- Research article
- Open Access
Effects of the C57BL/6 strain background on tauopathy progression in the rTg4510 mouse model
Molecular Neurodegeneration volume 9, Article number: 8 (2014)
Cross-breeding of transgenic mice is commonly used to assess gene-gene interactions, particularly in the context of disease. Strain background changes can influence the phenotype of mouse models and can confound crossbreeding studies. We sought to determine if changing the strain background of a commonly used mouse model of tauopathy (rTg4510) would significantly impact the originally reported phenotype. On the original F1 FVB/N x 129S6 background, rTg4510 mice present with progressive cognitive decline, increased insoluble tau, robust tau pathology and age-dependent neurodegeneration. One of the most common strains in mouse modeling is C57BL/6. We and others have previously reported that this strain background alters the phenotypes of various models, including the JNPL3 model of tauopathy. To determine if the phenotype of rTg4510 mice was similarly affected by the introduction of the C57BL/6 background, we compared rTg4510 mice on the original F1 FVB/N x 129S6 background to rTg4510 mice on an F1 FVB/N x C57BL/6NTac (B6/NTac) background, herein termed rTg4510B6.
Despite a small, but significant increase in soluble human tau levels, young rTg4510B6 mice had equivalent levels of tau phosphorylation, aggregation and cognitive impairments as age-matched rTg4510 mice. At 6.5 months of age, rTg4510B6 mice displayed hyperphosphorylated insoluble tau and robust cortical tau neuropathology that was equivalent to age-matched rTg4510 mice; however, 10.5-month-old rTg4510B6 mice had greater amounts of phospho-tau in the cortex and hippocampus when compared to age-matched rTg4510 mice. Non-transgenic (NT) littermates of rTg4510B6 (NTB6) mice also had greater amounts of cortical and hippocampal phospho-tau at 10.5 months of age when compared to NT littermates of rTg4510 mice. Additionally, older rTg4510B6 mice had gross forebrain neurodegeneration that was equivalent to age-matched rTg4510 mice.
Overall, our data shows that introduction of the C57BL/6 strain into the rTg4510 mouse background modestly alters the tau pathology that was originally reported in rTg4510 on the F1 FVB/129 background. In contrast, behavioral and neurodegenerative outcomes were not altered. These studies support the use of the rTg4510 mouse model on a partial C57BL/6 strain background without losing fidelity of the phenotype and suggest that the C57BL/6 background does not inherently protect against tauopathy.
Numerous transgenic mice expressing wild-type or mutant human tau have been created to model the neuropathology of tauopathies–a group of neurodegenerative diseases characterized by the accumulation of tau protein aggregates. Many of the behaviors and pathologies reported for these mouse models, even those that express the same tau protein, are different. Several factors may contribute to these differences, including the levels and regions of transgenic tau protein expression, the characteristics of the promoters used to drive transgenic tau expression, and the behavioral tests used to characterize the models. The strain background of transgenic mice can also alter disease progression and presentation.
JNPL3  and rTg4510  mice are two widely used, independent mouse models of human tauopathy that express the same human 0N4R tau protein using different promoter systems. Previously, Bolmont et al. crossed the JNPL3 mouse model from a mixed background onto an inbred C57BL/6 J background and found that the regional distribution of tauopathy was altered and that the timing of phenotype was significantly delayed . Studies have also suggested that the C57BL/6 background is protective against neurotoxicity in other disease models [4–7]. To test the hypothesis that crossing rTg4510 mice to a C57BL/6 strain background is protective against tauopathy, we have compared rTg4510 mice on the original F1 FVB/N x 129S6 background to rTg4510 on an F1 FVB/N x C57BL/6NTac background (rTg4510B6) (Figure 1). Here we compare the phenotypes of both young and old rTg4510 mice on each strain background.
Increased human tau levels in young rTg4510B6mice
Tau is normally a highly soluble protein and expression levels are generally measured in soluble protein extracts. In order to compare human tau expression levels in rTg4510B6 and rTg4510 mice, we prepared soluble brain extracts from mice at 2.5 months of age, prior to robust tau pathology and neuronal loss. rTg4510B6 mice had a small, but significant increase (0.32 ± 0.13; p < 0.05) in soluble human tau levels compared to rTg4510 mice at 2.5 months of age, suggesting that rTg4510B6 mice may have moderately elevated tau transgene expression (Figure 2). Using the Tau5 antibody that recognizes both the transgenic human tau and endogenous mouse tau, no differences in soluble total tau levels were found between rTg4510B6 and rTg4510 mice at 2.5 months of age. Human tau expression in the rTg4510 lines is controlled by the tetracycline transactivator (tTA). Although both the tTA129 mice used for rTg4510 mice and the tTAB6 mice used for rTg4510B6 mice originated from the same tTA line , this minor increase in tau expression could be due to minor changes in tTA expression on the two backgrounds. We were, however, unable to assess tTA expression due to the lack of a good tTA antibody, a problem that is consistent with data from others working with tTA mouse lines [5, 9, 10].
Tau was biochemically equivalent between young rTg4510B6and young rTg4510 mice
Normal tau function and solubility is regulated by phosphorylation (reviewed in ); therefore, we compared the phosphorylation of soluble tau in young rTg4510 mice on both strain backgrounds. To detect tau phosphorylated at S202 and S396/404–sites that are hyper-phosphorylated in human tauopathies–we used the phospho-tau antibodies CP13 and PHF1, respectively [2, 12–14]. Analysis of soluble brain extract with the CP13 and PHF1 antibodies revealed that young rTg4510B6 mice had similar phosphorylation of soluble tau as rTg4510 mice (Figure 2).
A central feature of human tauopathies is the loss of tau solubility and the accumulation of hyper-phosphorylated tau in aggregates that can be isolated from brain with sarkosyl extraction . Tau deposition in the sarkosyl-insoluble brain fraction can be detected as early as 2.5 months of age in rTg4510 mice. With increasing age and disease progression, insoluble tau shifts from a ~55 kDa species to a hyper-phosphorylated 64 kDa species  and we have previously demonstrated that 64 kDa tau is biochemically equivalent to NFTs in tau transgenic mice . At 2.5 months of age, there was no significant difference in the accumulation of insoluble human tau and the phosphorylation of insoluble tau in rTg4510B6 mice compared to rTg4510 mice (Figure 3). Importantly, we observed the initial aggregation of a 64 kDa tau species in rTg4510 mice on either strain background. There was considerable spread in the degree of insoluble tau found within each group, consistent with each animal being in slightly different stages of the initial, rapid development of tauopathy. We also examined the insoluble fraction with the Tau5 antibody, but were unable to obtain sufficient Tau5 antibody reactivity with the insoluble fraction from 2.5 month-old rTg4510 mice on either strain background (data not shown).
