Dysregulation of the ALS-associated gene TDP-43 leads to neuronal death and degeneration in mice (original) (raw)
Generation of Tg mice overexpressing hTDP-43-WT and hTDP-43-ΔNLS proteins. To create conditional mouse models of TDP-43 proteinopathies, we generated Tg mice expressing hTDP-43-ΔNLS and its control counterpart hTDP-43-WT using CaMK2α promoter elements to drive tet-off tTA (Camk2a-tTA) and a tetracycline responsive promoter to drive hTDP-43 expression (tetO-hTDP-43; Figure 1A) (21–23). Bigenic mice (Camk2a-tTA x tetO-hTDP-43) were maintained on Doxycycline (Dox) to inhibit transgene expression until 28 days of age when they were switched to a Dox-free diet and sacrificed at the designated time points off Dox (Figure 1B).
Generation and biochemical characterization of inducible TDP-43 Tg mice. (A) Generation of conditional Tg mice. Camk2a-tTA mice were crossed with tetO-TDP-WT or tetO-TDP-ΔNLS mice. In bigenic mice, Dox inhibits tTA binding to the tetracycline-responsive promoter element (tetO), repressing hTDP-43 expression. (B) Dox was removed at weaning (P28) followed by analysis at the indicated time points. (C) Expression of hTDP-43 in Tg mice. Immunoblot of hTDP-43 or total TDP-43 (h+mTDP-43) in cortical RIPA extracts (1 month off Dox) of nTg, tTA, tTA/TDP-WT (WT4, WT8, WT5 and WT12), and tTA/TDP-ΔNLS mice (ΔNLS4 and ΔNLS19) showed variable expression of hTDP-43. GAPDH is a loading control. Fold expression relative to nTg and tTA control mice is shown, as described in Methods. (D) Regional expression of hTDP-43. RIPA extracts from different brain regions of tTA/TDP-WT or tTA/TDP-ΔNLS mice (1 month off Dox) were immunoblotted for hTDP-43, h+m TDP-43, and GAPDH. Ctx, cerebral cortex; Hp, hippocampus; OB, olfactory bulb; Cb, cerebellum; Rest, brain stem plus subcortical gray regions; SC, spinal cord. (E) Low levels of insoluble hTDP-43. Sequential cortical extracts from tTA/TDP-WT and tTA/TDP-ΔNLS mice of increasing time off Dox were immunoblotted for hTDP-43 showing low levels of TDP-43 in urea fractions. Urea lysates were loaded at 4× relative to RIPA lysates so that the low level of insoluble TDP-43 could be seen. R, RIPA; U, urea. n = at least 3 animals per group analyzed in C–E.
We identified 2 lines overexpressing hTDP-43-ΔNLS (bigenic mice designated tTA/TDP-ΔNLS) and 4 lines overexpressing hTDP-43-WT (bigenic mice designated tTA/TDP-WT) that expressed differing levels of TDP-43, ranging from 8- to 9-fold over endogenous mTDP-43 for tTA/TDP-ΔNLS mice and from 0.4- to 1.7-fold over endogenous mTDP-43 for tTA/TDP-WT mice (Figure 1C). We selected 1 line of tTA/TDP-ΔNLS (ΔNLS4) for in-depth analysis with the tTA/TDP-WT12 line as a control line, although the other Tg lines also were studied to ensure consistency of the relationship between phenotype and expression levels. Single Tg mice (tetO-TDP-ΔNLS or tetO-TDP-WT) showed little to no hTDP-43 expression indicative of very low tetO activity or “leakiness” (data not shown).
