Confocal Laser Scanning Platform Combined With In Situ High‐Resolution Quantitative Phase Imaging

This paper introduces an advanced dual-modality imaging platform by integrating a confocal laser scanning/imaging module with flat-fielding quantitative phase contrast microscopy (FF-QPCM). The platform enables phase/fluorescence dual-modality imaging of the same samples with high resolution and contrast. Using this platform, we observed that confocal fluorescence excitation causes minimal damage to cells, whereas wide-field fluorescence excitation (WFE) results in significant damage, particularly mitochondrial fragmentation and notable alterations in phase values. Additionally, in situ quantitative phase imaging was conducted on live COS7 cells with a specific region irradiated by a confocal laser. The results demonstrated that 5-min continuous confocal laser irradiation affects only COS7 cells with fluorescently labeled mitochondria, causing mitochondrial dysfunction throughout the cell. These findings suggest that integrating FF-QPCM with a confocal laser scanning/imaging module offers a highly efficient, sensitive, and information-rich tool for cell biology research, with broad application potential.

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Publication Details

Journal
Journal of Biophotonics
Published
2025-03-07
DOI
https://doi.org/10.1002/jbio.202500010
Citations
1
Primary Topic
Advanced Fluorescence Microscopy Techniques
Type
article
Field-Weighted Citation Impact
1.63

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article

Confocal Laser Scanning Platform Combined With In Situ High‐Resolution Quantitative Phase Imaging

Peng Gao, Juanjuan Zheng, Hongfei Suo, Huaigang Cheng et al.
1 citations
Journal of Biophotonics
Advanced Fluorescence Microscopy Techniques
1.63
article

Confocal Laser Scanning Platform Combined With In Situ High‐Resolution Quantitative Phase Imaging

Peng Gao, Juanjuan Zheng, Hongfei Suo, Huaigang Cheng, Wenjing Feng, Yunze Lei, Sha An, Min Liu, Ying Ma
article en
1 citations

Abstract

This paper introduces an advanced dual-modality imaging platform by integrating a confocal laser scanning/imaging module with flat-fielding quantitative phase contrast microscopy (FF-QPCM). The platform enables phase/fluorescence dual-modality imaging of the same samples with high resolution and contrast. Using this platform, we observed that confocal fluorescence excitation causes minimal damage to cells, whereas wide-field fluorescence excitation (WFE) results in significant damage, particularly mitochondrial fragmentation and notable alterations in phase values. Additionally, in situ quantitative phase imaging was conducted on live COS7 cells with a specific region irradiated by a confocal laser. The results demonstrated that 5-min continuous confocal laser irradiation affects only COS7 cells with fluorescently labeled mitochondria, causing mitochondrial dysfunction throughout the cell. These findings suggest that integrating FF-QPCM with a confocal laser scanning/imaging module offers a highly efficient, sensitive, and information-rich tool for cell biology research, with broad application potential.

Journal of BiophotonicsVol. 18(6)
Ministry of Education of the People's Republic of China (CN), Xidian University (CN)
Key Research and Development Projects of Shaanxi Province
Openalex Percentile: Top 16%
Advanced Fluorescence Microscopy Techniques
1.63
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Confocal Laser Scanning Platform Combined With In Situ High‐Resolution Quantitative Phase Imaging — Peng Gao, Juanjuan Zheng, et al. · Journal of Biophotonics (2025) | TGRS Research Map | TGRS