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阿尔茨海默病:使用疾病模型和靶向 Tau 蛋白的表型方法。

Alzheimer's disease: phenotypic approaches using disease models and the targeting of tau protein.

机构信息

Alzheimer's Center at Temple, Lewis Katz School of Medicine, Temple University, Philadelphia, PA, USA.

出版信息

Expert Opin Ther Targets. 2020 Apr;24(4):319-330. doi: 10.1080/14728222.2020.1737012. Epub 2020 Mar 6.

Abstract

: Hyperphosphorylated and aggregated tau protein is the main hallmark of a class of neurodegenerative disorders known as tauopathies. Tau is a microtubule-binding protein which is important for microtubule assembly and stabilization, for proper axonal transport and overall neuronal integrity. However, in tauopathies, tau undergoes aberrant post-translational modifications that fundamentally affect its normal function. The etiology of these devastating diseases is unclear and there is no treatment for these disorders.: This review examines the neurobiology of tau, tau post-translational modifications, and tau pathophysiology. Progress regarding the effort to identify and assess novel tau-targeted therapeutic strategies in preclinical studies is also discussed. We performed a search on PubMed of the relevant literature published between 1995 and 2020.: Tau diversity and the lack of clinically available test to diagnose and identify tauopathies are major obstacles; they represent a possible reason for the lack of success of clinical trials. However, given the encouraging advances in PET tau imaging and tau neurobiology, we believe that a more personalized approach could be on the horizon and that this will be key to addressing the heterogeneity of tau pathology.

摘要

过度磷酸化和聚集的 tau 蛋白是一类被称为 tau 病的神经退行性疾病的主要标志。Tau 是一种微管结合蛋白,对于微管组装和稳定、适当的轴突运输和整体神经元完整性很重要。然而,在 tau 病中,tau 经历了异常的翻译后修饰,从根本上影响了其正常功能。这些破坏性疾病的病因尚不清楚,也没有针对这些疾病的治疗方法。

本文综述了 tau 的神经生物学、tau 的翻译后修饰以及 tau 的病理生理学。还讨论了在临床前研究中鉴定和评估新型 tau 靶向治疗策略的努力进展。我们在 PubMed 上搜索了 1995 年至 2020 年期间发表的相关文献。

tau 的多样性以及缺乏临床可用的诊断和鉴定 tau 病的方法是主要障碍;这可能是临床试验缺乏成功的原因。然而,鉴于正电子发射断层扫描(PET)tau 成像和 tau 神经生物学的令人鼓舞的进展,我们相信更个性化的方法可能即将出现,这将是解决 tau 病理学异质性的关键。

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