MRC Laboratory for Molecular Cell Biology, University College London.
MRC Laboratory for Molecular Cell Biology, University College London; NIHR Great Ormond Street Hospital Biomedical Research Centre, University College London.
J Vis Exp. 2022 Jun 9(184). doi: 10.3791/63496.
Transmission electron microscopy has been long considered to be the gold standard for the visualization of cellular ultrastructure. However, analysis is often limited to two dimensions, hampering the ability to fully describe the three-dimensional (3D) ultrastructure and functional relationship between organelles. Volume electron microscopy (vEM) describes a collection of techniques that enable the interrogation of cellular ultrastructure in 3D at mesoscale, microscale, and nanoscale resolutions. This protocol provides an accessible and robust method to acquire vEM data using serial section transmission EM (TEM) and covers the technical aspects of sample processing through to digital 3D reconstruction in a single, straightforward workflow. To demonstrate the usefulness of this technique, the 3D ultrastructural relationship between the endoplasmic reticulum and mitochondria and their contact sites in liver hepatocytes is presented. Interorganelle contacts serve vital roles in the transfer of ions, lipids, nutrients, and other small molecules between organelles. However, despite their initial discovery in hepatocytes, there is still much to learn about their physical features, dynamics, and functions. Interorganelle contacts can display a range of morphologies, varying in the proximity of the two organelles to one another (typically ~10-30 nm) and the extent of the contact site (from punctate contacts to larger 3D cisternal-like contacts). The examination of close contacts requires high-resolution imaging, and serial section TEM is well suited to visualize the 3D ultrastructural of interorganelle contacts during hepatocyte differentiation, as well as alterations in hepatocyte architecture associated with metabolic diseases.
透射电子显微镜长期以来一直被认为是可视化细胞超微结构的金标准。然而,分析通常仅限于二维,这限制了全面描述细胞器的三维(3D)超微结构和功能关系的能力。体视学电子显微镜(vEM)描述了一系列技术,这些技术可以在中尺度、微尺度和纳米尺度分辨率下对细胞超微结构进行 3D 检测。本方案提供了一种使用连续切片透射电子显微镜(TEM)获取 vEM 数据的简单、强大的方法,并涵盖了从样品处理到数字 3D 重建的各个技术方面,在单个简单的工作流程中完成。为了证明该技术的有用性,展示了肝实质细胞中内质网和线粒体之间的 3D 超微结构关系及其接触部位。细胞器之间的接触在细胞器之间离子、脂质、营养物质和其他小分子的转移中起着至关重要的作用。然而,尽管它们最初在肝细胞中被发现,但关于它们的物理特征、动态和功能仍有许多需要了解。细胞器之间的接触可以呈现出多种形态,彼此之间的两个细胞器的接近程度(通常为~10-30nm)和接触部位的大小(从点状接触到更大的 3D 腔状接触)各不相同。近距离接触的检查需要高分辨率成像,而连续切片 TEM 非常适合在肝细胞分化过程中可视化细胞器之间的 3D 超微结构,以及与代谢疾病相关的肝细胞结构的改变。