Brazilian Synchrotron Light Laboratory (LNLS), Brazilian Center for Research in Energy and Materials (CNPEM), Campinas 13083-970, Sao Paulo, Brazil.
Attocube Systems AG, Eglfinger Weg 2, 85540 Munich, Germany.
Cells. 2021 Sep 27;10(10):2559. doi: 10.3390/cells10102559.
Alzheimer's disease (AD) accounts for about 70% of neurodegenerative diseases and is a cause of cognitive decline and death for one-third of seniors. AD is currently underdiagnosed, and it cannot be effectively prevented. Aggregation of amyloid-β (Aβ) proteins has been linked to the development of AD, and it has been established that, under pathological conditions, Aβ proteins undergo structural changes to form β-sheet structures that are considered neurotoxic. Numerous intensive in vitro studies have provided detailed information about amyloid polymorphs; however, little is known on how amyloid β-sheet-enriched aggregates can cause neurotoxicity in relevant settings. We used scattering-type scanning near-field optical microscopy (s-SNOM) to study amyloid structures at the nanoscale, in individual neurons. Specifically, we show that in well-validated systems, s-SNOM can detect amyloid β-sheet structures with nanometer spatial resolution in individual neurons. This is a proof-of-concept study to demonstrate that s-SNOM can be used to detect Aβ-sheet structures on cell surfaces at the nanoscale. Furthermore, this study is intended to raise neurobiologists' awareness of the potential of s-SNOM as a tool for analyzing amyloid β-sheet structures at the nanoscale in neurons without the need for immunolabeling.
阿尔茨海默病(AD)约占神经退行性疾病的 70%,是三分之一老年人认知能力下降和死亡的原因。AD 目前诊断不足,且无法有效预防。淀粉样蛋白-β(Aβ)蛋白的聚集与 AD 的发展有关,并且已经确定,在病理条件下,Aβ蛋白发生结构变化,形成被认为具有神经毒性的β-折叠结构。大量的体外强化研究提供了有关淀粉样蛋白多形体的详细信息;然而,对于富含β-淀粉样蛋白的聚集物如何在相关环境中引起神经毒性,人们知之甚少。我们使用散射型近场光学显微镜(s-SNOM)在单个神经元中研究纳米级的淀粉样蛋白结构。具体来说,我们表明,在经过充分验证的系统中,s-SNOM 可以以纳米级的空间分辨率检测单个神经元中的淀粉样蛋白β-折叠结构。这是一项概念验证研究,旨在证明 s-SNOM 可用于在纳米尺度上检测细胞表面上的 Aβ-折叠结构,而无需免疫标记。此外,这项研究旨在提高神经生物学家对 s-SNOM 作为一种工具的认识,用于在神经元中分析纳米尺度上的淀粉样蛋白β-折叠结构,而无需免疫标记。