Increased Tau Phosphorylation and Tau Truncation, and Decreased Synaptophysin Levels in Mutant BRI2/Tau Transgenic Mice

Familial Danish dementia (FDD) is an autosomal dominant neurodegenerative disease caused by a 10-nucleotide duplication-insertion in the BRI2 gene. FDD is clinically characterized by loss of vision, hearing impairment, cerebellar ataxia and dementia. The main neuropathologic findings in FDD are the deposition of Danish amyloid (ADan) and the presence of neurofibrillary tangles (NFTs). Here we investigated tau accumulation and truncation in double transgenic (Tg-FDD-Tau) mice generated by crossing transgenic mice expressing human Danish mutant BRI2 (Tg-FDD) with mice expressing human 4-repeat mutant Tau-P301S (Tg-Tau). Compared to Tg-Tau mice, we observed a significant enhancement of tau deposition in Tg-FDD-Tau mice. In addition, a significant increase in tau cleaved at aspartic acid (Asp) 421 was observed in Tg-FDD-Tau mice. Tg-FDD-Tau mice also showed a significant decrease in synaptophysin levels, occurring before widespread deposition of fibrillar ADan and tau can be observed. Thus, the presence of soluble ADan/mutant BRI2 can lead to significant changes in tau metabolism and synaptic dysfunction. Our data provide new in vivo insights into the pathogenesis of FDD and the pathogenic pathway(s) by which amyloidogenic peptides, regardless of their primary amino acid sequence, can cause neurodegeneration.


Introduction
Two early-onset autosomal dominant diseases known as familial British dementia (FBD) and familial Danish dementia (FDD) are caused by mutations in the BRI 2 gene [1][2][3][4]. FBD was first reported by Worster-Drought and McMenemey in 1933, who described a British kindred with presenile dementia and spastic paralysis [1]. FDD was first described by Strömgren and collaborators in 1970, who described a Danish kindred with predominant clinical features of vision impairment, hearing loss, and progressive dementia [2]. The BRI 2 gene (also known as ITM2b) encodes a protein of 266 amino acids that belongs to a family of integral type II trans-membrane domain proteins [3][4][5][6]. Cleavage of the BRI 2 protein within its ectodomain (residue Arg243 and Glu244, KGIQKR Q EAS) by pro-protein convertases (PCs) [7][8][9] releases a 23 amino acid pro-peptide from the wildtype precursor protein and 34 amino acid long amyloid peptides in patients with FBD (ABri) and FDD (ADan) [3,4]. A large part of the remaining ectodomain, the BRICHOS domain, is shed by ADAM10 and released into the extracellular space. The remaining membrane associated N-terminal fragment (NTF) undergoes intramembrane proteolysis mediated by SPPL2a or SPPL2b. This cleavage generates an intracellular domain, which is liberated into the cytosol and a secreted C domain [10][11][12].
The clinical phenotype of FBD and FDD consists of progressive dementia and ataxia. The main neuropathologic findings are the presence of severe amyloid angiopathy and neurofibrillary tangles (NFTs). Patients with FBD have hippocampal extracellular perivascular amyloid plaques and intraneuronal formation of NFTs within the limbic regions. Amyloid plaques are primarily localized to the hippocampus and cerebellum. NFTs are numerous in the hippocampus. Extensive cerebral amyloid angiopathy (CAA) is observed in the leptomeningeal vessels and in gray and white matter vessels within the cerebrum, cerebellum, brainstem, and spinal cord; however, cerebral hemorrhage rarely occurs in FBD patients [3,13]. Neuropathologic findings of FDD closely resemble those of FBD; however, parenchymal deposits found in the hippocampus of patients with FDD are Congo red and Thioflavine S (ThS) negative. In addition, amyloid b (Ab) can be found co-deposited with the Danish amyloid [4,14]. Interestingly, tau deposits in FBD, FDD, Alzheimer disease (AD), and some forms of prion diseases are antigenically, ultrastructurally and biochemically similar [13][14][15][16][17]. NFTs in patients with FBD and FDD are composed of paired helical filaments (PHFs) as in patients with AD. Biochemical analyses of insoluble tau from FBD, FDD, and AD brains show a similar Western blot banding profile. The similarity between pathological lesions supports a unifying pathologic mechanism by which different amyloidogenic peptides could trigger a complex pathological cascade from soluble to filamentous insoluble tau protein [18].
Hyperphosphorylation and caspase-mediated truncation of tau at aspartic acid (Asp) residue 421 (Asp 421 or D421, longest human tau isoform) appears to play an important role in the assembly of tau into filaments [19,20]. In fact, several in vitro and in vivo studies suggest that caspase activation might be an early event in NFT formation [19][20][21]. Using in vivo multiphoton imaging, it was observed that fibrillar tau deposits are the consequence of a cellular degenerative process marked by caspase activation [22]. After the formation of a new tangle within the neuron, the cell remained alive and caspase activity seems to be suppressed. Importantly, NFT formation and cleavage of tau at amino acid Asp 421 can be triggered by Ab peptides, linking amyloid and tau [19].
Herein, we generated double transgenic (Tg-FDD-Tau) mice by crossing transgenic mice expressing human Danish mutant BRI 2 (Tg-FDD) with mice expressing human 4-repeat mutant Tau-P301S (Tg-Tau) to study in vivo the relationship between BRI 2 , ADan and tau. Our studies provide novel in vivo insights into the pathogenesis of FDD and a mechanistic link between ADan, tau, and synaptic pathology.

