Stem Cell-Based Human Blood-Brain Barrier Models for Drug Discovery and Delivery

被引:120
|
作者
Aday, S. [1 ,2 ,3 ]
Cecchelli, R. [4 ]
Hallier-Vanuxeem, D. [4 ]
Dehouck, M. P. [4 ]
Ferreira, L. [1 ,2 ,3 ]
机构
[1] Univ Coimbra, Ctr Neurosci & Cell Biol CNC, P-3004517 Coimbra, Portugal
[2] Ctr Innovat Biotechnol Biocant, P-3060197 Cantanhede, Portugal
[3] Univ Coimbra, Inst Interdisciplinary Res, IIIUC, P-3030789 Coimbra, Portugal
[4] Univ Artois, Blood Brain Barrier Lab, EA 2465, F-62307 Lens, France
关键词
ASTROCYTE-ENDOTHELIAL INTERACTIONS; TARGETED ABSOLUTE PROTEOMICS; P-GLYCOPROTEIN TRANSPORT; TIGHT JUNCTION STRANDS; PROTEIN EXPRESSION; QUANTITATIVE ATLAS; RECEPTORS; CLAUDIN-1; SYSTEMS; ADULT;
D O I
10.1016/j.tibtech.2016.01.001
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The development of novel neuropharmaceuticals requires the evaluation of blood-brain barrier (BBB) permeability and toxicity. Recent studies have highlighted differences in the BBB among different species, with the most important differences involving the expression of P-glycoprotein (P-gp), multi drug resistance-associated proteins, transporters, and claudins. In addition, functional studies have shown that brain pharmacokinetics of P-glycoprotein substrates are different in humans and rodents. Therefore, human BBB models may be an important platform for initial drug screening before in vivo studies. This strategy might help to reduce costs in drug development and failures in clinical studies. We review the differences in the BBB among species, recent advances in the generation of human BBB models, and their applications in drug discovery and delivery.
引用
收藏
页码:382 / 393
页数:12
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