Single cell transcriptomic profiling of a neuron-astrocyte assembloid tauopathy model.

Single cell transcriptomic profiling of a neuron-astrocyte assembloid tauopathy model.
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DOI:
10.1038/s41467-022-34005-1
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发表时间:
2022-10-21
影响因子:
16.6
通讯作者:
--
中科院分区:
综合性期刊1区
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使用iPSC衍生的脑类器官模型来研究神经退行性疾病受到缺乏在神经元-神经胶质相互作用的背景下准确且快速地概括发病机制的系统的阻碍。在这里,我们报告了一个系统的发展,称为AstTau,它在iPSC衍生的神经元-星形胶质细胞类胶质细胞中传播有毒的人tau寡聚体。AstTau系统发展了在tau蛋白病中观察到的许多神经元和星形胶质细胞病理学,包括错误折叠、磷酸化、寡聚和纤维状tau蛋白、强烈的神经变性和反应性星形胶质细胞增生。单细胞转录组学分析结合免疫化学表征了一个模型系统,可以更紧密地概括成人神经退行性变的晚期变化。转录组学研究表明,在疾病过程中,神经炎症和热休克蛋白(HSP)伴侣系统发生了显着变化。使用HSP 90抑制剂PU-H71的治疗用于解决假定的功能失调的HSP分子伴侣系统,并产生病理学和神经变性的强烈减少,突出了AstTau作为药物发现的快速和可重复工具的潜力。AstTau神经元-小行星tau蛋白样模型的单细胞RNA测序揭示了兴奋性神经元炎症特征和星形胶质细胞热休克反应,其类似于发生在患有tau蛋白病的个体的大脑中的反应,这可以用神经保护性HSP 90抑制剂来改善。
The use of iPSC derived brain organoid models to study neurodegenerative disease has been hampered by a lack of systems that accurately and expeditiously recapitulate pathogenesis in the context of neuron-glial interactions. Here we report development of a system, termed AstTau, which propagates toxic human tau oligomers in iPSC derived neuron-astrocyte assembloids. The AstTau system develops much of the neuronal and astrocytic pathology observed in tauopathies including misfolded, phosphorylated, oligomeric, and fibrillar tau, strong neurodegeneration, and reactive astrogliosis. Single cell transcriptomic profiling combined with immunochemistry characterizes a model system that can more closely recapitulate late-stage changes in adult neurodegeneration. The transcriptomic studies demonstrate striking changes in neuroinflammatory and heat shock protein (HSP) chaperone systems in the disease process. Treatment with the HSP90 inhibitor PU-H71 is used to address the putative dysfunctional HSP chaperone system and produces a strong reduction of pathology and neurodegeneration, highlighting the potential of AstTau as a rapid and reproducible tool for drug discovery. Single cell RNA-sequencing of the AstTau neuron-asteroid tau assembloid model reveals excitatory neuron inflammatory signatures and an astrocytic heat shock response similar to that occurring in the brains of individuals with tauopathies, which can be ameliorated with a neuroprotective HSP90 inhibitor.
DOI: 10.1038/s41588-022-01024-z
发表时间: 2022-04
期刊: NATURE GENETICS
影响因子: 30.8
作者:
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