Center for Molecular and Cellular Biosciences, School of Biological, Environmental and Earth Sciences, University of Southern Mississippi, 118 College Drive, #5018, Hattiesburg, Mississippi 39406, U.S.A.
Biochem J. 2021 Jul 30;478(14):2921-2925. doi: 10.1042/BCJ20210324.
Secretion of misfolded tau, a microtubule-binding protein enriched in nerve cells, is linked to the progression of tau pathology. However, the molecular mechanisms underlying tau secretion are poorly understood. Recent work by Lee et al. [Biochemical J. (2021) 478: 1471-1484] demonstrated that the transmembrane domains of syntaxin6 and syntaxin8 could be exploited for tau release, setting a stage for testing a novel hypothesis that has profound implications in tauopathies (e.g. Alzheimer's disease, FTDP-17, and CBD/PSP) and other related neurodegenerative diseases. The present commentary highlights the importance and limitations of the study, and discusses opportunities and directions for future investigations.
错误折叠的 tau 蛋白的分泌与 tau 病理的进展有关,tau 蛋白是一种富含于神经细胞中的微管结合蛋白。然而,tau 蛋白分泌的分子机制尚不清楚。最近,Lee 等人的研究表明,突触融合蛋白 6 和 8 的跨膜结构域可被用于 tau 蛋白的释放,这为测试一个具有深远意义的新假说奠定了基础,该假说与 tau 病(如阿尔茨海默病、FTDP-17 和 CBD/PSP)和其他相关神经退行性疾病有关。本评论强调了这项研究的重要性和局限性,并讨论了未来研究的机会和方向。