4.8 Article

Large-scale two-photon calcium imaging in freely moving mice

Journal

CELL
Volume 185, Issue 7, Pages 1240-+

Publisher

CELL PRESS
DOI: 10.1016/j.cell.2022.02.017

Keywords

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Funding

  1. European Research Council [951319]
  2. Research Council of Norway (RCN) FRIPRO grants [286225, 300394]
  3. RCN Centre of Excellence grant [223262, 295721]
  4. RCN National Infrastructure grant [223262, 295721]
  5. Ministry of Education and Research of Norway
  6. Kavli Foundation
  7. European Union's Horizon 2020 Research and Innovation Programme (Marie Sklodowska-Curie grant) [842006]
  8. EMBO postdoctoral fellowship [EMBO ALTF 1078-2020]
  9. Marie Curie Actions (MSCA) [842006] Funding Source: Marie Curie Actions (MSCA)
  10. European Research Council (ERC) [951319] Funding Source: European Research Council (ERC)

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We developed a miniaturized two-photon microscope (MINI2P) that can perform fast and high-resolution calcium imaging of over 1,000 neurons in multiple planes simultaneously. The microscope allows stable imaging without interfering with the behavior of freely moving mice, and its optical system design improves cell yield and enables recording of a large number of neurons.
We developed a miniaturized two-photon microscope (MINI2P) for fast, high-resolution, multiplane calcium imaging of over 1,000 neurons at a time in freely moving mice. With a microscope weight below 3 g and a highly flexible connection cable, MINI2P allowed stable imaging with no impediment of behavior in a variety of assays compared to untethered, unimplanted animals. The improved cell yield was achieved through a optical system design featuring an enlarged field of view (FOV) and a microtunable lens with increased z-scanning range and speed that allows fast and stable imaging of multiple interleaved planes, as well as 3D functional imaging. Successive imaging across multiple, adjacent FOVs enabled recordings from more than 10,000 neurons in the same animal. Large-scale proof-of-principle data were obtained from cell populations in visual cortex, medial entorhinal cortex, and hippocampus, revealing spatial tuning of cells in all areas.

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