- Open Access
Phosphorylated TDP-43 (pTDP-43) aggregates in the axial skeletal muscle of patients with sporadic and familial amyotrophic lateral sclerosis
© The Author(s). 2018
- Received: 17 March 2018
- Accepted: 19 March 2018
- Published: 13 April 2018
Muscle atrophy with weakness is a core feature of amyotrophic lateral sclerosis (ALS) that has long been attributed to motor neuron loss alone. However, several studies in ALS patients, and more so in animal models, have challenged this assumption with the latter providing direct evidence that muscle can play an active role in the disease. Here, we examined the possible role of cell autonomous pathology in 148 skeletal muscle samples from 57 ALS patients, identifying phosphorylated TAR DNA-binding protein (pTDP-43) inclusions in the muscle fibers of 19 patients (33.3%) and 24 tissue samples (16.2% of specimens). A muscle group-specific difference was identified with pTDP-43 pathology being significantly more common in axial (paraspinous, diaphragm) than appendicular muscles (P = 0.0087). This pathology was not significantly associated with pertinent clinical, genetic (c9ALS) or nervous system pathologic data, suggesting it is not limited to any particular subgroup of ALS patients. Among 25 non-ALS muscle samples, pTDP-43 inclusions were seen only in the autophagy-related disorder inclusion body myositis (IBM) (n = 4), where they were more diffuse than in positive ALS samples (P = 0.007). As in IBM samples, pTDP-43 aggregates in ALS were p62/ sequestosome-1-positive, potentially indicating induction of autophagy. Phospho-TDP-43-positive ALS and IBM samples also showed significant up-regulation of TARDBP and SQSTM1 expression. These findings implicate axial skeletal muscle as an additional site of pTDP-43 pathology in some ALS patients, including sporadic and familial cases, which is deserving of further investigation.
- Amyotrophic lateral sclerosis
- Skeletal muscle
- Inclusion body myositis
- Paraspinous muscle
- p62/ sequestosome-1
ALS is a progressive disorder characterized by motor neuron injury, muscle weakness, bulbar symptoms, such as dysarthria and dysphagia , and frontal-subcortical cognitive dysfunction in many patients [43, 44]. ALS has a lifetime risk of ~ 1 in 500 persons  and a prevalence in the United States reaching 17 per 100,000 individuals in the eighth decade . Survival is generally poor and patients typically live only three to five years after diagnosis .
Pathologic studies of ALS nervous tissue have emphasized cell autonomous and non-cell autonomous pathologies in upper and lower motor neuron groups, and more recently, in non-motor brain regions [18, 38]. These include neuronal and glial inclusions comprising misfolded and phosphorylated TAR DNA-binding protein 43 kDA (pTDP-43) [10, 17, 35] and fused-in-sarcoma (FUS) protein , as well as dipeptide repeat pathology in C9ORF72 expansion-associated ALS (c9ALS) . The critical role of glia and immune cells in disease progression is also recognized in human ALS and transgenic ALS models [26, 40, 58]. In contrast, since the original descriptions of ALS [16, 55], the secondary process of muscle atrophy following motor neuron loss and denervation has been emphasized. Indeed, electrophysiologic findings in ALS muscle are typically those of denervation atrophy [19, 29] and are accompanied by histopathologic changes of denervation, such as target fibers and fiber type grouping. At the same time, electrophysiological and functional studies of human ALS have supported an active and early role of skeletal muscle  and an early vulnerability of select muscle groups, such as paraspinous [29, 30]. Further, not all pathologies described in ALS muscle are those of denervation atrophy. Additional pathologies that have been described in some ALS muscle samples include myopathic features , fiber necrosis and inflammation , DNA fragmentation with expression of pro-apoptotic proteins , and reduced expression of mitochondrial proteins and mitochondrial DNA mutations/ deletions [4, 15, 56]. Studies of protein aggregates in human ALS muscle, that might indicate cell autonomous pathology, are much more limited. One study of 30 quadriceps biopsies did not identify pTDP-43 pathology in any samples . Another recent study of deltoid samples found p62-positive, pTDP-43-negative inclusions  and p62-positive, pTDP-43-negative inclusions were recently described in the gastrocnemius of a single c9ALS patient .
