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Modulated polarization microscopy: a promising new approach to visualizing cytoskeletal dynamics in living cells.

机译:调制偏振显微镜:一种在活细胞中可视化细胞骨架动力学的有前途的新方法。

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摘要

In an effort to visualize cytoskeletal filaments in living cells, we have developed modulated polarization microscopy. Modulated polarization microscopy visualizes cytoskeletal filaments based on their birefringence but differs from the standard polarization microscopy by exploiting the angle dependence of birefringence. A prototype instrument has been developed using two Faraday rotators under computer control to change the angle of plane polarized light at a known rate. By placing one Faraday rotator before and one after the specimen, rotation produced by the first Faraday rotator is cancelled by the second. This allows the use of fixed polarizer and analyzer in a crossed configuration and continuous imaging of the specimen between crossed polarizers. The variation in polarization angle of light illuminating the specimen causes birefringent elements to oscillate in brightness. Images acquired as polarization angle is varied are then processed by a Fourier filter image-processing algorithm. The Fourier filtering algorithm isolates those signals that vary at the proper rate, whereas static or random signals are removed. Here we show that the modulated polarization microscope can reveal cytoskeletal elements including stress fibers and microtubules in living cells.
机译:为了可视化活细胞中的细胞骨架丝,我们开发了调制偏振显微镜。调制偏振显微镜基于双折射使细胞骨架细丝可视化,但与标准偏振显微镜不同,其利用了双折射的角度依赖性。在计算机控制下,使用两个法拉第旋转器开发了一种原型仪器,以已知的速率改变平面偏振光的角度。通过在样品之前和之后放置一个法拉第转子,第二个法拉第转子产生的旋转被抵消。这允许以交叉配置使用固定偏振器和检偏器,并在交叉偏振器之间对样本进行连续成像。照射样品的光的偏振角的变化导致双折射元件的亮度振荡。随偏振角变化而获取的图像然后通过傅立叶滤波器图像处理算法进行处理。傅立叶滤波算法将那些以适当速率变化的信号隔离开,而静态或随机信号则被去除。在这里,我们显示调制偏振显微镜可以揭示活细胞中的细胞骨架元素,包括应激纤维和微管。

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