6 Sep 2012: Ke Y, Dramiga J, Schütz U, Kril JJ, Ittner LM, et al. (2012) Correction: Tau-Mediated Nuclear Depletion and Cytoplasmic Accumulation of SFPQ in Alzheimer's and Pick's Disease. doi: info:doi/10.1371/annotation/6650167a-7567-4c65-931f-4be7145a39fc View correction
Tau dysfunction characterizes neurodegenerative diseases such as Alzheimer's disease (AD) and frontotemporal lobar degeneration (FTLD). Here, we performed an unbiased SAGE (serial analysis of gene expression) of differentially expressed mRNAs in the amygdala of transgenic pR5 mice that express human tau carrying the P301L mutation previously identified in familial cases of FTLD. SAGE identified 29 deregulated transcripts including Sfpq that encodes a nuclear factor implicated in the splicing and regulation of gene expression. To assess the relevance for human disease we analyzed brains from AD, Pick's disease (PiD, a form of FTLD), and control cases. Strikingly, in AD and PiD, both dementias with a tau pathology, affected brain areas showed a virtually complete nuclear depletion of SFPQ in both neurons and astrocytes, along with cytoplasmic accumulation. Accordingly, neurons harboring either AD tangles or Pick bodies were also depleted of SFPQ. Immunoblot analysis of human entorhinal cortex samples revealed reduced SFPQ levels with advanced Braak stages suggesting that the SFPQ pathology may progress together with the tau pathology in AD. To determine a causal role for tau, we stably expressed both wild-type and P301L human tau in human SH-SY5Y neuroblastoma cells, an established cell culture model of tau pathology. The cells were differentiated by two independent methods, mitomycin C-mediated cell cycle arrest or neuronal differentiation with retinoic acid. Confocal microscopy revealed that SFPQ was confined to nuclei in non-transfected wild-type cells, whereas in wild-type and P301L tau over-expressing cells, irrespective of the differentiation method, it formed aggregates in the cytoplasm, suggesting that pathogenic tau drives SFPQ pathology in post-mitotic cells. Our findings add SFPQ to a growing list of transcription factors with an altered nucleo-cytoplasmic distribution under neurodegenerative conditions.
Citation: Ke Y, Dramiga J, Schütz U, Kril JJ, Ittner LM, Schröder H, et al. (2012) Tau-Mediated Nuclear Depletion and Cytoplasmic Accumulation of SFPQ in Alzheimer's and Pick's Disease. PLoS ONE 7(4): e35678. doi:10.1371/journal.pone.0035678
Editor: Koichi M. Iijima, Thomas Jefferson University, United States of America
Received: September 14, 2011; Accepted: March 20, 2012; Published: April 25, 2012
Copyright: © 2012 Ke et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: The authors acknowledge funding by the NHMRC (National Health & Medical Research Council), the ARC (Australian Research Council), and the J.O. & J.R. Wicking Trust, as well as the Center for Molecular Medicine Cologne (TV79). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Alzheimer's disease (AD) is characterized by both amyloid-β (Aβ) plaques and tau tangles in the brain while tau pathology in the absence of plaques occurs in a subset of frontotemporal lobar degeneration (FTLD-Tau) that includes FTDP-17 and Pick's disease (PiD) . Features of FTLD-Tau have been reproduced in transgenic mice expressing FTDP-17 mutant tau : P301L tau transgenic pR5 mice are characterized by tau hyperphosphorylation, tangle formation in the amygdala and hippocampus, and memory impairment .
To determine the consequences of tau pathology, both in animal models and human disease, we and others have applied the tools of functional genomics . Proteomic analysis, e.g., revealed separate and synergistic modes of Aβ and tau on mitochondrial functions ,  while in a transcriptomic study, we identified the detoxifying enzyme glyoxalase I as a target of tau toxicity . These studies were all done with total brain, while here we focused on the amygdala, a brain area with prominent tau pathology and affected early on in AD pathogenesis. Furthermore, instead of using gene arrays to identify differential gene expression, we used the unbiased, though less frequently applied SAGE (Serial Analysis of Gene Expression) method .
