Department of Neurology, Keio University School of Medicine, Tokyo 160-8582, Japan.
Department of Physiology, Keio University School of Medicine, Tokyo 160-8582, Japan.
Brain. 2024 Nov 4;147(11):3933-3948. doi: 10.1093/brain/awae224.
Advanced pathological and genetic approaches have revealed that mutations in fused in sarcoma/translated in liposarcoma (FUS/TLS), which is pivotal for DNA repair, alternative splicing, translation and RNA transport, cause familial amyotrophic lateral sclerosis (ALS). The generation of suitable animal models for ALS is essential for understanding its pathogenesis and developing therapies. Therefore, we used CRISPR-Cas9 to generate FUS-ALS mutation in the non-classical nuclear localization signal (NLS), H517D (mouse position: H509D) and genome-edited mice. Fus WT/H509D mice showed progressive motor impairment (accelerating rotarod and DigiGait system) with age, which was associated with the loss of motor neurons and disruption of the nuclear lamina and nucleoporins and DNA damage in spinal cord motor neurons. We confirmed the validity of our model by showing that nuclear lamina and nucleoporin disruption were observed in lower motor neurons differentiated from patient-derived human induced pluripotent stem cells (hiPSC-LMNs) with FUS-H517D and in the post-mortem spinal cord of patients with ALS. RNA sequence analysis revealed that most nuclear lamina and nucleoporin-linking genes were significantly decreased in FUS-H517D hiPSC-LMNs. This evidence suggests that disruption of the nuclear lamina and nucleoporins is crucial for ALS pathomechanisms. Combined with patient-derived hiPSC-LMNs and autopsy samples, this mouse model might provide a more reliable understanding of ALS pathogenesis and might aid in the development of therapeutic strategies.
先进的病理和遗传方法表明,融合肉瘤/翻译脂肪肉瘤(FUS/TLS)的突变,这对于 DNA 修复、选择性剪接、翻译和 RNA 运输至关重要,导致家族性肌萎缩侧索硬化症(ALS)。生成适合 ALS 的动物模型对于理解其发病机制和开发治疗方法至关重要。因此,我们使用 CRISPR-Cas9 在非经典核定位信号(NLS)、H517D(小鼠位置:H509D)中生成 FUS-ALS 突变,并对基因组编辑的小鼠进行了研究。Fus WT/H509D 小鼠随着年龄的增长表现出进行性运动障碍(加速旋转棒和 DigiGait 系统),这与运动神经元的丧失以及核层和核孔蛋白的破坏以及脊髓运动神经元中的 DNA 损伤有关。我们通过显示从具有 FUS-H517D 的患者来源的人诱导多能干细胞(hiPSC-LMN)分化的下运动神经元和 ALS 患者死后的脊髓中观察到核层和核孔蛋白破坏,证实了我们模型的有效性。RNA 序列分析显示,FUS-H517D hiPSC-LMN 中大多数核层和核孔蛋白连接基因显著减少。这一证据表明核层和核孔蛋白的破坏对于 ALS 发病机制至关重要。结合患者来源的 hiPSC-LMN 和尸检样本,这种小鼠模型可能提供对 ALS 发病机制的更可靠理解,并有助于开发治疗策略。