perfused lumbar spinal cords from 3 to 4 animals per genotype were serially sectioned, and every 6th section (30 μm) was analysed. Sections were mounted, dried, incubated overnight in 1:1 ethanol/chloroform to de-fat the sections, stained for 10 min in warm 0.1 % cresyl violet, dehydrated and coverslipped. To compare the number of motor neurons, large neurons greater than 30 μm in diameter (as assessed using the integrated morphometry analysis package in Metamorph 7.7, Molecular Devices, Wokingham, UK) in the anterior horn of the lumbar spinal cord were counted in 15 sections. Data were assessed statistically by one-way ANOVA, followed by the post-hoc Tukey test. For cortical neuron counts, perfused brains from 3 to 4 animals per genotype were serially sectioned, and every 12th section (30 μm) through the motor cortex was assessed. Sections were stained as for the lumbar spinal cord. To compare the number of neurons, cells greater than 5 μm in diameter (as assessed using the nuclear count analysis package in Metamorph) were counted in four images per section. Data were assessed statistically by one-way ANOVA, followed by the post-hoc Tukey test.
For muscle histology, gastrocnemius muscles (2–4 animals per age and genotype) were dissected fresh, immediately frozen in isopentane cooled in dry ice, and cryostat sections were cut onto slides and stained with haematoxylin and eosin. For the detection of neuromuscular junctions (NMJs), perfused gastrocnemius muscle (2–3 animals per age and genotype) was incubated in Alexa Fluor 555 α-bungarotoxin (1:500, Life Technologies) and rabbit anti-Synaptophysin 1 (1:500, Synaptic Systems). Sections were washed and incubated in donkey anti-rabbit IgG DyLight 488 secondary antibody (1:500, Thermo Scientific) and imaged on a Leica confocal microscope. To assess NMJ area, the total area stained by bungarotoxin was assessed in ImageJ, in 30–40 NMJs per animal. To calculate the number of intact NMJs, 70–100 were assessed per animal, and were considered intact if they demonstrated full colocalisation of bungarotoxin and synaptophysin staining. Data were assessed statistically by one-way ANOVA, followed by the post-hoc Tukey test.
Nerve root axon count
7 week old, end stage TDP-43WTxQ331K mice (n = 3–4 per genotype), and 24 month old single hemizygous mice (n = 3–6 per genotype) and their respective age-matched littermates were anaesthetised and transcardially perfused with PBS followed by a mixture of 2 % PFA and 2.5 % glutaraldehyde in 0.1 M cacodylate buffer. The L5 ventral roots were removed and post fixed in the same fixative at 4 °C overnight. The roots were then further fixed in 1 % osmium tetroxide in0.1 M cacodylate buffer for 4 h. Fixed tissue was then dehydrated in ethanol and embedded in Epox 812/Araldite 502 (TAAB). semi-thin sections (0.65 μm) were cut using an ultramicrotome (Reichart-Jung Ultracut-E) and collected onto glass slides. The sections were stained with 1 % toluidine blue for 15 s before mounting for viewing and examined under a light microscope. Axon measurements were made using the integrated morphometry package on Metamorph 7.7 (Molecular Devices, Wokingham, UK) and α-motor axons, defined as those with a diameter greater than 3.5 μm, were counted. Data was analysed statistically by way of ANOVA followed by the post-hoc Tukey test.
To assess expression levels of full length TDP-43, the 25 and 35 kDa TDP-43 fragments, and phospho-TDP-43, whole brains of 3–4 end stage hTDPWTxQ331K and 3–4 age-matched hTDPWT, hTDPQ331K and non-transgenic animals, were lysed in low salt buffer (10 mM Tris, 5 mM EDTA, 10 % sucrose) with protease inhibitors (Roche Diagnostics, UK). Total TDP-43 levels were also assessed in four 24 month old hTDPWT, hTDPQ331K and non-transgenic animals.
For cytoplasmic and nuclear fractionation, four brain samples for each age and genotype were prepared as described earlier . Briefly, snap-frozen tissue was weighed and homogenised in buffer containing 10 mM Hepes, 10 mM NaCl, 1 mM KH2PO4, 5 mM NaHCO3, 5 mM EDTA, 1 mM CaCl2, 0.5 mM MgCl2 and protease inhibitors (10x vol/weight). After 10 min on ice, 2.5 M sucrose (0.5x vol/weight) was added. Tissue was homogenized and centrifuged at 6300 g for 10 min. The supernatant was collected as the cytoplasmic fraction. The pellet was washed four times in TSE buffer (10 mM Tris, 300 mM sucrose, 1 mM EDTA, 0.1 % IGEPAL (Sigma) and protease inhibitors 10x vol/weight), homogenized and centrifuged at 4000 x g for 5 min. Finally the pellet was resuspended in RIPA buffer with 2 % SDS (5x vol/weight) as the nuclear fraction.
For insolubility assessment, four brain samples for each age and genotype underwent sequential extraction in buffers of increasing stringency, based on a modified protocol previously described . Briefly, snap-frozen tissue (500 mg/ml w/v) was extracted by repeated homogensiation and cetrifugation steps (120,000 g, 30 min 4 °C) in high salt buffer (50 mM Tris–HCl, 750 mM NaCl, 10 mM NaF, 5 mM EDTA, pH7.4), 1 % Triton X-100 in high salt buffer, RIPA buffer (50 mM Tris–HCl, 150 mM NaCl, 5 mM EDTA, 1 % NP-40 substitute, 0.5 % sodium deoxycholate, 0.1 % sodium dodecyl sulphate) and urea buffer (30 mM Tris HCl pH 8.5, 7 M Urea, 2 M Thiourea, 4%CHAPS). To prevent carry over, each extraction step was performed twice. Supernatants from the first extraction steps were analysed, while supernatants from the wash steps were discarded. Protease inhibitors were added to all buffers excluding the urea buffer prior to use.
