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In Situ Sensitive Fluorescence Imaging of Neurons Cultured on a Plasmonic Dish Using Fluorescence Microscopy

机译:使用荧光显微镜在等离子培养皿上培养的神经元的原位敏感荧光成像

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摘要

A plasmonic dish was fabricated as a novel cell-culture dish for in situ sensitive imaging applications, in which the cover glass of a glass-bottomed dish was replaced by a grating substrate coated with a film of silver. Neuronal cells were successfully cultured over a period of more than 2 weeks in the plasmonic dish. The fluorescence images of their cells including dendrites were simply observed in situ using a conventional fluorescence microscope. The fluorescence from neuronal cells growing along the dish surface was enhanced using the surface plasmon resonance field. Under an epi-fluorescence microscope and employing a donut-type pinhole, the fluorescence intensity of the neuron dendrites was found to be enhanced efficiently by an order of magnitude compared with that using a conventional glass-bottomed dish. In a transmitted-light fluorescence microscope, the surface-selective fluorescence image of a fine dendrite growing along the dish surface was observed; therefore, the spatial resolution was improved compared with the epi-fluorescence image of the identical dendrite.
机译:将等离子体激元皿制造为用于原位敏感成像应用的新型细胞培养皿,其中玻璃底皿的盖玻片被涂有银膜的光栅基板代替。将神经元细胞成功地在等离子培养皿中培养2周以上。使用常规荧光显微镜可以简单地在原位观察其细胞(包括树突)的荧光图像。利用表面等离振子共振场增强了沿培养皿表面生长的神经元细胞的荧光。在落射荧光显微镜下并且使用甜甜圈型针孔,发现神经元树突的荧光强度与使用常规玻璃底皿的荧光强度相比有效地提高了一个数量级。在透射荧光显微镜下,观察到沿着碟子表面生长的细枝晶的表面选择性荧光图像。因此,与相同枝晶的落射荧光图像相比,空间分辨率得到了改善。

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