We identified 29 differentially expressed genes in pR5 transgenic amygdala, of which 11 were up- and 18 down-regulated compared to non-transgenic controls. Among these was Sfpq that encodes a nuclear splicing factor and transcriptional regulator. Our subsequent analysis for the first time revealed a nucleo-cytoplasmic redistribution of SFPQ under pathological conditions, similar to what has been reported for TDP-43 that forms cytoplasmic aggregates in amytrophic lateral sclerosis (ALS) and FTLD-TDP , and FUS in ALS ,  and FTLD-FUS . This highlights the nucleo-cytoplasmic redistribution of transcription factors as a prominent pathomechanism in neurodegeneration. Our data suggest that pathological tau may cause neuronal dysfunction, at least in part, by mislocalizing proteins such as those implicated in mRNA processing and/or splicing.
SAGE analysis of P301L tau-expressing mice
In P301L mutant tau transgenic pR5 mice, NFT formation is initiated in the amygdala , . To determine differentially regulated genes in pR5 mice compared to non-transgenic control littermates, we isolated mRNAs from dissected amygdalae and performed an unbiased SAGE analysis. We obtained 92,000 sequenced tags (46,586/wild-type and 46,905/pR5), which allowed us to identify differentially expressed genes (Table 1). By disregarding repetitive elements and SAGE linkers, most of the mitochondrial genes in the library showed a reduced expression in the transgenic sample. This included both mitochondrial and nuclear encoded mitochondrial genes. Specifically, subunits 6 and 8 of ATP synthase F0 (mt-Atp6 and mt-Atp8) as well as subunit 3 of Cytochrome c oxidase (mt-Co3) were down-regulated, while subunit 1 of Cytochrome c oxidase (mt-Co1) was up-regulated. These genes are encoded by the mitochondrial genome. The nuclear encoded mitochondrial genes included isoforms 1 and 3 of the ATP synthase subunit c (Atp5g1 and Atp5g3, respectively). While in the wild-type sample, isoform 1 yielded 7 tags, in pR5 it yielded none; isoform 1 yielded 42 tags in wild-type and only 17 in pR5. This deregulation may contribute to the reduced mitochondrial activity that characterizes pR5 mice as shown by us previously, both at the level of the proteome and functionally , . In addition to mitochondrial genes, 24 genes were identified that reached a significance of p<0.01 of differential regulation (Table 1). Of these, 9 were up- and 14 down-regulated. They included genes with functions in mitochondrial/homeostasis, transcription/gene expression, transport, cell growth/division, signaling pathways, and others (Fig. 1A).
(A) Transcriptomic SAGE analysis of P301L tau mutant pR5 (TG) compared to wild-type (WT) amygdala identified differentially expressed genes within several functional categories (pie chart). The strongly deregulated ‘transcription’ genes (green) included Sfpq. (B) Scheme of the domain structure of the 707 amino acid-long nuclear protein SFPQ. The amino-terminal glutamic acid (E)/glutamine(Q)/proline(P)-rich domain is followed by two RNA/DNA-binding domains (RRMs).
We identified a total of 29 genes that were significantly deregulated in pR5 amygdala (Table 1). Importantly, several of these have been implicated in neurodegenerative diseases other than AD or FTD, in particular those with functions in mitochondria. For example, among the up-regulated genes in pR5 amygdala is Itm2c that encodes an integral membrane protein. Genetic variants of ITMC2 have been associated with hemorrhagic stroke in humans . Ttr encoding transthyretin is also up-regulated; gene mutations have been implicated in multiple forms of amyloid polyneuropathy, a disease characterized by systemic deposition of TTR amyloid , . Enpp2 is up-regulated; it encodes a phosphodiesterase also known by the name of autotaxin, that has a possible role in metastasis .
