L'esperance Oliver J, McGhee Josh, Davidson Garrett, Niraula Suraj, Smith Adam Steven, Sosunov Alexandre, Yan Shirley Shidu, Subramanian Jaichandar
bioRxiv. 2024 May 9:2023.01.05.522900. doi: 10.1101/2023.01.05.522900.
While Alzheimer's disease (AD) has been extensively studied with a focus on cognitive networks, sensory network dysfunction has received comparatively less attention despite compelling evidence of its significance in both Alzheimer's disease patients and mouse models. We recently found that neurons in the primary visual cortex of an AD mouse model expressing human amyloid protein precursor with the Swedish and Indiana mutations (hAPP mutations) exhibit aberrant c-Fos expression and altered synaptic structures at a pre-amyloid plaque stage. However, it is unclear whether aberrant c-Fos expression and synaptic pathology vary across the broader visual network and to what extent c-Fos abnormality in the cortex is inherited through functional connectivity. Using both sexes of 4-6-month AD model mice with hAPP mutations (J20[PDGF-APPSw, Ind]), we found that cortical regions of the visual network show aberrant c-Fos expression and impaired experience-dependent modulation while subcortical regions do not. Interestingly, the average network-wide functional connectivity strength of a brain region in wild type (WT) mice significantly predicts its aberrant c-Fos expression, which in turn correlates with impaired experience-dependent modulation in the AD model. Using in vivo two-photon and ex vivo imaging of presynaptic termini, we observed a subtle yet selective weakening of excitatory cortical synapses in the visual cortex. Intriguingly, the change in the size distribution of cortical boutons in the AD model is downscaled relative to those in WT mice, suggesting that synaptic weakening may reflect an adaptation to aberrant activity. Our observations suggest that cellular and synaptic abnormalities in the AD model represent a maladaptive transformation of the baseline physiological state seen in WT conditions rather than entirely novel and unrelated manifestations.
虽然阿尔茨海默病(AD)已被广泛研究,重点是认知网络,但感觉网络功能障碍尽管在AD患者和小鼠模型中具有重要意义的证据确凿,却相对较少受到关注。我们最近发现,在表达带有瑞典和印第安纳突变的人类淀粉样蛋白前体(hAPP突变)的AD小鼠模型的初级视觉皮层中,神经元在淀粉样前体斑块阶段就表现出异常的c-Fos表达和突触结构改变。然而,尚不清楚异常的c-Fos表达和突触病理学在更广泛的视觉网络中是否存在差异,以及皮层中的c-Fos异常通过功能连接在多大程度上是遗传性的。使用4至6个月大的带有hAPP突变的AD模型小鼠(J20[PDGF-APPSw, Ind])的雌雄两性,我们发现视觉网络的皮层区域显示出异常的c-Fos表达和经验依赖性调制受损,而皮层下区域则没有。有趣的是,野生型(WT)小鼠大脑区域的全网络平均功能连接强度显著预测其异常的c-Fos表达,而这反过来又与AD模型中经验依赖性调制受损相关。通过对突触前终末进行体内双光子和体外成像,我们观察到视觉皮层中兴奋性皮层突触有细微但选择性的减弱。有趣的是,AD模型中皮层轴突终扣大小分布的变化相对于WT小鼠有所缩小,这表明突触减弱可能反映了对异常活动的一种适应。我们的观察结果表明,AD模型中的细胞和突触异常代表了在WT条件下所见基线生理状态的适应不良转变,而不是全新的和不相关的表现。