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Ceruloplasmin inhibits the production of extracellular hepatitis B virions by targeting its middle surface protein.

Abstract
Ceruloplasmin (CP) is mainly synthesized by hepatocytes and plays an essential role in iron metabolism. Previous reports have shown that CP levels correlate negatively with disease progression in patients with chronic hepatitis B. However, the function of CP in the hepatitis B virus (HBV) life cycle and the mechanism underlying the above correlation remain unclear. Here, we report that CP can selectively inhibit the production of extracellular HBV virions without altering intracellular viral replication. HBV expression can also downregulate the expression of CP. Knockdown of CP using small interfering RNA significantly increased the level of extracellular HBV virions in both Huh7 and HepG2.2.15 cells, while overexpression of CP decreased this level. Mechanistically, CP could specifically interact with the HBV middle surface protein (MHB). Using an HBV replication-competent clone unable to express MHBs, we demonstrated that the overexpression of CP did not affect the production of extracellular HBV virions in the absence of MHBs. Furthermore, introduction of an MHB expression construct could rescue the impairment in virion production caused by CP. Taken together, our results suggest that CP may be an important host factor that targets MHBs during the envelopment and/or release of virions.
AuthorsKaitao Zhao, Chunchen Wu, Yongxuan Yao, Liang Cao, Zhenhua Zhang, Yifei Yuan, Yun Wang, Rongjuan Pei, Jizheng Chen, Xue Hu, Yuan Zhou, Mengji Lu, Xinwen Chen
JournalThe Journal of general virology (J Gen Virol) Vol. 98 Issue 6 Pg. 1410-1421 (Jun 2017) ISSN: 1465-2099 [Electronic] England
PMID28678687 (Publication Type: Journal Article)
Chemical References
  • Hepatitis B Surface Antigens
  • Ceruloplasmin
Topics
  • Adult
  • Cell Line
  • Ceruloplasmin (analysis, metabolism)
  • Female
  • Hepatitis B Surface Antigens (metabolism)
  • Hepatitis B virus (growth & development, immunology)
  • Hepatitis B, Chronic (virology)
  • Hepatocytes (virology)
  • Humans
  • Male
  • Middle Aged
  • Protein Interaction Mapping

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