Department of Biomedical Science and Technology, Konkuk University, Seoul 143-701, Republic of Korea.
Neurosci Res. 2011 Aug;70(4):339-48. doi: 10.1016/j.neures.2011.05.008. Epub 2011 May 20.
Progressive accumulation of specific protein aggregates is a defining feature of many major neurodegenerative diseases, including Alzheimer's disease, Parkinson's disease, fronto-temporal dementia, Huntington's disease, and Creutzfeldt-Jakob disease (CJD). Findings from several recent studies have suggested that aggregation-prone proteins, such as tau, α-synuclein, polyglutamine-containing proteins, and amyloid-β, can spread to other cells and brain regions, a phenomenon considered unique to prion disorders, such as CJD and bovine spongiform encephalopathy. Cell-to-cell propagation of protein aggregates may be the general underlying principle for progressive deterioration of neurodegenerative diseases. This may also have significant implications in cell replacement therapies, as evidenced by the propagation of α-synuclein aggregates from host to grafted cells in long-term transplants in Parkinson's patients. Here, we review recent progress in protein aggregate propagation in experimental model systems and discuss outstanding questions and future perspectives. Understanding the mechanisms of this pathological spreading may open the way to unique opportunities for development of diagnostic techniques and novel therapies for protein misfolding-associated neurodegenerative diseases.
特定蛋白质聚集体的逐渐积累是许多主要神经退行性疾病的一个特征,包括阿尔茨海默病、帕金森病、额颞叶痴呆、亨廷顿病和克雅氏病(CJD)。最近的几项研究结果表明,聚集倾向蛋白,如 tau、α-突触核蛋白、多聚谷氨酰胺蛋白和淀粉样β,可传播到其他细胞和脑区,这种现象被认为是朊病毒疾病(如 CJD 和牛海绵状脑病)所特有。蛋白质聚集体的细胞间传播可能是神经退行性疾病进行性恶化的普遍潜在原理。这在细胞替代疗法中也具有重要意义,正如帕金森病患者的长期移植中,宿主到移植细胞的 α-突触核蛋白聚集体的传播所证明的那样。在这里,我们回顾了实验模型系统中蛋白质聚集体传播的最新进展,并讨论了悬而未决的问题和未来的展望。了解这种病理性传播的机制可能为开发与蛋白质错误折叠相关的神经退行性疾病的诊断技术和新型疗法开辟独特的机会。