Active 3-D microscaffold system with fluid perfusion for culturing in vitro neuronal networks

被引:45
作者
Rowe, Laura
Almasri, Mahmoud
Lee, Kil
Fogleman, Nick
Brewer, Gregory J.
Nam, Yoonkey
Wheeler, Bruce C.
Vukasinovic, Jelena
Glezer, Ari
Frazier, A. Bruno
机构
[1] Georgia Inst Technol, Sch Elect & Comp Engn, Atlanta, GA 30332 USA
[2] So Illinois Univ, Sch Med, Dept Neurol & Med Microbiol, Carbondale, IL 62702 USA
[3] So Illinois Univ, Sch Med, Dept Immunol & Cell Biol, Carbondale, IL 62702 USA
[4] Univ Illinois, Dept Elect & Comp Engn, Urbana, IL 61801 USA
[5] Georgia Inst Technol, Sch Mech Engn, Atlanta, GA 30332 USA
关键词
D O I
10.1039/b700795g
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This work demonstrated the design, fabrication, packaging, and characterization of an active microscaffold system with fluid perfusion/nutrient delivery functionalities for culturing in vitro neuronal networks from dissociated hippocampal rat pup neurons. The active microscaffold consisted of an 8 6 8 array of hollow, microfabricated, SU-8 towers (1.0 mm or 1.5 mm in height), with integrated, horizontal, SU-8 cross-members that connect adjacent towers, thus forming a 3-D grid that is conducive to branching, growth, and increased network formation of dissociated hippocampal neurons. Each microtower in the microscaffold system contained a hollow channel and multiple fluid ports for media delivery and perfusion of nutrients to the in vitro neuronal network growing within the microscaffold system. Additionally, there were two exposed Au electrodes on the outer wall of each microtower at varying heights ( with insulated leads running within the microtower walls), which will later allow for integration of electrical stimulation/recording functionalities into the active microscaffold system. However, characterization of the stimulation/recording electrodes was not included in the scope of this paper. Design, fabrication, fluid packaging, and characterization of the active microscaffold system were performed. Furthermore, use of the active microscaffold system was demonstrated by culturing primary hippocampal embryonic rat pup neurons, and characterizing cell viability within the microscaffold system.
引用
收藏
页码:475 / 482
页数:8
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