Comparable cognitive deficits in young rTg4510B6and rTg4510 mice
The initial characterization of rTg4510 mice showed that human tau expressing mice had similar motor performance to tau negative mice on the F1 FVB/129S strain background at 2.5 months of age, before widespread neurodegeneration in the brain . Studies have shown, however, that non-transgenic (NT) mice on different strain backgrounds can have variable motor performance in a variety of behavioral tasks . To assess effects of the C57BL/6 strain background on sensorimotor function, 2.5-month-old rTg4510B6, rTg4510 and NT mice on both strain backgrounds performed the cued (visible platform) version of MWM. No differences in swim speed were observed across training between all groups (Figure 4A). Further, all groups improved performance over training, as indicated by the decreased search path to the platform [F (2, 32) = 35.91, p < 0.001], but rTg4510 mice on both strain backgrounds had longer search paths to reach the platform than NT mice [F (1, 16) = 5.39, p < 0.05] (Figure 4B). Post hoc analysis revealed that by the third day of visible platform training, all groups swam comparable distances to reach the platform. Equivalent results were found with measurements of the escape latency to reach the platform (data not shown). Importantly, no differences between strains were detected, signifying that mice on an F1 FVB/B6 background had similar sensorimotor function as mice on the F1 FVB/129 background.
Spatial learning and reference memory are hippocampal dependent functions . The hippocampus is one of the first regions affected by tauopathy in rTg4510 mice and cognitive deficits in the hidden platform version of MWM are detected as early as 2.5 months of age in rTg4510 on the original F1 FVB/129 strain background [2, 14]. Analysis of our 2.5-month-old rTg4510 and NT cohorts showed improvement in finding the hidden platform for all groups across training days [escape latency: F (4, 64) = 8.43, p < 0.001), search path: F (4, 64) = 5.77, p < 0.001] (Figure 5A-B). rTg4510 mice showed significantly less improvement in performance than NT mice as indicated by longer escape latencies [F (1, 16) = 61.78, p < 0.001)] (Figure 5A) and longer search paths to find the hidden platform [F(1, 16) = 48.83, p < 0.001)] (Figure 5B). Additionally, no strain background effect was detected for either parameter. Irrespective of strain background, rTg4510 mice showed increased thigmotaxic, or wall-hugging, swimming compared to NT mice [F (1, 16) = 24.70, p < 0.001]. The thigomotaxic behavior of rTg4510 mice decreased over training days [F (4, 64) = 19.07, p < 0.001]; however, it never reached the low levels of thigomotaxis observed in NT mice (Figure 5C). Spatial learning performance was also assessed by the percentage of distance swam in the target quadrant during the final probe trial–rTg4510 mice on both strain backgrounds were significantly impaired compared to NT mice (p < 0.0001) (Figure 5D). Overall, we found that crossing rTg4510 mice to a C57BL/6 strain background did not affect sensorimotor function or attenuate the cognitive decline that is characteristic of rTg4510 mice on the original strain background at 2.5 months of age.
Characterization of tau in older rTg4510B6brain extracts
Having found that the onset of tauopathy is unchanged in rTg4510B6 mice compared to the original rTg4510 mice, we then sought to determine if the C57BL/6 background alters late stage tauopathy in mice at 6.5 and 10.5 months of age. Unlike young mice, old rTg4510B6 mice had similar levels of soluble human tau and increased levels of total soluble tau (human and mouse) as rTg4510 mice (p < 0.01) (Figure 6). Further, while there was not a significant difference in the phosphorylation of soluble tau detected with CP13, analysis with PHF1 revealed that old rTg4510B6 mice had twice as much soluble tau phosphorylated at S396/404 compared to old rTg4510 mice (p < 0.01) (Figure 6). By late stage tauopathy, rTg4510 mice were characterized primarily by a 64 kDa species of tau in the sarkosyl-insoluble brain fraction, regardless of strain background and the accumulation of human tau in the insoluble fraction was similar between rTg4510B6 and rTg4510 mice (Figure 7). The accumulation of human and mouse tau in the sarkosyl-insoluble fraction, as assessed with the Tau5 antibody, was also similar between rTg4510B6 and rTg4510 mice (data not shown). The 64 kDa insoluble tau band from rTg4510 mice on either background was similarly phosphorylated at epitopes associated with human tauopathy when normalized to the amount of human tau (Figure 7) or human and mouse tau (data not shown) in the sarkosyl-insoluble fraction. Results from the biochemical analysis of tau in older rTg4510B6 and rTg4510 mice are summarized in Table 1.
rTg4510B6mice have increased tau pathology compared to rTg4510 mice
Immunohistochemical (IHC) staining with CP13 and PHF1 antibodies was used to compare tauopathy in rTg4510B6 and rTg4510 mice. Both CP13 and PHF1 detected striking amounts of tauopathy in the cortex and hippocampus of late stage rTg4510 mice on either background and tau pathology was found in both the cell body and the neuropil (Figures 8 and 9). The brainstem was minimally affected, reflecting the low levels of transgenic tau expression within this brain structure (Figures 8 and 9). Results from a two-way ANOVA (strain background x age) indicated that rTg4510B6 mice had increased cortical CP13-specific phospho-tau compared to rTg4510 mice [F (1, 13) = 8.60, p < 0.05], but there was an interaction of strain background and age [F (1, 13) = 8.40, p < 0.05] (Figure 8, Table 2). Post hoc analysis revealed that cortical CP13 burden was increased in rTg4510B6 mice at 10.5 months of age (p < 0.01), but not 6.5 months of age when compared to age-matched rTg4510 mice. Independent of age, CP13 burden was also significantly higher in the hippocampus of rTg4510B6 mice compared to rTg4510 mice [F (1, 13) = 15.00, p < 0.01] (Figure 8, Table 2). We also analyzed the brainstem of rTg4510B6 and rTg4510 mice and found that CP13 staining was increased with age but unaffected by the strain background of the mice (Figure 8, Table 2). Quantitation of regional PHF1 staining yielded similar results. Cortical PHF1 staining was increased in rTg4510B6 mice compared to rTg4510 mice [F (1, 13) = 9.20, p < 0.01], but there was an interaction of strain background and age [F (1, 13) = 9.40, p < 0.01] with PHF1 burden being significantly higher in rTg4510B6 mice over rTg4510 mice only at 10.5 months of age (p < 0.01) (Figure 9, Table 2). Additionally, PHF1 was significantly increased in the hippocampus of rTg4510B6 mice compared to rTg4510 mice at both 6.5 and 10.5 months of age [F (1, 13) = 23.00, p < 0.001] (Figure 9). Interestingly, there was also increased PHF1 immunoreactivity that was not seen with CP13 in the brainstem of rTg4510B6 mice when compared to rTg4510 mice on the original strain background [F (1, 13) = 21.00, p < 0.001] (Figure 9, Table 2). Overall, IHC analysis revealed age-dependent regional differences in phospho-tau pathology in mice crossed to a C57BL/6 background compared to mice on the original rTg4510 strain background.
