CNS-Wide over Expression of Fractalkine Improves Cognitive Functioning in a Tauopathy Model
Accumulating evidence increasingly implicates regulation of neuroinflammation as a potential therapeutic target in Alzheimer’s disease and other neurodegenerative disorders. Fractalkine (FKN) is a unique chemokine that is expressed and secreted by neurons and reduces expression of pro-inflammatory genes. To further demonstrate the utility of agents that increase FKN signaling throughout the central nervous system as possible therapies for AD, we assessed the impact of soluble FKN (sFKN) over expression on cognition in tau depositing rTg450 mice after the onset of cognitive deficits. Using adeno-associated virus serotype 4, we infected cells lining the ventricular system with soluble FKN to increase FKN signaling over a larger fraction of the brain than achieved with intraparenchymal injections. We found that soluble FKN over expression by cells lining the ventricles significantly improved cognitive performance on the novel mouse recognition and radial arm water maze tasks. These benefits were achieved without detectable reductions in tau hyperphosphorylation, hippocampal atrophy, or microglial CD45 expression. Utilizing qPCR, we report a significant increase in Vegfa expression, indicating an increase in trophic support and possible neovascularization in AAV-sFKN-injected mice. To our knowledge, this is the first demonstration that FKN over expression can rescue cognitive function in a tau depositing mouse line.
KeywordsAlzheimer’s disease Tauopathy Fractalkine CX3CL1 Microglia
Fractalkine (CX3CL1; FKN) is unique among chemokines because it is the only member of the CX3C motif family and has a one-to-one relationship with its receptor, CX3CR1 (Bazan et al. 1997; Imai et al. 1997; Pan et al. 1997). Produced as a transmembrane protein, FKN can undergo proteolytic cleavage by a disintegrin and metalloprotease (ADAM) 10/17 or cathepsin S to produce a secreted, soluble form of the protein (sFKN) (Garton et al. 2001; Hundhausen et al. 2003; Jones et al. 2013). There is evidence that the membrane-associated (full-length) and ectodomain (soluble) forms of FKN may have different functional roles and activate the receptor differently (Clark and Malcangio 2012; Kim et al. 2011). In the periphery, the full-length form is important for monocyte adhesion to endothelial cells while the soluble form may act as a chemoattractant for lymphocytes and monocytes (Imai et al. 1997). In the central nervous system (CNS), FKN is produced by neurons and its receptor is expressed only on microglia (Cardona et al. 2006; Harrison et al. 1998). FKN signaling in the CNS blunts microglial activation, reducing production of pro-inflammatory cytokines such as interleukin (IL)-1β, IL-6 and tumor necrosis factor-α (Lyons et al. 2009).
Fractalkine’s role in neurodegenerative diseases has been of considerable interest in the last few years. Initial work disrupting FKN signaling in animal models (receptor or ligand knockouts) demonstrated increased Parkinson’s disease pathology, tauopathy, and amyotrophic lateral sclerosis (Bhaskar et al. 2010; Cardona et al. 2006), suggesting that dysregulation of microglial activation can result in worsening of disease pathology and neurodegeneration. However, disrupting FKN signaling in amyloid-depositing mice showed amelioration of the pathology due to increased microglial phagocytosis of the extracellular amyloid plaques (Lee et al. 2010b). Conversely, studies investigating the over expression of FKN showed opposite results to disruptions in signaling, generally leading to favorable improvements in disease pathology. The soluble form of FKN was shown to be beneficial in multiple models of Parkinson’s disease (Morganti et al. 2012; Nash et al. 2015; Pabon et al. 2011). In Alzheimer’s disease, we reported that adeno-associated virus (AAV) over expression of sFKN in the hippocampus of the rTg4510 mouse model of tauopathy resulted in reduced tau pathology, amelioration of neuron loss, and reduction of microgliosis. However, there was no improvement in cognitive performance after sFKN over expression, which may be attributed to the limited distribution of the treatment which was targeted to the dentate gyrus of the hippocampus (Nash et al. 2013).
