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作 者:范月超[1] 冯力[1] 陈晨[1] 李中林[1] 谢满意[1] 苗发安[1]
机构地区:[1]徐州医学院附属医院神经外科,江苏徐州221002
出 处:《徐州医学院学报》2011年第10期654-657,共4页Acta Academiae Medicinae Xuzhou
基 金:基金项目:徐州市科技局科技计划项目(XM07C074)
摘 要:目的研究缺氧诱导因子-1a(HIF-1a)反义寡核苷酸(asODN)转染的树突状细胞(DC)与U251胶质瘤细胞融合后的抗胶质瘤活性。方法将HIF-1a asODN利用脂质体包裹转染DC,采用PEG化学融合方法将DC与U251胶质瘤细胞融合,通过MTT法及流式细胞仪检测胶质瘤细胞凋亡率。结果HIF-1a asODN转染DC组与各对照组相比细胞增殖下降,凋亡增加(P〈0.01)。结论HIF-1a asODN转染DC后,再与U251胶质瘤细胞融合能够比单纯使用HIF-1a asODN转染U251细胞或单纯使用DC细胞取得更好的抑制胶质瘤细胞生长及促进其凋亡的效果。Objective To antisense oligodeoxynucleotides (asODN) targeting hypoxia inducible factor - 1 a gene into dendritic cells (DC) , then fuse with glioma cell line U251 and to observe its effect of apoptosis inducing and growth restraining to U251 cells. Method The asODN targeting hypoxia inducible factor - 1a gene was transduced into DC by liposomes mediated transfection. Then the transduced DCs are fused with glioma cells. The growth of U251 cell was detected by 3 - (4,5 - dimethylthiazol - 2 - yl) - 2,5 - diphenyltetrazolium bromide (MTT) method. The change of cells apoptosis rate was measured by flow cytometry . Results MTT method revealed that the cell growth in the transfected group was inhibited most significantly (P 〈 0.01 ). Flow cytometry analysis revealed glioma cell line U251 suffered a more notable apoptosis than other group ( P 〈 0. 01 ). Conclusion After transduction of HIF - 1 a asODN into DC, the transduced DC can inhibited human glioma cell line U251 in vitro remarkably and the apoptosis of U251 cell can be induced significantly.
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