College of Optometry, University of Houston;
College of Optometry, University of Houston.
J Vis Exp. 2021 Mar 26(169). doi: 10.3791/62045.
Serial block-face scanning electron microscopy (SBF-SEM) allows for the collection of hundreds to thousands of serially-registered ultrastructural images, offering an unprecedented three-dimensional view of tissue microanatomy. While SBF-SEM has seen an exponential increase in use in recent years, technical aspects such as proper tissue preparation and imaging parameters are paramount for the success of this imaging modality. This imaging system benefits from the automated nature of the device, allowing one to leave the microscope unattended during the imaging process, with the automated collection of hundreds of images possible in a single day. However, without appropriate tissue preparation cellular ultrastructure can be altered in such a way that incorrect or misleading conclusions might be drawn. Additionally, images are generated by scanning the block-face of a resin-embedded biological sample and this often presents challenges and considerations that must be addressed. The accumulation of electrons within the block during imaging, known as "tissue charging," can lead to a loss of contrast and an inability to appreciate cellular structure. Moreover, while increasing electron beam intensity/voltage or decreasing beam-scanning speed can increase image resolution, this can also have the unfortunate side effect of damaging the resin block and distorting subsequent images in the imaging series. Here we present a routine protocol for the preparation of biological tissue samples that preserves cellular ultrastructure and diminishes tissue charging. We also provide imaging considerations for the rapid acquisition of high-quality serial-images with minimal damage to the tissue block.
连续块面扫描电子显微镜 (SBF-SEM) 可以采集数百到数千张连续注册的超微结构图像,提供组织微观解剖结构的前所未有的三维视图。虽然 SBF-SEM 在近年来的使用呈指数级增长,但适当的组织准备和成像参数等技术方面对于这种成像方式的成功至关重要。这种成像系统受益于设备的自动化性质,允许在成像过程中无人值守,一天内可以自动采集数百张图像。然而,如果没有适当的组织准备,细胞超微结构可能会发生改变,从而得出不正确或误导性的结论。此外,图像是通过扫描树脂包埋生物样本的块面生成的,这经常带来必须解决的挑战和考虑因素。在成像过程中,电子在块内的积累被称为“组织充电”,会导致对比度降低和无法欣赏细胞结构。此外,虽然增加电子束强度/电压或降低电子束扫描速度可以提高图像分辨率,但这也会产生不幸的副作用,即损坏树脂块并扭曲成像系列中的后续图像。在这里,我们提出了一种常规的生物组织样本制备方案,该方案可以保留细胞超微结构并减少组织充电。我们还提供了用于快速获取高质量的连续图像的成像注意事项,同时最大限度地减少对组织块的损伤。