Studies in ALS animal models have provided direct evidence that skeletal muscle can play a more active role in neurodegeneration. A variety of cell autonomous pathologies have been identified in the myofibers of transgenic (tg) mice expressing mutant Cu/Zn superoxide dismutase (mSOD1) . These include increased endoplasmic reticulum stress response early in disease , reduction of heat shock protein expression , mitochondrial dysfunction , and pro-apoptotic signaling with increased cytosolic levels of calcium and calcium-binding proteins . Aggregates of SOD1 protein have also been detected in the muscle of mSOD1 animals  and multiple studies have found an alteration in muscle expression of autophagy-related genes [14, 21]. The most compelling evidence to date for the active role of muscle in ALS is the finding that tg mice expressing G37R and G93A human SOD1 in skeletal muscle (hSOD1mus), but not in nervous tissue, develop neurologic and pathologic ALS , with the wildtype motor neurons developing ubiquitinated aggregates. Other muscle-specific tg models have also shown muscular atrophy and reduced strength  and motor neuron degeneration .
To further examine whether cell autonomous pathology is present in the muscle of human ALS patients, we studied 148 muscle specimens from 57 patients to identify the prevalence and muscle group distribution of pTDP-43, a well-characterized marker of ALS pathology in motor neurons. To extend the work of prior studies, we included samples not only of appendicular muscle (quadriceps, deltoid), but also diaphragm and paraspinous muscle groups. We also studied pTDP-43-positive samples to determine whether the autophagy-related protein p62/ Sequestosome-1 was present in myofiber inclusions. To determine the specificity of these findings, we compared the ALS samples to an additional 25 non-ALS muscle samples with neurogenic atrophy, including four samples of clinical and pathologic inclusion body myositis (IBM). Finally, we examined whether pTDP-43 pathology in muscle was associated with salient disease characteristics, including age, site of onset, disease duration, familial or c9ALS status, and the burden of nervous system TDP-43 pathology.
ALS muscle samples and clinical data
The 57 ALS patients with tissue examined in this study all underwent autopsy at our institution. The sample was representative of clinically diagnosed ALS patients seen at our institution with (1) pathologic confirmation and (2) skeletal muscle samples obtained at autopsy from one or multiple muscle groups. All pathologically confirmed ALS cases with skeletal muscle available for study were included. The majority of patients were evaluated in the clinic of two study authors (SHA, JWA). The study was conducted with the approval of the Institutional Review Board at Houston Methodist Hospital (IRB-(3 N)-0114–0013).
Clinical variables recorded included (a) disease duration, defined as the time between first symptoms and autopsy date, (b) age at death, (c) site of disease onset (“limb”, “bulbar”, or “multifocal/other”), and (d) whether the patient had familial (fALS) or sporadic ALS (sALS). As previously described , c9ALS status was identified (or confirmed) for the purposes of this retrospective study by the presence of TDP-43-negative, p62-positive inclusions on immunofluorescence (purified mouse anti-p62 Ick ligand, 1:50, BD Biosciences, San Jose, CA) in hippocampus and/or cerebellar granule cells. All c9ALS cases were confirmed using poly-GA (MABN889, EMD Millipore, 1:200, mouse monoclonal) and poly-GP (ABN455, EMD Millipore, 1:1000, rabbit polyclonal) antibodies. In 42 of the 57 patients in this study, the percentage of nervous system regions-of-interest (ROIs) with TDP-43 pathology, as previously reported , was also available.
Non-ALS muscle samples
Non-ALS patients (n = 25) included seventeen samples with neurogenic atrophy demonstrated on muscle biopsy. These non-ALS patients comprised four cases of biopsy-proven inclusion body myositis (IBM), one case with neurogenic atrophy in a patient with myasthenic symptoms, one case of denervation atrophy in a patient with nerve plexus injury, one case of steroid myopathy, and 10 biopsies with a range of mild neurogenic changes (scattered nuclear clumps, esterase-positive angulated and atrophic fibers). Eleven of the non-ALS biopsies were from quadriceps and the remainder were obtained from biceps (2), gastrocnemius (2), or an unspecified site (2). An additional eight samples were included that contained fairly abundant paraspinous muscle among the various tissues obtained at laminectomy and submitted for routine pathologic examination. Two such specimens were from cervical spine with the remainder from lumbar spine and diagnoses included synovial cyst (2), radiculopathy (1), spinal stenosis (4), and spondylolisthesis (1).
