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The age-related pathological cascade underlying intraneuronal tau formation in 3xTg-AD mice, which harbor the human APPSwe, PS1M126V , and TauP301L gene mutations, remains unclear. At 3 weeks of age, AT180, Alz50, MC1, AT8, and PHF-1 intraneuronal immunoreactivity appeared in the amygdala and hippocampus and at later ages in the cortex of 3xTg-AD mice. AT8 and PHF-1 staining was fixation dependent in young mutant mice. 6E10 staining was seen at all ages. Fluorescent immunomicroscopy revealed CA1 neurons dual stained for 6E10 and Alz50 and single Alz50 immunoreactive neurons in the subiculum at 3 weeks and continuing to 20 months. Although electron microscopy confirmed intraneuronal cytoplasmic Alz50, AT8, and 6E10 reaction product in younger 3xTg-AD mice, straight filaments appeared at 23 months of age in female mice. The present data suggest that other age-related biochemical mechanisms in addition to early intraneuronal accumulation of 6E10 and tau underlie the formation of tau filaments in 3xTg-AD mice.
During the last several years numerous transgenic animal models of Alzheimer's disease (AD) have been engineered to examine the effects of the two major AD neuropathological hallmarks, amyloid plaques, and neurofibrillary tangles (NFT) on neurodegeneration. The vast majority of these AD transgenic mice overexpress a mutant human amyloid-beta (Aβ) precursor protein (APP) gene alone or in combination with a mutated presenilin (PS) gene resulting in the presence of brain extracellular amyloid plaques, which are mainly formed by the accumulation of insoluble Aβ species [1–6]. Since overexpression of amyloid-beta peptide did not recapitulate all of the neuropathological features of AD, additional models were created adding mutant tau transgenes. For example, to further evaluate the pathogenic mechanisms underlying NFT formation, transgenic mouse models have been generated to harbor a mutant human tau gene found in frontotemporal dementia or Pick's disease (P301L or P301S). These mutant mouse models display NFT-like structures consisting of abnormal cytoskeletal tau protein aggregates in the central and peripheral nervous systems [4, 7–10]. Recently, a triple transgenic mouse (3xTg-AD) harboring the human APPSwe, PS1M146V, and TauP301L gene mutations was developed, displaying accumulation of both intracellular Aβand tau in an age-dependent manner within the cortex, hippocampus, and amygdala [11–14], and to a lesser degree, in the brainstem .
Immunohistochemical studies using immersion-fixed 3xTg-AD mouse tissue have shown that intracellular Aβprecedes the appearance of tau pathology, developing Aβ deposits at 6 months and intraneuronal tau pathology at 9 months of age [11, 12, 14]. Recent reports have demonstrated that the development of Aβ plaques differed between 3xTg-AD mouse colonies as well as between male and female mice [16, 17]. Furthermore, rostral-caudal differences in the onset of tau pathology have been reported, but only in male 3xTg-AD mice . Virtually no ultrastructural analysis of AD pathology in these mice has been described.
Therefore, in the present study we performed a systematic detailed evaluation of the evolution of tau conformation and phosphorylation events beginning at 3 weeks of age using perfusion-fixed tissue at the light and electron microscopic level to more completely define the cascade of amyloid and tau pathology in male and female 3xTg-AD mice. The data derived from this study provide novel information underlying the temporal progression of amyloid and tau pathology within the cortex, hippocampal/subicular complex, and the amygdala that is pivotal in determining the selective vulnerability of neurons during the life span of male and female 3xTg-AD mice. This data is critical for the design of future experiments to address pharmacological, mechanistic, behavioral, and gender questions in studies using this widely used mouse model of AD.
A colony of homozygous 3xTg-AD and nontransgenic (ntg) mice were generated from breeding pairs provided by Dr. Frank LaFerla, University of California Irvine. These transgenic mice harboring the human APPSwe, PS1M146V, and TauP301L mutations exhibit intraneuronal and extracellular amyloid pathology as well as tau pathology . At least 4 male and 4 female juvenile (3 weeks), young (2-3 months), adult (4–6 months), middle-aged (8-9 months), and old (18–20 months) 3xTg-AD and non-transgenic (ntg) mice were examined. In addition young, middle-aged and old female 3xTg-AD mice were used for electron microscopic examination. Animal care and procedures were conducted according to the National Institutes of Health Guide for Care and Use of Laboratory Animals.
Mice were anesthetized with an injection of ketamine/xylazine (100mg/kg/5.0mg/kg) and transcardially perfused for 2minutes with 0.9% physiological saline followed by a solution containing 4% paraformaldehyde and 0.1% glutaraldehyde in 0.1M phosphate buffer (PB) for 5minutes (~50ml) and then post-fixed in the same solution for 24hours at 4°C. Since many transgenic mice studies use immersion-fixed brain tissue and considering that tau antigenicity is time and fixation sensitive [18–26], another group of mice was transcardially perfused with physiological saline and their brains hemisected and immersion-fixed for 24hours in the same fixation solution. All brains were cryoprotected in 30% sucrose, sectioned on a sliding microtome at 40micron thickness, and stored in a solution consisting of 30% glycerin, 30% ethylene glycol, in 0.1M phosphate buffer at −20°C until processed for immunohistochemistry.
