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利用图案化基底控制神经突生长。

Controlling neurite outgrowth with patterned substrates.

机构信息

Department of Chemical and Materials Engineering University of Cincinnati Cincinnati, Ohio 45221, USA.

出版信息

J Biomed Mater Res A. 2011 Jun 15;97(4):451-6. doi: 10.1002/jbm.a.33082. Epub 2011 Apr 11.

Abstract

In vivo, neurons form neurites, one of which develops into the axon while others become dendrites. While this neuritogenesis process is well programmed in vivo, there are limited methods to control the number and location of neurite extension in vitro. Here we report a method to control neuritogenesis by confining neurons in specific regions using cell resistant poly(oligoethyleneglycol methacrylate-co-methacrylic acid (OEGMA-co-MA)) or poly(ethyleneglycol-block-lactic acid) PEG-PLA. Line patterned substrates reduce multiple extension of neurites and stimulate bi-directional neurite budding for PC12 and cortical neurons. PC12 cells on 20 and 30 μm line patterns extended one neurite in each direction along the line pattern while cortical neuron on 20 and 30 μm line patterns extended one or two neurites in each direction along the line pattern. Statistical analysis of neurite lengths revealed that PC12 cells and cortical neurons on line patterns extend longer neurites. The ability to guide formation of neurites on patterned substrates is useful for generating neural networks and promoting neurite elongation.

摘要

在体内,神经元形成突起,其中一个突起发育成轴突,而其他突起则成为树突。虽然这个突起生成过程在体内有很好的编程,但在体外控制突起延伸的数量和位置的方法有限。在这里,我们报告了一种通过使用细胞抗性聚(聚乙二醇甲基丙烯酸酯-co-甲基丙烯酸(OEGMA-co-MA))或聚(乙二醇-丙交酯)PEG-PLA 将神经元限制在特定区域来控制突起生成的方法。线图案化基底减少了突起的多次延伸,并刺激了 PC12 和皮质神经元的双向突起芽生。在 20 和 30 μm 线图案上的 PC12 细胞在沿着线图案的每个方向上延伸一个突起,而在 20 和 30 μm 线图案上的皮质神经元在沿着线图案的每个方向上延伸一个或两个突起。对突起长度的统计分析表明,在线图案上的 PC12 细胞和皮质神经元延伸出更长的突起。在线图案化基底上引导突起形成的能力对于生成神经网络和促进突起伸长很有用。

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Controlling neurite outgrowth with patterned substrates.利用图案化基底控制神经突生长。
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