Transgenic Mice
Transgenic (Tg) mice homozygous for human BRI 2 containing the 10 nucleotide duplication (787_796dupTTTAATTTGT) found in patients with FDD (Tg-FDD) [4,23], mice expressing the smallest 4-repeat human isoform of the microtubule-associated protein tau (MAPT) (0N4R) with the frontotemporal dementia with parkinsonism linked to chromosome 17 (FTDP-17) P301S mutation (Tg-Tau) [24,25], double homozygous Tg-FDD6Tg-Tau (Tg-FDD-Tau) [18] mice, and wild-type (WT) C57BL/6J mice were used. The P301S mutation was introduced into the smallest exon 10 containing MAPT cDNA by site-directed mutagenesis and ligated into XhoI digested pMoPrP.Xho vector [23]. The positive clones were analyzed for proper orientation and sequence. The resultant DNA was digested with NotI and given to the Indiana University Transgenic Core Facility for injection. The construct was free of all vector sequences prior to injection. Standard technique was used to generate the transgenic mice using C3HeB/FeJ mice. Transgenic pups were identified by amplifying tail DNA with human specific MAPT primers, 59-CTCCAAAAT-CAGGGGATCGC-39 and 59-CCTTGCTCAGGT-CAACTGGT-39. Eight founders were mated with C57BL/6 mice. Copy number and integration of the transgene was determined by Southern blotting of tail DNA from founder offspring and expression of the transgene was determined by Northern analyses. The offspring were backcrossed to C57BL/6 mice to establish lines. Tg-FDD-Tau mice were generated by mating Tg-FDD and Tg-Tau mice. Expression of the transgenes (BRI 2 and MAPT) is under the control of the murine Prnp promoter [18,23,24]. Tg-FDD-Tau and single Tg-FDD and Tg-Tau mice have the same genetic background: C57BL/6. The presence of the transgenes was detected by PCR amplification as described [23,24]. Body weight, coat appearance, posture, and tail suspension response were assessed in all mice as described [23,26]. Coats were deemed to be either normal (smooth and clean) or rough (matted and dirty) by observing the fur at the back of the neck. A hunched or arched posture that was apparent while the mouse was both sitting and walking was noted. The tail suspension response was observed and noted as normal if the mouse assumed a wide spread toes and legs position. Cupping of the paws and pulling of the legs in toward the body was noted as the cupping and pulling response [23,26].

Ethics Statement
This study was carried out in strict accordance with the Guidelines for the Care and Use of Laboratory Animals of the National Institutes of Health. The protocol was approved by the Indiana University School of Medicine Institutional Animal Care and Use Committee (Protocol Number: 10142). All surgeries were performed under anesthesia, and all efforts were made to minimize animal suffering.

Rotarod testing
Motor function of WT C57BL/6 (n = 7), Tg-FDD (n = 10), Tg-Tau (n = 11), and Tg-FDD-Tau (n = 9) mice, was tested at six months of age using a rotarod device (Columbus Instruments International, Columbus, OH) as described previously [26]. Only naive mice were used. Each trial lasted a maximum of 10 min, during which time the rotating rod underwent a linear acceleration from 4 to 40 rpm over the first 5 min of the trial and then remained at maximum speed for the remaining 5 min. Animals were scored for their latency to fall (in seconds) for each trial. Animals were rested a minimum of 30 min between trials to avoid fatigue and exhaustion. Each mouse performed four trials on each of four consecutive days.

Histology and immunohistochemistry
Mice were anesthetized and perfusion fixed with 4% paraformaldehyde in 0.1 M phosphate buffer, pH 7.2 (Sigma-Aldrich). Brains were removed, embedded in paraffin, and sectioned. Sections (8 mm thick) were cut and mounted on poly-l-lysinecoated slides and stained with hematoxylin and eosin [23,26,27]. Some sections were stained with Bodian silver staining. ThS was used to show the presence of amyloid deposits in the brain [23,27]. Immunohistochemical staining of mice sections were performed as previously described [23,27]. Cell counts were performed on four Tg-Tau and four Tg-FDD-Tau mice at 6 and 11 months of age.
Individual mice were coded, and for each animal, brains were serially cut in coronal sections (6 mm thick) and immunostained with AT8 and Tau-C3 Abs. The total number of positive neurons throughout the neocortex was estimated on 11 coronal sections at 180 mm intervals following a standard protocol [28]. Nerve cells were counted manually using a 206 or 406 objective. To avoid counting the same neuron in consecutive sections, only neurons with a nucleolus were included. Statistical analysis was done using GraphPad Prism version 5.04 (GraphPad Software, San Diego, CA).

