Co-culture Based Blood-brain Barrier In Vitro Model, a Tissue Engineering Approach using Immortalized Cell Lines for Drug Transport Study

被引:17
作者
Zhang, Zhiqi [1 ]
McGoron, Anthony J. [1 ]
Crumpler, Eric T. [1 ]
Li, Chen-Zhong [1 ]
机构
[1] Florida Int Univ, Dept Biomed Engn, Miami, FL 33174 USA
关键词
Blood-brain barrier; Co-culture; In vitro; Transport; Drug delivery; Membrane impedance; Western blot; Tight junction; Occludin; DOWN-REGULATION; OCCLUDIN; BIOLOGY; PERMEABILITY; CAFFEINE;
D O I
10.1007/s12010-010-9037-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This study evaluated the feasibility of using commercially available immortalized cell lines in building an in vitro blood-brain barrier (BBB) co-culture model for preliminary drug development studies. Astrocytes-derived acellular extracellular matrix (aECM) was introduced in the co-culture model to provide a novel biomimetic basement membrane for the endothelial cells to form tight junctions. Trans-Endothelial Electrical Resistance (TEER) and solute mass transport studies quantitatively evaluated the tight junction formation. Immuno-fluorescence microscopy and Western blot analysis qualitatively verified the expression of occludin, one of the tight junction proteins on the samples. Experimental data from a total of 13 experiments conclusively showed that the novel BBB in vitro co-culture model with aECM (CO + aECM) is promising in terms of establishing tight junction formation represented by TEER values, transport profiles, and tight junction protein expression when compared with traditional co-culture (CO) model setup or the endothelial cells cultured alone (EC). In vitro colorimetric sulforhodamine B (SRB) assay also revealed that the "CO + aECM" samples resulted in less cell loss on the basal sides of the insert membranes than traditional co-culture models. Our novel approach using immortalized cell lines with the addition of aECM was proven to be a feasible and repeatable alternative to the traditional BBB in vitro modeling.
引用
收藏
页码:278 / 295
页数:18
相关论文
共 38 条
[1]  
Abbott N Joan, 2004, Drug Discov Today Technol, V1, P407, DOI 10.1016/j.ddtec.2004.11.014
[2]   Astrocyte-endothelial interactions at the blood-brain barrier [J].
Abbott, NJ ;
Rönnbäck, L ;
Hansson, E .
NATURE REVIEWS NEUROSCIENCE, 2006, 7 (01) :41-53
[3]   High-throughput mapping of a dynamic signaling network in mammalian cells [J].
Barrios-Rodiles, M ;
Brown, KR ;
Ozdamar, B ;
Bose, R ;
Liu, Z ;
Donovan, RS ;
Shinjo, F ;
Liu, YM ;
Dembowy, J ;
Taylor, IW ;
Luga, V ;
Przulj, N ;
Robinson, M ;
Suzuki, H ;
Hayashizaki, Y ;
Jurisica, I ;
Wrana, JL .
SCIENCE, 2005, 307 (5715) :1621-1625
[4]  
DIGLIO CA, 1982, LAB INVEST, V46, P554
[5]   Development of the blood-brain barrier [J].
Engelhardt, B .
CELL AND TISSUE RESEARCH, 2003, 314 (01) :119-129
[6]   Drug permeability across a phospholipid vesicle based barrier: A novel approach for studying passive diffusion [J].
Flaten, GE ;
Dhanikula, AB ;
Luthman, K ;
Brandl, M .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2006, 27 (01) :80-90
[7]   In vitro models for the blood-brain barrier [J].
Garberg, P ;
Ball, M ;
Borg, N ;
Cecchelli, R ;
Fenart, L ;
Hurst, RD ;
Lindmark, T ;
Mabondzo, A ;
Nilsson, JE ;
Raub, TJ ;
Stanimirovic, D ;
Terasaki, T ;
Öberg, JO ;
Österberg, T .
TOXICOLOGY IN VITRO, 2005, 19 (03) :299-334
[8]   A relevant in vitro rat model for the evaluation of blood-brain barrier translocation of nanoparticles [J].
Garcia-Garcia, E ;
Gil, S ;
Andrieux, K ;
Desmaële, D ;
Nicolas, V ;
Taran, F ;
Georgin, D ;
Andreux, JP ;
Roux, F ;
Couvreur, P .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2005, 62 (12) :1400-1408
[9]   Mucociliary differentiation of serially passaged normal human tracheobronchial epithelial cells [J].
Gray, TE ;
Guzman, K ;
Davis, CW ;
Abdullah, LH ;
Nettesheim, P .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1996, 14 (01) :104-112
[10]   Distribution of integrin-like immunoreactivity on primate brain microvasculature [J].
Haring, HP ;
Akamine, P ;
Habermann, R ;
Koziol, JA ;
delZoppo, GJ .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1996, 55 (02) :236-245