Whole-Body Imaging with Single-Cell Resolution by Tissue Decolorization

The development of whole-body imaging at single-cell resolution enables system-level approaches to studying cellular circuits in organisms. Previous clearing methods focused on homogenizing mismatched refractive indices of individual tissues, enabling reductions in opacity but falling short of achieving transparency. Here, we show that an aminoalcohol decolorizes blood by efficiently eluting the heme chromophore from hemoglobin. Direct transcardial perfusion of an aminoalcohol-containing cocktail that we previously termed CUBIC coupled with a 10 day to 2 week clearing protocol decolorized and rendered nearly transparent almost all organs of adult mice as well as the entire body of infant and adult mice. This CUBIC-perfusion protocol enables rapid whole-body and whole-organ imaging at single-cell resolution by using light-sheet fluorescent microscopy. The CUBIC protocol is also applicable to 3D pathology, anatomy, and immunohistochemistry of various organs. These results suggest that whole-body imaging of colorless tissues at high resolution will contribute to organism-level systems biology.

[1]  Rajan P Kulkarni,et al.  Single-Cell Phenotyping within Transparent Intact Tissue through Whole-Body Clearing , 2014, Cell.

[2]  Ton G van Leeuwen,et al.  Light absorption of (oxy-)hemoglobin assessed by spectroscopic optical coherence tomography. , 2003, Optics letters.

[3]  Frank Bradke,et al.  Three-dimensional imaging of solvent-cleared organs using 3DISCO , 2012, Nature Protocols.

[4]  M. Hilton,et al.  Demineralized murine skeletal histology. , 2014, Methods in molecular biology.

[5]  Elo Leung,et al.  A TALE nuclease architecture for efficient genome editing , 2011, Nature Biotechnology.

[6]  W. Guido,et al.  ClearT: a detergent- and solvent-free clearing method for neuronal and non-neuronal tissue , 2013, Development.

[7]  K. Deisseroth,et al.  Advanced CLARITY for rapid and high-resolution imaging of intact tissues , 2014, Nature Protocols.

[8]  Philipp J. Keller,et al.  Shedding light on the system: studying embryonic development with light sheet microscopy. , 2011, Current Opinion in Genetics and Development.

[9]  M. Kinoshita,et al.  The see-through medaka: A fish model that is transparent throughout life , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[10]  Yamamura Ken-ichi,et al.  Efficient selection for high-expression transfectants with a novel eukaryotic vector , 1991 .

[11]  R. Weiler,et al.  Chemical Clearing and Dehydration of GFP Expressing Mouse Brains , 2012, PloS one.

[12]  S. Lukyanov,et al.  Fluorescent proteins and their applications in imaging living cells and tissues. , 2010, Physiological reviews.

[13]  S. Qadri,et al.  Oxyradical-induced GFP damage and loss of fluorescence. , 2008, International journal of biological macromolecules.

[14]  P. O'Byrne,et al.  A GABAergic system in airway epithelium is essential for mucus overproduction in asthma , 2007, Nature Medicine.

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

[16]  Tomoko Nakanishi,et al.  ‘Green mice’ as a source of ubiquitous green cells , 1997, FEBS letters.

[17]  Volker Brendel,et al.  TAL Effector-Nucleotide Targeter (TALE-NT) 2.0: tools for TAL effector design and target prediction , 2012, Nucleic Acids Res..

[18]  H. Kiyonari,et al.  Three inhibitors of FGF receptor, ERK, and GSK3 establishes germline‐competent embryonic stem cells of C57BL/6N mouse strain with high efficiency and stability , 2010, Genesis.

[19]  Kenji F. Tanaka,et al.  Expanding the repertoire of optogenetically targeted cells with an enhanced gene expression system. , 2012, Cell reports.

[20]  H Steinke,et al.  A modified Spalteholz technique with preservation of the histology. , 2001, Annals of anatomy = Anatomischer Anzeiger : official organ of the Anatomische Gesellschaft.

[21]  Takeshi Imai,et al.  SeeDB: a simple and morphology-preserving optical clearing agent for neuronal circuit reconstruction , 2013, Nature Neuroscience.

[22]  A. Schierloh,et al.  Ultramicroscopy: three-dimensional visualization of neuronal networks in the whole mouse brain , 2007, Nature Methods.

[23]  Kristin L. Hazelwood,et al.  Far-red fluorescent tags for protein imaging in living tissues. , 2009, The Biochemical journal.

[24]  R. Weissleder A clearer vision for in vivo imaging , 2001, Nature Biotechnology.

[25]  E. Susaki,et al.  Establishment of TSH β real-time monitoring system in mammalian photoperiodism , 2013, Genes to cells : devoted to molecular & cellular mechanisms.

[26]  K. Naruse,et al.  Effects of Body-Color Mutations on Vitality: An Attempt to Establish Easy-to-Breed See-Through Medaka Strains by Outcrossing , 2013, G3: Genes, Genomes, Genetics.

[27]  F. Teale,et al.  Cleavage of the haem-protein link by acid methylethylketone. , 1959, Biochimica et biophysica acta.

[28]  Johannes E. Schindelin,et al.  Fiji: an open-source platform for biological-image analysis , 2012, Nature Methods.

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

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

[31]  Hans-Ulrich Dodt,et al.  Light sheet microscopy of living or cleared specimens , 2012, Current Opinion in Neurobiology.

[32]  W. Webb,et al.  Dynamics of fluorescence fluctuations in green fluorescent protein observed by fluorescence correlation spectroscopy. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[33]  H. Hultin,et al.  Changes in trout hemoglobin conformations and solubility after exposure to acid and alkali pH. , 2004, Journal of agricultural and food chemistry.

[34]  G. Feng,et al.  Imaging Neuronal Subsets in Transgenic Mice Expressing Multiple Spectral Variants of GFP , 2000, Neuron.

[35]  Aileen J F King,et al.  The use of animal models in diabetes research , 2012, British journal of pharmacology.

[36]  James Sharpe,et al.  Tomographic molecular imaging and 3D quantification within adult mouse organs , 2007, Nature Methods.

[37]  Hiroshi Kiyonari,et al.  Establishment of conditional reporter mouse lines at ROSA26 locus for live cell imaging , 2011, Genesis.

[38]  H. Wolf,et al.  Alkaline haematin D-575, a new tool for the determination of haemoglobin as an alternative to the cyanhaemiglobin method. II. Standardisation of the method using pure chlorohaemin. , 1984, Clinica chimica acta; international journal of clinical chemistry.

[39]  H. Niwa,et al.  Efficient selection for high-expression transfectants with a novel eukaryotic vector. , 1991, Gene.