German Center for Neurodegenerative Diseases (DZNE), 81377, Munich, Germany.
Center for Neuropathology and Prion Research, Ludwig-Maximilians University Munich, 81377, Munich, Germany.
Commun Biol. 2021 Dec 7;4(1):1368. doi: 10.1038/s42003-021-02884-7.
Alzheimer's disease (AD) is associated with aberrant neuronal activity, which is believed to critically determine disease symptoms. How these activity alterations emerge, how stable they are over time, and whether cellular activity dynamics are affected by the amyloid plaque pathology remains incompletely understood. We here repeatedly recorded the activity from identified neurons in cortex of awake APPPS1 transgenic mice over four weeks during the early phase of plaque deposition using in vivo two-photon calcium imaging. We found that aberrant activity during this stage largely persisted over the observation time. Novel highly active neurons slowly emerged from former intermediately active neurons. Furthermore, activity fluctuations were independent of plaque proximity, but aberrant activity was more likely to persist close to plaques. These results support the notion that neuronal network pathology observed in models of cerebral amyloidosis is the consequence of persistent single cell aberrant neuronal activity, a finding of potential diagnostic and therapeutic relevance for AD.
阿尔茨海默病(AD)与异常的神经元活动有关,人们认为这种活动对疾病症状具有决定性作用。这些活动改变是如何出现的,它们在时间上的稳定性如何,以及细胞活动动态是否受到淀粉样斑块病理学的影响,这些仍然不完全清楚。在这里,我们使用体内双光子钙成像技术,在 APPPS1 转基因小鼠的皮层中,在淀粉样斑块沉积的早期阶段,反复记录了清醒的转基因小鼠的神经元的活动,时间长达四周。我们发现,在这个阶段,异常活动在很大程度上持续了整个观察时间。新的高度活跃的神经元从以前的中度活跃的神经元中缓慢出现。此外,活动波动与斑块的接近程度无关,但异常活动更有可能在斑块附近持续存在。这些结果支持这样一种观点,即在大脑淀粉样变性模型中观察到的神经元网络病理学是持续的单个细胞异常神经元活动的结果,这一发现对 AD 的诊断和治疗具有潜在的相关性。