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γ干扰素可增强肿瘤坏死因子所引起的DNA片段化和细胞毒性。

DNA fragmentation and cytotoxicity caused by tumor necrosis factor is enhanced by interferon-gamma.

作者信息

Dealtry G B, Naylor M S, Fiers W, Balkwill F R

出版信息

Eur J Immunol. 1987 May;17(5):689-93. doi: 10.1002/eji.1830170517.

Abstract

Recombinant human tumor necrosis factor (rhuTNF) induced DNA fragmentation in sensitive cell lines. This fragmentation was similar to that caused by lymphotoxin-containing cytotoxic T cell culture supernatants. The percentage of DNA cleaved correlated with the degree of cell growth inhibition shown by individual cell lines. DNA fragmentation was first seen after 12 h treatment, and increased slowly with time. The presence of 100 microM ZnSO4 inhibited the rhuTNF-induced DNA cleavage in MCF-7 cells. Recombinant interferon-gamma (rhuIFN-gamma) did not induce DNA cleavage, although it reduced the growth of all the cell lines used in this study. However, it interacted with rhuTNF to produce a doubling in the percentage of DNA fragmentation, and increased cytotoxicity in rhuTNF-sensitive cell lines. Pretreatment with rhuIFN-gamma for 1 h prior to rhuTNF treatment also enhanced DNA fragmentation and cell killing.

摘要

重组人肿瘤坏死因子(rhuTNF)可诱导敏感细胞系中的DNA片段化。这种片段化与含淋巴毒素的细胞毒性T细胞培养上清液所引起的片段化相似。DNA裂解的百分比与各个细胞系所表现出的细胞生长抑制程度相关。DNA片段化在处理12小时后首次出现,并随时间缓慢增加。100微摩尔硫酸锌的存在可抑制MCF-7细胞中rhuTNF诱导的DNA裂解。重组干扰素-γ(rhuIFN-γ)虽可降低本研究中所用所有细胞系的生长,但不会诱导DNA裂解。然而,它与rhuTNF相互作用,使DNA片段化的百分比加倍,并增加了rhuTNF敏感细胞系中的细胞毒性。在rhuTNF处理前用rhuIFN-γ预处理1小时也可增强DNA片段化和细胞杀伤作用。

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