Engineered 3D vascular and neuronal networks in a microfluidic platform

被引:128
作者
Osaki, Tatsuya [1 ]
Sivathanu, Vivek [1 ]
Kamm, Roger D. [1 ,2 ,3 ]
机构
[1] MIT, Dept Mech Engn, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[2] MIT, Dept Biol Engn, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[3] Singapore MIT Alliance Res & Technol, Singapore, Singapore
基金
美国国家科学基金会;
关键词
ENDOTHELIAL GROWTH-FACTOR; AMYOTROPHIC-LATERAL-SCLEROSIS; EMBRYONIC STEM-CELLS; NEUROTROPHIC FACTOR; MOTOR-NEURONS; NEURAL DIFFERENTIATION; NEUROVASCULAR UNIT; SHEAR-STRESS; ALS; EXPRESSION;
D O I
10.1038/s41598-018-23512-1
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Neurovascular coupling plays a key role in the pathogenesis of neurodegenerative disorders including motor neuron disease (MND). In vitro models provide an opportunity to understand the pathogenesis of MND, and offer the potential for drug screening. Here, we describe a new 3D microvascular and neuronal network model in a microfluidic platform to investigate interactions between these two systems. Both 3D networks were established by co-culturing human embryonic stem (ES)-derived MN spheroids and endothelial cells (ECs) in microfluidic devices. Co-culture with ECs improves neurite elongation and neuronal connectivity as measured by Ca2+ oscillation. This improvement was regulated not only by paracrine signals such as brain-derived neurotrophic factor secreted by ECs but also through direct cell-cell interactions via the delta-notch pathway, promoting neuron differentiation and neuroprotection. Bi-directional signaling was observed in that the neural networks also affected vascular network formation under perfusion culture. This in vitro model could enable investigations of neuro-vascular coupling, essential to understanding the pathogenesis of neurodegenerative diseases including MNDs such as amyotrophic lateral sclerosis.
引用
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页数:13
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