Expression of the subgenomic hepatitis C virus replicon alters iron homeostasis in Huh7 cells.

Abstract

BACKGROUND/AIMS:

Infection with hepatitis C virus (HCV) is associated with alterations in body iron homeostasis by poorly defined mechanisms. To seek for molecular links, we employed an established cell culture model for viral replication, and assessed how the expression of an HCV subgenomic replicon affects iron metabolism in host Huh7 hepatoma cells.

METHODS:

The expression of iron metabolism genes and parameters defining the cellular iron status were analyzed and compared between parent and replicon Huh7 cells.

RESULTS:

By using the IronChip microarray platform, we observed replicon-induced changes in expression profiles of iron metabolism genes. Notably, ceruloplasmin mRNA and protein expression were decreased in replicon cells. In addition, transferrin receptor 1 (TfR1) was also downregulated, while ferroportin levels were elevated, resulting in reduced iron uptake and increased iron release capacity of replicon cells. These responses were associated with an iron-deficient phenotype, manifested in decreased levels of the "labile iron pool" and concomitant induction of IRE-binding activity and IRP2 expression. Furthermore, hemin-treated replicon cells exhibited a defect in retaining iron. The clearance of the replicon by prolonged treatment with interferon-alpha only partially reversed the iron-deficient phenotype but almost completely restored the capacity of cured cells to retain iron.

CONCLUSIONS:

We propose that Huh7 cells undergo genetic reprogramming to permit subgenomic viral replication that results in reduction of intracellular iron levels. This response may provide a mechanism to bypass iron-mediated inactivation of the viral RNA polymerase NS5B.

• Authors: Carine Fillebeen, Martina Muckenthaler, Bill Andriopoulos, Martin Bisaillon, Zineb Mounir, Matthias W Hentze, Antonis E Koromilas, Kostas Pantopoulos
• Journal: Journal of hepatology (J Hepatol) Vol. 47 Issue 1 Pg. 12-22 (Jul 2007) ISSN: 0168-8278 [Print] Netherlands
• PMID: 17399844 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Antigens, CD
• CD71 antigen
• Receptors, Transferrin
• Hemin
• Iron
• Ceruloplasmin

Topics

• Antigens, CD (genetics, metabolism)
• Biological Transport
• Cell Line, Tumor
• Ceruloplasmin (genetics, metabolism)
• Down-Regulation
• Gene Expression Profiling
• Genome, Viral
• Hemin (pharmacology)
• Hepacivirus (genetics, physiology)
• Hepatocytes (drug effects, metabolism, virology)
• Homeostasis
• Humans
• Iron (metabolism)
• Receptors, Transferrin (genetics, metabolism)
• Replicon (genetics)
• Virus Replication (genetics)