Williams Aislinn J, Paulson Henry L
Program in Neuroscience and Medical Scientist Training Program, University of Iowa, 2206 MERF, Iowa City, IA 52242, USA.
Trends Neurosci. 2008 Oct;31(10):521-8. doi: 10.1016/j.tins.2008.07.004. Epub 2008 Sep 6.
Polyglutamine diseases are a major cause of neurodegeneration worldwide. Recent studies highlight the importance of protein quality control mechanisms in regulating polyglutamine-induced toxicity. Here we discuss a model of disease pathogenesis that integrates current understanding of the role of protein folding in polyglutamine disease with emerging evidence that alterations in native protein interactions contribute to toxicity. We also incorporate new findings on other age-related neurodegenerative diseases in an effort to explain how protein aggregation and normal aging processes might be involved in polyglutamine disease pathogenesis.
聚谷氨酰胺疾病是全球神经退行性变的主要原因。最近的研究突出了蛋白质质量控制机制在调节聚谷氨酰胺诱导的毒性中的重要性。在此,我们讨论一种疾病发病机制模型,该模型整合了当前对蛋白质折叠在聚谷氨酰胺疾病中作用的理解,以及新出现的证据,即天然蛋白质相互作用的改变会导致毒性。我们还纳入了关于其他与年龄相关的神经退行性疾病的新发现,以解释蛋白质聚集和正常衰老过程可能如何参与聚谷氨酰胺疾病的发病机制。