Wu Jiamin, Lu Zhi, Jiang Dong, Guo Yuduo, Qiao Hui, Zhang Yi, Zhu Tianyi, Cai Yeyi, Zhang Xu, Zhanghao Karl, Xie Hao, Yan Tao, Zhang Guoxun, Li Xiaoxu, Jiang Zheng, Lin Xing, Fang Lu, Zhou Bing, Xi Peng, Fan Jingtao, Yu Li, Dai Qionghai
Department of Automation, Tsinghua University, Beijing 100084, China; Institute for Brain and Cognitive Sciences, Tsinghua University, Beijing 100084, China; Beijing Key Laboratory of Multi-dimension & Multi-scale Computational Photography (MMCP), Tsinghua University, Beijing 100084, China; IDG/McGovern Institute for Brain Research, Tsinghua University, Beijing 100084, China.
State Key Laboratory of Membrane Biology, Tsinghua University-Peking University Joint Center for Life Sciences, Beijing Frontier Research Center for Biological Structure, School of Life Sciences, Tsinghua University, Beijing 100084, China.
Cell. 2021 Jun 10;184(12):3318-3332.e17. doi: 10.1016/j.cell.2021.04.029. Epub 2021 May 25.
Long-term subcellular intravital imaging in mammals is vital to study diverse intercellular behaviors and organelle functions during native physiological processes. However, optical heterogeneity, tissue opacity, and phototoxicity pose great challenges. Here, we propose a computational imaging framework, termed digital adaptive optics scanning light-field mutual iterative tomography (DAOSLIMIT), featuring high-speed, high-resolution 3D imaging, tiled wavefront correction, and low phototoxicity with a compact system. By tomographic imaging of the entire volume simultaneously, we obtained volumetric imaging across 225 × 225 × 16 μm, with a resolution of up to 220 nm laterally and 400 nm axially, at the millisecond scale, over hundreds of thousands of time points. To establish the capabilities, we investigated large-scale cell migration and neural activities in different species and observed various subcellular dynamics in mammals during neutrophil migration and tumor cell circulation.
在哺乳动物中进行长期亚细胞活体成像对于研究天然生理过程中多样的细胞间行为和细胞器功能至关重要。然而,光学异质性、组织不透明度和光毒性带来了巨大挑战。在此,我们提出一种计算成像框架,称为数字自适应光学扫描光场相互迭代断层扫描(DAOSLIMIT),其特点是具有高速、高分辨率3D成像、平铺波前校正以及采用紧凑系统实现低光毒性。通过同时对整个体积进行断层成像,我们在毫秒级时间尺度上,跨越数十万个时间点,获得了横向分辨率高达220 nm、轴向分辨率高达400 nm、尺寸为225×225×16μm的体积成像。为了确立其能力,我们研究了不同物种中的大规模细胞迁移和神经活动,并观察了哺乳动物中性粒细胞迁移和肿瘤细胞循环过程中的各种亚细胞动力学。