White J G, Squirrell J M, Eliceiri K W
LOCI, Laboratory of Molecular Biology, University of Wisconsin, Madison, WI 53706, USA.
Traffic. 2001 Nov;2(11):775-80. doi: 10.1034/j.1600-0854.2001.21105.x.
The endomembrane system of a cell is a highly dynamic, ephemeral structure that is difficult to visualize. Reconstructions from sections of fixed material can provide high-resolution information on intercellular membrane architecture, but such techniques are fraught with artifacts and are of little help in understanding the dynamics of intracellular membrane traffic. Recently, the availability of fluorescent membrane probes and the development of techniques for optically sectioning intact specimens have allowed glimpses of membrane dynamics to be visualized in living tissue. In this review we discuss the potential of a new optical sectioning technique, multiphoton imaging, for visualizing membrane dynamics in living cells. Multiphoton microscopy offers an unparalleled ability to obtain images from deep within specimens while minimizing the effects of phototoxicity.
细胞内膜系统是一种高度动态、短暂存在且难以可视化的结构。从固定材料切片进行的重建可以提供关于细胞内膜结构的高分辨率信息,但这些技术存在诸多人为因素,对于理解细胞内膜运输的动态过程帮助不大。最近,荧光膜探针的出现以及对完整标本进行光学切片技术的发展,使得在活组织中可视化膜动态成为可能。在本综述中,我们讨论了一种新的光学切片技术——多光子成像,用于在活细胞中可视化膜动态的潜力。多光子显微镜具有无与伦比的能力,能够从标本深处获取图像,同时将光毒性的影响降至最低。