Department of Chemistry and Bio-X, Stanford University, Stanford, CA, USA.
Department of Radiology and BRIC, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Nat Methods. 2019 Jun;16(6):545-552. doi: 10.1038/s41592-019-0398-7. Epub 2019 May 13.
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.
非侵入性深层组织三维光学成像活体哺乳动物具有高时空分辨率是有挑战性的由于光散射。我们开发了近红外 II (1000-1700nm) 光片显微镜激发和发射分别高达约 1320nm 和 1700nm,用于光学切片穿透深度约 750μm 活体组织无侵入性手术和甘油清除脑组织约 2mm 深。近红外 II 光片显微镜在正常和倾斜配置下,能够通过完整的组织对活体小鼠进行成像,揭示肿瘤微循环中异常的血流和 T 细胞运动,并以细胞分辨率绘制肿瘤中的程序性死亡配体 1 和程序性细胞死亡蛋白 1。通过完整的小鼠头部进行三维成像可以分辨颅骨和大脑皮层之间的血管通道,并允许监测巨噬细胞和小胶质细胞向创伤性脑损伤部位的募集。