Protein extraction
Brains were removed, dissected, quickly frozen on dry ice and stored at 280uC. Post-nuclear supernatants (PNS) were prepared by homogenizing the neocortex in 3 volumes of cold Hepessucrose buffer (20 mM Hepes, 1 mM EDTA, 1 mM EGTA, 0.25 M sucrose, all from Sigma) containing protease inhibitors (PI) (Complete, 1 mM pepstatin, 100 mM TLCK-HCl, 200 mM TPCK, and 1 mM leupeptin; all from Roche Molecular Biochemical, Indianapolis, IN). The homogenates were centrifuged at 1,000 g for 10 minutes and the supernatants (PNS) retained for western analysis. Soluble and sarkosyl insoluble fractions were prepared from the neocortex as previously described [29]. Tissue was homogenized in 3 volumes of Trissucrose buffer (25 mM Tris-HCl, 150 mM NaCl, 1 mM EDTA, 1 mM EGTA, 250 mM sucrose; buffer A) containing PI and phosphatase inhibitors (Phosphatase Inhibitor Cocktail 2, P5726, Sigma). Homogenates were centrifuged for 20 minutes at 15,000 g in a Beckman TLA 110 rotor (Beckman, Palo Alto, CA). The supernatant (soluble fraction) was reserved. The pellet was resuspended in a fresh volume of buffer A and centrifuged 15 minutes at 15,000 g. The supernatant was removed; the pellet was washed with 1 ml buffer A, and centrifuged 15 minutes at 15,000 g. The pellet was resuspended in 2 ml of buffer B (buffer A with 1% sarkosyl), incubated 1 hour at room temperature on a rotator, and centrifuged 30 minutes at 43,000 g at 4uC. The pellet was washed two times with 2 ml of buffer B and centrifuged 30 minutes at 43,000 g at 4uC. The pellet (sarkosyl insoluble fraction) was resuspended in 200 ml of Laemmli sample buffer (Bio-Rad, Philadelphia, PA).

Western blot analysis
Protein concentrations were determined with the BCA Protein Assay Kit (Pierce). Forty mg of protein from PNS and sarkosyl soluble samples were used for western blot analysis. Five mg tissue w/v (pre-processing tissue weight (mg)/200 ml of sample buffer) of the sarkosyl insoluble fractions were used for western blot analysis. Proteins were separated on Mini-Protean TGX Precast gels (Bio-Rad), run under denaturing conditions and electrotransferred to Immobilon PVDF membrane (Millipore). Membranes were blocked with 0.01% milk in PBS (10 mM phosphate, pH 7.4, 150 mM NaCl) with 0.05% Tween-20 (PBS-T, all from Sigma) using the SNAP ID protein detection system (Millipore) then incubated 2 hours or overnight with the primary Ab. Following washes with PBS-T buffer, membranes were incubated 1 hour with the appropriate HRP-conjugated secondary Ab and visualized using the Pierce ECL Pico kit (Pierce). To ensure equal protein loading of the soluble and PNS samples, blots were probed with anti-b-actin. Blots were scanned and quantified using Image J software from NIH. Statistical analysis was done using GraphPad Prism version 5.04 (GraphPad Software).

RNA isolation and multiplex expression analysis
For isolation of RNA, three (WT n = 6; Tg-FDD n = 4; Tg-Tau n = 4, and Tg-FDD-Tau n = 6), six (WT n = 6; Tg-FDD n = 5; Tg-Tau n = 5; and Tg-FDD-Tau n = 6), and nine (WT n = 6; and Tg-FDD-Tau n = 6)-month-old mice were anesthetized, perfused transcardially with 0.9% saline, and the brains removed. The hippocampus (HIP) and neocortex (CTX) were dissected, placed in 750 ul of RNA later (Qiagen, Valencia, CA) and frozen at 220 degrees. RNA was isolated from the HIP and CTX samples using RNeasy Lipid Tissue Mini Kit (Qiagen) according to the manufacturer protocol. Samples were treated on column with the RNase free DNase Kit (Qiagen) according to the manufacturer instructions. Reverse transcription was performed on 25 ng of total RNA for each sample followed by multiplex PCR, and fragment separation by capillary electrophoresis using the GeXP Chemistry Protocol (Beckman Coulter, Fullerton, CA). Fragments were separated using a CEQ 8000 Automated Capillary DNA sequencer/Genetic Analysis Systems (Beckman Coulter), and analyzed using the GenomeLab GeXP Genetic Analysis System (Beckman Coulter) using the following fragment analysis parameters: slope threshold = 0.9999, peak height threshold = 500 rfu, peak size,375, peak size.145, dye = D4. Multiplex-specific fragments were selected by applying exclusion filters and the data exported to eXpress Analysis software, where they were normalized against mouse polymerase II polypeptide A (Polr2a) as described [30]. Relative mRNA level values for each of the triplicates for each RNA sample were averaged and the mean for the replicates were compared by unpaired two-tailed t-tests using GraphPad Prism version 5.04 (GraphPad Software). Differences in relative mRNA levels with p-values,0.05 were considered statistically significant.