Protein samples were then separated by SDS/PAGE using 10 % polyacrylamide gels, and transferred to nitrocellulose membranes. Total TDP-43 and the 25 and 35 kDa fragments were recognised by a rabbit polyclonal antibody to TDP-43 (1:1000, Proteintech), and exogenous myc tagged human TDP-43 was recognised by a mouse monoclonal antibody to the myc tag (1:1000, Cell Signalling). Phospho-TDP-43 was recognised using a rabbit anti-phospho-Ser409/410-TDP-43 (1:1000, CosmoBio), and in these analyses, total TDP was recognised using a rat monoclonal antibody to TDP-43 (1:1000, BioLegend) . Fluorescent secondary antibodies conjugated to Dylight 680 nm or 800 nm (Thermo Scientific) were used to detect protein levels, and results were visualised using the Odyssey Imager (Licor). Data were normalised to GAPDH (1:5000, Sigma), actin (1:20,000, Abcam) or Lamin B1 (1:2000, Abcam). Quantitation of immunoblots was done using Image J software, and data were analysed statistically by way of ANOVA followed by the post-hoc Tukey test.
Overexpression of human wild-type and Q331K mutant TDP-43 causes progressive paralysis and death in mice
Mice expressing human WT (TDP-43WT) or Q331K mutant (TDP-43Q331K) TDP-43 were interbred to generate TDP-43WTxQ331K animals expressing both the WT and mutant protein. Initial breeding approximated a Mendelian distribution of genotypes on weaning. Because 3 week old TDP-43WTxQ331K animals struggled to compete for food against their single transgenic littermates we added wet mash food to their home cage prior to weaning which ensured survival.
Immunoblots of brain lysates from TDP-43 transgenic mice showed that the exogenous human TDP-43 protein had a slightly higher molecular weight than the endogenous mouse TDP-43, due to the presence of the myc tag (Fig. 1a). Quantification of expression indicated that total TDP-43 expression detected in the brains of young TDP-43WTxQ331K mice was 3.3 fold higher than non-transgenic animals (Figs. 1a–b), while expression in young TDP-43WT and TDP-43Q331K single hemizygous animals was 1.4 and 2.2 fold higher respectively. Levels of transgene encoded mouse TDP-43 were maintained during aging (Additional file 1: Figure S1). The increase in total TDP-43 observed in transgenic animals was associated with a proportionate downregulation of endogenous murine TDP-43 (Fig. 1c, Additional file 1: Figures S1 and S2), which is consistent with previous reports of autoregulation of TDP-43 mRNA levels [23, 25] and the absence of a key autoregulatory sequence  on our transgene encoded mRNA. Immunohistochemistry using a myc-tag antibody to selectively visualise only the human TDP-43 protein revealed expression throughout the spinal cord (Figs. 1d–g), and in the cortex (Fig. 1h–k) in all transgenic animals.
Motor function was assessed at multiple age points using the accelerating rotarod paradigm. Animals were born at Mendelian ratios, and were indistinguishable from their non-transgenic littermates until 3 weeks of age when the TDP-43WTxQ331K animals began to develop tremor. From 3 weeks of age, TDP-43WTxQ331K mice displayed a rapid decline in their motor function, with a significant reduction in performance on the accelerating rotarod at 5 weeks of age compared with non-transgenic, TDP-43WT and TDP-43Q331K littermates (Fig. 2a). TDP-43WTxQ331K animals developed progressive hind limb paralysis with a severely stilted gait, an inability to raise their pelvis off the ground (Additional file 2: Movie S1) and a failure to splay hind limbs normally when lifted by their tail (Fig. 2c). Following the onset of severe hind limb paralysis at 5–6 weeks, disease progressed rapidly in TDP-43WTxQ331K animals, necessitating euthanasia by 8–10 weeks because they were unable to obtain food or water, or had lost 25 % of their total body weight. The average survival time for TDP-43WTxQ331K mice was 64 ± 4 days (Fig. 2b). In contrast TDP-43WT animals displayed no significant motor dysfunction or signs of ill health out to 24 months. TDP-43Q331K animals displayed a mild but progressive motor dysfunction as assessed by the rotarod (Fig. 2a), accompanied by abnormal hind limb splay (Fig. 2d) and tremor but no evidence of early lethality (Fig. 2b). Previous studies have demonstrated intestinal blockage and/or megacolon as a major phenotype in prion-promoter driven TDP-43 mouse overexpression models [40, 41, 44] however, the TDP-43WTxQ331K mice displayed normal bowel movements throughout their lives, and physical examination of the intestines immediately following euthanasia did not detect any evidence of intestinal blockage or megacolon. In addition, the progressive decline in motor function observed in these mice resulted in increasing difficulty in accessing food and water. The provision of wet mash at floor level was sufficient to maintain them at a consistent weight until the last few days prior to euthanasia, when they increasingly struggled to access food, and began to lose weight. The progressive phenotype observed in these animals was more characteristic of the G93A SOD1 mouse model  than the TDP-43 A315T mice which display significant gut motility issues [40, 41, 44, 37].
ALS-like spinal cord pathology in TDP-43Q331K mice is potentiated by co-expression with wild type TDP-43
In the spinal cord of 8 week old TDP-43WTxQ331K mice, TDP-43 staining showed frequent globular cytoplasmic inclusions similar to globular punctate inclusions seen in human TDP-ALS patients [1, 2] (Fig. 3a), which were absent in age matched TDP-43WT and TDP-43Q331K single transgenic and non-transgenic animals (Additional file 1: Figure S3). Assessment using a mouse specific TDP-43 antibody also demonstrated that despite reduced levels of endogenous murine TDP-43, (Additional file 1: Figure S2), there was evidence of both cytoplasmic and nuclear aggregation of endogenous TDP-43 in 8 week old TDP-43WTxQ331K mice (Fig. 3b).
Ubiquitin (Fig. 3c, Additional file 1: Figure S4) and p62 (Fig. 3d, Additional file 1: Figure S4) immunohistochemistry also revealed multiple small globular inclusions present in the neuronal cytoplasm and neuropil of TDP-43WTxQ331K mouse ventral horns. Interestingly, there were a small number of p62 (sequestosome 1) positive inclusions in the spinal cord of 8 week old hTDPQ331K animals (Additional file 1: Figure S4). Consistent with this, 24 month old TDP-43Q331K mice demonstrated numerous small cytoplasmic p62 inclusions (Additional file 1: Figure S4), accompanied by occasional small TDP-43 inclusions in the neuropil (Additional file 1: Figure S3), although there was no evidence of any changes in ubiquitin staining in these animals. Co-labelling of myc-tagged TDP-43 with both ubiquitin and p62 demonstrated the presence of both proteins in TDP-43 inclusions (Figs. 3e-f) in TDP-43WTxQ331K mice. Assessment of myc and ubiquitin positive aggregate containing cells in TDP-43WTxQ331K animals (50–100 cells per mouse, n = 4; Fig. 3f) demonstrated that ~65 % of these cells displayed minimal nuclear myc-TDP staining, providing evidence of nuclear clearing in aggregate containing cells, which is supported by total and endogenous TDP-43 staining showing a loss of nuclear TDP-43 in a number of aggregate containing cells (Figs. 3a–b). In addition, co-staining studies showed the existence of many small p62 inclusions and a few small ubiquitin inclusions that did not colocalise with myc-TDP (Figs. 3e–f). Studies in other TDP-43 transgenic mouse models [34, 46] have shown evidence of eosinophilic aggregates consistent with mitochondrial aggregation, however, haemotoxylin and eosin staining did not reveal any overt signs of eosinophilic aggregates in our mice, regardless of genotype (Additional file 1: Figure S5) hence abnormal accumulation of mitochondria is unlikely to be a major pathological feature of these animals.