Tissues from immersion or perfusion fixed brains were processed as free-floating sections and immunostained for anti-hAPP/Aβ reactive amino acid residue 1–17 of beta-amyloid (6E10; 1:2,000 dilution, Covance, N.J.), the tau conformational antibodies Alz50 (66kD), MC1 (66kD) (1:10,000, 1:250 dilution, resp., both gifts from Dr. Peter Davies, Albert Einstein School of Medicine, N.Y.), and the phosphoepitope tau antibodies AT180 (~66 kD), AT8 (~66 kD) (both at 1:1000 dilution, Thermofisher, Waltham, MA) and PHF-1(57–67 kD) (1:10000 dilution; gift from Dr. Peter Davies, Albert Einstein College of Medicine) at each age examined. The specificity of each of the antibodies used in this study was previously characterized by western blot by others (6E10 (Covance), AT180 [27, 28], AT8 , PHF-1 [30–32], Alz50 [33–36], and MC1 [34, 35]). Prior to staining, sections were washed 3 × 10min in phosphate buffer and 3 × 10min in Tris-buffered saline (TBS) to remove cryoprotectant before a 20-minute incubation in 0.1M sodium metaperiodate (Sigma, St. Louis, MO) in TBS to quench endogenous peroxidase activity. Tissue was then permeablized 3 × 10minutes in TBS containing 0.25% Triton-X (Thermofisher, Waltham, MA) and blocked in the same solution containing 3% goat serum for 1hour. Sections were incubated with appropriate antibody dilutions overnight on an orbital shaker at 45 RPM at room temperature in 0.25% Triton X-100, 1% goat serum solution. The next day, tissue was washed 3 × 10min in TBS containing 1% goat serum prior to incubation with appropriate secondary antibody (see Table 1) at a 1:200 dilution for 1hr. Following 3 × 10minutes washes in TBS, sections were incubated in Vectastain ABC kit (Vector Labs, Burlingame, CA) in TBS for 1hour. Tissue was then rinsed 3 × 10minutes in 0.2M sodium acetate, 1.0M imidazol buffer, pH 7.4, and developed in acetate-imidazol buffer containing 0.05% 3,3'-diaminobenzidine tetrahydrochloride (DAB, Sigma, St Louis, MO). For comparison across ages sections from animals of different ages were immunostained at the same time and with the same duration of DAB reaction. The reaction was terminated in acetate-imidazol buffer, tissue mounted on glass slides, dehydrated through graded alcohols (70–95–100%, 3 × 5min), cleared in xylenes (3 × 5min), and coverslipped with DPX (Biochemica Fluka, Switzerland). Cytochemical control sections consisted of (1) tissue from ntg mice which were processed in a manner identical to the immunohistochemical procedures described above for 3xTg-AD animals, (2) tissue from 3xTg-AD as previously described with the exception of the primary antibody, and (3) a preadsorption control consisting of a 100 fold amount of Aβ 1-42 (US Peptides, Rancho Cucamonga, CA) incubated with 6E10 in TBS containing 0.25% Triton X-100, 1% goat serum overnight at room temperature. The preadsorbed serum was used in place of the 6E10 antibody in the immunohistochemistry protocol. Since the antigen used to create the tau monoclonal antibodies obtained from commercial sources was unavailable, only the 6E10 preadsorbtion control was performed. Brightfield images were acquired using a Nikon Optiphot microscope.
Selected sections were fluorescently double-labeled for 6E10 and Alz50 using the above protocol with the following modifications . All steps prior to incubation of primary antibody were as described above with the exclusion of the quenching of endogenous peroxidase activity with 0.1M sodium metaperiodate. Tissue was incubated with primary antibody overnight (6E10; 1:200 dilution). After rinsing 3 × 10minutes in TBS, tissue was incubated with Cy3-conjugated goat antimouse IgG Fcγ Subclass 1 specific secondary antibody (Jackson Immunoresearch; West Grove, PA) for 2hours in the dark. Sections were washed 3 × 10 minutes in TBS and then incubated with Alz50 (1:1000) overnight in the dark. Tissue was again rinsed 3 × 10minutes and then incubated in Cy2-conjugated goat antimouse IgM μ-chain specific secondary antibody (1:200 dilution) for 2hours in the dark. Immunofluorescence was visualized using a Zeiss Axioplan 2 microscope using excitation filters at wavelengths 489 and 555nm and emission filters at 505 and 570nm for Cy2 and Cy3, respectively. Florescent images were stored on a computer and brightness and contrast was enhanced using GIMP Version 2.6.7. Double immunofluorescence staining for 6E10 and phosphotau markers were not successfully achieved using methods to block the cross reactivity between monoclonal IgG1 subclass primary antibodies (see Table 1).
