Rapid 3D projection microscopy of neural circuit with two-photon glutamate uncaging
We introduce a rapid dual-view projection imaging technique with two-photon glutamate uncaging capabilities. This method significantly enhances volumetric imaging rates for neural studies over traditional light-sheet imaging. Furthermore, we integrated an independent laser scanning module for two-photon uncaging, allowing for simultaneous synaptic resolution stimulation and 100 Hz volumetric imaging of neural activity in deep tissue. Additionally, we provide imaging results from mouse brain slices undergoing two-photon glutamate uncaging.
Authors
- Dongli Xu (ORCID: https://orcid.org/0000-0002-9241-7131)
- Jun Ding (ORCID: https://orcid.org/0000-0003-0690-1312)
- Leilei Peng (ORCID: https://orcid.org/0000-0003-1400-4208)
Institutions
- University of Arizona (US)
- Stanford University (US)
Publication Details
- Published
- 2025-03-19
- DOI
- https://doi.org/10.1117/12.3046799
- Primary Topic
- Force Microscopy Techniques and Applications
- Type
- article
- Field-Weighted Citation Impact
- 0.00