Mice showed neuronal expression predominantly, albeit not exclusively, in forebrain structures, consistent with the properties of the Camk2a promoter (21, 22). To demonstrate the regional differences in TDP-43 expression, protein lysates were analyzed using antibodies specific for hTDP-43 and antibodies recognizing both hTDP-43 and endogenous mTDP-43 (h+mTDP-43). High TDP-43 expression was found in cortex, hippocampus, and olfactory bulb, while cerebellum, subcortical regions/brain stem, and spinal cord displayed no or barely detectable hTDP-43 (Figure 1D). Sequential extraction using RIPA and urea buffers of cortex from bigenic WT12 and ΔNLS4 Tg mice showed the majority of hTDP-43 and mTDP-43 protein was recovered in the RIPA fraction (Figure 1E). However, low levels of TDP-43 (<10%) were detected in the urea fraction (Figure 1E), and C-terminal TDP-43 fragments (CTFs) were not found in any line at any of the time points examined (Supplemental Figure 1; supplemental material available online with this article; doi:10.1172/JCI44867DS1). Importantly, all tTA/TDP-WT and tTA/TDP-ΔNLS lines showed nearly complete suppression of transgene under constant Dox treatment (data not shown).
tTA/TDP-WT mice show progressive neurodegeneration. Overexpression of TDP-43-WT protein is known to be neurotoxic (16–20). To determine whether hTDP-43-WT exhibited similar neurotoxicity in our conditional WT12 line, a time course of neuron loss and the distribution of hTDP-43-WT protein was assessed by histological and immunohistochemical (IHC) analyses of these mice (Figure 2). Although nTg and single Tg littermates never showed signs of neurodegeneration, H&E-stained sections of tTA/TDP-WT brain showed time-dependent neuron loss in the hippocampal dentate gyrus (DG) and neocortex beginning at about 1 month, and this became progressively more severe from 3 to 6 months (Figure 2, A and D). Quantification of DG neuron loss showed approximately 20% loss of DG neurons at 1 month and approximately 75% loss by 3 months after Dox removal, which was paralleled by progressive brain atrophy as assessed by histology and total brain weight (Figure 2, M and N). Astrocytic and microglial activation were seen in cortex and hippocampus by IHC with antibodies to glial fibrillary acidic protein (GFAP) and Iba-1 as early as 1 month off Dox (Supplemental Figure 2A and data not shown). Importantly, WT8 mice (low expressors) showed no detectable neuron loss at 3–4 months in contrast with WT4 mice (high expressors), which showed DG neurodegeneration as early as 7–10 days after Dox removal (data not shown). This suggests that there may be a threshold effect, with neurodegeneration occurring as a function of higher levels of exogenous hTDP-43 expression.
Neuron loss and cerebral atrophy in tTA/TDP-WT mice. (A–L) Expression of hTDP-43 and time-dependent cell loss in tTA/TDP-WT12 mice. (A–D) H&E sections of nTg (A) and tTA/TDP-WT12 (B–D) brain revealed time-dependent hippocampal neuron loss in bigenic mice. Note the loss of DG neurons as indicated by arrowheads. (E–L) Nuclear expression of hTDP-43. IHC for hTDP-43 (E–H) and h+mTDP-43 (I–L) showed mosaic nuclear expression of hTDP-43 in tTA/TDP-WT12 and a severe thinning of the DG cell layer after 3 to 6 months off Dox. Insets in E–L display higher magnification of DG neurons. Scale bars: 500 μm (A–D); 200 μm (E–L). (M) Loss of DG neurons in tTA/TDP-WT12 mice. Quantification of DG neurons shows progressive neuron loss in tTA/TDP-WT12 mice. (N) Time-dependent brain atrophy in tTA/TDP-WT12 mice. There was a progressive reduction in total brain weight in tTA/TDP-WT12 mice. Data in M and N represent mean ± SEM (n = 3–4 per group). *Significantly different from nTg (P < 0.001); ###significantly different from 1 month off Dox (P < 0.001); #significantly different from 1 month off Dox (P < 0.05); ‡significantly different from 3 months off Dox (P < 0.05).
