血脑屏障
周细胞
微血管
星形胶质细胞
药物输送到大脑
细胞生物学
紧密连接
药物输送
细胞外基质
人脑
生物
神经科学
内皮干细胞
体外
材料科学
血管生成
中枢神经系统
纳米技术
癌症研究
生物化学
作者
Marco Campisi,Yoojin Shin,Tatsuya Osaki,Cynthia Hajal,Valeria Chiono,Roger D. Kamm
出处
期刊:Biomaterials
[Elsevier]
日期:2018-07-13
卷期号:180: 117-129
被引量:529
标识
DOI:10.1016/j.biomaterials.2018.07.014
摘要
The blood-brain barrier (BBB) regulates molecular trafficking, protects against pathogens, and prevents efficient drug delivery to the brain. Models to date failed to reproduce the human anatomical complexity of brain barriers, contributing to misleading results in clinical trials. To overcome these limitations, a novel 3-dimensional BBB microvascular network model was developed via vasculogenesis to accurately replicate the in vivo neurovascular organization. This microfluidic system includes human induced pluripotent stem cell-derived endothelial cells, brain pericytes, and astrocytes as self-assembled vascular networks in fibrin gel. Gene expression of membrane transporters, tight junction and extracellular matrix proteins, was consistent with computational analysis of geometrical structures and quantitative immunocytochemistry, indicating BBB maturation and microenvironment remodelling. Confocal microscopy validated microvessel-pericyte/astrocyte dynamic contact-interactions. The BBB model exhibited perfusable and selective microvasculature, with permeability lower than conventional in vitro models, and similar to in vivo measurements in rat brain. This robust and physiologically relevant BBB microvascular model offers an innovative and valuable platform for drug discovery to predict neuro-therapeutic transport efficacy in pre-clinical applications as well as recapitulate patient-specific and pathological neurovascular functions in neurodegenerative disease.
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