Murine tau phosphorylation is influenced by strain background
As human tau transgene expression in the brainstem of the original rTg4510 mice is very low, it was surprising to detect increased PHF1 staining in the brainstem of old rTg4510B6 mice. The PHF1 antibody recognizes both phosphorylated human and mouse tau; therefore, it was possible that that addition of C57BL/6 into the strain background could increase phosphorylation of endogenous mouse tau. To test this, we analyzed PHF1 staining in NT mice on both the F1 FVB/B6 (NTB6) and the F1 FVB/129 (NT) strain backgrounds. Similarly to rTg4510 mice, PHF1 staining was increased in the cortex of NTB6 mice compared to NT mice [F (1, 14) = 18.00, p < 0.001], but there was an interaction of strain background and age [F (1, 14) = 14.00, p < 0.01] with PHF1 burden being significantly higher in NTB6 mice over NT mice only at 10.5 months of age (p < 0.001) (Figure 10, Table 3). Additionally, PHF1 staining was significantly increased in the hippocampus and brainstem of NTB6 mice compared to NT mice at both time points and independent of an interaction with age [hippocampus: F (1, 14) = 33.00, p < 0.0001; brainstem: F (1, 14) = 40.00, p < 0.0001] (Figure 10, Table 3). Analysis with the CP13 antibody revealed that old NTB6 mice had significantly more CP13 staining in the cortex [F (1, 14) = 9.90, p < 0.01], but not in the hippocampus or brainstem, compared to old NT mice (data not shown, Table 3).
Equivalent neurodegeneration in old rTg4510B6and rTg4510 mice
A pathological hallmark of rTg4510 mice is age-dependent neurodegeneration of the forebrain regions that is detected by 5.5 months of age [2, 14]. Consistent with this, 6.5-and 10.5-month-old rTg4510 mice on both strain backgrounds had significantly lower hemi-brain weights than NT mice [F (1, 24) = 158.72, p < 0.001] (Figure 11A). There was also a small, but significant decrease in the brain weight of all mice on an F1 FVB/B6 background compared to all mice on the original F1 FVB/129 background [F (1, 24) = 4.60, p < 0.05] that was independent of genotype. We then wanted to determine if there were differences in the size of regions specifically vulnerable to tau-related neurodegeneration in this model. Neuronal loss in forebrain regions of rTg4510 mice has been well characterized by work from Spires et al. that used stereological methods to demonstrate that the overall hippocampal formation has the greatest neuronal loss when compared to the cortical and striatal regions . To assess hippocampal atrophy in rTg4510B6 mice, we measured the area of the hippocampal formation in matched sagittal sections of 6.5-and 10.5-month-old rTg4510 mice and NT littermates on both strain backgrounds. Three factor ANOVA (age x strain x genotype) revealed that the area of the hippocampi were significantly affected by age, strain background and genotype [age: F (1, 27) = 7.57, p < 0.01; strain: F (1, 27) = 5.07, p < 0.05; genotype: F (1, 27) = 501.97, p < 0.001], and that there was an interaction between all three factors [F (1, 27) = 5.93, p < 0.05]. Post hoc analysis revealed that both 6.5-and 10.5-month-old rTg4510 mice had significantly smaller hippocampal areas compared to NT mice (ps < 0.0001), with no difference in size between rTg4510 mice on the original strain background and rTg4510B6 mice (Figure 11B). Additionally, at 6.5 months of age the area of the hippocampi in NTB6 mice was significantly smaller than NT mice (p < 0.01), but this difference was abrogated by 10.5 months of age (Figure 11B). We also examined the CA1 layer, as this hippocampal sub-region has been reported to have an 82% reduction of neurons by 8.5 months of age in rTg4510 mice on the original strain background . We calculated a CA1 index value for each mouse with a smaller index value indicating fewer CA1 neurons (see Methods). In agreement with previous data by Spires et al. , we found that rTg4510 mice had significantly smaller CA1 indices than NT mice [F (1, 27) = 96.54, p < 0.001], suggesting that rTg4510 mice have greater neuronal loss (Figure 11C). Additionally, there was no difference between strains, although the CA1 index value was found to significantly decreased with age [F (1, 27) = 8.67, p < 0.01], consistent with progressive neuronal loss previously reported in this model. Overall, histological analyses of rTg4510B6 brains at 6.5 and 10.5 months of age revealed substantial thinning of the neuronal cell layers of the CA1 and dentate gyrus hippocampal sub-regions, gross atrophy of the hippocampi and cortices and ventricle enlargement that was indistinguishable from age matched rTg4510 mice (Figure 11D).
rTg4510 mice that overexpress mutant human tau are widely used in both academia and industry to study modifiers of human tauopathy [19–33], yet rTg4510 mice on a different strain background have not been fully characterized. One of the most commonly used mouse strains is C57BL/6 and crossing to this background can affect a mouse model’s phenotype because of genetic and behavioral differences that exist amongst inbred mouse strains (reviewed in ). In this study we analyzed rTg4510 mice on a C57BL/6NTac background (rTg4510B6) near the onset of tauopathy at 2.5 months of age and during late stage tauopathy at 6.5 and 10.5 months of age. We found that at 2.5 months of age, rTg4510B6 mice had a small, but significant increase in soluble human tau levels and equivalent tau phosphorylation and aggregation as compared to age-matched rTg4510 mice on the original strain background. Further, cognition was equally impaired in young rTg4510B6 and rTg4510 mice as compared to NT littermates. During late stage tauopathy, rTg4510B6 mice displayed hyperphosphorylated insoluble tau and robust neurodegeneration that was equivalent to rTg4510 mice. Additionally, soluble phospho-tau detected with the PHF1 antibody was increased in rTg4510B6 mice compared to rTg4510 mice and 10.5-month-old rTg4510B6 mice had greater amounts of phospho-tau in the cortex and hippocampus when compared to age-matched rTg4510 mice. Finally, NT littermates of rTg4510B6 mice also had greater amounts of cortical and hippocampal phospho-tau at 10.5 months of age compared to NT littermates of rTg4510 mice. Interestingly, aged rTg4510 and NT mice containing a C57BL/6 background had greater variation in measured phospho-tau levels, therefore, a greater number of mice are needed to confirm that the findings of aged rTg4510B6 mice were not influenced by an outlier.
