Interferon alpha regulates MAPK and STAT1 pathways in human hepatoma cells

被引:23
|
作者
Zhao, Lan-Juan [1 ]
Hua, Xian [1 ]
He, Sheng-Fei [1 ]
Ren, Hao [1 ]
Qi, Zhong-Tian [1 ]
机构
[1] Second Mil Med Univ, Dept Microbiol, Shanghai Key Lab Med Biodef, Shanghai, Peoples R China
来源
VIROLOGY JOURNAL | 2011年 / 8卷
基金
中国国家自然科学基金;
关键词
HEPATITIS-C VIRUS; ACTIVATED PROTEIN-KINASE; SIGNALING PATHWAYS; ENVELOPE PROTEIN; HCV; E2; PHOSPHORYLATION; EXPRESSION; RECEPTORS; GAMMA;
D O I
10.1186/1743-422X-8-157
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Signaling events triggered by interferon (IFN) account for the molecular mechanisms of antiviral effect. JAK STAT pathway plays a critical role in IFN signaling, and other pathways are also implicated in IFN mediated antiviral effect. Changes in mitogen-activated protein kinase (MAPK) and STAT1 pathways were evaluated in human hepatoma cells Huh7 and HepG2 upon IFN alpha treatment. Results: Phosphorylation of ERK was significantly and specifically up-regulated, whereas enhanced phosphorylation of upstream kinase MEK was unobservable upon IFN alpha treatment. A mild increase in p38 MAPK, SAPK/JNK and downstream target ATF-2 phosphorylation was detectable after exposure to IFN alpha, indicating differential up-regulation of the MAPK signaling cascades. Moreover, STAT1 phosphorylation was strongly enhanced by IFN alpha. Conclusion: IFN alpha up-regulates MAPK and STAT1 pathways in human hepatoma cells, and may provide useful information for understanding the IFN signaling.
引用
收藏
页数:7
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