Zander Nicole E, Beebe Thomas P
US Army Research Laboratory, Weapons and Materials Research Directorate, Aberdeen Proving Ground, Maryland 21005.
Department of Chemistry and Biochemistry, University of Delaware, Newark, Delaware 19716.
Biointerphases. 2014 Mar;9(1):011003. doi: 10.1116/1.4857295.
Neuronal process growth is guided by extrinsic environmental cues such as extracellular matrix (ECM) proteins. Recent reports have described that the growth cone extension is superior across gradients of the ECM protein laminin compared to growth across uniformly distributed laminin. In this work, the authors have prepared gradients of laminin on aligned electrospun nanofibers for use as substrates for neuronal growth. The substrates therefore presented both topographical and chemical guidance cues. Step gradients were prepared by the controlled robotic immersion of plasma-treated polycaprolactone fibers reacted with N-hydroxysuccinimide into the protein solution. The gradients were analyzed using x-ray photoelectron spectroscopy and confocal laser scanning microscopy. Gradients with a dynamic range of protein concentrations were successfully generated and neurite outgrowth was evaluated using neuronlike pheochromocytoma cell line 12 (PC12) cells. After 10 days of culture, PC12 neurite lengths varied from 32.7 ± 14.2 μm to 76.3 ± 9.1 μm across the protein concentration gradient. Neurite lengths at the highest concentration end of the gradient were significantly longer than neurite lengths observed for cells cultured on samples with uniform protein coverage. Gradients were prepared both in the fiber direction and transverse to the fiber direction. Neurites preferentially aligned with the fiber direction in both cases indicating that fiber alignment has a more dominant role in controlling neurite orientation, compared to the chemical gradient.
神经元突起的生长受细胞外基质(ECM)蛋白等外在环境线索的引导。最近的报告描述,与在均匀分布的层粘连蛋白上生长相比,生长锥在ECM蛋白层粘连蛋白的梯度上延伸得更优。在这项工作中,作者在排列好的电纺纳米纤维上制备了层粘连蛋白梯度,用作神经元生长的底物。因此,这些底物呈现了地形学和化学引导线索。通过将经等离子体处理且与N-羟基琥珀酰亚胺反应的聚己内酯纤维用机器人控制浸入蛋白质溶液中来制备阶梯梯度。使用X射线光电子能谱和共聚焦激光扫描显微镜对梯度进行分析。成功生成了蛋白质浓度动态范围的梯度,并使用神经母细胞瘤细胞系12(PC12)细胞评估神经突生长。培养10天后,PC12神经突长度在蛋白质浓度梯度上从32.7±14.2μm变化到76.3±9.1μm。梯度最高浓度端的神经突长度明显长于在蛋白质均匀覆盖的样品上培养的细胞所观察到的神经突长度。在纤维方向和与纤维方向垂直的方向上都制备了梯度。在这两种情况下,神经突都优先与纤维方向对齐,这表明与化学梯度相比,纤维排列在控制神经突方向方面具有更主导的作用。