Yao Zhou, Mengmeng Li, Shimeng Gao, Fenghe Zhong, Peng Fei
{"title":"Resolution-Enhanced Mesoscopic Imaging With Cylindrical Lens-Corrected Oblique Plane Light-Sheet Microscopy.","authors":"Yao Zhou, Mengmeng Li, Shimeng Gao, Fenghe Zhong, Peng Fei","doi":"10.1002/jbio.202500262","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":94068,"journal":{"name":"Journal of biophotonics","volume":" ","pages":"e202500262"},"PeriodicalIF":2.3000,"publicationDate":"2025-08-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of biophotonics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/jbio.202500262","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
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.