THE EFFECT OF HCV F AND CORE PROTEIN ON THE APOPTOSIS OF HEPG2 CELLS

被引:0
|
作者
Chu Chunli [1 ,3 ]
Deng Xiaozhao [2 ]
Kong Jing [4 ]
Wei Juan [5 ]
Zhang Jinhai [2 ]
Yue Ming [1 ]
Lu Weidong [6 ]
Yu Xiaojie [5 ]
机构
[1] China Pharmaceut Univ, Nanjing 210009, Peoples R China
[2] Huadong Res Inst Med & Biotech, Nanjing 210002, Jiangsu, Peoples R China
[3] Nantong Tichen Hlth Sch, Nantong 220007, Peoples R China
[4] Huaiyin Inst Technol, Huaian 223300, Peoples R China
[5] Nanjing Med Univ, Nanjing 210029, Jiangsu, Peoples R China
[6] Kunming Med Coll, Kunming 650031, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Hepatitis C virus(HCV); F protein; core protein; Apoptosis; HEPATITIS-C VIRUS; GENOTYPE; 1B; INFLAMMATION;
D O I
暂无
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The F protein is expressed by a +1 ribosomal frameshift during HCV translation. Discovery of F protein expressed from the HCV core coding sequence challenges properties assigned to core protein. In this study, we aimed to investigate the functional role of F protein in the change of cell-cycle on cellular levels. Cells were stably transfected using Lipofectamine 2000 with a EGFP reporter construction of different plasmids, pEGFP-F or pEGFP-core. Fluorescence microscope and Western blotting assays were performed at 48h of post-transfection to confirm successful transfections. Cells transfected with pEGFP-F or pEGFP-core plasmids were selected and tested to show that differences in their growth rates are due to endogenous core or F expression. We concluded that F protein inhibits apoptosis of transfected cells, contrast to parent cells, but less than core protein.
引用
收藏
页码:223 / 225
页数:3
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