Suppr超能文献

阿尔茨海默病的干细胞模型:进展与挑战

Stem cell models of Alzheimer's disease: progress and challenges.

作者信息

Arber Charles, Lovejoy Christopher, Wray Selina

机构信息

Department of Molecular Neuroscience, UCL Institute of Neurology, 1 Wakefield Street, London, WC1N 1PJ, UK.

出版信息

Alzheimers Res Ther. 2017 Jun 13;9(1):42. doi: 10.1186/s13195-017-0268-4.

Abstract

A major challenge to our understanding of the molecular mechanisms of Alzheimer's disease (AD) has been the lack of physiologically relevant in vitro models which capture the precise patient genome, in the cell type of interest, with physiological expression levels of the gene(s) of interest. Induced pluripotent stem cell (iPSC) technology, together with advances in 2D and 3D neuronal differentiation, offers a unique opportunity to overcome this challenge and generate a limitless supply of human neurons for in vitro studies. iPSC-neuron models have been widely employed to model AD and we discuss in this review the progress that has been made to date using patient-derived neurons to recapitulate key aspects of AD pathology and how these models have contributed to a deeper understanding of AD molecular mechanisms, as well as addressing the key challenges posed by using this technology and what progress is being made to overcome these. Finally, we highlight future directions for the use of iPSC-neurons in AD research and highlight the potential value of this technology to neurodegenerative research in the coming years.

摘要

我们对阿尔茨海默病(AD)分子机制的理解面临的一个主要挑战是缺乏生理相关的体外模型,这些模型能够在感兴趣的细胞类型中,以感兴趣基因的生理表达水平捕捉精确的患者基因组。诱导多能干细胞(iPSC)技术,以及二维和三维神经元分化的进展,为克服这一挑战提供了独特的机会,并为体外研究提供了无限的人类神经元来源。iPSC-神经元模型已被广泛用于模拟AD,在本综述中,我们讨论了迄今为止使用患者来源的神经元来概括AD病理学关键方面所取得的进展,以及这些模型如何有助于更深入地理解AD分子机制,同时也讨论了使用该技术所面临的关键挑战以及为克服这些挑战所取得的进展。最后,我们强调了在AD研究中使用iPSC-神经元的未来方向,并突出了该技术在未来几年对神经退行性研究的潜在价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a54c/5470327/836650f6daba/13195_2017_268_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验