Kuhn J R, Wu Z, Poenie M
Division of Molecular Cell and Developmental Biology, University of Texas, Austin, Texas 78712, USA.
Biophys J. 2001 Feb;80(2):972-85. doi: 10.1016/S0006-3495(01)76076-6.
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.
为了观察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细胞骨架丝的双折射来观察它们,但与标准偏振显微镜不同的是,它利用了双折射的角度依赖性。我们开发了一种原型仪器,该仪器使用两个法拉第旋转器,并在计算机控制下以已知速率改变平面偏振光的角度。通过在样品之前和之后各放置一个法拉第旋转器,第一个法拉第旋转器产生的旋转被第二个法拉第旋转器抵消。这使得可以在正交配置中使用固定的起偏器和检偏器,并在正交偏振器之间对样品进行连续成像。照射样品的光的偏振角变化会导致双折射元件的亮度发生振荡。然后,通过傅里叶滤波器图像处理算法对随着偏振角变化而采集的图像进行处理。傅里叶滤波算法分离出以适当速率变化的那些信号,而去除静态或随机信号。在这里,我们表明调制偏振显微镜可以揭示活细胞中的细胞骨架成分,包括应力纤维和微管。