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首页> 外文期刊>Japanese Journal of Cancer Research >Reinforced cytotoxicity of lymphokine-activated killer cells toward glioma cells by transfection of the killer cells with the gamma-interferon gene.
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Reinforced cytotoxicity of lymphokine-activated killer cells toward glioma cells by transfection of the killer cells with the gamma-interferon gene.

机译:通过用γ-干扰素基因转染杀伤细胞,淋巴因子激活的杀伤细胞对神经胶质瘤细胞的细胞毒性增强。

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摘要

Lymphokine-activated killer (LAK) cells generated from peripheral blood lymphocytes incubated with recombinant interleukin-2 were transfected with the human gamma-interferon (HuIFN-gamma) gene by means of liposomes having a positive charge on their surface. The cells secreted significant amounts of HuIFN-gamma (reaching more than 5 U/ml) into the culture medium. The HuIFN-gamma produced by the cells induced intercellular adhesion molecule-1 (ICAM-1) and enhanced the expression of Fas antigen on the surface of human glioma cells. Also, LAK cells transfected with HuIFN-gamma gene exhibited reinforcement of cytotoxicity toward human glioma cell lines (U251-MG and SK-MG-1). Furthermore, the reinforcement was significantly quenched by anti-ICAM-1 and/or anti-TNF-alpha monoclonal antibody.
机译:由人γ干扰素(HuIFN-γ)基因通过在其表面具有正电荷的脂质体转染由与重组白介素2孵育的外周血淋巴细胞产生的淋巴因子激活的杀伤(LAK)细胞。细胞向培养基中分泌大量的HuIFN-γ(达到5U / ml以上)。细胞产生的HuIFN-γ诱导细胞间粘附分子-1(ICAM-1)并增强人胶质瘤细胞表面Fas抗原的表达。同样,用HuIFN-γ基因转染的LAK细胞表现出对人神经胶质瘤细胞系(U251-MG和SK-MG-1)的细胞毒性增强。此外,通过抗ICAM-1和/或抗TNF-α单克隆抗体显着淬灭了增强物。

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