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Tau P301S转基因小鼠出现模仿进行性核上性麻痹的步态和眼球运动障碍。

Tau P301S Transgenic Mice Develop Gait and Eye Movement Impairments That Mimic Progressive Supranuclear Palsy.

作者信息

Creed Rose B, Harris Scott C, Sridhar Sadhana, du Lac Sascha, Zee David S, Dunn Felice A, Bouvier Guy, Nelson Alexandra B

机构信息

Kavli Institute for Fundamental Neuroscience, UCSF, San Francisco, CA, 94158.

Weill Institute for Neuroscience, UCSF, San Francisco, CA, 94159.

出版信息

bioRxiv. 2024 Oct 31:2024.09.20.614197. doi: 10.1101/2024.09.20.614197.

DOI:10.1101/2024.09.20.614197
PMID:39386710
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11463522/
Abstract

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.

摘要

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。

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本文引用的文献

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A human Tau expressing zebrafish model of progressive supranuclear palsy identifies Brd4 as a regulator of microglial synaptic elimination.人类 Tau 表达的进行性核上性麻痹斑马鱼模型确定 Brd4 为小胶质细胞突触消除的调节剂。
Nat Commun. 2024 Sep 18;15(1):8195. doi: 10.1038/s41467-024-52173-0.
2
Optokinetic nystagmus: six practical uses.视动性眼球震颤:六种实用用途。
Pract Neurol. 2024 Jul 16;24(4):285-288. doi: 10.1136/pn-2023-003772.
3
Asymmetric retinal direction tuning predicts optokinetic eye movements across stimulus conditions.
视网膜方向调谐的不对称性预测了在不同刺激条件下的视动性眼球运动。
Elife. 2023 Mar 17;12:e81780. doi: 10.7554/eLife.81780.
4
Tau seeds from patients induce progressive supranuclear palsy pathology and symptoms in primates.患者的 Tau 种子可在灵长类动物中诱导进行性核上性麻痹的病理和症状。
Brain. 2023 Jun 1;146(6):2524-2534. doi: 10.1093/brain/awac428.
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The transcription factor Tbx5 regulates direction-selective retinal ganglion cell development and image stabilization.转录因子 Tbx5 调节方向选择性视网膜神经节细胞的发育和图像稳定。
Curr Biol. 2022 Oct 10;32(19):4286-4298.e5. doi: 10.1016/j.cub.2022.07.064. Epub 2022 Aug 22.
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Eye Movement Disorders in Movement Disorders.运动障碍中的眼球运动障碍
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Superior colliculus drives stimulus-evoked directionally biased saccades and attempted head movements in head-fixed mice.上丘驱动刺激诱发的有方向性偏向的扫视和头固定小鼠的头部运动尝试。
Elife. 2021 Dec 31;10:e73081. doi: 10.7554/eLife.73081.
8
Human wildtype tau expression in cholinergic pedunculopontine tegmental neurons is sufficient to produce PSP-like behavioural deficits and neuropathology.在胆碱能脑桥被盖脚核神经元中表达人类野生型 tau 足以产生 PSP 样行为缺陷和神经病理学。
Eur J Neurosci. 2021 Nov;54(10):7688-7709. doi: 10.1111/ejn.15496. Epub 2021 Nov 2.
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Modulation of motor behavior by the mesencephalic locomotor region.中脑运动区对运动行为的调制。
Cell Rep. 2021 Aug 24;36(8):109594. doi: 10.1016/j.celrep.2021.109594.
10
Best Practices in the Clinical Management of Progressive Supranuclear Palsy and Corticobasal Syndrome: A Consensus Statement of the CurePSP Centers of Care.进行性核上性麻痹和皮质基底节综合征临床管理的最佳实践:CurePSP护理中心的共识声明
Front Neurol. 2021 Jul 1;12:694872. doi: 10.3389/fneur.2021.694872. eCollection 2021.