Generation and behavioral analysis of Tg-FDD-Tau mice
Compared to WT mice, male and female Tg-FDD-Tau mice exhibited significant weight loss by 6 months of age (female, p = 0.0181; male, p = 0.0145); however, the weight of Tg-FDD-Tau mice was not significantly different from that of single Tg-FDD and Tg-Tau mice of the same age. Tg-FDD-Tau, Tg-FDD, and Tg-Tau mice exhibited abnormal grooming behavior starting around 9 months as apparent by their dull rough coats. By 12 months of age, Tg-FDD-Tau mice showed a hunched back or arched posture when sitting and walking, which could also be observed in some Tg-FDD mice. None of these abnormalities were seen in WT mice of the same age. Twelve month old Tg-FDD-Tau mice and Tg-FDD mice displayed an unusual gait in which the mouse holds its body near the walking surface and takes wide shortened steps, which was not observed in WT mice and Tg-Tau mice of the same age. At 12 months of age, 88% (n = 8) of Tg-FDD-Tau mice, 33% (n = 6) of the age-matched WT mice, 100% of Tg-Tau (n = 5), and 77% (n = 9) of Tg-FDD exhibited cupping of the hind paws and bilaterally pulling of the hind paws toward the abdomen when suspended by the tail (Fig. 1A-D). Beyond 12 months of age, the health of Tg-FDD-Tau mice, like that of single Tg-Tau mice, sharply declined and the mice had to be euthanized in accordance with institutional guidelines. At 10-14 months, Tg-Tau mice showed a precipitous decline in health, with deterioration of coat condition, hunched back, weight loss, and hind-limb dystonia. No significant differences were observed in the motor function between single Tg-Tau and single Tg-FDD mice (not shown) and Tg-FDD-Tau mice compared with WT mice at 6 months of age by rotarod analysis when male and female animals were analyzed together or when females and males were analyzed separately ( Fig. 1E-G). Additional rotarod analysis in older mice was not performed because the decline in motor performance that led to a reduced survival rate in Tg-Tau mice beginning around 9 months of age was also observed in Tg-FDD-Tau mice.

Transgene expression in Tg-FDD-Tau mice
Cleavage of the FDD mutant form of BRI 2 (ADanPP) between amino acids Arg243 and Glu244 by PCs releases the 34 amino acids ADan peptide ( Fig. 2A) and a mature form of BRI 2 (m-BRI 2 ) [9,18]. As previously reported for transfected cells and FDD knock-in mice [31], the ectodomain processing of the FDD mutant form of BRI 2 by PCs seems to be compromised in FDD, with an accumulation of full-length ADanPP as immature BRI 2 mutant protein (Fig. 2B). No significant difference was observed in the expression of ADanPP between Tg-FDD and Tg-FDD-Tau mice (Fig. 2B). Densitometric scanning and statistical analysis of the bands indicate that the levels of ADanPP and m-BRI 2 were not statistically different in Tg-FDD-Tau and in Tg-FDD mice. We observed that the higher molecular weight band, representing immature BRI 2 , and the lower molecular weight band, representing m-BRI 2 , had approximately the same intensity, suggesting that ,50% of the immature protein was being processed to m-BRI 2 protein in Tg-FDD-Tau and Tg-FDD mouse lines.
The integration and expression of the tau transgene was analyzed in Tg-Tau mice. Southern blot analyses of Tg-Tau mice showed one integration site and incorporation of ,60-70 copies of the transgene (not shown). Males only carried one copy of the transgene since transgene integration occurred on the murine X chromosome. Analysis of the expression of the tau transgene between single Tg-Tau and Tg-FDD-Tau mice by multiplex PCR did not reveal any significant differences in tau expression between the two lines ( Fig. S1).

