|Home | About | Journals | Submit | Contact Us | Français|
Neuronal intermediate filament inclusion disease and atypical frontotemporal lobar degeneration are rare diseases characterized by ubiquitin-positive inclusions lacking transactive response DNA-binding protein-43 and tau. Recently, mutations in the fused in sarcoma gene have been shown to cause familial amyotrophic lateral sclerosis and fused in sarcoma-positive neuronal inclusions have subsequently been demonstrated in neuronal intermediate filament inclusion disease and atypical frontotemporal lobar degeneration with ubiquitinated inclusions. Here we provide clinical, imaging, morphological findings, as well as genetic and biochemical data in 14 fused in sarcoma proteinopathy cases. In this cohort, the age of onset was variable but included cases of young-onset disease. Patients with atypical frontotemporal lobar degeneration with ubiquitinated inclusions all presented with behavioural variant frontotemporal dementia, while the clinical presentation in neuronal intermediate filament inclusion disease was more heterogeneous, including cases with motor neuron disease and extrapyramidal syndromes. Neuroimaging revealed atrophy of the frontal and anterior temporal lobes as well as the caudate in the cases with atypical frontotemporal lobar degeneration with ubiquitinated inclusions, but was more heterogeneous in the cases with neuronal intermediate filament inclusion disease, often being normal to visual inspection early on in the disease. The distribution and severity of fused in sarcoma-positive neuronal cytoplasmic inclusions, neuronal intranuclear inclusions and neurites were recorded and fused in sarcoma was biochemically analysed in both subgroups. Fused in sarcoma-positive neuronal cytoplasmic and intranuclear inclusions were found in the hippocampal granule cell layer in variable numbers. Cortical fused in sarcoma-positive neuronal cytoplasmic inclusions were often ‘Pick body-like’ in neuronal intermediate filament inclusion disease, and annular and crescent-shaped inclusions were seen in both conditions. Motor neurons contained variable numbers of compact, granular or skein-like cytoplasmic inclusions in all fused in sarcoma-positive cases in which brainstem and spinal cord motor neurons were available for study (five and four cases, respectively). No fused in sarcoma mutations were found in any cases. Biochemically, two major fused in sarcoma species were found and shown to be more insoluble in the atypical frontotemporal lobar degeneration with ubiquitinated inclusions subgroup compared with neuronal intermediate filament inclusion disease. There is considerable overlap and also significant differences in fused in sarcoma-positive pathology between the two subgroups, suggesting they may represent a spectrum of the same disease. The co-existence of fused in sarcoma-positive inclusions in both motor neurons and extramotor cerebral structures is a characteristic finding in sporadic fused in sarcoma proteinopathies, indicating a multisystem disorder.
Frontotemporal lobar degenerations are a group of neurodegenerative diseases known to have overlapping clinical syndromes, with a number of different underlying pathological phenotypes (Neary et al., 1998). The three best delineated clinical syndromes are behavioural variant frontotemporal dementia, progressive non-fluent aphasia and semantic dementia, although the clinical subtypes do not always predict the underlying degenerative disease.
As a result of recent advances in our understanding of the molecular mechanisms associated with frontotemporal lobar degeneration, this heterogeneous group of diseases are now subdivided on the basis of the presence of abnormal intracellular protein aggregates (Mackenzie et al., 2010). In approximately half of all cases with frontotemporal lobar degeneration, the hyperphosphorylated tau protein forms inclusions in neurons and in some forms also in glia. The majority of the tau-negative cases have neuronal inclusions originally identified by their immunoreactivity for ubiquitin and designated as frontotemporal lobar degeneration with ubiquitinated inclusions (FTLD-U) (Josephs et al., 2004; Mackenzie et al., 2006). The majority of the FTLD-U cases have been demonstrated to be associated with accumulation of the transactive response DNA-binding protein-43 (TDP-43), known as FTLD-TDP (Neumann et al., 2006). In a smaller group of FTLD-U cases with a distinct clinical and morphological phenotype, the ubiquitin-positive inclusions remained negative for TDP-43 and were designated as atypical FTLD-U (Roeber et al., 2008). Neuronal intermediate filament inclusion disease (NIFID) or neurofilament inclusion body disease has been defined as a rare form of frontotemporal lobar degeneration with ubiquitin-positive inclusions, a proportion of which are also immunoreactive for α-internexin and neurofilaments (Josephs et al., 2003; Cairns et al., 2007).
The fused in sarcoma (FUS) protein is composed of 526 amino acids with a molecular weight of 53kDa and is encoded by the FUS gene located on chromosome 16 (Crozat et al., 1993; Aman et al., 1996; Yang et al., 2010). The C-terminal region of the FUS protein contains multiple domains involved in RNA–protein interactions, while the N-terminus is involved in transcription activation (Prasad et al., 1994). FUS is a ubiquitously expressed protein (Aman et al., 1996) that binds RNA (Crozat et al., 1993) and DNA (Perrotti et al., 1998) and is involved in diverse cellular processes including cell proliferation (Bertrand et al., 1999), DNA repair (Baechtold et al., 1999) and RNA transport between intracellular compartments (Zinszner et al., 1997). The subcellular localization of the FUS protein is cell type dependent, for example FUS is present in proportionally larger amounts in the nucleus than in the cytoplasm of neurons while FUS expression is exclusively nuclear in glia (Andersson et al., 2008). The first association between neurodegeneration and FUS was shown in two studies reporting 14 different mutations in the FUS gene in 26 unrelated families with familial amyotrophic lateral sclerosis type 6 (Kwiatkowski et al., 2009; Vance et al., 2009). Pathologically, one study reported an increase in neuronal cytoplasmic FUS immunohistochemistry (Kwiatkowski et al., 2009), while the other reported the presence of FUS immunoreactive dystrophic neurites and neuronal cytoplasmic inclusions (Vance et al., 2009). Following these two studies, FUS was shown to be a component of the ubiquitin-positive neuronal cytoplasmic and intranuclear inclusions in a group of FTLDs designated as FTLD-FUS, which includes atypical FTLD-U, NIFID and basophilic inclusion body disease (Munoz et al., 2009; Neumann et al., 2009a, b; Urwin et al., 2010).
