老年供者尿液来源的细胞通过iPSCs进行神经细胞的2D/3D建模

IF 1.7 Q3 CLINICAL NEUROLOGY Aging brain Pub Date : 2023-01-01 DOI:10.1016/j.nbas.2023.100101
Sopak Supakul , Yuki Hatakeyama , Nicolas Leventoux , Maika Itsuno , Naoko Numata , Hayato Hiramine , Satoru Morimoto , Atsushi Iwata , Sumihiro Maeda , Hideyuki Okano
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引用次数: 0

摘要

由诱导多能干细胞(iPSCs)衍生的人类神经细胞模型已被广泛接受用于体外模拟各种神经退行性疾病,如阿尔茨海默病(AD)。虽然iPSCs最常见的来源是成纤维细胞和外周血单个核细胞,但这些细胞的收集是侵入性的。为了减轻供者的负担,我们建议使用尿源性细胞(UDCs),这种细胞可以从尿液样本中非侵入性地获得。然而,从患有年龄相关疾病(如AD)的老年供体收集UDCs尚未有报道,并且尚不清楚这些来自80岁以上供体的UDCs是否可以转化为iPSCs并分化为神经细胞。在本研究中,我们报道了一例使用来自89岁AD患者尿液样本的UDCs的病例,UDCs成功重编程为iPSCs,并以四种不同的方式分化为神经细胞:(i)通过神经祖细胞前体阶段用小分子双重抑制SMAD, (ii)不经过神经祖细胞阶段使用瞬时表达Ngn2和microrna的快速诱导方法,(iii)用于3D培养的皮质脑类器官,以及(iv)人类星形胶质细胞。磷酸化Tau蛋白的积累是阿尔茨海默病的病理标志,在老年供体UDCs产生的神经元模型中进行了检查。这种细胞源的应用将扩大利用iPS技术进行疾病建模的目标人群。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Urine-derived cells from the aged donor for the 2D/3D modeling of neural cells via iPSCs

Human neural cell models derived from induced pluripotent stem cells (iPSCs) have been widely accepted to model various neurodegenerative diseases such as Alzheimer’s disease (AD) in vitro. Although the most common sources of iPSCs are fibroblasts and peripheral blood mononuclear cells, the collection of these cells is invasive. To reduce the donor’s burden, we propose the use of urine-derived cells (UDCs), which can be obtained non-invasively from a urine sample. However, the collection of UDCs from elderly donors suffering from age-related diseases such as AD has not been reported, and it is unknown whether these UDCs from the donor aged over 80 years old can be converted into iPSCs and differentiated into neural cells. In this study, we reported a case of using the UDCs from the urine sample of an 89-year-old AD patient, and the UDCs were successfully reprogrammed into iPSCs and differentiated into neural cells in four different ways: (i) the dual SMAD inhibition with small-molecules via the neural progenitor precursor stage, (ii) the rapid induction method using transient expression of Ngn2 and microRNAs without going through the neural progenitor stage, (iii) the cortical brain organoids for 3D culture, and (iv) the human astrocytes. The accumulation of phosphorylated Tau proteins, which is a pathological hallmark of AD, was examined in the neuronal models generated from the UDCs of the aged donor. The application of this cell source will broaden the target population for disease modeling using iPS technology.

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Aging brain
Aging brain Neuroscience (General), Geriatrics and Gerontology
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