Phospho(409/410)-TDP43 antibody (1:500, rabbit polyclonal, 22309–1-AP, Proteintech, Rosemont, IL) was applied to all ALS samples, including paraspinous muscle (n = 44), deltoid (n = 34), diaphragm (n = 29), quadriceps (n = 26), skeletal muscle, NOS (n = 13), and one sample each of gastrocnemius and abdominal wall muscle. Immunostaining was performed on formalin-fixed, paraffin embedded (FFPE) tissue samples, sectioned at 4 μm, mounted on charged slides and dried for at least 2 h at 50–60 °C. Deparaffinization and rehydration were carried out using a series of xylenes, graded alcohols, and reagent grade water (ThermoFisher Scientific, Waltham, MA). Heat-based antigen retrieval was performed using a 1× antigen retrieval solution at pH 9 (Agilent Technologies, Santa Clara, CA) and was carried out for 1 h (30 min at 95 C0, followed by 30 min on ice). Subsequent washing steps were carried out using a commercial Tris-buffered saline solution (1×) containing Tween 20, pH 7.6 (Agilent Technologies) with a 3% hydrogen peroxide solution (VWR International, Radnor, PA) used to block endogenous peroxidase. Primary antibody was applied for a minimum of 1 h following a one-hour blocking step at room temperature with 2.5% horse serum (Vector Laboratories, Burlingame, CA). Slides were thoroughly washed and a species appropriate ImmPress™ HRP IgG detection kit (Vector Laboratories) was applied for 1 h at room temperature. Following additional washing steps, target antigen was visualized using DAB chromogen in substrate buffer (Agilent Technologies). Hematoxylin counterstain was applied and slides were taken to xylene and mounted with Permount™ (ThermoFisher Scientific). Negative and positive controls were used with all staining reactions. Positive controls comprised ALS spinal cord or medulla and performed appropriately.
Evaluation of pTDP-43 inclusion pathology
Myofibers, adipose tissue, and neurovascular tissue were assessed for pTDP-43-reactive inclusions. For myofibers, only cases with unequivocal staining in the subsarcolemmal region or within sarcoplasm were recorded as positive (no intranuclear inclusions were identified). Semi-quantitation of pTDP43-positive samples was also performed. For pTDP-43 density, the number of involved fibers was quantitated in a single 100× low-power field (LPF). For pTDP-43 extent, the number of LPFs with pTDP-43 pathology per slide was expressed as a percentage of all LPFs with myofibers in the sample (e.g., 15 fields with pTDP-43 inclusion pathology of 25 total LPFs of muscle = 60% of fields with at least one pTDP-43 inclusion).
p62 and FUS immunohistochemistry
Using the procedures described above, skeletal muscle samples that were positive for pTDP-43 were screened for inclusions of p62 (purified mouse anti-p62 Ick ligand, 1:100, BD Biosciences, San Jose, CA) and/or FUS/TLS (1:200, rabbit polyclonal, 11570–1-AP, Proteintech). Immunohistochemical procedures were identical to those described above. Negative and positive controls were used and performed appropriately. For p62, sections of spinal cord or medulla from ALS patients served as positive controls. For FUS, positive controls were sections of FTLD-FUS brain tissue.
Additional staining in a subset of cases
In a subset of ALS cases with pTDP-43 inclusions, double labeling immunofluorescence procedures were performed to assess co-expression of pTDP-43 (as above) with fast myosin (anti-mouse, 1:400, Sigma Aldrich, M4276), slow myosin (anti-mouse, 1:1000, Sigma Aldrich, M8421), or p62 (as above). Samples were incubated overnight with a mixture of primary antibodies at 4 °C following deparaffinization and rehydration steps, antigen retrieval procedures (10 mM citrate buffer), and a blocking step using 2.5% horse serum. After several washes with phosphate buffered saline, secondary antibodies (1:200) were applied for 1 h, including the secondary antibodies Alexa Fluor® 555 anti-rabbit IgG (Thermo Fisher, A-21429), Alexa Fluor® 555 anti-mouse IgG (Thermo Fisher, A32727), Alexa Fluor® 488 anti-mouse IgG (Thermo Fisher, A11001), and Alexa Fluor® 488 anti-rabbit IgG (Thermo Fisher, A-11034). Following further PBS washes, sections were mounted using Vectashield Antifade mounting media with DAPI (H-1200, Vector Laboratories, Burlingame, CA).
Additional staining for N-terminal TDP-43 antibody (1:1000, rabbit polyclonal, 10782–2-AP, Proteintech, Rosemont, IL), which stains both physiologic and pathologic TDP-43, was performed in three ALS samples with pTDP-43 inclusions (see Results), two ALS samples without pTDP-43 inclusions, and a control sample of frontotemporal lobar degeneration with TDP-43 inclusion pathology. 1% Thioflavin S staining was performed in the same five ALS samples undergoing N-terminal TDP-43 immunohistochemistry, as well as four samples of IBM, three samples of non-ALS, non-IBM neurogenic atrophy, and two control samples (Alzheimer’s disease).
Evaluation of immunofluorescence studies
All immunofluorescence studies were reviewed within 24 h of staining and images were captured in cellSens software 1.13 (Olympus America, Inc., Center Valley, PA) on an Olympus BX-43 Microscope using a DP71 camera, a EGFP FITC/Cy2 filter cube (set number 49002, Olympus, Center Valley, PA) and a CY3/TRITC filter cube (set number 49004, Olympus, Center Valley, PA). Slides were examined separately under DAPI, TRITC, and FITC filters, to facilitate examination of antibody/ fluorophore-specific signal versus structures with autofluorescence (e.g., pigment). Images were captured in cellSens software, including merged images combining all three channels.