IHC for hTDP-43-WT in line WT12 revealed predominantly nuclear localization (Figure 2, F–H), with a mosaic pattern ranging from neurons showing strong staining to those with negligible staining. This variability was corroborated with an antibody that detects both hTDP-43 and mTDP-43 (h+mTDP-43), as seen by comparing nTg in Figure 2I with hTDP-43-WT in Figure 2, J–L. The number of hTDP-43–expressing neocortical neurons appeared to increase with time off Dox so that approximately 50% of neurons expressed hTDP-43 by 3 months (see Supplemental Figure 7A). Notably, in all of the tTA/TDP-WT lines examined, only extremely rare TDP-43 inclusions were identified in cortical and hippocampal neurons (<0.1% of neurons; see Supplemental Figure 2B) using antibodies that recognize phosphorylated TDP-43 at Ser409 and 410 (p409/410) or ubiquitin. TDP-43 inclusions were not seen in nTg and single tetO-TDP-WT mice. Thus, hTDP-43-WT expression leads to dose- and time-dependent neuron loss in association with gliosis, cerebral atrophy, and rare TDP-43 aggregates.
Cytoplasmic TDP-43 expression leads to progressive neuron loss in tTA/TDP-ΔNLS mice. To evaluate the effects of TDP-43-ΔNLS overexpression in the cytoplasm, we assessed tTA/TDP-ΔNLS4 mice to determine whether neuron loss also occurred with time. Although DG neurodegeneration was variable 1 week after Dox removal, mice sacrificed later displayed increasing levels of neurodegeneration (Figure 3, A–D). Quantitative analyses indicated more acute neuron loss in ΔNLS4 mice such that approximately 50% of the DG neurons were gone at 1 month after induction (Figure 3K). Consistent with the prominent degeneration of neurons in both tTA/TDP-ΔNLS lines, IHC for GFAP and Iba-1 demonstrated massive gliosis in cortical and hippocampal regions, while areas of low transgene expression (i.e., cerebellum, spinal cord) with no evidence of neuron loss showed no gliosis (Supplemental Figure 3B and data not shown). Selective vulnerability of particular brain regions such as the DG and the deep neocortical layers was observed, while other regions with similar transgene expression such as the hippocampal CA1 subfield and the olfactory bulb were relatively resistant to neurodegeneration (Supplemental Figure 4). Further, IHC studies demonstrated cytoplasmic localization of hTDP-43-ΔNLS in most neurons (70%–90%) of the hippocampus (Figure 3, E–J) and cortex (Supplemental Figure 3A), although some hTDP-43 nuclear staining was observed (see also Supplemental Figure 7A). To better quantify the distribution of exogenous hTDP-43-ΔNLS protein, cortical extracts were separated into enriched nuclear and cytoplasmic fractions and immunoblotted for hTDP-43 and h+mTDP-43 (Figure 3L). Control monogenic tTA mice showed no exogenous hTDP-43 protein in either fraction, whereas endogenous mTDP-43 was predominantly nuclear. In contrast, in tTA/TDP-ΔNLS mice, exogenous protein was found in both nuclear and cytoplasmic fractions, indicating that the ΔNLS mutations were effective in misdirecting TDP-43 to the cytoplasm in concordance with the above IHC results. These findings demonstrated that overexpression of a ΔNLS mutant form of TDP-43 leads to cytoplasmic and nuclear TDP-43, neuron death, and gliosis in the hippocampus and cortex. The somewhat faster rate of neurodegeneration in tTA/TDP-ΔNLS mice relative to tTA/TDP-WT mice appeared to be due to the more widespread, uniform expression pattern of TDP-43-ΔNLS protein compared with the mosaic expression pattern of hTDP-43-WT.
Cytoplasmic hTDP-43 expression and progressive neuronal loss in tTA/TDP-ΔNLS mice. (A–D) Progressive neuron loss in tTA/TDP-ΔNLS4 mice. Hippocampal H&E sections of nTg (A) and tTA/TDP-ΔNLS (B) mice show a progressive DG neuron loss evident from 1 month off Dox (arrowhead highlights DG degeneration). (E–J) Cytoplasmic TDP-43 expression in tTA/TDP-ΔNLS hippocampus. IHC for hTDP-43 (E–G) or h+m TDP-43 (H–J) was performed on hippocampal sections from bigenic mice 1 week off Dox showing predominantly cytoplasmic expression of TDP-43. Insets show nTg mice with no hTDP-43 expression and nuclear h+mTDP-43 expression. Scale bars: 500 μm; (A–D, E and H); 200 μm (F, G, I, and J). (K) Loss of DG neurons in tTA/TDP-ΔNLS4 mice. Quantification of DG neurons shows progressive neuronal loss in tTA/TDP-ΔNLS mice. Data shown represent mean ± SEM (n = 3–4 per group). *Significantly different from nTg (P < 0.001). (L) Immunoblot analysis of enriched cytoplasmic (C) and nuclear (N) fractions isolated from cortical extracts of monogenic tTA and 2-month-old bigenic tTA/TDP-ΔNLS mice 10 days off Dox showing the presence of hTDP-43 in both fractions in tTA/TDP-ΔNLS. Note endogenous mTDP-43 is predominately nuclear. Nuclear hnRNP A2/B1 and cytoplasmic HSP90 indicated that the fractions are well separated.
