Downstream effects of plectin mutations in epidermolysis bullosa simplex with muscular dystrophy
Acta Neuropathologica Communications volume 4, Article number: 44 (2016)
Mutations of the human plectin gene (PLEC) on chromosome 8q24 cause autosomal recessive epidermolysis bullosa simplex with muscular dystrophy (EBS-MD). In the present study we analyzed the downstream effects of PLEC mutations on plectin protein expression and localization, the structure of the extrasarcomeric desmin cytoskeleton, protein aggregate formation and mitochondrial distribution in skeletal muscle tissue from three EBS-MD patients.
PLEC gene analysis in a not previously reported 35-year-old EBS-MD patient with additional disease features of cardiomyopathy and malignant arrhythmias revealed novel compound heterozygous (p.(Phe755del) and p.(Lys1040Argfs*139)) mutations resulting in complete abolition of plectin protein expression. In contrast, the other two patients with different homozygous PLEC mutations showed preserved plectin protein expression with one only expressing rodless plectin variants, and the other markedly reduced protein levels. Analysis of skeletal muscle tissue from all three patients revealed severe disruption of the extrasarcomeric intermediate filament cytoskeleton, protein aggregates positive for desmin, syncoilin, and synemin, degenerative myofibrillar changes, and mitochondrial abnormalities comprising respiratory chain dysfunction and an altered organelle distribution and amount.
Our study demonstrates that EBS-MD causing PLEC mutations universally result in a desmin protein aggregate myopathy phenotype despite marked differences in individual plectin protein expression patterns. Since plectin is the key cytolinker protein that regulates the structural and functional organization of desmin filaments, the defective anchorage and spacing of assembled desmin filaments is the key pathogenetic event that triggers the formation of desmin protein aggregates as well as secondary mitochondrial pathology.
Plectin, a multi-domain protein of exceptionally large size (>500 kDa), is abundantly expressed in a wide range of mammalian cells and tissues, most prominently in muscle, brain and stratified squamous epithelia . It acts as a multi-functional linker protein and signalling scaffold that centrally orchestrates the structural and functional organization of filamentous cytoskeletal networks, thereby contributing to fundamental biomechanical properties of mechanical stress-bearing tissue . The essential role of plectin in the latter is highlighted by the observation that mutations in the human plectin gene (PLEC) on chromosome 8q24 cause a variety of rare human disorders (referred to as “plectinopathies”), namely autosomal recessive epidermolysis bullosa simplex with muscular dystrophy (EBS-MD, MIM #226670), EBS-MD with myasthenic features (EBS-MD-MyS), limb girdle muscular dystrophy type 2Q (LGMD2Q, MIM #613723), EBS with pyloric atresia (EBS-PA, MIM #612138), and the autosomal dominant variant EBS-Ogna [23, 25]. While the skin blistering in plectinopathies has been attributed on the molecular level to a disruption of the normal keratin intermediate filament (IF) anchorage to hemidesmosomes , the downstream effects of plectin mutations in striated muscle are less clearly defined and to date have only been addressed in very few detailed studies [2, 17].
Here we report the clinical, genetic, myopathological, and biochemical findings in a not previously reported German EBS-MD patient with additional features of cardiomyopathy and malignant arrhythmias. Furthermore, we analyse the downstream effects of his novel disease-causing compound heterozygous PLEC mutations and two other homozygous PLEC mutations on i) plectin protein expression, ii) the structure of the extrasarcomeric desmin cytoskeleton, iii) protein aggregate formation and iv) the subcellular distribution and biochemical properties of mitochondria in skeletal muscle tissue.
Materials and methods
This study was approved by the local Ethics committees of each participating institution. Written informed consent was obtained from all participants. Patient 1 is a not previously reported, 35-year-old male patient of German origin with EBS-MD. Patient 2 is a previously reported German female with EBS-MD due to a homozygous 16-bp insertion frameshift-mutation c.13459_13474dup (NM_000445.3) in the 3′end of exon 32 of the PLEC gene, causing a premature termination codon (p.(Glu4492Glyfs*48))  (see also Fig. 1a). She had last been seen for clinical evaluation at the age of 25 years but subsequently had tragically died in a domestic fire accident. Patient 3 is a 24-year-old British female with EBS-MD caused by a homozygous 19-bp deletion frameshift-mutation c.5018_5036del (NM_000445.3) in exon 31, which causes a premature termination codon (p.(Leu1673Argfs*64))  (see also Fig. 1a). See Table 1 for more detailed clinical information of all three patients.
