ZFIN ID: ZDB-PUB-170512-4
Whole-brain serial-section electron microscopy in larval zebrafish
Hildebrand, D.G.C., Cicconet, M., Torres, R.M., Choi, W., Quan, T.M., Moon, J., Wetzel, A.W., Scott Champion, A., Graham, B.J., Randlett, O., Plummer, G.S., Portugues, R., Bianco, I.H., Saalfeld, S., Baden, A.D., Lillaney, K., Burns, R., Vogelstein, J.T., Schier, A.F., Lee, W.A., Jeong, W.K., Lichtman, J.W., Engert, F.
Date: 2017
Source: Nature   545(7654): 345-349 (Journal)
Registered Authors: Bianco, Isaac, Engert, Florian, Randlett, Owen, Schier, Alexander
Keywords: Classification and taxonomy, Cellular neuroscience, Imaging techniques, Characterization and analytical techniques, Data acquisition
MeSH Terms:
  • Anatomy, Artistic
  • Animals
  • Atlases as Topic
  • Axons/metabolism
  • Axons/ultrastructure
  • Brain/anatomy & histology
  • Brain/cytology
  • Brain/ultrastructure*
  • Datasets as Topic
  • Larva/anatomy & histology
  • Larva/cytology
  • Larva/ultrastructure
  • Microscopy, Electron*
  • Microscopy, Fluorescence, Multiphoton
  • Open Access Publishing
  • Zebrafish*/anatomy & histology
  • Zebrafish*/growth & development
PubMed: 28489821 Full text @ Nature
High-resolution serial-section electron microscopy (ssEM) makes it possible to investigate the dense meshwork of axons, dendrites, and synapses that form neuronal circuits. However, the imaging scale required to comprehensively reconstruct these structures is more than ten orders of magnitude smaller than the spatial extents occupied by networks of interconnected neurons, some of which span nearly the entire brain. Difficulties in generating and handling data for large volumes at nanoscale resolution have thus restricted vertebrate studies to fragments of circuits. These efforts were recently transformed by advances in computing, sample handling, and imaging techniques, but high-resolution examination of entire brains remains a challenge. Here, we present ssEM data for the complete brain of a larval zebrafish (Danio rerio) at 5.5 days post-fertilization. Our approach utilizes multiple rounds of targeted imaging at different scales to reduce acquisition time and data management requirements. The resulting dataset can be analysed to reconstruct neuronal processes, permitting us to survey all myelinated axons (the projectome). These reconstructions enable precise investigations of neuronal morphology, which reveal remarkable bilateral symmetry in myelinated reticulospinal and lateral line afferent axons. We further set the stage for whole-brain structure-function comparisons by co-registering functional reference atlases and in vivo two-photon fluorescence microscopy data from the same specimen. All obtained images and reconstructions are provided as an open-access resource.