Leibniz Institut für Analytische Wissenschaften-ISAS-e.V., Otto-Hahn-Str. 6b, 44227 Dortmund, Germany.
Lab Chip. 2011 Aug 21;11(16):2763-71. doi: 10.1039/c1lc20257j. Epub 2011 Jun 28.
Spatially defined neuronal networks have great potential to be used in a wide spectrum of neurobiology assays. We present an original technique for the precise and reproducible formation of neuronal networks. A PDMS membrane comprising through-holes aligned with interconnecting microchannels was used during oxygen plasma etching to dry mask a protein rejecting poly(ethylene glycol) (PEG) adlayer. Patterns were faithfully replicated to produce an oxidized interconnected array pattern which supported protein adsorption. Differentiated human SH-SY5Y neuron-like cells adhered to the array nodes with the micron-scale interconnecting tracks guiding neurite outgrowth to produce neuronal connections and establish a network. A 2.0 μm track width was optimal for high-level network formation and node compliance. These spatially standardized neuronal networks were used to analyse the dynamics of acrylamide-induced neurite degeneration and the protective effects of co-treatment with calpeptin or brain derived neurotrophic factor (BDNF).
具有特定空间分布的神经元网络在广泛的神经生物学检测中具有巨大的应用潜力。我们提出了一种精确且可重复形成神经元网络的新技术。在进行氧等离子体刻蚀时,使用包含与互连通孔对准的贯穿孔的 PDMS 膜,以对具有排斥蛋白质特性的聚乙二醇(PEG)的吸附层进行干掩模。通过等离子体刻蚀,图案被忠实地复制,从而产生了一个支持蛋白质吸附的氧化互联阵列图案。经过分化的人类 SH-SY5Y 神经元样细胞附着在阵列节点上,微米级的互连通路引导轴突生长,形成神经元连接并建立网络。2.0 μm 的轨道宽度对于高水平的网络形成和节点适应性最为理想。这些具有空间标准化的神经元网络可用于分析丙烯酰胺诱导的轴突退化的动态,以及用 calpeptin 或脑源性神经营养因子(BDNF)共同处理的保护作用。