Synchrotron microCT imaging of soft tissue in juvenile zebrafish reveals retinotectal projections

被引:0
作者
Xin, Xuying [1 ,2 ,3 ]
Clark, Darin [4 ]
Ang, Khai Chung [1 ,2 ,3 ]
van Rossum, Damian B. [1 ,2 ,3 ]
Copper, Jean [1 ,2 ,3 ]
Xiao, Xianghui [5 ]
La Riviere, Patrick J. [6 ]
Cheng, Keith C. [1 ,2 ,3 ]
机构
[1] Penn State Coll Med, Dept Pathol, Hershey, PA 17033 USA
[2] Jake Gittlen Labs Canc Res, Hershey, PA 17033 USA
[3] Penn State Consortium Interdisciplinary Image Inf, Berkeley, CA 94720 USA
[4] Duke Univ, Med Ctr, Dept Radiol, Ctr In Vivo Microscopy, Durham, NC 27708 USA
[5] Argonne Natl Lab, Adv Photon Source, Argonne, IL 60439 USA
[6] Univ Chicago, Dept Radiol, Chicago, IL 60637 USA
来源
OPTICAL BIOPSY XV: TOWARD REAL-TIME SPECTROSCOPIC IMAGING AND DIAGNOSIS | 2017年 / 10060卷
关键词
zebrafish; phenomics; 3D imaging; image visualization; soft tissue imaging; optic nerves; retinotectal projections; synchrotron microCT; VERTEBRATE DEVELOPMENT; DRUG DISCOVERY; VISUAL-SYSTEM; MODEL; CANCER; DISEASE; GENOME; TOOLS;
D O I
10.1117/12.2267477
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Biomedical research and clinical diagnosis would benefit greatly from full volume determinations of anatomical phenotype. Comprehensive tools for morphological phenotyping are central for the emerging field of phenomics, which requires high-throughput, systematic, accurate, and reproducible data collection from organisms affected by genetic, disease, or environmental variables. Theoretically, complete anatomical phenotyping requires the assessment of every cell type in the whole organism, but this ideal is presently untenable due to the lack of an unbiased 3D imaging method that allows histopathological assessment of any cell type despite optical opacity. Histopathology, the current clinical standard for diagnostic phenotyping, involves the microscopic study of tissue sections to assess qualitative aspects of tissue architecture, disease mechanisms, and physiological state. However, quantitative features of tissue architecture such as cellular composition and cell counting in tissue volumes can only be approximated due to characteristics of tissue sectioning, including incomplete sampling and the constraints of 2D imaging of 5 micron thick tissue slabs. We have used a small, vertebrate organism, the zebrafish, to test the potential of microCT for systematic macroscopic and microscopic morphological phenotyping. While cell resolution is routinely achieved using methods such as light sheet fluorescence microscopy and optical tomography, these methods do not provide the pancellular perspective characteristic of histology, and are constrained by the limited penetration of visible light through pigmented and opaque specimens, as characterizes zebrafish juveniles. Here, we provide an example of neuroanatomy that can be studied by microCT of stained soft tissue at 1.43 micron isotropic voxel resolution. We conclude that synchrotron microCT is a form of 3D imaging that may potentially be adopted towards more reproducible, large-scale, morphological phenotyping of optically opaque tissues. Further development of soft tissue microCT, visualization and quantitative tools will enhance its utility.
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页数:7
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