小胶质细胞
神经科学
人脑
神经炎症
诱导多能干细胞
生物
表型
疾病
电池类型
间隙
细胞
模式生物
转录组
神经退行性变
淀粉样蛋白(真菌学)
人类疾病
体内
中枢神经系统
神经胶质
细胞模型
神经干细胞
长时程增强
人诱导多能干细胞
阿尔茨海默病
细胞生物学
干细胞
β淀粉样蛋白
基因
神经免疫学
免疫疗法
脑病
星形胶质细胞
细胞分化
作者
Julien Klimmt,Carolina Cardoso Gonçalves,Jessica Valentina Montgomery,Stephan A. Müller,Merle Bublitz,Severin Filser,Lars Paeger,Brigitte Nuscher,Angelika Dannert,Sigrun Roeber,Veronica M. Pravatà,Martina Schifferer,Joshua Shrouder,Nathalie Schulz,Judit González-Gallego,Silvia Cappello,Thomas Misgeld,Nikolaus Plesnila,Eduardo Beltrán,Jochen Herms
标识
DOI:10.1038/s41593-026-02367-0
摘要
Stem-cell-based in vitro models offer promising potential to elucidate human brain cell functions and interactions, but limitations in reproducibility, maturation and cell-type diversity persist. Especially, prolonged incorporation of mature microglia and studies of neuroinflammation have proven challenging. Here, we developed a human induced pluripotent stem cell-based three-dimensional cortical brain tissue model (3BTM) containing neurons, astrocytes and microglia with high reproducibility, maturity and viability. 3BTMs show morphological, functional and proteomic maturation of all cell types, leading to high similarity to their in vivo counterparts. Incorporated microglia survive for over 6 months and display mature morphology, functions and gene expression. Importantly, when engineered to model Alzheimer's disease pathology, 3BTMs recapitulate key disease hallmarks, including amyloid deposition, increased phospho-tau levels and neuroinflammation, with microglia shifting their transcriptional landscape to disease-relevant signatures. Treatment of Alzheimer's disease 3BTMs with anti-Aβ immunotherapy cleared deposits and largely reversed disease signatures in glia. Together, our microglia-containing model provides a platform for studying physiological and pathological states of human brain tissue.
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