Here, we further investigate the therapeutic ability of sFKN by addressing two questions: does a more global distribution of CNS sFKN expression have a greater cognitive impact and can increased sFKN expression have an impact in animals that already have advanced tau pathology? The latter would be more clinically informative because most AD patients would have significant tau pathology at the time of their diagnosis. To achieve this, we used a novel delivery method into five-month old rTg4510 animals, which present with insoluble tau and cognitive deficits (Dickey et al. 2009; Santacruz et al. 2005). We utilized the unique capability of AAV serotype 4 to infect cells lining the ventricular system, combined with the soluble nature of our therapeutic gene product, to distribute sFKN to the CNS via secretion into the CSF. This has been achieved with other secreted proteins (Davidson et al. 2000b; Liu et al. 2005; Tenenbaum et al. 2004). We demonstrate here that elevated sFKN expression via AAV4, during late stage disease pathology, can partially rescue behavioral deficits but does not appear to alter disease progression.
Adeno-Associated Virus Production
The ectodomain (amino acids 1–336 containing the chemokine domain and mucin-like stalk) of mouse fractalkine was isolated from mouse cDNA and cloned into pTR2-MCS vector at the Age I and Nhe I sites as described previously (Morganti et al. 2012; Nash et al. 2013). This vector contained the AAV2 terminal repeats and hybrid cytomegalovirus-chicken β-actin (CBA) promoter. A C-terminal hemagglutinin (HA)-tag was added for protein detection. rAAV4 particles were generated as described previously (Carty et al. 2010) and quantified using a dot-blot method with a non-radioactive biotinylated probe for fractalkine generated by polymerase chain reaction (Burger and Nash 2016; Nash et al. 2013).
Transgenic Mice and Breeding
Animal experiments were conducted in accordance with the National Institute of Health Guide and Use of Laboratory Animals and were approved by the Institutional Animal Care and Use committee of the University of South Florida. Parental mutant tau and tetracycline-controlled transactivator protein strains were maintained separately and bred to produce rTg4510s and littermate nontransgenic (NonTg) and tetracycline-controlled transactivator protein (tTA) mice as previously described (Santacruz et al. 2005). Littermate tTA and NonTg mice were used as behavioral controls, as we observed modest differences in performance between tTA and NonTg mice. Study animals were given food and water ad libitum and maintained on a 12-h light/dark cycle.
Surgical Procedure and Tissue Collection
Immediately before surgery, mice were weighed and anesthetized with isoflurane. Surgeries were performed using a stereotaxic apparatus using convection enhanced delivery as described previously (Burger and Nash 2016; Carty et al. 2010; Nash and Gordon 2016). Animals receiving AAV4 sFKN (3.4 × 1012 vg/mL) were injected bilaterally into the lateral ventricles with 5 μL of virus in sterile PBS per site (coordinates from bregma: −0.4 mm anteroposterior, ±1.0 mm lateral, & -2.4 mm vertical). Control animals received AAV9 UF11 (5 × 1012 vg/mL) expressing green fluorescent protein (GFP) were injected as described previously (Carty et al. 2010).
Three months post-surgery, mice were weighed and overdosed with pentobarbital (200 mg/kg). CSF was collected as described (Liu and Duff 2008) and mice were perfused with 25 mL of 0.9% normal saline. Brains were collected immediately after perfusion. The right hemisphere was dissected and frozen on dry ice for biochemical analysis. The left hemisphere was immersion fixed in 4% paraformaldehyde for 24 h. The fixed hemisphere was cryoprotected with successive incubations in 10%, 20%, and 30% sucrose solutions for 24 h in each solution. Brains were frozen on a cold stage and sectioned horizontally (25 μm thick) on a sliding microtome and sections were stored in PBS with 10 mM sodium azide at 4 °C. For rTg4510 mice, every twelfth section was 50 μm.
