Impaired Autophagic Flux in Skeletal Muscle of Plectin‐Related Epidermolysis Bullosa Simplex With Muscular Dystrophy

ABSTRACT Background Plectin, a multifunctional cytolinker and intermediate filament stabilizing protein, is essential for muscle fibre integrity and function. Mutations in the human plectin gene (PLEC) cause autosomal recessive epidermolysis bullosa simplex with muscular dystrophy (EBS‐MD). The diso...

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Main Authors: Michaela M. Zrelski, Margret Eckhard, Petra Fichtinger, Sabrina Hösele, Andy Sombke, Leonid Mill, Monika Kustermann, Wolfgang M. Schmidt, Fiona Norwood, Ursula Schlötzer‐Schrehardt, Gerhard Wiche, Rolf Schröder, Lilli Winter
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Language:English
Published: Wiley 2025-08-01
Series:Journal of Cachexia, Sarcopenia and Muscle
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Online Access:https://doi.org/10.1002/jcsm.70001
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author Michaela M. Zrelski
Margret Eckhard
Petra Fichtinger
Sabrina Hösele
Andy Sombke
Leonid Mill
Monika Kustermann
Wolfgang M. Schmidt
Fiona Norwood
Ursula Schlötzer‐Schrehardt
Gerhard Wiche
Rolf Schröder
Lilli Winter
author_facet Michaela M. Zrelski
Margret Eckhard
Petra Fichtinger
Sabrina Hösele
Andy Sombke
Leonid Mill
Monika Kustermann
Wolfgang M. Schmidt
Fiona Norwood
Ursula Schlötzer‐Schrehardt
Gerhard Wiche
Rolf Schröder
Lilli Winter
author_sort Michaela M. Zrelski
collection DOAJ
description ABSTRACT Background Plectin, a multifunctional cytolinker and intermediate filament stabilizing protein, is essential for muscle fibre integrity and function. Mutations in the human plectin gene (PLEC) cause autosomal recessive epidermolysis bullosa simplex with muscular dystrophy (EBS‐MD). The disorganization and aggregation of desmin filaments in conjunction with degenerative changes of the myofibrillar apparatus are key features in the skeletal muscle pathology of EBS‐MD. We performed a comprehensive analysis addressing protein homeostasis in this rare protein aggregation disease by using human EBS‐MD tissue, plectin knock‐out mice and plectin‐deficient cells. Methods Protein degradation pathways were analysed in muscles from EBS‐MD patients, muscle‐specific conditional plectin knockout (MCK‐Cre/cKO) mice, as well as in plectin‐deficient (Plec−/−) myoblasts by electron and immunofluorescence microscopy. To obtain a comprehensive picture of autophagic processes, we evaluated the transcriptional regulation and expression levels of autophagic markers in plectin‐deficient muscles and myoblasts (RNA‐Seq, qRT‐PCR, immunoblotting). Autophagic turnover was dynamically assessed by measuring baseline autophagy as well as specific inhibition and activation in mCherry‐EGFP‐LC3B‐expressing Plec+/+ and Plec−/− myoblasts, and by monitoring primary Plec+/+ and Plec−/− myoblasts using organelle‐specific dyes. Wild‐type and MCK‐Cre/cKO mice were treated with chloroquine or metformin to assess the effects of autophagy inhibition and activation in vivo. Results Our study identified the accumulation of degradative vacuoles as well as LC3‐ and SQSTM1‐positive patches in EBS‐MD patients, MCK‐Cre/cKO mouse muscles and Plec−/− myoblasts. The transcriptional regulation of ~30% of autophagy‐related genes was altered, and protein levels of downstream targets of the autophagosomal degradation machinery were elevated in MCK‐Cre/cKO muscle lysates (e.g., LAMP2, BAG3 and SQSTM1 to ~160, ~150 and ~140% of controls, respectively; p < 0.05). Autophagosome turnover was compromised in mCherry‐EGFP‐LC3B‐expressing Plec−/− myoblasts (~40% reduction in median red:green ratio, reduced puncta number, smaller puncta; p < 0.01). By labelling autophagic compartments with CYTO‐ID dye or lysosomes with LYSO‐ID, we found reduced signal intensities in primary Plec−/− cells (p < 0.001). Treatment with chloroquine led to drastic swelling of autophagic vacuoles in primary Plec+/+ myoblasts, while the swelling in Plec−/− cells was moderate, establishing a defect in their autophagic clearance. Chloroquine treatment of MCK‐Cre/cKO mice corroborated that loss of plectin coincides with impaired autophagic clearance, while metformin amelioratively induced autophagic flux. Conclusions Our work demonstrates that the characteristic protein aggregation pathology in EBS‐MD is linked to an impaired autophagic flux. The obtained results open a new perspective on the understanding of the protein aggregation pathology in plectin‐related disorders and provide a basis for further pharmacological intervention.
