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Abnormal distribution, modification and aggregation of transactivation response DNA-binding protein 43 (TDP-43) are the hallmarks of multiple neurodegenerative diseases, especially frontotemporal lobar degeneration with ubiquitin-positive inclusions (FTLD-U) and amyotrophic lateral sclerosis (ALS). Researchers have identified 44 mutations in the TARDBP gene that encode TDP-43 as causative for cases of sporadic and familial ALS http://www.molgen.ua.ac.be/FTDMutations/. Certain mutant forms of TDP-43, such as M337V, are associated with increased low molecular weight (LMW) fragments compared to wild-type (WT) TDP-43 and cause neuronal apoptosis and developmental delay in chick embryos. Such findings support a direct link between altered TDP-43 function and neurodegeneration.
To explore the pathogenic properties of the M337V mutation, we generated and characterized two mouse lines expressing human TDP-43 (hTDP-43M337V) carrying this mutation. hTDP-43M337V was expressed primarily in the nuclei of neurons in the brain and spinal cord, and intranuclear and cytoplasmic phosphorylated TDP-43 aggregates were frequently detected. The levels of TDP-43 LMW products of ~25 kDa and ~35 kDa species were also increased in the transgenic mice. Moreover, overexpression of hTDP-43M337V dramatically down regulated the levels of mouse TDP-43 (mTDP-43) protein and RNA, indicating TDP-43 levels are tightly controlled in mammalian systems. TDP-43M337V mice displayed reactive gliosis, widespread ubiquitination, chromatolysis, gait abnormalities, and early lethality. Abnormal cytoplasmic mitochondrial aggregates and abnormal phosphorylated tau were also detected in the mice.
Our novel TDP-43M337V mouse model indicates that overexpression of hTDP-43M337V alone is toxic in vivo. Because overexpression of hTDP-43 in wild-type TDP-43 and TDP-43M337V mouse models produces similar phenotypes, the mechanisms causing pathogenesis in the mutant model remain unknown. However, our results suggest that overexpression of the hTDP-43M337V can cause neuronal dysfunction due to its effect on a number of cell organelles and proteins, such as mitochondria and TDP-43, that are critical for neuronal activity. The mutant model will serve as a valuable tool in the development of future studies designed to uncover pathways associated with TDP-43 neurotoxicity and the precise roles TDP-43 RNA targets play in neurodegeneration.
TDP-43 is the major component of ubiquitinated inclusions in most cases of ALS and FTLD-U [1,2], and the link between TDP-43 mutations and neurodegeneration was first established in 2008 [3,4]. Autosomal dominant mutations in TARDBP, the gene encoding TDP-43, are associated with sporadic and familial ALS [3-7]. TDP-43 is a ubiquitously expressed 414-amino acid nuclear protein and a highly conserved heterogeneous nuclear ribonucleoprotein (hnRNP). TDP-43 has high-binding affinity for the (TG)n motif and is involved in gene transcription, pre-mRNA splicing, mRNA stability, and mRNA transport [8,9]. Under disease conditions, TDP-43 is truncated, phosphorylated, ubiquitinated and aggregated both in the nucleus and cytoplasm. Under such conditions, cytoplasmic TDP-43 aggregation coincides with the depletion of nuclear TDP-43. The manner through which TDP-43 causes neurodegeneration has not been identified; however, recently TDP-43 mouse models generated by our group and others demonstrate that overexpression of TDP-43 [either wild-type, A315T mutant, G348C or ΔNLS (defective nuclear localization signal TDP-43)] is toxic and can cause neurodegeneration in the central nervous system [10-16]. That being said, the various TDP-43 transgenic models exhibit other similarities as well as differences. For instance, most transgenic models showed increased ubiquitin levels, TDP-43 fragmentation, phosphorylation, gliosis, motor functional impairments, and shortened lifespan. On the other hand, neuronal loss, caspase activation, redistribution of TDP-43 from nuclei to cytoplasm, cytoplasmic TDP-43 inclusions, down regulation of endogenous mTDP-43 and abnormal mitochondrial aggregation were either only seen in some of those TDP-43 transgenic mice, or not examined. To further confirm the toxic effect of TDP-43 overexpression and to specifically study mutant TDP-43, we generated transgenic mice expressing hTDP-43M337V under control of the mouse prion (PrP) promoter .