Tissue Homogenization, ELISA, and Western Blotting
Anterior cortex and hippocampal samples were homogenized in TBS with protease inhibitor cocktail (Sigma Aldrich, St. Louis, MO, USA; Cat. No. P8340), phosphatase inhibitor cocktails II and III (Sigma Aldrich, St. Louis, MO, USA; Cat. Nos. P5726 & P0044, respectively), and Benzonase (Sigma Aldrich, St. Louis, MO, USA; 25 U/mL final concentration) at 10 vol/wt of tissue. Tissue was homogenized with a rotating pestle and briefly sonicated (3 × 3 s). The samples were centrifuged for 10 min at 10,000 x g at 4 °C. An aliquot (15 μL) of the resulting supernatant was taken for FKN ELISA. The pellet was resuspended in the remaining supernatant and detergents added to a final concentration of 0.01% SDS, 0.1% NP40, and 0.05% sodium deoxycholate. Samples were then centrifuged at 40,000 x g for 30 min at 4 °C. The resulting pellet was resuspended in 70% formic acid (2 μL/mg tissue) and incubated for 60 min at room temperature. An equal volume of 1 M Tris pH 7.5 was added and the sample was neutralized to pH 7.5 with NaOH if needed. The soluble fraction was taken for Western blotting and total protein concentration was determined by Pierce BCA protein assay (ThermoFisher Scientific, Walthman, MA, USA). For Western blotting, 1 μg of protein was loaded for each sample. H150 (total tau; Sigma), anti-phospho-Ser199/202 tau (pSer199/202, Anaspec, Fremont, CA, USA), and anti-phosphoSer396 tau (pSer396, Anaspec, Fremont, CA, USA) were used to assess tau pathology. All signals were normalized to β-actin (ThermoFisher Scientific, Walthman, MA, USA). For the insoluble fraction, which does not contain actin, an equal volume of each sample was loaded. A fractalkine ELISA was obtained from R&D Systems and the manufacturer’s protocol was followed.
All behavioral tasks were conducted by an observer blinded to treatment condition and genotype of the mice. The open field was used as a general measure of activity and anxiety. Animals were recorded for 15 min in a 40 cm by 40 cm open field box with video tracking software (ANY-Maze, Stoelting, Wood Dale, IL, USA). General activity levels were evaluated by distance traveled in the open field.
Each animal was placed for a single, 5-min trial in a Y-maze and activity was recorded (ANY-Maze, Stoelting, Wood Dale, IL, USA). The number of arm entries and spontaneous alternation, entering each arm in sequence without repetition, was expressed as a percentage as previously described (Brownlow et al. 2014).
Short term memory was evaluated by the novel object recognition task. Two objects, similar in scale to the mice, were placed in the 40 cm × 40 cm open field arena approximately 3–5 cm from the outer wall. Each animal was given three 5-min familiarization trials with a 5-min inter-trial interval. On the fourth trial, one of the objects was switched for a novel object. Animals were given five minutes to explore the objects and their activity was recorded (ANY-Maze, Stoelting, Wood Dale, IL, USA). The objects and arena were cleaned between trials with 10% ethanol to minimize olfactory cues. Working memory was evaluated by measuring the time spent with familiar object and novel object on the final trial.
To overcome the disinterest the mice showed in the objects, the mice were also tested in a variant of the NOR task using unfamiliar mice as the stimuli as previously described (Brownlow et al. 2014). Briefly, the test mouse was given one 5-min habituation trial to its environment. It was then introduced to two sex-matched bait mice, located in the left or right chamber of the three-chambered arena. The test mouse had two five-minute trials with a five-minute inter-trial interval to familiarize itself with the bait mouse. On the fourth trial, one of the bait mice was switched for a novel bait mouse. The test mouse was given another five minutes to explore the arena and its activity was recorded (ANY-Maze, Stoelting, Wood Dale, IL, USA). Preference for the novel mouse was assessed by measuring time spent in the chamber of the arena containing the novel mouse.
Radial arm water maze (RAWM) has been described in detail, including sample score sheets, previously (Alamed et al. 2006). The radial arm water maze contained six arms radiating from an open central area with a hidden escape platform located at the end of one of the arms. Around the pool, several extra-maze cues were hung to allow for spatial navigation. On each trial, the mouse was allowed 60 s to find the platform. The platform was located in the same goal arm on each trial. On day one, the mice were given 15 trials alternating between a visible and hidden platform. On day two, mice were given 15 additional trials, all with a hidden platform. The start arm was varied for each trial, forcing mice to rely on the extra-maze spatial cues to find the platform instead of procedural memory. The goal arm for each mouse was different to avoid odor cues revealing the platform location. Entry into an incorrect arm (all four limbs in the arm) was counted as an error. Failure to enter an arm for 15 s was also counted as an error. The errors of blocks of three trials were averaged for data analysis. Mice that made one or fewer errors on the last block of Day 2 were considered to have learned the platform location.
On the third day, a reversal trial was performed with the goal arm moved 180° across the pool. The mice were again given 15 trials, all with the hidden platform, to learn its new location. On the fourth day, the arm insert was removed from the pool, the extra-maze cues were taken down, and the platform was raised above the surface of the water with a flag attached to confirm that all mice were able to see and capable of ascending the platform. Latency to find and ascend the platform was recorded with a maximum swim time of 60s.
