Light-field flow cytometry for high-resolution, volumetric and multiparametric 3D single-cell analysis

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作者
Xuanwen Hua
Keyi Han
Biagio Mandracchia
Afsane Radmand
Wenhao Liu
Hyejin Kim
Zhou Yuan
Samuel M. Ehrlich
Kaitao Li
Corey Zheng
Jeonghwan Son
Aaron D. Silva Trenkle
Gabriel A. Kwong
Cheng Zhu
James E. Dahlman
Shu Jia
机构
[1] Georgia Institute of Technology and Emory University,Wallace H. Coulter Department of Biomedical Engineering
[2] Parker H. Petit Institute for Bioengineering and Biosciences,Department of Chemical Engineering
[3] Georgia Institute of Technology,undefined
[4] Georgia Institute of Technology,undefined
[5] Georgia W. Woodruff School of Mechanical Engineering,undefined
[6] Georgia Institute of Technology,undefined
来源
Nature Communications | / 15卷
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摘要
Imaging flow cytometry (IFC) combines flow cytometry and fluorescence microscopy to enable high-throughput, multiparametric single-cell analysis with rich spatial details. However, current IFC techniques remain limited in their ability to reveal subcellular information with a high 3D resolution, throughput, sensitivity, and instrumental simplicity. In this study, we introduce a light-field flow cytometer (LFC), an IFC system capable of high-content, single-shot, and multi-color acquisition of up to 5,750 cells per second with a near-diffraction-limited resolution of 400-600 nm in all three dimensions. The LFC system integrates optical, microfluidic, and computational strategies to facilitate the volumetric visualization of various 3D subcellular characteristics through convenient access to commonly used epi-fluorescence platforms. We demonstrate the effectiveness of LFC in assaying, analyzing, and enumerating intricate subcellular morphology, function, and heterogeneity using various phantoms and biological specimens. The advancement offered by the LFC system presents a promising methodological pathway for broad cell biological and translational discoveries, with the potential for widespread adoption in biomedical research.
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