Hyperphosphorylated and ubiquitinated hTDP-43 aggregates in tTA/TDP-ΔNLS mice. To investigate whether the overexpression of hTDP-43-ΔNLS leads to the accumulation of hyperphosphorylated, ubiquitinated cytoplasmic aggregates similar to human TDP-43 proteinopathies (2, 24, 25), IHC was performed using antibodies to phosphorylated epitopes p409/410 and p403/404 of TDP-43 and ubiquitin as markers of pathologically modified TDP-43. Analysis of tTA/TDP-ΔNLS4 mice showed very rare TDP-43 aggregates in less than 1% of cortical neurons, which peaked at 1 month off Dox (Figure 4A). Aggregates in other brain regions, such as the hippocampus and striatum, also were rare to absent (<0.1% of neurons). In contrast, higher-expressing tTA/TDP-ΔNLS19 mice exhibited slightly more cytoplasmic aggregates in hippocampus (Figure 4, C–E) and cortex (Figure 4, B and F–H). These aggregates peaked at 1 week and 1 month off Dox for the hippocampus and neocortex, respectively, and decreased thereafter. No pathological aggregates were detected in nTg and single tetO-TDP-ΔNLS mice, or in cerebellum or brainstem of ΔNLS4 and ΔNLS19 mice (data not shown). Double-label immunofluorescence (IF) (Figure 4, I–N) using antibodies to p409/410 and ubiquitin demonstrated extensive colocalization in cytoplasmic TDP-43 aggregates. Hence, cytoplasmic expression of hTDP-43 triggers variable accumulation of hTDP-43-ΔNLS aggregates that are hyperphosphorylated and ubiquitinated. However, the paucity of aggregates in tTA/TDP43-ΔNLS4 mice indicated that cytoplasmic inclusions were not required for neuron death.
TDP-43 aggregates are phosphorylated and ubiquitinated in tTA/TDP-ΔNLS mice. (A–H) TDP-43 aggregates in cortex and hippocampus of tTA/TDP-ΔNLS mice. IHC of cortex from tTA/TDP-ΔNLS4 (A) and tTA/TDP-ΔNLS19 mice (B) at 1 month off Dox with p409/410 TDP-43 antibody shows relatively few aggregates in tTA/TDP-ΔNLS4 mice and higher number of inclusions in tTA/TDP-ΔNLS19 mice. Inclusions in the DG (C–E) and cortex (F–H) of tTA/TDP-ΔNLS19 mice 1 week off DOX were immunopositive for p409/410 TDP-43 (C and F), p403/404 TDP-43 (D and G), and ubiquitin (Ub) (E and H) antibodies. (I–N) Colocalization of pathologic epitopes in TDP-43 aggregates. IF staining with antibodies to ubiquitin (green) and p409/410 TDP-43 (red) demonstrated extensive colocalization within pathological cytoplasmic aggregates (arrows) in cortex (I–N) from tTA/TDP-ΔNLS19 mice 1 week off Dox. Scale bars: 50 μm (A and B); 20 μm (C–E).