To determine ultrastructural localization of intraneuronal Aβ and tau immunoreactivity, we performed an immunoelectron microscopic analysis of hippocampal/subicular neurons obtained from female homozygous at 2- (n = 2), 9- (n = 2), and 23- (n = 2) month-old 3xTg-AD mice. Each animal was transcardially perfused with 4% paraformaldehyde/0.1% glutaraldehyde in phosphate buffer, brains were removed from the skull and immersion post-fixed in the same fixative overnight at 4°C and cut into 80micron thick horizontal sections using a Vibratome-1500 (Vibratome, Saint-Louis, MO). Tissue containing the hippocampal/subicular complex was immunostained using the antibodies directed against Aβ/APP (6E10, 1:2000 dilution), the conformation specific tau antibody Alz50 (1:10,000 dilution), and the phosphospecific (Ser202/Thr205) antibody AT8 (1:1000 dilution). The chromogen DAB was used to visualize each antibody.
Immunostained sections were post-fixed in 1% OsO4 for 45–60minutes, dehydrated and embedded in Epoxy resin. Immunoreactive profiles within the hippocampal/subicular complex were selected using light microscopy, ultrathin sections (50–70nm) were cut using a Leica Ultracut UCT (Leica Microsystems Inc, Bannockburn, IL) microtome, and the majority of sections counter-stained with 2% uranyl acetate and lead citrate. TEM sections were viewed and photographed with a JEOL transmission electron microscope. Immunostaining appeared as an electron-dense precipitate (dark-black) in neurons and other profiles within hippocampal-subicular complex of mutant mice. Cortical brain tissue obtained at autopsy from an 82-year-old male AD patient was immersion fixed in 4% paraformaldehyde and processed for TEM without antibody staining to compare the ultrastructure of human AD pathology to that found in 3xTg-AD mice.
In the present study forebrain sections from male and female 3-week, 2–4, 5-6, 8-9, and 18–20-month-old 3xTg-AD and age-matched ntg mice were immunostained using well-characterized antibodies directed against 6E10, tau conformational epitopes (Alz50 and MC1), and phosphotau epitopes AT180 (phosphothreonine 231), AT8 (phosphoserine 202/205), and PHF-1 (phosphoserine 396/404). In general, an age-related increase in intraneuronal and neuropil immunoreactivity in the hippocampal-subicular complex and amygdala were seen for all antibodies examined (Figure 1). The exception was MC1, where immunoreactivity decreased after 2–4 months of age (see Figure 6). Our findings revealed that transcardial but not immersion fixation dramatically enhanced the immunovisualization of AT8 (Figures 1(e)–1(h)) and PHF-1 (Figures 1(f)–1(l)) as early as 3 weeks of age. By contrast, AT180 and Alz50 immunoreactivity was not affected by the fixation procedure. Therefore all morphological analyses and photomicrographs subsequent to Figure 1 were derived from transcardially fixed tissue. The colocalization of 6E10 and tau antibodies using fluorescence was achieved successfully for 6E10 (IgG1) and Alz50 (IgM), but not for 6E10 and AT180 (IgG1) or AT8 (IgG1) due to the cross reactivity of their primary antibodies. Therefore, the comparative analyses of the distribution of 6E10 and phosphotau markers were performed using DAB-reacted tissue sections at the light microscopic level. All immunohistochemical controls failed to display cellular or plaque reactivity beyond background levels for any tau antigen or 6E10 independent of fixation, age, and gender.
The 6E10 antibody, which recognizes amino acids 3–8 of the Aβ sequence, revealed the greatest number and topographic distribution of immunoreactive (-ir) neurons in 3xTg-AD mice compared to the other antibodies we examined. There was an age-related increase in the extent of 6E10-ir neurons in all regions examined (Figure 2). Beginning at 3 weeks of age, intraneuronal 6E10-ir neurons were found in lamina 3 and 5 of the fronto-parietal cortex, deep layers of the cingulate cortex, CA fields of the hippocampus, subiculum, and the basolateral amygdala (BLA) in 3xTg-AD mice at each age independent of gender (Figure 2). 6E10-ir neurons, particularly in the hippocampal CA1 subfield, appeared round or oval in shape with many cells showing a thin ring of immunoreactivity located within the somatodendritic compartment (Figures 3(a), 3(d), and 3(g)). However, a number of cells in the cortex and amygdala had thickened perinuclear staining (Figures 3(d) and 3(a)), which became more prominent by 9 months of age (Figure 3(b) and 3(h)). Beginning at 9 months of age there was neuronal shrinkage of 6E10-ir neurons in 3xTg-AD mice (Figures 3(b), 3(e), and 3(h)), which continued at least until 18–20 months of age where many neurons displayed blunted dendrites, as well.
Although no dramatic gender differences in intraneuronal 6E10 staining were seen prior to 8-9 months, Aβ plaque deposits were visualized for the first time in the subiculum of 8-9-month-old female, but not male mutant mice (data not shown). By 18–20 months both genders displayed Aβ plaque deposits in the subiculum (Figures 3(j), 3(k), 3(m), and 3(n)) and hippocampus (data not shown). Aβ plaques appeared smaller and more diffuse in male than seen in the female subiculum of 3xTg-AD mice (Figures 3(j) and 3(k)). In fact, female CA1 neurons lost their dendritic 6E10-ir extensions into the substantia radiatum (Figure 3(o)) while similar processes remained present in male mutant mice (Figures 3(l) and 3(o)).