The identification of the FUS protein in neuronal inclusions in atypical FTLD-U, NIFID and basophilic inclusion body disease led us to investigate 14 tau and TDP-43 negative FTLD cases identified in the extensive archives of FTLD cases of Queen Square Brain Bank, University College London Institute of Neurology and the Medical Research Council London Brain Bank for Neurodegenerative Diseases, Institute of Psychiatry. The original neuropathological diagnosis was NIFID and atypical FTLD-U in seven cases each. A detailed comparative clinical and neuropathological study was performed using semi-quantitative assessment of lesions identified by FUS immunohistochemistry. The electrophoretic migration pattern of the FUS protein was investigated using western blot analysis in the 10 cases for which frozen material was available. This study is the first to investigate the molecular composition of the FUS protein in the NIFID subgroup.
Brains were donated to the Queen Square Brain Bank for Neurological Disorders, UCL Institute of Neurology, University College London; the Medical Research Council London Brain Bank for Neurodegenerative Diseases, Institute of Psychiatry, King's College, London, UK; Neuropathology Department, Århus Kommunehospital, Århus, Denmark; and NeuroResource, UCL Institute of Neurology, University College London. Demographic and clinical data were obtained from a retrospective case notes review performed by an experienced cognitive neurologist. All patients had details of a standard clinical history and had undergone both neurological examination and cognitive assessment. Magnetic resonance brain imaging was available in six of the cases with NIFID (all but NIFID2) and four of the cases with atypical FTLD-U (Patients 2, 3, 5 and 6). All cases had previously been diagnosed as NIFID (n=7) or atypical FTLD-U (n=7) characterized by the presence of pathological inclusions immunoreactive for ubiquitin, but negative for both tau and TDP-43, with the NIFID subgroup also containing α-internexin-positive inclusions. Eight cases have been previously reported (see Table 1 for summary and references) and six are presented here for the first time. Two cases are from the same family; Patient aFTLD-U7 was the mother of Patient aFTLD-U3.
Tissue sections (7-µm thick) from a number of brain and spinal cord regions (Table 4) were used. Commercially available anti-FUS antibodies each recognizing different epitopes of the FUS protein were tested (Table 3). FUS immunohistochemistry required pressure cooker pretreatment in citrate buffer (pH 6.0). Endogenous peroxidase activity was blocked with 0.3% H2O2 in methanol and non-specific binding with 10% dried milk solution. Tissue sections were incubated with the primary FUS antibodies overnight at 4°C, followed by biotinylated anti-rabbit immunoglobulin G (1:200, 30min; Dako) and Avidin–biotin complex (30min; Dako). Colour was developed with diaminobenzidine/H2O2. Antibodies to the following proteins were also used: α-synuclein (Vector, 1:50), tau (AT8 clone; Autogen Bioclear, 1:600), TDP-43 (Abnova, 1:800), CD68 (Dako, 1:150), glial fibrillary acidic protein (Dako, 1:1000), p62 (BD Transduction Labs, 1:200) and ubiquitin (Dako, 1:200). Thioflavine-S staining was carried out as previously described (Holton et al., 2001). To test the specificity of FUS antibodies, tissue sections from cases with sporadic motor neuron disease with TDP-43-positive inclusions, Alzheimer′s disease, Parkinson's disease, multiple system atrophy, Pick's disease, corticobasal degeneration and progressive supranuclear palsy were also used.
The frontal cortex and hippocampal formation from all cases were stained using an anti-FUS antibody (1-50 aa) in combination with either an anti-p62, anti-α-internexin or anti-ubiquitin antibody. After appropriate pretreatment, tissue sections were incubated with the appropriate primary antibody as described above, followed by the secondary antibodies Alexa Fluor 488 and Alexa Fluor 568 (Invitrogen, 1:300) for 1h at room temperature and 4′-6-diamidino-2-phenylindol (DAPI) was used for nuclear counterstaining. Sections were viewed with a Leica TCS4D confocal microscope using a 3-channel scan head and argon/krypton laser or a fluorescent microscope (Zeiss Axioskop MC80DX).
The extent and severity of FUS-positive pathology was evaluated using a five-tiered semi-quantitative grading scale in which the pathological lesions were scored as ‘0’ that described the absence of FUS-positive neuronal cytoplasmic inclusions and neuronal intranuclear inclusions, score ‘+’ corresponded to 1–5 inclusions present in an average of at least five microscopic fields using a ×20 objective, score ‘++’ was given when the number of lesions was 6–10, while score ‘+++’ was given when the number of inclusions was between 11 and 20. Score ‘++++’ corresponded to >20 lesions. The different morphological neuronal cytoplasmic inclusion types were recorded in each region together with the neuronal intranuclear inclusions. The presence of FUS-positive neurites or glial inclusions was also documented.
The hippocampus and parahippocampus of both NIFID and FTLD-FUS cases were stained with anti-ubiquitin antibodies to reveal ubiquitin-positive inclusions. The inclusions of the granule cell layer of the dentate fascia were analysed and classified into two categories based on the intensity of staining: weak-to-moderate and strong staining categories. Up to 100 inclusions were counted and the difference between the number of weak-to-moderate and strongly staining inclusions for each case and disease subtype was compared and subjected to statistical analysis.
