Department of Biochemistry and Molecular Biophysics, Kansas State University, Manhattan, KS 66506, USA.
Division of Science, Yale-NUS College, Singapore 138527, Singapore.
Int J Mol Sci. 2023 Feb 21;24(5):4300. doi: 10.3390/ijms24054300.
Across the world a dementia case is diagnosed every three seconds. Alzheimer's disease (AD) causes 50-60% of these cases. The most prominent theory for AD correlates the deposition of amyloid beta (Aβ) with the onset of dementia. Whether Aβ is causative remains unclear due to findings such as the recently approved drug Aducanumab showing effective clearance of Aβ, but not improving cognition. New approaches for understanding Aβ function, are therefore necessary. Here we discuss the application of optogenetic techniques to gain insight into AD. Optogenetics, or genetically encoded, light-dependent on/off switches, provides precise spatiotemporal control to regulate cellular dynamics. This precise control over protein expression and oligomerization or aggregation could provide a better understanding of the etiology of AD.
全球每三秒钟就会诊断出一例痴呆症。阿尔茨海默病(AD)导致其中 50-60%的病例。AD 最突出的理论将淀粉样蛋白 β (Aβ) 的沉积与痴呆的发作联系起来。由于最近批准的药物 Aducanumab 显示出有效清除 Aβ,而对认知没有改善等发现,Aβ 是否具有因果关系尚不清楚。因此,有必要采用新的方法来了解 Aβ 的功能。在这里,我们讨论了应用光遗传学技术来深入了解 AD。光遗传学或基因编码的、依赖光的开/关开关为调节细胞动力学提供了精确的时空控制。这种对蛋白质表达和寡聚或聚集的精确控制可以更好地了解 AD 的病因。