Intracellular localization of the hepatitis B virus HBx protein

被引:131
作者
Henkler, F
Hoare, J
Waseem, N
Goldin, RD
McGarvey, MJ
Koshy, R
King, IA
机构
[1] Natl Inst Med Res, Div Membrane Biol, London NW7 1AA, England
[2] Univ London Imperial Coll Sci Technol & Med, Sch Med, Dept Med, London W2 1NY, England
[3] Univ London Imperial Coll Sci Technol & Med, Sch Med, Dept Histopathol, London W2 1NY, England
[4] NIAID, Hepatitis Viruses Sect, LID, NIH, Bethesda, MD 20892 USA
[5] Guys Kings & St Thomass Sch Med, Div Med & Mol Genet, London SE1 9RT, England
关键词
D O I
10.1099/0022-1317-82-4-871
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 hepatitis B virus (HBV) X protein (HBx) was originally suggested to be a viral transcriptional activator, but its functional mechanisms are still unclear. In this study we have analysed the intracellular localization of HBx in transfected cells and demonstrate that its compartmentalization is dependent on overall expression levels. HBx was exclusively or predominantly localized in the nuclei in weakly expressing cells. However, elevated cellular levels correlated with its accumulation in the cytoplasm, suggesting that the capacity of HBx for nuclear compartmentalization might be limited. Cytoplasmic HBx was detected either as punctate granular staining or in dispersed, finely granular patterns. We have further analysed the detailed cytoplasmic compartmentalization, using confocal microscopy, and show no association with the endoplasmic reticulum, plasma membrane or lysosomes, but a substantial association of HBx with mitochondria. However, a major fraction of cytoplasmic HBx did not localize in mitochondria, indicating the presence of two distinctly compartmentalized cytoplasmic populations. Furthermore, high levels of HBx expression led to an abnormal mitochondrial distribution, involving clumping and organelle aggregation, which was not observed at lower expression levels. The data presented here provide novel insights into the compartmentalization of HBx and may prove important for future evaluations of its functions, both in the viral life-cycle and in the pathology of HBV-related liver disease.
引用
收藏
页码:871 / 882
页数:12
相关论文
共 44 条