研究人类ipsc -小胶质细胞的3D模型的进展:对神经发育和神经系统疾病的见解

hLife Pub Date : 2025-05-01 DOI:10.1016/j.hlife.2025.02.002
Satish Kumar Tiwari , Florent Ginhoux
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引用次数: 0

摘要

小胶质细胞是中枢神经系统的免疫细胞,在大脑发育、体内平衡和疾病中起着至关重要的作用。当这些细胞功能失调时,它们会导致各种精神疾病和神经退行性疾病。为了增强我们对小胶质细胞功能的理解,研究人员越来越多地采用基于人类细胞的模型。这种方法显著改善了我们对这些复杂情况的调查,并有助于正在进行的药物开发工作。来源于疾病特异性诱导多能干细胞(iPSCs)的人小胶质细胞体外模型对于研究其在神经系统疾病中的作用至关重要。这些模型为研究小胶质细胞驱动的神经炎症和神经变性所涉及的细胞和分子过程提供了一个可控的环境。将小胶质细胞整合到三维(3D)类器官培养物中,产生了一个与人类大脑生理更相关的模型,从而推进了大脑发育和神经疾病病理学的研究。目前,脑类器官模型由于缺乏关键成分(如脉管系统)而受到限制,这限制了它们的生长,阻碍了神经发育的最佳建模,以及对小胶质细胞形式和功能的检查。这篇综述探讨了新开发的用于产生人类诱导的小胶质细胞的3D模型,并研究了这些体外系统的潜力,以提高我们对大脑发育及其中断所产生的疾病的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Advancements in 3D models for studying human iPSC-microglia: Insights into neurodevelopment and neurological disorders
Microglia are immune cells of the central nervous system, playing a vital role in brain development, homeostasis, and disease. When these cells become dysfunctional, they can contribute to various psychiatric disorders and neurodegenerative diseases. To enhance our understanding of microglial function, researchers are increasingly employing human cell-based models. This approach significantly improves our investigations into these complex conditions and aids in ongoing drug development efforts. In vitro models of human microglia, derived from disease-specific induced pluripotent stem cells (iPSCs), are essential for examining their roles in neurological disorders. These models provide a controlled environment for studying the cellular and molecular processes involved in microglia-driven neuroinflammation and neurodegeneration. Integrating microglia into three-dimensional (3D) organoid cultures yields a more physiologically relevant model of the human brain, thereby advancing the study of brain development and the pathology of neurological disorders. Currently, brain organoid models are limited by the absence of key components, such as vasculature, which restricts their growth and hinders the optimal modeling of neurodevelopment, as well as the examination of microglial forms and functions. This review explores newly developed 3D models for generating human-induced microglia and investigates the potential of these in vitro systems to improve our understanding of brain development and the disorders that emerge from its disruption.
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