The method for sequential extraction of proteins with increasing insolubility was an adapted and modified procedure as used in Neumann et al. (2009a). Frozen material was available in five patients with NIFID and five patients with atypical FTLD-U, three normal controls and two cases with FTLD-TDP. Tissue samples from frontal cortex (grey matter) or spinal cord (one case) were homogenized at a ratio of 1:2 (weight/volume) in high-salt buffer (50mM Tris–HCl, 750mM NaCl, 10mM NaF, 5mM EDTA) containing 1% Triton-X and protease and phosphatase inhibitors (Roche). Tissue homogenate was initially spun at 1000g to remove nuclear and membrane debris. The resulting supernatant was subjected to ultracentrifugation at 120000g for 30min at 4°C, following which the supernatant was retained (high-salt fraction). The pellet was subjected to further extractions with radioimmunoprecipitation buffer (50mM Tris–HCl, 150mM NaCl, 1% NP-40, 0.5% deoxycholate) containing 2% sodium dodecyl sulphate (SDS) and protease and phosphatase inhibitors as before, which was subjected to ultracentrifugation at 120000g for 30min at 15°C to avoid SDS precipitation, with the resulting supernatant being termed radioimmunoprecipitation-SDS fraction. The final pellet was resuspended in 8M urea containing 8% SDS (urea-soluble) fraction.
Protein concentrations from each fraction were determined by the bicinchoninic acid protein assay (Pierce) and 10, 5 and 0.6µg of protein from high-salt fraction, radioimmunoprecipitation-SDS fraction and urea fractions, respectively, from each case were loaded onto 10% Bis–Tris polyacrylamide gels (Invitrogen) and run at 200V with MES [2-(N-morpholino)ethanesulphonic acid] buffer (Invitrogen) under reducing conditions. Following electrophoresis, the proteins were transferred onto Hybond P membrane (GE Healthcare), blocked with 5% non-fat dried milk in phosphate-buffered saline containing 0.1% Tween and probed overnight with one of three anti-FUS antibodies, one recognizing the N-terminus (NB100-565; 1:4000), the second the C-terminus (NB100-562; 1:4000) while the third full-length FUS (HPA008784; 1:4000). Following washes in phosphate-buffered saline-Tween, blots were developed using horseradish peroxidase-conjugated secondary antibody (Santa Cruz) and visualized by enhanced chemiluminescence (Pierce) and captured onto Kodak, X-Omat (Sigma) membranes. ImageJ software was used for the semi-quantitative analysis of band density.
For the densitometric quantitation, the densities from the soluble fractions of both the 75 and 53kDa bands were analysed individually and combined, while for the insoluble component we combined the densities from SDS-soluble and urea-soluble fractions. Results have been expressed as a ratio of soluble/insoluble fractions (Fig. 7).
Genomic DNA was extracted using a standard method using proteinase K for digestion prior to phenol–chloroform extraction (Laird et al., 1991). The concentration and quality of extracted DNA were determined spectrophotometrically using a Nanodrop (Thermo Scientific). For sequencing of FUS, the entire open reading frame and exon–intron boundaries were sequenced; conditions are available on request. The sequences were analysed using the SeqScape software version 2.5 (Applied Biosystems).
Statistical analysis was performed using Graphpad Prism 5 software (GraphPad Software Inc.). Continuous variables were analysed using either a two-tailed t-test or a Mann–Whitney U test as appropriate, while continuous variables between several groups were compared using the Kruskal–Wallis test. The statistical significance level was established at P≤0.05.
The NIFID group consisted of five females and two males while the atypical FTLD-U group consisted of three females and four males. The mean age of onset was similar in both groups: mean 45.6 (SD 15.3) years old in the NIFID group and 47.0 (SD 5.1) years old in the atypical FTLD-U group. However, the variability of age of onset was greater in the NIFID group with a range of 28–69 years, with a much smaller range of 40–55 years in the atypical FTLD-U group. There was a significant difference between the disease duration from symptom onset to death between the groups with a shorter, relatively rapid, disease course in the NIFID group: mean 3.0 (SD 1.1) years compared with a longer disease duration in atypical FTLD-U of 7.3 (SD 2.9) years (Students t-test; P=0.003).
The most common syndromic diagnosis was the behavioural variant of frontotemporal dementia and all the patients with atypical FTLD-U had initial behavioural features with a combination of disinhibition, apathy, obsessive/compulsive behaviour and change in appetite (usually development of a ‘sweet tooth’). Patients later developed cognitive impairment with most prominently executive dysfunction and often episodic memory impairment as well. This group includes four cases previously reported in Rohrer et al. (2010) (aFTLD-U1, 3, 4 and 6). However, one patient with atypical FTLD-U (Case 5) developed falls, truncal rigidity, bradykinesia and rigidity in all four limbs as well as a vertical supranuclear gaze palsy consistent with a progressive supranuclear palsy syndrome [and previously reported as progressive supranuclear palsy with FTLD-U pathology, Case 2, in Paviour et al. (2004)]. In contrast, the clinical features of the NIFID cases were more heterogeneous, differing both within group and from the atypical FTLD-U group. Most strikingly, the diagnosis in the NIFID cases was often felt to be unclear initially and not fitting one particular clinical syndrome (all patients attended a specialist tertiary referral centre and were seen by experienced cognitive neurologists). In the youngest patient with NIFID [NIFID1, reported as Case FUS3 in Rohrer et al. (2010)], who had behavioural features consistent with the behavioural variant of frontotemporal dementia as well as inappropriate laughter, dysarthria and limb apraxia, this uncertainty led to a brain biopsy being performed. The clinical syndrome of Patient NIFID2 was felt to most closely fit a corticobasal syndrome because of the asymmetrical extrapyramidal syndrome with limb apraxia and alien limb as well as difficulty initiating saccadic eye movements but it was felt to be unusual for corticobasal syndrome because of the rapidity of progression of the disease. The case is reported in more detail as Case UK1 in Josephs et al. (2003). Patient NIFID3 [previously reported as Case D1 in Josephs et al. (2003)] initially had features consistent with