Cplx2 is among the down-regulated genes in pR5 amygdala. It encodes complexin 2, an essential protein with a role in synaptic vesicle fusion . Abnormal levels of CPLX2 have been implicated in Huntington's disease , while its levels are reduced in AD . Septin 3 and 5 are both down-regulated in pR5, with Septin 5 accumulating in Parkinson's disease (PD) brain . Septins play important roles in many cellular processes by providing rigidity to the cell membrane, serving as scaffolds to recruit proteins to specific subcellular loci, and creating membrane diffusion barriers to establish discrete cellular domains . Another down-regulated gene is Pja1 that encodes the E3 ubiquitin ligase Praja that is expressed abundantly in brain and that has been proposed as a candidate gene in X-linked mental retardation (MRX) . Pja1 is up-regulated in the basolateral amygdala during the formation of fear condition memory , and interestingly, it is in the basolateral amygdala where pR5 mice specifically accumulate tau . Finally, Dbn1 is down-regulated in the pR5 amygdala. This gene encodes the actin-binding postsynaptic protein drebrin1 that regulates synaptic plasticity. Its levels are reduced in hippocampal synapses in AD , and its mRNA levels were found to negatively correlate with PHF-tau, i.e. abnormally phosphorylated tau .
Deregulation of the gene encoding SFPQ
While several genes were identified as being deregulated based on just one tag, for others, up to four tags were represented in the SAGE library, increasing the confidence in the finding of deregulation (Table 2). The latter group included Sfpq (splicing factor proline/glutamine rich) that encodes a large nuclear protein, SFPQ, implicated in cellular processes such as transcriptional regulation and RNA splicing. The protein is also known as PSF (Polypyrimidine tract-binding protein-associated Splicing Factor) –. The 707 amino acid-long nuclear protein SFPQ is highly conserved and contains an amino-terminal glutamic acid(E)/glutamine(Q)/proline(P)-rich domain followed by two RNA/DNA-binding domains (RRMs) (Fig. 1B). SFPQ is expressed by neurons and glia, and in both it is confined to nuclei (Fig. 2).
Double immunofluorescence for SFPQ (green)/MAP2 (red) (A,B) and SFPQ (green)/GFAP (red) (C) reveals an exclusively nuclear localization in both neurons and astrocytes of WT mice.
Nuclear depletion of SFPQ in AD and PiD brain
We next analyzed SFPQ in human diseases with tau pathology, by staining paraffin-embedded sections from the hippocampal formation of six sporadic AD cases, six sporadic PiD cases, and eight non-demented CT controls. SFPQ was completely depleted from most nuclei in AD and PiD hippocampi, and accumulated in focal patches in the cytoplasm, resembling aggregates (Fig. 3A). Interestingly, double immunofluorescence (IF) for SFPQ/GFAP or SFPQ/MAP2 revealed that in both AD and PiD brain, SFPQ was depleted from nuclei in both neurons and astrocytes (Fig. 3B). Accordingly, neurons harboring either AD tangles or PiD Pick bodies were also depleted of SFPQ as shown by co-staining for phospho-tau (AT8), SFPQ and DAPI (Fig. 3C). Immunoblot analysis of human entorhinal cortex samples with Braak stage 0 (CT), entorhinal stages I–II (minimal AD pathology) and neocortical stages V–VI (terminal pathology) revealed 65.3±6.7% reduced SFPQ levels for stages I–II, and a 78.7±1.9% reduction for V–VI compared with CT (Fig. 3D). This suggests that the SFPQ pathology may progress together with the tau pathology in AD.
(A) Compared to controls (CT), SFPQ (green) is massively depleted from hippocampal nuclei in AD and PiD cases. It accumulates in patches (arrows) in the cytoplasm as shown by co-staining with nuclear DAPI (blue) at higher magnification (insets). (B) IF for SFPQ (green) and GFAP or MAP2 (red) reveals that in both AD and PiD brain, SFPQ is almost completely depleted from neuronal and astrocytic nuclei. (C) Neurons harboring AD tangles and PiD Pick bodies are similarly depleted of SFPQ (green) as shown by co-staining for phospho-tau (AT8, red) and DAPI (blue). (D) Immunoblot analysis of Braak stage 0 (CT), entorhinal stage I–II of AD pathology, and neocortical stage V–VI (terminal pathology) reveals massively reduced SFPQ levels as disease progresses (n = 6–8; *,p<0.01; **,p<0.001). Scale bars, 10 µm.
