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Investigation of neuronal pathfinding and construction of artificial neuronal networks on 3D-arranged porous fibrillar scaffolds with controlled geometry

机译:3D排列可控几何结构的多孔原纤维支架上神经元寻路的研究和人工神经元网络的构建

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摘要

Herein, we investigated the neurite pathfinding on electrospun microfibers with various fiber densities, diameters, and microbead islands, and demonstrated the development of 3D connected artificial neuronal network within a nanofiber-microbead-based porous scaffold. The primary culture of rat hippocampal embryonic neurons was deposited on geometry-controlled polystyrene (PS) fiber scaffolds while growth cone morphology, neurite outgrowth patterns, and focal adhesion protein expression were cautiously examined by microscopic imaging of immunostained and live neuronal cells derived from actin-GFP transgenic mice. It was demonstrated that the neurite outgrowth was guided by the overall microfiber orientation, but the increase in fiber density induced the neurite path alteration, thus, the reduction in neurite linearity. Indeed, we experimentally confirmed that growth cone could migrate to a neighboring, but, spatially disconnected microfiber by spontaneous filopodium extrusion, which is possibly responsible for the observed neurite steering. Furthermore, thinner microfiber scaffolds showed more pronounced expression of focal adhesion proteins than thicker ones, suggesting that the neuron-microfiber interaction can be delicately modulated by the underlying microfiber geometry. Finally, 3D connected functional neuronal networks were successfully constructed using PS nanofiber-microbead scaffolds where enhanced porosity and vertical fiber orientation permitted cell body inclusion within the scaffold and substantial neurite outgrowth in a vertical direction, respectively.
机译:在这里,我们调查了具有各种纤维密度,直径和微珠岛的静电纺微纤维上的神经突寻路,并证明了基于纳米纤维-微珠的多孔支架内3D连接的人工神经元网络的发展。大鼠海马胚胎神经元的原代培养物沉积在几何控制的聚苯乙烯(PS)纤维支架上,同时通过显微镜观察来自肌动蛋白的免疫染色和活神经元细胞的显微成像,仔细检查了生长锥的形态,神经突的生长方式和粘着斑蛋白的表达。 GFP转基因小鼠。结果表明,神经突的生长受整个微纤维取向的影响,但是纤维密度的增加引起了神经突路径的改变,从而降低了神经突的线性。实际上,我们通过实验证实,生长锥可以通过自发fi的挤压而迁移到相邻但空间上断开的微纤维,这可能是观察到的神经突转向的原因。此外,较薄的超细纤维支架比较厚的微纤维支架表现出更显着的粘着斑蛋白表达,表明神经元-超细纤维的相互作用可以被潜在的超细纤维几何形状精细地调节。最后,使用PS纳米纤维-微珠支架成功构建了3D连接的功能神经元网络,其中多孔性和垂直纤维取向增强,使得细胞体分别包含在支架中,并且在垂直方向上有大量的神经突向外生长。

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