Kilohertz two-photon fluorescence microscopy imaging of neural activity in vivo

Understanding information processing in the brain requires monitoring neuronal activity at high spatiotemporal resolution. Using an ultrafast two-photon fluorescence microscope empowered by all-optical laser scanning, we imaged neuronal activity in vivo at up to 3,000 frames per second and submicrom...

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Veröffentlicht in:Nature methods 2020-03, Vol.17 (3), p.287-290
Hauptverfasser: Wu, Jianglai, Liang, Yajie, Chen, Shuo, Hsu, Ching-Lung, Chavarha, Mariya, Evans, Stephen W., Shi, Dongqing, Lin, Michael Z., Tsia, Kevin K., Ji, Na
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Sprache:eng
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Zusammenfassung:Understanding information processing in the brain requires monitoring neuronal activity at high spatiotemporal resolution. Using an ultrafast two-photon fluorescence microscope empowered by all-optical laser scanning, we imaged neuronal activity in vivo at up to 3,000 frames per second and submicrometer spatial resolution. This imaging method enabled monitoring of both supra- and subthreshold electrical activity down to 345 μm below the brain surface in head-fixed awake mice. High-speed two-photon laser scanning microscopy using a passive laser scanner based on free-space angular-chirp-enhanced delay achieves frame rates suitable for voltage imaging in vivo in the mouse brain.
ISSN:1548-7091
1548-7105
DOI:10.1038/s41592-020-0762-7