Brendza Robert P, Bacskai Brian J, Cirrito John R, Simmons Kelly A, Skoch Jesse M, Klunk William E, Mathis Chester A, Bales Kelly R, Paul Steven M, Hyman Bradley T, Holtzman David M
Department of Neurology and Hope Center for Neurological Disorders, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
J Clin Invest. 2005 Feb;115(2):428-33. doi: 10.1172/JCI23269.
Neuritic plaques are a defining feature of Alzheimer disease (AD) pathology. These structures are composed of extracellular accumulations of amyloid-beta peptide (Abeta) and other plaque-associated proteins, surrounded by large, swollen axons and dendrites (dystrophic neurites) and activated glia. Dystrophic neurites are thought to disrupt neuronal function, but whether this damage is static, dynamic, or reversible is unknown. To address this, we monitored neuritic plaques in the brains of living PDAPP;Thy-1:YFP transgenic mice, a model that develops AD-like pathology and also stably expresses yellow fluorescent protein (YFP) in a subset of neurons in the brain. Using multiphoton microscopy, we observed and monitored amyloid through cranial windows in PDAPP;Thy-1:YFP double-transgenic mice using the in vivo amyloid-imaging fluorophore methoxy-X04, and individual YFP-labeled dystrophic neurites by their inherent fluorescence. In vivo studies using this system suggest that amyloid-associated dystrophic neurites are relatively stable structures in PDAPP;Thy-1:YFP transgenic mice over several days. However, a significant reduction in the number and size of dystrophic neurites was seen 3 days after Abeta deposits were cleared by anti-Abeta antibody treatment. This analysis suggests that ongoing axonal and dendritic damage is secondary to Abeta and is, in part, rapidly reversible.
神经炎性斑块是阿尔茨海默病(AD)病理学的一个决定性特征。这些结构由细胞外淀粉样β肽(Aβ)和其他与斑块相关的蛋白质聚集物组成,周围环绕着粗大、肿胀的轴突和树突(营养不良性神经突)以及活化的胶质细胞。营养不良性神经突被认为会破坏神经元功能,但这种损伤是静态的、动态的还是可逆的尚不清楚。为了解决这个问题,我们监测了活体PDAPP;Thy-1:YFP转基因小鼠大脑中的神经炎性斑块,该模型会发展出类似AD的病理学特征,并且在大脑中的一部分神经元中稳定表达黄色荧光蛋白(YFP)。使用多光子显微镜,我们通过颅骨视窗在PDAPP;Thy-1:YFP双转基因小鼠中使用体内淀粉样蛋白成像荧光团甲氧基-X04观察和监测淀粉样蛋白,并通过其固有荧光观察单个YFP标记的营养不良性神经突。使用该系统的体内研究表明,在PDAPP;Thy-1:YFP转基因小鼠中,与淀粉样蛋白相关的营养不良性神经突在数天内是相对稳定的结构。然而,在用抗Aβ抗体清除Aβ沉积物3天后,观察到营养不良性神经突的数量和大小显著减少。该分析表明,持续的轴突和树突损伤继发于Aβ,并且部分是可快速逆转的。