IMMUNOCYTOCHEMICAL AND ELECTRON-MICROSCOPIC STUDY OF HEPATITIS-B VIRUS-ANTIGEN AND COMPLETE PARTICLE-PRODUCTION IN HEPATITIS-B VIRUS-DNA TRANSFECTED HEPG2 CELLS

被引:37
作者
ROINGEARD, P
LU, S
SUREAU, C
FRESCHLIN, M
ARBEILLE, B
ESSEX, M
ROMETLEMONNE, JL
机构
[1] HARVARD UNIV, SCH PUBL HLTH, DEPT CANC BIOL, 665 HUNTINGTON AVE, BOSTON, MA 02115 USA
[2] CHR UNIV BRETONNEAU, DEPT BIOL HUMAINE, TOURS, FRANCE
关键词
D O I
10.1002/hep.1840110219
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The relationship between the presence of hepatitis B virus antigens, their localization and hepatitis B virus replication was studied in different clones of cultured HepG2 hepatoblastoma cells transfected with cloned hepatitis B virus DNA. Intracellular hepatitis B virus antigens were detected by immunofluorescence. The production of these antigens was evaluated in the culture media by enzyme‐linked immunoassay. Hepatitis B virus DNA was detected using dot‐blot hybridization. Three types of HBeAg staining were observed in transfected HepG2 cells: (a) cells with nuclear HBcAg, (b) cells with cytoplasmic HBcAg and (c) cells with both nuclear and cytoplasmic HBcAg. Cell types b and c also expressed hepatitis B virus DNA in their culture media. Our results suggest that cytoplasmic HBcAg may be more involved than nuclear HBcAg in hepatitis B virus replication. The site of hepatitis B virus formation in hepatocytes was studied by electron microscopic examination of a specific hepatitis B virus producer clone, thereby allowing detection of intracellular Dane particles more easily than liver biopsy samples from infected patients. Dane particles and HBsAg filaments were found in large, dilated structures probably related to the endoplasmic reticulum. Budding of core particles into cisternae of endoplasmic reticulum‐related structures appears to be a possible mechanism for hepatitis B virus formation; our results suggest that the exocytosis of cisternae to extracellular spaces may be a mechanism for release of hepatitis B virus particles. Copyright © 1990 American Association for the Study of Liver Diseases
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页码:277 / 285
页数:9
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