Iterative tomography with digital adaptive optics permits hour-long intravital observation of 3D subcellular dynamics at millisecond scale
Author(s) -
Jiamin Wu,
Zhi Lü,
Dong Jiang,
Yuduo Guo,
Hui Qiao,
Yi Zhang,
Tianyi Zhu,
Yeyi Cai,
Xu Zhang,
Karl Zhanghao,
Hao Xie,
Tao Yan,
Guoxun Zhang,
Xiaoxu Li,
Zheng Jiang,
Xing Lin,
Lu Fang,
Bing Zhou,
Peng Xi,
Jingtao Fan,
Li Yu,
Qionghai Dai
Publication year - 2021
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2021.04.029
Subject(s) - biology , millisecond , scale (ratio) , dynamics (music) , adaptive optics , intravital microscopy , tomography , biophysics , optics , physics , acoustics , quantum mechanics , astronomy , microbiology and biotechnology , in vivo
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 3 , 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.
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