In the TDP-43M337V mice, hTDP-43M337V is mainly expressed in the brain and spinal cord, a finding that is consistent with transgenic mice overexpressing wild-type TDP-43 that we previously reported . TDP-43M337V mice exhibited certain features similar to those seen in ALS, such as TDP-43 cleavage, phosphorylation, aggregation, increased ubiquitination, gliosis, gait disturbances, and early lethality; however, the mice also exhibited other features not yet reported in humans, which may be due to the effect of hTDP-43M337V overexpression. Such features include: down regulation of mTDP-43, abnormal mitochondrial aggregation and abnormal tau phosphorylation.
To explore the pathogenic properties of mutant (M337V) TDP-43, we generated transgenic mice using the mouse prion promoter to constitutively drive expression of full-length hTDP-43 carrying the M337V mutation. Three (Lines 1, 4, and 6) of eight independent founder lines showed germline transmission. The expression level of human TDP-43 was low in line 1 (~20% of endogenous levels), while lines 4 and line 6 had similar hTDP-43 expression levels to that of wild-type TDP-43 mice (TDP-43WT line 3c hereafter termed TDP-43WT), which we previously generated with the same promoter  (Figure 1A, B). Biochemical analyses of hTDP-43M337V showed that protein expression was highest in the brain and spinal cord, with low levels in other tissues (Figure (Figure1C).1C). The immunohistochemistry (IHC) of hemizygous mice showed that hTDP-43 M337V expression was primarily in nuclei and distributed throughout the gray matter of the spinal cord and brain (Figure 1D, E). Hemizygous mice from all lines were phenotypically, histologically, and immunohistochemically indistinguishable from NT mice up to 12 months of age, currently the oldest age available. Given the similar levels of expression between lines 4 and 6, the full characterization of line 4 is shown and all subsequent description of TDP-43M337V mice refer to homozygous mice from line 4 unless otherwise noted. The expression level of hTDP-43M337V in the brains of homozygous mice was about 1.9 ± 0.06 fold over that of hemizygous mice (Figure 2A, B). The total levels of TDP-43 protein (human and mouse TDP-43) in the brains of hemizygous and homozygous mice were 1.6 ± 0.03 and 2.7 ± 0.08 fold that of endogenous mouse TDP-43 in the non-transgenic mice (NT), respectively (Figure 2A, C). These results obtained from hTDP-43M337V compared with total TDP-43 indicated that endogenous mTDP-43 protein levels were likely down regulated in TDP-43M337V mice, in a dose-dependent fashion. We confirmed that mTDP-43 was similarly down regulated at the mRNA level (~ 20% and 30% reduction of mTDP-43, respectively, compared to NT mice) using real time-PCR analyses of hemizygous and homozygous brains (Figure (Figure2D).2D). The mRNA levels of hTDP-43 in the brain of homozygous mice were 1.86 ± 0.14 fold of that in the hemizygous mice (Figure (Figure2E),2E), consistent with the hTDP-43 protein levels. Moreover, the ~25 kDa and ~35 kDa TDP-43 LMW species also increased significantly in the hemizygous and homozygous mice, and their levels correlated with the levels of full-length TDP-43 (Figure 2F, G).
At approximately post-natal day 21, homozygous TDP-43M337V mice began to have body tremors and difficulty recruiting their hindlimbs (not shown). They failed to show proper escape extension by splaying their hindlimbs upon elevation, as shown by their NT counterparts (Figure 3A, B). They displayed an irregular, dragging gait pattern, due at least in part to limb weakness (Figure 3C, D). By ~ 1 month old, homozygous TDP-43M337V mice had significantly lower brain and body weight compared with their NT and hemizygous littermates (Figure 3E, F). Due in part to muscle weakness, homozygous TDP-43M337V mice were unable to feed from a food hopper, lost the ability to right themselves, became moribund and required euthanasia. Approximately 70% of the homozygous TDP-43M337V mice became moribund by 1 month of age, which was statistically significant compared with NT and hemizygous littermates (Figure (Figure3G).3G). We had previous success (unpublished) extending the lifespan of mouse models that showed early lethality through the use of intensive care such as delayed weaning and supplementing diets with gel and dough. We have now employed similar measures in an effort to prolong the lives of homozygous TDP-43M337V transgenic mice. The phenotype of the homozygous TDP-43M337V mice from line 6 (not shown) was similar to that described for line 4.
