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Optical Sectioning of Live Mammal with Near-Infrared Light Sheet

Feifei Wang, Hao Wan, Jingying Yue, Mingxi Zhang, Zhuoran Ma, Qinchao Sun, Liangqiong Qu, Huilong Ma, Yeteng Zhong, Ye Tian, Guosong Hong, Wen Jung Li, Yongye Liang, Lianqing Liu, Hongjie Dai
doi: https://doi.org/10.1101/447433
Feifei Wang
1Department of Chemistry and Bio-X, Stanford University, Stanford, CA 94305, USA.
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Hao Wan
1Department of Chemistry and Bio-X, Stanford University, Stanford, CA 94305, USA.
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Jingying Yue
1Department of Chemistry and Bio-X, Stanford University, Stanford, CA 94305, USA.
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Mingxi Zhang
1Department of Chemistry and Bio-X, Stanford University, Stanford, CA 94305, USA.
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Zhuoran Ma
1Department of Chemistry and Bio-X, Stanford University, Stanford, CA 94305, USA.
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Qinchao Sun
1Department of Chemistry and Bio-X, Stanford University, Stanford, CA 94305, USA.
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Liangqiong Qu
2Department of Radiology and BRIC, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
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Huilong Ma
3Department of Materials Science and Engineering, South University of Science and Technology of China, 518055 Shenzhen, China.
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Yeteng Zhong
1Department of Chemistry and Bio-X, Stanford University, Stanford, CA 94305, USA.
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Ye Tian
1Department of Chemistry and Bio-X, Stanford University, Stanford, CA 94305, USA.
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Guosong Hong
1Department of Chemistry and Bio-X, Stanford University, Stanford, CA 94305, USA.
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Wen Jung Li
4Department of Mechanical and Biomedical Engineering, City University of Hong Kong, Kowloon Tong 999077, Hong Kong.
5State Key Laboratory of Robotics, Shenyang Institute of Automation, Chinese Academy of Sciences, Shenyang 110016, China.
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Yongye Liang
2Department of Radiology and BRIC, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
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Lianqing Liu
5State Key Laboratory of Robotics, Shenyang Institute of Automation, Chinese Academy of Sciences, Shenyang 110016, China.
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Hongjie Dai
1Department of Chemistry and Bio-X, Stanford University, Stanford, CA 94305, USA.
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  • For correspondence: hdai@stanford.edu
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Abstract

Deep-tissue three-dimensional optical imaging of live mammals in vivo with high spatiotemporal resolution in non-invasive manners has been challenging due to light scattering. Here, we developed near-infrared (NIR) light sheet microscopy (LSM) with optical excitation and emission wavelengths up to ~ 1320 nm and ~ 1700 nm respectively, far into the NIR-II (1000-1700 nm) region for 3D optical sectioning through live tissues. Suppressed scattering of both excitation and emission photons allowed one-photon optical sectioning at ~ 2 mm depth in highly scattering brain tissues. NIR-II LSM enabled non-invasive in vivo imaging of live mice, revealing never-before-seen dynamic processes such as highly abnormal tumor microcirculation, and 3D molecular imaging of an important immune checkpoint protein, programmed-death ligand 1 (PD-L1) receptors at the single cell scale in tumors. In vivo two-color near-infrared light sheet sectioning enabled simultaneous volumetric imaging of tumor vasculatures and PD-L1 proteins in live mammals.

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Posted October 18, 2018.
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Optical Sectioning of Live Mammal with Near-Infrared Light Sheet
Feifei Wang, Hao Wan, Jingying Yue, Mingxi Zhang, Zhuoran Ma, Qinchao Sun, Liangqiong Qu, Huilong Ma, Yeteng Zhong, Ye Tian, Guosong Hong, Wen Jung Li, Yongye Liang, Lianqing Liu, Hongjie Dai
bioRxiv 447433; doi: https://doi.org/10.1101/447433
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Optical Sectioning of Live Mammal with Near-Infrared Light Sheet
Feifei Wang, Hao Wan, Jingying Yue, Mingxi Zhang, Zhuoran Ma, Qinchao Sun, Liangqiong Qu, Huilong Ma, Yeteng Zhong, Ye Tian, Guosong Hong, Wen Jung Li, Yongye Liang, Lianqing Liu, Hongjie Dai
bioRxiv 447433; doi: https://doi.org/10.1101/447433

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