Format

Send to

Choose Destination
J Virol. 2008 Mar;82(5):2120-9. Epub 2007 Dec 12.

Cellular determinants of hepatitis C virus assembly, maturation, degradation, and secretion.

Author information

1
The Scripps Research Institute, Maildrop SBR-10, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.

Abstract

Intracellular infectious hepatitis C virus (HCV) particles display a distinctly higher buoyant density than do secreted virus particles, suggesting that the characteristic low density of extracellular HCV particles is acquired during viral egress. We took advantage of this difference to examine the determinants of assembly, maturation, degradation, and egress of infectious HCV particles. The results demonstrate that HCV assembly and maturation occur in the endoplasmic reticulum (ER) and post-ER compartments, respectively, and that both depend on microsomal transfer protein and apolipoprotein B, in a manner that parallels the formation of very-low-density lipoproteins (VLDL). In addition, they illustrate that only low-density particles are efficiently secreted and that immature particles are actively degraded, in a proteasome-independent manner, in a post-ER compartment of the cell. These results suggest that by coopting the VLDL assembly, maturation, degradation, and secretory machinery of the cell, HCV acquires its hepatocyte tropism and, by mimicry, its tendency to persist.

PMID:
18077707
PMCID:
PMC2258938
DOI:
10.1128/JVI.02053-07
[Indexed for MEDLINE]
Free PMC Article

Supplemental Content

Full text links

Icon for HighWire Icon for PubMed Central
Loading ...
Support Center