先进的光学显微成像技术成像淀粉样蛋白和阿尔茨海默病的发病机制

iRadiology Pub Date : 2025-03-06 DOI:10.1002/ird3.70002
Shiju Gu, Chongzhao Ran
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引用次数: 0

摘要

阿尔茨海默病(AD)是一种以认知功能进行性下降为特征的神经退行性疾病。鉴于阿尔茨海默病损害了数百万人的生活质量,并且无症状期延长,探索阿尔茨海默病的全部发病机制并寻求最佳治疗方案已变得至关重要和势在必行。这使得研究人员能够干预、延缓并潜在地预防阿尔茨海默病的进展。一些临床影像学方法被常规用于诊断和监测AD,如磁共振成像(MRI)、功能磁共振成像(fMRI)、正电子发射断层扫描(PET)和单光子发射计算机断层扫描(SPECT)。然而,由于其固有的缺点和限制,如辐射问题、成本高、采集时间长、空间分辨率低,限制了它们在AD研究中的应用,特别是在细胞和分子水平上的应用。相比之下,光学显微成像方法克服了这些局限性,为研究人员提供了多种具有独特优势的方法来探索不同模型的阿尔茨海默病病理。在这篇综述中,我们全面概述了AD研究中常用的光学显微成像技术,并介绍了它们在成像β淀粉样蛋白(a β)物种方面的贡献。这些技术包括荧光显微镜(FM)、共聚焦显微镜(CM)、双光子荧光显微镜(TPFM)、超分辨率显微镜(SRM)、扩展显微镜(ExM)和光片荧光显微镜(LSFM)。此外,我们还介绍了一些相关的主题,如近红外(NIR) Aβ探针的发展,Aβ斑块假说和Aβ低聚物假说,以及小胶质细胞和星形胶质细胞在AD进展中的作用。我们相信光学显微成像方法在破译AD的全部发病机制和推进治疗策略方面继续发挥着不可或缺的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Advanced Optical Microscopic Imaging Techniques for Imaging Amyloid Beta and Deciphering Alzheimer's Disease Pathogenesis

Advanced Optical Microscopic Imaging Techniques for Imaging Amyloid Beta and Deciphering Alzheimer's Disease Pathogenesis

Alzheimer's disease (AD) is a neurodegenerative disease characterized by a progressive decline in cognitive functions. Given that AD undermines the quality of life for millions and has an extended asymptomatic period, exploring the full AD pathogenesis and seeking the optimal therapeutic solution have become critical and imperative. This allows researchers to intervene, delay, and potentially prevent AD progression. Several clinical imaging methods are utilized routinely to diagnose and monitor AD, such as magnetic resonance imaging (MRI), functional magnetic resonance imaging (fMRI), positron emission tomography (PET), and single photon emission computed tomography (SPECT). Nevertheless, due to their intrinsic drawbacks and restrictions, such as radiation concerns, high cost, long acquisition time, and low spatial resolution, their applications in AD research are limited, especially at the cellular and molecular levels. In contrast, optical microscopic imaging methods overcome these limitations, offering researchers a variety of approaches with distinct advantages to explore AD pathology on diverse models. In this review, we provide a comprehensive overview of commonly utilized optical microscopic imaging techniques in AD research and introduce their contributions to image amyloid beta (Aβ) species. These techniques include fluorescence microscopy (FM), confocal microscopy (CM), two-photon fluorescence microscopy (TPFM), super-resolution microscopy (SRM), expansion microscopy (ExM), and light-sheet fluorescence microscopy (LSFM). In addition, we introduce some related topics, such as the development of near-infrared (NIR) Aβ probes, the Aβ plaque hypothesis, and Aβ oligomer hypothesis, and the roles of microglia and astrocytes in AD progression. We believe optical microscopic imaging methods continue to play an indispensable role in deciphering the full pathogenesis of AD and advancing therapeutic strategies.

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