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鼠诱导多能干细胞衍生的阿尔茨海默病大脑类器官培养和神经分化障碍。

Mouse induced pluripotent stem cells-derived Alzheimer's disease cerebral organoid culture and neural differentiation disorders.

机构信息

National Health Commission Key Laboratory of Birth Defects Prevention, Scientific and Technical Institute of Population and Family Planning, Zhengzhou, China; School of Life Science, Henan University, Kaifeng, China; Luohe Medical College, Luohe, China.

School of Life Science, Henan University, Kaifeng, China.

出版信息

Neurosci Lett. 2019 Oct 15;711:134433. doi: 10.1016/j.neulet.2019.134433. Epub 2019 Aug 14.

Abstract

Alzheimer's disease (AD) is a progressive neurodegenerative disease, characterized by cognitive impairment. However, the pathogenesis of AD are very complicated, and the theories of Aβ and neurofibrillary tangles cannot explain all pathological alterations and clinical symptoms. Here, we used three-dimensional (3D) neural organoids culture derived from mouse induced pluripotent stem cells (iPSCs) to investigate the pathological mechanisms of AD. In this study, AD cerebral organoids were generated by overexpressing familial AD mutations (APP and PS1 genes) in mouse induced pluripotent stem cells, so that the early pathogenesis of AD could be investigated well with protein and cellular phenotype analyses. The results showed that AD cerebral organoids appeared some AD pathological alterations, and high levels of Aβ and p-Tau were induced as well. Furthermore, the number of GFAP-positive astrocytes and glutamatergic excitatory neurons increased significantly, but the number of GABAergic interneurons decreased. In conclusion, we suggest that cerebral organoids are a suitable AD model for scientific study, and that will provide us a novel insight into the understanding of the pathogenesis of AD.

摘要

阿尔茨海默病(AD)是一种进行性神经退行性疾病,以认知障碍为特征。然而,AD 的发病机制非常复杂,Aβ 和神经原纤维缠结的理论不能解释所有的病理改变和临床症状。在这里,我们使用源自小鼠诱导多能干细胞(iPSCs)的三维(3D)神经类器官培养物来研究 AD 的病理机制。在这项研究中,通过在小鼠诱导多能干细胞中过表达家族性 AD 突变(APP 和 PS1 基因)来生成 AD 脑类器官,从而可以通过蛋白质和细胞表型分析很好地研究 AD 的早期发病机制。结果表明,AD 脑类器官出现了一些 AD 病理改变,并诱导了高水平的 Aβ 和 p-Tau。此外,GFAP 阳性星形胶质细胞和谷氨酸能兴奋性神经元的数量显著增加,而 GABA 能中间神经元的数量减少。总之,我们认为脑类器官是一种适合 AD 科学研究的模型,为我们深入了解 AD 的发病机制提供了新的视角。

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