The Jake Gittlen Laboratories for Cancer Research, Penn State College of Medicine, Hershey, United States; Division of Experimental Pathology, Department of Pathology, Penn State College of Medicine, Hershey, United States; Medical Scientist Training Program, Penn State College of Medicine, Hershey, United States
The Jake Gittlen Laboratories for Cancer Research, Penn State College of Medicine, Hershey, United States; Division of Experimental Pathology, Department of Pathology, Penn State College of Medicine, Hershey, United States
The Jake Gittlen Laboratories for Cancer Research, Penn State College of Medicine, Hershey, United States; Division of Experimental Pathology, Department of Pathology, Penn State College of Medicine, Hershey, United States
The Jake Gittlen Laboratories for Cancer Research, Penn State College of Medicine, Hershey, United States; Division of Experimental Pathology, Department of Pathology, Penn State College of Medicine, Hershey, United States; Medical Scientist Training Program, Penn State College of Medicine, Hershey, United States
The Jake Gittlen Laboratories for Cancer Research, Penn State College of Medicine, Hershey, United States; Division of Experimental Pathology, Department of Pathology, Penn State College of Medicine, Hershey, United States
Darin P Clark
Center for In Vivo Microscopy, Duke University, Durham, United States
Phillip Vargas
Department of Radiology, The University of Chicago, Chicago, United States
Xuying Xin
The Jake Gittlen Laboratories for Cancer Research, Penn State College of Medicine, Hershey, United States; Division of Experimental Pathology, Department of Pathology, Penn State College of Medicine, Hershey, United States
Jean E Copper
The Jake Gittlen Laboratories for Cancer Research, Penn State College of Medicine, Hershey, United States; Division of Experimental Pathology, Department of Pathology, Penn State College of Medicine, Hershey, United States
The Jake Gittlen Laboratories for Cancer Research, Penn State College of Medicine, Hershey, United States; Division of Experimental Pathology, Department of Pathology, Penn State College of Medicine, Hershey, United States
The Jake Gittlen Laboratories for Cancer Research, Penn State College of Medicine, Hershey, United States; Division of Experimental Pathology, Department of Pathology, Penn State College of Medicine, Hershey, United States
Yuxin Wang
Imaging Group, Omnivision Technologies, Inc., Santa Clara, United States
Xianghui Xiao
National Synchrotron Light Source II, Brookhaven National Laboratory, Upton, United States
Francesco De Carlo
Advanced Photon Source, Argonne National Laboratory, Lemont, United States
Damian B van Rossum
The Jake Gittlen Laboratories for Cancer Research, Penn State College of Medicine, Hershey, United States; Division of Experimental Pathology, Department of Pathology, Penn State College of Medicine, Hershey, United States
The Jake Gittlen Laboratories for Cancer Research, Penn State College of Medicine, Hershey, United States; Division of Experimental Pathology, Department of Pathology, Penn State College of Medicine, Hershey, United States
Organismal phenotypes frequently involve multiple organ systems. Histology is a powerful way to detect cellular and tissue phenotypes, but is largely descriptive and subjective. To determine how synchrotron-based X-ray micro-tomography (micro-CT) can yield 3-dimensional whole-organism images suitable for quantitative histological phenotyping, we scanned whole zebrafish, a small vertebrate model with diverse tissues, at ~1 micron voxel resolutions. Micro-CT optimized for cellular characterization (histotomography) allows brain nuclei to be computationally segmented and assigned to brain regions, and cell shapes and volumes to be computed for motor neurons and red blood cells. Striking individual phenotypic variation was apparent from color maps of computed densities of brain nuclei. Unlike histology, the histotomography also allows the study of 3-dimensional structures of millimeter scale that cross multiple tissue planes. We expect the computational and visual insights into 3D cell and tissue architecture provided by histotomography to be useful for reference atlases, hypothesis generation, comprehensive organismal screens, and diagnostics.