[Entry of HCV into target cells].
F Helle, L Cocquerel
Abstract
F Helle, L Cocquerel
Abstract
To replicate its genome, a virus needs to cross the plasma membrane of a host cell and get access to cytosolic and/or nuclear components. For an enveloped virus, this involves binding to the plasma membrane, followed by migration of the virion to a microdomain or an endosomal vesicle where fusion between the virion envelope and a host cell membrane occurs. Although we are still far from understanding the details of hepatitis C virus (HCV) entry, recent data show that this virus enters into target cells in a slow and complex multistep process involving the presence of several entry factors. Initial attachment of the virion may involve glycosaminoglycans and the low-density lipoprotein receptor, and it is followed by the sequential interaction with the scavenger receptor BI, the tetraspanin CD81 and the tight junction protein Claudin-1, -6 or -9. The current knowledge accumulated on HCV entry is summarized in this review.
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To replicate its genome, a virus needs to cross the plasma membrane of a host cell and get access to cytosolic and/or nuclear components. For an enveloped virus, this involves binding to the plasma membrane, followed by migration of the virion to a microdomain or an endosomal vesicle where fusion between the virion envelope and a host cell membrane occurs. Although we are still far from understanding the details of hepatitis C virus (HCV) entry, recent data show that this virus enters into target cells in a slow and complex multistep process involving the presence of several entry factors. Initial attachment of the virion may involve glycosaminoglycans and the low-density lipoprotein receptor, and it is followed by the sequential interaction with the scavenger receptor BI, the tetraspanin CD81 and the tight junction protein Claudin-1, -6 or -9. The current knowledge accumulated on HCV entry is summarized in this review.
Key concepts: CD81, Tetraspanin, Viral entry, Viral envelope, Cell biology, Lipid bilayer fusion, Endosome, Hepatitis C virus