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Biofunctionalized3D Nanopillar Arrays Fostering CellGuidance and Promoting Synapse Stability and Neuronal Activity inNetworks

机译:生物功能化3D Nanopillar阵列培育细胞指导并促进突触稳定性和神经元活动网路

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摘要

A controlled geometry of in vitro neuronal networks allows investigation of the cellular mechanisms that underlie neuron-to-neuron and neuron–extracellular matrix interactions, which are essential to biomedical research. Herein, we report a selective guidance of primary hippocampal neurons by using arrays of three-dimensional vertical nanopillars (NPs) functionalized with a specific adhesion-promoting molecule—poly-dl-ornithine (PDLO). We show that 90% of neuronal cells are guided exclusively on the combinatorial PDLO/NP substrate. Moreover, we demonstrate the influence of the interplay between nanostructures and neurons on synapse formation and maturation, resulting in increased expression of postsynaptic density-95 protein and enhanced network cellular activity conferred by the endogenous c-fos expression. Successful guidance to foster synapse stability and cellular activity on multilevel cues of surface topography and chemical functionalization suggests the potential to devise technologies to control neuronal growth on nanostructures for tissue engineering, neuroprostheses, and drug development.
机译:体外神经元网络的受控几何结构可以研究构成神经元与神经元以及神经元与细胞外基质相互作用基础的细胞机制,这对于生物医学研究至关重要。本文中,我们报告了通过使用三维阵列的三维垂直纳米柱(NPs)选择性引导原代海马神经元的功能,这些纳米柱具有特定的促黏附分子-聚-dl-鸟氨酸(PDLO)。我们显示90%的神经元细胞仅在组合PDLO / NP底物上被引导。此外,我们证明了纳米结构和神经元之间的相互作用对突触形成和成熟的影响,导致内源性c-fos表达赋予了突触后密度95蛋白增加的表达和增强的网络细胞活性。在表面形貌和化学功能化的多层次线索上促进突触稳定性和细胞活性的成功指南表明,有潜力开发出控制纳米结构上神经元生长的技术,以用于组织工程,神经假体和药物开发。

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