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      Atacama Clear for Complex 3D Imaging of Organs

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          Abstract

          3D reconstructive imaging is a powerful strategy to interrogate the global architecture of tissues. We developed Atacama Clear (ATC), a novel method that increases 3D imaging signal-to-noise ratios (SNRs) while simultaneously increasing the capacity of tissue to be cleared. ATC potentiated the clearing capacity of all tested chemical reagents currently used for optical clearing by an average of 68%, and more than doubled SNRs. This increased imaging efficacy enabled multiplex interrogation of tough fibrous tissue and specimens that naturally exhibit high levels of background noise, including the heart, kidney, and human biopsies. Indeed, ATC facilitated visualization of previously undocumented adjacent nephron segments that exhibit notoriously high autofluorescence, elements of the cardiac conduction system, and the distinct human glomerular tissue layers, at single cell resolution. Moreover, ATC was validated to be compatible with fluorescent reporter proteins in murine, zebrafish, and 3D stem cell model systems. These data establish ATC for 3D imaging studies of challenging tissue types.

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          Most cited references32

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          SeeDB: a simple and morphology-preserving optical clearing agent for neuronal circuit reconstruction.

          We report a water-based optical clearing agent, SeeDB, which clears fixed brain samples in a few days without quenching many types of fluorescent dyes, including fluorescent proteins and lipophilic neuronal tracers. Our method maintained a constant sample volume during the clearing procedure, an important factor for keeping cellular morphology intact, and facilitated the quantitative reconstruction of neuronal circuits. Combined with two-photon microscopy and an optimized objective lens, we were able to image the mouse brain from the dorsal to the ventral side. We used SeeDB to describe the near-complete wiring diagram of sister mitral cells associated with a common glomerulus in the mouse olfactory bulb. We found the diversity of dendrite wiring patterns among sister mitral cells, and our results provide an anatomical basis for non-redundant odor coding by these neurons. Our simple and efficient method is useful for imaging intact morphological architecture at large scales in both the adult and developing brains.
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            Structural and molecular interrogation of intact biological systems.

            Obtaining high-resolution information from a complex system, while maintaining the global perspective needed to understand system function, represents a key challenge in biology. Here we address this challenge with a method (termed CLARITY) for the transformation of intact tissue into a nanoporous hydrogel-hybridized form (crosslinked to a three-dimensional network of hydrophilic polymers) that is fully assembled but optically transparent and macromolecule-permeable. Using mouse brains, we show intact-tissue imaging of long-range projections, local circuit wiring, cellular relationships, subcellular structures, protein complexes, nucleic acids and neurotransmitters. CLARITY also enables intact-tissue in situ hybridization, immunohistochemistry with multiple rounds of staining and de-staining in non-sectioned tissue, and antibody labelling throughout the intact adult mouse brain. Finally, we show that CLARITY enables fine structural analysis of clinical samples, including non-sectioned human tissue from a neuropsychiatric-disease setting, establishing a path for the transmutation of human tissue into a stable, intact and accessible form suitable for probing structural and molecular underpinnings of physiological function and disease.
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              Whole-brain imaging with single-cell resolution using chemical cocktails and computational analysis.

              Systems-level identification and analysis of cellular circuits in the brain will require the development of whole-brain imaging with single-cell resolution. To this end, we performed comprehensive chemical screening to develop a whole-brain clearing and imaging method, termed CUBIC (clear, unobstructed brain imaging cocktails and computational analysis). CUBIC is a simple and efficient method involving the immersion of brain samples in chemical mixtures containing aminoalcohols, which enables rapid whole-brain imaging with single-photon excitation microscopy. CUBIC is applicable to multicolor imaging of fluorescent proteins or immunostained samples in adult brains and is scalable from a primate brain to subcellular structures. We also developed a whole-brain cell-nuclear counterstaining protocol and a computational image analysis pipeline that, together with CUBIC reagents, enable the visualization and quantification of neural activities induced by environmental stimulation. CUBIC enables time-course expression profiling of whole adult brains with single-cell resolution. Copyright © 2014 Elsevier Inc. All rights reserved.
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                Author and article information

                Journal
                bioRxiv
                BIORXIV
                bioRxiv
                Cold Spring Harbor Laboratory
                23 January 2024
                : 2024.01.22.576689
                Affiliations
                [1 ]Department of Surgery, Weill Cornell Medicine, New York, NY, USA
                [2 ]Department of Medicine, Weill Cornell Medicine, New York, NY, USA
                [3 ]Human Therapeutic Organoid Core Facility, Weill Cornell Medicine, New York, NY USA
                [4 ]Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA
                [5 ]Weill Cornell Center for Genomic Health
                Author notes
                [*]

                These authors contributed equally

                AUTHOR CONTRIBUTIONS

                Study conception, R.H.; Technological Conception and Development, R.H.; Experiment Design, R.H., T.E., E.A.J; Experiments, R.H., N.D.S., L.L.; Intellectual Contributions, R.H., T.E., E.A.J.; Manuscript Writing, R.H. with input from T.E., E.A.J.

                [+ ] Corresponding Author Lead Contact: Romulo Hurtado, Ph.D., Assistant Professor of Cell and Developmental Biology Research, Department of Surgery, Weill Medical College of Cornell University, 1300 York Avenue, New York, NY 10021, roh2002@ 123456med.cornell.edu
                Article
                10.1101/2024.01.22.576689
                10849539
                38328217
                8ef0bdc3-d595-4314-99e9-54a4fa1a17f3

                This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.

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