The Alz50 antibody recognizes an early stage conformational tau epitope that labels neurons undergoing early degenerative events associated with NFT formation but has also been shown to label neurons in normal brains [33–37]. Similar to 6E10 staining, the number of Alz50-ir neurons increased with age in all regions examined (Figure 4). As early as 3 weeks of age Alz50-ir staining was seen predominantly within the more caudal and ventral aspects of the hippocampal CA1 pyramidal and subicular neurons, whereas a few scattered Alz50-ir neurons were found in the neocortex and BLA (Figures 4(a)–4(d)). In addition, Alz50-ir neurons were also found in the septal but not temporal portions of the hippocampal formation (data not shown). Beginning at 2–4 months of age a few scattered Alz50-ir neurons were found in layers 3 and 5 of the fronto-parietal and the deep layers of the cingulate and retrosplenial cortex in 3xTg-AD mice (Figures 4(e)–4(h)). By 5-6 months of age there was an apparent increase in the number of Alz50-ir neurons in the ventral hippocampus and amygdala (Figures 4(i)-4(l)), as well as more intense neuropil staining (Figures 1(q) and 1(r)). However, unlike the continuous distribution of 6E10-ir pyramidal neurons in the hippocampal complex, the topographic distribution of labeled Alz50-ir CA1 pyramidal neurons spread in dorsal and anterior directions from the ventral and caudal regions of the brain (Figure 4). At 3 weeks of age Alz50-ir neurons in the cortex, hippocampus, and amygdala appeared round or oval and displayed a dense rim of perinuclear staining (Figures 5(a), 5(d), and 5(g)) with long dendrites extending into the neuropil. At 9 months of age many Alz50-ir neurons appeared shrunken with a distorted cellular morphology in the hippocampal complex and amygdala (Figures 5(e) and 5(h)). Interestingly, some cells no longer displayed perinuclear staining but became completely filled with Alz50 reaction product (Figure 5(h)) or were dystrophic (data not shown). While the presence of Alz50-ir dystrophic neurites appeared concomitantly with the onset of Aβ plaque deposition between 8 and 9 months of age in female mutant mice, dramatic differences between male and female Alz50 staining were only apparent by 18–20 months of age. The dorsal and anterior subicular region adjacent to the CA1 neurons was most affected with Alz50-ir dystrophic neurites in male and female 18–20-month-old 3xTg-AD mice (Figures 5(j) and 5(m)). In general, numerous large and globular dystrophic Alz50-ir neurites were seen surrounded by plaques in both male and female mice (Figures 5(m) and 5(n)). In female transgenic mice many plaques displayed a rim of dark Alz50-ir dystrophic neurites with a clear center (Figure 5(k)), while in males this neuritic organization was less obvious (Figure 5(n)). In addition, in 18–20-month-old female 3xTg-AD mice dark, swollen, Alz50-ir dystrophic neurons were found in abundance among more lightly stained CA1 pyramidal cells (Figures 5(m) and 5(o)). Furthermore, the amygdala displayed similar neuronal perinuclear staining in male and female transgenic mice with an occasional rim of Alz50-ir dystrophic neurites surrounding plaques only in female mutant mice (data not shown).
The MC1 antibody recognizes early stage conformational epitopes similar to Alz50 but does not react with normal neuronal tau [34, 35, 37]. In contrast to Alz50 staining, lightly stained MC1-ir neurons were found only in the CA1 pyramidal cells of the ventral hippocampus in 3-week-old 3xTg-AD mice (Figure 6(a)). By 2–4 months, lightly stained MC1-ir neurons were seen throughout the CA1 subfield of the ventral hippocampus (Figure 6(b)). A few darkly stained MC1 neurons were seen, some of which appeared shrunken with blunted dendrites within the hippocampus. On the other hand, no MC1-ir neurons were seen in the BLA at 3 weeks of age (Figure 6(d)). In 2–4-month-old mutant mice, scattered round-or-oval shaped lightly stained MC1-ir neurons were found embedded within the MC1 immuopositive neuropil of the BLA. Interestingly, MC1-ir neuropil and neuronal labeling decreased in the hippocampus and BLA in 8-9-month-old mutant mice (Figures 6(c) and 6(f)). MC1-ir profiles were not detected in the neo- and limbic cortex up to 9 months of age. By 18–20 months, MC1 labeling matched Alz50 immunoreactivity in male and female 3xTg-AD mice. Although plaque-like structures were hard to detect, globular MC1-ir dystrophic neurites and neurons were found mainly throughout the female subiculum (Figures 6(j), 6(k), and 6(l)). Some dystrophic neurons appeared to have eccentrically located dark cytoplasmic neuronal inclusions (Figures 6(i), 6(k), and 6(l)).
