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顺铂对鼻咽癌细胞NKG2D配体表达和NK细胞杀伤活性的增强作用[J]. 肿瘤防治研究, 2009, 36(12): 996-998. DOI: 10.3971/j.issn.1000-8578.2009.12.002
引用本文: 顺铂对鼻咽癌细胞NKG2D配体表达和NK细胞杀伤活性的增强作用[J]. 肿瘤防治研究, 2009, 36(12): 996-998. DOI: 10.3971/j.issn.1000-8578.2009.12.002
Cisplatin Induces Up-regulation of NKG2D Ligands and Enhances Natural Killer Cell Lysis of Nasopharyngeal Carcinoma Cells[J]. Cancer Research on Prevention and Treatment, 2009, 36(12): 996-998. DOI: 10.3971/j.issn.1000-8578.2009.12.002
Citation: Cisplatin Induces Up-regulation of NKG2D Ligands and Enhances Natural Killer Cell Lysis of Nasopharyngeal Carcinoma Cells[J]. Cancer Research on Prevention and Treatment, 2009, 36(12): 996-998. DOI: 10.3971/j.issn.1000-8578.2009.12.002

顺铂对鼻咽癌细胞NKG2D配体表达和NK细胞杀伤活性的增强作用

Cisplatin Induces Up-regulation of NKG2D Ligands and Enhances Natural Killer Cell Lysis of Nasopharyngeal Carcinoma Cells

  • 摘要: 目的 研究顺铂(Cisplatin, DDP)作用前后人鼻咽癌细胞CNE2 NKG2D配体和HLA-Ⅰ类分子表达的改变及NK细胞杀伤活性的变化。 方法 MTT法测定DDP对CNE2细胞的50%抑制量(IC50);以此浓度DDP作用CNE2细胞24h,乳酸脱氢酶释放法检测效靶比20∶1时,NK细胞对DDP作用前后的CNE2细胞的杀伤活性;流式细胞仪检测DDP作用前后的CNE2细胞表面NKG2D配体(MICA/B、ULBP1、ULBP2、ULBP3)和HLA-Ⅰ类分子表达的变化。 结果 DDP对CNE2细胞的IC50为5mg/L。效靶比20∶1时,NK细胞对5mg/L DDP作用前后的CNE2细胞的杀伤活性分别为(38.11±1.41)%,(47.71±1.53)%,差异有统计学意义(P<0.05),DDP作用后CNE2细胞表面MICA/B、ULBP1、ULBP3表达显著升高,与作用前相比差异有统计学意义(P<0.05)。ULBP2、HLA-Ⅰ类分子无明显变化(P>0.05)。 结论 DDP能提高CNE2细胞NKG2D配体(MICA/B、ULBP1、ULBP3)的表达,从而增强CNE2细胞对NK细胞杀伤的敏感度。

     

    Abstract: Objective To explore the effects of Cisplatin(DDP) on the expression of NKG2D ligands and HLA-class Ⅰ molecules on human nasopharyngeal carcinoma cell line (CNE2) and natural killer (NK)cells cytotoxicity. Methods The IC50 of DDP against CNE2 cells were measured by MTT assay. Cytotoxicities of NK cells isolated from 3 healthy volunteers against CNE2 cells before and after cultured by DDP were analyzed by LDH releasing assay at effector-to-target cell ratio(E∶T) of 20∶1. The expression of NKG2D ligands(MICA/B, ULBP1, ULBP2, ULBP3), HLA-classⅠmolecules before and after treated by DDP were assayed by flow cytometery. Results DDP could decrease the proliferation and survival rate of CNE2 cells. The IC50 was 5mg/L. The cytotoxicity of NK cells against CNE2 cells cultured by DDP was significantly enhanced. The expression of NKG2D ligands(MICA/B, ULBP1, ULBP3) of CNE2 cells were up-expressed after cultured with DDP. There were no significant difference of expression of ULBP2 and HLA-classⅠmolecules before and after treated by DDP(P>0.05). Conclusion The results indicate that DDP up-regulated the expressions of MICA/B, ULBP-1, ULBP-3, which enhanced the susceptibility of CNE2 cells to natural killer cell-mediated lysis.

     

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