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Modulation of hepatitis B surface antigen secretion by annexin II expressed in hepatitis B virus-producing hepatoma cells

机译:乙肝病毒生产性肝癌细胞中表达的膜联蛋白II对乙肝表面抗原分泌的调节

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The role of annexin II in hepatitis B virus (HBV)-associated hepatocellular carcinoma (HCC) remains to be elucidated. Intracellular hepatitis B surface antigen (HBsAg)-retention contributes to the induction of hepatocarcinogenesis. The present study aimed to investigate the regulation of HBsAg secretion by annexin II expressed in HBV-producing hepatoma cells. The expression of annexin II was analyzed using western blot analysis in SMMC-7721, HepG2, HepG2.2.15, 293T and Chinese hamster ovary (CHO) cells. CHO cells transfected with an annexin II plasmid were used as a positive control. The localization of annexin II and HBsAg was observed in the HepG2 and HepG2.2.15 cells using indirect immunofluorescence. HepG2.2.15 cells were transfected with a human immunodeficiency virus-type 1 viral infectivity factor-hemagglutinin (Vif-HA) plasmid or a control vector and, 24 h post-transfection, MG132 was added to the Vif-complemented HepG2.2.I5 cells. Western blot analysis was performed to detect the expression of annexin II and Vif-HA. HepG2 cells were cotransfected with HBV and annexin II expression vectors. Western blot analysis was performed to examine the expression of annexin II and an Abbott chemiluminescence immunoassay was used to assess the levels of HBsAg. The expression of annexin II was lower in the HepG2.2.I5 cells compared with the SMMC-7721 and HepG2 cells and the fluorescence signal of annexin II in the HepG2 cells was brighter than in the HepG2.2.15 cells. Annexin II colocalized with HBsAg in the cytosol of the HepG2.2.15 cells. MG132 was not able to increase the stability of annexin II expression in HepG2.2.15 cells. Annexin II reduced the secretion of HBsAg when compared with the control-transfected HepG2 cells. In conclusion, HBV downregulated the expression of annexin II and annexin II decreased the secretion of HBsAg in HBV-producing hepatoma cells in favor of intracellular HBsAg storage.
机译:Annexin II在乙型肝炎病毒(HBV)相关的肝细胞癌(HCC)中的作用尚待阐明。细胞内乙型肝炎表面抗原(HBsAg)的保留有助于诱导肝癌的发生。本研究旨在调查在产生HBV的肝癌细胞中表达的膜联蛋白II对HBsAg分泌的调节。使用蛋白质印迹分析法分析膜联蛋白II在SMMC-7721,HepG2,HepG2.2.15、293T和中国仓鼠卵巢(CHO)细胞中的表达。用膜联蛋白II质粒转染的CHO细胞用作阳性对照。使用间接免疫荧光在HepG2和HepG2.2.15细胞中观察到膜联蛋白II和HBsAg的定位。用人免疫缺陷病毒1型病毒感染因子血凝素(Vif-HA)质粒或对照载体转染HepG2.2.15细胞,转染后24小时,将MG132添加到Vif补充的HepG2.2.I5中细胞。进行蛋白质印迹分析以检测膜联蛋白II和Vif-HA的表达。 HepG2细胞与HBV和膜联蛋白II表达载体共转染。进行蛋白质印迹分析以检查膜联蛋白II的表达,并使用Abbott化学发光免疫分析法评估HBsAg的水平。与SMMC-7721和HepG2细胞相比,膜联蛋白II在HepG2.2.I5细胞中的表达更低,并且膜联蛋白II在HepG2细胞中的荧光信号要比在HepG2.2.15细胞中亮。 Annexin II与HBsAg在HepG2.2.15细胞的胞质溶胶中共定位。 MG132不能增加HepG2.2.15细胞中膜联蛋白II表达的稳定性。与对照转染的HepG2细胞相比,膜联蛋白II减少了HBsAg的分泌。总之,HBV下调了膜联蛋白II的表达,膜联蛋白II降低了产生HBV的肝癌细胞中HBsAg的分泌,有利于细胞内HBsAg的储存。

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