Creed Rose B, Harris Scott C, Sridhar Sadhana, du Lac Sascha, Zee David S, Dunn Felice A, Bouvier Guy, Nelson Alexandra B
Kavli Institute for Fundamental Neuroscience, UCSF, San Francisco, CA, 94158.
Weill Institute for Neuroscience, UCSF, San Francisco, CA, 94159.
bioRxiv. 2024 Oct 31:2024.09.20.614197. doi: 10.1101/2024.09.20.614197.
Progressive supranuclear palsy (PSP) is a neurodegenerative disorder with an estimated prevalence of 5-7 people in 100,000. Clinically characterized by impairments in gait, balance, and eye movements, as well as aggregated Tau pathology, PSP leads to death in approximately 5-8 years. No disease-modifying treatments are currently available. The contribution of Tau pathology to the symptoms of patients with PSP is poorly understood, in part due to lack of a rodent model that recapitulates characteristic aspects of PSP. Here, we assessed the hTau.P301S mouse for key clinical features of PSP, finding progressive impairments in balance and gait coordination. Additionally, we found impairments in fast vertical eye movements, one of the most distinctive features of PSP. Across animals, we found that Tau pathology in motor control regions correlated with motor deficits. These findings highlight the utility of the hP301S mouse in modeling key aspects of PSP.
进行性核上性麻痹(PSP)是一种神经退行性疾病,估计患病率为每10万人中有5至7人。临床上以步态、平衡和眼球运动障碍以及Tau蛋白病理聚集为特征,PSP患者通常在约5至8年内死亡。目前尚无改善病情的治疗方法。Tau蛋白病理在PSP患者症状中的作用尚不清楚,部分原因是缺乏能重现PSP特征的啮齿动物模型。在此,我们评估了hTau.P301S小鼠是否具有PSP的关键临床特征,发现其平衡和步态协调性存在进行性损害。此外,我们还发现快速垂直眼球运动存在障碍,这是PSP最显著的特征之一。在所有动物中,我们发现运动控制区域的Tau蛋白病理与运动缺陷相关。这些发现突出了hP301S小鼠在模拟PSP关键方面的实用性。