诱导多能干细胞
血脑屏障
神经科学
药物发现
人脑
生物
细胞生物学
干细胞
中枢神经系统
内皮干细胞
体内
体外
胚胎干细胞
生物信息学
生物技术
生物化学
基因
作者
Matthew J. Stebbins,Hannah K. Wilson,Scott G. Canfield,Tongcheng Qian,Sean P. Palecek,Eric V. Shusta
出处
期刊:Methods
[Elsevier]
日期:2015-10-27
卷期号:101: 93-102
被引量:138
标识
DOI:10.1016/j.ymeth.2015.10.016
摘要
The blood-brain barrier (BBB) is a critical component of the central nervous system (CNS) that regulates the flux of material between the blood and the brain. Because of its barrier properties, the BBB creates a bottleneck to CNS drug delivery. Human in vitro BBB models offer a potential tool to screen pharmaceutical libraries for CNS penetration as well as for BBB modulators in development and disease, yet primary and immortalized models respectively lack scalability and robust phenotypes. Recently, in vitro BBB models derived from human pluripotent stem cells (hPSCs) have helped overcome these challenges by providing a scalable and renewable source of human brain microvascular endothelial cells (BMECs). We have demonstrated that hPSC-derived BMECs exhibit robust structural and functional characteristics reminiscent of the in vivo BBB. Here, we provide a detailed description of the methods required to differentiate and functionally characterize hPSC-derived BMECs to facilitate their widespread use in downstream applications.
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