Clasping motoric phenotype and CST degeneration in tTA/TDP-ΔNLS mice. Previous studies showed that the overexpression of hTDP-43-WT and mutants associated with ALS in spinal cord motor neurons led to motor impairments (16–20). Since the Camk2a promoter does not direct hTDP-43 expression in spinal cord motor neurons (see Figure 1), we asked whether hTDP-43-ΔNLS expression in motor cortex is sufficient to cause motor impairments. Abnormal “clasping” is a measure of spastic motor impairment (26–28), and the tTA/TDP-ΔNLS mice displayed abnormal limb clasping as early as 1 week after induction and throughout their life spans until sacrifice at 6 months after induction (Figure 5A). In contrast, the tTA/TDP-WT mice showed less robust and more variable clasping, which was detected only after approximately 1–3 months after induction (Figure 5A). No clasping phenotype was observed in nTg or single Tg littermates.
Motor dysfunction and CST degeneration in tTA/TDP mice. (A) Prevalence of abnormal limb-clasping motor phenotype. tTA/TDP-ΔNLS4 mice showed an early and time-dependent increase in abnormal clasping behavior, with all mice showing motor impairment within 3 weeks off Dox. A lower proportion of tTA/hTDP-WT mice (aggregate data for all WT lines) showed motor impairment only after several months off Dox. This clasping behavior corresponds to spasticity that occurs in PLS and ALS. (B) Axonal loss and gliosis of the CST after 1 month off Dox. IHC analysis of the cervical spinal cord using antibodies against phosphorylated NF-H (top row: RMO217) and phosphorylated NF-H+M (second row: TA51) showed loss of axons in the CST (ventral portion of the dorsal columns, top rows). Higher-power view of this region stained with a rabbit anti-NFL antibody in nTg mice showed numerous puncta corresponding to axons in cross-section, which is reduced in tTA/TDP-ΔNLS4 mice (third row). GFAP IHC demonstrated moderate gliosis in tTA-TDP-WT (both WT5 and WT12) and severe gliosis in tTA/hTDP-ΔNLS4 mice. H&E sections of the proximal and distal forelimb and hind limb showed no evidence of atrophy or grouping. Representative sections of biceps are shown. Scale bars: 100 μm (top 2 rows); 10 μm (third row); 50 μm (bottom 2 rows).
To determine whether upper motor neuron pathology is responsible for this motoric phenotype, sections of brain, spinal cord, and skeletal muscle were examined for evidence of degeneration. Gliosis was noted at all levels of the CST in tTA/TDP-ΔNLS mice, including the striatum, cerebral peduncles, medullary pyramids, and cervical spinal cord (Supplemental Figure 5). Using antibodies to phosphorylated and phosphorylation-independent neurofilament (NF) subunits as axonal markers, we observed select loss of CST axons in cervical spinal cord associated with gliosis (Figure 5B). Lower motor neuron loss was not observed, consistent with the absence of gliosis of the spinal cord ventral horn, and the absence of grouped atrophy or other abnormalities of the proximal and distal forelimb and hind limb striated muscles (Figure 5B). Thus, our findings support that degeneration of motor neurons in the cortex is sufficient to elicit a motoric phenotype reminiscent of both FTLD-TDP and PLS due to the selective involvement of upper but not lower motor neurons.
Nuclear or cytoplasmic overexpression of hTDP-43 leads to downregulation of endogenous mTDP-43. Since the profound neurodegeneration in tTA/TDP-ΔNLS mice could not be accounted for by rare cytoplasmic TDP-43 inclusions and since previous studies have shown that hTDP-43-WT or hTDP-43-ΔNLS expression reduces endogenous mTDP-43 levels in cultured nonneuronal cells (11), we asked whether overexpression of hTDP-43 decreases endogenous mTDP-43. To this end, we developed what we believe is a novel mouse-specific TDP-43 polyclonal antibody raised to a synthetic peptide corresponding to residues 203–219 of mTDP-43 (only 58% sequence identity with hTDP-43). Triple-affinity purification of the polyclonal antisera showed that it reacted specifically with mTDP-43 and not hTDP-43 by immunoblot and by IHC analyses (Supplemental Figure 6). Double-label IF using antibodies specific for hTDP-43 and mTDP-43 showed the absence or a reduction of endogenous mTDP-43 in neurons that expressed hTDP-43 in both tTA/TDP-WT (Figure 6, A–C) and tTA/TDP-ΔNLS (Figure 6, D–F) mice. Indeed, higher-power images showed that neurons expressing exogenous hTDP-43 protein exhibited reduced immunostaining of endogenous mTDP-43 (Figure 6, G–I). Interestingly, since tTA/TDP-ΔNLS mice show more uniform transgene expression, greater numbers of DG neurons were devoid of mTDP-43 expression, in contrast with the mosaic expression of hTDP-43-WT and the concomitant mosaic reduction of mTDP-43 in tTA/TDP-WT mice (compare Figure 6, A–C with D–F). Notably, neurodegeneration was only seen in regions in which there was a reduction of nuclear mTDP-43 staining. Regions with low or no transgene expression or neurodegeneration, such as the ventral motor neuron pool in spinal cord, showed no change in endogenous nuclear mTDP-43 staining (data not shown). Interestingly, very rare cells with mTDP-43 nuclear inclusions were identified (Figure 6J). Significantly, we also did not observe sequestration of endogenous mTDP-43 into hTDP-43 inclusions in our hTDP-43 Tg mice.
