Rummens Jens, Khalil Bilal, Yıldırım Günseli, Silva Pedro, Zorzini Valentina, Peredo Nicolas, Wojno Marta, Ramakers Meine, Van Den Bosch Ludo, Van Damme Philip, Davie Kristofer, Hendrix Jelle, Rousseau Frederic, Schymkowitz Joost, Da Cruz Sandrine
Laboratory of Neurophysiology in Neurodegenerative Disorders, VIB-KU Leuven Center for Brain & Disease Research, Department of Neurosciences, KU Leuven, Leuven Brain Institute, 3000 Leuven, Belgium.
Laboratory of Neurophysiology in Neurodegenerative Disorders, VIB-KU Leuven Center for Brain & Disease Research, Department of Neurosciences, KU Leuven, Leuven Brain Institute, 3000 Leuven, Belgium; Switch Laboratory, VIB-KU Leuven Center for Brain & Disease Research, Department of Cellular and Molecular Medicine, KU Leuven, 3000 Leuven, Belgium.
Neuron. 2025 May 21;113(10):1597-1613.e8. doi: 10.1016/j.neuron.2025.03.004. Epub 2025 Mar 28.
Cytoplasmic aggregation and nuclear depletion of TAR DNA-binding protein 43 (TDP-43) are hallmarks of several neurodegenerative disorders. Yet, recapitulating both features in cellular systems has been challenging. Here, we produced amyloid-like fibrils from recombinant TDP-43 low-complexity domain and demonstrate that sonicated fibrils trigger TDP-43 pathology in human cells, including induced pluripotent stem cell (iPSC)-derived neurons. Fibril-induced cytoplasmic TDP-43 inclusions acquire distinct biophysical properties, recapitulate pathological hallmarks such as phosphorylation, ubiquitin, and p62 accumulation, and recruit nuclear endogenous TDP-43, leading to its loss of function. A transcriptomic signature linked to both aggregation and nuclear loss of TDP-43, including disease-specific cryptic splicing, is identified. Cytoplasmic TDP-43 aggregates exhibit time-dependent heterogeneous morphologies as observed in patients-including compacted, filamentous, or fragmented-which involve upregulation/recruitment of protein clearance pathways. Ultimately, cell-specific progressive toxicity is provoked by seeded TDP-43 pathology in human neurons. These findings identify TDP-43-templated aggregation as a key mechanism driving both cytoplasmic gain of function and nuclear loss of function, offering a valuable approach to identify modifiers of sporadic TDP-43 proteinopathies.
TAR DNA结合蛋白43(TDP - 43)的细胞质聚集和核内缺失是几种神经退行性疾病的标志。然而,在细胞系统中重现这两个特征一直具有挑战性。在这里,我们从重组TDP - 43低复杂性结构域产生了淀粉样纤维,并证明超声处理的纤维会引发人类细胞中的TDP - 43病理变化,包括诱导多能干细胞(iPSC)衍生的神经元。纤维诱导的细胞质TDP - 43包涵体具有独特的生物物理特性,重现了诸如磷酸化、泛素化和p62积累等病理特征,并招募核内源性TDP - 43,导致其功能丧失。我们鉴定了一种与TDP - 43的聚集和核内缺失相关的转录组特征,包括疾病特异性的隐蔽剪接。细胞质TDP - 43聚集体表现出与患者中观察到的时间依赖性异质形态,包括致密的、丝状的或碎片化的,这涉及蛋白质清除途径的上调/招募。最终,在人类神经元中,种子TDP - 43病理引发了细胞特异性的进行性毒性。这些发现确定TDP - 43模板化聚集是驱动细胞质功能获得和核功能丧失的关键机制,为鉴定散发性TDP - 43蛋白病的修饰因子提供了一种有价值的方法。