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NK细胞杀伤人胶质瘤起始细胞的体外研究

Studies on Cytotoxicity of Natural Killer (NK) Cells against Glioma Initiating Cells in Vitro
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摘要 背景与目的:越来越多的证据支持人脑胶质瘤来源于胶质瘤起始细胞/干细胞(glioma initiating cell/stem cell,GIC/GSC)的假说,鉴于干细胞特性,常规手术和放化疗难以清除GIC,本研究试图用体外活化的自然杀伤(natural killer,NK)细胞对GIC细胞进行杀伤研究。方法:以体外长期培养于干细胞培养基的CD133阳性胶质瘤细胞作为GIC,用免疫磁珠从胶质瘤患者(或健康人)的外周血中分离NK细胞,常规IL2/PHA活化NK细胞后,应用LDH释放法检测其体外杀伤GIC细胞的活性,以K562细胞为阳性对照。结果:体外实验中,异体NK细胞可以在GIC的培养基里生长和活化,且其杀伤GIC细胞的能力随效靶比增高而增强,同一效靶比时,活化的NK细胞杀伤GIC细胞的活性明显高于未活化(静止)NK细胞的活性(P<0.01)。结论:异体NK细胞可以在GIC的培养环境中活化并表现出针对GIC的杀伤能力,为NK细胞用于脑胶质瘤起始细胞的临床清除提供可能性。 BACKGROUND & OBJECTIVE:There are increasing evidence to support the hypothesis that human gliomas originated fi'om glioma initiating cells or stem cells (GIC/GSC). These cells can not be eradicated by conventional surgeu, chemotherapy and radiotherapy because of their "stem-like" properties. In this study, the cytotoxicity of activated natural killer (NK) cells against GIC in vitro was investigated. METHODS : NK cells were isolated from peripheral blood monormelear cells of glioma patients or heahhy donors by Miltenyi magnetic beads, and were activated with IL2/PHA. Their in vitro cytotoxicity against GIC was assessed by lactate dehydrogenase (LDH) assay. RESULT: The allogeneic NK cells were vital and cotdd be activated with GIC-cuhured medium. Increased cytolytie activity against GIC was obsep,ed with the higher E:T ratio. At the same E:T ratio, activated NK cells showed remarkable higher cytolytic activity against GIC than that of resting NK cells. CONCLUSIONS : Allogeneic NK cells demonstrate killing effect against GIC. It is suggested that activated NK cells may be promising to eradicate GIC.
出处 《中国神经肿瘤杂志》 2009年第4期227-230,共4页 Chinese Journal of Neuro-Oncology
基金 国家自然科学基金(Νο.30772551)
关键词 活化NK细胞 胶质瘤起始细胞/干细胞 细胞杀伤 LDH实验 Activating NK cell GIC/GSC Cytotoxicity LDH assay
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  • 1Anhua Wu,Steve Wiesner,Jing Xiao,Katya Ericson,Wei Chen,Walter A. Hall,Walter C. Low,John R. Ohlfest. Expression of MHC I and NK ligands on human CD133+ glioma cells: possible targets of immunotherapy[J] 2007,Journal of Neuro - Oncology(2):121~131

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