Contrary to our findings with rTg4510 mice, previous work with JNPL3 mice showed that backcrossing onto C57BL/6 strain background significantly delayed the onset of disease and altered the pathological presentation of the original model . Although JNPL3 mice express the same P301L 0N4R tau as rTg4510 mice, there are several important differences between the models that may explain the disparate effects of the C57BL/6 strain on tauopathy in each model. The tau transgenic integration sites in JNPL3 and rTg4510 mice have not been published, but it is likely that the incorporation of the human tau cDNA into the murine genome occurred at different locations for each model. Based on the integration site of the transgenes and the endogenous activity of that chromosomal region, strain background could differentially affect promoter activity in each model . Moreover, the transgenic tau expression in JNPL3 mice is controlled by the mouse prion promoter, resulting in human mutant tau that predominantly affects neurons in the spinal cord and hindbrain. In contrast, tau expression in rTg4510 mice is ultimately controlled by the CaMKIIα promoter, which results in high tau expression in neurons in the forebrain region. The promoter affects which populations of neurons are expressing the transgene and different neuronal populations may be differently affected in each strain background. Additionally, the C57BL/6 sub-strain utilized in each study could also contribute to the difference. In this study, we crossed tau-expressing mice to a C57BL/6NTac (B6/NTac) sub-strain while Bolmont et al. crossed tau-expressing mice to a C57BL/6 J (B6/J) sub-strain. The B6/NTac sub-strain from Taconic was originally derived from the B6/J strain from Jackson laboratory, but over time genetic and phenotypic differences have developed between the two sub-strains [36–38]. Although we detected significant, but relatively modest changes in the tauopathy of rTg4510 mice on a B6/NTac background, it is possible that modifiers of tauopathy exist on the B6/J strain. Finally, the C57BL/6 strain zygosity has been shown to affect transgenic phenotype [4, 5] and the Bolmont et al. study used congenic C57BL/6 mice while our studies used hybrid F1 C57BL/6 mice. If a recessive gene were responsible for altering tauopathy in JNPL3, such effects would not be detected in F1 rTg4510B6 mice.
In addition to the concerns detailed above, differences in transgenic protein levels could confound comparisons of the same model on different strain backgrounds (i.e. rTg4510B6 vs. rTg4510). By comparing tau protein levels between rTg4510B6 and rTg4510 mice prior to substantial neuronal loss, we found that rTg4510B6 mice have a small, but significant, increase in soluble human tau. Interestingly, this difference in soluble human tau levels was not detected using an antibody specific for both human and mouse tau, which may reflect a difference in endogenous tau levels between the two strain backgrounds. It should be noted though, that it is currently unclear if the Tau5 antibody has equal affinity for human and mouse tau, confounding such an interpretation. Increased soluble human tau in young rTg4510B6 mice could result from decreased tau degradation or from increased tau transgene expression. Because the tau responder line utilized in the rTg4510B6 and rTg4510 lines were identical, it is unlikely that the difference in transgenic tau expression arose from the tau responder line, per se. Since human tau expression in the rTg4510 model is dependent on both the tau and the tTA transgenes, elevated levels of tTA expression could underlie the increased human tau levels. The CaMKIIα-tTA mice used in rTg4510 and rTg4510B6 mice originated from the same line and laboratory  and they were subsequently backcrossed to different mouse strains by the two different laboratories from which we acquired the mice. It is possible that change of transgene copy number may have occurred between the two tTA sub-lines, and this could influence our findings. This can occur if there is inherent instability of the transgene locus . We attempted to use commercially available antibodies raised against tTA to determine if tTA levels were changed between rTg4510B6 and rTg4510 mice, but like others, we were unsuccessful in detecting tTA protein using these antibodies [5, 9, 10]. We, therefore, were unable to determine if altered tTA expression underlies the modestly increased tau levels in young rTg4510B6 mice.
Despite increased human tau expression in 2.5-month-old rTg4510B6 mice, we did not detect differences in tau phosphorylation or aggregation at this age. Furthermore, rTg4510B6 and rTg4510 mice were similarly cognitively impaired. The hidden platform version of MWM revealed that cognition was equivalently impaired in 2.5-month-old rTg4510 mice across strain backgrounds. Interestingly, performance in the cued version of the MWM task showed a difference in the swim path to the visible platform between rTg4510 and NT mice across all days. Closer analysis of individual training days revealed that although rTg4510 mice on both backgrounds took significantly longer paths to reach the platform on days 1 and 2, by day 3 they performed comparably to NT littermates. This suggests that rTg4510 mice took a longer time to learn the cue, but once learned, were able to perform comparably to NT mice so that the deficits observed in rTg4510 mice on both backgrounds strains can be accredited to cognitive deficits rather than an inability to complete the task. Overall, although behavioral differences have been reported between C57BL/6 and 129S6 inbred strains [40, 41], we found no differences in sensorimotor function or spatial dependent learning in mice of the same genotype and on an F1 FVB/B6 versus an F1 FVB/129 strain background.
Interestingly, aged (6.5-and 10.5-month-old) rTg4510B6 mice did not have significantly different human tau levels, as evaluated by soluble human tau. Total soluble tau levels, though, were significantly increased in aged rTg4510B6 mice as compared to rTg4510 mice when an antibody specific to both human and mouse tau was used. Assessment of tau protein production in old mice, however, is complicated by significant neurodegeneration as those neurons expressing human tau are likely the neurons that have died or will die. Given this, the modest but significantly elevated levels of human tau expression in the 2.5-month-old rTg4510B6 mice compared to rTg4510 are likely to be more accurate.
In old mice, the biochemical analysis of tau revealed increased phospho-tau in the soluble brain fraction of rTg4510B6 mice compared to rTg4510 mice using the PHF1 antibody. Additionally, IHC analysis revealed that PHF1 staining was increased in both the forebrain and hindbrain of rTg4510B6 mice, while CP13 burden was increased in forebrain regions (cortex and hippocampus), but not in the brainstem of old rTg4510B6 mice compared to old rTg4510 mice. Furthermore, NTB6 mice also had increased PHF1 and CP13 staining compared to NT mice that was spatiotemporally parallel to the increased PHF1 and CP13 staining in rTg4510B6 mice versus rTg4510 mice. Importantly, analysis of 64 kDa tau in the biochemically abnormal, sarkosyl-insoluble fraction and gross assessments of neurodegeneration through hemi-brain weights, hippocampal areas, and CA1 neuronal thickness, indicated no differences between rTg4510 mice on different strain backgrounds. Taken together, these results suggest that the differences we observed in soluble phosphorylated tau levels and phospho-tau burden of rTg4510B6 mice could be attributed to increased phosphorylation of endogenous mouse tau rather than transgenic human tau. Regardless, the enhanced murine tau phosphorylation does not appear to alter to ultimate neurodegenerative phenotype observed in rTg4510B6 mice. Interestingly, it has been reported that Dab1 deficient mice on a C57BL/6 strain background have increased murine tau phosphorylation compared to Dab1 deficient mice on a BALB/cByJ strain background . Further, the increased murine phospho-tau has been correlated with higher expression of a novel modifier of tau phosphorylation, Stk25, in C57BL/6 mice . In Dab1 deficient mice on a C57BL/6 background, increased phosphorylation of mouse tau was not associated with overt neurodegeneration. These findings highlight a critical consideration when studying phospho-tau alterations in mice that contain both mouse and human tau.
