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Imbalances in protein homeostasis caused by mutant desmin.

L WinterA UngerC BerwangerM SpörrerM TürkF ChevessierK-H StrucksbergU Schlötzer-SchrehardtI WittigW H GoldmannK MarcusW A LinkeChristoph Stephan ClemenR Schröder
Published in: Neuropathology and applied neurobiology (2018)
Our findings demonstrate that the presence of R349P mutant desmin causes a general imbalance in skeletal muscle protein homeostasis via aberrant activity of all major protein quality control systems. The augmented activity of these systems and the subcellular shift of essential heat shock proteins may deleteriously contribute to the previously observed increased turnover of desmin itself and desmin-binding partners, which triggers progressive dysfunction of the extrasarcomeric cytoskeleton and the myofibrillar apparatus in the course of the development of desminopathies.
Keyphrases
  • heat shock
  • skeletal muscle
  • quality control
  • protein protein
  • binding protein
  • multiple sclerosis
  • amino acid
  • oxidative stress
  • heat stress
  • small molecule
  • human immunodeficiency virus
  • wild type