A modular approach to create a neurovascular unit-on-a-chip

被引:154
作者
Achyuta, Anil Kumar H. [1 ]
Conway, Amy J. [1 ]
Crouse, Richard B. [1 ,2 ]
Bannister, Emilee C. [1 ,2 ]
Lee, Robin N. [1 ]
Katnik, Christopher P. [2 ]
Behensky, Adam A. [2 ]
Cuevas, Javier [2 ]
Sundaram, Shivshankar S. [1 ]
机构
[1] Charles Stark Draper Lab, Ctr Bioengn, Tampa, FL USA
[2] Univ S Florida, Tampa, FL USA
关键词
BLOOD-BRAIN-BARRIER; IN-VITRO MODEL; ASTROCYTE-ENDOTHELIAL INTERACTIONS; IMMORTALIZED CELL-LINE; NEURAL STEM-CELLS; ALZHEIMERS-DISEASE; HIPPOCAMPAL-NEURONS; NEURODEGENERATION; TISSUE; MECHANISMS;
D O I
10.1039/c2lc41033h
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In this work, we describe the fabrication and working of a modular microsystem that recapitulates the functions of the "Neurovascular Unit". The microdevice comprised a vertical stack of a poly(dimethylsiloxane) (PDMS) neural parenchymal chamber separated by a vascular channel via a microporous polycarbonate (PC) membrane. The neural chamber housed a mixture of neurons (similar to 4%), astrocytes (similar to 95%), and microglia (similar to 1%). The vascular channel was lined with a layer of rat brain microvascular endothelial cell line (RBE4). Cellular components in the neural chamber and vascular channel showed viability (>90%). The neural cells fired inhibitory as well as excitatory potentials following 10 days of culture. The endothelial cells showed diluted-acetylated low density lipoprotein (dil-a-LDL) uptake, expressed von Willebrand factor (vWF) and zonula occludens (ZO-1) tight junctions, and showed decreased Alexafluor (TM)-conjugated dextran leakage across their barriers significantly compared with controls (p < 0.05). When the vascular layer was stimulated with TNF-alpha for 6 h, about 75% of resident microglia and astrocytes on the neural side were activated significantly (p < 0.05 compared to controls) recapitulating tissue-mimetic responses resembling neuroinflammation. The impact of this microsystem lies in the fact that this biomimetic neurovascular platform might not only be harnessed for obtaining mechanistic insights for neurodegenerative disorders, but could also serve as a potential screening tool for central nervous system (CNS) therapeutics in toxicology and neuroinfectious diseases.
引用
收藏
页码:542 / 553
页数:12
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