Institute of Neuroscience and Center for Integrated Protein Science, Technical University Munich, Biedersteinerstr. 29, 80802 Munich, Germany.
Nat Commun. 2012 Apr 10;3:774. doi: 10.1038/ncomms1783.
The accumulation of amyloid-β in the brain is an essential feature of Alzheimer's disease. However, the impact of amyloid-β-accumulation on neuronal dysfunction on the single cell level in vivo is poorly understood. Here we investigate the progression of amyloid-β load in relation to neuronal dysfunction in the visual system of the APP23×PS45 mouse model of Alzheimer's disease. Using in vivo two-photon calcium imaging in the visual cortex, we demonstrate that a progressive deterioration of neuronal tuning for the orientation of visual stimuli occurs in parallel with the age-dependent increase of the amyloid-β load. Importantly, we find this deterioration only in neurons that are hyperactive during spontaneous activity. This impairment of visual cortical circuit function also correlates with pronounced deficits in visual-pattern discrimination. Together, our results identify distinct stages of decline in sensory cortical performance in vivo as a function of the increased amyloid-β-load.
淀粉样蛋白-β在大脑中的积累是阿尔茨海默病的一个重要特征。然而,淀粉样蛋白-β积累对体内单个神经元功能障碍的影响在很大程度上仍不清楚。在这里,我们研究了 APP23×PS45 阿尔茨海默病小鼠模型的视觉系统中淀粉样蛋白-β负荷与神经元功能障碍的进展关系。通过在视觉皮层进行体内双光子钙成像,我们证明了神经元对视觉刺激方向的调谐逐渐恶化与淀粉样蛋白-β负荷的年龄依赖性增加平行发生。重要的是,我们仅在自发活动期间过度活跃的神经元中发现这种恶化。这种视觉皮层回路功能的损害也与视觉模式识别的明显缺陷相关。总之,我们的研究结果确定了随着淀粉样蛋白-β负荷的增加,体内感觉皮层性能下降的不同阶段。