To assess thermal hyperalgesia, mice were placed on a hot plate at 50 °C. Latency to hind paw withdrawal was measured (Woolfe and Macdonald 1944).
Six to eight sections approximately 200 μm apart spanning the hippocampus were chosen for analysis. Immunohistochemical experiments were performed as described previously (Gordon et al. 2002). Briefly, sections for each animal were placed into a multisample staining tray. Endogenous peroxidases were blocked (10% methanol, 3% hydrogen peroxide in PBS for 15 min) and tissue was permeabilized (0.2% lysine, 0.1% Triton X-100 in PBS for 30 min). Sections were incubated overnight in appropriate primary antibody: anti-pSer396 (Anaspec, Fremont, CA, USA); anti-CD45 (ThermoFisher Scientific, Walthman, MA, USA); anti-IBA-1 (Wako, Richmond, VA, USA); or HRP-conjugated anti-HA (Roche, Indianapolis, IN, USA). Sections were washed three times in PBS, then incubated for two hours with corresponding biotinylated secondary antibody (Vector Laboratories, Burlingame, CA, USA), if necessary. The tissue was again washed and incubated with Vectastain Elite ABC Kit (Vector Laboratories) for enzyme conjugation. Finally, sections were stained using 0.05% diaminobenzidine and 0.03% hydrogen peroxide for five minutes. Each immunohistochemical assay omitted some sections from primary antibody incubation to evaluate nonspecific binding of the secondary. Sections were mounted onto slides, dehydrated, and coverslipped.
Gallyas staining was performed as previously described (Lee et al. 2010a). Staining was performed on pre-mounted tissue sections that had been dried for a minimum of 24 h. Prior to staining sections were rehydrated for 30 s. Slides were treated with 5% periodic acid for five minutes, washed with water, and incubated sequentially in silver iodide (1 min) and 0.5% acetic acid (10 min) prior to being placed in developer solution (2.5% sodium carbonate, 0.1% ammonium nitrate, 0.1% silver nitrate, 1% tungstosilicic acid, 0.7% formaldehyde). Slides were incubated in developer solution until color developed after which they were placed in 0.5% acetic acid to stop the reaction (3 min). Slides were incubated in 0.1% gold chloride solution (5 min), washed with water, and incubated in 1% sodium thiosulphate solution (5 min). After a final wash, slides were dehydrated and coverslipped.
Stained sections were imaged using a Zeiss Axioscan.Z1 scanning microscope and Neurocyte IAE software (created by Andrew Lesniak) was used for analysis. The area of positive staining in the hippocampus was analyzed. The software used hue, saturation, and intensity to segment the images and these values were held constant for analysis of every section of every animal in each stain. These values were established on sections of high and low levels of staining to identify positive staining over background (Gordon et al. 2002).
RNA Isolation and Real-Time PCR
RNA was isolated from posterior cortex using the Zymo Quick-RNA Miniprep Plus kit (Zymo Research, Irvine, CA, USA; cat. no. R1057) per the manufacturer’s recommended protocol. EXPRESS One-Step Superscript qRT-PCR Kit (cat. no. 11718200) and TaqMan Gene Expression Assays were purchased from ThermoFisher (Walthman, MA, USA). Primers for the target genes Tnf (Mm00443256_m1), Il1b (Mm00434228_m1), Il6 (Mm00446190_m1), Il12a (Mm00434169_m1), Il10 (Mm01288386_m1), Vegfa (Mm00437306_m1), Il4 (Mm00445259_m1), Marco (Mm00440265_m1), Itgam (Mm00434455_m1), CD68 (Mm03047343_m1), Arg1 (Mm00475988_m1), Nos2 (Mm00440502_m1), C1qa (Mm00432142_m1), Itgax (Mm00498701_m1), and the housekeeping gene Pgk1 (Mm00435617_m1) were used per the manufacturer’s recommended protocol. Fifty nanograms of RNA were loaded per well and data collected in a Bio-Rad CFX96 thermal cycler (50 °C for 15 min, 95 °C for 2 min, 40 cycles of: 95 °C for 15 s, 60 °C for 1 min). Data was analyzed using the ΔΔCT method (Schmittgen and Livak 2008).