Electron microscopy of FFPE tissue
A protocol at our institution available for the ultrastructural study of specimens from FFPE blocks not fixed with glutaraldehyde was used to study four ALS muscle samples with comparatively extensive pTDP-43 inclusion pathology (see Results). A region of maximal pTDP-43 inclusion pathology was identified microscopically and marked on the tissue block face. A core of tissue was sampled from the corresponding tissue focus, deparaffinized and post fixed in buffered 2% osmium tetroxide. Tissues were dehydrated in a graded ethanol series, followed by resin infiltration with propylene oxide and EMbed 812 mixture (Electron Microscopy Sciences, Hatfield, PA). Samples were embedded overnight at 60 oC. Semi-thick and ultrathin sections were collected using a LEICA EM UC7 (Leica Microsystems, Buffalo Grove, IL). Stained thin sections were imaged with JEOL 1400 transmission electron microscope (JEOL Ltd., Tokyo, Japan) and AMT Imaging Software (Advanced Microscopy Techniques, Corp., Woburn, MA).
RNA isolation and real-time PCR
To examine SQSTM1 (p62/ sequestosome-1) and TARDBP gene expression, RNA was isolated from four successive 10-μm sections of paraffin-embedded muscle tissue using an RNeasy® FFPE Kit (Qiagen, catalogue number 73504, Hilden, Germany) according to the manufacturer’s protocol. RNA was isolated from five ALS samples (p62 and pTDP-43-positive), three IBM samples (p62 and pTDP-43-positive), and three samples of non-ALS, non-IBM neurogenic atrophy (p62 and pTDP-43-negative). Quantification of RNA was performed using a Nanodrop ND 100 spectrophotometer (Thermo Fisher Scientific).
Real-time PCR primer assays were performed using SYBR® Green dye-based chemistry (Bio-Rad, catalogue # 1725151, Hercules, CA, USA) with commercially available and experimentally validated PCR primer pairs for SQSTM1 (Bio-Rad, catalogue # qHsaCED0045925) and TARDBP (Bio-Rad, catalogue # qHsaCED0043888). Housekeeping genes utilized for normalization of transcript levels included GAPDH (Bio-Rad, catalogue # qHsaCED0038674) and RPS18 (Bio-Rad, catalogue # qHsaCED0037454). Each real-time PCR experiment included eleven ALS, IBM, and atrophy muscle RNA samples plus a no template control (12 experimental wells per primer × 4 primers). This experiment was duplicated in the other half of the 96-well plate and then repeated, again in duplicate, using a new 96-well plate. A one-step real-time PCR protocol was performed on a CFX96 Touch (Bio-Rad, Hercules, CA, USA), including a melt curve step to exclude non-specific amplification. Experiments were analyzed in CFX Maestro™ software for Mac (Bio-Rad, Hercules, CA, USA). TARDBP and SQSTM1 expression were normalized to both reference genes (GAPDH, RS18) and relative normalized gene expression was compared between patient groups. Significance testing was performed using an unpaired t-test.
Descriptive statistics and statistical analyses
Fisher exact tests were used to determine the strength of association between pTDP-43 inclusion pathology in muscle fibers and individual muscle groups (deltoid, quadriceps, paraspinous, and diaphragm), as well as axial (diaphragm, paraspinous) versus appendicular (deltoid, quadriceps) musculature. Fisher exact tests were also used to examine the association between pTDP-43 inclusion pathology and c9ALS status, fALS status, and onset (limb versus bulbar). The strength of these associations was recorded by the P-value and odds ratio (OR).
Wilcoxon rank sum tests (Mann-Whitney U) were applied to examine the equality of medians in pTDP-43-positive and negative ALS patients with respect to age at death, disease duration, and percentage of central nervous system regions-of-interest (ROIs) positive for TDP-43 pathology . As previously reported, the last of these measures was the percentage of 34 different brain regions positive for TDP-43 inclusions (using Proteintech 10782–2-AP) (ranging between 27.3 and 100%) and these data were available for 42 of the 57 patients studied here . Similarly, Wilcoxon rank sum tests were applied to examine the equality of medians between IBM and ALS patients with respect to pTDP-43 density and pTDP-43 extent in positive skeletal muscle samples. Statistical testing was implemented in Matlab R2015b  and statistical significance was set at P ≤ 0.01.
