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Status: Bibliographieeintrag

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Verfasst von:Alvisi, Gualtiero [VerfasserIn]   i
 Madan Renes, Vanesa [VerfasserIn]   i
 Bartenschlager, Ralf [VerfasserIn]   i
Titel:Hepatitis C virus and host cell lipids
Titelzusatz:An intimate connection
Verf.angabe:Gualtiero Alvisi, Vanesa Madan and Ralf Bartenschlager
E-Jahr:2011
Jahr:01 Mar 2011
Umfang:12 S.
Fussnoten:Gesehen am 02.03.2022
Titel Quelle:Enthalten in: RNA biology
Ort Quelle:Philadelphia, Pa. : Taylor & Francis, 2004
Jahr Quelle:2011
Band/Heft Quelle:8(2011), 2, Seite 258-269
ISSN Quelle:1555-8584
Abstract:Hepatitis C virus (HCV) is a major human pathogen, persistently infecting more than 170 million individuals worldwide. The recent establishment of fully permissive culture systems allowed unraveling the close link between host cell lipids and HCV, at each step of the viral replication cycle. HCV entry is triggered by the timely coordinated interaction of virus particles with cell surface receptors, including the low-density lipoprotein receptor. Viral RNA replication strictly depends on fatty acids and cholesterol biosynthesis. This process occurs on modified intracellular membranes, forming a membranous web. Their biogenesis is induced by the viral nonstructural proteins (NS) 4B and NS5A and requires the activity of cellular lipid kinases belonging to the phosphatidylinositol-4-kinase III family. A hallmark of HCV-induced membranes is thus the presence of phosphatidylinositol-4-phosphate (PI4P), which is synthesized by these kinases. Intriguingly, certain recently identified HCV dependency factors selectively bind to PI derivatives, suggesting a crucial role for PIPs in viral RNA replication and assembly. The latter occurs on the surface of lipid droplets and is tightly connected to the very low density lipoprotein pathway leading to the formation of unique lipoviro particles. Thus, HCV exploits lipid metabolism in many ways and may therefore serve as a model system to gain insights into membrane biogenesis, lipid droplet formation and lipid trafficking.
DOI:doi:10.4161/rna.8.2.15011
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.4161/rna.8.2.15011
 DOI: https://doi.org/10.4161/rna.8.2.15011
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:1794369597
Verknüpfungen:→ Zeitschrift

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