Construction and Functional Evaluation of a Three-Dimensional Blood-Brain Barrier Model Equipped With Human Induced Pluripotent Stem Cell-Derived Brain Microvascular Endothelial Cells (Apr, 10.1007/s11095-022-03249-3, 2022)

被引:0
|
作者
Kurosawa, Toshiki [1 ]
Sako, Daiki [1 ]
Tega, Yuma [1 ]
Debori, Yasuyuki [1 ,2 ]
Tomihara, Yumi [2 ]
Aoyama, Kazunobu [2 ]
Kubo, Yoshiyuki [1 ]
Amano, Nobuyuki [2 ]
Deguchi, Yoshiharu [1 ]
机构
[1] Teikyo Univ, Fac Pharma Sci, Lab Drug Disposit & Pharmacokinet, Itabashi Ku, 2-11-1 Kaga, Tokyo 1738605, Japan
[2] Axcelead Drug Discovery Partners Inc, 26-1 Muraoka Higashi 2 Chome Fujisawa, Fujisawa, Kanagawa 2510012, Japan
基金
日本学术振兴会;
关键词
3D culture; blood–brain barrier; human iPS cells; organ-on-a-chip; transporter;
D O I
10.1007/s11095-022-03264-4
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Purpose: The purpose of this study was to construct and validate an in vitro three-dimensional blood–brain barrier (3DBBB) model system equipped with brain microvascular endothelial cells derived from human induced pluripotent stem cells (hiPS-BMECs). Methods: The 3D-BBB system was constructed by seeding hiPS-BMECs onto the capillary lane of a MIMETAS OrganoPlate® 3-lane coated with fibronectin/collagen IV. hiPS-BMECs were incubated under continuous switchback flow with an OrganoFlow® for 2 days. The 3D capillary structure and expression of tight-junction proteins and transporters were confirmed by immunocytochemistry. The mRNA expression of transporters in the 3D environment was determined using qRT-PCR, and the permeability of endogenous substances and drugs was evaluated under various conditions. Results and Discussion: The expression of tight-junction proteins, including claudin-5 and ZO-1, was confirmed by immunohistochemistry. The permeability rate constant of lucifer yellow through hiPS-BMECs was undetectably low, indicating that paracellular transport is highly restricted by tight junctions in the 3D-BBB system. The mRNA expression levels of transporters and receptors in the 3D-BBB system differed from those in the 2D-culture system by 0.2- to 5.8-fold. The 3D-cultured hiPS-BMECs showed asymmetric transport of substrates of BCRP, CAT1 and LAT1 between the luminal (blood) and abluminal (brain) sides. Proton-coupled symport function of MCT1 was also confirmed. Conclusion: The 3D-BBB system constructed in this study mimics several important characteristics of the human BBB, and is expected to be a useful high-throughput evaluation tool in the development of CNS drugs. © 2022, The Author(s).
引用
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页码:1661 / 1661
页数:1
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