Tau induces cytoplasmic sequestration of SFPQ
To determine the effects of pathological tau on SFPQ directly, we stably expressed both wild-type and P301L human tau in human SH-SY5Y neuroblastoma cells, a cell culture model of tau pathology , followed by either mitomycin C (Mito C)-mediated cell cycle arrest or neuronal differentiation with retinoic acid (RA). Confocal microscopy revealed that SFPQ was confined to nuclei in non-transfected wild-type cells, whereas in both wild-type and P301L tau-expressing cells, irrespective of the differentiation method, it formed vesicular aggregates in the cytoplasm (Fig. 4A). These were more pronounced in the mutant, and were remarkably similar to those identified in P301L tau-expressing cells. Within the sensitivity of the Western blot assay, total levels of SFPQ were not altered under any of these conditions (Fig. 4B). Together this suggests that pathogenic tau drives SFPQ pathology in post-mitotic cells. How tau causes the altered nucleo-cytoplasmic distribution of SFPQ remains to be determined.
(A) Mitomycin C (Mito C)-mediated cell cycle arrest or neuronal differentiation with retinoic acid (RA) of V5-tagged wild-type or P301L tau-expressing SH-SY5Y compared to untransfected (CT) SH-SY5Y neuroblastoma cells reveals SFPQ aggregates (arrows) in the cytoplasm that are not seen in CT. Insets: detailed view of vesicular SFPQ in the cytoplasm. Nuclear staining: DAPI (blue). (B) Western blotting reveals that total levels of SFPQ are not altered under any of these conditions. Actin has been used for normalisation.
By using SAGE as an unbiased transcriptomic approach we identified Sfpq as a downstream target of tau. We further found a nucleo-cytoplasmic redistribution of the nuclear protein SFPQ in AD and PiD pointing at a putative role for deregulated transcription factors in neurodegeneration. For both TDP-43 and FUS, a similar redistribution has been reported in ALS, and FTLD-TDP or FTD-FUS, respectively , . SFPQ promotes neuronal survival in development , and increased SFPQ levels sensitize neurons to excitotoxic damage in vitro . Hence, although tau itself may have nuclear functions , the nuclear depletion of SFPQ identified here suggests that pathological tau may cause neuronal dysfunction, at least in part, by mislocalizing proteins with nuclear functions. This extends the molecular targets of pathological tau beyond axons and dendritic processes , .
SFPQ is a transcriptional repressor of several genes, by inhibiting transcriptional co-activators or by binding to a consensus palindromic sequence (CTGAGTC) in the promoter region , . Two of these sequences are found in the putative Sfpq promoter suggesting that SFPQ may repress its own transcription. SFPQ not only functions as a repressor of gene transcription, but it can also up-regulate gene expression by increasing mRNA stability as shown for the inducible Cyclooxygenase-2 (Cox-2) gene .
Arresting P301L tau-expressing SH-SY5Y cells with either mitomycin C (mito C) or retinoic acid (RA), which causes a cytoplasmic accumulation of SFPQ in P301L tau-expressing cells and not, untransfected controls, rules out a direct role for mitosis in the altered localization of SFPQ. In addition, neurons are post-mitotic so the cytoplasmic localization found by us for SFPQ in AD and PiD brains cannot be due to mitosis. SFPQ redistribution could eventually induce cell death by contributing to apoptosis or mitosis, since a nuclear redistribution of SFPQ into aggregates has been observed in apoptotic cells, and a cytoplasmic redistribution in mitotic cells , . It is therefore possible that stressed neurons try to cope with elevated tau levels by cytoplasmic sequestration of SFPQ.
