Ozer A, Khaoustov V I, Mearns M, Lewis D E, Genta R M, Darlington G J, Yoffe B
Department of Medicine, Veterans Affairs Medical Center, Baylor College of Medicine, Houston, Texas, USA.
Gastroenterology. 1996 May;110(5):1519-28. doi: 10.1053/gast.1996.v110.pm8613059.
BACKGROUND & AIMS: Interrelationship between hepatitis B virus (HBV) replication and the stage of hepatocyte proliferation and differentiation may play an important role in the pathogenesis of HBV infection. The aim of this study was to assess the effect of hepatocyte proliferation and/or cell arrest on HBV replication.
Hepatoblastoma cells transfected with HBV were subjected to serum deprivation or treatment with aphidicolin or camptothecin. Cell cycle analysis was performed using flow cytometry, and cellular DNA synthesis was analysed by assessing 5-bromo-2'-deoxyuridine incorporation. Distribution of episomal HBV DNA and proliferating cell nuclear antigen in liver specimens was assessed by simultaneous in situ hybridization and immunohistochemistry.
Serum deprivation inhibited cellular DNA synthesis and increased levels of HBV messenger RNA (mRNA). Aphidicolin treatment resulted in cell arrest in C1, with concomitant increases in levels of HBV mRNA and viral DNA. Cell entry into S phase inhibited expression of HBV mRNA. Camptothecin induced G2 cell arrest and inhibited cellular DNA synthesis with increased amounts of viral replication and levels of HBV mRNA. In vivo studies showed an inverse correlation between expression of proliferating cell nuclear antigen and presence of episomal HBV DNA in individual hepatocytes.
HBV replication is cell cycle dependent, supporting the concept of enhanced viral replication in quiescent hepatocytes. The results may explain the mechanism of viral elimination during cell regeneration.
乙型肝炎病毒(HBV)复制与肝细胞增殖和分化阶段之间的相互关系可能在HBV感染的发病机制中起重要作用。本研究的目的是评估肝细胞增殖和/或细胞停滞对HBV复制的影响。
用HBV转染的肝母细胞瘤细胞进行血清剥夺或用阿非迪霉素或喜树碱处理。使用流式细胞术进行细胞周期分析,并通过评估5-溴-2'-脱氧尿苷掺入来分析细胞DNA合成。通过同时进行原位杂交和免疫组织化学来评估肝标本中游离型HBV DNA和增殖细胞核抗原的分布。
血清剥夺抑制细胞DNA合成并增加HBV信使核糖核酸(mRNA)水平。阿非迪霉素处理导致细胞停滞于C1期,同时HBV mRNA和病毒DNA水平增加。细胞进入S期抑制HBV mRNA的表达。喜树碱诱导G2期细胞停滞并抑制细胞DNA合成,同时病毒复制量和HBV mRNA水平增加。体内研究表明,单个肝细胞中增殖细胞核抗原的表达与游离型HBV DNA的存在呈负相关。
HBV复制是细胞周期依赖性的,支持静止肝细胞中病毒复制增强的概念。这些结果可能解释了细胞再生过程中病毒清除的机制。