Here we report that introduction of the C57BL/6 strain into the rTg4510 mouse background minimally alters the presentation of tau pathology that was originally reported in rTg4510 on the F1 FVB/129 background. At 2.5 months of age, rTg4510B6 mice had minor increases in human tau expression compared to rTg4510 mice, but cognitive decline and phosphorylation of tau was equivalent in rTg4510 mice on both strain backgrounds. Late stage tauopathy in rTg4510B6 mice was robust with equivalent insoluble tau aggregation and gross neurodegeneration to rTg4510 mice. Additionally, we observed minor, but significant, increases in tau phosphorylation in both older rTg4510B6 mice as compared to rTg4510 mice, and in older NTB6 mice as compared to NT mice. Overall, these studies provide evidence that rTg4510 mice can be crossed to a B6/NTac background without loss or delay of the original phenotype.
The generation of the rTg4510 mouse model that uses a system of responder and activator transgenes to express human mutant (P301L) tau has been previously described . Briefly, mice carrying a responder gene with human tauP301L cDNA downstream of a tetracycline response element (TRE) were maintained on an FVB/N background while mice carrying an activator gene with the tetracycline transactivator (tTA) downstream of a calcium/calmodulin kinase IIα (CaMKIIα) promoter were maintained on a 129S6 background (tTA129S). TRE-tau responder mice are crossed with tTA129S activator mice to produce rTg4510 mice on an F1 FVB/129S background with human mutant tau expression focused within forebrain. tTA129S mice were obtained by crossing offspring carrying the CaMKIIα-tTA transgene  with 129S6/SvEv mice purchased from Taconic  (Figure 1). The original tTA129S mice were acquired from George Carlson. Concurrently, tTA mice were maintained on a B6 background (tTAB6) by crossing the CaMKIIα-tTA mice  to C57BL/6NTac mice (Taconic) for more than ten generations . The original tTAB6 mice were acquired from Li-Huei Tsai. To test the effects of the B6 strain background on the progression of tauopathy in the rTg4510 mouse model, we crossed TRE-tau responder mice to tTAB6 activator mice to produce rTg4510B6 mice on an F1 FVB/B6 genetic background (Figure 1). The initial characterization of rTg4510 indicated that single transgenic (tau only and tTA only) and non-transgenic (NT) littermates have similar performances in Morris water maze, so to maximize the number of rTg4510 mice that could be run within the same test, only NT mice were used as controls. Cohorts included 2.5-, 6.5-and 10.5-month-old rTg4510, rTg4510B6 and NT littermates of both sexes (see Table 4 for details). Grubb’s analysis of the western blot of sarkosyl-insoluble tau (see protocol below) identified one 2.5-month-old male rTg4510 mouse as an outlier due to extremely high tau aggregation. All western blot data from this mouse was excluded from the final results as this may have been a tissue preparation error.
Mice were housed and treated in accordance with the NIH Guide for the Care and Use of Laboratory Animals. All animal procedures were approved and conducted in accordance with the Mayo Clinic Institutional Animal Care and Use committee and the University of Florida Animal Care and Use committee. Mice were maintained in a pathogen-free facility on a 12 hour light/dark cycle with water and food provided ad libitum.
Morris water maze
rTg4510, rTg4510B6 and NT littermates of both sexes underwent Morris water maze (MWM) testing at 2.5 months of age. Mice were handled for 6 days prior to the initiation of behavioral training. MWM testing was performed in a 60 cm high and 1.5 m diameter circular pool filled with water maintained between 24 and 26°C and that was made opaque using non-toxic paint. The swim path of each mouse was recorded by a video camera suspended 2.5 m over the center of the pool and connected to the video tracking system (HVS Image Advanced Tracker VP2000, HVS Image, Buckingham, UK). Curtains surrounding a portion of the pool were used to block the view of the computer. Both the curtains and walls of the room contained dark, geometric shapes to be used as visual cues.
MWM testing occurred over 6 consecutive days with task acquisition training on days 1 through 5 and with probe trials to evaluate spatial memory on day 3, prior to the onset of the training session, and on day 6. For training sessions, a 15 cm diameter platform was submerged 1 cm under the surface of the water in the middle of the target quadrant. The hidden escape platform was located in the same target quadrant for each session for each mouse. The mouse was transported to the pool in a holding container and released facing the wall of the pool from each of the cardinal directions in a semi-random fashion. Once released, the mouse had 60 seconds to locate the hidden platform. If a mouse failed to find the platform, then it was gently guided to the platform and each mouse was allowed to remain on the platform for 10 seconds. Each mouse received 4 training trials per day. During the probe trials on days 3 and 6, the hidden platform was removed from the pool and each animal searched for the hidden platform for 60 seconds.
Prior to the start of the MWM, the 2.5-month-old cohort underwent a visible cued test to evaluate sensorimotor function. A curtain surrounded the MWM tank so that spatial cues could not be referenced and a platform 0.5 cm above the water that contained a visual cue (a tall black rod) was placed in the tank. Both the quadrant location of the visible cued platform and the mouse release points were changed semi randomly for each trial to prevent habituation to a particular quadrant. Mice were given 90 seconds to reach the platform before being gently guided to the platform where the mice remained for 10 seconds. Each mouse was tested 4 times per day for 3 days.
Tissue harvest and preparation
Mice were euthanized by cervical dislocation and the brains were rapidly removed and cut down the midline. The left hemisphere was drop fixed in 10% formalin for immunohistochemical analysis and the right hemisphere was frozen on dry ice and then stored at-80°C. For tau biochemical analysis, sarkosyl fractionation was performed on the frozen brains as previously described . Specifically, each whole hemisphere was homogenized in 10 volumes of homogenate buffer [50 mM Tris–HCl, 274 mM NaCl, 5 mM KCl, 1% protease inhibitor mixture (Sigma), 1% phosphatase inhibitor cocktails I and II (Sigma), and 1 mM phenylmethylsulfonyl fluoride (PMSF), (pH 8.0)] and 200 μl of homogenate was then centrifuged at 150,000 x g for 15 minutes at 4°C. The supernatant, which contains the soluble tau species, was collected and the protein concentration determined using a standard BCA protein assay (Pierce). Pellets were further homogenized in 3 volumes (600 μl) of Buffer B [10 mM Tris–HCl (pH 7.4), 0.8 M NaCl, 10% Sucrose, 1 mM EGTA and 1 mM PMSF] and centrifuged for 15 minutes at 150,000 x g at 4°C. The supernatants were incubated with 1% sarkosyl (Sigma) for one hour at 37°C and then centrifuged at 150,000 x g for 30 minutes at 4°C. The sarkosyl-insoluble pellet was re-suspended in 20 μl TE buffer [10 mM Tris–HCl (pH 8.0), 1 mM EDTA] to obtain the biochemical equivalent of neurofibrillary tangles.
Tau antibodies used included the polyclonal antibody E1 (specific for amino acids 19-33 of human tau)  and the monoclonal antibody Tau5 (provided by Dr. Lester I. Binder, Northwestern University Medical School) for western blot analysis and the monoclonal tau antibodies CP13 (specific for pS202 tau) and PHF1 (specific for pS396/404 tau) (provided by Dr. Peter Davies, The Einstein Institute for Medical Research, Manhasset, NY) for both western blot and immunohistochemical analysis. Anti-GAPDH (Biodesign) was used as a loading control for western blot analysis.
