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Effect of Gene Transfer of Tumor Necrosis Factor Receptors into Human Lung Carcinoma Cell Line

机译:肿瘤坏死因子受体基因转移到人肺癌细胞株中的作用

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摘要

The human lung adenocarcinoma cell line A549 is known to be resistant to tumor necrosis factor alpha (TNF‐α)‐mediated tumor cell lysis in spite of the expression of 55 kDa TNF receptor (TNF‐R55) mRNA and its cell surface protein. In this study, we investigated the mechanism of TNF‐α resistance and the role of two types of TNF receptors (TNF‐R55 and TNF‐R75 (75 kDa TNF receptor)). TNF‐R55 or TNF‐R75 cDNA was transfected into A549 cells. In addition, a C‐terminal deletion mutant of TNF‐R75 which lacks the intracellular domain of TNF‐R75 was also transfected into A549 cells. We assessed the TNF‐α‐mediated tumor cell lysis of these transfected clones, and found that the cytotoxic effect increased in transfected clones highly expressing TNF‐R55, but not in low‐expression clones. As for TNF‐R75, the cytotoxic effect of TNF‐α was observed in TNF‐R75‐transfected clones even when expression was low. Furthermore, the cytotoxic effect was also observed in clones transfected with the deletion mutant of TNF‐R75, as well as the complete TNF‐R75. These results indicate that a certain level of expression of TNF‐R55 is necessary for obtaining TNF‐α‐mediated tumor cell lysis in the absence of TNF‐R75. On the other hand, the expression of TNF‐R75 strongly induces TNF‐α‐mediated cytotoxicity through TNF‐R55 in the absence of an intracellular signal via TNF‐R75.
机译:尽管存在55 kDa TNF受体(TNF-R55)mRNA及其细胞表面蛋白的表达,但已知人肺腺癌细胞A549对肿瘤坏死因子α(TNF-α)介导的肿瘤细胞裂解具有抗性。在这项研究中,我们研究了TNF-α抵抗的机制以及两种类型的TNF受体(TNF-R55和TNF-R75(75 kDa TNF受体)的作用。 TNF-R55或TNF-R75 cDNA被转染到A549细胞中。此外,缺少TNF-R75胞内结构域的TNF-R75的C端缺失突变体也被转染到A549细胞中。我们评估了这些转染克隆的TNF-α介导的肿瘤细胞裂解,发现在高表达TNF-R55的转染克隆中细胞毒性作用增强,而在低表达克隆中则没有。至于TNF-R75,即使表达水平低,在TNF-R75转染的克隆中也观察到TNF-α的细胞毒性作用。此外,在转染了TNF-R75缺失突变体的克隆以及完整的TNF-R75中也观察到了细胞毒性作用。这些结果表明,在不存在TNF-R75的情况下,获得TNF-α介导的肿瘤细胞裂解需要一定水平的TNF-R55表达。另一方面,在没有通过TNF-R75的细胞内信号的情况下,TNF-R75的表达通过TNF-R55强烈诱导TNF-α介导的细胞毒性。

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