Hyperphosphorylated microtubule-associated protein tau is the major component of the paired helical filament seen in the NFT. The monoclonal antibody AT8 marks tau phosphorylation at both serine 202 and threonine 205 . AT8-ir neurons were found in the neocortex, amygdala, and hippocampal formation in both male and female 3xTg-AD mice at all ages examined (Figure 7). Like the distribution of Alz50-ir neurons, hippocampal and subicular regions contained the highest number of AT8-ir neurons compared to the cortex and amygdala in 3-week-old 3xTg-AD mice (Figures 7(a)–7(d)). A few AT8-ir neurons were observed in layer 5 of the fronto-parietal cortex and BLA (Figures 7(a)–7(c)). As mutant mice age, the extent of neuronal AT8 labeling in the hippocampal complex increased in a ventral to dorsal and posterior to anterior gradient (Figures 7(e)–7(l)), but unlike the Alz50-ir profiles at 5-6 months of age, anterior portions of the hippocampal complex did not appear to be affected (Figures 7(c), 7(g), and 7(k)). At 3 weeks of age, AT8-ir neurons displayed more diffuse cytoplasmic staining in the cortex, hippocampus, and BLA (Figures 8(a), 8(d), and 8(g)), rather than the dense perinuclear staining observed in Alz50-ir neurons in these regions. However by 9 months of age AT8-ir neurons appeared shrunken, distorted, and showed thicker perinuclear staining, especially in the amygdala (Figures 8(b), 8(e), and 8(h)). Some neurons in the hippocampus (Figure 8(e)), BLA (Figure 8(h)), and subiculum displayed blunted AT8-ir dendrites. AT8 dystrophic neurons were more abundant in the female subiculum and constituted the greatest difference between male and female pathology at 18–20 months of age (Figures 8(j)–8(o)). While the entire extent of the female subiculum showed numerous AT8-ir dystrophic neurites, the male subiculum contained less neuritic dystrophy (Figure 8(j) versus Figure 8(m)). AT8-ir pyramidal cells displayed an asymmetric accumulation of dense perinuclear staining (Figures 8(k) and 8(o)), and AT8-ir dystrophic neurites were associated with plaques (Figures 8(l), 8(n)).
AT180 detects tau phosphorylation at the Thr231 site, an early event in the assembly of tau into filaments [27, 28]. AT180-ir neurons displayed the greatest number and spatial distribution of all tau antibodies examined at 3 weeks of age in 3xTg-AD mice. AT180-ir neurons were found in layer 5 of the fronto-parietal cortex, BLA, CA1 ventral hippocampus, and subiculum (Figures 9(a), 9(d), and 9(g)). Qualitatively there was an age-related increase in the number of AT180-ir neurons within each brain region examined as well as in the intensity of neuropil staining in the ventral hippocampus and BLA (Figures 1(s)–1(x)). At 3 weeks of age AT180 immunostaining appeared as diffuse cytoplasmic reactivity in round or oval pyramidal cells of the neocortex, hippocampus (Figure 9(a) and 9(d)) and BLA (Figure 9(g)) in 3xTg-AD mice. Some neurons embedded in the CA1 pyramidal cell layer, BLA, and subiculum displayed perinuclear staining (Figures 9(d) and 9(g)). By 9 months, AT180-ir hippocampal and BLA neurons revealed blunted staining in dendrites (Figure 9(e)). In the BLA, a number of neurons exhibited thickened perinuclear staining (Figure 9(h)). Differences between male and female AT180 staining occurred in the hippocampal CA1 neurons and the subiculum at older ages. Specifically, at 18–20 months of age AT180-ir dystrophic neurites were more widespread within the subiculum in female compared to male 3xTg-AD mice (Figures 9(j) and 9(m)). However, in male mice, AT180-ir dystrophic pathology was mainly found in the subiculum closest to the border with the CA1 pyramidal cell layer. In addition, CA1 pyramidal neurons displayed a dense perinuclear staining and blunted dendrites (Figures 9(l) and 9(o)).
PHF-1 recognizes tau phosphorylated at serine residues 396 and 404 and is generally considered a late marker in the evolution of PHF positive NFTs [30–32]. At 3 weeks of age only a few lightly stained PHF-1-ir neurons were observed in the CA1 region of the ventral hippocampus and the BLA in perfusion fixed 3xTg-AD mice (Figures 10(d) and 10(g)). At 2-3 months, a few PHF-ir neurons were seen at the CA1/subicular interface of the dorsal hippocampus (data not shown). By 9 months, the number of PHF-1-ir ventral hippocampal CA1 pyramidal and BLA neurons increased (Figures 10(e) and 10(h)). The distribution of PHF-ir neurons in the hippocampal complex followed a ventral to dorsal gradient. Up to 9 months of age, an occasional PHF-1-ir neuron was visible in the neocortex (Figure 10(b)). PHF-1 dystrophic neurons and neurites were more prevalent in the subiculum of aged females (Figures 10(m) and 10(n)) compared to aged males (Figures 10(j) and 10(k)). PHF-1-ir CA1 neurons displayed distorted cellular morphology, with broken, asymmetric, but strongly stained perinuclear staining in the female subiculum (Figure 10(o)). In contrast, PHF-1-ir neurons in the male subiculum showed similarly stained dark neurons but retained somatodendritic staining (Figure 10(l)).
