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利用脑类器官和其他三维培养系统模拟神经退行性疾病:以阿尔茨海默病为例。

Modeling neurodegenerative diseases with cerebral organoids and other three-dimensional culture systems: focus on Alzheimer's disease.

机构信息

Department of Neuroscience, The Ohio State University Wexner Medical Center, 616 Biomedical Research Tower, 460 W. 12th Ave, Columbus, OH, 43210, USA.

The Steve and Cindy Rasmussen Institute for Genomic Medicine, Abigail Wexner Research Institute at Nationwide Children's Hospital, 575 Children's Crossroad, Columbus, OH, 43215, USA.

出版信息

Stem Cell Rev Rep. 2022 Feb;18(2):696-717. doi: 10.1007/s12015-020-10068-9. Epub 2020 Nov 12.

Abstract

Many neurodegenerative diseases (NDs) such as Alzheimer's disease, Parkinson's disease, frontotemporal dementia, amyotrophic lateral sclerosis and Huntington's disease, are characterized by the progressive accumulation of abnormal proteinaceous assemblies in specific cell types and regions of the brain, leading to cellular dysfunction and brain damage. Although animal- and in vitro-based studies of NDs have provided the field with an extensive understanding of some of the mechanisms underlying these diseases, findings from these studies have not yielded substantial progress in identifying treatment options for patient populations. This necessitates the development of complementary model systems that are better suited to recapitulate human-specific features of ND pathogenesis. Three-dimensional (3D) culture systems, such as cerebral organoids generated from human induced pluripotent stem cells, hold significant potential to model NDs in a complex, tissue-like environment. In this review, we discuss the advantages of 3D culture systems and 3D modeling of NDs, especially AD and FTD. We also provide an overview of the challenges and limitations of the current 3D culture systems. Finally, we propose a few potential future directions in applying state-of-the-art technologies in 3D culture systems to understand the mechanisms of NDs and to accelerate drug discovery. Graphical abstract.

摘要

许多神经退行性疾病(NDs),如阿尔茨海默病、帕金森病、额颞叶痴呆、肌萎缩侧索硬化症和亨廷顿病,其特征是异常蛋白聚集体在大脑的特定细胞类型和区域中进行性积累,导致细胞功能障碍和脑损伤。尽管基于动物和体外的 NDs 研究为该领域提供了对这些疾病一些潜在机制的广泛理解,但这些研究的结果并没有在确定患者群体的治疗选择方面取得实质性进展。这就需要开发互补的模型系统,这些系统更适合重现 ND 发病机制的人类特异性特征。三维(3D)培养系统,如源自人类诱导多能干细胞的大脑类器官,具有在复杂的组织样环境中对 NDs 进行建模的巨大潜力。在这篇综述中,我们讨论了 3D 培养系统和 NDs 的 3D 建模的优势,特别是 AD 和 FTD。我们还概述了当前 3D 培养系统的挑战和局限性。最后,我们提出了在应用 3D 培养系统中的最先进技术来理解 NDs 的机制并加速药物发现方面的一些潜在未来方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d3c/7658915/6dd2836c4de2/12015_2020_10068_Figa_HTML.jpg

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