Pathological analysis of Tg-FDD-Tau mice
A similar progression and distribution of ADan deposition was observed between the Tg-FDD-Tau and the Tg-FDD lines [23]. Beginning at around 6-7 months of age, Tg-FDD-Tau mice showed amyloid deposition primarily in leptomeningeal cerebellar vessels, developing later extensive amyloid lesions in the parenchyma and vasculature of the neocortex, hippocampus, and cerebellum ( Fig. 3A-C). Parenchymal amyloid deposition in the hippocampus was most prominent in the CA3 and CA2 regions and the hilus, consistent with the neuropathological findings in Tg-FDD mice [23]. Anti-ADan Abs immunolabeled amyloid plaques, diffuse ADan deposits, and vascular deposits in Tg-FDD-Tau mice (Fig. 3D,E). Immunohistochemistry using anti-ADan Abs (which also recognize the C-terminus of ADanPP) in Tg-FDD mice revealed the presence of parenchymal and vascular amyloid deposits, as well as intracellular deposits [23]. By using Abs against the N-terminus of BRI 2 ( Fig. 2A) we observed the presence of clusters of swollen neuritic profiles at the periphery of ADan plaques, in addition to intracellular BRI 2 deposits (Fig. 3F-H). DNs were made up of large and rounded processes, strongly immunolabelled with the Abs against the N-terminus of BRI 2 but were not recognized by anti-ADan Abs. These profiles appear to be associated with fibrillar ADan amyloid cores, although some clusters of DNs were also observed in the absence of ADan deposits (Fig. 3G,H). Similar immunoreactive profiles were observed using the BRI 2 -N-terminal Ab BRI-11-26 (not shown) [32]. No immunoreactivity was seen when the primary Ab was omitted. Increased expression of glial fibrillary acidic protein (Gfap), which occurs during activation of astrocytes, was observed by immunohistochemistry (Fig. 4A,B). In addition, 5D4-immunopositive microglia was observed throughout neocortical areas and the hippocampus of Tg-FDD-Tau mice (Fig. 4C). These immunohistochemical observations were confirmed by gene expression analysis. A significant increase in the expression levels of Gfap and the microglial-specific ionized calcium binding adapter molecule 1 (Iba1) was observed in Tg-FDD-Tau mice compared to WT mice (Fig. S2). We also observed an increase in the expression of the complement protein C1q, and the pro-inflammatory chemokines macrophage inflammatory protein-1a (Ccl3) and Ccl5/RANTES (Fig. S2). The distribution of tau deposits was compared between single Tg-Tau and Tg-FDD-Tau mice. Tau deposits in Tg-FDD-Tau mice were found predominantly in the hippocampus, piriform cortex, brain stem, spinal cord, and the cerebellum (Fig. 4D-F), as in single Tg-Tau mice (Fig. S3) [24]. Tau accumulation was detected with the phosphorylation-dependent tau Ab AT8 and was never found in control animals. In FDD, amyloid-b (Ab) may co-deposit with ADan, mainly in vascular and perivascular amyloid lesions [4,14]. However, immunohistochemical analysis using Abs against Ab did not show any immunopositivity in brain sections from single Tg-FDD and Tg-FDD-Tau mice (not shown).

Enhanced tau pathology and cleavage of tau at D421 in Tg-FDD-Tau mice
Extracellular amyloid deposition in combination with NFT formation may be seen only in a limited number of human neurodegenerative diseases, including FDD [3,4,[15][16][17][18]. To assess the influence of the expression of the Danish mutant form of BRI 2 on tau pathology, we analyzed AT8 detectable p-tau in neuronal cell bodies of Tg-Tau and Tg-FDD-Tau mice (Fig. 5A,B). At 6 months of age, we observed by immunohistochemistry a statistically significant difference in the number of AT8-positive (p,0.0001) neuronal perikarya between Tg-FDD-Tau mice and single Tg-Tau mice (Fig. 5C). This change occurred at an age before any significant ADan deposition can be observed in Tg-FDD-Tau mice. Since truncation of tau has been proposed to cause filament formation [19][20][21][22], the presence of caspasetruncated tau at Asp 421 was assessed using Ab Tau-C3. Immunohistochemical studies showed a significant increase in the number of Tau-C3-positive neuronal perikarya in Tg-FDD-Tau mice compared to single Tg-Tau mice at 6 months of age (Fig. 6A,C,E) and at 11 months of age (Fig. 6B,D,F). The number of Tau-C3-positive neuronal perikarya in Tg-FDD-Tau mice increased progressively with age, as it was also statistically significant between 6 and 11 months of age (Fig. 6A,B,G). Analysis of pro-caspase-3 levels by immunoblot showed no significant differences between WT, Tg-Tau, Tg-FDD-Tau and Tg-FDD mice (Fig. 6H). Soluble and sarkosyl-insoluble tau prepared from the brain of Tg-Tau and Tg-FDD-Tau mice were analyzed by western blot. In the soluble brain fraction, we observed strong immunoreactivity using phosphorylation-independent (d29) and phosphorylation-dependent (AT8) Abs, but not using the phosphorylation-dependent Ab AT100 (Fig. 7A) and the Ab specific for tau truncated at Asp 421 (Tau-C3, not shown). Sarkosyl-insoluble tau was detected using the phosphorylation-independent Ab d29, . Processing by ADAM10 in the ectodomain of BRI 2 releases the BRICHOS domain and an N-terminal fragment (NTF). The NTF is also the subject of additional proteolysis by SPPL2, releasing an intracellular domain (ICD) and a C-terminal peptide fragment (BRI2 C-peptide) [18]. Disulfide bonded loops in the BRICHOS domain and in the carboxy-terminus of BRI 2 (amino acids 5 and 22 of the ADan peptide) are indicated. The figure shows the localization of the Abs used. Western blot analysis of PNS from neocortex of Tg-FDD-Tau (2x, n = 6) mice, Tg-FDD (FDD, n-6) mice, and wild-type (WT, n = 6) control mice using the BRI 2 -amino-terminal antibody 14307 (B). The ectodomain processing of the FDD mutant form of BRI 2 by PCs seems to be compromised in FDD. In Tg-FDD mice, two bands can be observed corresponding to full-length ADanPP and m-BRI 2 , while in WT mice most of the detectable BRI 2 protein can be seen as m-BRI 2 . Samples were run in triplicates. Representative samples are shown. The densitometric values of the bands representing ADanPP and m-BRI 2 immunoreactivity were normalized to the values of the corresponding actin band using ImageJ software. No significant differences were observed between Tg-FDD-Tau and Tg-FDD mice (independent t test). doi:10.1371/journal.pone.0056426.g002 and the phosphorylation-dependent Abs AT8 and AT100 (Fig. 7B). A faint immunoreactive band corresponding to tau protein truncated at Asp 421 was observed only in the sarkosyl-insoluble fraction of Tg-FDD-Tau mice using Ab Tau-C3.