DNA of patient 1 and his parents was fragmented and enriched using the TruSight one enrichment kit (Illumina, San Diego, USA). Sequencing was performed on a MiSeq (Illumina, San Diego, USA) in paired-end reads (2× 200 bp). After duplicate removal and quality control the sequence reads were mapped with the BWA aligner  to the reference genome (hg19). Variants were called using 5 different calling programs (GATK, SNVer, CASAVA, SOAPSNP and SOAPindel) and filtered based on population frequency (<0.001 in 94 in house controls and exomes of the ExAC consortium), position (exon and splice site) and mutational effect (CADD score, Polyphen2, SIFT, MutationTaster). Graphical presentation of the mapped sequences was viewed with the Integrative Genomics Viewer (IGV) . The resulting variants were Sanger sequenced and the segregation in the family confirmed.
Muscle biopsies and myopathological analyses
Patient 1 had a diagnostic muscle biopsy from his left triceps brachii muscle in 2013. Skeletal muscle tissue (left quadriceps) from patient 2 obtained as part of the diagnostic process in 2001 was reevaluated. Patient 3 underwent a muscle biopsy from her left biceps humeri in 2014. Skeletal muscle tissue was used for histochemical studies by standard methods . Immunofluorescence microscopy was performed on frozen muscle sections (5 μm) using guinea pig antiserum (AS) to plectin (Progen, GP-21; recognizing the C-terminal domain of plectin, aa 4367–4684 in exon 32), mouse monoclonal antibodies (mAbs) to plectin (KeraFAST, PN643; recognizing the N-terminal actin binding domain, aa 171–595), mAbs to desmin (Dako, clone D33), rabbit AS to synemin 3 (D. Paulin, France, ), goat AS to syncoilin (Santa Cruz Biotechnology Inc., sc-162284), and mAbs to complex IV (subunit I, Invitrogen, #459600) in combination with donkey anti-guineapig IgG Alexa Fluor 555, goat anti-mouse IgG Alexa Fluor 488, donkey anti-mouse IgG Alexa Fluor 555, donkey anti-rabbit IgG Alexa Fluor 488, and donkey anti-goat IgG Alexa Fluor 488 (all from Life Technologies). Images were acquired using a Zeiss LSM 780 confocal laser scanning microscope.
Western blot analyses
Skeletal muscle tissue was homogenized in lysis buffer (pH 6.8) containing 5 mM Tris, 10 % SDS, 0.2 M DTT, 1 mM EDTA, 100 mM NaF, 50 mM ß-glycerphosphate, 2 mM Na3VO4, 1 mM PMSF, and Complete mini protease inhibitor cocktail (Roche) using a TissueLyser II (Qiagen; 30×/s, 2 min; three repetitions). The homogenate was centrifuged for 10 min at 13,000 rpm and the supernatant was stored at −20 °C. For gel electrophoresis, the tissue homogenate was mixed with SDS-sample buffer, denatured at 95 °C for 5 min, and loaded onto 4–15 % Mini-PROTEAN® TGX™ Precast Gels (BioRad). Proteins were transferred onto nitrocellulose membranes, and the following primary antibodies were used for immunoblot analyses: guinea pig AS to plectin (Progen, GP-21; recognizing the C-terminal domain of plectin, aa 4367–4684 in exon 32), rabbit AS to plectin (#9, G. Wiche, Austria; recognizing plectin exons 9–12, ), rabbit AS to desmin (Abcam, ab8592), rabbit AS to synemin 3 (D. Paulin, France, ), goat AS to syncoilin (Santa Cruz Biotechnology Inc., sc-162284), mAbs to α-actinin (Sigma, #7811), mAbs to GAPDH (Sigma, G8795), mAbs to complex II (70 kDa Fp Subunit, Invitrogen, # 459200), mAbs to complex V (α-subunit, Invitrogen, #439800). For detection, HRP-conjugated secondary antibodies (all from BioRad) in combination with Pierce SuperSignal West Pico Chemiluminescent Substrate (Thermo Scientific) were used.