behavioural variant frontotemporal dementia, but later developed parkinsonian and pyramidal features as well as cognitive impairment, leading to an additional diagnosis of a corticobasal syndrome-like syndrome. Patient NIFID7 was also felt to fit most closely to the diagnosis of corticobasal syndrome, and also developed severe dysarthria and a vertical supranuclear gaze palsy. Patients NIFID4, NIFID5 and NIFID6 all eventually had features of motor neuron disease but the initial clinical features differed between the patients and were often non-specific although with relatively intact cognition. Patient NIFID4 presented with right arm weakness, dysarthria and dysphagia. On examination, he was found to have bradykinesia and rigidity in all four limbs without any tremor as well as brisk deep tendon reflexes and a brisk jaw jerk. He developed a vertical supranuclear gaze palsy as well as difficulty initiating saccades. He also had an orofacial apraxia and became anarthric. Two years into the illness, he had an electromyogram showing denervation suggestive of motor neuron disease. Patient NIFID5 presented with progressive impairment of speech production that was slow and monotonous with articulatory difficulties and evidence of phonological errors, although with relatively intact naming. Within the next year, she developed dysphagia and a mixed spastic and flaccid dysarthria. On examination, there was wasting and fasciculations of the tongue and wasting of the left deltoid muscle with brisk deep tendon reflexes and jaw jerk. Electromyography demonstrated chronic partial denervation in all four limbs suggestive of motor neuron disease. The patient became anarthric and writing demonstrated agrammatism and phonological errors. Cognition was otherwise relatively intact in non-linguistic domains, and there were no changes in behaviour or personality. Patient NIFID6 presented with a 12-month history of progressive dysarthria and unsteadiness. She had suffered several falls and required a stick to walk. Neurological examination revealed perioral dyskinesiae, spastic dysarthria with a brisk jaw jerk, hypometric saccades, mild bilateral limb ataxia, retained tendon reflexes and flexor plantar responses, a normal sensory examination and gait ataxia. There was executive dysfunction but otherwise relatively intact cognition. She was reassessed 6 months after her initial presentation: wasting and fasciculations of the tongue and deltoid were noted although an electromyogram was not performed as she was anticoagulated. A clinical diagnosis of motor neuron disease was made at this time.
In the atypical FTLD-U cases, all three patients with imaging had atrophy of the frontal lobe (particularly orbitofrontal cortex), anterior temporal lobe and caudate. Atrophy was asymmetrical with either right- or left-sided predominant atrophy (Fig. 1). As with the clinical features of the group of patients with NIFID, the imaging findings were variable: Patients NIFID 4, 5, 6 and 7 did not have cortical or brainstem atrophy when imaged at the first assessment. Similar to the atypical FTLD-U cases, Patient NIFID1 showed asymmetrical frontotemporal atrophy although to a lesser extent than the atypical FTLD-U cases (Fig. 1). Patient NIFID3 showed caudate atrophy when initially scanned as well as signal change in the striatum although with only mild cortical atrophy. Although MRI was normal initially in Patient NIFID7, a subsequent fluorodeoxyglucose-PET showed asymmetrical reduced uptake in the frontal lobe, worse in the left hemisphere, and an 18F dihydroxyphenylalanine-PET showed reduced uptake in the putamen bilaterally and the left caudate.
In the subgroup of patients with NIFID, the brain weight ranged from 1030 to 1570g (mean 1256g) and 780–1274g (mean 1027g) in the a subgroup of patients with atypical FTLD-U (P=0.1). The cortical atrophy involved the frontal and anterior temporal lobes, but the parietal and occipital lobes appeared well preserved in all cases. The atrophy was particularly prominent in Patients aFTLD-U3, 5 and 6, in which the most affected gyri had a ‘knife-edge’ appearance. While some degree of macroscopic changes, indicative of hippocampal sclerosis, were observed in all the cases with atypical FTLD-U, no such macroscopic abnormality was seen in the cases with NIFID. The caudate nucleus was of normal bulk and appearance in all but two patients with NIFID (Cases 2 and 3), which showed severe atrophy and discolouration of this nucleus. In contrast, the caudate nucleus appeared thinned and discoloured in all cases with atypical FTLD-U. In general, the putamen was preserved apart from Patients aFTLD-U5 and 7, in which both the putamen and pallidum were reduced in size and showed greyish discolouration. Spinal cord was available in four cases with NIFID and three cases with atypical FTLD-U. The cord was described macroscopically as unremarkable in the NIFID cases, but discolouration of the lateral columns was documented in the atypical FTLD-U cases.
All cases showed superficial spongiosis affecting the frontal and temporal cortices to varying degrees with subpial and white matter gliosis. FUS-positive crescent-shaped neuronal cytoplasmic inclusions were present in all patients, but were more frequent in the cases with NIFID (Fig. 2A) than in the subgroup with atypical FTLD-U (Table 4, Fig. 2F). The superficial cortical layers appeared affected more severely than the deeper cortical laminae in both subgroups. However, the reduced number of inclusions may, at least partially, be the result of the severe cell loss found in the cortex in the subgroup with atypical FTLD-U. In the subgroup with NIFID, further FUS-positive neuronal cytoplasmic inclusion types included large globular or Pick body-like (Table 5) homogenous inclusions and flame-shaped, tangle-like inclusions, which often extended into the apical dendrites of pyramidal neurons. In the subgroup with atypical FTLD-U, bean-like, crescent and annular-shaped FUS-positive inclusions were also present (Table 5; Fig. 2H). An occasional rod-shaped and vermiform neuronal intranuclear inclusion were found in the subgroup with NIFID (Fig. 2D and E), but not in the cortex of the cases with atypical FTLD-U. FUS-positive neurites were found in the white matter of the subgroup with atypical FTLD-U, but not in the subgroup with NIFID. A minority of the neuronal cytoplasmic inclusions were positive for α-internexin in NIFID but they were entirely negative in the cases with atypical FTLD-U (Fig. 4G).
