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干扰素-γ调节人结肠癌细胞中TRAIL介导的细胞凋亡。

Interferon-gamma modulates TRAIL-mediated apoptosis in human colon carcinoma cells.

作者信息

Langaas V, Shahzidi S, Johnsen J I, Smedsrød B, Sveinbjørnsson B

机构信息

Department of Experimental Pathology, University of Tromsø, Norway.

出版信息

Anticancer Res. 2001 Nov-Dec;21(6A):3733-8.

Abstract

BACKGROUND

Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) is expressed by immune cells and has been shown to play an important role in tumor surveillance due to its ability to induce apoptosis in various transformed cells. Interferon gamma (IFN-gamma), a multipotent cytokine with broad stimulatory effects on anti-tumoral immune reactions, may exert its cytotoxic activity directly on tumor cells or indirectly via stimulation of effector cells. This study was designed to determine the effect of IFN-gamma on TRAIL-mediated apoptosis in human colon carcinoma cell lines.

MATERIALS AND METHODS

Cytotoxicity was assessed by MTT-assay. Expression of death receptors was measured by reverse transcriptase polymerase chain reaction. Apoptosis was assessed by caspase-8 immunoblot, DNA fragmentation and morphological studies.

RESULTS

Treatment with TRAIL resulted in detectable cytotoxicity within 5 hours and was enhanced in a dose-dependent manner. When cells were pretreated with IFN-gamma, the cytotoxic effect of TRAIL increased significantly. Treated cells showed a typical apoptotic morphology that was accompanied by internucleosomal cleavage of DNA. Up-regulation of caspase-8 expression and activation were detected as a result of pretreatment with IFN-gamma and subsequent apoptosis mediated by TRAIL.

CONCLUSION

Our results demonstrated that IFN-gamma sensitises human colon carcinoma cells to TRAIL-mediated apoptosis, partly by elevated caspase-8 expression.

摘要

背景

肿瘤坏死因子相关凋亡诱导配体(TRAIL)由免疫细胞表达,由于其能够诱导各种转化细胞凋亡,已被证明在肿瘤监测中发挥重要作用。干扰素γ(IFN-γ)是一种对抗肿瘤免疫反应具有广泛刺激作用的多能细胞因子,它可能直接对肿瘤细胞发挥细胞毒活性,或通过刺激效应细胞间接发挥作用。本研究旨在确定IFN-γ对人结肠癌细胞系中TRAIL介导的凋亡的影响。

材料与方法

通过MTT法评估细胞毒性。通过逆转录聚合酶链反应测量死亡受体的表达。通过半胱天冬酶-8免疫印迹、DNA片段化和形态学研究评估凋亡。

结果

用TRAIL处理在5小时内导致可检测到的细胞毒性,并呈剂量依赖性增强。当细胞用IFN-γ预处理时,TRAIL的细胞毒性作用显著增加。处理后的细胞呈现典型的凋亡形态,并伴有DNA的核小体间切割。检测到由于用IFN-γ预处理以及随后由TRAIL介导的凋亡导致半胱天冬酶-8表达上调和激活。

结论

我们的结果表明,IFN-γ使人类结肠癌细胞对TRAIL介导的凋亡敏感,部分原因是半胱天冬酶-8表达升高。

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