Serial optical coherence microscopy for label-free volumetric histopathology

被引:11
作者
Min, Eunjung [1 ]
Ban, Sungbea [2 ]
Lee, Junwon [2 ]
Vavilin, Andrey [2 ]
Baek, Songyee [2 ]
Jung, Sunwoo [2 ]
Ahn, Yujin [2 ]
Park, Kibeom [2 ]
Shin, Sungwon [2 ]
Han, SoHyun [3 ]
Cho, Hyungjoon [2 ]
Lee-Kwon, Whaseon [2 ]
Kim, Jeehyun [4 ]
Lee, C. Justin [5 ]
Jung, Woonggyu [2 ]
机构
[1] Max Planck Inst Biol Cybernet, D-72076 Tubingen, Germany
[2] Ulsan Natl Inst Sci & Technol UNIST, Dept Biomed Engn, Ulsan 44919, South Korea
[3] Martinos Ctr Biomed Imaging, Charlestown, MA 02129 USA
[4] Kyungpook Natl Univ, Sch Elect Engn, Daegu 41566, South Korea
[5] Inst for Basic Sci Korea, Ctr Cognit & Social, Daejeon 34126, South Korea
基金
新加坡国家研究基金会;
关键词
SINGLE-CELL RESOLUTION; BRAIN; TOMOGRAPHY; TISSUES;
D O I
10.1038/s41598-020-63460-3
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The observation of histopathology using optical microscope is an essential procedure for examination of tissue biopsies or surgically excised specimens in biological and clinical laboratories. However, slide-based microscopic pathology is not suitable for visualizing the large-scale tissue and native 3D organ structure due to its sampling limitation and shallow imaging depth. Here, we demonstrate serial optical coherence microscopy (SOCM) technique that offers label-free, high-throughput, and large-volume imaging of ex vivo mouse organs. A 3D histopathology of whole mouse brain and kidney including blood vessel structure is reconstructed by deep tissue optical imaging in serial sectioning techniques. Our results demonstrate that SOCM has unique advantages as it can visualize both native 3D structures and quantitative regional volume without introduction of any contrast agents.
引用
收藏
页数:8
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