Immunohistochemistry was performed on both line 4 and line 6 of TDP-43M337V and NT mice. The results showed that TDP-43 was mostly in nuclei in the brain and spinal cord of TDP-43M337V and NT mice and that the TDP-43M337V mice specifically expressed high levels of hTDP-43 that were not seen in the controls (Figure 4A-C). Cytoplasmic TDP-43 was detected with either a human TDP-43 specific antibody or total TDP-43 antibody that recognized both human and mouse TDP-43. Cytoplasmic TDP-43 was detected in spinal cord neurons and less frequently in the brainstem and cortex of TDP-43M337V mice (Figure 4A, B, D and and4E4E arrowhead, Table Table1).1). Abnormally phosphorylated (pS403/pS404) TDP-43 (pTDP-43) was frequently located within nuclear bodies or diffusely within the cytoplasm of motor neurons in the anterior horns of the spinal cord of TDP-43M337V mice (Figure 4G, H arrowheads, arrows) but not in the NT mice (Figure (Figure4I).4I). Far less cytoplasmic pTDP-43 was detected in the posterior horn of TDP-43M337V mice and in the brainstem (< 5 neurons/section; Table Table1).1). pTDP-43-immunoreactive nuclear bodies were not detected in the brains of TDP-43M337V mice (Table (Table1).1). Multiple small, distinct, cytoplasmic inclusions that were immunoreactive for pTDP-43 were frequently observed within neurons in layer V of the cortex of TDP-43M337V mice (Figure 4J, K, arrows) that were not observed in NT controls (Figure (Figure4L).4L). The extent and distribution of these features in the TDP-43M337V mice was similar to that observed in our previously reported TDP-43WT mice .
A striking histological feature in TDP-43M337V mice was the presence of cytoplasmic eosinophilic aggregates (Figure (Figure5A)5A) located within the neurons of the anterior horn of the spinal cord and less frequently in the posterior horn and brainstem. These aggregates were absent from NT mice (Figure (Figure5B).5B). Neuronal loss due to apoptosis was not detected in TDP-43M337V mice, as assessed by TUNEL staining and staining for activated caspase 3 (data not shown); however, increased ubiquitination and reactive gliosis were observed in TDP-43M337V mice and not in NT mice (Figure 5C-J). Ubiquitination was both widespread, and generally increased, in both the nucleus and cytoplasm of neurons in spinal cord and brain (Figure 5C, E). Ubiquitination was more widespread than cytoplasmic TDP-43 or phospho-TDP-43 aggregates (Table (Table1),1), and co-immunoprecipitation studies indicated that hTDP-43 was not ubiquitinated (Additional file 1). Reactive gliosis was also seen in the TDP-43M337V mice, as GFAP-positive astrocytes and IBA-1-positive microglia were elevated in the spinal cord and brainstem of TDP-43M337V mice compared with NT mice (Figure 5G-J; Table Table1).1). Each of these features observed in the TDP-43M337V mice was similar to that observed in our previously reported TDP-43WT model . Homozygous TDP-43M337V mice from line 4 and 6 (not shown) showed similar pathological changes.
The eosinophilic aggregates in spinal motor neurons of TDP-43M337V mice were immunoreactive for the mitochondrial marker, COX-IV (Figure (Figure6A),6A), which indicates the aggregates were composed of abnormal clusters of mitochondria. NT mice (Figure (Figure6B)6B) did not show altered redistribution of COX-IV immunostaining into the juxtanuclear pattern observed in the TDP-43M337V mice. Electron microscopic (EM) results confirmed that the majority of neuronal cytoplasmic inclusions in the spinal motor neurons of TDP-43M337V mice contained aggregates of mitochondria (Figure (Figure6C)6C) that were occasionally surrounded by a core of microtubules (20 nm) in random orientations (Figure (Figure6D).6D). The aggregated mitochondria showed variable degrees of loss of inner cristae and vacuolization (Figure (Figure6E).6E). The degenerating mitochondria in TDP-43M337V mice (Figure (Figure6E)6E) were smaller than those in NT mice (Figure (Figure6F).6F). In NT mice, mitochondria were usually admixed with other cytoplasmic organelles such as endoplasmic reticulum and ribosome (Figure (Figure6F);6F); however, this intervening organelles were absent in the neuronal aggregates of TDP-43M337V mice (Figure (Figure6E).6E). The mitochondrial aggregates in the TDP-43M337V mice were frequent in the spinal cord and brainstem, less frequent in the cortex, and rare in other brain regions (Table (Table1).1). Homozygous TDP-43M337V mice from line 6 also developed juxtanuclear mitochondrial aggregates (not shown).
