A large field-of-view, single-cell-resolution two- and three-photon microscope for deep and wide imaging

• Published in: eLight Vol. 4; no. 1; pp. 20 - 14
• Main Authors: Mok, Aaron T., Wang, Tianyu, Zhao, Shitong, Kolkman, Kristine E., Wu, Danni, Ouzounov, Dimitre G., Seo, Changwoo, Wu, Chunyan, Fetcho, Joseph R., Xu, Chris
• Format: Journal Article
• Language: English
• Published: Singapore Springer Nature Singapore 01-12-2024; Springer Nature B.V; SpringerOpen
• Subjects: Aperture; Brain imaging; DEEPscope; Efficiency; Large field of view; Lasers; Microscopes; Microscopy; Neurons; Optical Devices; Optics; Photonics; Physics; Physics and Astronomy; Research Article; Scanners; Three-photon microscopy; Two-photon microscopy; Two-photon microscopy; Brain imaging; DEEPscope; Three-photon microscopy; Large field of view
• ISSN: 2097-1710; 2662-8643
• DOI: 10.1186/s43593-024-00076-4

In vivo imaging of large-scale neuronal activity plays a pivotal role in unraveling the function of the brain's circuitry. Multiphoton microscopy, a powerful tool for deep-tissue imaging, has received sustained interest in advancing its speed, field of view and imaging depth. However, to avoid thermal damage in scattering biological tissue, field of view decreases exponentially as imaging depth increases. We present a suite of innovations to optimize three-photon microscopy for large field-of-view imaging at depths unreachable by two-photon microscopy. These techniques enable us to image neuronal activities of transgenic animals expressing protein calcium sensors in a ~ 3.5-mm diameter field-of-view with single-cell resolution in the deepest cortical layer of mouse brains. We further demonstrate simultaneous large field-of-view two-photon and three-photon imaging, subcortical imaging in the mouse brain, and whole-brain imaging in adult zebrafish. The demonstrated techniques can be integrated into typical multiphoton microscopes to enlarge field of view for system-level neural circuit research.