Kolotuev Irina, Bumbarger Daniel J, Labouesse Michel, Schwab Yannick
Institut de Génétique et Développement de Rennes, UMR 6290 CNRS, Université Rennes 1, Faculté de Medecine/1, 35043 Rennes Cedex, France.
Methods Cell Biol. 2012;111:203-22. doi: 10.1016/B978-0-12-416026-2.00011-X.
Correlative light and electron microscopy (CLEM) is used when one needs to combine both imaging modalities on the same sample. When working on living small model organisms, such as Caenorhabditis elegans, specific CLEM protocols are required to acquire high-resolution light microscopic images of a region of interest and thereafter to relocate and study the same object at the ultrastructural level using a transmission electron microscope. In this chapter, we describe how to process living specimens from the confocal microscope to the transmission electron microscopy (TEM), focusing on an improved ultramicrotomy technique that allows a precise and reliable targeting of the object of interest. This improvement significantly reduces the time consuming and frequently frustrating search for the region of interest. Our targeted ultramicrotomy protocol is versatile enough to be applied on a variety of bulk specimens, such as fly and fish embryos, or mouse tissues.
当需要在同一样本上结合两种成像方式时,会使用 correlative light and electron microscopy (CLEM,相关光电子显微镜)。在处理活的小型模式生物(如秀丽隐杆线虫)时,需要特定的 CLEM 方案来获取感兴趣区域的高分辨率光学显微镜图像,然后使用透射电子显微镜在超微结构水平上重新定位并研究同一物体。在本章中,我们将描述如何将活标本从共聚焦显微镜处理到透射电子显微镜 (TEM),重点介绍一种改进的超薄切片技术,该技术可以精确、可靠地定位感兴趣的物体。这一改进显著减少了寻找感兴趣区域的耗时且常常令人沮丧的过程。我们的靶向超薄切片方案通用性很强,可应用于各种大块标本,如苍蝇和鱼类胚胎或小鼠组织。