Volumetric chemical imaging by clearing-enhanced stimulated Raman scattering microscopy

被引:115
作者
Wei, Mian [1 ]
Shi, Lingyan [1 ]
Shen, Yihui [1 ]
Zhao, Zhilun [1 ]
Guzman, Asja [1 ]
Kaufman, Laura J. [1 ]
Wei, Lu [1 ,3 ]
Min, Wei [1 ,2 ]
机构
[1] Columbia Univ, Dept Chem, New York, NY 10027 USA
[2] Columbia Univ, Kavli Inst Brain Sci, New York, NY 10027 USA
[3] CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA
关键词
volumetric imaging; stimulated Raman scattering; tissue clearing; metabolic imaging; cancer metabolism; IN-VIVO; GLIOBLASTOMA; CANCER; METASTASIS; HALLMARKS; IDISCO; ORGANS; CELLS;
D O I
10.1073/pnas.1813044116
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
Three-dimensional visualization of tissue structures using optical microscopy facilitates the understanding of biological functions. However, optical microscopy is limited in tissue penetration due to severe light scattering. Recently, a series of tissue-clearing techniques have emerged to allow significant depth-extension for fluorescence imaging. Inspired by these advances, we develop a volumetric chemical imaging technique that couples Raman-tailored tissue-clearing with stimulated Raman scattering (SRS) microscopy. Compared with the standard SRS, the clearing-enhanced SRS achieves greater than 10-times depth increase. Based on the extracted spatial distribution of proteins and lipids, our method reveals intricate 3D organizations of tumor spheroids, mouse brain tissues, and tumor xenografts. We further develop volumetric phasor analysis of multispectral SRS images for chemically specific clustering and segmentation in 3D. Moreover, going beyond the conventional label-free paradigm, we demonstrate metabolic volumetric chemical imaging, which allows us to simultaneously map out metabolic activities of protein and lipid synthesis in glioblastoma. Together, these results support volumetric chemical imaging as a valuable tool for elucidating comprehensive 3D structures, compositions, and functions in diverse biological contexts, complementing the prevailing volumetric fluorescence microscopy.
引用
收藏
页码:6608 / 6617
页数:10
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