Jens Rummens, Bilal Khalil, Günseli Yıldırım, Pedro Silva, Valentina Zorzini, Nicolas Peredo, Marta Wojno, Meine Ramakers, Ludo Van Den Bosch, Philip Van Damme, Kristofer Davie, Jelle Hendrix, Frederic Rousseau, Joost Schymkowitz, Sandrine Da Cruz
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引用次数: 0
摘要
TAR dna结合蛋白43 (TDP-43)的细胞质聚集和核耗损是几种神经退行性疾病的标志。然而,在细胞系统中再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淀粉样原纤维,并证明超声原纤维在人类细胞中触发TDP-43病理,包括诱导多能干细胞(iPSC)衍生的神经元。原纤维诱导的细胞质TDP-43包涵体具有独特的生物物理特性,再现了磷酸化、泛素和p62积累等病理特征,并招募核内源性TDP-43,导致其功能丧失。鉴定了与TDP-43的聚集和核损失相关的转录组学特征,包括疾病特异性的隐剪接。在患者中观察到,细胞质TDP-43聚集体表现出时间依赖性的异质形态,包括致密、丝状或碎片状,这涉及蛋白质清除途径的上调/募集。最终,细胞特异性进行性毒性是由人类神经元的TDP-43病理引起的。这些发现确定了TDP-43模板聚集是驱动细胞质功能获得和细胞核功能丧失的关键机制,为鉴定散发性TDP-43蛋白病变的修饰因子提供了有价值的方法。
TDP-43 seeding induces cytoplasmic aggregation heterogeneity and nuclear loss of function of TDP-43.
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.
期刊介绍:
Established as a highly influential journal in neuroscience, Neuron is widely relied upon in the field. The editors adopt interdisciplinary strategies, integrating biophysical, cellular, developmental, and molecular approaches alongside a systems approach to sensory, motor, and higher-order cognitive functions. Serving as a premier intellectual forum, Neuron holds a prominent position in the entire neuroscience community.