Inhibition of NF-kappa B can enhance Fas-mediated apoptosis in leukemia cell line HL-60.

Frontiers of medicine in China Pub Date : 2010-09-01 Epub Date: 2010-04-24 DOI:10.1007/s11684-010-0026-5
Li Wang, Shi Zhao, Hong-Xiang Wang, Ping Zou
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引用次数: 6

Abstract

This study explored the effects of nuclear factor-kappa B (NF-κB) inhibitor Bay 11-7082 on Fas/FasL system and Fas-mediated apoptosis in cell line HL-60 cells. The mRNA and protein levels of Fas, FasL, and X-linked inhibitor of apoptosis protein (XIAP) were detected by reverse transcription-polymerase chain reaction (RT-PCR) and flow cytometry (FCM); the level of sFasL was evaluated by enzyme-linked immunosorbent assay (ELISA); and apoptosis was determined by FCM. After treatment with Bay 11-7082, the mRNA and protein levels of FasL and XIAP in HL-60 cells were significantly lower than in the controls (P<0.05), but the mRNA and protein levels of Fas and sFasL did not change significantly (P>0.05). Apoptotic rate of HL-60 cells treated with Bay 11-7082 was significantly higher than in the controls (P<0.05). Therefore, we conclude that Bay 11-7082 can enhance Fas-mediated apoptosis in HL-60 cells by downregulating FasL and XIAP levels.

抑制nf - κ B可促进fas介导的白血病HL-60细胞凋亡。
本研究探讨核因子κB (NF-κB)抑制剂Bay 11-7082对HL-60细胞Fas/FasL系统及Fas介导的细胞凋亡的影响。采用逆转录聚合酶链式反应(RT-PCR)和流式细胞术(FCM)检测Fas、FasL和x -连锁凋亡抑制蛋白(XIAP) mRNA和蛋白水平;采用酶联免疫吸附法(ELISA)检测血清sFasL水平;流式细胞仪检测细胞凋亡。经Bay 11-7082处理后,HL-60细胞中FasL和XIAP的mRNA和蛋白水平均显著低于对照组(P0.05)。Bay 11-7082处理后HL-60细胞的凋亡率显著高于对照组(P
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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