Imbalances in protein homeostasis caused by mutant desmin

Winter L, Unger A, Berwanger C, Spörrer M, Türk M, Chevessier F, Strucksberg KH, Schlötzer-Schrehardt U, Wittig I, Goldmann W, Marcus K, Linke WA, Clemen CS, Schröder R (2019)

Publication Type: Journal article

Publication year: 2019

Journal

Book Volume: 45

Pages Range: 476-494

Journal Issue: 5

DOI: 10.1111/nan.12516

Abstract

Aims: We investigated newly generated immortalized heterozygous and homozygous R349P desmin knock-in myoblasts in conjunction with the corresponding desminopathy mice as models for desminopathies to analyse major protein quality control processes in response to the presence of R349P mutant desmin. Methods: We used hetero- and homozygous R349P desmin knock-in mice for analyses and for crossbreeding with p53 knock-out mice to generate immortalized R349P desmin knock-in skeletal muscle myoblasts and myotubes. Skeletal muscle sections and cultured muscle cells were investigated by indirect immunofluorescence microscopy, proteasomal activity measurements and immunoblotting addressing autophagy rate, chaperone-assisted selective autophagy and heat shock protein levels. Muscle sections were further analysed by transmission and immunogold electron microscopy. Results: We demonstrate that mutant desmin (i) increases proteasomal activity, (ii) stimulates macroautophagy, (iii) dysregulates the chaperone assisted selective autophagy and (iv) elevates the protein levels of αB-crystallin and Hsp27. Both αB-crystallin and Hsp27 as well as Hsp90 displayed translocation patterns from Z-discs as well as Z-I junctions, respectively, to the level of sarcomeric I-bands in dominant and recessive desminopathies. Conclusions: 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.

Authors with CRIS profile

Involved external institutions

Ruhr-Universität Bochum (RUB) Germany (DE) Berufsgenossenschaftliches Universitätsklinikum Bergmannsheil Germany (DE) Universitätsklinikum Frankfurt am Main (KGU) Germany (DE) Universität zu Köln Germany (DE)

How to cite

APA:

Winter, L., Unger, A., Berwanger, C., Spörrer, M., Türk, M., Chevessier, F.,... Schröder, R. (2019). Imbalances in protein homeostasis caused by mutant desmin. Neuropathology and Applied Neurobiology, 45(5), 476-494. https://dx.doi.org/10.1111/nan.12516

MLA:

Winter, L., et al. "Imbalances in protein homeostasis caused by mutant desmin." Neuropathology and Applied Neurobiology 45.5 (2019): 476-494.

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