Hooper Nigel M, Turner Anthony J
Institute of Molecular and Cellular Biology, Faculty of Biological Sciences, University of Leeds, Leeds, UK.
Trends Biochem Sci. 2008 Apr;33(4):151-5. doi: 10.1016/j.tibs.2008.01.004. Epub 2008 Mar 17.
Alzheimer's disease is a major neurodegenerative disease of the brain, the incidence of which increases dramatically in old age. Currently, no drugs are available to halt or slow the progression of this disease, which poses an ever-expanding burden on health services, families and society. The prion protein has become infamous owing to its role as the causative agent of the transmissible spongiform encephalopathies such as Creutzfeldt-Jakob disease in humans. However, our view of the prion protein as an unwanted, harmful entity has been challenged recently. New data indicate that the normal cellular form of the prion protein might have a crucial role in suppressing the production of the amyloid-beta peptide, the neurotoxic molecule involved in the pathogenesis of Alzheimer's disease.
阿尔茨海默病是一种主要的脑部神经退行性疾病,其发病率在老年时会急剧上升。目前,尚无药物能够阻止或减缓这种疾病的进展,这给医疗服务、家庭和社会带来了日益沉重的负担。朊病毒蛋白因其作为人类可传播性海绵状脑病(如克雅氏病)的病原体而声名狼藉。然而,我们将朊病毒蛋白视为有害的多余物质的观点最近受到了挑战。新数据表明,朊病毒蛋白的正常细胞形式可能在抑制β-淀粉样肽的产生方面发挥关键作用,β-淀粉样肽是一种参与阿尔茨海默病发病机制的神经毒性分子。