Deterioration of mitochondrial bioenergetics and ultrastructure impairment in skeletal muscle of a transgenic minipig model in the early stages of Huntington's disease

0512108 - ÚŽFG 2020 RIV GB eng J - Článek v odborném periodiku
Rodinová, M. - Křížová, J. - Štufková, H. - Bohuslavová, Božena - Askeland, G. - Dosoudilová, Z. - Juhás, Štefan - Juhásová, Jana - Ellederová, Zdeňka - Zeman, J. - Eide, L. - Motlík, Jan - Hansíková, H.
Deterioration of mitochondrial bioenergetics and ultrastructure impairment in skeletal muscle of a transgenic minipig model in the early stages of Huntington's disease.
Disease Models & Mechanisms. Roč. 12, č. 7 (2019), č. článku dmm038737. ISSN 1754-8403. E-ISSN 1754-8411
Grant CEP: GA MŠMT(CZ) LO1609; GA MŠMT 7F14308
Institucionální podpora: RVO:67985904
Klíčová slova: Huntington´s disease * mitochondrial function * ultrastructure * HD large animal model
Obor OECD: Cell biology
Impakt faktor: 4.651, rok: 2019
Způsob publikování: Open access
https://dmm.biologists.org/content/12/7/dmm038737

Skeletal muscle wasting and atrophy is one of the more severe clinical impairments resulting from the progression of Huntington's disease (HD). Mitochondrial dysfunction may play a significant role in the etiology of HD, but the specific condition of mitochondria in muscle has not been widely studied during the development of HD. To determine the role of mitochondria in skeletal muscle during the early stages of HD, we analyzed quadriceps femoris muscle from 24-, 36-, 48- and 66-month-old transgenic minipigs that expressed the N-terminal portion of mutated human huntingtin protein (TgHD) and age-matched wild-type (WT) siblings. We found altered ultrastructure of TgHD muscle tissue and mitochondria. There was also significant reduction of activity of citrate synthase and respiratory chain complexes (RCCs) I, II and IV, decreased quantity of oligomycin-sensitivity conferring protein (OSCP) and the E2 subunit of pyruvate dehydrogenase (PDHE2), and differential expression of optic atrophy 1 protein (OPA1) and dynamin-related protein 1 (DRP1) in the skeletal muscle of TgHD minipigs. Statistical analysis identified several parameters that were dependent only on HD status and could therefore be used as potential biomarkers of disease progression. In particular, the reduction of biomarker RCCII subunit SDH30 quantity suggests that similar pathogenic mechanisms underlie disease progression in TgHD minipigs and HD patients. The perturbed biochemical phenotype was detectable in TgHD minipigs prior to the development of ultrastructural changes and locomotor impairment, which become evident at the age of 48 months. Mitochondrial disturbances may contribute to energetic depression in skeletal muscle in HD, which is in concordance with the mobility problems observed in this model.
Trvalý link: http://hdl.handle.net/11104/0302315