Neuronal cell counting demonstrated a significant (~70 %) loss of α-motor neurons in the anterior horn of the lumbar spinal cord in TDP-43WTxQ331K animals compared to their age-matched TDP-43WT (p < 0.001), TDP-43Q331K (p < 0.001) and non-transgenic (p < 0.001) littermates (Fig. 4). In the anterior horn, this was associated with a robust increase in astrogliosis, accompanied by mild microgliosis (Additional file 1: Figure S6) A moderate level of microgliosis was also found in the white matter tracts, and there was evidence of mild increases in astrogliosis in the anterior horn of single transgenic age-matched animals (Additional file 1: Figure S6). In 24 month old animals, a non-significant 25 % loss (p = 0.074) of α-motor neurons in the anterior horn (Additional file 1: Figure S7) was accompanied by a robust increase in astrogliosis in the TDP-43Q331K transgenic animals compared to their non-transgenic and TDP-43WT aged –matched littermates. These changes were accompanied by a modest microglial increase in the white matter tracts (Additional file 1: Figure S6), In addition, assessment of large caliber α-motor axons (>3.5 μm diameter) in the L5 nerve root demonstrated a significant (~46 %) loss in TDP-43WTxQ331K mice at 8 weeks (Additional file 1: Figure S8), with no significant change observed in single transgenic animals at either age. Interestingly, there was a decline in the number of motor axons in all genotypes at 24 months of age, which is consistent with previous reports suggesting that C57Bl/6 mice display a subclinical loss of myelin during aging . A trend to a further reduction (~12 %; p = 0.25; Additional file 1: Figure S8) in numbers of motor axons was seen in the phenotypic 24 month old TDP-43Q331K animals. The loss of myelin reported in C57Bl/6 mice may partially mask the reduction in α-motor axons in aged TDP-43Q331K animals. The loss of α-motor axons in TDP-43WTxQ331K animals is accompanied by degenerating axons, characterised by the appearance of vacuolization and myelin defects (Additional file 1: Figure S8).
Muscle histology from end-stage TDP-43WTxQ331K mice showed group atrophy of muscle fibres (Additional file 1: Figure S8) characteristic of denervation seen in muscle from ALS patients, while age-matched single transgenic animals were not significantly different from their non-transgenic littermates. Analysis of aged TDP-43Q331K animals revealed a mild disorganisation of muscle fibres compared to age-matched littermates (Additional file 1: Figure S8) and immunoflourescent analysis revealed a significant reduction in the number of intact neuromuscular junctions (NMJ) in TDP-43WTxQ331K mice (~60 %; p < 0.001; Additional file 1: Figure S8) coupled with significant structural disruption, indicated by a reduction in NMJ area (Table S1) compared to their non-transgenic and TDP-43WT littermates. There was also a mild, reduction in NMJs in age-matched TDP-43Q331K animals (~15 %; p = 0.06; Additional file 1: Figure S8). Consistent with data from young animals, 24 month old TDP-43Q331K animals displayed a significant reduction in the number of intact NMJs (~35 %; p < 0.05; Additional file 1: Figure S8), accompanied by a reduction in area (Table S1), demonstrating an age-dependent degeneration of the NMJs in the TDP-43Q331K animals.
Brain pathology in TDP-43Q331K mice is potentiated by co-expression with TDP-43WT without loss of nuclear TDP-43
TDP-43 positive puncta without loss of nuclear TDP-43 were identified in layer V of the motor and somatosensory cortices in TDP-43WTxQ331K mice (Fig. 5a, Additional file 1: Figure S9), which were not apparent in age-matched non-transgenic, TDP-43WT or TDP-43Q331K single transgenic littermates (Additional file 1: Figure S9). Ubiquitin and p62 staining in the TDP-43WTxQ331K animals shows similar small inclusions together with occasional larger inclusions in the same region (Figs. 5b–c, Additional file 1: Figure S9), accompanied by an increase in diffuse ubiquitin staining in the pyramidal cells compared to age matched single and non-transgenic littermates (Additional file 1: Figure S9). As seen in the cord, cortices from 8 week old TDP-43Q331K animals contain occasional small cytoplasmic p62 inclusions, together with occasional small ubiquitin inclusions while phenotypic 24 month old TDP-43Q331K animals also display evidence of small ubiquitin and p62 inclusions (Additional file 1: Figure S10) that are not apparent in age-matched non-transgenic or TDP-43WT animals. There is also evidence of small TDP-43 inclusions in the aged TDP-43Q331K mice (Additional file 1: Figure S9) that are not apparent in aged non-transgenic or TDP-43WT mice. Co-labelling of myc-TDP and ubiquitin (Fig. 5d) demonstrates a clear colocalisation of these proteins in large inclusions identified in the cortex of TDP-43WTxQ331K mice, together with partial colocalisation in smaller puncta. In contrast, although there is evidence of occasional perinuclear TDP-43 and p62 colocalisation, multiple small cytoplasmic p62 inclusions throughout the cortex show no evidence of myc-TDP colocalisation (Fig. 5e), again suggesting that this p62 may be targeting some other, as yet unidentified protein or proteins.