The pathology seen in the hippocampus varied significantly within the two subgroups. Neuronal loss mainly affecting the CA1 hippocampal subregion and subiculum was present in patients NIFID2 and 3, while good preservation of the neuronal population was seen in the hippocampi, subiculum and mediotemporal cortices in the remaining cases with NIFID. The granule cell layer of the dentate fascia and neurons of the subiculum contained large numbers of FUS-positive, bean-shaped or Pick body-like cytoplasmic and intranuclear inclusions in both patients NIFID2 and 3 (Table 5; Fig. 3A and B). Intranuclear inclusions were also frequent in neurons of the granule cell layer of these cases and it was noted that some neurons contained both cytoplasmic and intranuclear inclusions. FUS-positive oligodendroglial coiled body-like inclusions were also seen in the white matter of these two cases. The remainder of the cases with NIFID demonstrated an occasional crescent-shaped FUS-positive neuronal cytoplasmic inclusion in the granule cell layer of the dentate fascia (Fig. 3C and D), but unlike Patients NIFID2 and 3, no neuronal intranuclear inclusions were seen in the granule cell layer in these cases.
All cases with atypical FTLD-U showed some degree of hippocampal sclerosis. Profound cell loss with marked astrogliosis was seen in the CA1 hippocampal subregion of Patients aFTLD-U3, 6 and 7, which also extended into the subiculum. FUS immunohistochemistry showed that there were frequent neuronal intranuclear inclusions in the granule cell layer of the dentate fascia, which outnumbered the bean-shaped cytoplasmic inclusions found in the same anatomical region in Patients aFTLD-U2, 3 and 4 (Fig. 3D). It is of note that the remaining cases contained only an occasional neuronal cytoplasmic inclusion in the same anatomical area (Fig. 3A). In the CA1 subregion, which was affected by neuronal loss of different degree in all cases, a proportion of the remaining neurons contained cytoplasmic inclusions, intranuclear inclusions or both. Abnormal neurites were also present in the entorhinal cortex and fusiform gyrus.
Patients NIFID2 and 4 showed moderate gliosis in the caudate and putamen, whereas in the remaining cases with NIFID, the basal ganglia appeared unremarkable. FUS immunohistochemistry revealed frequent bean-shaped or ring-like neuronal cytoplasmic inclusions and abnormal neurites in all cases with NIFID in the caudate nucleus and putamen (Table 5). Neuronal vermiform intranuclear inclusions were occasionally observed in Patients NIFID 4 and 5, but were not observed in the other cases with NIFID. In the subgroup with atypical FTLD-U, severe neuronal loss with astrocytosis was seen in the caudate nucleus, putamen and claustrum. Bean and annular-shaped neuronal cytoplasmic inclusions were found in some of the remaining neurons. FUS-positive neuritic profiles were also a prominent feature in the basal ganglia of the subgroup with atypical FTLD-U.
In Patients NIFID5 and 6, the substantia nigra was well populated with neurons and showed only minimal pigment incontinence with an occasional α-synuclein-positive Lewy body and Lewy neurite. The remaining cases with NIFID showed mild neuronal loss in the substantia nigra with extracellular neuromelanin pigment. Globular FUS-positive neuronal cytoplasmic inclusions were found in all cases in the substantia nigra and their number varied from occasional to frequent (Table 4). Apart from Patient NIFID6, where the locus coeruleus remained unaffected, there was neuronal loss in the locus coeruleus in all the cases and several of the remaining neurons contained cytoplasmic inclusions. The neurons of the pontine base were affected in all cases by occasional globular or bean-shaped cytoplasmic inclusions. Although the 12th nerve nucleus showed good preservation of its neuronal population in all cases with NIFID, the majority of the motor neurons contained either compact or filamentous skein-like FUS-positive cytoplasmic inclusions (Fig. 3E–G).
In the subgroup with atypical FTLD-U, the substantia nigra showed severe neuronal loss in all cases with astrocytosis and extraneuronal neuromelanin pigment, together with dense globular FUS-positive neuronal cytoplasmic inclusions. The locus coeruleus also showed cell loss in all cases but this was less severe than that seen in the substantia nigra. An occasional FUS-positive neuronal cytoplasmic inclusion was found in three cases with atypical FTLD-U in the locus coeruleus, whereas two cases remained unaffected (Table 4). The 12th nerve nucleus was available in Patients aFTLD-U5 and 6 where at least half of the motor neurons demonstrated large FUS-positive skein-like filamentous inclusions along with dense globular cytoplasmic inclusions (Fig. 3H).
Purkinje cell loss and frequent axonal torpedoes were seen in the cerebellar cortex in all cases with NIFID. Purkinje cells contained an occasional FUS-positive intranuclear inclusion in Patient NIFID2. The cerebellar white matter was unremarkable in all cases, but the dentate nucleus showed mild to moderate astrogliosis with occasional globular FUS-positive neuronal cytoplasmic inclusions. Apart from Patients aFTLD-U4 and 7, in which the cerebellum was preserved, the remaining cases with atypical FTLD-U showed loss of Purkinje cells with accompanying Bergmann gliosis and axonal torpedoes. There was mild to moderate astrocytosis in the cerebellar dentate nucleus with occasional dentate nerve cells containing FUS-positive cytoplasmic inclusions.
Spinal cord was available for assessment from four patients with NIFID. Patient NIFID4 demonstrated pallor of the lateral columns, but the anterior horn cells were preserved in numbers. CD68 immunohistochemistry showed an increase in microglia and macrophages in the lateral columns of the thoracic cord bilaterally in Patient NIFID5, indicating degeneration of the corticospinal tracts. The motor neurons in the thoracic and lumbar cord of Patient NIFID6 and the lumbar cord of Patient NIFID3 showed neuronal cell loss accompanied by increased numbers of microglial and astrocytic cells. A proportion of the motor neurons in all cases with NIFID contained FUS-positive cytoplasmic inclusions, which were either filamentous skein-like, compact, dot-like or had a loose ‘cotton wool-like’ architecture (Fig. 3I and J). Spinal cord was available for examination in three cases with atypical FTLD-U. The cervical segments showed mild anterior horn cell loss with occasional remaining neurons containing FUS-positive cytoplasmic inclusions. Patient aFTLD-U5 showed degeneration of the crossed and uncrossed corticospinal tracts, while in Patient aFTLD-U7 the spinal cord appeared normal. Skein-like, FUS immunoreactive cytoplasmic inclusions were found in the motor neurons at all levels in all cases (Fig. 3K and L).
