Medical College of Wisconsin, Department of Cell Biology, Neurobiology & Anatomy, Milwaukee, Wisconsin, USA.
Medical College of Wisconsin, Department of Physiology, Milwaukee, Wisconsin, USA.
Compr Physiol. 2019 Mar 14;9(2):565-611. doi: 10.1002/cphy.c180025.
Neurological disorders have emerged as a predominant healthcare concern in recent years due to their severe consequences on quality of life and prevalence throughout the world. Understanding the underlying mechanisms of these diseases and the interactions between different brain cell types is essential for the development of new therapeutics. Induced pluripotent stem cells (iPSCs) are invaluable tools for neurological disease modeling, as they have unlimited self-renewal and differentiation capacity. Mounting evidence shows: (i) various brain cells can be generated from iPSCs in two-dimensional (2D) monolayer cultures; and (ii) further advances in 3D culture systems have led to the differentiation of iPSCs into organoids with multiple brain cell types and specific brain regions. These 3D organoids have gained widespread attention as in vitro tools to recapitulate complex features of the brain, and (iii) complex interactions between iPSC-derived brain cell types can recapitulate physiological and pathological conditions of blood-brain barrier (BBB). As iPSCs can be generated from diverse patient populations, researchers have effectively applied 2D, 3D, and BBB models to recapitulate genetically complex neurological disorders and reveal novel insights into molecular and genetic mechanisms of neurological disorders. In this review, we describe recent progress in the generation of 2D, 3D, and BBB models from iPSCs and further discuss their limitations, advantages, and future ventures. This review also covers the current status of applications of 2D, 3D, and BBB models in drug screening, precision medicine, and modeling a wide range of neurological diseases (e.g., neurodegenerative diseases, neurodevelopmental disorders, brain injury, and neuropsychiatric disorders). © 2019 American Physiological Society. Compr Physiol 9:565-611, 2019.
神经系统疾病近年来成为主要的医疗保健关注点,因为它们对生活质量和全球患病率都有严重影响。了解这些疾病的潜在机制和不同脑细胞类型之间的相互作用对于开发新的治疗方法至关重要。诱导多能干细胞(iPSC)是神经疾病建模的宝贵工具,因为它们具有无限的自我更新和分化能力。越来越多的证据表明:(i)可以从 iPSC 在二维(2D)单层培养物中生成各种脑细胞;(ii)3D 培养系统的进一步进展导致 iPSC 分化为具有多种脑细胞类型和特定脑区的类器官。这些 3D 类器官作为体外工具,能够重现大脑的复杂特征,因此受到广泛关注,(iii)iPSC 衍生的脑细胞类型之间的复杂相互作用可以再现血脑屏障(BBB)的生理和病理状态。由于 iPSC 可以从不同的患者群体中产生,因此研究人员有效地应用 2D、3D 和 BBB 模型来重现遗传上复杂的神经疾病,并揭示神经疾病的分子和遗传机制的新见解。在这篇综述中,我们描述了从 iPSC 生成 2D、3D 和 BBB 模型的最新进展,并进一步讨论了它们的局限性、优点和未来的发展方向。这篇综述还涵盖了 2D、3D 和 BBB 模型在药物筛选、精准医学和模拟广泛的神经疾病(例如神经退行性疾病、神经发育障碍、脑损伤和神经精神障碍)中的应用现状。