University of Rochester, Rochester, NY, USA.
Adv Exp Med Biol. 2019;1184:57-68. doi: 10.1007/978-981-32-9358-8_5.
Efficient quality control mechanisms are essential for a healthy, functional neuron. Recognition and degradation of misfolded, damaged, or potentially toxic proteins, is a crucial aspect of protein quality control. Tau is a protein that is highly expressed in neurons, and plays an important role in modulating a number of physiological processes. Maintaining appropriate levels of tau is key for neuronal health; hence perturbations in tau clearance mechanisms are likely significant contributors to neurodegenerative diseases such as Alzheimer's disease and frontotemporal lobar degeneration. In this chapter we will first briefly review the two primary degradative mechanisms that mediate tau clearance: the proteasome system and the autophagy-lysosome pathway. This will be followed by a discussion about what is known about the contribution of each of these pathways to tau clearance. We will also present recent findings on tau degradation through the endolysosomal system. Further, how deficits in these degradative systems may contribute to the accumulation of dysfunctional or toxic forms of tau in neurodegenerative conditions is considered.
有效的质量控制机制对于健康、功能正常的神经元至关重要。识别和降解错误折叠、受损或潜在有毒的蛋白质是蛋白质质量控制的一个关键方面。Tau 是一种在神经元中高度表达的蛋白质,在调节许多生理过程中发挥着重要作用。维持适当的 Tau 水平对于神经元的健康至关重要;因此,Tau 清除机制的干扰可能是阿尔茨海默病和额颞叶痴呆等神经退行性疾病的重要贡献因素。在本章中,我们将首先简要回顾介导 Tau 清除的两种主要降解机制:蛋白酶体系统和自噬溶酶体途径。接下来将讨论关于这些途径对 Tau 清除的贡献的已知内容。我们还将介绍最近关于通过内溶酶体系统降解 Tau 的发现。此外,还考虑了这些降解系统的缺陷如何导致神经退行性疾病中功能失调或有毒形式的 Tau 积累。