For tau protein analysis, 1-5 μg of the soluble fraction and 3 μl (6.5-and 10.5-month-old mice) or 4.5 μl (2.5-month-old mice) of the sarkosyl-insoluble fraction were loaded in each well. Brain lysates were diluted in Novex Tris-glycine SDS-sample buffer (Invitrogen) with β-mercaptoethanol and heat denatured at 95°C for 5 minutes before being loaded onto 26-well 10% Tris-glycine gels (Invitrogen) and separated by SDS-PAGE. Protein was transferred in CAPS transfer buffer (Sigma) to PVDF membranes. Membranes were then blocked in Tris buffered saline plus 0.1% TritonX-100 (TBS-T) with 5% non-fat milk and incubated overnight with antibody diluted in TBS-T/5% milk. Membranes were washed in TBS-T, incubated with peroxidase-conjugated goat anti-mouse HRP or goat anti-rabbit HRP secondary antibodies (Jackson ImmunoResearch) for 1 hour at room temperature and washed again in TBS-T. Membranes were developed using Western Lightning Plus (Perkin Elmer) and imaged using a FluorChem E System (ProteinSimple). The relative levels of immunoreactivity were determined by densitometry using the software AlphaView SA (ProteinSimple). Relative soluble tau and phospho-tau levels were quantified by normalizing protein levels to GAPDH levels. The relative levels of phospho-tau in the sarkosyl-insoluble fraction were determined by normalizing CP13 and PHF1 levels with E1 levels and Tau5 levels (data not shown) for each mouse to correct for the amount of tau aggregated in the sarkosyl-insoluble fraction of that animal. Tau and phospho-tau levels are presented relative to 6.5-month-old rTg4510 mice for the older cohorts (6.5 and 10.5 months of age) and relative to 2.5-month-old rTg4510 mice for the young cohort (2.5 months of age).
Fixed mouse brains were paraffin embedded and cut into 5 μm sagittal sections. Hematoxylin and eosin (H&E) staining was performed on at least two brain sections from each mouse to align all brains to approximately 1.3 mm lateral to the midline using a mouse brain atlas . Stained slides were digitally scanned using a Scanscope XT scanner. Hippocampal area measurements were performed on a sagittal section stained with H&E obtained for each mouse. The hippocampal formation was then outlined using ImageScope version 10 software (Aperio, Vista, CA) and the resultant area value for each animal was used to generate group means. The same section used for hippocampal area measurements per animal was also used to calculate the CA1 index. Three lines were pseudo-randomly drawn perpendicular to the main axis of the CA1 cell layer and the number of intact neuronal cell bodies touching each line was blindly counted. Each of the counts was summed to obtain a “CA1 index” value per animal.
Standard immunohistochemical procedures were used to immunostain tissues with PHF1 and CP13 antibodies and counterstain with hematoxylin using the Dako Universal Autostainer with DAKO Envision + HRP system (Dako). Stained slides were digitally scanned using a Scanscope XT scanner and were analyzed using ImageScope software. Positive pixel count algorithms were created to measure the percent positivity of the secondary antibody, specifically chromogen DAB, in a selected region. Distinct algorithms were used for burden analysis of each primary antibody in either rTg4510 or NT littermates. The brain regions analyzed included the cortex and the hippocampal formation, which expressed high levels of human tau, and the brain stem, which has very low human tau expression in rTg4510 mice.
Results for MWM training are displayed as the group mean ± SEM and were analyzed using multifactorial repeated measures (RM) ANOVA, with strain background and genotype as between subject factors and training days as within subject factors. When appropriate, post hoc comparisons were performed. The probe trial for MWM was analyzed using two-way ANOVA (genotype x strain) with post hoc Bonferroni’s multiple comparisons test. Western blot results from 2.5-month-old mice were analyzed with an unpaired, two tailed Student’s t-test. Assessments of gross neuropathology in 6.5- and 10.5-month-old rTg4510 and rTg4510B6 mice and NTB6 littermates were analyzed using one-way ANOVA with post hoc analysis with Bonferroni’s multiple comparison tests. Western blot and IHC data from 6.5- and 10.5-month-old rTg4510 and rTg4510B6 mice were analyzed using two-way ANOVA with strain background and age as independent variables and post hoc analysis with Bonferroni’s multiple comparison test. Grubb’s analysis was used to identify outliers in the western blot analysis of sarkosyl-insoluble tau. Analyses were performed using GraphPad Prism version 6.00 software (GraphPad Software) and SPSS version 20.0 (IBM). In all cases, p < 0.05 was considered to be statistically significant.
Tetracycline response element
Calcium/calmodulin kinase IIα
C57BL/6 mouse strain
Non-transgenic mice on an FVB/N x 129S6 strain background
Non-transgenic mice on an FVB/N x C57BL/6 N strain background
Mice with a tTA transgene on a 129S6 strain background
Mice with a tTA transgene on a C57BL/6 N strain background
Mice with tau responder and tTA transgenes on an FVB/N x 129S6 strain background
Mice with tau responder and tTA transgenes on an FVB/N x C57BL/6 N strain background
Morris water maze
Lewis J, McGowan E, Rockwood J, Melrose H, Nacharaju P, Van Slegtenhorst M, Gwinn-Hardy K, Paul Murphy M, Baker M, Yu X, et al: Neurofibrillary tangles, amyotrophy and progressive motor disturbance in mice expressing mutant (P301L) tau protein. Nat Genet. 2000, 25: 402-405. 10.1038/78078.
Santacruz K, Lewis J, Spires T, Paulson J, Kotilinek L, Ingelsson M, Guimaraes A, DeTure M, Ramsden M, McGowan E, et al: Tau suppression in a neurodegenerative mouse model improves memory function. Science (New York, NY). 2005, 309: 476-481. 10.1126/science.1113694.
Bolmont T, Clavaguera F, Meyer-Luehmann M, Herzig MC, Radde R, Staufenbiel M, Lewis J, Hutton M, Tolnay M, Jucker M: Induction of tau pathology by intracerebral infusion of amyloid-beta-containing brain extract and by amyloid-beta deposition in APP x Tau transgenic mice. Am J Pathol. 2007, 171: 2012-2020. 10.2353/ajpath.2007.070403.
McKinney BC, Schneider JS, Schafer GL, Lowing JL, Mohan S, Zhao MX, Heng MY, Albin RL, Seasholtz AF, Akil H, Murphy GG: Decreased locomotor activity in mice expressing tTA under control of the CaMKII alpha promoter. Genes, Brain, Behavior. 2008, 7: 203-213. 10.1111/j.1601-183X.2007.00339.x.