Downregulation of endogenous nuclear mTDP-43 in neurons overexpressing cytoplasmic or nuclear hTDP-43. (A–I) hTDP-43 downregulates mTDP-43. IF for hTDP-43 (green) or mTDP-43 (red) in DG of tTA/TDP-WT12 (A–C) or tTA/TDP-ΔNLS4 (D–F) 1 month off Dox showed neurons expressing hTDP-43 with loss of mTDP-43 staining (insets: higher magnification). (G–I) IF for hTDP-43 (red) or mTDP-43 (green) of cortex from tTA/TDP-WT12 mice 1 month off Dox showed loss of mTDP-43 expression in neurons expressing hTDP-43 (arrows). (J) Intranuclear mTDP-43 aggregates. IHC of tTA/TDP-ΔNLS19 cortex for mTDP-43 showed rare intranuclear aggregates (insets: higher magnification of boxed regions). Note the absence of mTDP-43 in neurons with aggregates (*) compared with a cell with reduced (**) or normal (***) mTDP-43 expression. Scale bars: 200 μm (A–F); 20 μm (G–I); 50 μm (J). (K) Reduced mTDP-43 protein in tTA/TDP mice. Immunoblot for hTDP-43, mTDP-43, and h+mTDP-43 of cortical RIPA extracts from tTA/TDP-WT12 or tTA/TDP-ΔNLS4 at various times off Dox showed increased hTDP-43 and reduced mTDP-43 protein relative to nTg (–/–) and tetO-TDP monogenic (+/–) mice. GAPDH is a loading control. (L) Quantification of immunostained sections of DG from tTA/TDP-WT12, tTA/TDP-ΔNLS4 mice, and control nTg and monogenic (tTA only or tetO-TDP only) mice (n = 29). The percentage of neurons with inclusions (green, p409/410 stained sections), percentage of neurons with reduced mTDP-43 expression (red, anti-mTDP43 stained sections) and percentage of neuronal degeneration (blue, H&E sections as in Figures 2 and 3) are shown as mean ± SEM versus time off Dox (t = 0 represents control mice).
The reduction of endogenous mTDP-43 secondary to exogenous hTDP-43 expression was confirmed by immunoblotting. Endogenous mTDP-43 protein was decreased in tTA/TDP-WT12 mice at 6 months off Dox, whereas mTDP-43 protein was reduced as early as 1 month off Dox in tTA/hTDP-ΔNLS4 mice (Figure 6K). The delayed biochemical detection of mTDP-43 reduction was consistent with the slower onset and mosaic expression pattern of tTA/TDP-WT12 mice. To confirm that endogenous nuclear TDP-43 protein was reduced in Tg mice, immunoblotting of nuclear versus cytoplasmic enriched fractions was performed, which showed that in control mice, endogenous mTDP-43 is detected only in nuclear enriched fractions and that nuclear mTDP-43 protein levels are reduced in tTA/TDP-ΔNLS4 mice (Figure 3L). Given the neuronal specificity of the Camk2a promoter, the decrease in mTDP-43 protein levels in whole cortical lysates is indicative of a marked reduction of mTDP-43 protein in affected cells.
