Lin Lan-yi, Li Shu-chen, Lû Shu-lan
Department of Infectious Diseases, The Second Hospital of Harbin Medical University, Harbin 150086, China.
Zhonghua Nei Ke Za Zhi. 2003 Jun;42(6):392-5.
To study the suppressive effect of HCV nonstructural 5A (NS5A) protein on tumor necrosis factor alpha (TNF alpha) mediated apoptosis of HepG2 cells.
NS5A gene fragment was amplified by reverse transcription and nested polymerase chain reaction from serum samples positive for anti-HCV. The PCR product was directly cloned using TA cloning kit, and 2 independent clones were isolated, digested and sequenced. Then we constructed HCV NS5A expression plasmid (pcDNA3.1-NS5A), stably transfected into HepG2 cells with lipofectamine. Successful transfection of NS5A gene and expression of NS5A protein were confirmed by Western blot. Transfected cells were incubated with TNFalpha for 48 h, then labeled with Annexin V and visualized by fluorescence microscopy. To examine the effects of NS5A protein on the apoptotic signaling pathway, caspase-3 cleavages and release of cytochrome C were investigated in the transfectant treated with TNF alpha for 48 h and the cell cytosol was subjected to SDS-PAGE and Western blot analysis.
The stable transfectant of HepG2 cells lines for HCV NS5A protein expression was achieved. The NS5A protein blocked the activation of caspase-3 and the release of cytochrome C in the TNF alpha treated cells.
HCV NS5A protein inhibits TNF alpha mediated apoptosis of HepG2 cells in vitro.
研究丙型肝炎病毒非结构蛋白5A(NS5A)对肿瘤坏死因子α(TNFα)介导的HepG2细胞凋亡的抑制作用。
采用逆转录巢式聚合酶链反应从抗HCV阳性血清样本中扩增NS5A基因片段。使用TA克隆试剂盒直接克隆PCR产物,分离出2个独立克隆,进行酶切和测序。然后构建HCV NS5A表达质粒(pcDNA3.1-NS5A),用脂质体稳定转染HepG2细胞。通过蛋白质免疫印迹法确认NS5A基因的成功转染和NS5A蛋白的表达。将转染细胞与TNFα孵育48小时,然后用膜联蛋白V标记,通过荧光显微镜观察。为了研究NS5A蛋白对凋亡信号通路的影响,在用TNFα处理48小时的转染细胞中研究caspase-3的切割和细胞色素C的释放,并对细胞胞质溶胶进行SDS-PAGE和蛋白质免疫印迹分析。
成功构建了稳定表达HCV NS5A蛋白的HepG2细胞系。NS5A蛋白可阻断TNFα处理细胞中caspase-3的激活和细胞色素C的释放。
HCV NS5A蛋白在体外可抑制TNFα介导的HepG2细胞凋亡。