Han HJ, Allen CC, Buchovecky CM, Yetman MJ, Born HA, Marin MA, Rodgers SP, Song BJ, Lu HC, Justice MJ, et al: Strain background influences neurotoxicity and behavioral abnormalities in mice expressing the tetracycline transactivator. J Neurosci. 2012, 32: 10574-10586. 10.1523/JNEUROSCI.0893-12.2012.
Qiao G, Li Z, Minto AW, Shia J, Yang L, Bao L, Tschopp J, Gao JX, Wang J, Quigg RJ, Zhang J: Altered thymic selection by overexpressing cellular FLICE inhibitory protein in T cells causes lupus-like syndrome in a BALB/c but not C57BL/6 strain. Cell Death Differ. 2010, 17: 522-533. 10.1038/cdd.2009.143.
Clark AG, Fan Q, Brady GF, Mackin KM, Coffman ED, Weston ML, Foster MH: Regulation of basement membrane-reactive B cells in BXSB, (NZBxNZW)F1, NZB, and MRL/lpr lupus mice. Autoimmunity. 2013, 46: 188-204. 10.3109/08916934.2012.746671.
Mayford M, Bach ME, Huang YY, Wang L, Hawkins RD, Kandel ER: Control of memory formation through regulated expression of a CaMKII transgene. Science (New York, NY). 1996, 274: 1678-1683. 10.1126/science.274.5293.1678.
Krestel HE, Mayford M, Seeburg PH, Sprengel R: A GFP-equipped bidirectional expression module well suited for monitoring tetracycline-regulated gene expression in mouse. Nucleic Acids Res. 2001, 29: E39-10.1093/nar/29.7.e39.
Zhou H, Huang C, Yang M, Landel CP, Xia PY, Liu YJ, Xia XG: Developing tTA transgenic rats for inducible and reversible gene expression. Int J Biol Sci. 2009, 5: 171-181.
Iqbal K, Liu F, Gong CX, Alonso Adel C, Grundke-Iqbal I: Mechanisms of tau-induced neurodegeneration. Acta Neuropathol. 2009, 118: 53-69. 10.1007/s00401-009-0486-3.
Otvos L, Feiner L, Lang E, Szendrei GI, Goedert M, Lee VM: Monoclonal antibody PHF-1 recognizes tau protein phosphorylated at serine residues 396 and 404. J Neurosci Res. 1994, 39: 669-673. 10.1002/jnr.490390607.
Weaver CL, Espinoza M, Kress Y, Davies P: Conformational change as one of the earliest alterations of tau in Alzheimer’s disease. Neurobiol Aging. 2000, 21: 719-727. 10.1016/S0197-4580(00)00157-3.
Ramsden M, Kotilinek L, Forster C, Paulson J, McGowan E, SantaCruz K, Guimaraes A, Yue M, Lewis J, Carlson G, et al: Age-dependent neurofibrillary tangle formation, neuron loss, and memory impairment in a mouse model of human tauopathy (P301L). J Neurosci. 2005, 25: 10637-10647. 10.1523/JNEUROSCI.3279-05.2005.
Greenberg SG, Davies P: A preparation of Alzheimer paired helical filaments that displays distinct tau proteins by polyacrylamide gel electrophoresis. Proc Natl Acad Sci U S A. 1990, 87: 5827-5831. 10.1073/pnas.87.15.5827.
O’Leary TP, Gunn RK, Brown RE: What are we measuring when we test strain differences in anxiety in mice?. Behav Genet. 2013, 43: 34-50. 10.1007/s10519-012-9572-8.
Aggleton JP, Sanderson DJ, Pearce JM: Structural learning and the hippocampus. Hippocampus. 2007, 17: 723-734. 10.1002/hipo.20323.
Spires TL, Orne JD, SantaCruz K, Pitstick R, Carlson GA, Ashe KH, Hyman BT: Region-specific dissociation of neuronal loss and neurofibrillary pathology in a mouse model of tauopathy. Am J Pathol. 2006, 168: 1598-1607. 10.2353/ajpath.2006.050840.
Berger Z, Roder H, Hanna A, Carlson A, Rangachari V, Yue M, Wszolek Z, Ashe K, Knight J, Dickson D, et al: Accumulation of pathological tau species and memory loss in a conditional model of tauopathy. J Neurosci. 2007, 27: 3650-3662. 10.1523/JNEUROSCI.0587-07.2007.
Ramalho RM, Viana RJ, Castro RE, Steer CJ, Low WC, Rodrigues CM: Apoptosis in transgenic mice expressing the P301L mutated form of human tau. Mol Med. 2008, 14: 309-317.
Spires-Jones TL, de Calignon A, Matsui T, Zehr C, Pitstick R, Wu HY, Osetek JD, Jones PB, Bacskai BJ, Feany MB, et al: In vivo imaging reveals dissociation between caspase activation and acute neuronal death in tangle-bearing neurons. J Neurosci. 2008, 28: 862-867. 10.1523/JNEUROSCI.3072-08.2008.
Dickey C, Kraft C, Jinwal U, Koren J, Johnson A, Anderson L, Lebson L, Lee D, Dickson D, de Silva R, et al: Aging analysis reveals slowed tau turnover and enhanced stress response in a mouse model of tauopathy. Am J Pathol. 2009, 174: 228-238. 10.2353/ajpath.2009.080764.
Lee DC, Rizer J, Selenica ML, Reid P, Kraft C, Johnson A, Blair L, Gordon MN, Dickey CA, Morgan D: LPS- induced inflammation exacerbates phospho-tau pathology in rTg4510 mice. J Neuroinflammation. 2010, 7: 56-10.1186/1742-2094-7-56.
Rocher AB, Crimins JL, Amatrudo JM, Kinson MS, Todd-Brown MA, Lewis J, Luebke JI: Structural and functional changes in tau mutant mice neurons are not linked to the presence of NFTs. Exp Neurol. 2010, 223: 385-393. 10.1016/j.expneurol.2009.07.029.
Fox LM, William CM, Adamowicz DH, Pitstick R, Carlson GA, Spires-Jones TL, Hyman BT: Soluble tau species, not neurofibrillary aggregates, disrupt neural system integration in a tau transgenic model. J Neuropathol Exp Neurol. 2011, 70: 588-595. 10.1097/NEN.0b013e318220a658.
Barten DM, Fanara P, Andorfer C, Hoque N, Wong PY, Husted KH, Cadelina GW, Decarr LB, Yang L, Liu V, et al: Hyperdynamic microtubules, cognitive deficits, and pathology are improved in tau transgenic mice with low doses of the microtubule-stabilizing agent BMS-241027. J Neurosci. 2012, 32: 7137-7145. 10.1523/JNEUROSCI.0188-12.2012.
Ljungberg MC, Ali YO, Zhu J, Wu CS, Oka K, Zhai RG, Lu HC: CREB-activity and nmnat2 transcription are down-regulated prior to neurodegeneration, while NMNAT2 over-expression is neuroprotective, in a mouse model of human tauopathy. Hum Mol Genet. 2012, 21: 251-267. 10.1093/hmg/ddr492.