Pyramidal neuron counts in layer V reveal a significant reduction in number in the cortex of TDP-43WTxQ331K mice (~28 %; p = 0.007) compared to their single and non-transgenic littermates (Fig. 6). This loss is accompanied by a profound increase in GFAP immunoreactive astrogliosis specific to layer V in TDP-43WSTxQ331K mice (Additional file 1: Figure S11). Interestingly, young TDP-43Q331K single transgenic animals also show a mild increase in astrogliosis in this region (Additional file 1: Figure S11), despite the lack of motor phenotype at this age. There is also a trend towards a reduction in pyramidal neurons in the cortex of these animals (~12 %), but this does not reach significance (p = 0.253). In contrast, young TDP-43WT single transgenic animals do not differ from their non-transgenic littermates (Fig. 6). The increase in astrogliosis in TDP-43WTxQ331K mice is accompanied by a mild increase in CD68 positive microglioisis in the same region (Additional file 1: Figure S11), demonstrating a significant pathological impact of coexpression of the WT and mutant transgenes on the cortex, specifically the motor cortex and upper motor neurons, in TDP-43WTxQ331K animals. Consistent with the data from young animals, 24 months old TDP-43Q331K single transgenic animals show increased astro- and microgliosis in the layer V of the cortex compared to their non-transgenic and TDP-43WT littermates (Additional file 1: Figure S11). These increases in the cortical neuroinflammatory response are accompanied by a loss of pyramidal neurons from the cortex (~14 %, p = 0.035; Additional file 1: Figure S12).
Motor dysfunction and death in WTxQ331K mice is accompanied by a significant increase in pathogenic TDP-43
Immunoblot analysis of phosphorylated TDP-43 (pTDP) reveals a significant increase in levels in end-stage TDP-43WTxQ331K animals compared to age-matched single and non-transgenic littermates (Figs. 7a-b). This is accompanied by an increase in the levels of both 25 and 35 kDa fragments of TDP-43 (Figs. 7c-d) providing further evidence of a pathological profile similar to that seen in human patients in these compound transgenic mice. Lesser, but still significant increases in both TDP-43 fragments are also present in 8 week old TDP-43Q331K animals in the absence of significant increases in pTDP.
Assessment of TDP-43 cellular localisation reveals a significant increase in the level of both cytoplasmic and nuclear TDP-43 in all transgenic animals compared to age matched non-transgenic littermates (Figs. 8a-c, Additional file 1: Figure S12). TDP-43WTxQ331K and TDP-43Q331K animals both displayed a significant increase in cytoplasmic TDP-43 levels compared to TDP-43WT mice indicating that the presence of the TDP-43Q331K mutation enhances this mislocalisation. In contrast, there was no significant increase in nuclear TDP levels between the various transgenic animals (Fig. 8c, Additional file 1: Figure S13). This suggests that levels of nuclear TDP-43 are tightly regulated and could not account for neurodegenerative pathology.
Analysis of TDP-43 solubility demonstrates that although the majority of the protein is present in the high salt fraction, as previously reported , there is also a significant increase in the amount of TDP-43 identified in the urea fraction in the TDP-43WTxQ331K mice (Figs. 8d–e), compared to their non-transgenic, TDP-43WT and TDP-43Q331K single transgenic littermates. This is consistent with the identification of TDP-43 positive inclusions in the brain and cord of these mice. These animals also display a general increase in TDP-43 insolubility, with increases also observed in the Triton and RIPA fractions. In addition, both young and aged TDP-43Q331K single transgenic animals display an increase in detergent insoluble TDP-43 compared to age-matched non-transgenic animals (Figs. 8d–e, Additional file 1: Figure S13), hence there appears to be a correlation between levels of detergent insoluble TDP-43 and the degenerative pathological and behavioural motor phenotype observed in these mice.
TDP-43 is a predominantly nuclear protein but also shuttles to the cytoplasm fulfilling multiple roles in RNA processing [48, 49, 50]. Cytoplasmic TDP-43 inclusions are the pathological hallmark in ~90 % of ALS and 55 % of FTLD cases, [1, 2] and in many surviving neurons levels of nuclear TDP-43 are greatly reduced. Wild-type TDP-43 mis-accumulation can arise from many different gene defects which account for ~10 % of all cases. Multiple lines of evidence from cellular and animal studies indicate that the mis-accumulation of TDP-43 is directly toxic to neurons and glia but whether the mechanism is due to a loss of nuclear TDP-43 function or toxicity due to cytoplasmic aggregation, or a combination of the two, is unclear.
Here we describe the behavioural and pathological features of a line of transgenic mice expressing the ALS-linked mutant TDP-43Q331K. Single hemizygous TDP-43-43Q331K animals developed a late-onset, age-dependent, progressive motor deficit detectable by reduced rotarod performance from 3 months of age, which slowly declines out to 24 months, but is not fatal. Aged TDP-43Q331K mice have a mild loss of pyramidal neurons from cortical layer V and α-motor neurons from the lumbar spinal cord, often with TDP-43, ubiquitin and p62 inclusions in surviving cells. This is accompanied by a mild loss of motor axons and neuromuscular junctions peripherally and moderate micro- and astrogliosis in the cortex and spinal cord centrally. The presence of insoluble cytoplasmic TDP-43 inclusions without a reduction of nuclear TDP-43, implies that it is cytoplasmic TDP-43 aggregation that exerts a neurotoxic effect. Neurodegeneration in TDP-43Q331K mice began much earlier as some layer V cortical neurons had ubiquitin and p62 inclusions with mild neuronal loss and astrocytosis even at 8 weeks. Histological changes in the spinal cord however were less marked, suggesting that TDP-43 toxicity may preferentially affect the motor cortex in these animals, progressing to motor neurons in the spinal cord as disease progresses.
Most surprisingly, while TDP-43WT mice are indistinguishable from their non-transgenic littermates both behaviourally and pathologically, when crossed with the TDP-43Q331K mutant, the compound hemizygotes produce an early-onset, rapidly progressive motor phenotype manifesting with tremor at 3–4 weeks, very poor rotarod performance and progressive hind limb paralysis, necessitating euthanasia by 8–10 weeks.. End-stage pathology revealed severe lower motor neuron loss from the lumbar spinal cord, accompanied by a loss of large calibre motor axons, and neuromuscular junctions with atrophic muscles. Many surviving spinal cord neurons contained TDP-43, ubiquitin and p62 positive cytoplasmic inclusions, and there was microglial and astrocytic activation in the anterior horn and throughout the white matter. In addition, increased levels of pTDP and 25 and 35 kDa fragments of TDP-43 were detected in these animals. Interestingly, brains from end-stage TDP-43WTxQ331K mice also demonstrated key pathological features of patient tissues , including a moderate loss of pyramidal neurons in layer V of the cortex, accompanied by marked microglial and astrocytic activation, insoluble TDP-43, ubiquitin and p62 inclusions in surviving cortical neurons. Thus, these mice have many of the pathological hallmarks of ALS patient tissues [51, 1, 52].