Demographics and clinical characteristics
Demographic, clinical, and sample characteristics in 57 ALS patients
Entire cohort a
61 years (IQR, 56–68), range 39–86 b
1090 days (IQR, 781–1565), range 315–4886
39 men (68.4%)/ 18 women (31.6%)
fALS c/ sALS/ C9ALS
10 fALS (18.2%)/ 45 sALS (81.8%)/ 13 C9ALS
Onset site c
38 Limb (66.7%)/ 12 Bulbar (21.1%)/ 6 Multifocal (10.5%)
Axial muscle samples
44 Paraspinous (29.7%)/ 29 Diaphragm (19.6%)
Append. Muscle samples
34 Deltoid (22.9%)/ 26 Quadriceps (17.6%)
Other muscle samples
13 NOS d (8.8%)/ 1 gastrocnemius/ 1 abdominus rectus
Prevalence, distribution, and quantitation of pTDP-43 muscle pathology in ALS
Quantitatively, a range of inclusion density and spatial extent was seen across pTDP-43-positive ALS samples. The median number of pTDP-43 inclusions per 100× field was 2 (IQR, 2 to 14.3 inclusions, range of 1 to 64). The majority of positive samples had multiple LPFs of pTDP-43 pathology, with a median of 5 LPFs per case having pTDP-43 inclusions (IQR, 2–7 LPFs, range of 1 to 15). A median of 10% of all microscopic LPFs that included skeletal muscle had pTDP-43 pathology (range of 3%–60%), reflecting that the inclusion pathology was patchy and not typically diffuse.
Co-localization of pTDP-43 inclusion pathology was examined with respect to fast- and slow-myosin heavy chain expression in 5 ALS cases and 1 IBM sample. In ALS cases, a median of 2 pTDP-43-immunoreactive inclusions was seen in the positive high-power field studied (range of 1–14). Phospho-TDP-43 inclusions in both slow- and fast-myosin positive fibers were seen in two cases (one with 78.5% in fast-myosin expressing fibers, the other with 80% in slow-myosin expressing fibers). The remaining ALS cases had pTDP-43 positive inclusions only in slow fibers (2 cases) or fast fibers (1 case). The single IBM sample tested had 83.3% of pTDP-43-positive inclusions in myofibers expressing fast myosin.
p62 and FUS IHC in pTDP-43-positive ALS samples
All but one pTDP-43-positive ALS sample (23 of 24 samples) had pathologic inclusions of p62 in myofibers in the same distribution (Fig. 1). As in IBM cases, p62 was a more sensitive marker, revealing more extensive inclusion pathology than pTDP-43 alone. FUS immunohistochemistry was negative in all 24 ALS samples.
Muscle group distribution of pTDP-43 positive samples in ALS
Among the 24 pTDP-43-positive ALS muscle samples, 10 were obtained from paraspinous musculature (41.7% of positive samples), 7 from diaphragm (29.2%), three from deltoid (12.5%), and one from gastrocnemius (4.2%). Three positive samples were from a muscle group not specified in the original autopsy report (12.5%) and were simply designated as “muscle, NOS.”
Among the 19 ALS patients with any pTDP-43-positive muscle sample, 4 patients had multiple pTDP-43-positive samples (7% of the cohort, 21% of positive samples). The combinations of pTDP-43-positive samples included: diaphragm and paraspinous (2 patients), diaphragm, paraspinous, and deltoid (1 patient), and diaphragm and deltoid (1 patient). Three of these patients had clinically-designated sALS (75%) and c9ALS was present in two of these four (50%).
Clinical and pathologic associations of pTDP-43 muscle pathology
Characteristics of muscle samples with and without pTDP-43 pathology
pTDP-43 Positive (n = 19)
pTDP-43 Negative (n = 38)
17 Axial, 4 Appendicular b
56 Axial, 57 Appendicular b
64 years (IQR, 58.5–69.5)
59.5 years (IQR, 54.3–66.5)
1114 days (IQR, 840–2134)
1085 days (IQR, 723–1390)
CNS TDP+ ROI c
58.3% TDP+ (IQR, 45.5–79.4)
50.0% TDP+ (IQR, 42.3–76.5)
13 men, 6 women
26 men, 12 women
3 fALS, 16 sALS
7 fALS, 29 sALS
11 Limb, 5 Bulb, 3 Multifocal
27 Limb, 7 Bulb, 3 Multifocal
No significant differences were identified between ALS patients with and without pTDP-43 muscle pathology with respect to age (z = 1.7, P = 0.1) or disease duration (z = 0.95, P = 0.34). Likewise, no significant association was seen between pTDP-43 status in muscle and fALS status (OR = 0.78), c9ALS status (OR = 0.8), or site of symptom onset (OR = 0.57). Utilizing data from an earlier study , ALS cases with pTDP-43 muscle pathology had a median of 58.3% and 50.0% of brain regions involved by TDP-43 inclusion pathology, respectively (z = 0.42, P = 0.67).
