Chen Claire C, Liu Linan, Ma Fengxia, Wong Chi W, Guo Xuning E, Chacko Jenu V, Farhoodi Henry P, Zhang Shirley X, Zimak Jan, Ségaliny Aude, Riazifar Milad, Pham Victor, Digman Michelle A, Pone Egest J, Zhao Weian
Department of Pharmaceutical Sciences, Sue and Bill Gross Stem Cell Research Center, Chao Family Comprehensive Cancer Center and Edwards Life sciences Center for Advanced Cardiovascular Technology, 845 Health Sciences Road, University of California-Irvine, Irvine, California, 92697, USA; Department of Biomedical Engineering, University of California-Irvine, Irvine, California, 92697, USA.
Department of Pharmaceutical Sciences, Sue and Bill Gross Stem Cell Research Center, Chao Family Comprehensive Cancer Center and Edwards Life sciences Center for Advanced Cardiovascular Technology, 845 Health Sciences Road, University of California-Irvine, Irvine, California, 92697, USA; Department of Biomedical Engineering, University of California-Irvine, Irvine, California, 92697, USA; State Key Laboratory of Experimental Hematology, Institute of Hematology and Blood Disease Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin 300020, China.
Cell Mol Bioeng. 2016 Dec;9(4):509-529. doi: 10.1007/s12195-016-0458-3. Epub 2016 Jul 7.
The delivery of therapeutics to the central nervous system (CNS) 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) under conditions that mimic the healthy and inflamed BBB . 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 . This study encourages further development of engineered exosomes as drug delivery vehicles or tracking tools for treating or monitoring neurological diseases.
由于血脑屏障(BBB)的存在,向中枢神经系统(CNS)递送治疗药物仍然是一项重大挑战。最近,细胞衍生的囊泡,特别是外泌体,已成为将药物靶向大脑的一种有吸引力的载体,但它们是否以及如何穿过血脑屏障仍不清楚。在这里,我们研究了在模拟健康和炎症性血脑屏障的条件下外泌体与脑微血管内皮细胞(BMECs)之间的相互作用。Transwell分析显示,携带荧光素酶的外泌体可以在类似中风的炎症条件下(TNF-α激活)穿过BMEC单层,但在正常条件下则不能。共聚焦显微镜显示,外泌体通过内吞作用被BMECs内化,与内体共定位,实际上主要利用跨细胞途径穿过。这些结果共同表明,细胞衍生的外泌体可以在类似中风的条件下穿过血脑屏障模型。这项研究鼓励进一步开发工程化外泌体作为治疗或监测神经疾病的药物递送载体或追踪工具。