Novel compound heterozygous PLEC mutations lead to EBS-MD plus cardiomyopathy and life-threatening arrhythmias
Patient 1 is a 35-year-old German male with a past medical history of skin blistering (Fig. 1b) and nail dystrophy (Fig. 1c) since birth. At the age of 27 he first experienced recurrent episodes of dizziness and sudden loss of consciousness. Cardiological evaluation at that time revealed a dilated cardiomyopathy with markedly reduced left ventricular ejection fraction (20–30 %), as well as episodes characterized by self-limiting ventricular fibrillation and torsades. Since the cardiac arrhythmias were graded as life-threatening, a single-chamber cardioverter defibrillator was implanted (see asterisk in Fig. 1d). Slowly progressive muscle weakness and myalgia were first noted soon after the manifestation of cardiac problems. Neurological examination at the age of 32 revealed muscle weakness and wasting predominantly affecting shoulder-girdle and lower leg muscles with an associated marked steppage gait (Fig. 1d and e). Needle electromyography revealed a myopathic pattern in proximal and distal muscles of both the upper and lower limbs. CK levels were markedly elevated (up to 3782 IU/l). PLEC sequencing revealed two novel heterozygous variants, a maternally inherited in-frame deletion c.2264_2266delTCT/p.(Phe755del) in exon 19 and a paternally inherited frameshift deletion c.3119_3120delAA/p.(Lys1040Argfs*139) in exon 24 (see Additional file 1: Figure S1 and Table 1). Both are classified as pathogenic according to the ACMG criteria and are therefore considered disease causing variants.
Impact of PLEC mutations on skeletal muscle morphology and plectin protein levels: no plectin, less plectin, or expression of rodless plectin
Myopathological analyses of skeletal muscle specimens from all three EBS-MD patients with genetically confirmed PLEC mutations revealed a marked myodegenerative pattern with increased endomysial connective and fatty tissue, highly variable fiber size diameters (5 to 145 μm), predominance of type 1 fibers, fiber splitting as well as de- and regenerating fibers (Fig. 2a). Quantification of muscle fibers with internally located myonuclei demonstrated an abnormal myonuclear positioning in 47 % of fibers in patient 1, in 55 % of fibers in patient 2 and in 10 % of fibers in patient 3. Muscle biopsy from patient 2 additionally showed multiple muscle fibers with rimmed vacuoles (data not shown). To investigate the effects of the three different PLEC mutations on plectin protein expression in skeletal muscle, we performed indirect immunofluorescence microscopy and immunoblot analyses using plectin-specific antibodies (Fig. 2b-d). These analyses showed a marked variation of plectin protein levels among the three EBS-MD cases. Immunofluorescence analysis using antibodies directed against the N-terminal or the C-terminal part of plectin demonstrated the complete absence of specific immunostaining in patient 1, whereas the other two EBS-MD muscle specimens displayed markedly reduced plectin staining in comparison to normal controls (Fig. 2b). Plectin immunoblot analysis of normal human skeletal muscle detected two bands, one with a strong signal intensity corresponding to a molecular mass of approximately 500 kDa and a second, very faint signal at 390 kDa. While the former represents the full length plectin protein species, the latter corresponds to rodless plectin variants . Analysis of patient 1 showed a complete absence of plectin, whereas patient 2 displayed a marked reduction in the signal intensities of both bands. In contrast, analysis of the muscle probe from patient 3 resulted in the sole detection of rodless plectin variants (Fig. 2c and d, and Table 1). Thus, the PLEC mutations in our three EBS-MD patients led to marked individual differences in plectin protein expression in skeletal muscle.
Aberrant plectin expression leads to destruction of the desmin network and desmin protein aggregation pathology
One major function of plectin in skeletal muscle is the proper organization and anchorage of the three-dimensional, extrasarcomeric IF network, which – in addition to plectin - is mainly composed of the IF proteins desmin, syncoilin, synemin [7, 16]. In contrast to the regular IF staining pattern in normal controls, our immunofluorescence analyses on muscle tissue from EBS-MD patients using corresponding antibodies demonstrated a marked disruption of the endogenous desmin network in conjunction with subsarcolemmal and sarcoplasmic desmin-, syncoilin-, and synemin-positive protein aggregates in nearly all muscle fibers (Fig. 3a and b). Subsequent immunoblot analyses of all three EBS-MD probes revealed significantly increased desmin protein levels (180 % in patient 1; 156 % in patient 2 and 242 % in patient 3), whereas the levels of syncoilin and synemin were unchanged (Fig. 3c and d). Thus, irrespective of the individual PLEC mutations and their corresponding plectin protein expression pattern, these patients universally exhibited destruction of the desmin filament network and desmin-positive protein aggregates, which are the hallmarks of the EBS-MD muscle pathology.