Inclusion pathology in IBM and non-IBM, non-ALS muscle
Four cases of IBM (clinically suspected and pathologically confirmed) were from three males and one female with a median age of 59 years. Among these samples, only IBM cases (100%) had pTDP-43 inclusions, which were also p62-immunoreactive (Fig. 1). Three non-ALS, non-IBM cases with mild neurogenic atrophy had granular, non-specific p62 immunoreactivity (pTDP-43 negative) that did not resemble that seen in either ALS or IBM patients. Likewise, in non-ALS paraspinous samples, p62 occasionally showed immunoreactive structures, but these were uniformly pTDP-43-negative and did not resemble those in ALS or IBM muscle. In IBM patients, within the focus of maximum pTDP-43 pathology (100× field), IBM cases had a median of 10 involved myofibers (IQR of 7–11.8), whereas for ALS cases the median was 2 (IQR of 2–14.3) (z = − 1.1, P = 0.26). However, IBM and ALS patients with pTDP-43 inclusions did significantly differ in the spatial extent of pathology, with IBM patients having a median of 67% of LPFs involved (z = − 2.7, P = 0.007).
pTDP-43 replication study in a subset of cases
A subset of 5 pTDP-43-positive muscle samples, two from patients with IBM and three from patients with ALS, were sent to an independent research laboratory for separate evaluation using their pTDP-43 immunohistochemistry protocol (phospho-TDP-43, 1D3 clone, 1:500). Five unstained sections, cut at 4 μm and labeled “ALS1–3” and “IBM1–2”, were shipped to the laboratory. Their results matched the spatial distribution and staining intensity of pTDP-43 in all IBM and ALS samples (see Online Resource Additional file 1: Figure S1).
This study demonstrates that aggregates of phosphorylated TDP-43 may be identified in the skeletal muscle of both sALS and fALS patients, including patients with and without c9ALS. This implicates axial skeletal muscle as an additional site of pTDP-43 pathology in ALS. A muscle group-specific difference in muscle pathology was also suggested by the finding that pTDP-43 inclusions were significantly more frequent in samples from axial muscle groups than appendicular groups (the absence of inclusion pathology in quadriceps samples is also consistent with the negative result of an earlier study  that did not assess axial muscle groups). Our finding that pTDP-43-positive (FUS-negative) aggregates in ALS samples are also positive for the autophagy pathway protein p62/ sequestosome-1 suggests the possibility of an engagement of endogenous autophagic mechanisms in ALS muscle, as in motor neurons. Indeed, this pattern resembled the co-localization of pTDP-43 and p62 inclusions in IBM [9, 31], an intrinsic myopathy in the differential diagnosis of ALS  with pathologic protein aggregates, progressive and asymmetrical weakness , and impairments in autophagy. Other characteristic features of IBM, however, were not identified in our ALS samples and there was significantly more extensive pTDP-43 inclusion pathology in IBM muscle than in ALS. Nonetheless, pTDP-43 aggregates in ALS and IBM muscle may arise through similar mechanisms, including impairments in autophagy and proteostasis.
To our knowledge this is the first study to systematically demonstrate the presence of pTDP-43 aggregates in the myofibers of ALS patients, particularly in axial muscle groups. This implicates ALS muscle as an additional site of pTDP-43 pathology, as previously demonstrated in motor neurons, non-motor neurons, and glia. The downstream effects of cytoplasmic pTDP-43 pathology in ALS muscle cells requires further study, though studies in transgenic animals expressing mutant human TDP-43 have identified a toxic gain-of-function from cytoplasmic aggregation, leading to transcriptional dysregulation, including within histone processing genes . Several results of this study raise the question as to whether pTDP-43 in ALS muscle represents a cell autonomous pathology. First, the presence of pTDP-43 inclusions in muscle did not associate at all with disease duration or the burden of central nervous system TDP-43 pathology . If cell-to-cell spread were the sole mechanisms explaining muscle pTDP-43 pathology, one would expect significant positive associations between muscle fiber inclusion pathology and either duration or the burden of nervous system TDP-43 pathology. Second, pTDP-43 co-localized with p62 in affected muscle fibers and a concomitant up-regulation of TARDBP and SQSTM1 gene expression was seen by real-time PCR. Co-localization with an autophagy pathway protein (p62), and up-regulation in gene expression (for TDP-43 and p62), suggests this may be an endogenous pathology in muscle that engages the autophagy pathway. Increased expression of p62 has also been seen in non-ALS, non-IBM muscle diseases, including genetically driven forms of muscular dystrophy , so it may not implicate autophagy in all cases. Third, pTDP-43 co-localized with both fast- and slow-myosin expressing fibers in the same ALS sample (motor neurons innervating fibers of a single type) and was distributed within multiple fascicles rather than a single fascicle. However, it is also important to recognize that the majority of skeletal muscle samples were negative for pTDP-43. One reason for this may be that our study used single tissue samples obtained from between one and four muscle groups per patient. This approach is distinctly different from the postmortem examination of ALS nervous systems, where all anatomic regions (brain, spinal cord) are amenable to sampling and diagnostic pTDP-43 that may actually be quite limited in spatial extent. Recent autopsies at our institution, not included in this study, with paraspinous samples at multiple spinal levels, have indeed shown patchy, multifocal and segmental involvement of muscle (see Online Resource Additional file 1: Figure S2). This suggests that the true prevalence of pTDP-43 pathology in muscle cannot be ascertained from single biopsy-size samples and may be underestimated even in the present study.
