bioRxivBioengineeringPreprint
Optical Sectioning of Live Mammal with Near-Infrared Light Sheet
Feifei WangiD, Hao Wan, Jingying Yue, Mingxi Zhang, Zhuoran Ma, Qinchao Sun, Liangqiong QuiD, Huilong Ma, Yeteng Zhong, Ye Tian, Guosong Hong, Wen Jung Li, Yongye Liang, Lianqing Liu, Hongjie DaiiD
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.
- organism: mouse
- assay: imaging
- research focus: cell type annotation
- approach: microscopy & imaging analysis
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