Loss of nuclear SFPQ and/or its cytoplasmic accumulation may contribute to cellular degeneration also directly: The Sfpq homologue whitesnake is required for cell survival and normal brain development in zebrafish, where it is mostly detected in regions enriched with neuronal precursors: this suggests that an impairment in SFPQ function could contribute to neuronal cell death . Sfpq overexpression per se may contribute to neuronal death since SFPQ sensitizes neurons to neurotransmitter-induced death in vitro . Furthermore, studies in a cancer cell line identified SFPQ as a tumor suppressor suggesting that an altered distribution and depletion from nuclei could affect transcription of target genes .
Together, our finding of an aberrant cytoplasmic localisation of SFPQ in both AD and PiD brains and P301L tau-expressing SH-SY5Y neuroblastoma cells suggests a role for SFPQ in neurodegeneration with a tau pathology. Our study further links FTLD-Tau with the cytoplasmic aggregation of the nuclear protein SFPQ to FTLD-TDP with the cytoplasmic aggregation of the nuclear protein TDP-43 , , highlighting RNA mismanagement as a general pathomechanism .
Materials and Methods
Human brain tissue was obtained from the Australian Brain Bank Network's Sydney Brain Bank, with approval from the Human Ethics Review Committee of the University of Sydney. Written informed consent was obtained from donors or donors next of kin for brain donation. The animal experiments were approved by the Animal Ethics Committee (AEC) of the University of Sydney and the Animal Care Committee of the University of Cologne (approval number K00/1-2009/3/4914).
The pR5 mouse strain expresses the longest human tau isoform together with the FTLD-Tau (FTDP-17) pathogenic mutation P301L in neurons, with NFT formation occurring first in the amygdala and then in the hippocampus , , .
For the SAGE analysis, amygdalae were dissected from ten 10 month-old male pR5 mice and ten wild-type male littermate controls. At 5–6 months of age, NFT formation is initiated in the amygdala, with numbers increasing as the mice age. Phenotypically the mice show no obvious impairment, neither at 5 nor at 10 months of age , . Brains were homogenized in Trizol (Invitrogen, Carlsbad, CA) to isolate high quality RNA, following the manufacturer's instructions. To remove contaminating DNA, the RNA was incubated with RNase-free DNase I (Promega, Wisconsin, MD) and quantified by UV spectroscopy at 260 nm. Between 10 and 30 µg of RNA was obtained from each amygdala, and RNA integrity was confirmed by gel electrophoresis using Bioanalyser chromatography (Agilent, Santa Clara, CA).
Construction of the SAGE library
SAGE libraries were established by Memorec Stoffel GmbH (Cologne, Germany) as described , using 20 µg of total RNA pooled from the two genotypes. Enrichment of mRNA was achieved by affinity chromatography, using oligo-dT-coupled Dynabeads (Dynal, Invitrogen, Carlsbad, CA). In brief, mRNA was converted to cDNA using oligo-d(T)25 primers (Invitrogen) and Superscript II reverse transcriptase (Gibco BRL, Carlsbad, CA). The single-stranded cDNA was converted to double-stranded cDNA and digested with Nla III as the anchoring enzyme. After ligation of linkers to the Nla III-compatible sticky ends, the cDNA fragments were digested with the tagging enzyme BsmF I (a site present in the linkers) for 1 h at 65°C, thus generating 10 bp (base pairs) SAGE cDNA tags attached to the linkers. After blunting of the linker cDNA products with Klenow enzyme, dimerization and PCR amplification using primers directed against linker sequences, the linkers were excised by Nla III digestion. The released ditag was purified from the excised linkers by polyacrylamide gel electrophoresis (PAGE) and ligated to long multimers of ditags separated by Nla III sites. After size separation by PAGE, the 0.7- to 2-kb fraction was excised from the gel, purified, and cloned into the pZero-1.1 vector (Invitrogen). Competent TOP10 E. coli (Invitrogen) were transformed, and colonies screened by PCR for inserts using M13F and M13R primers. Positive clones were sequenced until 46,000 tags/genotype were obtained. SAGE data were analyzed using the SAGE™ software (Memorec Stoffel GmbH, Cologne, Germany), an extensive proprietary tag database that establishes automatic annotations derived from EST/genomic data and, in addition, contains 700 manually annotated tags elusive to the automated mapping. The program extracts 11 bp SAGE tags and guarantees a more reliable assignment to UniGene clusters than programs working with 10 bp tags. Proprietary filtering algorithms eliminate SAGE artifacts resulting from polymorphic tags, ribosomal RNA, linker tags and LINE/SINE tags. For comparison, all SAGE libraries were normalized to 100,000 tags. The calculation of statistical significance levels in SAGE is based on a formula developed by Audic and Claverie . Significance was ascribed for p<0.01.