We have previously demonstrated that mitochondrial clustering in neurons of TDP-43WT mice is accompanied by changes in protein levels and/or phosphorylation of proteins that regulate mitochondrial fission and fusion . Given the similarity between mitochondrial aggregates in TDP-43M337V mice and our previously described TDPWT mice, we sought to determine if mitochondrial fission and fusion proteins were altered in the TDP-43M337V mice. Surprisingly, the alterations to pDLP1 (Ser616), Fis1, and MFN1 that were observed in the TDP-43WT mice, regardless of line, were not present in the TDP-43M337V mice, despite the comparable mitochondrial aggregation in each transgenic model (Additional file 2).
In the spinal motor neuron of TDP-43M337V mice, Nissl bodies became dispersed (Figure (Figure7A)7A) compared to NT mice (Figure (Figure7B).7B). There was disintegration of chromophil substance primarily within the cell bodies of the spinal cords of TDP-43M337V mice (Figure (Figure7C)7C) that was not observed in NT mice (Figure (Figure7D).7D). Ultrastructural analysis showed reduced cytoplasmic density and less cytoplasmic organelles in TDP-43M337V mice (Figure (Figure7E)7E) compared to NT mice (Figure (Figure7F).7F). These finding are indicative of chromatolysis and suggest that neurons in TDP-43M337V mice are undergoing perikaryal response to axonal degeneration.
Abnormal, phosphorylated tau was found in the brains of both TDP-43WT and TDP-43M337V mice. Immunohistochemical analyses of the cortices of TDP-43M337V (Figure (Figure8A)8A) and TDP-43WT mice (Figure (Figure8B)8B) showed significantly elevated phosphorylated tau (CP13) immunoreactivity throughout the neuropil of the brain compared with NT mice (Figure (Figure8C).8C). Additionally, cytoplasmic tau accumulations were found in the TDP-43WT mice and much less frequently in the TDP-43M337V mice (Figure 8A, B). Western blots of brain lysates showed that the levels of phosphorylated tau (CP13) were significantly increased in both the TDP-43WT and TDP-43M337V mice (Figure (Figure8D),8D), while the level of dephosphorylated tau (Tau-1) was dramatically decreased. There was no significant change in the level of total tau (Tau-5) (Figure (Figure8D).8D). To explore the mechanism for tau phosphorylation, we examined protein kinases and phosphatases and found significant increases in phospho-(Ser) PKC substrate in both TDP-43WT and TDP-43M337V mice, indicating PKC activation may be responsible for such abnormal tau phosphorylation (Figure (Figure8D).8D). The levels of other tau kinases, such as GSK-3β and CDK5, and the tau phosphatase PP2A were not significantly changed in the TDP-43M337V and TDP-43WT mice (data not shown). Abnormally phosphorylated tau was rarely found in the spinal cord (data not shown). The regional distribution of hyperphosphorylated tau is summarized in Table Table11.
In the current study, we generated and characterized a novel transgenic mouse model that overexpresses hTDP-43 carrying the M337V mutation under the mouse prion promoter. Homozygous TDP-43 M337V mice (referred to as TDP-43M337V mice) develop phenotypic and pathologic features including gait disturbances, gliosis, increased ubiquitination, TDP-43 truncation, phosphorylation, and both nuclear and cytoplasmic phosphorylated inclusions.