No labelling of abnormal pathological structures with the anti-FUS antibody was seen in four normal controls and cases with alternative neurodegenerative diseases (sporadic motor neuron disease with TDP-43-positive inclusions, Alzheimer's disease, Parkinson's disease, multiple system atrophy, Pick's disease, corticobasal degeneration and progressive supranuclear palsy).
The inclusions were thioflavine-S-negative in all cases with NIFID and atypical FTLD-U indicating that the FUS protein is not in β-pleated sheet-rich conformation in these diseases.
Double-label immunofluorescence with a combination of anti-FUS and anti-p62 antibodies confirmed that these two antigens co-localize in the neuronal cytoplasmic inclusions (Fig. 4A–F) in both diseases. Double-labelling for FUS and α-internexin (Fig. 4G–I) in the cases with NIFID demonstrated that the co-localization of these two proteins was rather poor within individual inclusions containing both α-internexin and FUS. The majority of the FUS-positive neuronal cytoplasmic and intranuclear inclusions were also labelled with the anti-ubiquitin antibody (Fig. 4N–S), although the ubiquitin staining varied considerably between inclusions in both the NIFID and the atypical FTLD-U cases. Neuronal vermiform intranuclear inclusions were highlighted on thicker sections with FUS immunohistochemistry (Fig. 4J), with an occasional neuron also found to contain a double intranuclear inclusion (Fig. 4K). Several neurons were also noted to contain both cytoplasmic and intranuclear inclusions (Fig. 4L and M).
All cases showed positivity to both ubiquitin and p62 to varying degrees, staining neuronal cytoplasmic and intranuclear inclusions in a manner similar to that observed in FUS immunohistochemistry. The intensity of the ubiquitin staining of the inclusions showed considerable variation. The ratio of weakly/moderately and strongly stained inclusions, determined by semi-quantitative analysis in the granule cell layer of the dentate fascia, showed no significant difference in the intensity between the subgroups with NIFID and atypical FTLD-U (t-test P=0.75; Fig. 5A and B).
To characterize FUS biochemically, protein was sequentially extracted from flash-frozen frontal cortex from patients with atypical FTLD-U, NIFID, FTLD associated with TDP-43 and controls, using buffers containing increasing detergent strength. FUS immunoreactive bands were consistently detected at ~75 and ~53kDa in the soluble fraction (high-salt fraction), whereas with some variability in the insoluble fractions (radioimmunoprecipitation-SDS and urea fractions) in all cases using the anti-FUS antibody recognizing 1–50 aa (N-terminus). The specificity of the bands was confirmed by (i) an antibody pre-absorption experiment using the relevant synthetic peptide and (ii) omission of the anti-FUS (but not the secondary) antibody (Fig. 6). In these experiments, both the ~75 and the ~53kDa bands were absent confirming the specificity of the antibody binding and also that the faster migrating 53kDa band did not represent immunoglobulin recognized by the relevant secondary antibody. Further characterization with two additional antibodies, one recognizing the C-terminus of FUS and the other the full-length protein, also identified the same two bands (data not shown). Further analysis of the immunoblots revealed that in the NIFID cases, the two major bands representing FUS were less abundant in the SDS-soluble fraction than in the soluble (high-salt) fraction. In the urea fraction, while the higher 75kDa band was abundant, the faster migrating 53kDa band was absent or very weak in the cases with NIFID (Fig. 6). In contrast, the 75 and 53kDa bands were represented in all three fractions in atypical FTLD-U. In one case, Patient aFTLD4 (Fig. 6), both bands were stronger in the urea-soluble fraction than those in the SDS-soluble fraction. The 53-kDa bands in both the SDS- and urea-soluble fractions were relatively strong in atypical FTLD-U. The electrophoretic migration pattern of FUS in normal controls (Fig. 6) and FTLD-TDP (data not shown) was similar to that seen in NIFID. Using densitometry for the quantitation of the different bands, a ratio of insoluble (SDS and urea soluble together) to soluble (high-salt soluble) FUS was calculated, which was used as a measure of FUS solubility in each case. This was calculated for the 53 and 75kDa bands individually and with both bands being pooled together (Fig. 7). Analysing the bands individually, there was a significant overlap between the NIFID, atypical FTLD-U and control groups. However, when the analysis was repeated, combining the bands of the cases with atypical FTLD-U had a statistically significant higher mean ratio of insoluble to soluble FUS (mean=1.77) than cases with NIFID (mean=0.64) or controls (mean=0.96) (Kruskal–Wallis test P=0.01), indicating a decreased solubility of FUS in atypical FTLD-U. However, the difference identified with this approach disappeared when the SDS and urea fractions were analysed independently (SDS/soluble FUS P=0.0602 and urea/soluble FUS P=0.0884).
Sequencing of all exons of FUS did not identify any mutations in the five cases with NIFID and five cases with atypical FTLD-U, where frozen brain tissue was available for DNA extraction and genetic analysis.
In this study, we performed a comparative clinicopathological study of seven cases with atypical FTLD-U and seven cases with NIFID and demonstrated a difference between the two subgroups in clinical presentation, pathological features and solubility of FUS. Clinically, all the patients with atypical FTLD-U presented with a behavioural variant of frontotemporal dementia, while the clinical presentation in NIFID was more heterogeneous, including cases with motor neuron disease and extrapyramidal syndromes. Neuroimaging reflected this different clinical pattern with atrophy of the frontal and anterior temporal lobes and caudate in atypical FTLD-U, whereas cases with NIFID were often normal to visual inspection early on in the disease. Our qualitative and semi-quantitative morphological and biochemical analysis of FUS not only showed significant overlap between atypical FTLD-U and NIFID, but also confirmed both morphological and biochemical differences which are characteristic only for either of the two diseases with FUS pathology. We were unable to demonstrate a mutation in the FUS gene in 10 cases in which DNA was available for genetic analysis. This is of interest as the cases tested included one of two members of a family (Patients aFTLD-U3 and aFTLD-U7) with confirmed FUS pathology, in whom (Patient aFTLD-U3) no mutation was found in the MAPT, GRN or TARDBP genes either (Rohrer et al., 2009).
