Structural Genomics Consortium, University of Toronto, MaRS South Tower, Suite 700, 101 College Street, Toronto, Ontario M5G 1L7, Canada.
Department of Pharmacology and Toxicology, University of Toronto, Toronto, Ontario M5G 1L7, Canada.
Acta Pharmacol Sin. 2018 May;39(5):754-769. doi: 10.1038/aps.2018.11. Epub 2018 Apr 5.
Many neurodegenerative diseases are characterized by impairment of protein quality control mechanisms in neuronal cells. Ineffective clearance of misfolded proteins by the proteasome, autophagy pathways and exocytosis leads to accumulation of toxic protein oligomers and aggregates in neurons. Toxic protein species affect various cellular functions resulting in the development of a spectrum of different neurodegenerative proteinopathies, including Huntington's disease (HD). Playing an integral role in proteostasis, dysfunction of the ubiquitylation system in HD is progressive and multi-faceted with numerous biochemical pathways affected, in particular, the ubiquitin-proteasome system and autophagy routes for protein aggregate degradation. Unravelling the molecular mechanisms involved in HD pathogenesis of proteostasis provides new insight in disease progression in HD as well as possible therapeutic avenues. Recent developments of potential therapeutics are discussed in this review.
许多神经退行性疾病的特征是神经元细胞中蛋白质质量控制机制受损。蛋白酶体、自噬途径和胞吐作用清除错误折叠蛋白的效率降低,导致有毒的蛋白质寡聚物和聚集体在神经元中积累。有毒的蛋白质种类会影响各种细胞功能,导致一系列不同的神经退行性蛋白病的发展,包括亨廷顿病(HD)。泛素化系统在蛋白质稳态中起着至关重要的作用,HD 中的泛素化系统功能障碍是进行性的和多方面的,受影响的生化途径众多,特别是影响了泛素-蛋白酶体系统和蛋白质聚集体降解的自噬途径。阐明 HD 中蛋白质稳态发病机制中的分子机制,为 HD 疾病进展以及可能的治疗途径提供了新的见解。本文讨论了潜在治疗方法的最新进展。