Ghosh Ujjayini, Tse Eric, Yang Hyunjun, Shi Marie, Caro Christoffer D, Wang Feng, Merz Gregory E, Prusiner Stanley B, Southworth Daniel R, Condello Carlo
Institute for Neurodegenerative Diseases, University of California San Francisco, San Francisco, CA, USA.
Department of Biochemistry and Biophysics, University of California San Francisco, San Francisco, CA, USA.
Acta Neuropathol Commun. 2024 Jun 12;12(1):94. doi: 10.1186/s40478-024-01806-y.
Down syndrome (DS) is a common genetic condition caused by trisomy of chromosome 21. Among their complex clinical features, including musculoskeletal, neurological, and cardiovascular disabilities, individuals with DS have an increased risk of developing progressive dementia and early-onset Alzheimer's disease (AD). This dementia is attributed to the increased gene dosage of the amyloid-β (Aβ) precursor protein gene, the formation of self-propagating Aβ and tau prion conformers, and the deposition of neurotoxic Aβ plaques and tau neurofibrillary tangles. Tau amyloid fibrils have previously been established to adopt many distinct conformations across different neurodegenerative conditions. Here, we report the characterization of brain samples from four DS cases spanning 36-63 years of age by spectral confocal imaging with conformation-specific dyes and cryo-electron microscopy (cryo-EM) to determine structures of isolated tau fibrils. High-resolution structures revealed paired helical filament (PHF) and straight filament (SF) conformations of tau that were identical to those determined from AD cases. The PHFs and SFs are made of two C-shaped protofilaments, each containing a cross-β/β-helix motif. Similar to filaments from AD cases, most filaments from the DS cases adopted the PHF form, while a minority (approximately 20%) formed SFs. Samples from the youngest individual with no documented dementia had sparse tau deposits. To isolate tau for cryo-EM from this challenging sample we used a novel affinity-grid method involving a graphene oxide surface derivatized with anti-tau antibodies. This method improved isolation and revealed that primarily tau PHFs and a minor population of chronic traumatic encephalopathy type II-like filaments were present in this youngest case. These findings expand the similarities between AD and DS to the molecular level, providing insight into their related pathologies and the potential for targeting common tau filament folds by small-molecule therapeutics and diagnostics.
唐氏综合征(DS)是一种由21号染色体三体性引起的常见遗传疾病。在其复杂的临床特征中,包括肌肉骨骼、神经和心血管方面的残疾,DS患者患进行性痴呆和早发性阿尔茨海默病(AD)的风险增加。这种痴呆归因于淀粉样β(Aβ)前体蛋白基因的基因剂量增加、自传播Aβ和tau朊病毒构象体的形成,以及神经毒性Aβ斑块和tau神经原纤维缠结的沉积。此前已确定tau淀粉样原纤维在不同的神经退行性疾病中呈现多种不同的构象。在此,我们通过使用构象特异性染料的光谱共聚焦成像和冷冻电子显微镜(cryo-EM)对4例年龄在36至63岁之间的DS病例的脑样本进行表征,以确定分离出的tau原纤维的结构。高分辨率结构揭示了tau的双螺旋丝(PHF)和直丝(SF)构象,与从AD病例中确定的构象相同。PHF和SF由两条C形原纤维组成,每条原纤维都包含一个交叉β/β螺旋基序。与AD病例的纤维相似,DS病例的大多数纤维采用PHF形式,而少数(约20%)形成SF。来自最年轻且无痴呆记录的个体的样本中tau沉积物稀少。为了从这个具有挑战性的样本中分离出用于cryo-EM分析的tau,我们使用了一种新型的亲和网格方法,该方法涉及用抗tau抗体衍生化的氧化石墨烯表面。这种方法改进了分离效果,并揭示在这个最年轻的病例中主要存在tau PHF和少量II型慢性创伤性脑病样纤维。这些发现将AD和DS之间的相似性扩展到分子水平,为它们相关的病理学以及通过小分子疗法和诊断靶向常见tau纤维折叠的潜力提供了见解。