Institute of Human Genetics, University of Cologne, Cologne, Germany.
Faculty of Medicine, University Hospital Cologne, Cologne, Germany.
Adv Exp Med Biol. 2019;1184:69-77. doi: 10.1007/978-981-32-9358-8_6.
Tau is a microtubule-associated protein (MAP) that is mainly sorted into the axons in physiological conditions, but missorted in Alzheimer Disease and related tauopathies. The mechanism(s) of axonal targeting of Tau protein are still a matter of debate. Several possibilities for the axonal localization of Tau protein have been proposed: (1) Targeting of Tau mRNA into axons which is then translated locally. (2) Preferred axonal translation of Tau mRNA. (3) Specific dendritic degradation of Tau protein. (4) Active axonal sorting of somatically translated Tau protein. (5) Axonal retention of Tau protein by specific association of Tau protein with axonal structures, namely particularly modified microtubules. (6) Restriction of Tau diffusion by a selective filter function of the Axon Initial Segment (AIS). In our research we focused on the Tau Diffusion Barrier (TDB), located within the AIS, which controls anterograde and retrograde propagation of Tau. It shows both sensitivity to size of the Tau protein isoforms, and to disruption of the molecular structure of the AIS. Here, we review proposed mechanisms of axonal targeting of Tau and potential influences of the TDB/AIS on the subcellular distribution of Tau.
tau 是一种微管相关蛋白 (MAP),在生理条件下主要分拣到轴突中,但在阿尔茨海默病和相关的 tau 病中分拣错误。tau 蛋白的轴突靶向的机制仍存在争议。tau 蛋白的轴突定位有几种可能:(1)tau mRNA 靶向进入轴突,然后在局部翻译。(2)tau mRNA 优先在轴突中翻译。(3)tau 蛋白的特定树突降解。(4)tau 蛋白的主动轴突分拣。(5)tau 蛋白通过与轴突结构,特别是修饰的微管的特异性结合,在轴突中保留。(6)通过轴突起始段 (AIS) 的选择性过滤功能限制 tau 扩散。在我们的研究中,我们专注于位于 AIS 内的 tau 扩散屏障 (TDB),它控制 tau 的顺行和逆行传播。它既对 tau 蛋白同工型的大小敏感,也对 AIS 的分子结构的破坏敏感。在这里,我们综述了 tau 的轴突靶向的提出的机制,以及 TDB/AIS 对 tau 的亚细胞分布的潜在影响。