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Imaging of cell/substrate contacts of living cells with surface plasmon resonance microscopy.

机译:用表面等离子体共振显微镜对活细胞的细胞/底物接触进行成像。

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摘要

We have developed a new method for observing cell/substrate contacts of living cells in culture based on the optical excitation of surface plasmons. Surface plasmons are quanta of an electromagnetic wave that travel along the interface between a metal and a dielectric layer. The evanescent field associated with this excitation decays exponentially perpendicular to the interface, on the order of some hundreds of nanometers. Cells were cultured on an aluminum-coated glass prism and illuminated from below with a laser beam. Because the cells interfere with the evanescent field, the intensity of the reflected light, which is projected onto a camera chip, correlates with the cell/substrate distance. Contacts between the cell membrane and the substrate can thus be visualized at high contrast with a vertical resolution in the nanometer range. The lateral resolution along the propagation direction of surface plasmons is given by their lateral momentum, whereas perpendicular to it, the resolution is determined by the optical diffraction limit. For quantitative analysis of cell/substrate distances, cells were imaged at various angles of incidence to obtain locally resolved resonance curves. By comparing our experimental data with theoretical surface plasmon curves we obtained a cell/substrate distance of 160 +/- 10 nm for most parts of the cells. Peripheral lamellipodia, in contrast, formed contacts with a cell substrate/distance of 25 +/- 10 nm.
机译:我们已经开发了一种基于表面等离激元的光激发观察培养中活细胞的细胞/基质接触的新方法。表面等离子体激元是沿着金属和介电层之间的界面传播的电磁波的量子。与该激发相关的逝场垂直于界面呈指数衰减,约为数百纳米。将细胞在涂有铝的玻璃棱镜上培养,并从下方用激光束照射。因为单元会干扰渐逝场,所以投射到相机芯片上的反射光的强度与单元/基板的距离相关。因此,可以以高对比度以纳米范围内的垂直分辨率可视化细胞膜与基底之间的接触。沿表面等离子体激元的传播方向的横向分辨率由其横向动量给出,而垂直于该方向的分辨率由光学衍射极限确定。为了定量分析细胞/底物的距离,对细胞以各种入射角成像以获得局部分辨的共振曲线。通过将我们的实验数据与理论表面等离激元曲线进行比较,我们得到了大部分细胞的细胞/基质距离为160 +/- 10 nm。相反,周围的层状脂膜病形成与细胞底物/距离为25 +/- 10nm的接触。

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