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Hepatitis C virus receptor expression in normal and diseased liver tissue
Author(s) -
Reynolds Gary M.,
Harris Helen J.,
Jennings Adam,
Hu Ke,
Grove Joe,
Lalor Patricia F.,
Adams David H.,
Balfe Peter,
Hübscher Stefan G.,
McKeating Jane A.
Publication year - 2008
Publication title -
hepatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.488
H-Index - 361
eISSN - 1527-3350
pISSN - 0270-9139
DOI - 10.1002/hep.22028
Subject(s) - virology , hepatitis c virus , virus , biology , liver tissue , receptor , hepatitis a virus , medicine , hepatitis virus , pathology
Abstract The principal site of hepatitis C virus (HCV) replication is the liver. HCV pseudoparticles infect human liver derived cell lines and this suggests that liver‐specific receptors contribute to defining HCV hepatotropism. At least three host cell molecules have been reported to be important for HCV entry: the tetraspanin CD81, scavenger receptor class B member I (SR‐BI), and the tight junction (TJ) protein Claudin 1 (CLDN1). Hepatocytes in liver tissue coexpress CD81, SR‐BI, and CLDN1, consistent with their ability to support HCV entry. CLDN1 localized at the apical‐canalicular TJ region and at basolateral‐sinusoidal hepatocyte surfaces in normal tissue and colocalized with CD81 at both sites. In contrast, CLDN1 appeared to colocalize with SR‐BI at the basolateral‐sinusoidal surface. CLDN1 expression was increased on basolateral hepatocyte membranes in HCV‐infected and other chronically inflamed liver tissue compared with normal liver. In contrast, CLDN4 hepatocellular staining was comparable in normal and diseased liver tissue. Conclusion : HCV infection of Huh‐7.5 hepatoma cells in vitro significantly increased CLDN1 expression levels, consistent with a direct modulation of CLDN1 by virus infection. In HCV infected livers, immunohistochemical studies revealed focal patterns of CLDN1 staining, suggesting localized areas of increased CLDN1 expression in vivo which may potentiate local viral spread within the liver. (H EPATOLOGY 2007.)