Center for Biological Imaging, Institute of Biophysics, Chinese Academy of Sciences, 15 Datun Road, Beijing 100101, China; National Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, 15 Datun Road, Beijing 100101, China.
Center for Biological Imaging, Institute of Biophysics, Chinese Academy of Sciences, 15 Datun Road, Beijing 100101, China; National Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, 15 Datun Road, Beijing 100101, China; University of Chinese Academy of Sciences, 19 Yuquan Road, Beijing 100049, China.
J Struct Biol. 2017 Nov;200(2):87-96. doi: 10.1016/j.jsb.2017.09.010. Epub 2017 Oct 1.
Large scale, high resolution three dimensional (3D) ultrastructural reconstruction of cells and tissues has become increasingly important to our understanding of complex biological systems. There have been a few partial 3D ultra-structures of Caenorhabditis elegans (C. elegans) reported, however 3D reconstruction of a whole nematode has never been achieved. Here, we independently developed a technique called automatic collector of ultrathin sections scanning electron microscopy and using this methodology, generated a 3D reconstruction of an entire C. elegans larva with 100 nm axial and 15 nm lateral resolution. Compared to the current available ATUM (automated tape-collecting ultramicrotome) technique, our work provides another alternative complete solution that can be applied to obtain large scale 3D ultrastructure of tissues. Our workflow includes an automated hardware system for high throughput serial section collection, a software package for automatic SEM imaging, and an image reconstruction program. These combined techniques can now be used together to rapidly provide access to understand the anatomy of the whole nematodes.
对细胞和组织进行大规模、高分辨率的三维(3D)超微结构重建,对于我们理解复杂的生物系统变得越来越重要。已经有一些关于秀丽隐杆线虫(C. elegans)的部分 3D 超微结构的报道,然而,整个线虫的 3D 重建从未实现过。在这里,我们独立开发了一种称为超薄切片扫描电子显微镜自动采集器的技术,并使用这种方法,以 100nm 的轴向和 15nm 的横向分辨率生成了整个 C. elegans 幼虫的 3D 重建。与当前可用的 ATUM(自动带收集超薄切片机)技术相比,我们的工作提供了另一种可应用于获取组织大规模 3D 超微结构的完整替代方案。我们的工作流程包括一个用于高通量连续切片采集的自动化硬件系统、一个用于自动 SEM 成像的软件包和一个图像重建程序。这些组合技术现在可以一起使用,快速提供对整个线虫解剖结构的理解。