An alternative mechanism explaining pTDP-43 aggregates in ALS muscle is a “prion-like” transfer of pTDP-43 protein, possibly through anterograde axonal transport. This model of neuron-to-neuron spread has been proposed to explain dissemination of pTDP-43 pathology in brain and spinal cord . If trans-synaptic spread between neurons indeed takes place in ALS, then spread along the axons of motor neurons, across the neuromuscular junction, and into myofibers is plausible. A distance-dependent interaction between motor neurons and muscle, possibly acting in concert with muscle-specific pathology, may explain the enrichment of pTDP-43 inclusions in axial muscle. This question deserves further investigation, possibly through studies examining the density of spinal cord motor neuron pTDP-43 pathology in tandem with paraspinous muscle samples at the same spinal level.
Our study also identified co-localization of p62/ sequestosome-1 in pTDP-43 inclusions of ALS muscle, which suggests the possibility that the autophagy pathway is activated. This recapitulates pathology well described in inclusion body myositis (IBM). Further comparison of ALS and IBM muscle samples may provide insight as to how pTDP-43 inclusions arise in vulnerable ALS muscle groups. To date, there have been few studies of pTDP-43 (or p62) pathology in ALS muscle. None of these, to our knowledge, have examined both axial and appendicular muscle groups or compared findings in ALS and IBM, and non-ALS, non-IBM samples with neurogenic atrophy. Previous studies do include a negative study of ALS quadriceps biopsies from 30 patients  (the 26 quadriceps samples studied here were also negative), a study of 31 deltoid biopsies finding p62-immunoreactive, pTDP-43-negative foci in 25.8% of samples , and a case report of a c9ALS patient with blocky p62 inclusions in gastrocnemius . Inclusion pathologies have been much more extensively studied in IBM, where β-amyloid, α-synuclein, and p-tau inclusions have also been described . IBM inclusions are also reported to be positive for Thioflavin S, a finding identified here in all four IBM samples studied and in three pTDP-43-positive ALS samples examined (see Online Resource Additional file 1: Figure S3). In IBM, p62 appears to be the most sensitive marker of inclusion pathology  and these additional inclusions have not been seen in all studies . Nonetheless, these findings have led to the hypothesis that protein aggregates in IBM muscle result from impairments in autophagy, the cellular process by which misfolded protein aggregates are degraded [25, 31]. Supporting this hypothesis are the increased expression of the endosome marker clathrin, the autophagy-related protein ATG5, the microtubule-associated protein light chain (LC3), and beclin-1  in IBM samples. IBM samples also demonstrate more frequent LC3-reactive fibers than in pTDP-43-negative, non-IBM inflammatory myopathy (e.g., polymyositis), which indicates that alterations in autophagy are critical in IBM and not linked to inflammation per se. For ALS, autophagy impairments in motor neurons, as in IBM muscle fibers, have been proposed as a mechanism leading to cell degeneration and toxic protein aggregates [11, 45]. Moreover, mutations in fALS have been reported in autophagy-related genes, including optineurin (OPTN) , ubiquilin 2 (UBQLN2), sequestosome 1 (SQSTM1) , and ubiquitin segregase (VCP)  (the last of these also being described in familial IBM). In ALS nervous systems, p62- and LC3-reactive inclusions have also been identified in spinal cord motor neurons , in addition to TDP-43 . The findings of the current study, which extends the spectrum of pTDP-43 and p62 inclusion pathology to ALS skeletal muscle, particularly in axial muscles, suggests that impairments in autophagy may also involve ALS muscle. Future studies are needed to determine whether other autophagy-related proteins, such as LC3, beclin-1, and optineurin, are over- or under-expressed in ALS muscle.
