Resolution‐Enhanced Mesoscopic Imaging With Cylindrical Lens‐Corrected Oblique Plane Light‐Sheet Microscopy
Single-objective light sheet fluorescence microscopy (LSFM) excels in high-speed imaging of large samples, but its limited fluorescence collection angle would degrade system resolution due to the fluorescence loss at low magnifications. To address this issue, we introduce a new method using a coaxial modulation module. By combining two sets of cylindrical lenses with the camera's rolling shutter, we achieve 3D imaging with an optimized fluorescence collection angle in low-magnification mode. Compared to advanced single-objective LSFM, our method provides a practical solution for low-NA oblique plane microscopy (NA 0.5) and enhances resolution by ~30% along the light propagation axis. We validated the system's resolution with fluorescent microspheres, achieving sub-micron lateral and sub-cellular axial resolutions. Furthermore, we have demonstrated its feasibility using GFP-labeled neurons and Siha cervical cancer cell samples for cell counting.
Authors
- Fenghe Zhong (ORCID: https://orcid.org/0000-0002-1281-9465)
- Shimeng Gao
- Yao Zhou (ORCID: https://orcid.org/0000-0001-6422-7528)
- Peng Fei (ORCID: https://orcid.org/0000-0003-3764-817X)
- Mengmeng Li (ORCID: https://orcid.org/0000-0002-2788-0314)
Institutions
- Wuhan National Laboratory for Optoelectronics (CN)
Publication Details
- Journal
- Journal of Biophotonics
- Published
- 2025-08-10
- DOI
- https://doi.org/10.1002/jbio.202500262
- Primary Topic
- Advanced Fluorescence Microscopy Techniques
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China
- China Postdoctoral Science Foundation
- National Key Research and Development Program of China
- Fundamental Research Funds for the Central Universities