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由乙肝病毒X蛋白通过核因子κB途径介导的死亡受体5(DR5)表达增强,与肿瘤坏死因子-α相关凋亡诱导配体(TRAIL)诱导的肝癌细胞凋亡有关。

The enhanced expression of death receptor 5 (DR5) mediated by HBV X protein through NF-kappaB pathway is associated with cell apoptosis induced by (TNF-α related apoptosis inducing ligand) TRAIL in hepatoma cells.

作者信息

Kong Fanyun, You Hongjuan, Zhao Jinjin, Liu Wen, Hu Lei, Luo Wenya, Hu Wei, Tang Renxian, Zheng Kuiyang

机构信息

Department of Pathogenic Biology and Immunology, Laboratory of Infection and Immunity, Xuzhou Medical College, 209 Tongshan Road, Xuzhou, Jiangsu, 221004, China.

出版信息

Virol J. 2015 Nov 17;12:192. doi: 10.1186/s12985-015-0416-z.

Abstract

BACKGROUND

HBV X protein (HBX) is associated with cell apoptosis mediated by TNF-α related apoptosis inducing ligand (TRAIL), while the role of HBX on the expressions of TRAIL receptors death receptor 4 (DR4) and DR5 are unclear. In this study, we detected the cell apoptosis induced by TRAIL as well as gene and protein expressions of DR4 and DR5 in Huh-7 cells steadily transfected with HBX (Huh-7-HBX cells). In addition, we investigated the activation of different pathways associated with the expressions of TRAIL receptors in Huh-7-HBX cells.

METHODS

The apoptosis of Huh-7-HBX cells induced by TRAIL was evaluated by flow cytometry analysis. The levels of DR4 and DR5 expression in cells were determined by real-time PCR and western blotting analysis. The activities of JNK pathway and NF-kappaB (NF-κB) pathway were demonstrated by western blotting assay.

RESULTS

Compared to control cells, the percentage of cell apoptosis was increased in Huh-7-HBX cells. The increased expressions of DR4 and DR5 on gene and protein levels were observed in Huh-7-HBX cells. Further researches suggested that activation of JNK pathway was increased but not involved in the expression of TRAIL receptors in HBX positive cells. The activation of NF-κB pathway increased and was responsible for DR5 expression and cell apoptosis in HBX positive cells.

CONCLUSIONS

These results demonstrate that increased apoptosis induced by TRAIL is associated with increased expression of DR5 that mediated by HBX through NF-κB pathway. This finding provides a critical insight into the mechanism of hepatocyte apoptosis mediated by HBX in HBV infection.

摘要

背景

乙肝病毒X蛋白(HBX)与肿瘤坏死因子-α相关凋亡诱导配体(TRAIL)介导的细胞凋亡有关,而HBX对TRAIL受体死亡受体4(DR4)和DR5表达的作用尚不清楚。在本研究中,我们检测了TRAIL诱导的细胞凋亡以及稳定转染HBX的Huh-7细胞(Huh-7-HBX细胞)中DR4和DR5的基因及蛋白表达。此外,我们研究了Huh-7-HBX细胞中与TRAIL受体表达相关的不同信号通路的激活情况。

方法

通过流式细胞术分析评估TRAIL诱导的Huh-7-HBX细胞凋亡。通过实时定量PCR和蛋白质印迹分析确定细胞中DR4和DR5的表达水平。通过蛋白质印迹法检测JNK通路和核因子κB(NF-κB)通路的活性。

结果

与对照细胞相比,Huh-7-HBX细胞的凋亡百分比增加。在Huh-7-HBX细胞中观察到DR4和DR5在基因和蛋白水平上的表达增加。进一步研究表明,JNK通路的激活增加,但不参与HBX阳性细胞中TRAIL受体的表达。NF-κB通路的激活增加,并负责HBX阳性细胞中DR5的表达和细胞凋亡。

结论

这些结果表明,TRAIL诱导的凋亡增加与HBX通过NF-κB通路介导的DR5表达增加有关。这一发现为乙肝病毒感染中HBX介导的肝细胞凋亡机制提供了重要的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9ff/4650207/e6f4ec66da02/12985_2015_416_Fig1_HTML.jpg

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