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在人肝癌细胞系中丁型肝炎病毒的产生及辅助性乙型肝炎病毒的抑制

Production of hepatitis delta virus and suppression of helper hepatitis B virus in a human hepatoma cell line.

作者信息

Wu J C, Chen P J, Kuo M Y, Lee S D, Chen D S, Ting L P

机构信息

Division of Gastroenterology, Veterans General Hospital, Taipei, Taiwan, Republic of China.

出版信息

J Virol. 1991 Mar;65(3):1099-104. doi: 10.1128/JVI.65.3.1099-1104.1991.

Abstract

The hepatitis delta virus (HDV) is a defective virus with a coat composing of the surface antigen of its helper virus, hepatitis B virus (HBV). Replication of HDV in the absence of HBV has been shown in cell cultures by transient transfection of the HDV plasmid. However, the formation and release of HDV virions have not been observed. In this report, a human hepatoma cell line HuH-7 was transiently cotransfected with HDV and HBV plasmids. The production of monomeric and multimeric antigenomic RNAs of HDV in the transfected cells indicated replication of the HDV genome. The major 3.5- and 2.1-kb RNAs of HBV were also expressed. Virions of both HDV and HBV were released from the cotransfected cells, as shown by the detection of monomeric genomic HDV RNA and partially double-stranded HBV DNA in the culture medium. Thus, this is the first report that describes the assembly and the release of HDV viral particles in an in vitro cell culture. The HDV virions released possessed physicochemical properties identical to those of the HDV virions found in infected human serum. Furthermore, expression of both the 3.5- and 2.1-kb RNAs of HBV was shown to be dramatically decreased by the presence of HDV, indicating suppression of the expression of HBV genes by HDV. The amount of HBV virions released was similarly suppressed by HDV. Cotransfection of HBV with an expression plasmid of the HDV delta antigen remarkably reduced the levels of the 3.5- and 2.1-kb HBV RNAs, indicating that suppression of the expression of HBV RNAs by HDV occurs via the action of the delta antigen. This HBV- and HDV-cotransfected human hepatoma cell line should provide an excellent system for the study of the function of the delta antigen and the interaction between HDV and its helper, HBV.

摘要

丁型肝炎病毒(HDV)是一种缺陷病毒,其衣壳由其辅助病毒乙型肝炎病毒(HBV)的表面抗原组成。通过HDV质粒的瞬时转染,已在细胞培养物中证明HDV在没有HBV的情况下也能复制。然而,尚未观察到HDV病毒粒子的形成和释放。在本报告中,将人肝癌细胞系HuH-7与HDV和HBV质粒进行瞬时共转染。转染细胞中HDV单体和多聚体反基因组RNA的产生表明HDV基因组发生了复制。HBV的主要3.5 kb和2.1 kb RNA也得到了表达。如在培养基中检测到单体基因组HDV RNA和部分双链HBV DNA所示,HDV和HBV的病毒粒子均从共转染细胞中释放出来。因此,这是第一份描述在体外细胞培养中HDV病毒颗粒组装和释放的报告。释放的HDV病毒粒子具有与感染人血清中发现的HDV病毒粒子相同的物理化学性质。此外,HDV的存在显著降低了HBV 3.5 kb和2.1 kb RNA的表达,表明HDV抑制了HBV基因的表达。HDV同样抑制了释放的HBV病毒粒子的数量。将HBV与HDV δ抗原表达质粒共转染显著降低了3.5 kb和2.1 kb HBV RNA的水平,表明HDV对HBV RNA表达的抑制是通过δ抗原的作用实现的。这种HBV和HDV共转染的人肝癌细胞系应为研究δ抗原的功能以及HDV与其辅助病毒HBV之间的相互作用提供一个优良的系统。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/143a/239875/70c5744db539/jvirol00046-0061-a.jpg

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