From cytoskeletal to mitochondrial pathology in EBS-MD muscle tissue
Structural and functional alterations of mitochondrial networks have previously been described in skeletal muscle specimens from EBS-MD patients [10, 17] as well as muscle-restricted conditional plectin knockout mice . Succinate dehydrogenase (SDH) and cytochrome oxidase (COX) stains of muscle specimens from our EBS-MD patients clearly demonstrated an abnormal pattern with less ordered, often coarse, and thread-like appearing mitochondrial networks (Fig. 4a). Moreover, in a subset of fibers, large sarcoplasmic areas with markedly attenuated enzyme staining (“rubbed-out” lesions) became apparent (Fig. 4a, arrows). In addition, several COX-negative/SDH-positive fibers were identified in the muscle biopsy from patient 3 (Fig. 4a, arrowheads). However, no classical ragged-red fibers were seen in Gomori-Trichrome stains (data not shown). In keeping with the enzymatic COX stains, immunofluorescence analysis using a complex IV antibody showed reduced signal intensities in all EBS-MD samples (Fig. 4b). Furthermore, immunoblotting with antibodies directed against complex II and V of respiratory chain enzymes revealed a dramatic decrease of the respective expression levels in all EBS-MD samples (Fig. 4c). Expression levels of complex II were reduced to 42 % (patient 1), 52 % (patient 2), or 67 % (patient 3), and complex V to to 41 % (patient 1), 50 % (patient 2), or 44 % (patient 3) compared to control levels (Fig. 4d). In addition to changes in the subcellular distribution of mitochondria, the decrease in the levels of complex II, IV and V suggest a reduction in the total amount of mitochondria in EBS-MD muscle tissue.
Our genetic analysis in patient 1 identified two novel compound heterozygous PLEC mutations. In addition to the skin and skeletal muscle involvement characteristic of the disease, this patient developed a dilated cardiomyopathy and life-threatening episodes of cardiac arrhythmias necessitating the implantation of a single-chamber cardioverter defibrillator. Plectin-related cardiac disease comprising mild left ventricular hypertrophy , reduced ejection fraction in combination with artrial fibrillation , dilated cardiomyopathy , and left ventricular non-compaction cardiomyopathy  have previously been described in a subset of EBS-MD patients. However, this is the first report indicating that even life-threatening cardiac disease manifestations may occur before the onset of skeletal muscle symptoms, suggesting that regular cardiological assessments including electrophysiological and cardiac imaging studies should be part of the diagnostic work-up of all EBS-MD patients.
To characterize the downstream effects of PLEC mutations, we analysed skeletal muscle tissue from the newly-reported patient in comparison to muscle biopsies from two other previously reported EBS-MD patients, in whom the homozygous disease-causing mutations reside in exon 31 and exon 32 of the PLEC gene, respectively. Our immunoblot studies demonstrated a heterogenous pattern of plectin expression with complete abolition of plectin protein expression in patient 1, markedly reduced plectin levels in patient 2, and the sole presence of rodless plectin variants in patient 3. Rodless plectin isoforms, lacking the central rod domain due to alternative splicing of exon 31 , are expressed in normal human skeletal muscle and skin tissue, though in relatively low amounts [8, 16]. A recent study in plectin knock-in mice indicated that rodless plectin might functionally compensate for the loss of full-length plectin in murine skin and skeletal muscle tissue . However, this notion is clearly contradicted by our findings in patient 3, who - despite expressing rather high levels of rodless plectin in muscle – developed a severe form of muscular dystrophy.
Irrespective of the individual PLEC mutations and their varying consequences on plectin protein expression, our analyses revealed a rather uniform picture of EBS-MD muscle pathology, characterized by degenerative myofibrillar changes, subsarcolemmal and sarcoplasmic desmin-positive protein aggregates, and mitochondrial abnormalities. Since these myopathological alterations are also the morphological hallmark of myofibrillar myopathies [15, 18], EBS-MD can thus be classified as a subtype of these protein aggregate myopathies.