Expression of TDP-43WT , TDP-43Q331K or TDP-43WTxQ331K resulted in a ~40–65 % reduction in endogenous mouse TDP-43 levels as has been previously reported [36, 53] but this was not associated with neurodegeneration in WT mice, hence this reduction per se is unlikely to be responsible for the variable phenotypes and pathology seen. In all mutant and WT transgenic lines studied the levels of nuclear TDP-43 was increased ~1 times greater than non-transgenic littermates at 8 weeks and 0.5 times greater at 24 months (Fig. 8, Additional file 1: Figure S13). Thus, neither a decrease in endogenous mouse TDP-43 nor an increase in nuclear human TDP-43 is likely to be pathogenic. Neurodegeneration was only associated with an increase in cytoplasmic TDP-43 at either time point. Remarkably both early and late-onset mice recapitulate many of the pathological features of TDP-43 proteinopathy that typifies ALS providing a powerful model to explore disease mechanisms and conduct preclinical trials.
Evidence of “nuclear clearing” of TDP-43 from neurons containing cytoplasmic inclusions, similar to that seen in two-thirds of surviving aggregate containing cells in the TDP-43WTxQ331K animals, has been reported in ALS and FTLD patients [4, 5] and in other mouse models [32, 38]. Correspondingly, while animals with one endogenous TDP-43 allele inactivated are generally healthy, but have mildly impaired grip strength  homozygous deletion of TDP-43 in mice is embryonic lethal [27, 28]. It is not surprising therefore that focused depletion of a vital gene such as TDP-43 results in a paralytic neurodegeneration . Similarly, a reduction in nuclear TDP-43 in mouse forebrain causes neuronal loss and abnormal hind-limb clasping . By comparing the pathological changes in TDP-43WTxQ331K (cytoplasmic aggregation and nuclear clearing) and aged TDP-43Q331K mice (only cytoplasmic aggregation) one might conclude that while the loss of nuclear TDP-43 may accelerate disease, it is not essential, whereas cytoplasmic aggregation of TDP-43 into insoluble inclusions in cortical and spinal neurons, as seen in aged TDP-43Q331K and TDP-43WTxQ331K mice, is sufficient to cause neurodegeneration, as has previously been reported in another line of mice expressing Q331K (2).
The simplest explanation for differences in the severity of phenotype and pathology is a dose-threshold effect. A comparison of protein levels, phenotype and survival in mice transgenic for human TDP-43 under PrP promoter (Fig. 9) shows that mice expressing human mutant TDP-43 appear to develop a phenotype at lower protein levels than those overexpressing the human WT as measured by western blot. This is consistent with previous reports suggesting that overexpression of disease mutant TDP-43 results in a more aggressive phenotype than human WT TDP-43 expressed at comparable levels . Comparison of PrP driven overexpression shows that lethality is seen when TDP-43 is >2.3 fold for mutant or WT lines compared to non-transgenic endogenous mouse TDP-43. This is consistent with data from our lines (blue symbols in Fig. 9) where levels of TDP-43 in the brains of TDP-43WT were 1.4 above endogenous in non-transgenic littermates, while TDP-43Q331K mice were 2.2 fold and TDP-43WTxQ331K 3.3 fold. Caution must be taken when interpreting these data however, as the methodology used to assess protein levels was not consistent between each study, hence a general dose effect, regardless of mutation status, cannot be ruled out. In the current study, we show that the addition of a ‘dose’ of human WT TDP-43 appears to trigger massive TDP-43 aggregation in TDP-43Q331K mice and dramatically increases the toxicity such that 50 % of the mice are dead by 8 weeks. Assessment of the single transgenic animals used in this study have suggested that Q331K mutant TDP-43 has a greater tendency to aggregate in the cytoplasm than WT on its own, thus we hypothesise that Q331K aggregates provide a potent seed for the recruitment of human WT and endogenous mouse TDP-43 that results in nuclear clearing and rapid neurodegeneration. This hypothesis is supported by our finding that despite a general reduction in levels, endogenous mouse TDP-43 appears to be recruited to aggregates in the TDP-43WTxQ331K mice. Although there is no overt evidence of endogenous TDP-43 aggregation in the TDP-43Q331K single transgenic animals, the pathology seen in these mice is significantly reduced compared to the TDP-43WTxQ331K animals, and this, combined with the reduction seen in endogenous TDP-43 is likely to make detection of any potential recruitment problematic.
Our mice recapitulate many aspects of the clinical phenotype and pathological features of TDP-43-linked ALS with slow and rapidly progressive motor phenotypes. Although the occurrence of ALS-causing TDP-43 mutations is rare in the patient population, the close correlation between the pathology observed in these mice and that seen in the majority of TDP-ALS patients suggests that these animals provide a viable model for studying the impact and progression of TDP-43 pathology in the central nervous system, and help to elucidate mechanisms that may underlie disease progression. The aggregation of TDP-43 into insoluble cytoplasmic inclusions in cortical and spinal neurons was a feature of both aged TDP-43Q331K and TDP-43WTxQ331K mice while nuclear clearance was only seen in spinal cord motor neurons in TDP-43WTxQ331K mice. Thus while nuclear clearance of TDP-43 may accelerate disease it does not appear to be essential to cause neurodegeneration and loss of nuclear TDP-43 function may not be a primary or disease-critical event. A more detailed exploration of disease mechanisms in slow and rapid disease models of TDP-43 proteinopathy will help elucidate novel drug targets and provide a more informative platform for preclinical trials.
