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J Comp Neurol. 2016 Jan 1;524(1):23-38. doi: 10.1002/cne.23852. Epub 2015 Aug 11.

Three-dimensional immersive virtual reality for studying cellular compartments in 3D models from EM preparations of neural tissues.

Author information

1
Biological and Environmental Science and Engineering division, King Abdullah University of Science and Technology, 23955-6900 Thuwal, Saudi Arabia.
2
Heidelberg Collaboratory for Image Processing (HCI), University of Heidelberg, 69115 Heidelberg, Germany.
3
KAUST Visualization Lab (KVL), King Abdullah University of Science and Technology, 23955-6900 Thuwal, Saudi Arabia.
4
Brain Mind Institute, École Polytechnique Fédérale de Lausanne (EPFL), 1005 Lausanne, Switzerland.

Abstract

Advances in the application of electron microscopy (EM) to serial imaging are opening doors to new ways of analyzing cellular structure. New and improved algorithms and workflows for manual and semiautomated segmentation allow us to observe the spatial arrangement of the smallest cellular features with unprecedented detail in full three-dimensions. From larger samples, higher complexity models can be generated; however, they pose new challenges to data management and analysis. Here we review some currently available solutions and present our approach in detail. We use the fully immersive virtual reality (VR) environment CAVE (cave automatic virtual environment), a room in which we are able to project a cellular reconstruction and visualize in 3D, to step into a world created with Blender, a free, fully customizable 3D modeling software with NeuroMorph plug-ins for visualization and analysis of EM preparations of brain tissue. Our workflow allows for full and fast reconstructions of volumes of brain neuropil using ilastik, a software tool for semiautomated segmentation of EM stacks. With this visualization environment, we can walk into the model containing neuronal and astrocytic processes to study the spatial distribution of glycogen granules, a major energy source that is selectively stored in astrocytes. The use of CAVE was key to the observation of a nonrandom distribution of glycogen, and led us to develop tools to quantitatively analyze glycogen clustering and proximity to other subcellular features.

KEYWORDS:

3D analysis; 3D navigation; fast 3D reconstruction; glycogen clustering; glycogen spatial distribution; volume analysis

PMID:
26179415
PMCID:
PMC5042088
DOI:
10.1002/cne.23852
[Indexed for MEDLINE]
Free PMC Article

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