Ondracek Caitlin R, Rushing Christel N, Reese Vanessa C, Oropeza Claudia E, McLachlan Alan
Department of Microbiology and Immunology, College of Medicine, University of Illinois at Chicago, 909 South Wolcott Avenue, Chicago, Illinois 60612, USA.
J Virol. 2009 Dec;83(23):12535-44. doi: 10.1128/JVI.01623-09. Epub 2009 Sep 30.
Hepatitis B virus (HBV) biosynthesis involves the transcription of the 3.5-kb viral pregenomic RNA, followed by its reverse transcription into viral DNA. Consequently, the modulation of viral transcription influences the level of virus production. Nuclear receptors are the only transcription factors known to support viral pregenomic RNA transcription and replication. The coactivator peroxisome proliferator-activated receptor gamma coactivator 1alpha (PGC1alpha) and corepressor small heterodimer partner (SHP) have central roles in regulating energy homeostasis in the liver by modulating the transcriptional activities of nuclear receptors. Therefore, the effect of PGC1alpha and SHP on HBV transcription and replication mediated by nuclear receptors was examined in the context of individual nuclear receptors in nonhepatoma cells and in hepatoma cells. This analysis indicated that viral replication mediated by hepatocyte nuclear factor 4alpha, retinoid X receptor alpha (RXRalpha) plus peroxisome proliferator-activated receptor alpha (PPARalpha), and estrogen-related receptor (ERR) displayed differential sensitivity to PGC1alpha activation and SHP inhibition. The effects of PGC1alpha and SHP on viral biosynthesis in the human hepatoma cell line Huh7 were similar to those observed in the nonhepatoma cells expressing ERRalpha and ERRgamma. This suggests that these nuclear receptors, potentially in combination with RXRalpha plus PPARalpha, may have a major role in governing HBV transcription and replication in this cell line. Additionally, this functional approach may help to distinguish the transcription factors in various liver cells governing viral biosynthesis under a variety of physiologically relevant conditions.
乙型肝炎病毒(HBV)的生物合成涉及3.5 kb病毒前基因组RNA的转录,随后将其逆转录为病毒DNA。因此,病毒转录的调节会影响病毒产生的水平。核受体是已知支持病毒前基因组RNA转录和复制的唯一转录因子。共激活因子过氧化物酶体增殖物激活受体γ共激活因子1α(PGC1α)和共抑制因子小异二聚体伴侣(SHP)通过调节核受体的转录活性在调节肝脏能量稳态中起核心作用。因此,在非肝癌细胞和肝癌细胞中,针对单个核受体研究了PGC1α和SHP对核受体介导的HBV转录和复制的影响。该分析表明,由肝细胞核因子4α、视黄酸X受体α(RXRα)加过氧化物酶体增殖物激活受体α(PPARα)以及雌激素相关受体(ERR)介导的病毒复制对PGC1α激活和SHP抑制表现出不同的敏感性。PGC1α和SHP对人肝癌细胞系Huh7中病毒生物合成的影响与在表达ERRα和ERRγ的非肝癌细胞中观察到的相似。这表明这些核受体,可能与RXRα加PPARα结合,可能在该细胞系中控制HBV转录和复制方面起主要作用。此外,这种功能方法可能有助于区分在各种生理相关条件下控制病毒生物合成的各种肝细胞中的转录因子。