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Genetically targeted 3D visualisation of Drosophila neurons under Electron Microscopy and X-Ray Microscopy using miniSOG.
Ng, Julian; Browning, Alyssa; Lechner, Lorenz; Terada, Masako; Howard, Gillian; Jefferis, Gregory S X E.
Affiliation
  • Ng J; Department of Zoology, Downing Street, Cambridge, CB2 3EJ, United Kingdom.
  • Browning A; Neurobiology Division, MRC Laboratory of Molecular Biology, Francis Crick Avenue, CB2 0QH, United Kingdom.
  • Lechner L; Carl Zeiss X-ray Microscopy Inc., 4385 Hopyard Rd., Suite 100, Pleasanton, CA 94588, USA.
  • Terada M; Carl Zeiss X-ray Microscopy Inc., 4385 Hopyard Rd., Suite 100, Pleasanton, CA 94588, USA.
  • Howard G; Carl Zeiss X-ray Microscopy Inc., 4385 Hopyard Rd., Suite 100, Pleasanton, CA 94588, USA.
  • Jefferis GSXE; Cell Biology Division, MRC Laboratory of Molecular Biology, Francis Crick Avenue, CB2 0QH, United Kingdom.
Sci Rep ; 6: 38863, 2016 12 13.
Article in En | MEDLINE | ID: mdl-27958322
ABSTRACT
Large dimension, high-resolution imaging is important for neural circuit visualisation as neurons have both long- and short-range patterns from axons and dendrites to the numerous synapses at terminal endings. Electron Microscopy (EM) is the favoured approach for synaptic resolution imaging but how such structures can be segmented from high-density images within large volume datasets remains challenging. Fluorescent probes are widely used to localise synapses, identify cell-types and in tracing studies. The equivalent EM approach would benefit visualising such labelled structures from within sub-cellular, cellular, tissue and neuroanatomical contexts. Here we developed genetically-encoded, electron-dense markers using miniSOG. We demonstrate their ability in 1) labelling cellular sub-compartments of genetically-targeted neurons, 2) generating contrast under different EM modalities, and 3) segmenting labelled structures from EM volumes using computer-assisted strategies. We also tested non-destructive X-ray imaging on whole Drosophila brains to evaluate contrast staining. This enabled us to target specific regions for EM volume acquisition.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Microscopy, Electron / Imaging, Three-Dimensional / Drosophila / Neurons Limits: Animals Language: En Journal: Sci Rep Year: 2016 Type: Article Affiliation country: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Microscopy, Electron / Imaging, Three-Dimensional / Drosophila / Neurons Limits: Animals Language: En Journal: Sci Rep Year: 2016 Type: Article Affiliation country: United kingdom