Three-Dimensional Histology of Whole Zebrafish by Sub-Micron Synchrotron X-ray Micro-Tomography

Histological studies providing cellular insights into tissue architecture have been central to biological discovery and remain clinically invaluable today. Extending histology to three dimensions would be transformational for research and diagnostics. However, three-dimensional histology is impractical using current techniques. We have customized sample preparation, synchrotron X-ray tomographic parameters, and three-dimensional image analysis to allow for complete histological phenotyping using whole larval and juvenile zebrafish. The resulting digital zebrafish can be virtually sectioned and visualized in any plane. Whole-animal reconstructions at subcellular resolution also enable computational characterization of the zebrafish nervous system by region-specific detection of cell nuclei and quantitative assessment of individual phenotypic variation. Three-dimensional histological phenotyping has potential use in genetic and chemical screens, and in clinical and toxicological tissue diagnostics. One Sentence Summary Synchrotron X-ray micro-tomography can be used to rapidly create 3-dimensional images of fixed and stained specimens without sectioning, enabling computational histological phenotyping at cellular resolution.

[1]  Keith C. Cheng,et al.  Rigid Embedding of Fixed and Stained, Whole, Millimeter-Scale Specimens for Section-free 3D Histology by Micro-Computed Tomography , 2018, Journal of visualized experiments : JoVE.

[2]  F. Pfeiffer,et al.  Three-dimensional virtual histology enabled through cytoplasm-specific X-ray stain for microscopic and nanoscopic computed tomography , 2018, Proceedings of the National Academy of Sciences.

[3]  James A. Gagnon,et al.  Simultaneous single-cell profiling of lineages and cell types in the vertebrate brain , 2018, Nature Biotechnology.

[4]  Darin P Clark,et al.  Comparative analysis of fixation and embedding techniques for optimized histological preparation of zebrafish. , 2017, Comparative biochemistry and physiology. Toxicology & pharmacology : CBP.

[5]  Michael J. T. Stubbington,et al.  The Human Cell Atlas: from vision to reality , 2017, Nature.

[6]  Gregory A Gibson,et al.  Ribbon scanning confocal for high-speed high-resolution volume imaging of brain , 2017, PloS one.

[7]  Fabian J Theis,et al.  The Human Cell Atlas , 2017, bioRxiv.

[8]  Won-Ki Jeong,et al.  Whole-brain serial-section electron microscopy in larval zebrafish , 2017, Nature.

[9]  Mary E. Dickinson,et al.  Three-dimensional microCT imaging of mouse development from early post-implantation to early postnatal stages , 2016, Developmental biology.

[10]  Steve D. M. Brown,et al.  High-throughput discovery of novel developmental phenotypes , 2017 .

[11]  Lauren Kim,et al.  Essentials of anatomic pathology , 2016, Journal of Clinical Pathology.

[12]  Thomas P. Burghardt,et al.  In vivo myosin step-size from zebrafish skeletal muscle , 2016, Open Biology.

[13]  Konrad P. Körding,et al.  Quantifying Mesoscale Neuroanatomy Using X-Ray Microtomography , 2016, eNeuro.

[14]  William R. Gray Roncal,et al.  Saturated Reconstruction of a Volume of Neocortex , 2015, Cell.

[15]  Jon C. Aster,et al.  Robbins & Cotran Pathologic Basis of Disease , 2014 .

[16]  E. Susaki,et al.  Whole-Brain Imaging with Single-Cell Resolution Using Chemical Cocktails and Computational Analysis , 2014, Cell.

[17]  Jürg Schönenberger,et al.  Plant Tissues in 3D via X-Ray Tomography: Simple Contrasting Methods Allow High Resolution Imaging , 2013, PloS one.

[18]  Tilo Baumbach,et al.  X-ray phase-contrast in vivo microtomography probes new aspects of Xenopus gastrulation , 2013, Nature.

[19]  Anton J. Enright,et al.  The zebrafish reference genome sequence and its relationship to the human genome , 2013, Nature.

[20]  Aaron S. Andalman,et al.  Structural and molecular interrogation of intact biological systems , 2013, Nature.

[21]  Matteo Pellegrini,et al.  A large-scale zebrafish gene knockout resource for the genome-wide study of gene function , 2013, Genome research.

[22]  B. S. Manjunath,et al.  Corrigendum: Biological imaging software tools , 2012, Nature Methods.

[23]  Thomas Brox,et al.  Erratum: ViBE-Z: a framework for 3D virtual colocalization analysis in zebrafish larval brains , 2012, Nature Methods.

[24]  Thomas Brox,et al.  ViBE-Z: a framework for 3D virtual colocalization analysis in zebrafish larval brains , 2012, Nature Methods.

[25]  Atsushi Miyawaki,et al.  Scale: a chemical approach for fluorescence imaging and reconstruction of transparent mouse brain , 2011, Nature Neuroscience.

[26]  Darin P Clark,et al.  Whole-animal imaging, gene function, and the Zebrafish Phenome Project. , 2011, Current opinion in genetics & development.

[27]  M. Al-Abbadi,et al.  Basics of cytology , 2011, Avicenna Journal of Medicine.

[28]  Arrate Muñoz-Barrutia,et al.  3D reconstruction of histological sections: Application to mammary gland tissue , 2010, Microscopy research and technique.

[29]  B. Metscher MicroCT for comparative morphology: simple staining methods allow high-contrast 3D imaging of diverse non-mineralized animal tissues , 2009, BMC Physiology.

[30]  B. Metscher MicroCT for developmental biology: A versatile tool for high‐contrast 3D imaging at histological resolutions , 2009, Developmental dynamics : an official publication of the American Association of Anatomists.

[31]  G. Johnson,et al.  In vivo small-animal imaging using micro-CT and digital subtraction angiography , 2008, Physics in medicine and biology.

[32]  A. Arner,et al.  Structure and Function of Skeletal Muscle in Zebrafish Early Larvae , 2008, The Journal of general physiology.

[33]  P. Cloetens,et al.  Imaging applications of synchrotron X‐ray phase‐contrast microtomography in biological morphology and biomaterials science. I. General aspects of the technique and its advantages in the analysis of millimetre‐sized arthropod structure , 2007, Journal of microscopy.

[34]  Marco Stampanoni,et al.  Synchrotron X-ray tomographic microscopy of fossil embryos , 2006, Nature.

[35]  M. Wullimann,et al.  Atlas of Early Zebrafish Brain Development: A Tool for Molecular Neurogenetics , 2005 .

[36]  D. Holdsworth,et al.  Ex vivo characterization of articular cartilage and bone lesions in a rabbit ACL transection model of osteoarthritis using MRI and micro-CT. , 2004, Osteoarthritis and cartilage.

[37]  Christopher P Austin,et al.  The Knockout Mouse Project , 2004, Nature Genetics.

[38]  K. Cheng,et al.  Histology‐based screen for zebrafish mutants with abnormal cell differentiation , 2003, Developmental dynamics : an official publication of the American Association of Anatomists.

[39]  R. Ketcham,et al.  Acquisition, optimization and interpretation of X-ray computed tomographic imagery: applications to the geosciences , 2001 .

[40]  K. Cheng,et al.  Whole-Organism Cellular Pathology: A Systems Approach to Phenomics. , 2016, Advances in genetics.

[41]  The Mouse Phenotype Database Integration Consortium The Knockout Mouse Project , 2004 .

[42]  G. Watts From vision to reality. , 1991, Nursing.

[43]  Marianne Cooper,et al.  Introduction and overview , 1988, J. Am. Soc. Inf. Sci..