Recently, FUS has emerged as a pathological protein in neurodegenerative diseases with striking functional similarities to TDP-43, which together with tau is the most significant pathological protein involved in frontotemporal lobe degeneration and is the most common pathological protein in amyotrophic lateral sclerosis (Neumann et al., 2006). FUS and TDP-43 are DNA/RNA binding proteins involved in gene expression, transcription regulation, RNA splicing, transport and translation (Crozat et al., 1993; Prasad et al., 1994; Aman et al., 1996; Zinszner et al., 1997; Perrotti et al., 1998; Buratti and Baralle, 2008; Yang et al., 2010) continuously shuttling between the nucleus and cytoplasm, although under normal physiological conditions both proteins are predominantly located in the nucleus (Zinszner et al., 1997). The similarities between the two proteins also extend into their roles in disease, as similar to TDP-43, FUS is also implicated in both amyotrophic lateral sclerosis (Neumann et al., 2006; Kwiatkowski et al., 2009; Vance et al., 2009) and FTLD (Neumann et al., 2006, 2009). Mutations of both genes are associated with autosomal-dominant forms of amyotrophic lateral sclerosis with most pathogenic mutations affecting the highly conserved C-termini of the two proteins (Arai et al., 2006; Neumann et al., 2006; Davidson et al., 2007; Kwiatkoski et al., 2009; Vance et al., 2009). One of the significant differences between the TDP-43 and FUS proteinopathies is that under pathological conditions TDP-43 redistributes from the nucleus to the cytoplasm of neurons possessing cytoplasmic inclusions while data from previous (Neumann et al., 2009a, b) and also by our current investigations indicate that some of the FUS protein is retained within the nucleus of neurons affected by inclusion formation in the FUS proteinopathies.
Although there was overlap between the clinical features of the atypical FTLD-U and NIFID cases, there were a number of key distinctions. Patients with atypical FTLD-U had a mean disease duration of 7 years (similar to other FTLD pathologies) in comparison to the relatively rapid course of the NIFID cases with a mean disease duration of 3 years. Age of onset was often younger than characteristic of FTLD with onset in their 40s or 50s for atypical FTLD-U and although more variable for NIFID, this group included a very young onset case starting in their late 20s. It has previously been suggested that very early onset frontotemporal dementia (<40 years) is a strong predictor for FUS pathology (Loy et al., 2010). The clinical presentation was relatively homogeneous in the atypical FTLD-U cases, all presenting with behavioural variant of frontotemporal dementia and having asymmetrical orbitofrontal, anterior temporal and caudate atrophy. In contrast, patients with NIFID had a much more heterogeneous clinical presentation with a combination of behavioural, cognitive and motor symptoms. The motor features consisted of either motor neuron disease or an extrapyramidal syndrome (with features of either a corticobasal syndrome or progressive supranuclear palsy syndrome seen) (Table 2). In comparison to the atypical FTLD-U cases, little cortical or brainstem atrophy was seen early on in many NIFID cases.
The findings of our study using several antibodies to different epitopes of the FUS protein support previous reports showing that FUS is a major pathological protein in neuronal inclusions in both NIFID and atypical FTLD-U (Neumann et al., 2009b; Urwin et al., 2010). This also unequivocally redefines NIFID as a FUS proteinopathy, in which only a minority of the inclusions are immunoreactive for α-internexin (Cairns et al., 2004). A number of different neuronal inclusion types were seen in both NIFID and atypical FTLD-U with a significant overlap, and also characteristic differences between the two disease types (Table 5). FUS-positive inclusions were also p62 positive; however, considerable variability was seen in the intensity of staining with ubiquitin immunohistochemistry in both NIFID and atypical FTLD-U. Our semi-quantitative analysis of the intensity of the ubiquitin staining in the granule cell layer of the dentate fascia revealed no difference between NIFID and atypical FTLD-U. Variable labelling of pre-inclusions and larger inclusions with anti-ubiquitin antibodies has also been shown in TDP-43 proteinopathies (Mori et al., 2008; Giordana et al., 2010). According to in vitro studies, FUS appears to be one of an unknown number of proteins recognized and degraded by the proteasome without itself undergoing ubiquitination and it is, therefore, possible that the association of FUS with other ubiquitinated molecules is a prerequisite for targeting FUS for proteasomal degradation (Perrotti et al., 1998).