Decreased levels of synaptophysin in Tg-FDD-Tau mice precede ADan plaque formation and significant tau deposition
Losses of the pre-synaptic vesicle protein synaptophysin have been shown to correlate with cognitive decline in AD cases [33,34]. Several groups have shown a decrease in dendritic spine density and synaptophysin-positive synapses radiating out from the surface of plaques in mouse models [35][36][37][38]. To assess the effect of tau and ADan on synapses, we performed biochemical analysis by Western blot on PNS-soluble brain fractions. The relative amount of protein was quantified by densitometry and normalized with actin. No significant differences in the levels of synaptophysin and the post-synaptic density protein 95 (PSD-95) were observed at the young ages tested, 2 (not shown) and 3 months between control mice and Tg-FDD-Tau mice (Fig. 8A). Remarkably, we observed a clear decrease in synaptophysin levels in Tg-FDD-Tau mice (p = 0.005) at 6 months of age (Fig. 8B). Synaptophysin levels were found to be slightly decreased in single transgenic mice at 6 months of age, but the decrease did not reach statistical significance (Fig. 8B). Synaptophysin immunostaining did not show a remarkable difference in immunostaining between controls and single FDD and Tau transgenic mice in hippocampal CA1. A decrease in immunostaining was observed only in Tg-FDD-Tau mice (Fig. S4). Quantitative studies using stereological techniques will be needed to evaluate synaptic pathology in Tg-FDD-Tau mice. In older animals (9 months of age), synaptophysin levels were found to be decreased in all transgenic mice lines. The decrease was particularly significant in single Tg-Tau mice, but it was also statistically significant in single Tg-FDD mice (Fig. 8C). No significant difference in synaptophysin levels was observed between single Tg-Tau and Tg-FDD-Tau mice at 9 months of age; however, the difference in synaptophysin levels between single transgenic mice (Tg-FDD and Tg-Tau) and between Tg-FDD and Tg-FDD-Tau reached statistical significance.

