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NeuroscienceCell
Peer-reviewed journal article

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

Weijian ZongiD, Horst Andreas ObenhausiD, Emilie Ranheim Skytøen, Hanna EneqvistiD, Nienke L. de Jong, Ruben Duque do ValeiD, Marina JorgeiD, May‐Britt MoseriD, Edvard Ingjald MoseriD

Abstract

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 3g and a highly flexible connection cable, MINI2P allowed imaging to proceed with no impediment of behavior in half-hour free-foraging trials compared to untethered, unimplanted animals. The improved cell yield was achieved through a new optical system design featuring an enlarged field of view (FOV) and a new micro-tunable lens with increased z-scanning range and speed that allowed for fast and stable imaging of multiple, interleaved planes as well as 3D functional imaging. A novel technique for 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, including visual cortex. HighlightsWe developed a lightweight 2-photon miniscope for imaging in freely-foraging mice Activity can be monitored in volumes of over 1,000 visual or entorhinal-cortex cells A new z-scanning module allows fast imaging across multiple interleaved planes Successive imaging from adjacent regions enables imaging from more than 10,000 cells

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