期刊名称：Proceedings of the National Academy of Sciences
印刷版ISSN：0027-8424
电子版ISSN：1091-6490
出版年度：2022
卷号：119
期号：8
DOI：10.1073/pnas.2118068119
语种：English
出版社：The National Academy of Sciences of the United States of America
摘要：Significance
This article demonstrates a high-throughput technique to map cell images to cell positions. The technology uses a three-dimensional (3D) imaging flow cytometer to record multiparameter 3D cell images at a throughput of 1,000 cells/s and a cell placement robot to place the exiting cells from the imaging system on a filter plate in a first-in–first-out manner so the cells on the plate have the same order as the cells that are imaged. Innovative algorithms were developed to match the cell sequences from the imaging and placement modules to detect and eliminate errors to ensure high accuracy. The technology forms an unprecedented bridge between single-cell molecular analysis and single-cell image analysis to connect phenotype and genotype analysis with single-cell resolution.
We develop a high-throughput technique to relate positions of individual cells to their three-dimensional (3D) imaging features with single-cell resolution. The technique is particularly suitable for nonadherent cells where existing spatial biology methodologies relating cell properties to their positions in a solid tissue do not apply. Our design consists of two parts, as follows: recording 3D cell images at high throughput (500 to 1,000 cells/s) using a custom 3D imaging flow cytometer (3D-IFC) and dispensing cells in a first-in–first-out (FIFO) manner using a robotic cell placement platform (CPP). To prevent errors due to violations of the FIFO principle, we invented a method that uses marker beads and DNA sequencing software to detect errors. Experiments with human cancer cell lines demonstrate the feasibility of mapping 3D side scattering and fluorescent images, as well as two-dimensional (2D) transmission images of cells to their locations on the membrane filter for around 100,000 cells in less than 10 min. While the current work uses our specially designed 3D imaging flow cytometer to produce 3D cell images, our methodology can support other imaging modalities. The technology and method form a bridge between single-cell image analysis and single-cell molecular analysis.
