BioEM Facility, Centre of Electron Microscopy, EPFL, Lausanne, Switzerland.
PLoS One. 2013;8(2):e57405. doi: 10.1371/journal.pone.0057405. Epub 2013 Feb 28.
Correlating in vivo imaging of neurons and their synaptic connections with electron microscopy combines dynamic and ultrastructural information. Here we describe a semi-automated technique whereby volumes of brain tissue containing axons and dendrites, previously studied in vivo, are subsequently imaged in three dimensions with focused ion beam scanning electron microcopy. These neurites are then identified and reconstructed automatically from the image series using the latest segmentation algorithms. The fast and reliable imaging and reconstruction technique avoids any specific labeling to identify the features of interest in the electron microscope, and optimises their preservation and staining for 3D analysis.
将神经元及其突触连接的体内成像与电子显微镜相结合可以获得动态和超微结构信息。本文描述了一种半自动技术,该技术可对之前在体内研究过的包含轴突和树突的脑组织体积进行三维聚焦离子束扫描电子显微镜成像。然后,使用最新的分割算法自动从图像序列中识别和重建这些神经突。这种快速可靠的成像和重建技术避免了任何特定的标记来识别电子显微镜中感兴趣的特征,并优化了它们的保存和染色,以进行 3D 分析。