Minimum Transendothelial Electrical Resistance Thresholds for the Study of Small and Large Molecule Drug Transport in a Human in Vitro Blood-Brain Barrier Model

被引:62
|
作者
Mantle, Jennifer L.
Min, Lie
Lee, Kelvin H. [1 ]
机构
[1] Univ Delaware, Dept Chem & Biomol Engn, 15 Innovat Way, Newark, DE 19711 USA
基金
美国国家科学基金会;
关键词
blood-brain barrier; drug transport; human induced pluripotent stem cells; IgG transport; human brain microvascular endothelial cells; Alzheimer's disease; CELLS; PERMEABILITY; OPTIMIZATION; DERIVATION; CULTURE;
D O I
10.1021/acs.molpharmaceut.6b00818
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
A human cell-based in vitro model that can accurately predict drug penetration into the brain as well as metrics to assess these in vitro models are valuable for the development of new therapeutics. Here, human induced pluripotent stem cells (hPSCs) are differentiated into a polarized monolayer that express blood brain barrier (BBB)-specific proteins and have transendothelial electrical resistance (TEER) values greater than 2500 Omega.cm(2). By assessing the permeabilities of several known drugs, a benchmarking system to evaluate brain permeability of drugs was established. Furthermore, relationships between TEER and permeability to both small and large molecules were established, demonstrating that different minimum TEER thresholds must be achieved to study the brain transport of these two classes of drugs. This work demonstrates that this hPSC-derived BBB model exhibits an in vivo-like phenotype, and the benchmarks established here are useful for assessing functionality of other in vitro BBB models.
引用
收藏
页码:4191 / 4198
页数:8
相关论文
共 50 条
  • [1] Glycerophosphoinositol and dexamethasone improve transendothelial electrical resistance in an in vitro study of the blood-brain barrier
    Cucullo, L
    Hallene, K
    Dini, G
    Dal Toso, R
    Janigro, D
    BRAIN RESEARCH, 2004, 997 (02) : 147 - 151
  • [2] Establishment of a simplified in vitro porcine blood-brain barrier model with high transendothelial electrical resistance
    Patabendige, Adjanie
    Skinner, Robert A.
    Abbott, N. Joan
    BRAIN RESEARCH, 2013, 1521 : 1 - 15
  • [3] Development of a humanized in vitro blood-brain barrier model to study drug resistance
    Janigro, Damir
    Rapp, Ed
    Hossein, Mohammed
    Batra, Ayush
    Mayberg, Marc
    Marchi, Nicola
    Manders, Toby
    Cucullo, Luca
    STROKE, 2007, 38 (02) : 585 - 585
  • [4] In vitro model for evaluating drug transport across the blood-brain barrier
    Cecchelli, R
    Dehouck, B
    Descamps, L
    Fenart, L
    Buée-Scherrer, V
    Duhem, C
    Lundquist, S
    Rentfel, M
    Torpier, G
    Dehouck, MP
    ADVANCED DRUG DELIVERY REVIEWS, 1999, 36 (2-3) : 165 - 178
  • [5] Murine in vitro model of the blood-brain barrier for evaluating drug transport
    Shayan, Gilda
    Choi, Yong Seok
    Shusta, Eric V.
    Shuler, Michael L.
    Lee, Kelvin H.
    EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2011, 42 (1-2) : 148 - 155
  • [6] Development of Real-Time Transendothelial Electrical Resistance Monitoring for an In Vitro Blood-Brain Barrier System
    Tu, Kai-Hong
    Yu, Ling-Shan
    Sie, Zong-Han
    Hsu, Han-Yi
    Al-Jamal, Khuloud T.
    Wang, Julie Tzu-Wen
    Chiang, Ya-Yu
    MICROMACHINES, 2021, 12 (01) : 1 - 11
  • [7] The in vitro blood-brain barrier: the assessment of drug transport to the brain
    Dehouck, MP
    Fenart, L
    Dehouck, B
    Cecchelli, R
    ANIMAL ALTERNATIVES, WELFARE, AND ETHICS, 1997, 27 : 869 - 872
  • [8] An in vitro model for vitamin A transport across the human blood-brain barrier
    Est, Chandler B.
    Murphy, Regina M.
    ELIFE, 2023, 12
  • [9] Alterations in Transendothelial Electrical Resistance by Vasoactive Agonists and Cyclic AMP in a Blood-Brain Barrier Model System
    Roger D. Hurst
    John B. Clark
    Neurochemical Research, 1998, 23 : 149 - 154
  • [10] Alterations in transendothelial electrical resistance by vasoactive agonists and cyclic AMP in a blood-brain barrier model system
    Hurst, RD
    Clark, JB
    NEUROCHEMICAL RESEARCH, 1998, 23 (02) : 149 - 154