Discussion
In the present study, we have characterized a double transgenic mouse model that over-expresses the FDD-mutant form of BRI 2 (ADanPP) and the smallest 4-repeat isoform of mutant tau (P301S), with both transgenes being driven by the murine Prnp promoter. The Tg-FDD-Tau model was designed to reproduce the neuropathologic features of FDD and to test, in vivo, the ability of ADan to modify tau pathology. Tg-FDD-Tau mice displayed clasping and limb retraction when lifted by the tail, revealing a motor impairment that is age-dependent. On immunohistochemical examination, Tg-FDD-Tau mice exhibited an age-dependent accumulation of both ADan and tau; however, the results of this study show that expression of human mutant BRI 2 enhances tau phosphorylation and C-terminal cleavage of neuronal tau, while ADan deposition remained comparable to its parental strain. Enhancement of tau accumulation in Tg-FDD-Tau mice occurs before extracellular deposition of ADan can be detected; suggesting that soluble ADan species or abnormal function of mutant BRI 2 may mediate tau pathology. Sarkosyl-insoluble tau extracted from both Tg-FDD-Tau and Tg-Tau mice contained a major hyperphosphorylated species migrating at 64 kD. Although the levels of sarkosyl-insoluble tau extracted from Tg-FDD-Tau mice were elevated compared to Tg-Tau mice, the change did not reach statistical significance at the age analyzed. These data is in agreement with previous observations of enhanced tau pathology in mutant tau-expressing mice injected with Ab 42 peptides [39] or co-expressing mutant AbPP or BRI 2 in their brains [40][41][42], Representative immunoblots of tris-soluble and sarkosyl-insoluble fractions from 9 month old Tg-FDD-Tau (2x) and Tg-Tau (Tau) (four to five mice per group were analyzed). Samples were run on SDS-PAGE and immunoblotted with anti-tau Abs d29, AT8, AT100 and Tau-C3. bactin was used to normalize protein loading. doi:10.1371/journal.pone.0056426.g007 supporting the hypothesis that amyloidosis facilitates tauopathy in AD. However, the exact mechanism(s) involved in promoting accelerated neurofibrillary degeneration in double amyloid/tau mouse models remains to be determined. Tau truncation by caspases has been proposed as an early and crucial step in the development and maturation of NFTs [43]. Caspase activation may precede and lead to tangle formation with tangle-bearing neurons representing survivors of caspase attack [22]. By immunohistochemistry, we detected intracellular accumulation of tau truncated at Asp 421 in single Tg-Tau and Tg-FDD-Tau mice. The number of Tau-C3 positive cells was significantly higher in Tg-FDD-Tau mice compared to single Tg-Tau mice; however, the number of Tau-C3 positive cells represented only a small fraction of the number of neurons that were labeled by using Ab AT8 on the same section in both mouse lines. Truncation of tau at Asp 421 was not detected by western blot using the Ab Tau-C3 in single Tg-Tau mice, as previously reported on P301S transgenic mice [21,44]. Low levels of insoluble truncated tau were observed only in the sarkosyl-insoluble fraction of Tg-FDD-Tau mice brains, which may reflect the higher number of cells that were detected using Ab Tau-C3 by immunohistochemistry in Tg-FDD-Tau mice compared to Tg-Tau mice. Although tau truncation appears to play an important role in the assembly of tau into filaments, it is still controversial whether tau truncation is primary or secondary to tau hyperphosphorylation. Our data, in agreement with previous reports on single Tau transgenic and double transgenic models expressing mutant tau and amyloid precursor protein [19][20][21][22]44], strongly suggest that ADan and Ab may act on a similar cellular degenerative pathway, marked by caspase activation and tau fibrillar deposition and neurodegeneration [19,45].
One prominent finding in FDD as well as in AD and non-AD tauopathies [14,46,47] is the presence of a neuroinflammative process. Immunohistochemical and gene expression studies showed clear evidence of neuroinflammation in Tg-FDD-Tau mice. Activated astrocytes and microglia were seen frequently present in close proximity of amyloid deposits and NFTs. Interestingly, activated microglia was detected even before ADan deposition was observed and correlated with tau deposition in both Tg-Tau and Tg-FDD-Tau mice. The finding of an inflammatory process in association with tau deposition is in agreement with previous work done in transgenic mouse models expressing mutant tau protein and may constitute a general response of neurons to the accumulation of aggregated tau [46][47][48][49]. We observed that ADan amyloid cores in Tg-FDD mice are surrounded by DNs consisting of large globular processes that were labeled by Abs against the N-terminus of BRI 2 . The lack of immunoreactivity of DNs using a C-terminal Ab against ADan in Tg-FDD mice suggests that the accumulation of BRI 2 involves a form of BRI 2 generated after PC processing. This BRI 2 accumulation may be associated with disruption of axoplasmic transport by the presence of abnormal tau near amyloid deposits [34,50,51]. These globular processes have been shown to contain large numbers of clustered vesicles that can be labeled by Abs against pre-synaptic proteins [35,52]. Further studies will determine whether the large dystrophic processes identified by BRI 2 immunostaining also overlap with AbPP and ubiquitin immunoreactivity, and whether they play a role in neurodegeneration.