Importantly, the novel findings described in the current manuscript and the counterpart TDP-43WT mice manuscript , demonstrate expression of human TDP-43 at similar levels results in remarkably similar phenotypes and pathologies, suggesting that the phenotypes of both models are due to TDP-43 overexpression, and not specifically due to this mutation. Previously published findings regarding TDP-43 overexpression in mouse models strongly suggested that overexpression of TDP-43 itself is toxic; however, none of these studies have included mutant TDP-43 lines that were comparable in expression level and pattern, promoter system, and strain to WT TDP-43 counterparts [10-16]. In constitutive transgenic rat studies, Zhou and colleagues reported that mutant M337V TDP-43 appeared to be more toxic than wild-type TDP-43  even though the animals expressed the hTDP-43 protein at similar levels. It is unclear why there is a discrepancy between our mutant and wild-type TDP-43 transgenic models and those in the rat. One possibility could be the difference of promoters utilized in the studies. Additionally, Zhou and colleagues did not look at endogenous rat TDP-43 levels in response to the hTDP-43 overexpression ; therefore, it is possible that differences in endogenous TDP-43 played a role in the rat phenotype. Moreover, in contrast to our hTDP-43 cDNA construct, the constitutive hTDP-43 construct utilized by Zhou and colleagues is a hTDP-43 minigene , which appears to contain 3'UTR and binding regions that have been shown recently to be required for autoregulation of TDP-43 [19,20]. Given this, it is possible that the hTDP-43 in the constitutive rat model is also autoregulated and that the presence of the mutation in the hTDP-43 minigene prevents autoregulation of the mutant, but not the wild-type, hTDP-43. Finally, in the TDP-43 rat models, there appears to be extensive hTDP-43 immunoreactivity in both the nucleus and the cytoplasm, regardless of mutation; whereas, TDP-43 mainly localized in the nuclei in both of our TDP-43M337V and TDP-43WT mice. The toxicity that we observe in our TDP-43 transgenic mice is therefore likely to be due, at least in part, to the impact of high TDP-43 levels on nuclear functions. Overexpression of TDP-43 in the nuclei of TDP-43 mice may interfere with interaction with its DNA and RNA targets, disrupt normal substrate metabolism and lead to neuronal dysfunction. Recent efforts to identify neuronal RNA targets of TDP-43 implicated in neurodegeneration led to the identification of FUS/TLS, progranulin, tau and ataxin1 and -2 and TDP-43 itself [20-22]. Additional studies are needed to explore the precise roles of TDP-43 DNA/RNA targets at work in these mouse models. Both TDP-43 LMW species and cytoplasmic TDP-43 are present in our TDP-43 mice, and they may also contribute to the pathologies and abnormal behavior.
Our results showed that overexpression of hTDP-43M337V can down regulate endogenous mouse TDP-43 levels, which is consistent with the property of TDP-43 autoregulation. TDP-43 can autoregulate its mRNA level, in part by directly binding to the 3'UTR of its own transcript, thereby triggering exosome-mediated degradation or nonsense-mediated RNA degradation [19,20]. The C-terminal region (a.a 321-366) of TDP-43 is required for autoregulation . Recent reports allow for the possibility that mutation of TDP-43 within the C-terminus may affect the efficiency of autoregulation; however, the presence of the M337V mutant within hTDP-43 did not impair its ability to regulate endogenous mTDP-43. The loss of nuclear mTDP-43 in response to hTDP-43M337V overexpression has been proposed to play a role in the pathogenesis observed in another TDP-43 transgenic mouse model . Considering the substantial homology between the hTDP-43M337V and mTDP-43 proteins, it would seem likely that hTDP-43M337V might functionally compensate for the loss of mTDP-43, but we cannot exclude the possibility that loss of nuclear mTDP-43 may contribute to the phenotype of hTDP-43M337V transgenic mice.
Abnormal mitochondrial accumulation has now been observed in both our TDP-43M337V and TDP-43WT mice  and in another wild-type TDP-43 overexpressing mouse model driven by Thy1.2 promoter , suggesting that TDP-43 can regulate mitochondrial dynamics. In addition to clustering of mitochondria, the size and the ultrastructural integrity of neuronal mitochondria was reduced in our TDP-43 mice compared with mitochondria of NT mice. In the TDP-43WT mice, we had previously identified changes in levels and the phosphorylation state for proteins that critically regulate mitochondrial fission and fusion and suggested that these changes may contribute to the abnormal aggregation and morphology of mitochondria. Surprisingly, we did not find similar changes in mitochondrial fission and fusion proteins in the TDP-43M337V mice, suggesting that mitochondrial aggregation observed in both TDP-43 models may result from another pathogenic processes, such as axonal degeneration.