To examine the relationship among neurodegeneration, TDP-43 aggregates, and the downregulation of endogenous mTDP-43, quantification of percentage of neuron loss, percentage of neurons with TDP-43 aggregates, and percentage neurons with reduced mTDP-43 protein was performed (Figure 6L). TDP-43 aggregates in DG were extremely rare at all time points and therefore bear no relationship with neuron loss. In contrast, the reduction in mTDP-43 protein appeared to correlate with the extent of neurodegeneration. Significantly, more rapid degeneration in tTA/TDP-ΔNLS mice compared with tTA/TDP-WT mice was matched with more uniform and rapid loss of mTDP-43 protein. Moreover, the number of neurons with loss of mTDP-43 protein decreased relative to the number of unaffected neurons as a function of time off Dox, suggesting that neurons with reduced mTDP-43 protein are selectively vulnerable. Hence, these data indicate that overexpression of hTDP-43 leads to a downregulation of endogenous nuclear mTDP-43 expression, which correlates with the rate and extent of neurodegeneration, suggesting that dysregulation of endogenous TDP-43 activity may be linked to neuron death.
tTA/TDP-ΔNLS mice demonstrate substantial alterations in gene expression, particularly affecting chromatin assembly pathways. Thus far, our data suggest that endogenous mTDP-43 expression is strongly affected by exogenous hTDP-43 expression. Presumably, this tight regulation is required for the normal physiologic functions of endogenous TDP-43. To better understand the consequences of these observed changes, in particular the genome-wide effects of expressing hTDP-43-ΔNLS and perturbing mTDP-43, we used microarrays to evaluate global gene expression in the cortices of tTA/TDP-ΔNLS and tTA/TDP-WT animals relative to single Tg mice and nTg littermates. The inducible system allows analysis of relatively rapid changes in gene expression to avoid unrelated developmental effects and before secondary reactive changes due to neurodegeneration confound our analysis. Mice were studied at 2 weeks off Dox, a time point when tTA/TDP-ΔNLS mice showed uniform hTDP-43 expression and widespread reduction in mTDP-43, but prior to onset of significant gliosis and massive cell loss. It is worth noting that the widespread hTDP-43 expression observed in tTA/TDP-ΔNLS mice at this 2-week time point stands in contrast with tTA/TDP-WT mice, which showed mosaic hTDP-43 expression in less than 10% of neurons (Supplemental Figure 7A). The differing levels of transgene expression in the tTA/TDP-ΔNLS and tTA/TDP-WT mice were corroborated by both hTDP-43 mRNA (Supplemental Figure 7B) and protein levels (Supplemental Figure 7C), which showed robust hTDP-43 expression in tTA/TDP-ΔNLS mice relative to tTA/TDP-WT mice at early time points after Dox removal.
In cortical samples from tTA/TDP-ΔNLS4 (at 2 weeks when there is minimal confounding changes due to gliosis and neuron loss), all the tTA/TDP-ΔNLS animals (n = 5), regardless of sex, showed a dramatically different global gene expression profile compared with the other mouse lines (Figure 7, A and B). In all, more than 4,700 genes were differentially expressed between tTA/TDP-ΔNLS and nTg mice (false discovery rate [FDR] < 0.05), with 197 showing fold change (FC) differences greater than 2. Differentially expressed genes were evenly distributed between those increased versus decreased in tTA/TDP-ΔNLS mice (Figure 7B), making it unlikely that neuron loss alone could account for these findings. Biological pathway analysis of differentially expressed genes further revealed a number of dysregulated pathways (Figure 7C), with the relatively nonspecific category “response to stimulus” showing the greatest enrichment in dysregulated genes, followed by the category “macromolecular complex organization,” with a highly significant enrichment score of 8.3, corresponding to a P value of less than 10–8. Within this category, genes involved in chromatin assembly accounted for the significant enrichment of the entire category (Figure 7D), with 4 of the top 10 genes in this category coding for histones (Table 1). Remarkably, all 4 histone genes were upregulated in the tTA/TDP-ΔNLS mice.
