具有免疫能力的脑类器官-小胶质细胞进入发育阶段

IF 5 Q1 ENGINEERING, BIOMEDICAL
Sònia Sabaté-Soler, M. Bernini, J. Schwamborn
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引用次数: 1

摘要

小胶质细胞是大脑的免疫细胞,是神经退行性疾病研究的焦点。同样,关于诱导多能干细胞(iPSC)衍生的全脑和区域特异性类器官的研究也在增加。在类器官中,培养系统的复杂性增加,更好地模仿人类大脑中的实际情况。此外,动物模型并不总是概括人类神经变性,与类器官系统相比,它们意味着更多的伦理问题。近年来,ipsc衍生的小胶质细胞已被整合到脑类器官中,芯片技术已将重点放在小胶质细胞与神经细胞的相互作用上。本文就小胶质细胞融入脑类器官的研究进展作一综述。我们研究了小胶质细胞的细胞组织、超微结构和细胞信号传导,以及它们在类器官中其他细胞类型的功能。这里特别关注的是与中脑和多巴胺能系统的相互作用。最后,我们讨论了迄今为止关于神经炎症和疾病建模的成就,以及在3D系统中针对小胶质细胞和神经炎症的可能治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunocompetent brain organoids—microglia enter the stage
Microglia, the immune cells of the brain, are a focus of studies in neurodegenerative diseases. Similarly, research about induced pluripotent stem cell (iPSC)-derived whole brain and region-specific organoids is increasing. In organoids, the complexity of the culture systems increases, mimicking better the actual scenario in the human brain. Furthermore, animal models do not always recapitulate human neurodegeneration, and they imply more ethical concerns compared to organoid systems. Recently the integration of iPSC-derived microglia into brain organoids has been achieved, and on-chip technologies have been focusing on microglia interaction with neural cells. In this review, we discuss the achievements on integrating microglia into brain organoids. We study the cell organization, ultrastructure and cell signalling of microglia with respect to other cell types in organoids as well as their functionality in the system. A particular focus here is on the interaction with the midbrain and dopaminergic systems. Finally, we discuss the achievements until now concerning neuroinflammation and disease modelling, and the possible therapeutic approaches targeting microglia and neuroinflammation in 3D systems.
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CiteScore
9.40
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