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Updated: May 18, 2026

A Flow Cytometry-Based Cytotoxicity Assay for the Assessment of Human NK Cell Activity
Published on: August 9, 2017
[K562 cells induces apoptosis of activated NK cells in vitro]
Yan Cao1, Lianning Duan, Chengrong Lu
1Graduate Department, Hebei North University, Zhangjiakou 075000, China. cao.yan.happy@163.com
Objective:
To investigate the apoptosis of NK cells induced by the erythroleukemia cell line K562 in vitro.
Methods:
Primary NK cells isolated from the peripheral blood of healthy donors by magnetic-activated cell sorting were cultured with stem cell medium containing recombinant human interleukin-2 (rhIL-2). The NK cells and K562 cells were mixed and co-cultured at different E:T ratios for different time lengths. The apoptosis of NK cells and K562 cells were detected using PE-AnnexinV/7-AAD labeling and flow cytometry.
Results:
The purity of isolated NK cells reached (93.99∓4.22)%. At the same E: T ratio, the apoptotic rate of NK cells induced by K562 cells increased significantly with time. As the E:T ratio reduced, the apoptotic rate of the NK cells increased and their cytotoxic activity against K562 cells was attenuated.
Conclusion:
K562 cells can induce the apoptosis of activated NK cells, which is one of the probable mechanisms of immune escape of tumors.
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