Spires-Jones TL, Fox LM, Rozkalne A, Pitstick R, Carlson GA, Kazantsev AG: Inhibition of sirtuin 2 with sulfobenzoic acid derivative AK1 is non-toxic and potentially neuroprotective in a mouse model of frontotemporal dementia. Front Pharmacol. 2012, 3: 42-
Abisambra JF, Jinwal UK, Blair LJ, O’Leary JC, Li Q, Brady S, Wang L, Guidi CE, Zhang B, Nordhues BA, et al: Tau accumulation activates the unfolded protein response by impairing endoplasmic reticulum-associated degradation. J Neurosci. 2013, 33: 9498-9507. 10.1523/JNEUROSCI.5397-12.2013.
Nash KR, Lee DC, Hunt JB, Morganti JM, Selenica ML, Moran P, Reid P, Brownlow M, Guang-Yu Yang C, Savalia M, et al: Fractalkine overexpression suppresses tau pathology in a mouse model of tauopathy. Neurobiol Aging. 2013, 34: 1540-1548. 10.1016/j.neurobiolaging.2012.12.011.
Selenica ML, Brownlow M, Jimenez JP, Lee DC, Pena G, Dickey CA, Gordon MN, Morgan D: Amyloid oligomers exacerbate tau pathology in a mouse model of tauopathy. Neurodegener Dis. 2013, 11: 165-181. 10.1159/000337230.
Clippinger AK, D’Alton S, Lin WL, Gendron TF, Howard J, Borchelt DR, Cannon A, Carlomagno Y, Chakrabarty P, Cook C, et al: Robust cytoplasmic accumulation of phosphorylated TDP-43 in transgenic models of tauopathy. Acta Neuropathol. 2013, 126: 39-50. 10.1007/s00401-013-1123-8.
Perez PD, Hall G, Kimura T, Ren Y, Bailey RM, Lewis J, Febo M, Sahara N: In vivo functional brain mapping in a conditional mouse model of human tauopathy (tau(P301L)) reveals reduced neural activity in memory formation structures. Mol Neurodegeneration. 2013, 8: 9-10.1186/1750-1326-8-9.
Bothe GW, Bolivar VJ, Vedder MJ, Geistfeld JG: Genetic and behavioral differences among five inbred mouse strains commonly used in the production of transgenic and knockout mice. Genes, Brain, Behavior. 2004, 3: 149-157. 10.1111/j.1601-183x.2004.00064.x.
Krezowski J, Knudson D, Ebeling C, Pitstick R, Giri RK, Schenk D, Westaway D, Younkin L, Younkin SG, Ashe KH, Carlson GA: Identification of loci determining susceptibility to the lethal effects of amyloid precursor protein transgene overexpression. Hum Mol Genet. 2004, 13: 1989-1997. 10.1093/hmg/ddh210.
Bryant CD, Zhang NN, Sokoloff G, Fanselow MS, Ennes HS, Palmer AA, McRoberts JA: Behavioral differences among C57BL/6 substrains: implications for transgenic and knockout studies. J Neurogenet. 2008, 22: 315-331. 10.1080/01677060802357388.
Mekada K, Abe K, Murakami A, Nakamura S, Nakata H, Moriwaki K, Obata Y, Yoshiki A: Genetic differences among C57BL/6 substrains. Exp Anim. 2009, 58: 141-149. 10.1538/expanim.58.141.
Zurita E, Chagoyen M, Cantero M, Alonso R, Gonzalez-Neira A, Lopez-Jimenez A, Lopez-Moreno JA, Landel CP, Benitez J, Pazos F, Montoliu L: Genetic polymorphisms among C57BL/6 mouse inbred strains. Transgenic Res. 2011, 20: 481-489. 10.1007/s11248-010-9403-8.
Pravtcheva DD, Wise TL: Transgene instability in mice injected with an in vitro methylated Igf2 gene. Mutation Res. 2003, 529: 35-50. 10.1016/S0027-5107(03)00110-6.
Holmes A, Wrenn CC, Harris AP, Thayer KE, Crawley JN: Behavioral profiles of inbred strains on novel olfactory, spatial and emotional tests for reference memory in mice. Genes, Brain, Behavior. 2002, 1: 55-69. 10.1046/j.1601-1848.2001.00005.x.
Clapcote SJ, Roder JC: Survey of embryonic stem cell line source strains in the water maze reveals superior reversal learning of 129S6/SvEvTac mice. Behav Brain Res. 2004, 152: 35-48.
Brich J, Shie FS, Howell BW, Li R, Tus K, Wakeland EK, Jin LW, Mumby M, Churchill G, Herz J, Cooper JA: Genetic modulation of tau phosphorylation in the mouse. J Neurosci. 2003, 23: 187-192.
Matsuki T, Zaka M, Guerreiro R, van der Brug MP, Cooper JA, Cookson MR, Hardy JA, Howell BW: Identification of Stk25 as a genetic modifier of Tau phosphorylation in Dab1-mutant mice. PloS one. 2012, 7: e31152-10.1371/journal.pone.0031152.
Cruz JC, Tseng HC, Goldman JA, Shih H, Tsai LH: Aberrant Cdk5 activation by p25 triggers pathological events leading to neurodegeneration and neurofibrillary tangles. Neuron. 2003, 40: 471-483. 10.1016/S0896-6273(03)00627-5.
Crowe A, Ksiezak-Reding H, Liu WK, Dickson DW, Yen SH: The N terminal region of human tau is present in Alzheimer’s disease protein A68 and is incorporated into paired helical filaments. Am J Pathol. 1991, 139: 1463-1470.
Paxinos G, Franklin KBJ: The mouse brain in stereotaxic coordinates. 2001, San Diego: Academic Press, 2
We would like to acknowledge support by NINDS (NIH 1F31NS078896-01-A1) to RMB and (P50NS072187) to DWD. Additional support was provided from Mayo Clinic to DWD and JL and the University of Florida Department of Neuroscience and Center for Translational Research in Neurodegenerative Disease to NS and JL.
JL holds IP and has received royalties in excess of $10,000 NIH threshold for significant conflict of interest in the past year from the rTg4510 mouse model.
RMB, carried out animal breeding and harvests, tissue processing, immunohistochemical studies, data analysis, manuscript write up and aided in conceptualization of study. JH, performed animal behavioral tests, western blotting, data analysis and contributed to manuscript write up. JK, carried out animal breeding and harvesting. NS, contributed to western blotting. DWD, contributed to the generation of stained mouse brain sections for immunohistochemical analysis and manuscript editing. JL, conceived study and interpreted data, contributed research animals and performed manuscript editing. All authors read and approved the final manuscript.
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Bailey, R.M., Howard, J., Knight, J. et al. Effects of the C57BL/6 strain background on tauopathy progression in the rTg4510 mouse model. Mol Neurodegeneration 9, 8 (2014). https://doi.org/10.1186/1750-1326-9-8
- Transgenic mouse models
- Strain background
- Morris water maze