4.8 Article

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

Journal

NATURE METHODS
Volume 17, Issue 3, Pages 287-+

Publisher

NATURE RESEARCH
DOI: 10.1038/s41592-020-0762-7

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Funding

  1. Howard Hughes Medical Institute
  2. American Epilepsy Society predoctoral fellowship
  3. China Scholarship Council Joint PhD Training Program
  4. Stanford Neuroscience PhD Program training grant [5T32MH020016]
  5. Post-9/11 GI Bill
  6. Research Grants Council of the Hong Kong Special Administrative Region of China [17209017, 17259316, 17207715]
  7. NIH BRAIN Initiative [1U01NS103464, 1RF1MH114105, 1UF1NS107696]

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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 mu m 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.

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