在直接重编程的人类神经元中再现内源性4R tau表达和不溶性tau的形成。

Lucia Capano, C. Sato, E. Ficulle, A. Yu, Kanta Horie, Ji-Sun Kwon, Kyle F. Burbach, Nicolas R. Barthélemy, Susan G. Fox, C. Karch, R. Bateman, H. Houlden, R. Morimoto, D. Holtzman, K. Duff, A. Yoo
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引用次数: 11

摘要

Tau是一种在神经元中表达的微管结合蛋白,在正常成人脑功能中,4-repeat (4R)和3-repeat (3R)亚型的比例是相等的。3R:4R比例失调导致tau病变,人类神经元在健康和疾病中概括tau亚型,将为阐明涉及tau病理学的致病过程提供一个平台。我们对成人成纤维细胞的微rna诱导的神经元重编程衍生的人类神经元中表达的tau亚型进行了广泛的表征。转录物和蛋白质分析显示miR神经元表达所有6种亚型,其3R:4R亚型的比例与成人大脑中检测到的相同。此外,来自3R:4R比例改变突变的家族性tau病患者的miR神经元显示4R tau增加,并形成具有播种活性的不溶性tau。我们的研究结果共同证明了mirna诱导的神经元重编程在概括内源性tau调节方面的作用,与成人大脑在健康和疾病方面的作用相当。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recapitulation of endogenous 4R tau expression and formation of insoluble tau in directly reprogrammed human neurons.
Tau is a microtubule-binding protein expressed in neurons, and the equal ratios between 4-repeat (4R) and 3-repeat (3R) isoforms are maintained in normal adult brain function. Dysregulation of 3R:4R ratio causes tauopathy, and human neurons that recapitulate tau isoforms in health and disease will provide a platform for elucidating pathogenic processes involving tau pathology. We carried out extensive characterizations of tau isoforms expressed in human neurons derived by microRNA-induced neuronal reprogramming of adult fibroblasts. Transcript and protein analyses showed that miR neurons expressed all six isoforms with the 3R:4R isoform ratio equivalent to that detected in human adult brains. Also, miR neurons derived from familial tauopathy patients with a 3R:4R ratio altering mutation showed increased 4R tau and the formation of insoluble tau with seeding activity. Our results collectively demonstrate the utility of miRNA-induced neuronal reprogramming to recapitulate endogenous tau regulation comparable with the adult brain in health and disease.
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