Neumann M, Sampathu DM, Kwong LK, Truax AC, Micsenyi MC, Chou TT, Bruce J, Schuck T, Grossman M, Clark CM, McCluskey LF, Miller BL, Masliah E, Mackenzie IR, Feldman H, Feiden W, Kretzschmar HA, Trojanowski JQ, Lee VM (2006) Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science 314:130–133
Arai T, Hasegawa M, Akiyama H, Ikeda K, Nonaka T, Mori H, Mann D, Tsuchiya K, Yoshida M, Hashizume Y, Oda T (2006) TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Biochem Biophys Res Commun 351:602–611
Buratti E, Baralle FE (2010) The multiple roles of TDP-43 in pre-mRNA processing and gene expression regulation. RNA Biol 7:420–429
Van Deerlin VM, Leverenz JB, Bekris LM, Bird TD, Yuan W, Elman LB, Clay D, Wood EM, Chen-Plotkin AS, Martinez-Lage M, Steinbart E, McCluskey L, Grossman M, Neumann M, Wu IL, Yang WS, Kalb R, Galasko DR, Montine TJ, Trojanowski JQ, Lee VM, Schellenberg GD, Yu CE (2008) TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis. Lancet Neurol 7:409–416. doi:10.1016/S1474-4422(08)70071-1
Igaz LM, Kwong LK, Xu Y, Truax AC, Uryu K, Neumann M, Clark CM, Elman LB, Miller BL, Grossman M, McCluskey LF, Trojanowski JQ, Lee VM (2008) Enrichment of C-terminal fragments in TAR DNA-binding protein-43 cytoplasmic inclusions in brain but not in spinal cord of frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Am J Pathol 173:182–194. doi:10.2353/ajpath.2008.080003
Sreedharan J, Blair IP, Tripathi VB, Hu X, Vance C, Rogelj B, Ackerley S, Durnall JC, Williams KL, Buratti E, Baralle F, de Belleroche J, Mitchell JD, Leigh PN, Al-Chalabi A, Miller CC, Nicholson G, Shaw CE (2008) TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis. Science 319:1668–1672. doi:10.1126/science.1154584
Gitcho MA, Baloh RH, Chakraverty S, Mayo K, Norton JB, Levitch D, Hatanpaa KJ, White CL 3rd, Bigio EH, Caselli R, Baker M, Al-Lozi MT, Morris JC, Pestronk A, Rademakers R, Goate AM, Cairns NJ (2008) TDP-43 A315T mutation in familial motor neuron disease. Ann Neurol 63:535–538. doi:10.1002/ana.21344
Kabashi E, Valdmanis PN, Dion P, Spiegelman D, McConkey BJ, Vande Velde C, Bouchard JP, Lacomblez L, Pochigaeva K, Salachas F, Pradat PF, Camu W, Meininger V, Dupre N, Rouleau GA (2008) TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis. Nat Genet 40:572–574. doi:10.1038/ng.132
Mackenzie IR (2007) The neuropathology and clinical phenotype of FTD with progranulin mutations. Acta Neuropathol 114:49–54. doi:10.1007/s00401-007-0223-8
Neumann M, Mackenzie IR, Cairns NJ, Boyer PJ, Markesbery WR, Smith CD, Taylor JP, Kretzschmar HA, Kimonis VE, Forman MS (2007) TDP-43 in the ubiquitin pathology of frontotemporal dementia with VCP gene mutations. J Neuropathol Exp Neurol 66:152–157. doi:10.1097/nen.0b013e31803020b9 00005072-200702000-00007
Deng HX, Chen W, Hong ST, Boycott KM, Gorrie GH, Siddique N, Yang Y, Fecto F, Shi Y, Zhai H, Jiang H, Hirano M, Rampersaud E, Jansen GH, Donkervoort S, Bigio EH, Brooks BR, Ajroud K, Sufit RL, Haines JL, Mugnaini E, Pericak-Vance MA, Siddique T (2011) Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia. Nature 477:211–215. doi:10.1038/nature10353
De Jesus-Hernandez M, Mackenzie IR, Boeve BF, Boxer AL, Baker M, Rutherford NJ, Nicholson AM, Finch NA, Flynn H, Adamson J, Kouri N, Wojtas A, Sengdy P, Hsiung GY, Karydas A, Seeley WW, Josephs KA, Coppola G, Geschwind DH, Wszolek ZK, Feldman H, Knopman DS, Petersen RC, Miller BL, Dickson DW, Boylan KB, Graff-Radford NR, Rademakers R (2011) Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS. Neuron 72:245–256. doi:10.1016/j.neuron.2011.09.011
Renton AE, Majounie E, Waite A, Simon-Sanchez J, Rollinson S, Gibbs JR, Schymick JC, Laaksovirta H, van Swieten JC, Myllykangas L, Kalimo H, Paetau A, Abramzon Y, Remes AM, Kaganovich A, Scholz SW, Duckworth J, Ding J, Harmer DW, Hernandez DG, Johnson JO, Mok K, Ryten M, Trabzuni D, Guerreiro RJ, Orrell RW, Neal J, Murray A, Pearson J, Jansen IE, et al (2011) A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. Neuron 72:257–268. doi:S0896-6273(11)00797-5 10.1016/j.neuron.2011.09.010
Vance C, Rogelj B, Hortobagyi T, De Vos KJ, Nishimura AL, Sreedharan J, Hu X, Smith B, Ruddy D, Wright P, Ganesalingam J, Williams KL, Tripathi V, Al-Saraj S, Al-Chalabi A, Leigh PN, Blair IP, Nicholson G, de Belleroche J, Gallo JM, Miller CC, Shaw CE (2009) Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6. Science 323:1208–1211. doi:10.1126/science.1165942
Kwiatkowski TJ Jr, Bosco DA, Leclerc AL, Tamrazian E, Vanderburg CR, Russ C, Davis A, Gilchrist J, Kasarskis EJ, Munsat T, Valdmanis P, Rouleau GA, Hosler BA, Cortelli P, de Jong PJ, Yoshinaga Y, Haines JL, Pericak-Vance MA, Yan J, Ticozzi N, Siddique T, McKenna-Yasek D, Sapp PC, Horvitz HR, Landers JE, Brown RH Jr (2009) Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis. Science 323:1205–1208. doi:10.1126/science.1166066
Wang HY, Wang IF, Bose J, Shen CK (2004) Structural diversity and functional implications of the eukaryotic TDP gene family. Genomics 83:130–139
Ayala YM, Pantano S, D’Ambrogio A, Buratti E, Brindisi A, Marchetti C, Romano M, Baralle FE (2005) Human, Drosophila, and C.elegans TDP43: nucleic acid binding properties and splicing regulatory function. J Mol Biol 348:575–588. doi:10.1016/j.jmb.2005.02.038