On occasion, mitochondrial clusters within the neurons of the TDP-43M337V mice were associated with microtubules. TDP-43 may alter the microtubule-based mitochondrial transportation system and lead to both microtubule and mitochondrial aggregation and dysfunction. While there are a number of ways through which this could occur, it was interesting to find that the microtubule associated protein tau was abnormally hyperphosphorylated in the brain of both our TDP-43WT and TDP-43M337V mice. Tau functions to stabilize microtubules and to facilitate axonal transport. Abnormal phosphorylation of tau can reduce its ability to bind microtubules . A number of kinases can phosphorylate tau, and one of these kinases, PKC, was activated in both TDP-43M337V and TDP-43WT mice. Tau hyperphosphorylation might be partially due to PKC activation in the mice; however, the paradigm through which TDP-43 overexpression resulted in tau hyperphosphorylation and/or PKC activation is still unclear. One possibility is that exacerbated TDP-43 autoregulation disrupts the homeostasis of other key proteins and eventually leads to dysfunction. Alternatively, PKC activation and tau hyperphosphorylation could be secondary or unrelated to mitochondrial clustering. There is a large body of evidence suggesting that axonal transport is disrupted in ALS [24,25], which includes evidence that SOD1 mutations impair axonal transport [26,27]. Interestingly, depletion of kinesin heavy chain (kif5B) results in mitochondrial perinuclear clusters similar to those described in our TDP-43 models .
One limitation of our model is that although many of the features are consistent with those observed in ALS, there are several features of this model that are incongruous with the human disease. Phenotypically, our mice show retarded growth from early life; whereas, humans with ALS typically show progressive disease after initially normal development into adulthood. While our TDP-43M337V mice show early lethality, the age at death for the mice is significantly younger in comparison to the lifespan of humans with ALS due to mutations in TDP-43. We did not see loss of nuclear TDP-43 immunoreactivity similar to that observed in affected neurons in ALS, even in cells with cytoplasmic TDP-43 inclusions. It is possible that mTDP-43 underwent redistribution as recently reported in another TDP-43 mouse model ; however, we are unable to confirm this due to unavailability of mTDP-43-specific antibody. We also observed considerable chromatolysis in the TDP-43M337V mice; however, chromatolysis is infrequent in end stage human ALS, and often only detected in cases with rapid disease progression . TDP-43M337V mice also exhibit other pathologies not frequently seen in humans, such as abnormal mitochondrial aggregation. Interestingly, increased phospho-tau has been reported in ALS patients, especially those with cognitive impairment [30,31], which suggests that further analysis of a potential relationship between TDP-43 and tau in mouse models and in human cases might be warranted. The motor, biochemical, and pathological features observed in TDP-43M337V mice (line 4) were also noted in a second independent line of TDP-43M337V mice (line 6), suggesting that these features were not simply due to transgene insertional effects.
We observed some regional differences in our TDP-43 transgenic models, despite the relatively uniform expression of the TDP-43 proteins throughout the gray matter of the brain and spinal cord. For example, nuclear pTDP-43 inclusions, abnormal mitochondrial aggregation and chromatolysis were mainly observed in spinal cord, while cytoplasm pTDP-43 inclusions and tau phosphorylation were primarily seen in the brain. This indicates that the mechanisms regulating TDP-43 and being regulated by TDP-43 are likely to be different in the brain and spinal cord and warrant further investigation.
In summary, this novel TDP-43M337V mouse model indicates that overexpression of hTDP-43M337V alone is toxic in vivo. TDP-43M337V mice recapitulate certain pathologic features seen in neurodegenerative diseases, including TDP-43 fragmentation, phosphorylation, aggregation, increased ubiquitination and gliosis. While these features could also indicate general neuronal dysfunction, the mice also exhibit down regulation of mouse TDP-43, abnormal mitochondria aggregation and abnormal tau phosphorylation. Because overexpression of mutant hTDP-43 produces phenotypes similar to the wild-type TDP-43 model, the mechanisms causing pathogenesis in the mutant model remain unknown. However, these results should not be surprising, given the mutant TDP-43 and wild-type TDP-43 biochemically are similar in human disease. As such, the TDP-43M337V mice may serve as a valuable tool for future studies of yet-to-be-examined disease pathways and the precise roles TDP-43 RNA targets play in neurodegeneration.
