Department of Biological Sciences, Konkuk University, Seoul 05029, Korea.
Department of Biochemistry, Chungbuk National University College of Medicine, Cheongju 28644, Korea.
Int J Mol Sci. 2020 Jan 30;21(3):884. doi: 10.3390/ijms21030884.
Alzheimer's disease (AD), a main cause of dementia, is the most common neurodegenerative disease that is related to abnormal accumulation of the amyloid β (Aβ) protein. Despite decades of intensive research, the mechanisms underlying AD remain elusive, and the only available treatment remains symptomatic. Molecular understanding of the pathogenesis and progression of AD is necessary to develop disease-modifying treatment. , as the most advanced genetic model, has been used to explore the molecular mechanisms of AD in the last few decades. Here, we introduce AD models based on human Aβ and summarize the results of their genetic dissection. We also discuss the utility of functional genomics using the system in the search for AD-associated molecular mechanisms in the post-genomic era.
阿尔茨海默病(AD)是痴呆的主要病因,是最常见的神经退行性疾病,与淀粉样β(Aβ)蛋白的异常积累有关。尽管经过几十年的深入研究,AD 的发病机制仍不清楚,并且唯一可用的治疗方法仍然是对症治疗。要开发出能改变疾病进程的治疗方法,就需要对 AD 的发病机制和进展有更深入的分子层面的理解。作为最先进的遗传模型, 在过去几十年中被用于探索 AD 的分子机制。在这里,我们介绍了基于人 Aβ的 AD 模型,并总结了它们的遗传剖析结果。我们还讨论了在后基因组时代使用 系统进行功能基因组学研究以寻找 AD 相关分子机制的效用。