Virology Journal (Dec 2012)

Altered of apoptotic markers of both extrinsic and intrinsic pathways induced by hepatitis C virus infection in peripheral blood mononuclear cells

  • Albertoni Guilherme,
  • Arnoni Carine Prisco,
  • Latini Flávia Roche Moreira,
  • Andrade Sheila Siqueira,
  • Araújo Patrícia Regina Barboza,
  • Rodrigues Flaviane Kesia,
  • Rozenchan Patrícia Bortman,
  • Mendes-Correa Maria Cássia,
  • Leite Olavo Henrique Munhoz,
  • Schor Nestor,
  • Girão Manoel João Castelo Batista,
  • Barreto José

DOI
https://doi.org/10.1186/1743-422X-9-314
Journal volume & issue
Vol. 9, no. 1
p. 314

Abstract

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Abstract Background Chronic hepatitis C (CHC) has emerged as a leading cause of cirrhosis in the U.S. and across the world. To understand the role of apoptotic pathways in hepatitis C virus (HCV) infection, we studied the mRNA and protein expression patterns of apoptosis-related genes in peripheral blood mononuclear cells (PBMC) obtained from patients with HCV infection. Methods The present study included 50 subjects which plasma samples were positive for HCV, but negative for human immunodeficiency virus (HIV) or hepatitis B virus (HBV). These cases were divided into four groups according to METAVIR, a score-based analysis which helps to interpret a liver biopsy according to the degree of inflammation and fibrosis. mRNA expression of the studied genes were analyzed by reverse transcription of quantitative polymerase chain reaction (RT-qPCR) and protein levels, analyzed by ELISA, was also conducted. HCV genotyping was also determined. Results HCV infection increased mRNA expression and protein synthesis of caspase 8 in group 1 by 3 fold and 4 fold, respectively (p group 4 HCV infection increased mRNA expression and protein synthesis of caspase 9 by 2 fold and 1,5 fold, respectively (p group 1 by 4 fold and 5 fold, respectively, and in group 4 by 6 fold and 7 fold, respectively (p Conclusions HCV induces alteration at both genomic and protein levels of apoptosis markers involved with extrinsic and intrinsic pathways.

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