Abstract

Hepatitis C virus (HCV) infection of hepatocytes promotes liver fibrosis by activation of hepatic stellate cells (HSCs) and excessive deposition of extracellular matrix in liver tissue. Whether or not host factors released from the HCV-infected hepatocytes play role in HSCs activation is unclear. In this study, HSCs were activated by the conditioned medium derived from HCV replicon cells. Secretomic profiling of HCV replicon cells and the parental Huh7 cells revealed ubiquitin carboxy-terminal hydrolase L1 (UCHL1) as a novel secreted protein from HCV-infected hepatocytes. UCHL1 expression in hepatocytes was induced by HCV infection. UCHL1 was expressed in the liver and found in the plasma of patients with chronic hepatitis C. Molecular analysis by use of the anti-UCHL1 neutralization antibody and purified UCHL1 protein showed that secreted UCHL1 protein was bound to the cell surface of HSCs and activated JNK signaling leading to overexpression of alpha-smooth muscle actin and the activation of HSCs. These results provide further for understanding the underlying mechanism in HCV-mediated hepatic fibrogenesis.

Highlights

  • More than 170 million people are infected with hepatitis C virus (HCV) worldwide[1]

  • LX2) and rat (HSC-T6) hepatic stellate cells (HSCs) were grown in the conditioned medium collected from the culture of Hepatitis C virus (HCV) Con[1] replicon cells, HCVcc-infected cells, and the control Huh[7] cells, respectively, to evaluate whether HCV infection of hepatocytes induces secretion of factors playing a role in HSCs activation

  • The conditioned medium from Con[1] and HCVcc-infected cells and the HSCs activator TGF-β25 induced the expression of procollagen I transcript and α-SMA protein, the markers for HSCs activation and hepatic fibrosis[26] in the three types of HSCs

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Summary

Introduction

More than 170 million people are infected with hepatitis C virus (HCV) worldwide[1]. Chronic hepatitis C (CHC) infection may result in liver damage that is characterized by liver fibrosis due to excessive deposition of extracellular matrix (ECM)[2, 3]. Results Conditioned medium from HCV replicon cells stimulated HSCs activation. Identification of proteins secreted from HCV Con[1] replicon cells that induced HSC activation.

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