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作 者:王磊[1] 王辉[1] 宋军[1] 李慧忠 李连涛 郑骏年 徐为[1]
机构地区:[1]徐州医学院附属医院胃肠外科,江苏221002 [2]江苏省肿瘤生物治疗重点实验室
出 处:《中华实验外科杂志》2012年第9期1756-1758,共3页Chinese Journal of Experimental Surgery
摘 要:目的观察增殖细胞核抗原(PCNA)表佗肽融合白细胞介素18(IL-18)基㈥的树突状细胞(1)Cs)刺激的T淋巴细胞对结肠癌细胞凋亡的影响。方法实验分为DCs组、空载体组、PCNA表佗肽组、PCNA表化肽融合IL-18基因组。将空质粒(plRES—EGFP)、PCNA表位肽质粒[pIRES—EGFP-PCNA(6)]和PCNA表位肽融合IL-18基因质粒[pIRES—EGFP—PCNA(6)/IL-18]分别转染DCs。Objective To investigate the apoptosis of colonic cancer cells co-cultured with T lym- phocytes induced by dendritic cells modified by proliferating cell nuclear antigen (PCNA)-Epitope and inter- leukin-18 (IL-18) genes. Methods The experiment was divided into four groups, including DCs group, empty vector group, PCNA-Epitope transfection group, and PCNA-Epitope plus IL-18 gene group. Every group was operated according to DCs vs. T ratio (1: 10). The empty vector plasmid (plRES-EGFP), PCNA-Epitope plasmid [ plRES-EGFP-PCNA(6) ] and plasmid loaded with PCNA-Epitope and IL-18 gene plRES-EGFP-PCNA(6)/IL-18 ] were transfeeted into peripheral blood-derived dendritic cells by non-lip- id polymer-based reagent, then co-euhured with T lymphoeytes, respectively. The supernatants of immuno- cytes were cultured with colonic cancer cells according to the ratio of T lymphoeytes vs. colonic cancer cells (5:1, 10:1, 20:1, 40:1 ). The apoptosis of colonic cancer cells was examined by using flow eytometry. Results The apoptosis of colonic cancer (:ells couht be induced in every group. The apoptosis in the plRES-EGFP-PCNA (6)/IL-18 group was significantly higher than in DCs group, empty vector group, and PCNA-Epitope transtetion group. The optimal ratio of T lymphoeytes vs. colonic cancer (;ells was 40: 1. Conclusion The supernatants of T lymphocytes induced by DCs that were treated with the PCNA-Epitope and 1L-18 gene can induce apoptosis of more colonic cancer cells.
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