Abstract
Two-photon light-sheet fluorescence microscopy enables high-resolution imaging of neural activity in brain tissue at a high frame rate. Traditionally, light-sheet microscopy builds up a 3D stack by multiple depth scans with uniform spatial intervals, which substantially limits the volumetric imaging speed. Here, we introduce the depth random-access light-sheet microscopy, allowing rapid switching scanning depth for light-sheet imaging. With a low-cost electrically tunable lens and minimum modification of an existing two-photon light-sheet imaging instrument, we demonstrated fast random depth hopping light-sheet imaging at 100 frames per second in the live brain slice. Through depth random-access, calcium activities for an astrocyte were recorded on four user-selected detection planes at a refreshing rate of 25 Hz.
Original language | English (US) |
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Pages (from-to) | 26396-26406 |
Number of pages | 11 |
Journal | Optics Express |
Volume | 30 |
Issue number | 15 |
DOIs | |
State | Published - Jul 18 2022 |
ASJC Scopus subject areas
- Atomic and Molecular Physics, and Optics
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Visualization 3.mp4
Xu, D. (Creator), Ding, J. B. (Creator) & Peng, L. (Creator), Optica Publishing Group, 2022
DOI: 10.6084/m9.figshare.19214469, https://opticapublishing.figshare.com/articles/media/Visualization_3_mp4/19214469
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Visualization 2.mp4
Xu, D. (Creator), Ding, J. B. (Creator) & Peng, L. (Creator), Optica Publishing Group, 2022
DOI: 10.6084/m9.figshare.19214472.v1, https://opticapublishing.figshare.com/articles/media/Visualization_2_mp4/19214472/1
Dataset
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Visualization 2.mp4
Xu, D. (Creator), Ding, J. B. (Creator) & Peng, L. (Creator), Optica Publishing Group, 2022
DOI: 10.6084/m9.figshare.19214472, https://opticapublishing.figshare.com/articles/media/Visualization_2_mp4/19214472
Dataset