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spelling doaj-art-6c8c7aedd9f64015baca8fff0567dba32025-08-22T07:30:52ZengWileyJournal of Cachexia, Sarcopenia and Muscle2190-59912190-60092025-08-01164n/an/a10.1002/jcsm.70001Impaired Autophagic Flux in Skeletal Muscle of Plectin‐Related Epidermolysis Bullosa Simplex With Muscular DystrophyMichaela M. Zrelski0Margret Eckhard1Petra Fichtinger2Sabrina Hösele3Andy Sombke4Leonid Mill5Monika Kustermann6Wolfgang M. Schmidt7Fiona Norwood8Ursula Schlötzer‐Schrehardt9Gerhard Wiche10Rolf Schröder11Lilli Winter12Division of Cell and Developmental Biology, Center for Anatomy and Cell Biology Medical University of Vienna Vienna AustriaDivision of Cell and Developmental Biology, Center for Anatomy and Cell Biology Medical University of Vienna Vienna AustriaDivision of Cell and Developmental Biology, Center for Anatomy and Cell Biology Medical University of Vienna Vienna AustriaDivision of Cell and Developmental Biology, Center for Anatomy and Cell Biology Medical University of Vienna Vienna AustriaDivision of Cell and Developmental Biology, Center for Anatomy and Cell Biology Medical University of Vienna Vienna AustriaMIRA Vision Microscopy GmbH Wangen GermanyNeuromuscular Research Group, Division of Cell and Developmental Biology, Center for Anatomy and Cell Biology Medical University of Vienna Vienna AustriaNeuromuscular Research Group, Division of Cell and Developmental Biology, Center for Anatomy and Cell Biology Medical University of Vienna Vienna AustriaDepartment of Neurology, Ruskin Wing King's College Hospital London UKDepartment of Ophthalmology, University Hospital Erlangen Friedrich‐Alexander University Erlangen‐Nürnberg Erlangen GermanyDepartment of Biochemistry and Cell Biology, max Perutz Laboratories University of Vienna Vienna AustriaInstitute of Neuropathology, University Hospital Erlangen Friedrich‐Alexander University Erlangen‐Nürnberg Erlangen GermanyDivision of Cell and Developmental Biology, Center for Anatomy and Cell Biology Medical University of Vienna Vienna AustriaABSTRACT Background Plectin, a multifunctional cytolinker and intermediate filament stabilizing protein, is essential for muscle fibre integrity and function. Mutations in the human plectin gene (PLEC) cause autosomal recessive epidermolysis bullosa simplex with muscular dystrophy (EBS‐MD). The disorganization and aggregation of desmin filaments in conjunction with degenerative changes of the myofibrillar apparatus are key features in the skeletal muscle pathology of EBS‐MD. We performed a comprehensive analysis addressing protein homeostasis in this rare protein aggregation disease by using human EBS‐MD tissue, plectin knock‐out mice and plectin‐deficient cells. Methods Protein degradation pathways were analysed in muscles from EBS‐MD patients, muscle‐specific conditional plectin knockout (MCK‐Cre/cKO) mice, as well as in plectin‐deficient (Plec−/−) myoblasts by electron and immunofluorescence microscopy. To obtain a comprehensive picture of autophagic processes, we evaluated the transcriptional regulation and expression levels of autophagic markers in plectin‐deficient muscles and myoblasts (RNA‐Seq, qRT‐PCR, immunoblotting). Autophagic turnover was dynamically assessed by measuring baseline autophagy as well as specific inhibition and activation in mCherry‐EGFP‐LC3B‐expressing Plec+/+ and Plec−/− myoblasts, and by