Cao Yan, Duan Lianning, Lu Chengrong, Luo Yuan, Xiang Peide, Yan Shu, Ge Shujing, Zhang Yanjun
Graduate Department, Hebei North University, Zhangjiakou 075000, China.
Nan Fang Yi Ke Da Xue Xue Bao. 2012 Sep;32(9):1245-9.
To investigate the apoptosis of NK cells induced by the erythroleukemia cell line K562 in vitro.
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.
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.
K562 cells can induce the apoptosis of activated NK cells, which is one of the probable mechanisms of immune escape of tumors.
研究红白血病细胞系K562在体外诱导自然杀伤(NK)细胞凋亡的情况。
通过磁珠分选法从健康供者外周血中分离出原代NK细胞,用含重组人白细胞介素-2(rhIL-2)的干细胞培养基进行培养。将NK细胞与K562细胞按不同的效靶比混合并共培养不同时间。采用PE-AnnexinV/7-AAD标记和流式细胞术检测NK细胞和K562细胞的凋亡情况。
分离出的NK细胞纯度达到(93.99±4.22)%。在相同效靶比下,K562细胞诱导的NK细胞凋亡率随时间显著增加。随着效靶比降低,NK细胞凋亡率升高,其对K562细胞的细胞毒活性减弱。
K562细胞可诱导活化的NK细胞凋亡,这可能是肿瘤免疫逃逸的机制之一。