光学切片
薄层荧光显微镜
显微镜
材料科学
微循环
临床前影像学
活体显微镜检查
光学
生物物理学
生物医学工程
病理
体内
生物
医学
扫描共焦电子显微镜
放射科
物理
生物技术
作者
Feifei Wang,Hao Wan,Zhuoran Ma,Yeteng Zhong,Qinchao Sun,Ye Tian,Liangqiong Qu,Haotian Du,Mingxi Zhang,Lulin Li,Huilong Ma,Jian Luo,Yongye Liang,Wen J. Li,Guosong Hong,Lianqing Liu,Hongjie Dai
出处
期刊:Nature Methods
[Nature Portfolio]
日期:2019-05-13
卷期号:16 (6): 545-552
被引量:183
标识
DOI:10.1038/s41592-019-0398-7
摘要
Non-invasive deep-tissue three-dimensional optical imaging of live mammals with high spatiotemporal resolution is challenging owing to light scattering. We developed near-infrared II (1,000-1,700 nm) light-sheet microscopy with excitation and emission of up to approximately 1,320 nm and 1,700 nm, respectively, for optical sectioning at a penetration depth of approximately 750 μm through live tissues without invasive surgery and at a depth of approximately 2 mm in glycerol-cleared brain tissues. Near-infrared II light-sheet microscopy in normal and oblique configurations enabled in vivo imaging of live mice through intact tissue, revealing abnormal blood flow and T-cell motion in tumor microcirculation and mapping out programmed-death ligand 1 and programmed cell death protein 1 in tumors with cellular resolution. Three-dimensional imaging through the intact mouse head resolved vascular channels between the skull and brain cortex, and allowed monitoring of recruitment of macrophages and microglia to the traumatic brain injury site.
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