monitoring primary Plec+/+ and Plec−/− myoblasts using organelle‐specific dyes. Wild‐type and MCK‐Cre/cKO mice were treated with chloroquine or metformin to assess the effects of autophagy inhibition and activation in vivo. Results Our study identified the accumulation of degradative vacuoles as well as LC3‐ and SQSTM1‐positive patches in EBS‐MD patients, MCK‐Cre/cKO mouse muscles and Plec−/− myoblasts. The transcriptional regulation of ~30% of autophagy‐related genes was altered, and protein levels of downstream targets of the autophagosomal degradation machinery were elevated in MCK‐Cre/cKO muscle lysates (e.g., LAMP2, BAG3 and SQSTM1 to ~160, ~150 and ~140% of controls, respectively; p < 0.05). Autophagosome turnover was compromised in mCherry‐EGFP‐LC3B‐expressing Plec−/− myoblasts (~40% reduction in median red:green ratio, reduced puncta number, smaller puncta; p < 0.01). By labelling autophagic compartments with CYTO‐ID dye or lysosomes with LYSO‐ID, we found reduced signal intensities in primary Plec−/− cells (p < 0.001). Treatment with chloroquine led to drastic swelling of autophagic vacuoles in primary Plec+/+ myoblasts, while the swelling in Plec−/− cells was moderate, establishing a defect in their autophagic clearance. Chloroquine treatment of MCK‐Cre/cKO mice corroborated that loss of plectin coincides with impaired autophagic clearance, while metformin amelioratively induced autophagic flux. Conclusions Our work demonstrates that the characteristic protein aggregation pathology in EBS‐MD is linked to an impaired autophagic flux. The obtained results open a new perspective on the understanding of the protein aggregation pathology in plectin‐related disorders and provide a basis for further pharmacological intervention.https://doi.org/10.1002/jcsm.70001autophagydesminepidermolysis bullosa simplex with muscular dystrophymyofibrillar myopathyplectinskeletal muscle
spellingShingle Michaela M. Zrelski
Margret Eckhard
Petra Fichtinger
Sabrina Hösele
Andy Sombke
Leonid Mill
Monika Kustermann
Wolfgang M. Schmidt
Fiona Norwood
Ursula Schlötzer‐Schrehardt
Gerhard Wiche
Rolf Schröder
Lilli Winter
Impaired Autophagic Flux in Skeletal Muscle of Plectin‐Related Epidermolysis Bullosa Simplex With Muscular Dystrophy
Journal of Cachexia, Sarcopenia and Muscle
autophagy
desmin
epidermolysis bullosa simplex with muscular dystrophy
myofibrillar myopathy
plectin
skeletal muscle
title Impaired Autophagic Flux in Skeletal Muscle of Plectin‐Related Epidermolysis Bullosa Simplex With Muscular Dystrophy
title_full Impaired Autophagic Flux in Skeletal Muscle of Plectin‐Related Epidermolysis Bullosa Simplex With Muscular Dystrophy
title_fullStr Impaired Autophagic Flux in Skeletal Muscle of Plectin‐Related Epidermolysis Bullosa Simplex With Muscular Dystrophy
title_full_unstemmed Impaired Autophagic Flux in Skeletal Muscle of Plectin‐Related Epidermolysis Bullosa Simplex With Muscular Dystrophy
title_short Impaired Autophagic Flux in Skeletal Muscle of Plectin‐Related Epidermolysis Bullosa Simplex With Muscular Dystrophy
title_sort impaired autophagic flux in skeletal muscle of plectin related epidermolysis bullosa simplex with muscular dystrophy
topic autophagy
desmin
epidermolysis bullosa simplex with muscular dystrophy
myofibrillar myopathy
plectin
skeletal muscle
url https://doi.org/10.1002/jcsm.70001
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