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作 者:李超[1] 石芳琼[1] 杨丹[1] 王洁[2] 翦新春[1] 蒋灿华[1]
机构地区:[1]中南大学湘雅医院口腔颌面外科 [2]中南大学湘雅医学院免疫学系,长沙410078
出 处:《华西口腔医学杂志》2012年第1期32-35,共4页West China Journal of Stomatology
基 金:国家自然科学基金资助项目(30772437);湖南省科技计划一般基金资助项目(06sk3026,06sk3044)
摘 要:目的探讨口腔鳞癌细胞过表达MHC-Ⅰ类链相关蛋白A(MICA)对自然杀伤细胞(NK)与细胞毒性T淋巴细胞(CTL)杀伤活性的影响。方法通过绘制细胞生长曲线、检测细胞周期、进行平板集落形成率及裸鼠皮下成瘤等方法对稳定转染并过表达MICA的口腔鳞癌细胞株进行生物学特性鉴定。采用乳酸脱氢酶释放法及流式细胞术分析口腔鳞癌细胞过表达MICA对NK与CTL细胞杀伤活性及自然杀伤细胞2族成员D(NKG2D)受体表达的影响。结果口腔鳞癌细胞转染MICA基因后主要生物学特性未发生改变,但能显著增强NK与CTL细胞杀伤活性并上调其表面NKG2D的表达,与未转染及转染空白载体的细胞比较,差异有统计学意义(P<0.05)。结论 MICA可作为口腔鳞癌免疫基因治疗的潜在靶标,值得进一步研究。Objective To investigate the effect on natural killer (NK) and cytotoxic T lymphocyte (CTL)-mediated cytotoxicity by genetic overexpression of MHC class I chain-related protein A (MICA) in oral squamous cell carcinoma (OSCC). Methods The OSCC cells by genetic overexpression of MICA were detected to identify the biological features including cell growth curve, cell cycle distribution, plate clone forming rate and tumorigenicity in nude mice. The expression of natural killer group 2, member D (NKG2D) receptor and the cytotoxicity to target tumor cells of NK92 and CTL cells, which co-cultured with the transfected OSCC cells or the non-transfeeted or blank vector-transfected controls, were measured by flow cytometry and lactate dehydrogenase(LDH) release assay. Results There was no dif- ference in biological features before and after MICA gene transfection to OSCC cells. Flow cytometry and LDH release assay showed that MICA-overexpressed OSCC cells enhanced the eytotoxicity to target tumor cells and up-regulated the expression of NKG2D on NK92 and CTL(P〈0.05). Conclusion MICA may be considered as a promising immunotherapy target of OSCC.
关 键 词:口腔 鳞状细胞癌 MHC-Ⅰ类链相关蛋白A 杀伤活性 基因治疗
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