Human brain samples
Human brains were collected within 80 hours of death and frozen at −80°C for biochemical analysis or paraffin-embedded for immunofluorescence (IF) staining. For histology tissue from six sporadic AD (age range 63–78, mean 69.7±6.0), six sporadic PiD (age range 62–78, mean 69.8±6.3) and eight control (CT) cases (age range 62–79, mean 70.8±6.3) was used. Frozen entorhinal cortex from six sporadic AD cases at neocortical Braak stages V–VI (age range 76–98, mean 86.3±9.0), six clinically silent cases, histologically at transentorhinal Braak stages I–II (age range 92–103, mean 99.0±5.4) and six control cases without tangles (age range 79–93, mean 85.7±6) was used for biochemical analysis. Controls were free from psychiatric, neurological or neuropathological diseases. None of the AD or PiD cases had a family history suggestive of an autosomal dominant disease.
The following antibodies were used: a rabbit polyclonal antibody (Abcam #ab38148; WB (immunoblotting) 1/1000; IF (immunofluorescence) 1/200) was used to detect SFPQ. Mouse anti-glyceraldehyde-3-phosphate dehydrogenase (GAPDH; Abcam, Cambridge, MA) and a mouse anti-α-actin antibody were used as loading control (Chemicon, North Ryde, NSW, Australia). Tau13 was used to detect human tau (Abcam; #ab24634; IF 1/1000), a mouse monoclonal antibody against GFAP to stain astrocytes (Sigma, St Louis, MO; #G3893; IF 1/1000), a mouse monoclonal MAP2 antibody to stain neurons (Sigma; #M4403; IF 1/500), and mouse monoclonal antibody to detect the V5 tag (Invitrogen, IF 1/400). Secondary antibodies were coupled to Alexa-488 (Molecular Probes, USA, red, 1/200) or −555 (green, 1/200) for confocal microscopy. DAPI (4′,6-diamidino-2-phenylindole, dihydrochloride) (Molecular Probes, Invitrogen) was used for nuclear staining.
Immunofluorescence and Western blot analysis
Immunofluorescence and Western blot analysis of murine and human tissue were done as described previously .
Cell lines and immunofluorescence staining
SH-SY5Y is human neuroblastoma cell line . P301L-expressing SH-SY5Y cells and mock controls were generated using lentiviral gene transfer . The cells were grown in DMEM (Invitrogen) containing 10% of heat inactivated fetal bovine serum (FBS) and penicillin/streptomycin (Invitrogen) with or without blasticidin (Invitrogen) . Growth arrest was achieved by incubating cells for 2 h with 10 µg/ml mitomycin C (mito C) followed by a 24 h recovery, and neuronal differentiation by incubation with 20 µM all-trans-retinoic acid for 24 h, respectively. For immunofluorescence staining, cells were plated at a density of 20.000 cells per cm2 on 13 mm plastic cover slips (Sarstedt, Ingle Farm, SA, Australia), followed by fixation in 4% PFA. Blocking and permeabilization was done in 10% BSA and 0.3% Triton X-100 in 0.1 M PBS for 1 h. Primary antibodies were incubated overnight at 4°C in 5% BSA, 0.1 M PBS. Secondary antibodies were coupled to Alexa-488 or -555 (Molecular Probes, USA), followed by confocal microscopy.
We thank Ms Sandra Fok for confocal microscopy and Dr Stoffel (University of Cologne) for support.
Conceived and designed the experiments: HS LMI JG. Performed the experiments: YK JD US. Analyzed the data: JD LMI HS JG. Contributed reagents/materials/analysis tools: JJK. Wrote the paper: JG.
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