An intriguing finding of this study was that pTDP-43 pathology was significantly enriched in axial muscle samples. It is known that physiologic abnormalities in paraspinous muscle by electromyography (EMG) are reliable in confirming the clinical diagnosis of ALS and help to distinguish the disease from its mimics . Paraspinous abnormalities have also been described as being present early in the disease . Denervation changes by EMG in paraspinous muscle are also associated with features of diaphragm denervation – an association possibly explained by the medial position of the relevant motor neurons in the ventral horn . A recent study of multiple muscle groups, including thoracic (T10), lumbar (L3, L5), and sacral (S1) paraspinous muscle has also shown non-contiguous abnormalities by needle EMG (e.g., fibrillation potentials). This finding suggests the possibility of multifocal and discontinuous initiation of disease in different motor neuron pools. More extensive sampling of paraspinous muscle groups at autopsy will help to determine if pTDP-43 pathology is similarly multifocal and discontinuous. Further, a limitation of this study, to be addressed in future studies, is that autopsy-derived diaphragm and paraspinous muscle samples from non-ALS patients with other critical illnesses or neurological diseases were not available for study. Paraspinous muscle and muscle biopsy specimens from a range of non-ALS, non-IBM neurologic diagnoses did not show pTDP-43 pathology, but these specimens were not from patients with critical illnesses, such as ALS.
Studies in the mSOD1 mouse model of ALS have provided direct evidence that cell autonomous pathology in muscle can drive the development of the disease . The muscle of mSOD1 animals has been reported to have alterations in the endoplasmic reticulum stress response  and heat shock protein expression , as well as mitochondrial dysfunction , pro-apoptotic signaling, and increased cytosolic levels of calcium and calcium-binding proteins . Aggregates of SOD1 protein have also been detected in gastrocnemius, soleus, and flexor digitorum longus of the transgenic animal . Further, as in IBM, increased gene expression of autophagy components LC3 and SQSTM1 is reported in mSOD1 muscle . Most critically, studies of transgenic ALS mice have revealed that muscle-restricted and muscle-initiated pathologies may induce motor neuron degeneration. Specifically, expression of G37R and G93A human SOD1 in skeletal muscle (hSOD1mus), but not nervous tissue, can lead to neurologic and pathologic ALS  with ubiquitinated aggregates in wild type neurons. Models with a muscle-restricted distribution of SOD1 G93A mutation also show progressive muscular atrophy, mitochondrial dysfunction, and reduced muscle strength  and the atrophic muscles of these mice up-regulate autophagy genes, including LC3.
In summary, this study implicates axial skeletal muscle (diaphragm and paraspinous muscles) as an additional site of pTDP-43 pathology in ALS. Up-regulation of TARDBP and SQSTM1 expression by real-time PCR supports this as a possible cell autonomous pathology in ALS, though future studies using unbiased techniques with a wide range of transcripts for normalization are needed (e.g., RNA-Seq). Additional studies utilizing tissue dedicated for electron microscopy study, with registration to histologic data, are required to clarify the ultrastructural features of the pTDP-43-positive material in ALS muscle. Nonetheless, our findings suggest that the impaired clearance of misfolded proteins in ALS, a well-recognized mechanism in motor neuron degeneration, may play an important role in pTDP-43 pathology in ALS muscle.
We appreciate the efforts of Ms. Claire Haueter of the Houston Methodist Hospital elecrtron microscopy core laboratory, who assisted in the preparation and ultrastructural examination of specimens. We appreciate the efforts of the neuropathology core at the University of Kentucky Alzheimer’s Disease Center that assisted in external pTDP-43 staining in a subset of IBM and ALS samples, as well as the constructive feedback of core director Dr. Peter T. Nelson. We are grateful to the ALS patients and their family members for the donations that made this work possible.
Data collection, analysis, and interpretation, as well as writing of the manuscript, was supported by a Clinician-Scientist Research Award from the Institute of Academic Medicine in the Houston Methodist Research Institute (HMRI) of the Houston Methodist Hospital (to author MDC).
Availability of data and materials
The datasets obtained during and/or analyzed during the study are available from the corresponding author on reasonable request.
MDC conceived of the study, performed pathological and statistical analyses, and drafted the initial and final versions of the manuscript, tables, and figures, including supplementary material. SZP and ALR reviewed salient pathologic characteristics with MDC, assisted MDC in performing the primary autopsy examination in the patients studied herein, and reviewed the manuscript. ASA assisted MDC in the laboratory, including critical staining experiments, and critically evaluated the manuscript. SHA and JWA provided clinical data and expert clinical input and SHA provided critical feedback that improved study design. All authors read and approved the final manuscript.
Ethics approval and consent to participate
All procedures performed in this retrospective study were in accordance with the ethical standards of the institutional research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. The study was also carried out with IRB approval from Houston Methodist Hospital (IRB-(3 N)-0114–0013).
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
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