To evaluate whether neurons expressing 6E10 also contained tau epitopes we performed dual immunofluorescence and comparative light microscopic experiments on adjacent hippocampal subicular sections at 3-week, 9-, and 18–20-month old male and female 3xTg-AD mice. Although it would have been interesting to double stain for 6E10 and other tau makers (AT180 and AT8), all three antibodies are murine IgG1s. Therefore, dual immunofluorescence experiments were performed only for 6E10 and Alz50, an IgM. In these experiments we observed two bands of 6E10 immnoreactivity located within ventrally located within CA1 hippocampal and subiculum neurons of female mutant mice at all ages examined (Figures 11(a), 11(d), and 11(g)). By contrast, Alz50-ir neurons were only observed in the CA1 pyramidal cell layer, and as neuropil staining in the subiculum (Figures 11(b), 11(e), and 11(h)). In general, Alz50-ir neurons were found to be colocalized with 6E10-ir neurons at each age examined in the ventral hippocampus (Figures 11(c), 11(f), and 11(i)).
Because 6E10, AT180, or AT8 are all of the murine IgG1 subclass, adjacent sections through the CA1 and subicular fields were reacted with individual antibodies and visualized using peroxidase/DAB. In contrast to the single layer of Alz50-ir neurons in the CA1 pyramidal cell layer (Figures 12(b), 12(e), and 12(h)), numerous AT180, AT8, and 6E10 immunopositive neurons were seen in both CA1 and subicular fields in the ventral hippocampus at each age examined (Figure 12).
At the ultrastructural level, unstained tissue sections revealed plaques within the hippocampal/subicular complex that displayed numerous fibrillar branches, which were surrounded by dystrophic neurites in 9-month-old 3xTg-AD mice (Figure 13(a)). In 23-month-old female 3xTg-AD mice, the majority of neuritic plaques displayed a central core surrounded by many more fibrillar branches and dystrophic neurites, similar to that seen in human AD plaques (Figure 13(c)). The neuropil contained dystrophic neurites of different sizes displaying various accumulations of electron-dense cytoplasmic material, multilaminar, multivesiclular, and dense-core bodies in both 9-and 23-month-old 3xTg-AD mice (Figures 13(a) and 13(b)), similar to that seen in an AD plaque (Figure 13(d)). TEM analysis of intraneuronal 6E10 immunoreactivity revealed staining mainly confined to the periphery of the nucleus within CA1 hippocampal/subicular neurons in 2-month-old 3xTg-AD mice (Figure 14(a)). At 9 months of age this perinuclear 6E10 reaction product appeared more intense and extended into the cytoplasm (Figure 14(b)).
At the ultrastructural level, Alz50 and AT8-ir were seen in the soma and dendrites of CA1 neurons in female 2-month-old mutant mice (Figures 14(c) and 14(d)). Intraneuronal electron dense Alz50 and AT8-ir cytoplasmic staining was more widespread and increased in intensity in 9 month-old-mutant mice (Figures 14(e) and 14(f)). Interestingly, cytoplasmic Alz50-ir appeared more extensive than AT8 immunoreactivity in these neurons at both 2 and 9 months of age (Figures 14(c), 14(d), 14(e), and 14(f)). Despite the presence of AT8 and Alz50-ir cytoplasmic labeling within hippocampal/subicular CA1 neurons, TEM failed to reveal any type of filamentous aggregates in 2- or 9-month-old 3xTg-AD mice (Figures 14(c), 14(d), 14(e), 14(f), 14(l), and 14(m)). In contrast, at 23 months of age both male and female 3xTg-AD mice displayed Alz50 and AT8-ir straight filaments with a 19–20nm diameter within the hippocampal-subicular complex (Figures 14(i)–14(m)).
Previous studies have shown widespread amyloid but not tau pathology at 6 months of age in the hippocampus [3, 12, 13, 17], and behavioral studies using the Morris Water Maze have demonstrated memory retention deficits dependent upon the appearance of amyloid pathology at 6- but not 2-month-old 3xTg-AD mice . Our study found that (1) the appearance of 6E10 immunoreactivity was concomitant with conformation (Alz50 and MC1) and phosphorylation (AT8, AT180, and PHF-1) events in the neurons of the hippocampal-subicular complex and amygdala as early as 3 weeks of age; (2) the detection of the two phospho-epitopes AT8 and PHF-1 was fixation dependent at all ages; (3) the number of Aβ plaques, as well as neuritic and neuronal dystrophy, increased with age in the cortex, hippocampus, and subicular area in 3xTg-AD mice; (4) aged female mice displayed more plaque and tau pathology than aged male 3xTg-AD mice; a finally (5) straight tau filaments were found only in 23-month-old female 3xTg-AD mice.
In the present study, 6E10-ir neurons were seen as early as 3 weeks of age in lamina 3 and 5 of the fronto-parietal cortex, deep layers of the cingulate cortex, CA1 pyramidal neurons of the hippocampus, subiculum, and BLA in 3xTg-AD mice independent of gender. These data indicate that intraneuronal 6E10 immunoreactivity occurs extremely early in the development of these mice (3 weeks) and are in contrast to previous investigations showing that 6E10 intraneuronal staining occurred between 3 and 6 months of age in the hippocampus of these mice [12, 17]. Because the 6E10 epitope resides in amino acids 3–8 of the N-terminal portion of the Aβ sequence, it does not preclude binding to full length APP or its amyloidgenic derivatives. Consequently, the exact amyloid species revealed within neurons at 3 weeks of age in 3xTg-AD mice and at other ages examined is unclear. Oligomeric Aβ species may, in part, underlie cellular degeneration [3, 11, 38–48].
