LARGE expression in different types of muscular dystrophies other than dystroglycanopathy
Alpha-dystroglycan (αDG) is an extracellular peripheral glycoprotein that acts as a receptor for both extracellular matrix proteins containing laminin globular domains and certain arenaviruses. An important enzyme, known as Like-acetylglucosaminyltransferase (LARGE), has been shown to transfer repeating units of -glucuronic acid-β1,3-xylose-α1,3- (matriglycan) to αDG that is required for functional receptor as an extracellular matrix protein scaffold. The reduction in the amount of LARGE-dependent matriglycan result in heterogeneous forms of dystroglycanopathy that is associated with hypoglycosylation of αDG and a consequent lack of ligand-binding activity. Our aim was to investigate whether LARGE expression showed correlation with glycosylation of αDG and histopathological parameters in different types of muscular dystrophies, except for dystroglycanopathies.
The expression level of LARGE and glycosylation status of αDG were examined in skeletal muscle biopsies from 26 patients with various forms of muscular dystrophy [Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), sarcoglycanopathy, dysferlinopathy, calpainopathy, and merosin and collagen VI deficient congenital muscular dystrophies (CMDs)] and correlation of results with different histopathological features was investigated.
Despite the fact that these diseases are not caused by defects of glycosyltransferases, decreased expression of LARGE was detected in many patient samples, partly correlating with the type of muscular dystrophy. Although immunolabelling of fully glycosylated αDG with VIA4–1 was reduced in dystrophinopathy patients, no significant relationship between reduction of LARGE expression and αDG hypoglycosylation was detected. Also, Merosin deficient CMD patients showed normal immunostaining with αDG despite severe reduction of LARGE expression.
Our data shows that it is not always possible to correlate LARGE expression and αDG glycosylation in different types of muscular dystrophies and suggests that there might be differences in αDG processing by LARGE which could be regulated under different pathological conditions.
KeywordsLARGE Alpha-dystroglycan Hypoglycosylation Muscular dystrophy Skeletal muscle
Becker muscular dystrophy
Congenital muscular dystrophy
Duchenne muscular dystrophy
Fukuyama congenital muscular dystrophy
Haematoxylin and eosin
Limb-girdle muscular dystrophy
Protein-O-mannose ß2-N-acetylglucosaminyltransferase 1
Protein-O-mannosyl transferase 1
Protein-O-mannosyl transferase 2
Quantitative real-time PCR
Dystroglycan (DG), a heterodimeric transmembrane glycoprotein, is a central component of the dystrophin-glycoprotein complex (DGC) and responsible for a variety of physiological and developmental processes, including muscle stabilization, basement membrane assembly, cell migration and signalling . The protein is synthesized as a precursor molecule that is post-translationally cleaved into a cell surface α- and a transmembrane β- subunits . The extracellular subunit, alpha-dystroglycan (αDG), is a highly glycosylated basement membrane protein that acts as a receptor for non-collagenous proteins in the extracellular matrix (ECM) containing laminin globular domains, and for Old World arenaviruses [1, 3, 4, 5]. Mutations in the DG-encoding gene (DAG1) [6, 7] and several other genes whose products are involved, directly or indirectly, in glycosylation pathway of αDG  have been identified in various forms of congenital and limb-girdle muscular dystrophies (CMD/ LGMDs). These disorders are all associated with hypoglycosylation of αDG and a consequent lack of ligand-binding activity and thus are collectively termed as dystroglycanopathies .