The human wild-type TDP-43 cDNA was generated as previously described  and was inserted into the XhoI site of the pcDNA 3.1. To generate the M337V mutation, site directed mutagenesis was performed using Quikchange kit (Strategene). The primers used for the mutation were: 5'-CAGTTGGGGTATGGTGGGCATGTTAGC-3' and 5'-GCTAACATGCCCACCATACCCCAACTG-3'. After confirming the mutation by sequencing, the M337V TDP-43 cDNA was inserted into the XhoI site of MoPrP vector . Following sequencing, the construct was linearized with NotI, gel purified and digested with β-agarose. DNA was filtered, concentrated and diluted to 3 ng/μl in microinjection buffer. The transgene was microinjected into fertilized C57BL/6 (B6) mouse eggs and re-implanted into pseudopregnant females. Eight founders were mated with B6 mice to determine germline transmission and establish expression levels. TDP-43 founder lines (line 4 and 6) that have similar transgene levels to the TDP-43WT mice we previously described , were used for all subsequent experiments. Homozygous mice were produced through a crossbreeding of transgenic mice from the same line. At no time were lines 4 and 6 intercrossed. Procedures were performed in accordance with the Mayo Institutional Animal Care and Use Committee.
Transgenic mice were identified by PCR using hTDP-43-specific primers: 5'- TGGAGAAGTTCTTATGGTGCAGGTC-3' and 5'-GGTATTAGCCTATGGGGGACAC-3' against control actin-specific primers (5'-CGGAACCGCTCATTGCC-3' and 5'-ACCCACACTGTGCCCATCTA-3'). Homozygous mice were identified by Quantitative real-time PCR (see Quantitative real-time PCR section).
Levels of human and mouse TDP-43 transcripts were determined via TaqMan® Gene Expression Assays (Applied Biosystems, Carlsbad, CA). Total RNA was isolated either from tail samples for identification of homozygous mice or from brain or spinal cord tissue to determine the levels of human and mouse TDP-43 transcripts. TRIzol (Invitrogen, Carlsbad, CA) and Pure Link™ RNA Mini Kit (Invitrogen, Carlsbad, CA) were used for RNA extraction. 3 μg RNA were used to synthesize cDNA using the High Capacity cDNA Reverse Transcription Kit (Applied Biosystems, Carlsbad, CA). The qPCR assay used the following: hTDP-43 Hs00606522_m1, mTDP-43 Mm00523866_m and 18S rRNA Hs99999901_s1. The PCR was run on the ABI 7900 and data analyzed using Software RQ Manager 1.2 (Applied Biosystems, Carlsbad, CA).
Sagittal half brain and spinal column were immersion fixed in 10% formalin for immunohistochemistry, and the other half brain was frozen on dry ice for biochemistry. After 24 hours, the spinal cord was removed from the vertebral column and fixed overnight.
Tissues were homogenized at 10 ml/g (volume/weight) in lysis buffer (50 mM Tris-HCl, pH 7.4, 300 mM NaCl, 1% Triton X-100, 5 mM EDTA, 2% SDS, PMSF, and protease and phosphatase inhibitor). Following centrifugation, supernatant was assessed by BCA assay (Pierce, Rockford, IL). Following western blotting, membranes were incubated with mouse monoclonal TDP-43 antibody, which was generated using amino acids 1 to 261 of hTDP-43 as the immunogen and was found to recognize amino acids 205-222 of hTDP-43 by epitope mapping ; rabbit polyclonal TDP-43 antibody against amino acids 288-441; mouse CP13; mouse Tau 5; mouse tau-1; mouse monoclonal glyceraldehyde-3-phosphate dehydrogenase (GAPDH) antibody; Phospho-(Ser) PKC Substrate Antibody; mouseDLP1 antibody; rabbit phospho-DLP1(Ser616) antibody; rabbit Fis1 antibody; or mouse mitofusin 1 antibody. See Additional file 3 for a complete list of primary antibodies used. Following incubation with an appropriate secondary antibody, immunoreactivity was visualized by ECL and exposure to film.
Tissues were embedded in paraffin, sectioned (5 μm thick) and mounted on glass slides. Sections were deparaffinized in xylene and rehydrated in a graded series of alcohol, followed by dH20. Antigen retrieval was performed in a dH2O steam bath for 30 min. Tissues were immunostained with monoclonal TDP-43 antibody or antibodies toward pS403/S404-phosphorylated TDP-43, ubiquitin, glial fibrillary acidic protein (GFAP), ionized calcium-binding adaptor molecule 1 (IBA-1), cytochrome oxidase subunit IV (COX-IV), or phospho-tau (CP13; pS202 tau) using the DAKO Autostainer (Dako Auto Machine Corporation) and the DAKO EnVision+ HRP system. DAKO Liquid DAB Substrate-Chromogen system was the chromogen. See Additional file 3 for a complete list of primary antibodies used. After immunostaining, sections were briefly counterstained with hematoxylin to stain cell nuclei and coverslipped. Paraffin-embedded sections were also stained with hematoxylin and eosin.
