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阿尔茨海默病相关tau 修饰物选择性破坏 Drp1 非依赖性自噬体和线粒体溶酶体运输在新型秀丽隐杆线虫模型中的作用。

Selective disruption of Drp1-independent mitophagy and mitolysosome trafficking by an Alzheimer's disease relevant tau modification in a novel Caenorhabditis elegans model.

机构信息

Department of Anesthesiology & Perioperative Medicine, University of Rochester, Rochester, NY 14642, USA.

Department of Pathology and Laboratory Medicine, University of Rochester, Rochester, NY 14642, USA.

出版信息

Genetics. 2022 Aug 30;222(1). doi: 10.1093/genetics/iyac104.

Abstract

Accumulation of inappropriately phosphorylated tau into neurofibrillary tangles is a defining feature of Alzheimer's disease, with Tau pT231 being an early harbinger of tau pathology. Previously, we demonstrated that expressing a single genomic copy of human phosphomimetic mutant tau (T231E) in Caenorhabditis elegans drove age-dependent neurodegeneration. A critical finding was that T231E, unlike wild-type tau, completely and selectively suppressed oxidative stress-induced mitophagy. Here, we used dynamic imaging approaches to analyze T231E-associated changes in mitochondria and mitolysosome morphology, abundance, trafficking, and stress-induced mitophagy as a function of mitochondrial fission mediator dynamin-related protein 1, which has been demonstrated to interact with hyper phosphorylated tau and contribute to Alzheimer's disease pathogenesis, as well as Pink1, a well-recognized mediator of mitochondrial quality control that works together with Parkin to support stress-induced mitophagy. T231E impacted both mitophagy and mitolysosome neurite trafficking with exquisite selectivity, sparing macroautophagy as well as lysosome and autolysosome trafficking. Both oxidative-stress-induced mitophagy and the ability of T231E to suppress it were independent of drp-1, but at least partially dependent on pink-1. Organelle trafficking was more complicated, with drp-1 and pink-1 mutants exerting independent effects, but generally supported the idea that the mitophagy phenotype is of greater physiologic impact in T231E. Collectively, our results refine the mechanistic pathway through which T231E causes neurodegeneration, demonstrating pathologic selectivity for mutations that mimic tauopathy-associated post-translational modifications, physiologic selectivity for organelles that contain damaged mitochondria, and molecular selectivity for dynamin-related protein 1-independent, Pink1-dependent, perhaps adaptive, and mitophagy.

摘要

tau 蛋白过度磷酸化形成神经纤维缠结是阿尔茨海默病的一个明确特征,tau pT231 是 tau 病理学的早期标志。以前,我们证明在秀丽隐杆线虫中表达单个人类磷酸化突变体 tau(T231E)的基因组拷贝会导致年龄依赖性神经退行性变。一个关键发现是,与野生型 tau 不同,T231E 完全且选择性地抑制氧化应激诱导的线粒体自噬。在这里,我们使用动态成像方法分析 T231E 相关的线粒体和溶酶体形态、丰度、运输以及应激诱导的线粒体自噬变化,作为与过度磷酸化 tau 相互作用并导致阿尔茨海默病发病机制的 dynamin 相关蛋白 1(DRP1)的功能,以及 Pink1,一种公认的线粒体质量控制的介质,与 Parkin 一起工作以支持应激诱导的线粒体自噬。T231E 对线粒体自噬和溶酶体神经突运输都有极高的选择性影响,而不影响巨自噬以及溶酶体和自溶酶体运输。氧化应激诱导的线粒体自噬和 T231E 抑制它的能力都独立于 drp-1,但至少部分依赖于 pink-1。细胞器运输更为复杂,drp-1 和 pink-1 突变体产生独立的影响,但总体上支持这样的观点,即 T231E 中的线粒体自噬表型具有更大的生理影响。总的来说,我们的结果细化了 T231E 导致神经退行性变的机制途径,证明了对模拟 tau 病相关翻译后修饰的突变具有病理性选择性,对含有受损线粒体的细胞器具有生理性选择性,以及对 dynamin 相关蛋白 1 非依赖性、Pink1 依赖性、可能是适应性的和线粒体自噬的分子选择性。

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