In AD, the relationship among amyloid deposition, NFT formation, and synaptic loss remains obscure [33][34][35][36]. Early loss of synaptic contacts has been associated with the initiation of cognitive decline, followed by neuritic damage, and neuronal cell loss [53], with loss of hippocampal synaptophysin correlating with cognitive decline in AD [34]. Synaptic and cognitive dysfunction have been documented in several transgenic models of AD before amyloid plaque formation occurs [54,55], suggesting that oligomeric forms of Ab may play a role in synapse loss in AD [56]. To characterize changes in synaptic integrity in Tg-FDD-Tau mice, we measured levels of the pre-synaptic marker synaptophysin in brains of WT, Tg-FDD, Tg-Tau and Tg-FDD-Tau mice. We observed that at 6 months of age, brain synaptophysin levels were significantly decreased in Tg-FDD-Tau mice compared with control and single transgenic mice, while synaptophysin levels of Tg-FDD and Tg-Tau mice were not significantly different from those of age-matched non-transgenic controls. As animal aged, synaptophysin levels of single Tg-FDD and Tg-Tau mice also decreased significantly from those of age-matched non-transgenic controls. Together, these results show an age-dependent synaptic degeneration occurring in single Danish and tau transgenic mice that is particularly significant in double Tg-FDD-Tau mice, where the presence of the Danish mutant form of BRI 2 and the P301S mutant form of tau lead to an earlier and more severe loss of synaptophysin. The loss of synaptophysin in Tg-FDD-Tau mice occurs before amyloid plaques can be detected and significant tau pathology is present. Oligomeric forms of ADan, which were described in single Tg-FDD mice [23], may directly or indirectly interact with mutant tau leading to a reduction of tau binding to microtubules and consequent impairment in transport [48], and perhaps to BRI 2 accumulation in DNs. Several studies using animal models have shown that tau plays an important role in synaptic loss and synaptic dysfunction, with synaptic dysfunction appearing before the formation of NFTs, possibly involving oligomeric forms of tau [43,57]. In addition, Tg-FDD and Tg-FDD-Tau mice show an abnormal processing pattern of BRI 2 , with accumulation of immature mutant BRI 2 . Abnormal processing of BRI 2 can lead to a decrease in m-BRI 2 levels and accumulation of murine amyloid b precursor protein (Abpp) Cterminal fragments [58], which together with mutant tau may cause synaptic dysfunction in Tg-FDD-Tau mice, independent of the presence of ADan oligomers. Work done using knock-in mice with the Danish mutation (FDD-KI) and the British mutation (FBD-KI) in the murine Bri 2 gene, and with mice with a knock-out of one allele of murine Bri 2 (Bri 2 +/2 ) has shown that these mice exhibit abnormal synaptic plasticity and memory deficits that is independent of the presence of the amyloid peptides [31,[59][60][61]. The finding of a reduction of m-Bri 2 in synaptic membranes of FDD KI/+ mice in the absence of ADan and tau deposition is consistent with the hypothesis that FDD may begin as a synaptic disease, associated with a Bri 2 loss of function [31].
In summary, this study has shown the interrelationship between ADan (and BRI 2 ) and cytoskeletal changes that may be at play in FDD. Importantly, we observed enhanced tauopathy, tau truncation, and synaptic loss prior to ADan deposition in the brain of Tg-FDD-Tau mice. This model recapitulates major pathologic characteristics of FDD and may be particularly useful to study early stages of FDD by providing evidence supporting a role for plaque-independent amyloid toxicity in the pathogenesis of FDD. Figure S1 Multiplex RT-PCR expression analysis of tau transgene expression. Bar graphs depict differential tau transgene expression levels between Tg-Tau (Tau, n = 5) and Tg-FDD-Tau (2x, n = 6) mice at 6 months of age. Multiplex RT-PCR analysis was performed on mRNA isolated from the hippocampus (A) and from the neocortex (B). Analysis was performed in triplicate and normalized to the Polr2a gene. Group averages are reported as relative mRNA levels (means6sem). No significant expression differences were found by 2-tailed t test. (EPS) Figure S2 Analysis of inflammatory changes by multiplex RT-PCR expression analysis. Bar graphs depict relative expression levels in wild-type (WT, n = 6) and Tg-FDD-Tau (2x, n = 6) mice at 9 months of age. A significant increase in the expression levels of GFAP in Tg-FDD-Tau mice compared to WT mice is observed in the hippocampus (A) and in the neocortex (B). The expression of the complement protein C1q (C), the proinflammatory chemokines macrophage inflammatory protein-1a (Mip1-a or Ccl3) (D) and Ccl5/RANTES (E), and the microglial-specific ionized calcium binding adapter molecule 1 (Iba1) (F) were also significantly increased in Tg-FDD-Tau mice compared to WT mice. Multiplex RT-PCR analysis was performed on mRNA isolated from the hippocampus (A, C-F) and from the neocortex (B). Analysis was performed in triplicate and normalized to the Polr2a gene. Group averages are reported as relative mRNA levels (means6sem). Significant expression differences were found by 2tailed t test. (EPS) Figure S3 Neuropathologic examination of transgenic mice expressing the P301S mutation (Tg-Tau). ThS-fluorescent (A) and argentophilic (B) deposits in neurons of the frontal and temporal lobes, hippocampus, piriform cortex, brain stem and spinal cord. Neurons of the temporal cortex show argentophilia in the perikaryon extending into cell processes (B). Phosphorylationdependent anti-tau Abs showed the presence of tau-immunopositive deposits in both nerve (C, neurons of the frontal cortex) and glial (D, oligodendroglial cells of the white matter; E, astrocytes) cells in several areas of the central nervous system with deposition beginning in the temporal lobe, amygdala and hypothalamus. At the age of 5-14 months, tau positive inclusions were observed in the cingulate, somatosensory, motor, and entorhinal cortices as well as the hippocampus, caudate nucleus, putamen, cerebellum, midbrain, pons, medulla, and the anterior and posterior gray horns of the spinal cord (F, hippocampus; G, temporal cortex). Neuronal loss was observed in the temporal lobe, amygdala and hippocampal pyramidal layer. Sections were from a 10 month old homozygous female (A, B)