Jagadeesan Srikanth, Workman Michael J, Herland Anna, Svendsen Clive N, Vatine Gad D
The Department of Physiology and Cell Biology, Faculty of Health Sciences, Ben-Gurion University of the Negev; The Regenerative Medicine and Stem Cell (RMSC) Research Center, Ben-Gurion University of the Negev; The Zlotowski Center for Neuroscience, Ben-Gurion University of the Negev.
The Board of Governors Regenerative Medicine Institute, Cedars-Sinai Medical Center.
J Vis Exp. 2020 Mar 2(157). doi: 10.3791/60925.
The blood brain barrier (BBB) is formed by neurovascular units (NVUs) that shield the central nervous system (CNS) from a range of factors found in the blood that can disrupt delicate brain function. As such, the BBB is a major obstacle to the delivery of therapeutics to the CNS. Accumulating evidence suggests that the BBB plays a key role in the onset and progression of neurological diseases. Thus, there is a tremendous need for a BBB model that can predict penetration of CNS-targeted drugs as well as elucidate the BBB's role in health and disease. We have recently combined organ-on-chip and induced pluripotent stem cell (iPSC) technologies to generate a BBB chip fully personalized to humans. This novel platform displays cellular, molecular, and physiological properties that are suitable for the prediction of drug and molecule transport across the human BBB. Furthermore, using patient-specific BBB chips, we have generated models of neurological disease and demonstrated the potential for personalized predictive medicine applications. Provided here is a detailed protocol demonstrating how to generate iPSC-derived BBB chips, beginning with differentiation of iPSC-derived brain microvascular endothelial cells (iBMECs) and resulting in mixed neural cultures containing neural progenitors, differentiated neurons, and astrocytes. Also described is a procedure for seeding cells into the organ chip and culturing of the BBB chips under controlled laminar flow. Lastly, detailed descriptions of BBB chip analyses are provided, including paracellular permeability assays for assessing drug and molecule permeability as well as immunocytochemical methods for determining the composition of cell types within the chip.
血脑屏障(BBB)由神经血管单元(NVUs)构成,这些单元保护中枢神经系统(CNS)免受血液中一系列可能破坏脆弱脑功能的因素影响。因此,血脑屏障是治疗药物输送至中枢神经系统的主要障碍。越来越多的证据表明,血脑屏障在神经疾病的发生和发展中起关键作用。因此,迫切需要一种能够预测中枢神经系统靶向药物渗透情况并阐明血脑屏障在健康和疾病中作用的血脑屏障模型。我们最近将芯片器官技术和诱导多能干细胞(iPSC)技术相结合,生成了完全针对人类个性化定制的血脑屏障芯片。这个新型平台展现出适合预测药物和分子跨人类血脑屏障转运的细胞、分子和生理特性。此外,利用患者特异性血脑屏障芯片,我们构建了神经疾病模型,并展示了个性化预测医学应用的潜力。本文提供了一份详细方案,展示如何生成iPSC来源的血脑屏障芯片,从iPSC来源的脑微血管内皮细胞(iBMECs)的分化开始,最终得到包含神经祖细胞、分化神经元和星形胶质细胞的混合神经培养物。还描述了将细胞接种到器官芯片中并在可控层流条件下培养血脑屏障芯片的步骤。最后,提供了血脑屏障芯片分析的详细描述,包括用于评估药物和分子通透性的细胞旁通透性测定以及用于确定芯片内细胞类型组成的免疫细胞化学方法。