Although the precise glycosylation pathway of αDG is not fully understood, the function of Like-acetylglucosaminyltransferase (LARGE) enzyme has been of particular interest. It is encoded by one of the largest genes (LARGE) in the human genome [10, 11, 12], which is mutated in the myodystrophy mouse (LARGE-myd) [10, 13] and in patients affected by MDC1D, a subclass of CMD associated with skeletal muscle and structural brain involvement . The mentioned enzyme is a bifunctional glycosyltransferase, with both xylosyltransferase and glucuronyltransferase activities and plays an important role in the glycosylation pathway of αDG. It transfers a novel heteropolysaccharide structure, repeating units of -glucuronic acid-β1,3-xylose-α1,3- to the basement membrane receptor DG . This structure has been recently termed as matriglycan, which is bound to the αDG through a phosphorylated O-mannosyl glycan anchored at Thr317 and Thr319 in the mucin-like domain [8, 15, 16]. It is required for the αDG to bind laminin-G domain-containing ECM ligands including laminin, agrin, perlecan and neurexin [4, 17, 18, 19]. It has been reported that LARGE-dependent matriglycan structure plays an important role for normal skeletal muscle function and the consequent reduction in the amount of glycans on αDG causes structural alterations of the basement membrane, immature neuromuscular junctions and dysfunctional muscle predisposed to dystrophy . Uniquely, transient overexpression of LARGE has been shown to increase glycosylation of αDG as evaluated by increased immunoreactivity to antibodies IIH6 and VIA4–1 both of which are known to recognize carbohydrate moieties and leads to a recovery of receptor function in cells derived from patients diagnosed as Fukuyama CMD (FCMD), muscle-eye-brain disease (MEB) and Walker–Warburg syndrome (WWS) . Also, the identical results has been reported in vivo, after adenovirus or adeno-associated virus mediated gene transfer of LARGE in Fukutin (FKTN), Fukutin-related protein (FKRP) and Protein-O-mannose ß2-N-acetylglucosaminyltransferase 1 (POMGNT1) deficient mice models [21, 22, 23]. Although a recent study demonstrates that fukutin is required for the ability of LARGE to hyperglycosylate αDG , this strategy is already regarded as a promising therapeutic approach for preventing/slowing progression of a broad range of dystroglycanopathies regardless of the causative gene defects. However, it remains crucial to analyze such a strategy in different types of muscular dystrophies other than dystroglycanopathy.
In this study, we analyzed the influence of LARGE gene expression profile on VIA4–1 immunoreactivity in different types of muscular dystrophies, except for dystroglycanopathies [i.e. Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), sarcoglycanopathy, dysferlinopathy, calpainopathy, and merosin and collagen VI deficient CMDs]. Correlation between different histopathological features, LARGE expression profile and glycosylation status of αDG was investigated. We detected reduced expression level of LARGE in different types of muscular dystrophies, partly correlating with the severity of dystrophic changes, but we did not find any significant relationship between reduction of LARGE expression and VIA4–1 immunoreactivity.
Patients and muscle biopsies
The study protocol was approved by the Hacettepe University Faculty of Medicine Ethical Review Board (FON 10/35–11). As the legal age of consent is 18 years of age in Turkey, written informed consent was obtained from patients’ parents or legal guardians at the time of diagnostic muscle biopsy. Skeletal muscle biopsies from 3 controls and 26 patients with clinicopathological and/or molecular diagnosis of various forms of muscular dystrophy other than dystroglycanopathy were included in this study. The number of patients in each disease type is indicated in parentheses; DMD (3), BMD (4), sarcoglycanopathy (5), dysferlinopathy (1), calpainopathy (1), Merosin deficient CMD (4), Collagen VI deficient CMD (3), unclassified CMD (2), and unclassified MD (3). All patients have been investigated in the Department of Pediatrics at Hacettepe University Faculty of Medicine and open biopsies were taken from vastus lateralis muscle at the time of diagnosis. The muscle biopsy specimens were rapidly frozen in isopentane cooled in liquid nitrogen and kept at − 80 °C until use. Serial transverse muscle sections were cut by cryostat for histochemical staining. Standard histological and histochemical techniques were applied to cryostat sections, including Haematoxylin and eosin (H&E), modified Gomori trichrome, periodic acid Schiff, oil-red-O, nicotinamide adenine dinucleotide dehydrogenase-tetrazolium reductase, succinic dehydrogenase, cytochrome-c oxidase and ATPase. Immunohistochemical and/or immunofluorescent studies were done at the time of diagnosis, using antibodies against dystrophins, sarcoglycans, dysferlin, laminin α2 (merosin), collagen VI, and αDG, as appropriate.
