IFNγ基因修饰的骨髓基质细胞体外抗白血病作用的实验研究
基因治疗,,Ad,hIFNγ;骨髓基质细胞;基因治疗;IFNγ,1材料与方法,2结果,3讨论,参考文献:
摘要:目的 研究重组人IFNγ腺病毒(Ad/hIFNγ)在CML病人骨髓基质细胞(BMSCs)中的转染效率、IFNγ表达,并进一步观察转染Ad/hIFNγ的骨髓基质细胞体外抗白血病细胞株K562增殖和诱导K562细胞凋亡的作用。 方法 以Ad/hIFNγ重组腺病毒按感染复数(MOI)为50转染CML病人骨髓基质细胞,RTPCR、ELISA及Western blot分别检测转染Ad/hIFNγ的人骨髓基质细胞(BMSCs)中IFNγ mRNA和IFNγ的表达;转染Ad/hIFNγ的骨髓基质细胞与K562细胞共培养,通过绘制K562细胞生长曲线分析其对K562细胞增殖的影响;并进一步通过流式细胞学分析其对K562细胞周期的影响和诱导凋亡的作用。结果 RTPCR、Western blot及ELISA方法都分别检测到转染Ad/hIFNγ的人骨髓基质细胞(BMSCs)中IFNγ mRNA和IFNγ的表达;与对照组相比,转染Ad/hIFNγ的人骨髓基质细胞的实验组具有明显的抑制K562细胞增殖的作用(P=0.000),在细胞周期G1期的K562细胞比例明显增加,而S期K562细胞比例显著下降(P<0.01),并显著诱导K562细胞的凋亡(P<0.01)。结论 Ad/hIFNγ转染人骨髓基质细胞后可获得IFNγ有效的表达,并在体外能有效地发挥抗白血病细胞作用。关键词:Ad/hIFNγ;骨髓基质细胞;基因治疗;IFNγ
In vitro antileukemic effects of bone marrow stromal cells modified with Ad/hIFNγ
LI Xiaoqing, HUANG Wenlin, XU Haipeng, CHEN Xiaoqin, GENG Qirong, LU Yue
(1. Cancer Prevention Center, Sun Yatsen University, Guangzhou 510060,China; 2. Laboratory Department, Cancer Prevention Center/State Key Laboratory of Cancer Prevention , Sun Yatsen University, Guangzhou 510060,China)
Abstract: Objective This study was designed to explore the efficiency of recombinant adenovirusmediated human Gamma Interferon (hIFNγ) gene transferred into BMSCs and the expression of IFNγ in vitro. We further studied the antiproliferation and induction of apoptosis effects on the human leukemia cell line K562 cells by Ad/hIFNγ transduced BMSCs in vitro. Methods On transduction of BMSCs by Ad/hIFNγ at a MOI of 50, we detected the expression of IFNγ mRNA and IFNγ by RTPCR, cell immunohistochemical staining, ELISA and Western blot. After incubation of K562 cells with Ad/hIFNγ transduced BMSCs, The cellular proliferation of K562 cells was determined by the growth curve and MTT assay. Apoptosis and cell cycle status of K562 cells were analyzed by flow cytometry. Results We can detect the expression of IFNγ mRNA and IFNγ by RTPCR, cell immunohistochemical staining, ELISA and Western blot. Ad/hIFNγ transduced BMSCs markedly inhibited the proliferation of K562 cells compared with control groups after incubation with K562 cells (P=0.000). As compared with control groups, the percentage of K562 cells in the G1 phase of cell cycle can be increased by treatment of hIFNγ produced by Ad/hIFNγ transduced BMSCs, but the percentage of K562 cells in the S phase of cell cycle can be decreased in the same time (P<0.01, student ttest). The apoptosis effects can be induced by Ad/hIFNγ transduced BMSCs (P<0.01, student ttest). Conclusion on transduction of BMSCs by Ad/hIFNγ, IFNγ expression can be acquired and local production of IFNγ showed antileukemic effects in vitro. ......
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