Blood brain barrier: A tissue engineered microfluidic chip

被引:24
作者
Musafargani, Sikkandhar [1 ]
Mishra, Sachin [1 ]
Gulyas, Miklos [2 ]
Mahalakshmi, P. [3 ]
Archunan, Govindaraju [4 ]
Padmanabhan, Parasuraman [1 ]
Gulyas, Balks [1 ]
机构
[1] Nanyang Technol Univ, Lee Kong Chian Sch Med, 59 Nanyang Dr, Singapore 636921, Singapore
[2] Uppsala Univ, Rudbeck Lab, Dept Immunol Genet & Pathol, Dag Hammarskolds Vag 20, SE-75185 Uppsala, Sweden
[3] VIT Univ, Sch Elect Engn, Vellore 632014, Tamil Nadu, India
[4] Bharathidasan Univ, Ctr Pheromone Technol, Deportment Anim Sci, Tiruchirappalli 620024, Tamil Nadu, India
关键词
BBB-on-a-Chip; Blood-brain barrier; Microfluidics; Shear stress; Permeability; ENDOTHELIAL-CELLS; SHEAR-STRESS; DRUG PERMEABILITY; CEREBRAL-CORTEX; STEM-CELLS; MODEL; SYSTEMS; PLATFORM; MATRIX; MICROENVIRONMENT;
D O I
10.1016/j.jneumeth.2019.108525
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
With the increasing concern of neurological diseases, the improvised therapy for neurodegenerative disorders such as Alzheimer's disease is crucial. Yet, the efficacious delivery of drug across blood-brain barrier (BBB) remains a formidable challenge. BBB acts as a gate keeper to prevent the ingress of harmful foreign agents into the brain. It has built a great interest in designing BBB models to boost the field of neurotherapeutics. Recently, microfluidic systems are gaining ground in cell culture and bio-system analysis. It creates a new era of micro engineered laboratory onto a chip by combining the benefits of both in vitro and in vivo models. The high-fidelity microfluidic BBB-on-a-Chip possess the engineered physiological microenvironment for real time monitoring of barrier properties with human derived stem cells. These emerging models have intrinsic merits of regulating micro-scale fluid delivery and versatile fabrication. Moreover, the progress of 3D printing technology and versatility of stem cells assist in fabricating these robust and reproducible models. This review revolves around the various approaches of modelling microfluidic BBBs and emphasises on the limitations of existing models and technology. It contributes to the interdisciplinary engineering aspects of BBB research and its magnificent impact on drug development.
引用
收藏
页数:11
相关论文
共 93 条
[1]   Astrocyte-endothelial interactions at the blood-brain barrier [J].
Abbott, NJ ;
Rönnbäck, L ;
Hansson, E .
NATURE REVIEWS NEUROSCIENCE, 2006, 7 (01) :41-53
[2]   A modular approach to create a neurovascular unit-on-a-chip [J].
Achyuta, Anil Kumar H. ;
Conway, Amy J. ;
Crouse, Richard B. ;
Bannister, Emilee C. ;
Lee, Robin N. ;
Katnik, Christopher P. ;
Behensky, Adam A. ;
Cuevas, Javier ;
Sundaram, Shivshankar S. .
LAB ON A CHIP, 2013, 13 (04) :542-553
[3]   A 3D neurovascular microfluidic model consisting of neurons, astrocytes and cerebral endothelial cells as a blood-brain barrier [J].
Adriani, Giulia ;
Ma, Dongliang ;
Pavesi, Andrea ;
Kamm, Roger D. ;
Goh, Eyleen L. K. .
LAB ON A CHIP, 2017, 17 (03) :448-459
[4]   Characterization of human fetal brain endothelial cells reveals barrier properties suitable for in vitro modeling of the BBB with syngenic co-cultures [J].
Andrews, Allison M. ;
Lutton, Evan M. ;
Cannella, Lee A. ;
Reichenbach, Nancy ;
Razmpour, Roshanak ;
Seasock, Matthew J. ;
Kaspin, Steven J. ;
Merkel, Steven F. ;
Langford, Dianne ;
Persidsky, Yuri ;
Ramirez, Servio H. .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2018, 38 (05) :888-903
[5]  
[Anonymous], [No title captured]
[6]  
[Anonymous], [No title captured]
[7]   Contrary to adult, neonatal rats show pronounced brain uptake of corticosteroids [J].
Arya, Vikram ;
Demarco, Vincent G. ;
Issar, Manish ;
Hochhaus, Gunther .
DRUG METABOLISM AND DISPOSITION, 2006, 34 (06) :939-942
[8]   3D-Printed Microfluidics [J].
Au, Anthony K. ;
Huynh, Wilson ;
Horowitz, Lisa F. ;
Folch, Albert .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2016, 55 (12) :3862-3881
[9]   Shear stress-induced redistribution of the glycocalyx on endothelial cells in vitro [J].
Bai, Ke ;
Wang, Wen .
BIOMECHANICS AND MODELING IN MECHANOBIOLOGY, 2014, 13 (02) :303-311
[10]   Development of tight junction molecules in blood vessels of germinal matrix, cerebral cortex, and white matter [J].
Ballabh, P ;
Hu, FO ;
Kumarasiri, M ;
Braun, A ;
Nedergaard, M .
PEDIATRIC RESEARCH, 2005, 58 (04) :791-798