微泡
血脑屏障
内吞作用
外体
内体
细胞生物学
跨细胞
体外
体内
跨细胞
生物
神经科学
中枢神经系统
细胞
医学
细胞内
小RNA
生物技术
基因
生物化学
遗传学
作者
Claire C. Chen,Linan Liu,Fengxia Ma,Chi W. Wong,Xuning Emily Guo,Jenu V. Chacko,Henry P. Farhoodi,Shirley X. Zhang,Jan Zimak,Aude I. Ségaliny,Milad Riazifar,Victor Pham,Michelle A. Digman,Egest J. Pone,Weian Zhao
标识
DOI:10.1007/s12195-016-0458-3
摘要
The delivery of therapeutics to the central nervous system remains a major challenge in part due to the presence of the blood–brain barrier (BBB). Recently, cell-derived vesicles, particularly exosomes, have emerged as an attractive vehicle for targeting drugs to the brain, but whether or how they cross the BBB remains unclear. Here, we investigated the interactions between exosomes and brain microvascular endothelial cells (BMECs) in vitro under conditions that mimic the healthy and inflamed BBB in vivo. Transwell assays revealed that luciferase-carrying exosomes can cross a BMEC monolayer under stroke-like, inflamed conditions (TNF-α activated) but not under normal conditions. Confocal microscopy showed that exosomes are internalized by BMECs through endocytosis, co-localize with endosomes, in effect primarily utilizing the transcellular route of crossing. Together, these results indicate that cell-derived exosomes can cross the BBB model under stroke-like conditions in vitro. This study encourages further development of engineered exosomes as drug delivery vehicles or tracking tools for treating or monitoring neurological diseases.
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