Alzheimer's Center at Temple, Lewis Katz School of Medicine, Temple University, Philadelphia, PA, USA.
Expert Opin Ther Targets. 2020 Apr;24(4):319-330. doi: 10.1080/14728222.2020.1737012. Epub 2020 Mar 6.
: 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.
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。