Lippmann Ethan S, Al-Ahmad Abraham, Azarin Samira M, Palecek Sean P, Shusta Eric V
Department of Chemical and Biological Engineering, University of Wisconsin-Madison, Madison, WI, USA.
Sci Rep. 2014 Feb 24;4:4160. doi: 10.1038/srep04160.
Blood-brain barrier (BBB) models are often used to investigate BBB function and screen brain-penetrating therapeutics, but it has been difficult to construct a human model that possesses an optimal BBB phenotype and is readily scalable. To address this challenge, we developed a human in vitro BBB model comprising brain microvascular endothelial cells (BMECs), pericytes, astrocytes and neurons derived from renewable cell sources. First, retinoic acid (RA) was used to substantially enhance BBB phenotypes in human pluripotent stem cell (hPSC)-derived BMECs, particularly through adherens junction, tight junction, and multidrug resistance protein regulation. RA-treated hPSC-derived BMECs were subsequently co-cultured with primary human brain pericytes and human astrocytes and neurons derived from human neural progenitor cells (NPCs) to yield a fully human BBB model that possessed significant tightness as measured by transendothelial electrical resistance (~5,000 Ωxcm(2)). Overall, this scalable human BBB model may enable a wide range of neuroscience studies.
血脑屏障(BBB)模型常用于研究血脑屏障功能和筛选具有脑穿透性的治疗药物,但构建具有最佳血脑屏障表型且易于扩展的人类模型一直具有挑战性。为应对这一挑战,我们开发了一种人类体外血脑屏障模型,该模型由源自可再生细胞源的脑微血管内皮细胞(BMEC)、周细胞、星形胶质细胞和神经元组成。首先,视黄酸(RA)被用于显著增强人多能干细胞(hPSC)衍生的BMEC中的血脑屏障表型,特别是通过黏附连接、紧密连接和多药耐药蛋白调节。随后,将经RA处理的hPSC衍生的BMEC与原代人脑海周细胞以及源自人神经祖细胞(NPC)的人星形胶质细胞和神经元共培养,以产生一个完全人类的血脑屏障模型,该模型通过跨内皮电阻(约5000Ωxcm²)测量具有显著的紧密性。总体而言,这种可扩展的人类血脑屏障模型可能有助于开展广泛的神经科学研究。