Hepatitis B virus surface antigen (HBsAg) could be studied until recently only by isolating it from the blood of carriers, thus making incorporation of radioactive precursors into this protein(s) impossible. The isolation of a cell line producing HBsAg [Alexander et al, 1978] has eliminated this obs
Enhancement of hepatitis-B surface-antigen expression by 5-azacytidine in a hepatitis-B-virus-transfected cell line
โ Scribed by Eiji Miyoshi; Junichi Fujii; Norio Hayashi; Keiji Ueda; Takahiro Towata; Hideyuki Fusamoto; Takenobu Kamada; Naoyuki Taniguchi
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- French
- Weight
- 495 KB
- Volume
- 52
- Category
- Article
- ISSN
- 0020-7136
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โฆ Synopsis
The human hepatoblastoma-derived cell line HB6 I I secretes hepatitis-B surface antigen (HBsAg) and hepatitis-B e antigen (HBeAg) into the medium. Hepatitis-B-virus(HBV) DNA integrated into the cellular genome was found to be hypermethylated. When the cells were treated with 5-azacytidine for 3 days, the level of HBsAg in the medium increased, while the level of HBeAg remained constant. The level of alphafetoprotein (AFP) decreased with the 5-azacytidine treatment. Southern blot analysis of DNA digested with Hpall or Mspl showed that 5-azacytidine treatment resulted in hypomethylation of the integrated HBV DNA, suggesting that 5-azacytidine increased HBsAg production in the cells through hypomethylation of the HBV genomic DNA.
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