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1000 Titel
  • Homozygous expression of the myofibrillar myopathy-associated p.W2710X filamin C variant reveals major pathomechanisms of sarcomeric lesion formation
1000 Autor/in
  1. Schuld, Julia |
  2. Orfanos, Zacharias |
  3. Chevessier, Frédéric |
  4. Eggers, Britta |
  5. Heil, Lorena |
  6. Uszkoreit, Julian |
  7. Unger, Andreas |
  8. Kirfel, Gregor |
  9. van der Ven, Peter |
  10. Marcus, Katrin |
  11. Linke, Wolfgang A. |
  12. Clemen, Christoph S. |
  13. Schröder, Rolf |
  14. Fürst, Dieter O. |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-09-04
1000 Erschienen in
1000 Quellenangabe
  • 8(1):154
1000 Copyrightjahr
  • 2020
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s40478-020-01001-9 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7650280/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Filamin C (FLNc) is mainly expressed in striated muscle cells where it localizes to Z-discs, myotendinous junctions and intercalated discs. Recent studies have revealed numerous mutations in the FLNC gene causing familial and sporadic myopathies and cardiomyopathies with marked clinical variability. The most frequent myopathic mutation, p.W2710X, which is associated with myofibrillar myopathy, deletes the carboxy-terminal 16 amino acids from FLNc and abolishes the dimerization property of Ig-like domain 24. We previously characterized 'knock-in' mice heterozygous for this mutation (p.W2711X), and have now investigated homozygous mice using protein and mRNA expression analyses, mass spectrometry, and extensive immunolocalization and ultrastructural studies. Although the latter mice display a relatively mild myopathy under normal conditions, our analyses identified major mechanisms causing the pathophysiology of this disease: in comparison to wildtype animals (i) the expression level of FLNc protein is drastically reduced; (ii) mutant FLNc is relocalized from Z-discs to particularly mechanically strained parts of muscle cells, i.e. myotendinous junctions and myofibrillar lesions; (iii) the number of lesions is greatly increased and these lesions lack Bcl2-associated athanogene 3 (BAG3) protein; (iv) the expression of heat shock protein beta-7 (HSPB7) is almost completely abolished. These findings indicate grave disturbances of BAG3-dependent and -independent autophagy pathways that are required for efficient lesion repair. In addition, our studies reveal general mechanisms of lesion formation and demonstrate that defective FLNc dimerization via its carboxy-terminal domain does not disturb assembly and basic function of myofibrils. An alternative, more amino-terminally located dimerization site might compensate for that loss. Since filamins function as stress sensors, our data further substantiate that FLNc is important for mechanosensing in the context of Z-disc stabilization and maintenance.
1000 Sacherschließung
lokal Homozygote [MeSH]
lokal Myofibrillar myopathy
lokal Sarcomeres/pathology [MeSH]
lokal Mutation [MeSH]
lokal Myopathies, Structural, Congenital/genetics [MeSH]
lokal Myopathies, Structural, Congenital/metabolism [MeSH]
lokal Autophagy
lokal Gene Knock-In Techniques [MeSH]
lokal Pathophysiology
lokal Animals [MeSH]
lokal Filamins/genetics [MeSH]
lokal Muscle damage
lokal Myofibrillar lesions
lokal Myopathies, Structural, Congenital/pathology [MeSH]
lokal Mice [MeSH]
lokal Filamin
lokal Mouse model
lokal Research
lokal Sarcomeres/metabolism [MeSH]
lokal HSPB7
lokal BAG3
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/U2NodWxkLCBKdWxpYQ==|https://frl.publisso.de/adhoc/uri/T3JmYW5vcywgWmFjaGFyaWFz|https://frl.publisso.de/adhoc/uri/Q2hldmVzc2llciwgRnLDqWTDqXJpYw==|https://frl.publisso.de/adhoc/uri/RWdnZXJzLCBCcml0dGE=|https://frl.publisso.de/adhoc/uri/SGVpbCwgTG9yZW5h|https://frl.publisso.de/adhoc/uri/VXN6a29yZWl0LCBKdWxpYW4=|https://frl.publisso.de/adhoc/uri/VW5nZXIsIEFuZHJlYXM=|https://frl.publisso.de/adhoc/uri/S2lyZmVsLCBHcmVnb3I=|https://orcid.org/0000-0002-9750-8913|https://frl.publisso.de/adhoc/uri/TWFyY3VzLCBLYXRyaW4=|https://frl.publisso.de/adhoc/uri/TGlua2UsIFdvbGZnYW5nIEEu|https://frl.publisso.de/adhoc/uri/Q2xlbWVuLCBDaHJpc3RvcGggUy4=|https://frl.publisso.de/adhoc/uri/U2NocsO2ZGVyLCBSb2xm|https://frl.publisso.de/adhoc/uri/RsO8cnN0LCBEaWV0ZXIgTy4=
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