真菌学研究中的共聚焦显微镜

Kirk J. Czymmek , Joanne H. Whallon , Karen L. Klomparens
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引用次数: 50

摘要

真菌学研究中的共聚焦显微镜。真菌学学报,18,275-293。共聚焦显微镜是光学显微镜的革命性进步。利用最新的激光、计算机和成像技术,该技术为生物学家提供了一种独特的细胞和/或亚细胞可视化形式。共聚焦显微镜的主要特点是,它允许“光学切片”,而不是机械切片薄和相对较厚的显微镜标本在荧光和反射成像模式;所得到的图像具有比传统光学显微镜更好的分辨率和对比度。这种能力是通过在扫描光栅中使用单色激光来实现的。当在样品和检测器之间的光路中放置一个共聚焦针孔时,大多数失焦光被去除。数字化共聚焦图像可以通过图像处理和三维重建进一步分析或改进。激光扫描共聚焦显微镜可以成功地应用于各种真菌问题,包括细胞动力学,真菌-宿主相互作用,细胞器结构和功能,或细胞骨架定位和细胞化学,使用各种报告器阵列,在几乎任何可以通过常规光学显微镜观察的样品中。这对于检查厚真菌样品或在真菌深埋在宿主组织中的宿主-病原体相互作用特别有利。与任何技术一样,一些人工制品和困难与激光扫描显微镜和计算机处理所产生的图像固有地相关。在确定其用于特定真菌学样品的潜在应用时,必须考虑共聚焦显微镜的优点和缺点
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Confocal microscopy in mycological research

Confocal microscopy in mycological research. Experimental Mycology 18, 275-293. Confocal microscopy is a revolutionary advance in light microscopy. Utilizing the latest laser, computer, and imaging technologies, the technique offers biologists a unique form of cell and/or subcellular visualization. The principal feature of confocal microscopy is that it permits “optical sectioning” rather than mechanical sectioning of both thin and relatively thick microscope specimens in fluorescence and reflection imaging modes; the resulting images have far better resolution and contrast than can be obtained with a conventional light microscope. This capability is achieved by using a monochromatic laser light in a scanning raster across a specimen. When a confocal pinhole is placed in the light path between the sample and the detector, most out-of-focus light is removed. Digitized confocal images may be further analyzed or improved by image processing and 3-D reconstruction. Laser scanning confocal microscopy can be successfully applied to a variety of fungal problems including cell dynamics, fungus-host interactions, organelle structure and function, or cytoskeletal localization and cytochemistry using an array of various reporters, in virtually any sample that can be viewed by conventional light microscopy. It is particularly advantageous for examining thick fungal samples or in host-pathogen interactions where the fungus is embedded deep within the host tissue. As with any technique, some artifacts and difficulties are inherently associated with laser scanning microscopy and computer processing of the resulting images. The advantages and disadvantages of confocal microscopy must be considered when determining its potential applications for specific mycological samples

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