Analysis of global mRNA expression. (A) Principal component (PC) analysis revealed a distinct global gene expression signature for tTA/TDP-ΔNLS (tTA/TDP-ΔNLS4, blue, n = 5), while other groups (nTg n = 8, tTA/TDP-WT n = 4, and monogenic ΔNLS n = 4) were relatively admixed. Data shown as PC1 versus PC2 for each individual mouse. (B) Hierarchical cluster analysis of the genes differentially expressed between tTA/TDP-ΔNLS and nTg mice (FDR < 0.05, with absolute value of FC > 2, shown here, n = 197 genes) corroborated PC analysis. Genes dysregulated in tTA/TDP-ΔNLS mice were evenly split between those downregulated (blue) and upregulated (red). Columns on heat map correspond to individual animals designated as follows: tTA/TDP-ΔNLS (blue), nTg (green), tTA/TDP-WT (purple), and monogenic ΔNLS (red). Rows correspond to individual probe sets, with blue indicating lower, gray indicating intermediate, and red indicating higher expression. (C) Biological pathway analysis of genes dysregulated in tTA/TDP-ΔNLS mice revealed many enriched pathways. The top 5 enrichment scores (negative log10 χ2_P_ value) are shown (higher score indicates greater enrichment). (D) Within the second-most-enriched pathway (macromolecular complex assembly, blue bar in C), most of the genes were involved in DNA-protein complex assembly. (E) Microarray and qRT-PCR results showed good concordance (r2 of 0.7959, and no discordant directions of change), as shown by plotting log2 FC values for microarray data (x axis) versus qRT-PCR results (y axis). The 6 genes that differed significantly between tTA/TDP-ΔNLS and nTg littermates (red squares) and 8 genes that did not differ significantly between groups (black circles) are shown (see Table 2). A negative value denotes lower expression in the tTA/TDP-ΔNLS mice.
Top 10 genes in the DNA-protein complex assembly pathway
In contrast with the tTA/TDP-ΔNLS animals, the tTA/TDP-WT mice (n = 4), which express much lower levels of transgene and have correspondingly less repression of endogenous mTDP-43, showed more modest changes in global gene expression (Figure 7A). While these animals did separate from nTg mice, their global gene expression signature appeared to be intermediate between the nTg and tTA/TDP-ΔNLS mice (Figure 7, A and B).
To validate our microarray findings as well as interrogate the expression of genes previously reported to be affected by TDP-43, we performed quantitative RT-PCR (qRT-PCR) on select genes. As shown in Figure 7E, microarray and qRT-PCR results were concordant (r2 of 0.7959 across 14 genes tested on both platforms). Of note, while some genes previously reported to be affected by TDP-43 (e.g., Nefl) were dysregulated in both our microarray and qRT-PCR experiments, this was not true for other genes reported to be transcriptionally affected by TDP-43 (e.g., Hdac6 and Cdk6) (29–31). In addition, the mouse Tardbp gene itself is downregulated by log2 FC of –0.55 (32% reduction) by qRT-PCR in tTA/TDP-ΔNLS mice relative to nTg littermates (Table 2). This finding is concordant with our IF and immunoblot studies demonstrating that endogenous mTDP-43 is downregulated in the presence of exogenous hTDP-43 and implies that at least part of this regulatory effect occurs at the mRNA level. Significantly, we noted that mRNA markers of astrocytes (Gfap), microglia (Cd34), and neurons (Nefm) did not differ substantially between the tTA/TDP-ΔNLS mice and their nTg littermates, thereby indicating that gliosis, microglial infiltration, and neuron loss were not responsible for the gene expression changes seen here.
qRT-PCR verification of microarray results
Taken together, these data indicate that tTA/TDP-ΔNLS mice show significantly altered global gene expression affecting specific pathways such as chromatin assembly. Although tTA/TDP-WT mice showed a somewhat intermediate profile, their pattern of gene expression was closer to that of nTg mice, presumably due to their mosaic hTDP-43 expression pattern affecting only a small subset of neurons at the time point studied. Regardless, specific biological pathways, in particular those involved in chromatin assembly, were linked to the dysregulation of endogenous TDP-43 and downstream neurodegeneration.