Increased Prooxidant Production and Enhanced Susceptibility to Glutathione Depletion in HepG2 Cells Co-expressing HCV Core Protein and CYP2E1

Feng Wen, Maher Y. Abdalla, Costica Aloman, Jinhua Xiang, Iman M. Ahmad, Jose Walewski, Michael L. McCormick, Kyle E. Brown, Andrea D. Branch, Douglas R. Spitz, Bradley E. Britigan, Warren N. Schmidt

Research output: Contribution to journalArticle

39 Citations (Scopus)

Abstract

Hepatitis C virus (HCV) and HCV core protein are hypothesized to induce hepatic oxidative stress and exacerbate injury caused by other toxins such as ethanol that induce the cytochrome P450 enzyme, CYP2E1. In the current study, the effects of HCV core protein [sequence genotype 1b, (nt 342-915)] on parameters indicative of oxidative stress were evaluated in HepG2 cells stably over expressing CYP2E1 (E47), or vector controls (C34). Stable (>10 passages) expression of HCV core protein and CYP2E1 was confirmed in clonal cell lines at the level of mRNA and immunoreactive protein. Prooxidant production, as determined by cellular oxidation of dichlorodihydrofluorescin and dihydroethidium (HE), was increased by expression of HCV core protein in the presence or absence of CYP2E1. Depletion of glutathione (GSH) with buthionine sulfoximine (BSO) enhanced prooxidant production in both C34 and E47 cells. In addition, prooxidant production was greater in BSO-treated cells expressing HCV core protein, and this effect was further enhanced in cells expressing both HCV core and CYP2E1. The CYP2E1 inhibitor, 4-methylpyrazole, could suppress increased prooxidant production in E47 cells. Finally, cells co-expressing both CYP2E1 and HCV core protein showed significantly decreased viability following GSH depletion. These studies show simultaneous expression of HCV core protein and CYP2E1 increases parameters indicative of oxidative stress as well as sensitization to cell injury induced by GSH depletion. These results support the hypothesis that enhanced injury in hepatocytes over expressing both HCV core protein and CYP2E1 is mediated by increases in oxidative stress.

Original languageEnglish (US)
Pages (from-to)230-240
Number of pages11
JournalJournal of Medical Virology
Volume72
Issue number2
DOIs
StatePublished - Feb 1 2004

Fingerprint

Cytochrome P-450 CYP2E1
Hep G2 Cells
Glutathione
Oxidative Stress
Buthionine Sulfoximine
Hepacivirus
Cytochrome P-450 Enzyme System
Wounds and Injuries
Hepatitis C virus nucleocapsid protein
Hepatocytes
Ethanol
Genotype
Cell Line
Messenger RNA
Liver

Keywords

  • Buthionine sulfoximine
  • CYP2E1
  • Glutathione
  • Hepatitis C core protein
  • Oxidative stress
  • Prooxidant production

ASJC Scopus subject areas

  • Virology
  • Infectious Diseases

Cite this

Increased Prooxidant Production and Enhanced Susceptibility to Glutathione Depletion in HepG2 Cells Co-expressing HCV Core Protein and CYP2E1. / Wen, Feng; Abdalla, Maher Y.; Aloman, Costica; Xiang, Jinhua; Ahmad, Iman M.; Walewski, Jose; McCormick, Michael L.; Brown, Kyle E.; Branch, Andrea D.; Spitz, Douglas R.; Britigan, Bradley E.; Schmidt, Warren N.

In: Journal of Medical Virology, Vol. 72, No. 2, 01.02.2004, p. 230-240.

Research output: Contribution to journalArticle

Wen, Feng ; Abdalla, Maher Y. ; Aloman, Costica ; Xiang, Jinhua ; Ahmad, Iman M. ; Walewski, Jose ; McCormick, Michael L. ; Brown, Kyle E. ; Branch, Andrea D. ; Spitz, Douglas R. ; Britigan, Bradley E. ; Schmidt, Warren N. / Increased Prooxidant Production and Enhanced Susceptibility to Glutathione Depletion in HepG2 Cells Co-expressing HCV Core Protein and CYP2E1. In: Journal of Medical Virology. 2004 ; Vol. 72, No. 2. pp. 230-240.
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AU - Ahmad, Iman M.

AU - Walewski, Jose

AU - McCormick, Michael L.

AU - Brown, Kyle E.

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AU - Schmidt, Warren N.

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