Abstract
Cell–cell fusion is an important biological and pathological event. There are limited techniques for studying both the process of cell–cell fusion and the fate of fused cells. We have developed a non-invasive assay for the temporal analysis of cell–cell fusion, quantification of fused cells, and isolation of fused cells. Briefly, cells are transfected with either the T7 bacteriophage RNA polymerase, or yellow fluorescent protein (YFP) driven by a T7 specific promoter. Cells are mixed and induced to fuse. When cells expressing T7 RNA polymerase and T7 promoter driven YFP (T7-YFP) fuse and the cellular contents mix, the YFP is expressed. These YFP-positive cells can be detected with a fluorescent microscope, quantified by flow cytometry, or collected using fluorescence associated cell sorting. Isolated YFP-positive cells can be monitored to determine the fate of fused cells, specifically for the rates of growth, transformation, and changes in chromosome number.
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Acknowledgments
This work was funded by OCAST Grant HR03-014; The Mary Kay Ash Foundation, and NIH grant P20 RR017703.
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Hu, L., Plafker, K., Henthorn, J. et al. A non-invasive technique for quantifying and isolating fused cells. Cytotechnology 58, 113–118 (2008). https://doi.org/10.1007/s10616-009-9186-z
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DOI: https://doi.org/10.1007/s10616-009-9186-z