Statistical analysis was performed using SPSS Statistics (IBM, Armonk, NY, USA). For behavioral tasks, all groups were assessed using a one-way analysis of variance (ANOVA) was performed with Fisher’s LSD post-hoc analysis. For the novel object recognition task, a two-tailed Student’s t test was used to compare time spent with the familiar object to time spent with the novel object on trial four. The novel mouse recognition task was analyzed with a two-way ANOVA and Fisher’s LSD with Group and Chamber as fixed factors. For tau western blotting and immunostaining, where there was no signal from mice lacking P301L tau expression, a two-tailed Student’s t test was utilized to compare sFKN-treated mice to GFP-injected controls. Immunostaining for CD45 and IBA-1 was analyzed with a one-way ANOVA and Fisher’s LSD post-hoc analysis comparing all groups. The threshold for significance was set at p = 0.05.
Intraventricular Injection of AAV4 Increased Soluble FKN
Increased Soluble FKN Expression Ameliorated Hyperactivity and Improved Cognition
Increased Soluble FKN Signaling Did Not Reduce Tauopathy
Increased Soluble FKN Signaling Did Not Reduce Microglial Markers
Microglia play a key role in Alzheimer’s disease pathogenesis. Previous studies showed that increasing microglial activation exacerbates tau pathology while reducing microglial activation can reduce tau pathology (Cho et al. 2011; Herber et al. 2007; Lee et al. 2010a, 2010b). We previously demonstrated that increasing soluble fractalkine agonism in the rTg4510 mouse model of tauopathy reduced pathology and neurodegeneration. However, the treatment was administered at a preventative timepoint, with administration of virus prior to significant tau pathology formation (injection at 3 months of age). In this study we wanted to examine if sFKN could have beneficial effects when administered at a more therapeutic timepoint, by administering virus after significant disease pathology and memory deficits had already been established (injection at 5 months of age). This would reflect a more clinically relevant setting where diagnosed patients would already exhibit significant tau deposition. The current study also differed from our previous work in that our delivery method in the previous study targeted only the hippocampus with injections directly into the parenchyma; here we sought to maximize treated brain regions while minimizing the number of injections required with the use of AAV4. We envisioned that intracerebroventricular (ICV) injections would reduce tissue damage to brain regions already burdened with pathology, neuron loss, and gliosis while maximizing distribution of the therapeutic gene product, another key consideration for translation to the clinic.
Previous studies showed the rAAV4 vector can efficiently infect cells of the lateral ventricle (Davidson et al. 2000a; Liu et al. 2005). More importantly, it has been reported that ICV and intrathecal delivery of AAV4 and AAV2 vectors encoding lysosomal enzymes, which were also secreted from transduced cells, has proven very effective in providing therapeutic levels of enzyme throughout the CNS in adult mouse models of lysosomal storage disease (Liu et al. 2005; Watson et al. 2006). ICV delivery of an AAV4 vector encoding hIFN-β has also been shown to be an effective approach to curb glioblastoma tumor growth (Meijer et al. 2009). These data suggest that secretion of sFKN from a lateral ventricle injection may be sufficient to provide therapeutic levels of sFKN protein throughout the CNS. In this study, we show that AAV4 sFKN infected the cells lining the lateral ventricles and increased sFKN levels in the CSF and hippocampus of injected mice. We observed sFKN expression in cells throughout the ventricular system including the cerebral aqueduct, 3rd and 4th ventricles. Using this method, we achieved an approximately 2-fold increase of soluble FKN over endogenous levels.
Previous reports have implicated fractalkine signaling in neuropathic pain in the spinal cord (Clark and Malcangio 2012; Milligan et al. 2004). Since we secreted sFKN into the CSF, potentially increasing FKN signaling in the spinal cord, we were concerned this may have detrimental effects and thus examined the animals for thermal hyperalgesia on a hot plate. Animals over expressing sFKN had no change in latency to hind paw withdrawal as compared with GFP-injected controls (Fig. 3), indicating that either the levels of sFKN reaching the spinal cord are insufficient to cause hyperalgesia or the species (ADAM 10/17 product) of soluble FKN (aa 1–336) we over expressed does not participate in mediating neuropathic pain. The latter would be consistent with the data published by Clark and Malcangio (2012). They demonstrated that intrathecal administration of a peptide of the chemokine domain (amino acids 1–110 only) results in mechanical hypersensitivity whereas an injection of the sFKN protein does not alter sensitivity (Clark and Malcangio 2012). Furthermore, induction of allodynia in spinal lesion models has been shown to be mediated, in part, by FKN and requires cathepsin S (Clark et al. 2007, 2009). These findings implicate the cathepsin S cleavage product of FKN, which migrates at a lower apparent molecular weight by SDS-PAGE than the ADAM 10/17 cleavage product used in the current study, in the induction of neuropathic pain (Fonovic et al. 2013).
