Publication

Quantifying mesoscale neuroanatomy using X-ray microtomography

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Last modified
  • 05/21/2025
Type of Material
Authors
    Eva Dyer, Emory UniversityWilliam Gray Roncal, The Johns Hopkins University Applied Physics LaboratoryJudy A. Prasad, University of ChicagoHugo L. Fernandes, Northwestern UniversityDoga Gürsoy, Argonne National LaboratoryVincent De Andrade, Argonne National LaboratoryKamel Fezzaa, Argonne National LaboratoryXianghui Xiao, Argonne National LaboratoryJoshua T. Vogelstein, Johns Hopkins UniversityChris Jacobsen, Argonne National LaboratoryKonrad P. Körding, University of PennsylvaniaNarayanan Kasthuri, University of Chicago
Language
  • English
Date
  • 2017-09-01
Publisher
  • Society for Neuroscience
Publication Version
Copyright Statement
  • © 2017 Dyer et al.
License
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 2373-2822
Volume
  • 4
Issue
  • 5
Start Page
  • ENEURO.0195-17.2017
End Page
  • ENEURO.0195-17.2017
Grant/Funding Information
  • Support was provided by NIH U01MH109100 (E.L.D., H.L.F., D.G., X.X., C.J., N.K., and K.P.K.), the IARPA MICRONS project under IARPA Contract D16PC0002 (N.K.), an educational Fellowship from the Johns Hopkins University Applied Physics Laboratory (W.G.R.), the Defense Advanced Research Projects Agency (DARPA) SIMPLEX program through SPAWAR contract N66001-15-C-4041, and DARPA GRAPHS N66001-14-1-4028.
  • This research used resources from the US Department of Energy (DOE) Office of Science User Facilities operated for the DOE Office of Science by Argonne National Laboratory under contract no. DE-AC02-06CH11357.
Abstract
  • Methods for resolving the three-dimensional (3D) microstructure of the brain typically start by thinly slicing and staining the brain, followed by imaging numerous individual sections with visible light photons or electrons. In contrast, X-rays can be used to image thick samples, providing a rapid approach for producing large 3D brain maps without sectioning. Here we demonstrate the use of synchrotron X-ray microtomography (μCT) for producing mesoscale (~1 μm 3 resolution) brain maps from millimeter-scale volumes of mouse brain. We introduce a pipeline for μCT-based brain mapping that develops and integrates methods for sample preparation, imaging, and automated segmentation of cells, blood vessels, and myelinated axons, in addition to statistical analyses of these brain structures. Our results demonstrate that X-ray tomography achieves rapid quantification of large brain volumes, complementing other brain mapping and connectomics efforts.
Author Notes
  • Correspondence should be addressed to either of the following: Eva L. Dyer, Georgia Institute of Technology 313 Ferst Drive NW Atlanta, GA 30332. E-mail: evadyer@gatech.edu; or Narayanan Kasthuri. E-mail: bobbykasthuri@anl.gov.
Keywords
Research Categories
  • Engineering, Biomedical

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