Studies in primary human differentiating skeletal muscle cells and various transgenic plectin mouse models indicate that plectin exerts a pivotal role in the structural and functional organization of the three-dimensional desmin IF network, with an essential role in mechanosensing and in protecting skeletal muscle cells against mechanical stress [7, 16, 24]. Our study demonstrates universal disruption of the endogenous desmin-, synemin-, and syncoilin-IF networks in nearly all EBS-MD skeletal muscle fibers. Hence, the faulty subcellular spacing and anchorage of preformed desmin filaments is the primary pathogenic key event in EBS-MD striated muscle tissue. In keeping with this notion, the only reported histopathological study of cardiac muscle from an EBS-MD patient with dilated cardiomyopathy revealed a disruption of the regular desmin and plectin staining pattern at the level of Z-discs and intercalated discs as well as the presence of desmin-positive protein aggregates . Furthermore, our previously reported desmin immogold EM analysis of patient 2 demonstrated the presence of subsarcolemmal and sarcoplasmic protein aggregates, which are composed of preformed but highly disordered desmin filaments . Our new immunoblot studies further highlighted increased desmin protein levels in all EBS-MD samples indicating alterations in the overall desmin protein homeostasis. Thus, increased desmin protein levels in conjunction with the defective anchorage and spacing of preformed desmin filaments are the basis for the formation of subsarcolemmal and sarcoplasmic protein aggregates, which are composed of desmin, synemin-, and syncoilin IFs.
Previous studies in plectin and desmin knock-out mice convincingly demonstrated that the formation of endogenous plectin-desmin IF networks is pivotal for the normal organization, content, function and regulation of mitochondrial networks [7, 12, 22]. Hence, the observed changes in the subcellular distribution and amount of mitochondria as well as respiratory chain dysfunction in EBS-MD muscle are likely to be a direct consequence of the primary and omnipresent disruption of the plectin-desmin IF networks, rather than being an nonspecific secondary effect of muscle degeneration. Thus, our study strongly implies that the mitochondrial pathology is a fundamental pathogenic mechanism that contributes to the progressive and severe muscle damage in EBS-MD.
Our study demonstrates that EBS-MD causing PLEC mutations, though leading to marked differences in the individual plectin protein expression pattern, all result in a desmin protein aggregate myopathy phenotype. Since plectin is the key cytolinker protein that regulates the structural and functional organization of the desmin filaments, the defective anchorage and spacing of assembled desmin filaments is the key pathogenetic event that triggers the formation of desmin protein aggregates as well as the secondary mitochondrial pathology.
Ethics approval and consent to participate
This study was approved by the local Ethics committees of each participating institution. Written informed consent was obtained from all participants.
Consent for publication
Consent for publishing personal data was obtained from patient 1.
Availability of data and materials
The datasets supporting the conclusions of this article are included within the article and its additional file.
epidermolysis bullosa simplex with muscular dystrophy
epidermolysis bullosa simplex with muscular dystrophy with myasthenic features
epidermolysis bullosa simplex with pyloric atresia
limb girdle muscular dystrophy
mouse monoclonal antibody
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The authors thank Prof. Gerhard Wiche (Max F. Perutz Laboratories, University of Vienna, Austria) and Prof. Denise Paulin (Pierre and Marie Curie Universitè, France) for providing antibodies. We acknowledge support by Deutsche Forschungsgemeinschaft and Friedrich-Alexander University Erlangen-Nürnberg (FAU) within the funding programme Open Access Publishing.
We acknowledge grant support by the German Research Foundation (DFG) within the framework of the multi-location research group FOR1228 (SCHR 562/13-1 to Rolf Schröder).
The authors declare that they have no competing interests.
LW, MT, and RS initiated this study, generated the study concept and design, and prepared the manuscript. LW, MT, CT, USS carried out laboratory studies and interpretation of data. PH, MM, CK, FN, HJ provided patient samples for the study and interpretation of data. All authors read and approved the final manuscript.
Sanger confirmation of the identified PLEC mutations in patient 1. Plectin mutation analyses using genomic DNA derived from patient 1 and his parents compared to a healthy control individual presenting the maternally inherited non-frameshift deletion c.2264_2266delTCT and the paternally inherited frameshift deletion c.3119_3120delAA. (TIF 1670 kb)
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Winter, L., Türk, M., Harter, P.N. et al. Downstream effects of plectin mutations in epidermolysis bullosa simplex with muscular dystrophy. acta neuropathol commun 4, 44 (2016). https://doi.org/10.1186/s40478-016-0314-7