We also observed many shrunken 6E10-ir neurons beginning at 8-9 month of age in each brain area examined in both male and female 3xTg-AD mice. This phenotype was most pronounced in CA1 hippocampal neurons of older female 3xTg-AD mice. These neurons exhibited loss of dendritic 6E10 immunoreactivity when compared to CA1 neurons in male mutant mice. These gender differences in Aβ intraneuronal pathology lend support to prior investigations showing that female 3xTg-AD mice display earlier and more severe plaque pathology , which may be related to progesterone and estrogen-mediated signaling . However, other factors may contribute to the discrepancies in AD-like pathology reported in studies using different colonies of 3xTg-AD mice, including a loss of phenotype related to successive breeding, founder effects between colonies, or differential expression of transgenes . Together or separately, variations in transgenic animal strain or amyloid species may affect both pathological and behavioral observations reported in studies using 3xTg-AD mice.
Of interest was the observation that the immunohistochemical localization of phosphospecific tau proteins AT8 and PHF-1 was fixation dependent, whereas Alz50, MC1, AT180, and 6E10 immunoreactivity was fixation independent in young, juvenile, and middle age 3xTg-AD mice. Notably, neurons containing the phospho-epitope AT8 were seen in layer 5 of frontoparietal cortex, ventral hippocampal pyramidal, and amygdala neurons, whereas PHF-1-ir intraneuronal staining was seen only in the ventral hippocampus in perfusion-fixed 3-week-old 3xTg-AD mice. Previous biochemical and immunohistochemical studies indicate that fixative composition affects the ability to detect various cytoskeletal proteins [18, 22, 23]. The process of aldehyde fixation relies upon a slow cross-linking of carbonyl aldehyde to functional protein groups. While perfusion fixation rapidly exposes proteins to fixative through the vasculature, immersion fixation relies upon a slow 1mm per hour diffusion rate to penetrate tissue . It is possible during immersion fixation that proteolysis or dephosphorylation of the tau phospho-epitopes recognized by AT8 and PHF-1 occurs prior to the full penetration of the fixative. Since immersion-fixed tissue reacts with C-terminal, N-terminal, and internal tau antibodies, proteoloysis of tau is unlikely [25, 50]. A more plausible possibility is the destruction of AT8 and PHF-1 epitopes by the action of endogenous phosphatases during slow immersion fixation [51–53]. However, AT180 immunoreactivity remained robust even in immersion-fixed tissue. Likely, phosphatases act differentially depending on the individual tau phosphoepitopes ; hence, it is possible that the AT180 phospho-epitope is less sensitive to phosphatase activity than either AT8 or PHF-1 phosphorylation sites, resulting in a more robust staining in immersion-fixed tissue. Although long postmortem intervals reduce phospho-tau antigenicity due to active phosphatases, [19, 50, 55], this was not a confounding variable in the present study since all animals were sacrificed and perfused with fixative within 5 minutes of anesthetization. The potential effect of fixation on the immunolocalization of tau and other proteins  represents an important caveat that may provide an explanation for the underlying differences in tau antigenicity reported in previous studies using the 3xTg-AD mouse model [3, 12–14, 16, 57, 58].
Although a previous report described intraneuronal MC1-ir CA1 dorsal hippocampal neurons only in 12–15-month-old 3xTg-AD mice , the present study displayed weak MC1 immunoreactive neurons in the ventral hippocampus even as early as 3 weeks of age. We also observed Alz50 immunoreactive CA1 pyramidal and subicular neurons in the ventral aspect of the hippocampal/subicular complex at 3 weeks of age. Although both MC1 and Alz50 antibodies recognize similar epitopes, they are not identical. Overall, Alz50 immunoreactivity was much more intense and labeled a greater distribution of immunoreactive neurons than with the MC1 antibody. While Alz50 immunoreactivity increased in an age dependent manner in the neocortex, hippocampus, and amygdala, MC1 immunoreactivity exhibited a biphasic response, peaking initially between 2 and 4 months, declining at 9 months and then peaking again at 18–20 months in numerous swollen, tangle-like appearing CA1 hippocampal and subicular neurons. Interestingly, both MC1 and Alz50-ir neurons were found in the CA1 pyramidal but not the subicular cell layer in the ventral hippocampal formation at the ages examined suggesting that Alz50 is labeling similar populations of neurons.
Unlike previous studies where various phosphotau epitopes were immunohistochemically detectable by 15 months of age in 3xTg-AD mice [12, 17, 49], we observed tau-ir neurons primarily in the ventral CA1 hippocampal pyramidal and subicular neurons at 3-weeks of age. This occurred well before the onset of plaque deposition in 8-9-month-old 3xTg-AD mice . The current findings indicate that intraneuronal amyloid and tau co-occur or appear concurrent in the same neurons at least as early as 3 weeks of age suggesting that these mutant mice are born with the dual expression of these proteins within select populations of brain cells. The early appearance of tau-ir neurons in the forebrain of 3xTg-AD mice is not surprising since overexpression of mutant P301L four repeat tau and the APPswe amyloid mutation together  or tau P301L alone  induces an age dependent onset of MC1, AT8, and PHF-ir neurofibrillary tangles (NFTs) in the telencephalon of mutant mice as young as 2.5 months of age .