Spinal cords from 4%-paraformaldehyde-perfused mice were immersed in 2.5% glutaraldehyde-0.1 M cacodylate buffer, post-fixed in 1% OsO4, dehydrated in alcohol and propylene oxide, and finally infiltrated and embedded in Epon 812. Ultrathin sections mounted on copper grids were stained with uranyl acetate and lead citrate. Images were obtained with a Gatan CCD camera using a Philips 208S electron microscope.
Front paws were painted red, and hind feet were painted blue with nontoxic paint. The mice were placed in a plastic tunnel with a strip of white paper covering the floor. At the end of the tunnel was an enclosed black box to encourage mice to cross the paper and into the box. The test was repeated until mice left at least five pairs of adjacent footprints.
One-way ANOVA with Tukey's posthoc analysis were used to compare measures among 3 groups. Student's t-test analysis was used to compare measures between 2 groups. Kaplan-Meier methods were used for survival analysis. For data presentation, normalized values were averaged and presented as mean ± standard error of means (SEM). Values of p < 0.05 were considered statistically significant.
ALS: amyotrophic lateral sclerosis; FTLD-U: frontotemporal lobar degeneration with ubiquitin-positive inclusions; TDP-43: TAR DNA binding protein-43; hTDP-43: human TDP-43; mTDP-43: mouse TDP-43. pTDP-43: phospho-TDP-43.
YX, YZ, JL, and LP are inventors of this and related mouse models; however, no royalties have been generated from this invention.
YX and YZ performed experiments, data analysis and co-wrote the manuscript. XC performed experiments, WL performed Electron Microscopy study. CS edited the manuscript. JL, DWD and LP conceived of the study, participated in its design and coordination and edited the manuscript. All authors read and approved the final manuscript.
Figure A1: Increased ubiquitin levels in TDP-43M337V mice but hTDP-43 itself is not ubiquitinated. Human TDP-43 was immunoprecipitated from brain homogenates derived from nontransgenic and homozygous TDP-43m337v mice. Briefly, brain homogenates containing 500 μg protein were incubated with 1.5 μg mouse monoclonal TDP-43 antibody overnight at 4°C with gentle shaking. Protein G agarose was added for 4 h at 4°C then pelleted by centrifugation. Protein thus captured was eluted using sample loading buffer and resolved by SDS/PAGE for Western blot analysis. Shown are immunoblots of the inputs and the immunoprecipitated proteins, probed using an antibody to ubiquitin or to total TDP-43. Note that a marked increase in ubiquitin levels is observed in the homogenates derived from homozygous mice prior to immunoprecipitation. Nonetheless, the immunoprecipitated human TDP-43 is not immunopositive for ubiquitin. Arrow = IgG Heavy Chain.
Figure A2: No mitochondrial fission and fusion protein changes in TDP-43M337V mice. Immunoblot analysis of Ser616-phosphorylated DLP1, DLP1, Fis1, and mitofusin 1 (MFN1) expression level in brain lysates of nontransgenic(NT), hemizygous(Hemi), and homozygous(Homo) TDP-43M337V mice of both line 4 and line 6. There are no significant protein changes among different mice groups.
Additional Table: Primary Antibody List. Full list of the primary antibodies used in this study.
This work was supported by the AFAR Affiliate Research Grant Program (YZ), Mayo Clinic Foundation (DWD, JL, LP), National Institutes of Health/National Institute on Aging [5R01AG026251-04 and P01-AG17216-08 (LP)], National Institutes of Health/National Institute of Neurological Disorders and Stroke [R01 NS 063964-01 (LP) and 1R21NS071097-01 (JL)], Amyotrophic Lateral Sclerosis Association (LP, JL) and Department of Defense [USAMRMC PR080354 (LP, JL) and AL093108 (LP)]. We would like to thank Jimei Tong, Cindy Yu, Monica Castanedes-Casey, Linda Rousseau and Virginia Phillips for technical support.