MRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge, United Kingdom.
Institute of Biochemistry and Molecular Medicine, University of Bern, Bern, Switzerland.
Elife. 2021 Oct 26;10:e70269. doi: 10.7554/eLife.70269.
During brain development, axons must extend over great distances in a relatively short amount of time. How the subcellular architecture of the growing axon sustains the requirements for such rapid build-up of cellular constituents has remained elusive. Human axons have been particularly poorly accessible to imaging at high resolution in a near-native context. Here, we present a method that combines cryo-correlative light microscopy and electron tomography with human cerebral organoid technology to visualize growing axon tracts. Our data reveal a wealth of structural details on the arrangement of macromolecules, cytoskeletal components, and organelles in elongating axon shafts. In particular, the intricate shape of the endoplasmic reticulum is consistent with its role in fulfilling the high demand for lipid biosynthesis to support growth. Furthermore, the scarcity of ribosomes within the growing shaft suggests limited translational competence during expansion of this compartment. These findings establish our approach as a powerful resource for investigating the ultrastructure of defined neuronal compartments.
在大脑发育过程中,轴突必须在相对较短的时间内延伸很长的距离。生长轴突的亚细胞结构如何维持如此快速构建细胞成分的要求仍然难以捉摸。人类轴突在接近自然状态的高分辨率下进行成像一直特别难以实现。在这里,我们提出了一种结合冷冻相关的光显微镜和电子断层扫描与人类类器官技术的方法,用于可视化生长的轴突轨迹。我们的数据揭示了大量关于大分子、细胞骨架成分和延伸轴突中的细胞器排列的结构细节。特别是,内质网的复杂形状与其在满足支持生长的脂质生物合成的高需求中的作用一致。此外,在生长轴突中核糖体的稀缺性表明在该隔室扩张期间翻译能力有限。这些发现确立了我们的方法作为研究特定神经元隔室超微结构的有力资源。