In keeping with data from a recent study, which compared the FUS pathology in atypical FTLD-U, NIFID and basophilic inclusion body disease (Mackenzie et al., 2010), our semi-quantitative assessment of inclusion frequency has confirmed that the FUS pathology was overall considerably more severe in cerebral cortex, medial temporal lobe structures such as subiculum, entorhinal cortex and fusiform gyrus (but not in the granule cell layer of the dentate fascia), subcortical and brainstem nuclei in NIFID than in the same anatomical regions in atypical FTLD-U (Table 4). A greater cell loss in anatomical regions, such as the frontal and temporal cortices and caudate nucleus in the atypical FTLD-U cases may, at least partly, account for the lower numbers of inclusions in these areas, although no such difference in the degree of cell loss could be detected in other subcortical grey and brainstem nuclei, to explain the overall higher number of FUS inclusions in NIFID (Table 4). Hippocampal sclerosis has been described to be a prominent feature of atypical FTLD-U (Roeber et al., 2008; Mackenzie et al., 2010; Urwin et al., 2010) and this was a constant feature of all our cases with atypical FTLD-U and was only present in two of the NIFID cases. With the exception of one case with NIFID the granule cell layer of the dentate fascia was always affected by FUS-positive neuronal inclusions in both disease groups, but it is of note that the number of inclusions tended to be lower or they were even absent in NIFID cases with a clinical presentation indicating motor neuron disease. The overall common and often severe involvement of the neurons of the granule cell layer by FUS-positive inclusions may be due to the reported higher level of cytoplasmic FUS expression within these neurons (Belly et al., 2005), which may render them more vulnerable to inclusion formation (Armstrong et al., 2011). Although only two of our NIFID cases manifested clinically as motor neuron disease, our data indicate that involvement of motor neurons is a general feature of the FUS proteinopathies. Various numbers of FUS-positive neuronal inclusions were seen in motor neurons of the 12th cranial nerve nucleus and of the anterior horns of the spinal cords in NIFID and atypical FTLD-U cases in which the lower brainstem and/or spinal cord were available for neuropathological assessment (five and four cases, respectively). FUS-positive inclusions in motor neurons were morphologically rather diverse and their morphological appearances ranged from granular hazy, cotton wool-like deposits to better defined globular or characteristic skein-like inclusions. The inclusions in motor neurons were also p62 positive, but were only weakly stained with anti-ubiquitin antibody. The finding of constant involvement of motor neurons by FUS-positive inclusions in both NIFID and atypical FTLD-U indicates an increased vulnerability of such neurons to FUS protein aggregation. In post-natal life, a differentially higher level of expression of FUS in motor neurons has been demonstrated in rodents (Huang et al., 2010), the relevance of which needs to be confirmed in human disease.
Genetic analysis of exons and splice sites of the FUS gene, performed in 10/14 pathologically confirmed cases (five NIFID and five atypical FTLD-U), revealed no mutations. It is of note that DNA extracted from frozen tissue was available for genetic analysis in one (Patient aFTLD-U3) of the two atypical FTLD-U cases that belong to the same family (Patient aFTLD-U7 is the mother of aFTLD-U3) with a history of an autosomal dominant dementing disorder (Rohrer et al., 2010). This observation is in keeping with findings of a recent study reporting two brothers with a dementing illness in one of whom neuropathological examination confirmed FTLD-FUS, but without mutation in the FUS gene (Urwin et al., 2010). It remains to be seen whether a mutation in the non-coding region of the FUS gene or, analogous with TDP-43 pathology in families with mutation in the GRN gene (Baker et al., 2006; Cruts et al., 2006), a mutation in another gene functionally linked to FUS is responsible for a familial form of FTLD-FUS.
Using western blots, we were able to perform a comparative biochemical analysis of the FUS protein in NIFID and atypical FTLD-U. Using anti-FUS antibodies recognizing different epitopes, our studies demonstrated two strong bands at 53 and 75kDa in NIFID, atypical FTLD-U and controls, the specificity of which was confirmed with appropriate experiments (Fig. 6). As the calculated molecular weight of FUS is 53kDa (Yang et al., 2010), one of the possibilities is that this faster migrating band represents full-length FUS protein without post-translational modifications while the 75-kDa band is a post-translationally modified protein or a protein complex. However, as FUS isolated from cultured cells mainly runs at 75kDa, it is possible that the 53kDa band represents a modified protein species. In view of previous findings suggesting the absence of post-translational modifications of FUS (Perrotti et al., 1998) and previous western blot analysis of atypical FTLD-U only demonstrating the slower migrating band (Neumann et al., 2009a), further studies are required to clarify the composition of both the 53 and 75kDa FUS protein species. Quantitative analysis of the western blots of our cases demonstrated a significant decrease in solubility of the FUS protein in atypical FTLD-U, but not in NIFID and controls. Our finding of a change in solubility of FUS in atypical FTLD-U is in agreement with a previous report (Neumann et al., 2009a) but, in addition, our findings also indicate that there may be biochemical differences between the two major subgroups of FUS proteinopathies. To date this shift in solubility of FUS in atypical FTLD-U, shown by Neumann et al. (2009) and confirmed by our current study, is the only evidence of disease-associated modification of FUS. As the difference in solubility of FUS between the atypical FTLD-U and NIFID could suggest that the underlying disease mechanisms may also be different in these two forms of FUS proteinopathy, further biochemical investigations are required.
In summary, our study confirms that both NIFID and atypical FTLD-U can be classified under the umbrella term FTLD-FUS. Neuropathologically, they are both characterized by widespread FUS immunoreactive inclusions, affecting several major anatomical areas, including cerebral cortex, subcortical and brainstem nuclei and spinal cord. The distribution and types of FUS inclusions not only show considerable overlap, but also distinct differences in the two diseases. No FUS mutations were found in our NIFID and atypical FTLD-U cases, although two of the cases are from the same family raising the possibility of an alternative genetic abnormality. We demonstrated biochemically that FUS is more insoluble in atypical FTLD-U than in NIFID indicating that differences may exist in the underlying mechanisms resulting in aggregation of the FUS protein.
Alzheimer's Research UK to T.R., J.L.H., A.J.L. and M.N.R.; Reta Lila Weston Institute for Neurological Studies to J.L.H.; Wellcome Trust Senior Clinical Fellowship to J.D.W.; J.L.H., T.R. and A.J.L. receive research grants from the Multiple System Atrophy Trust and Parkinson’s UK. The Dementia Research Centre is an Alzheimer's Research Trust Coordinating Centre and has also received equipment funded by the Alzheimer's Research UK.
The authors would like to thank the patients and their families for their generosity and goodwill, as without their support none of this research would have been possible. This work was undertaken at UCLH/UCL with a proportion of funding from the Department of Health's NIHR Biomedical Research Centres funding scheme. The Queen Square Brain Bank, UCL Institute of Neurology is supported by the Reta Lila Weston Institute of Neurological Studies and the Progressive Supranuclear Palsy (Europe) Association.