Examining the behavioral phenotype of rTg4510s, we observed FKN expression above basal levels ameliorates several behavioral abnormalities. As reported previously, rTg4510s are known to be hyperactive and this hyperactivity may be due to pathological tau (Joly-Amado et al. 2016). Here, we observed a significant reduction in locomotor activity as measured in both the open field and Y-maze (Fig. 2). We also observed a significant improvement in novel mouse recognition, however, not novel object recognition (Fig. 2). This may be due to the greater motivation to interact with another mouse as opposed to an inanimate object (Brownlow et al. 2014). In the RAWM task, we observed that increased sFKN levels significantly improved hippocampal-dependent spatial learning and memory (Fig. 4). Animals over expressing sFKN made significantly fewer errors on Day 2 of the task than GFP-injected rTg4510s. However, we observed no improvement in the Reversal task, suggesting that this spatial learning improvement was partial. This may be due to the severe pathology that these animals already exhibited prior to start of sFKN treatment. This would suggest that earlier intervention, prior to significant neuropathology and neurodegeneration, may be a more beneficial therapeutic strategy.
We believe that the improvements we observed in behavior are due to alterations in the inflammatory milieu brought about by sFKN over expression. Previous studies have demonstrated that Cx3cr1−/− mice have deficits in cognition and neurogenesis that was reversed with IL-1 Receptor Antagonist (IL-1RA) administration (Bachstetter et al. 2011; Rogers et al. 2011). Microglial-specific cytotoxicity in an adoptive transfer model was also blocked by genetic ablation of IL-1 signaling (Cardona et al. 2006). Similarly, tau hyperphosphorylation induced by adoptive transfer of activated microglia from LPS-challenged hTau;Cx3cr1−/− mice into naïve wild-type mice was blocked by administration of the IL-1R antagonist Kineret (Maphis et al. 2015). Antagonism of IL-1R has also been shown to improve cognitive deficits in the 3xTg model of AD (Kitazawa et al. 2011). Finally, a recent report showed that activated microglia can induce a neurotoxic phenotype in astrocytes, that these activated astrocytes are present in AD tissue, and blockage of the transformation of astrocytes into neurotoxic astrocytes can be neuroprotective (Liddelow et al. 2017). Given that FKN agonism reduces pro-inflammatory gene expression, FKN agonism may promote an environment more permissive to learning and memory (Lyons et al. 2009).
Besides cytokine secretion, microglia are also directly involved in synaptic homeostasis. Depletion of microglia caused cognitive deficits and removal of microglial-derived brain derived neurotrophic factor recapitulated these effects, implicating microglial neurotrophic support in learning and memory (Parkhurst et al. 2013). Furthermore, microglia are involved in synaptic engulfment, both in disease and homeostasis (Hong et al. 2016; Schafer et al. 2012). Microglial dysfunction and senescence have been implicated in AD and clearance of senescent glial cells has recently been shown to improve recognition memory in the PS19 model of tauopathy (Bussian et al. 2018; Miller and Streit 2007). Increased FKN agonism may return microglia to a homeostatic state, facilitating learning.
Interestingly, we did not observe changes in microglial pan markers (CD45 and IBA-1), but this is consistent with what we have observed in previous studies in Parkinson’s disease where we showed a neuroprotective effect of sFKN over expression but no concomitant reduction in MHC-II expression (Nash et al. 2015). A likely explanation is that we are altering the microglial state with the addition of sFKN rather than decreasing the level of activation, as these markers can be increased in both proinflammatory and alternative activated states (Lee et al. 2013). We believe that the sFKN subtly altered microglial activation in a such a way that is more permissive to learning without altering expression of either CD45 or IBA-1. We would predict that this altered state would be less pro-inflammatory and possibly more neuroprotective.