H&E stained archive sections were examined to identify the severity of various dystrophic changes, including necrosis, regeneration, adiposis, endomysial and perimysial fibrosis and inflammation. These pathological changes were scored from 0 (absent) to 4 (severe).
For immunofluorescent staining, skeletal muscle cryosections of 7 μm were immunostained with primary antibodies [1/10 for mouse anti-α-Dystroglycan antibody (clone VIA4–1 against fully glycosylated form of αDG, Millipore), 1/50 for sheep anti-α-Dystroglycan core antibody (R&D Systems: AF6868), 1/100 for mouse anti-Spectrin (NCL-SPEC1 Clone: RBC2/3D5, Novocastra), 1:20 for anti-Beta-Dystroglycan (βDG) (NCL-b-DG Clone 43DAG1/8D5, Novocastra) and 1:1000 for mouse anti-laminin α2 (MAB1922 Chemicon (Millipore)] for 1 h at room temperature, followed by incubation with Alexa Fluor 488 goat anti-mouse or donkey anti-sheep IgG antibodies (Molecular Probes) at 1:1000 dilution for 45 min at room temperature. All dilutions and washing steps were made in phosphate buffered saline. Immunostained sections were then mounted and observed with epifluorescence using a Nicon Eclipse E400 microscope. The fluorescent labeling was scored from 0 (absent) to 3 (intense) using a scale based on the proportion of positive fibers and intensity relative to the control muscle sections.
Quantitative real-time PCR (qRT-PCR)
In order to assess the expression of LARGE, total RNA was extracted from liquid nitrogen fresh-frozen skeletal muscle tissues (3 mm3) from 26 patiens and 3 control samples using RNeasy® fibrous tissue mini kit (Qiagen) and cDNA was synthesized from 500 ng RNA using QuantiTect Reverse Transcription kit (Qiagen) according to manufacturer’s guidelines. Real-time PCR was then performed using SYBR Green JumpStart TaqReadyMix kit (Sigma) on Rotor-Gene 6000™ (Corbett Research) with the following conditions: 2 min at 94 °C, followed by 40 cycles of 5 s at 94 °C, 10 s at 58 °C, and 15 s at 72 °C. Reactions were performed in a total volume of 10 μL, including 5 μL SYBR Green JumpStart TaqReadyMix kit (Sigma), 1.2 μl of 25 mM MgCl2 (Sigma), 0.4 μl each of 10 mM forward and reverse primers and 1 μl of template cDNA. Mastermix with no cDNA was used as the no template control whereas water was used as the negative control. The relative amount of mRNA, normalized to an internal control human beta-actin (ACTB) and relative to a calibrator (control), was calculated by 2-∆∆CT. Primers used were as follows: LARGE-F: 5’-TGAGCCGTATGTTGTTGTGAGAC-3′; LARGE-R: 5’-GATGCGGTATTGCTTGTTGGAAC-3′ and ACTB-F: 5′- CGCAAAGACCTGTACGCCAAC -3′; ACTB-R: 5′- GAGCCGCCGATCCACACG -3′. All reactions were performed in triplicate and optimal threshold in 95–100% efficiency. All data was analyzed using Rotor-Gene 6000 Series Software 1.7 (Corbett Research).
All experiments performed at least three times and data were evaluated as means ± SD. The significance of differences between experimental groups was determined using Mann-Whitney U test. p values less than 0.05 were considered statistically significant.
