Dementia Research Centre and Department of Biomedical Sciences, Faculty of Medicine, Health and Human Sciences, Macquarie University, Sydney, NSW 2109, Australia.
University of New South Wales, Sydney, NSW 2052, Australia.
Biochem J. 2021 Apr 16;478(7):1471-1484. doi: 10.1042/BCJ20200664.
Tau pathology initiates in defined brain regions and is known to spread along neuronal connections as symptoms progress in Alzheimer's disease (AD) and other tauopathies. This spread requires the release of tau from donor cells, but the underlying molecular mechanisms remained unknown. Here, we established the interactome of the C-terminal tail region of tau and identified syntaxin 8 (STX8) as a mediator of tau release from cells. Similarly, we showed the syntaxin 6 (STX6), part of the same SNARE family as STX8 also facilitated tau release. STX6 was previously genetically linked to progressive supranuclear palsy (PSP), a tauopathy. Finally, we demonstrated that the transmembrane domain of STX6 is required and sufficient to mediate tau secretion. The differential role of STX6 and STX8 in alternative secretory pathways suggests the association of tau with different secretory processes. Taken together, both syntaxins, STX6 and STX8, may contribute to AD and PSP pathogenesis by mediating release of tau from cells and facilitating pathology spreading.
tau 病理学始于特定的脑区,已知在阿尔茨海默病 (AD) 和其他 tau 病中,随着症状的进展,tau 会沿着神经元连接扩散。这种扩散需要 tau 从供体细胞中释放,但潜在的分子机制尚不清楚。在这里,我们建立了 tau 的 C 端尾部区域的相互作用组,并确定突触结合蛋白 8 (STX8) 作为 tau 从细胞中释放的介质。同样,我们还发现了 STX8 所在的 SNARE 家族的一部分突触结合蛋白 6 (STX6) 也有助于 tau 的释放。STX6 先前与进行性核上性麻痹 (PSP) 这种 tau 病有关。最后,我们证明 STX6 的跨膜结构域是介导 tau 分泌所必需和充分的。STX6 和 STX8 在不同分泌途径中的差异作用表明 tau 与不同的分泌过程有关。总之,这两种突触结合蛋白 STX6 和 STX8 可能通过介导 tau 从细胞中释放并促进病理学的扩散,从而导致 AD 和 PSP 的发病机制。