Ou SH, Wu F, Harrich D, Garcia-Martinez LF, Gaynor RB (1995) Cloning and characterization of a novel cellular protein, TDP-43, that binds to human immunodeficiency virus type 1 TAR DNA sequence motifs. J Virol 69:3584–3596
Buratti E, Baralle FE (2001) Characterization and functional implications of the RNA binding properties of nuclear factor TDP-43, a novel splicing regulator of CFTR exon 9. J Biol Chem 276:36337–36343. doi:10.1074/jbc.M104236200
Winton MJ, Igaz LM, Wong MM, Kwong LK, Trojanowski JQ, Lee VM (2008) Disturbance of nuclear and cytoplasmic TAR DNA-binding protein (TDP-43) induces disease-like redistribution, sequestration, and aggregate formation. J Biol Chem 283:13302–13309. doi:10.1074/jbc.M800342200
D’Ambrogio A, Buratti E, Stuani C, Guarnaccia C, Romano M, Ayala YM, Baralle FE (2009) Functional mapping of the interaction between TDP-43 and hnRNP A2 in vivo. Nucleic Acids Res 37:4116–4126. doi:10.1093/nar/gkp342
Buratti E, Brindisi A, Giombi M, Tisminetzky S, Ayala YM, Baralle FE (2005) TDP-43 binds heterogeneous nuclear ribonucleoprotein A/B through its C-terminal tail: an important region for the inhibition of cystic fibrosis transmembrane conductance regulator exon 9 splicing. J Biol Chem 280:37572–37584
Polymenidou M, Lagier-Tourenne C, Hutt KR, Huelga SC, Moran J, Liang TY, Ling SC, Sun E, Wancewicz E, Mazur C, Kordasiewicz H, Sedaghat Y, Donohue JP, Shiue L, Bennett CF, Yeo GW, Cleveland DW (2011) Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43. Nat Neurosci 14:459–468. doi:10.1038/nn.2779
Tollervey JR, Curk T, Rogelj B, Briese M, Cereda M, Kayikci M, Konig J, Hortobagyi T, Nishimura AL, Zupunski V, Patani R, Chandran S, Rot G, Zupan B, Shaw CE, Ule J (2011) Characterizing the RNA targets and position-dependent splicing regulation by TDP-43. Nat Neurosci 14:452–458. doi:10.1038/nn.2778
Ayala YM, De Conti L, Avendano-Vazquez SE, Dhir A, Romano M, D’Ambrogio A, Tollervey J, Ule J, Baralle M, Buratti E, Baralle FE (2011) TDP-43 regulates its mRNA levels through a negative feedback loop. EMBO J 30:277–288. doi:10.1038/emboj.2010.310
Sephton CF, Good SK, Atkin S, Dewey CM, Mayer P 3rd, Herz J, Yu G (2010) TDP-43 is a developmentally regulated protein essential for early embryonic development. J Biol Chem 285:6826–6834. doi:10.1074/jbc.M109.061846
Kraemer BC, Schuck T, Wheeler JM, Robinson LC, Trojanowski JQ, Lee VM, Schellenberg GD (2010) Loss of murine TDP-43 disrupts motor function and plays an essential role in embryogenesis. Acta Neuropathol 119:409–419. doi:10.1007/s00401-010-0659-0
Wu LS, Cheng WC, Hou SC, Yan YT, Jiang ST, Shen CK (2010) TDP-43, a neuro-pathosignature factor, is essential for early mouse embryogenesis. Genesis 48:56–62. doi:10.1002/dvg.20584
Chiang PM, Ling J, Jeong YH, Price DL, Aja SM, Wong PC (2010) Deletion of TDP-43 down-regulates Tbc1d1, a gene linked to obesity, and alters body fat metabolism. Proc Natl Acad Sci U S A 107:16320–16324. doi:10.1073/pnas.1002176107
Wu LS, Cheng WC, Shen CK (2012) Targeted depletion of TDP-43 expression in the spinal cord motor neurons leads to the development of amyotrophic lateral sclerosis-like phenotypes in mice. J Biol Chem 287:27335–27344. doi:10.1074/jbc.M112.359000
Iguchi Y, Katsuno M, Niwa J, Takagi S, Ishigaki S, Ikenaka K, Kawai K, Watanabe H, Yamanaka K, Takahashi R, Misawa H, Sasaki S, Tanaka F, Sobue G (2013) Loss of TDP-43 causes age-dependent progressive motor neuron degeneration. Brain 136:1371–1382. doi:10.1093/brain/awt029
Wils H, Kleinberger G, Janssens J, Pereson S, Joris G, Cuijt I, Smits V, Ceuterick-de Groote C, Van Broeckhoven C, Kumar-Singh S (2009) TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration. Proc Natl Acad Sci U S A 107:3858–3863. doi:10.1073/pnas.0912417107
Stallings NR, Puttaparthi K, Luther CM, Burns DK, Elliott JL (2010) Progressive motor weakness in transgenic mice expressing human TDP-43. Neurobiol Dis 40:404–414. doi:10.1016/j.nbd.2010.06.017
Xu YF, Gendron TF, Zhang YJ, Lin WL, D’Alton S, Sheng H, Casey MC, Tong J, Knight J, Yu X, Rademakers R, Boylan K, Hutton M, McGowan E, Dickson DW, Lewis J, Petrucelli L (2010) Wild-type human TDP-43 expression causes TDP-43 phosphorylation, mitochondrial aggregation, motor deficits, and early mortality in transgenic mice. J Neurosci 30:10851–10859. doi:10.1523/JNEUROSCI.1630-10.2010
Xu YF, Zhang YJ, Lin WL, Cao X, Stetler C, Dickson DW, Lewis J, Petrucelli L (2011) Expression of mutant TDP-43 induces neuronal dysfunction in transgenic mice. Mol Neurodegener 6:73. doi:10.1186/1750-1326-6-73
Arnold ES, Ling SC, Huelga SC, Lagier-Tourenne C, Polymenidou M, Ditsworth D, Kordasiewicz HB, McAlonis-Downes M, Platoshyn O, Parone PA, Da Cruz S, Clutario KM, Swing D, Tessarollo L, Marsala M, Shaw CE, Yeo GW, Cleveland DW (2013) ALS-linked TDP-43 mutations produce aberrant RNA splicing and adult-onset motor neuron disease without aggregation or loss of nuclear TDP-43. Proc Natl Acad Sci U S A 110:E736–745. doi:10.1073/pnas.1222809110
Wegorzewska I, Bell S, Cairns NJ, Miller TM, Baloh RH (2009) TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degeneration. Proc Natl Acad Sci U S A 106:18809–18814. doi:10.1073/pnas.0908767106
Janssens J, Wils H, Kleinberger G, Joris G, Cuijt I, Ceuterick-de Groote C, Van Broeckhoven C, Kumar-Singh S (2013) Overexpression of ALS-associated p.M337V human TDP-43 in mice worsens disease features compared to wild-type human TDP-43 mice. Mol Neurobiol 48:22–35. doi:10.1007/s12035-013-8427-5