The clinicopathological diagnosis and histopathological characteristics of the patients (Assessment scores: 0: absent; 1: rare; 2: mild; 3: moderate; 4: severe)
In order to determine correlations between LARGE expression, glycosylation of αDG and histopathological parameters, we analyzed LARGE gene expression profile and glycosylation status of αDG in various forms of muscular dystrophies, except for dystroglycanopathies. The expression level of LARGE was analyzed by qRT-PCR in skeletal muscle biopsies from 26 patients diagnosed as different forms of muscular dystrophy with various histopathological phenotypes (Table 1). Our findings indicated that most of the patients with severe histopathological phenotype (DMD and merosin deficient CMD) have decreased LARGE expression levels compared to control skeletal muscle (Fig. 1). We then evaluated whether there was a relationship between LARGE expression and αDG glycosylation. The functional glycosylation of αDG is associated with the binding of either IIH6 and/or VIA4–1 antibodies to αDG. Thus, immunofluorescence staining was done using the widely used VIA4–1 antibody. Our findings indicate that irrespective of the muscular dystrophy type, the degree of hypoglycosylation varied (Figs. 2 and 3) and there was generally no correlation with clinical/histopathological severity. Similar results have previously been reported in dystroglycanopathy patients with Protein-O-mannosyl transferase 1 (POMT1), Protein-O-mannosyl transferase 2 (POMT2), POMGnT1, FKTN and FKRP mutations . Also, our results were not consistent with the findings which suggests a correlation between a reduction in αDG labeling and the clinical severity in mild, late-onset LGMD type 2I and severe CMD [20, 26]. On the other hand, we observed a severe reduction of αDG glycosylation in skeletal muscle biopsies of dystrophinopathy patients as a secondary finding, which has already been shown in DMD patients and mdx mouse [27, 28]. In contrast to those findings, the labelling obtained using the αDG core antibody was preserved in all patients, which suggested that the glycosylation of αDG is affected independently of DG protein expression.
In dystroglycanopathies, the effects of decreased glycosylation on laminin binding are variable [4, 11]. Therefore, further studies are necessary to evaluate if hypoglycosylation of αDG affects laminin binding or other functions of αDG in different types of muscular dystrophies other than dystroglycanopathy. Campbell and colleagues have previously demonstrated that short LARGE-glycan repeats reduces normal physiological function of muscle and predisposes it to dystrophy and showed that upregulation of LARGE and DG facilitates extension of LARGE-glycan repeat chains in differentiating mouse muscle . However, consistent with our preliminary findings , we did not find any significant relationship between reduction of LARGE expression and αDG hypoglycosylation (Figs. 1 and 3), except for DMD. Our results suggest that LARGE enzyme may have an additional function in skeletal muscle fibers that is probably distinct from adding a critical sugar chain onto αDG. Equally likely is that the RNA changes in LARGE, while present, are not related at all to the MD phenotype. Transcriptional changes are difficult to interpret in prediction effects downstream.
Glycosylation of αDG undergoes tissue and developmental stage specific changes, which indicates that it may have different roles in developing and fully differentiated skeletal muscle [4, 30]. αDG glycosylation is likely to be regulated by developmental and differential expression of numerous enzymes, including LARGE. Therefore the detected LARGE expression profiles in various form of muscular dystrophies may still reflect responses to pathological processes of skeletal muscle related to αDG glycosylation. Our cohort encompassed a wide range of muscular dystrophies, suggesting that a different pathomechanism may explain the relationship between LARGE expression and αDG glycosylation in the pathogenesis of different types of muscular dystrophies and highlighting the need for further studies.
This study was supported by a grant from Hacettepe University Scientific Research Projects Coordination Unit (grant number 011 D01 101 003).
Availability of data and materials
The datasets analyzed and/or generated during the current study are available from the corresponding author on reasonable request.
BBH drafted the manuscript, obtained funding for this study, designed and performed the experiments. BT provided biopsy specimens, evaluated the histopathological data and revised the manuscript. PD contributed to the design and implementation of the study. GK contributed to the evaluation of the histopathological data and made a significant intellectual contribution to this study. All authors discussed the results and contributed to the final manuscript.
Ethics approval and consent to participate
This study was performed with the approval of the Ethical Review Board of Hacettepe University Faculty of Medicine, Ankara, Turkey (FON 10/35–11). As the legal age of consent is 18 years of age in Turkey, written informed consent was obtained from patients’ parents or legal guardians at the time of diagnostic muscle biopsy. All studies were conducted in accordance with the principles of the Declaration of Helsinki.
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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