However, it remains to be determined whether amyloid interacts with tau over time to induce the apparent age-related perikaryal degeneration seen in these mice. Studies are underway to test the hypothesis that depletion of intraneuronal amyloid at an early age would prevent or slow the degeneration of neurons in these mice. It is interesting to note that tau containing straight filaments were seen in 18–20-month-old mutant mice suggesting that late-stage tau neuronal aggregation also plays a key role in the ultimate demise of neurons in 3xTg-AD mice. Although no studies to date have shown frank neuronal cell loss, a recent report described a reduction in the number of neurons containing 6E10 and tau markers in the brainstem of these mutant mice .
To more fully understand the vulnerability of hippocampal complex neurons, we colocalized 6E10 and Alz50 using immunofluorescence. A previous study colocalized HT7, a human specific pan tau antibody and M71/3 (oligomeric Aβ) in the dorsal hippocampus in 3xTg-AD mice . However, at earlier ages conformation or phosphospecific tau antibodies were not evaluated. Our immunofluorescence colocalization experiments demonstrated that virtually all ventral CA1 pyramidal but not all subicular neurons contained both Alz50 and 6E10 from 3 weeks to at least 18–20 months of age, suggesting that CA1 neurons are more vulnerable to Alz50 pathology. Although we were unable to perform colocalization experiments between 6E10 and our tau antibodies, we performed a comparative light microscopic analysis of adjacent hippocampal sections. This study revealed AT180 and AT8-ir neurons in the caudal aspects of the subicular region where we failed to visualize Alz50-ir neurons across all ages examined. The reason for the selective appearance of AT180 and AT8 in the ventral subiculum remains unknown. One possibility is that neurofibrillary pathology proceeds according to a sequence of tau conformational and phosphorylation events [61–64], which may vary between neuronal populations. In AD, as tau transitions to a more hyperphosphorylated state, it undergoes a self-assembly process forming PHF structures reducing the microtubule stability of the neuronal cytoskeleton [65, 66]. More specifically, the evolution of NFTs in AD follows a progression of phosphorylated tau modifications from TG3 (phosphospecific at Thr231), found in preneurofibrillary tangles (preNFTs), to AT8 and PHF-1 in intraneuronal and extraneuronal NFTs . This progression may be dynamic since intraneuronal AT180 and AT8 precedes Alz50 tau formation before the appearance of fibrillar tau [63, 64]. We suggest that the sequence of cellular tau conformation and phosphorylation events may also be dynamic in 3xTg-AD mice since Alz50-ir neurons were found only in CA1 neurons in the hippocampus but not in the underlying subiculum.
Despite differences in tau intraneuronal epitope expression, we found age-related changes in neuronal morphology in the 3xTg-AD mouse to be similar to the NFT neuronal phenotypes described in the human AD brain [67, 68]. Some AT8-ir neurons at 9 months of age displayed blunted dendrites (see Figure 8(e)) or tortuous proximal dendrites and thickened perinuclear staining reminiscent of Braak type 2 neurons . In our aged mutant mice, proximal and distal dendrites lost AT8 immunoreactivity and neurons appeared more globose and dystrophic similar to Braak type 3 neurons, which accumulate fibrillar material in the human AD brain . Furthermore, the present ultrastructural analysis revealed, for the first time, the presence of AT8 and Alz50 positive straight tau filamentous aggregates in female aged 23-month-old, but not in young or middle-age 3xTg-AD mice of the same gender, which are similar to those seen in tangle bearing neurons in the human AD brain. Similar tau filaments have been described in single transgenic mice overexpressing the mutant P301L human tau gene [10, 59] as well as in the double mutant (TAPP) mouse expressing APPswe and P301L mutant forms of tau . NFT formation was enhanced in young and middle age TAPP mutant mice with respect to single tau transgenic mice . Although young and middle-aged 3xTg-AD mice carry the same APPswe, and TauP301L mutations as the TAPP mouse, 3xTg-AD mice did not accumulate filamentous aggregates at younger ages. In this regard, mice overexpressing human genomic and cDNA tau genes also do not display intraneuronal filamentous structures at young ages . These findings suggest that factors other than the accumulation of tau underlie the filamentous tangle bearing phenotype seen in human AD. Factors that may influence the formation of AD filaments include differences in the abundance or ratio of specific tau isotypes  in different cohorts of neurons and/or minor alterations in proteases, kinases, phosphatases that alter the structure of these proteins during the life span of the neuron , and/or the promoter system designed for specific transgene expression in particular brain regions. Since age is a major risk factor for AD, aging itself may be a crucial variable in the formation of intraneuronal filaments in 3xTg-AD mice. Despite differences in the evolution of tau biochemistry, there are morphological similarities between neurons containing tau in 3xTg-AD mice and human AD indicating the usefulness of these mice for studies of the mechanism(s) underlying select aspects of AD pathology.
This work is supported in part by AG10688 (EJM), AG014449 (LIB), Shapiro Foundation (EJM), and Rush University Medical Center Research Council (SEP). The authors thank Linda Juarez for her excellent electron microscopic work.