Caged neuron MEA: A system for long-term investigation of cultured neural network connectivity

被引:84
作者
Erickson, Jonathan [1 ]
Tooker, Angela [2 ]
Tai, Y. -C. [2 ]
Pine, Jerome [3 ]
机构
[1] CALTECH, Dept Bioengn, Pasadena, CA 91125 USA
[2] CALTECH, Dept Elect Engn, Pasadena, CA 91125 USA
[3] CALTECH, Div Phys Math & Astron, Pasadena, CA 91125 USA
关键词
Neurochip; Multi-electrode array; Parylene; Connectivity;
D O I
10.1016/j.jneumeth.2008.07.023
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Traditional techniques for investigating cultured neural networks, such as the patch clamp and multi-electrode array, are limited by: (1) the number of identified cells which can be simultaneously electrically contacted, (2) the length of time for which cells can be studied, and (3) the lack of one-to-one neuron-to-electrocle specificity. Here, we present a new device - the caged neuron multi-electrode array which overcomes these limitations. This micro-machined device consists of an array of neurocages which mechanically trap a neuron near an extracellular electrode. While the cell body is trapped, the axon and dendrites can freely grow into the Surrounding area to form a network. The electrode is bi-directional, capable of both stimulating and recording action potentials. This system is non-invasive, so that all constituent neurons of a network can be studied over its lifetime with stable one-to-one neuron-to-electrode correspondence. Proof-of-concept experiments are described to illustrate that functional networks form in a neurochip system of 16 cages in a 4 x 4 array, and that suprathreshold connectivity can be fully mapped over several weeks. The neurochip opens a new domain in neurobiology for studying small cultured neural networks. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 16
页数:16
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