Zhou H, Huang C, Chen H, Wang D, Landel CP, Xia PY, Bowser R, Liu YJ, Xia XG (2010) Transgenic rat model of neurodegeneration caused by mutation in the TDP gene. PLoS Genet vol 6. 2010/04/03 edn. doi:10.1371/journal.pgen.1000887
Guo Y, Wang Q, Zhang K, An T, Shi P, Li Z, Duan W, Li C (2012) HO-1 induction in motor cortex and intestinal dysfunction in TDP-43 A315T transgenic mice. Brain Res 1460:88–95. doi:10.1016/j.brainres.2012.04.003
Esmaeili MA, Panahi M, Yadav S, Hennings L, Kiaei M (2013) Premature death of TDP-43 (A315T) transgenic mice due to gastrointestinal complications prior to development of full neurological symptoms of amyotrophic lateral sclerosis. Int J Exp Pathol 94:56–64. doi:10.1111/iep.12006
Mitchell JC, McGoldrick P, Vance C, Hortobagyi T, Sreedharan J, Rogelj B, Tudor EL, Smith BN, Klasen C, Miller CC, Cooper JD, Greensmith L, Shaw CE (2012) Overexpression of human wild-type FUS causes progressive motor neuron degeneration in an age- and dose-dependent fashion. Acta Neuropathol 125:273–288. doi:10.1007/s00401-012-1043-z
Neumann M, Bentmann E, Dormann D, Jawaid A, DeJesus-Hernandez M, Ansorge O, Roeber S, Kretzschmar HA, Munoz DG, Kusaka H, Yokota O, Ang LC, Bilbao J, Rademakers R, Haass C, Mackenzie IR (2011) FET proteins TAF15 and EWS are selective markers that distinguish FTLD with FUS pathology from amyotrophic lateral sclerosis with FUS mutations. Brain 134:2595–2609. doi:10.1093/brain/awr201
Herdewyn S, Cirillo C, Van Den Bosch L, Robberecht W, Vanden Berghe P, Van Damme P (2014) Prevention of intestinal obstruction reveals progressive neurodegeneration in mutant TDP-43 (A315T) mice. Mol Neurodegener 9:24. doi:10.1186/1750-1326-9-24
Gurney ME, Pu H, Chiu AY, Dal Canto MC, Polchow CY, Alexander DD, Caliendo J, Hentati A, Kwon YW, Deng HX et al (1994) Motor neuron degeneration in mice that express a human Cu, Zn superoxide dismutase mutation. Science 264:1772–1775
Shan X, Chiang PM, Price DL, Wong PC (2010) Altered distributions of Gemini of coiled bodies and mitochondria in motor neurons of TDP-43 transgenic mice. Proc Natl Acad Sci U S A 107:16325–16330. doi:10.1073/pnas.1003459107
Dib M, Vital A, Vital C, Georgescault D, Baquey A, Bezian J (1987) The C57BL mice: an animal model for inflammatory demyelinating polyneuropathy. J Neurol Sci 81:101–111
Ayala YM, Zago P, D’Ambrogio A, Xu YF, Petrucelli L, Buratti E, Baralle FE (2008) Structural determinants of the cellular localization and shuttling of TDP-43. J Cell Sci 121:3778–3785. doi:10.1242/jcs.038950
Godena VK, Romano G, Romano M, Appocher C, Klima R, Buratti E, Baralle FE, Feiguin F (2011) TDP-43 regulates Drosophila neuromuscular junctions growth by modulating Futsch/MAP1B levels and synaptic microtubules organization. PLoS One 6:e17808. doi:10.1371/journal.pone.0017808
McDonald KK, Aulas A, Destroismaisons L, Pickles S, Beleac E, Camu W, Rouleau GA, Vande Velde C (2011) TAR DNA-binding protein 43 (TDP-43) regulates stress granule dynamics via differential regulation of G3BP and TIA-1. Hum Mol Genet 20:1400–1410. doi:10.1093/hmg/ddr021
Kawamata T, Akiyama H, Yamada T, McGeer PL (1992) Immunologic reactions in amyotrophic lateral sclerosis brain and spinal cord tissue. Am J Pathol 140:691–707
Mizuno Y, Amari M, Takatama M, Aizawa H, Mihara B, Okamoto K (2006) Immunoreactivities of p62, an ubiqutin-binding protein, in the spinal anterior horn cells of patients with amyotrophic lateral sclerosis. J Neurol Sci 249:13–18
Igaz LM, Kwong LK, Lee EB, Chen-Plotkin A, Swanson E, Unger T, Malunda J, Xu Y, Winton MJ, Trojanowski JQ, Lee VM (2011) Dysregulation of the ALS-associated gene TDP-43 leads to neuronal death and degeneration in mice. J Clin Invest 121:726–738. doi:10.1172/JCI44867
This research was funded principally by a Strategic Grant Award from the Medical Research Council and the Wellcome Trust (grant reference 089701/Z/09/2) to CES, with additional support from The Motor Neuron Disease Association, Heaton Ellis Trust, Psychiatry Research Trust and American Amyotrophic Lateral Sclerosis Association. Support was also received from an ARRA grant from the National Institutes of Health to DWC. CL was the recipient of a Career Development Award from the Muscular Dystrophy Association. DWC and CL receive salary support from the Ludwig Institute.
The authors declare that they have no competing interests.
JCM designed and carried out the experiments and drafted the manuscript. RC and ES helped with the experiments. CV, ELS and TH advised on the experiments. LG performed the neuron counting. ESA, SCL, MM, SDC, MP, LT, DWC contributed to mouse line generation. CES directed the research and drafted the manuscript. All authors read and approved the final manuscript.
This file contains supplementary results as detailed in the manuscript.
This video shows a representative example of hind limb paralysis in a 6 week old TDP-43WTxQ331K mouse, displaying a severely stilted gait, and an inability to lift their pelvis from the ground.
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Mitchell, J.C., Constable, R., So, E. et al. Wild type human TDP-43 potentiates ALS-linked mutant TDP-43 driven progressive motor and cortical neuron degeneration with pathological features of ALS. acta neuropathol commun 3, 36 (2015). https://doi.org/10.1186/s40478-015-0212-4
- Amyotrophic lateral sclerosis