To further investigate alterations in microglial activation, we examined a panel of immune-related genes by qPCR and observed a significant increase in Vegfa expression in animals over expressing sFKN. While vascular endothelial growth factor (VEGF) is most known for angiogenesis, it can also impact neurogenesis and promote neuron survival. VEGF has been shown to protect primary hippocampal neurons from excitotoxicity in vitro and promote neurogenesis in vivo (Jin et al. 2002; Matsuzaki et al. 2001). In neurodegenerative diseases, VEGF has been shown to be neuroprotective in Parkinson’s disease, amyotrophic lateral sclerosis, and Alzheimer’s disease models (Dodge et al. 2010; Religa et al. 2013; Tian et al. 2007). Neuroprotective effects are mediated both by direct anti-apoptotic signaling in neurons, neurogenesis, and through increased trophic support (Jin et al. 2001, 2002; Storkebaum and Carmeliet 2004; Sun et al. 2003). We hypothesize this increase in trophic support improved neuronal function, which may explain the improvement in cognitive performance observed in this study. Closer examination of the microglial profile with sFKN agonism is the focus of our current investigations.
rTg4510 mice begin to show tau pathology as early as 3–4 months of age with behavioral deficits starting as early as 2.5 months (Dickey et al. 2009; Santacruz et al. 2005). By 6 months of age, rTg4510s have significant insoluble tau deposits and marked neuron loss and behavioral deficits. Furthermore, accumulation of insoluble tau species plateaus from 5.5 months of age onward, as does accumulation of a 64 kDa soluble phospho-tau species (Dickey et al. 2009; Santacruz et al. 2005). Examining the tau pathology in the sFKN treated animals, we observed no significant change in soluble total tau or soluble phospho-tau species, but interestingly we did observe a significant small increase in insoluble total tau in animals over expressing sFKN. When we examined tau pathology by immunohistochemical means, we observed no increase in pSer396 phospho-tau and no increase in Gallyas-positive tau tangles. The inability of sFKN over expression to slow tau pathology here is possibly due to achievement of stable, plateau levels of pathology already present at the time of injection (Dickey et al. 2009; Santacruz et al. 2005; Spires et al. 2006). Alternatively, it may also require higher elevations of sFKN than we obtained here to reduce the accumulation of tau in these mice.
It is also important to note that our results are similar to those reported where the tau transgene expression was suppressed with doxycycline at 5.5 months of age (Ramsden et al. 2005; Santacruz et al. 2005). The mice on doxycycline improved in spatial learning tasks at 7 and 9.5 months compared to those without doxycycline, but the treated mice had no reductions in neurofibrillary tangles, PHF-1 positive neurons, or neuron number in the CA1 subfield (Santacruz et al. 2005). The recovery of memory in this mouse model, by doxycycline and now sFKN treatment, suggests that irreversible structural degeneration may not be responsible for initial memory deficits and that there is potential to recover some cognitive function in early stages of the disease. Indeed, this uncoupling of insoluble tau deposition from neuron loss and cognitive deficits is not unique to this model, as NFT formation does not correlate well with neuron loss in the human brain (Berger et al. 2007; Gomez-Isla et al. 1997; Spires-Jones et al. 2011). This could open the door for some medications to have profound improvements in quality of life for patients and delay the need and reduce the cost of extensive residential care. It has been estimated that a five-year delay in AD could lead to a 40% reduction in costs by 2050 (Zissimopoulos et al. 2014).
We have previously demonstrated that sFKN can be beneficial in a preventative approach in rTg4510 mice with administration at three months of age, prior to significant pathology. Here we shown that delivery of sFKN, using AAV4, can have a beneficial cognitive effect in rTg4510 mice with advanced pathology, at five months of age. In this study, we show the utility of delivering AAV4 to the lateral ventricles and over expressing a soluble immunomodulator into the CSF to achieve broad delivery of a therapeutic gene product to treat tauopathy. We have shown that this delivery method can meaningfully increase sFKN concentrations in the hippocampus as well as ameliorate behavioral deficits in the rTg4510 mouse model of tauopathy with advanced tau pathology. These data suggest that immunomodulation could have significant benefits in AD patients which already show tau pathology.
This study was funded by Alzheimer’s Association grant ZEN-15-321311 and the UK Dementia Consortium.
Compliance with Ethical Standards
Conflicts of Interest
The authors declare that they have no conflicts of interest.
All procedures performed in studies involving animals were in accordance with the ethical standards of the institution at which studies were conducted.
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