Shelkovnikova T A, Kulikova A A, Tsvetkov F O, Peters O, Bachurin S O, Bukhman V L, Ninkina N N
Mol Biol (Mosk). 2012 May-Jun;46(3):402-15.
A number of neurodegenerative disorders have recently been coalesced into a group of proteinopathies because of the similarity of molecular mechanisms underlying their pathogenesis. A key step in the development of proteinopathies is a structural change that triggers aggregation of proteins, which are intrinsically prone to form aggregates due to their physical and chemical properties. Present review is devoted to the recent progress in the field of proteinopathies with specific focus on properties of aggregate-prone proteins, main stages of the development of molecular pathology and the role of cellular clearance systems in progression of neurodegeneration. Recent modifications in the nomenclature of neurodegenerative diseases will also be addressed.
由于多种神经退行性疾病发病机制背后的分子机制具有相似性,最近它们被归为一组蛋白病。蛋白病发展的关键步骤是结构变化引发蛋白质聚集,由于其物理和化学性质,这些蛋白质本身就容易形成聚集体。本综述致力于蛋白病领域的最新进展,特别关注易聚集蛋白的特性、分子病理学发展的主要阶段以及细胞清除系统在神经退行性变进展中的作用。还将讨论神经退行性疾病命名法的最新修订。