Department of Pathology and Laboratory Medicine, Center for Neurodegenerative Disease Research, Institute on Aging, University of Pennsylvania, Philadelphia, PA, USA.
Department of Pathology and Laboratory Medicine, Center for Neurodegenerative Disease Research, Institute on Aging, University of Pennsylvania, Philadelphia, PA, USA.
Alzheimers Dement. 2016 Oct;12(10):1051-1065. doi: 10.1016/j.jalz.2016.06.006.
A group of neurodegenerative diseases referred to as tauopathies are characterized by the presence of brain cells harboring inclusions of pathological species of the tau protein. These disorders include Alzheimer's disease and frontotemporal lobar degeneration due to tau pathology, including progressive supranuclear palsy, corticobasal degeneration, and Pick's disease. Tau is normally a microtubule (MT)-associated protein that appears to play an important role in ensuring proper axonal transport, but in tauopathies tau becomes hyperphosphorylated and disengages from MTs, with consequent misfolding and deposition into inclusions that mainly affect neurons but also glia. A body of experimental evidence suggests that the development of tau inclusions leads to the neurodegeneration observed in tauopathies, and there is a growing interest in developing tau-directed therapeutic agents. The following review provides a summary of strategies under investigation for the potential treatment of tauopathies, highlighting both the promises and challenges associated with these various therapeutic approaches.
一组被称为 tau 病的神经退行性疾病的特征是存在含有病理性 tau 蛋白的脑细胞包涵体。这些疾病包括阿尔茨海默病和由于 tau 病理学引起的额颞叶痴呆,包括进行性核上性麻痹、皮质基底节变性和匹克病。Tau 蛋白通常是一种微管(MT)相关蛋白,似乎在确保适当的轴突运输中发挥重要作用,但在 tau 病中,tau 蛋白过度磷酸化并与 MT 分离,随后错误折叠并沉积到主要影响神经元但也影响神经胶质的包涵体中。大量实验证据表明,tau 包涵体的形成导致了 tau 病中观察到的神经退行性变,人们越来越有兴趣开发针对 tau 的治疗药物。以下综述提供了正在研究的潜在治疗 tau 病的策略摘要,强调了这些各种治疗方法的前景和挑战。