Host cell kinases and the hepatitis C virus life cycle.
Identifieur interne : 002C98 ( Main/Curation ); précédent : 002C97; suivant : 002C99Host cell kinases and the hepatitis C virus life cycle.
Auteurs : Che C. Colpitts [France] ; Joachim Lupberger [France] ; Christian Doerig [Australie] ; Thomas F. Baumert [France]Source :
- Biochimica et biophysica acta [ 0006-3002 ] ; 2015.
Descripteurs français
- KwdFr :
- Animaux, Antigènes mineurs d'histocompatibilité, Assemblage viral (génétique), Hepacivirus (génétique), Hepacivirus (pathogénicité), Humains, Hépatite C (génétique), Hépatite C (virologie), Hépatocytes (enzymologie), Hépatocytes (virologie), Interactions hôte-pathogène (génétique), Phosphotransferases (Alcohol Group Acceptor) (génétique), Protéines virales non structurales (génétique), Pénétration virale, Récepteur EphA2 (génétique), Récepteur du facteur de croissance épidermique (génétique), Récepteur du facteur de croissance épidermique (métabolisme), Étapes du cycle de vie (génétique).
- MESH :
- enzymologie : Hépatocytes.
- génétique : Assemblage viral, Hepacivirus, Hépatite C, Interactions hôte-pathogène, Phosphotransferases (Alcohol Group Acceptor), Protéines virales non structurales, Récepteur EphA2, Récepteur du facteur de croissance épidermique, Étapes du cycle de vie.
- métabolisme : Récepteur du facteur de croissance épidermique.
- pathogénicité : Hepacivirus.
- virologie : Hépatite C, Hépatocytes.
- Animaux, Antigènes mineurs d'histocompatibilité, Humains, Pénétration virale.
English descriptors
- KwdEn :
- Animals, Hepacivirus (genetics), Hepacivirus (pathogenicity), Hepatitis C (genetics), Hepatitis C (virology), Hepatocytes (enzymology), Hepatocytes (virology), Host-Pathogen Interactions (genetics), Humans, Life Cycle Stages (genetics), Minor Histocompatibility Antigens, Phosphotransferases (Alcohol Group Acceptor) (genetics), Receptor, EphA2 (genetics), Receptor, Epidermal Growth Factor (genetics), Receptor, Epidermal Growth Factor (metabolism), Viral Nonstructural Proteins (genetics), Virus Assembly (genetics), Virus Internalization.
- MESH :
- chemical , genetics : Phosphotransferases (Alcohol Group Acceptor), Receptor, EphA2, Receptor, Epidermal Growth Factor, Viral Nonstructural Proteins.
- chemical , metabolism : Receptor, Epidermal Growth Factor.
- chemical : Minor Histocompatibility Antigens.
- enzymology : Hepatocytes.
- genetics : Hepacivirus, Hepatitis C, Host-Pathogen Interactions, Life Cycle Stages, Virus Assembly.
- pathogenicity : Hepacivirus.
- virology : Hepatitis C, Hepatocytes.
- Animals, Humans, Virus Internalization.
Abstract
Hepatitis C virus (HCV) infection relies on virus-host interactions with human hepatocytes, a context in which host cell kinases play critical roles in every step of the HCV life cycle. During viral entry, cellular kinases, including EGFR, EphA2 and PKA, regulate the localization of host HCV entry factors and induce receptor complex assembly. Following virion internalization, viral genomes replicate on endoplasmic reticulum-derived membranous webs. The formation of membranous webs depends on interactions between the HCV NS5a protein and PI4KIIIα. The phosphorylation status of NS5a, regulated by PI4KIIIα, CKI and other kinases, also acts as a molecular switch to virion assembly, which takes place on lipid droplets. The formation of lipid droplets is enhanced by HCV activation of IKKα. In view of the multiple crucial steps in the viral life cycle that are mediated by host cell kinases, these enzymes also represent complementary targets for antiviral therapy. This article is part of a Special Issue entitled: Inhibitors of Protein Kinases.
DOI: 10.1016/j.bbapap.2015.04.011
PubMed: 25896387
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pubmed:25896387Le document en format XML
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<term>Hepacivirus (pathogenicity)</term>
<term>Hepatitis C (genetics)</term>
<term>Hepatitis C (virology)</term>
<term>Hepatocytes (enzymology)</term>
<term>Hepatocytes (virology)</term>
<term>Host-Pathogen Interactions (genetics)</term>
<term>Humans</term>
<term>Life Cycle Stages (genetics)</term>
<term>Minor Histocompatibility Antigens</term>
<term>Phosphotransferases (Alcohol Group Acceptor) (genetics)</term>
<term>Receptor, EphA2 (genetics)</term>
<term>Receptor, Epidermal Growth Factor (genetics)</term>
<term>Receptor, Epidermal Growth Factor (metabolism)</term>
<term>Viral Nonstructural Proteins (genetics)</term>
<term>Virus Assembly (genetics)</term>
<term>Virus Internalization</term>
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<term>Antigènes mineurs d'histocompatibilité</term>
<term>Assemblage viral (génétique)</term>
<term>Hepacivirus (génétique)</term>
<term>Hepacivirus (pathogénicité)</term>
<term>Humains</term>
<term>Hépatite C (génétique)</term>
<term>Hépatite C (virologie)</term>
<term>Hépatocytes (enzymologie)</term>
<term>Hépatocytes (virologie)</term>
<term>Interactions hôte-pathogène (génétique)</term>
<term>Phosphotransferases (Alcohol Group Acceptor) (génétique)</term>
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<term>Récepteur EphA2 (génétique)</term>
<term>Récepteur du facteur de croissance épidermique (génétique)</term>
<term>Récepteur du facteur de croissance épidermique (métabolisme)</term>
<term>Étapes du cycle de vie (génétique)</term>
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<term>Receptor, EphA2</term>
<term>Receptor, Epidermal Growth Factor</term>
<term>Viral Nonstructural Proteins</term>
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<keywords scheme="MESH" type="chemical" xml:lang="en"><term>Minor Histocompatibility Antigens</term>
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<keywords scheme="MESH" qualifier="enzymologie" xml:lang="fr"><term>Hépatocytes</term>
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<keywords scheme="MESH" qualifier="enzymology" xml:lang="en"><term>Hepatocytes</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Hepacivirus</term>
<term>Hepatitis C</term>
<term>Host-Pathogen Interactions</term>
<term>Life Cycle Stages</term>
<term>Virus Assembly</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Assemblage viral</term>
<term>Hepacivirus</term>
<term>Hépatite C</term>
<term>Interactions hôte-pathogène</term>
<term>Phosphotransferases (Alcohol Group Acceptor)</term>
<term>Protéines virales non structurales</term>
<term>Récepteur EphA2</term>
<term>Récepteur du facteur de croissance épidermique</term>
<term>Étapes du cycle de vie</term>
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<front><div type="abstract" xml:lang="en">Hepatitis C virus (HCV) infection relies on virus-host interactions with human hepatocytes, a context in which host cell kinases play critical roles in every step of the HCV life cycle. During viral entry, cellular kinases, including EGFR, EphA2 and PKA, regulate the localization of host HCV entry factors and induce receptor complex assembly. Following virion internalization, viral genomes replicate on endoplasmic reticulum-derived membranous webs. The formation of membranous webs depends on interactions between the HCV NS5a protein and PI4KIIIα. The phosphorylation status of NS5a, regulated by PI4KIIIα, CKI and other kinases, also acts as a molecular switch to virion assembly, which takes place on lipid droplets. The formation of lipid droplets is enhanced by HCV activation of IKKα. In view of the multiple crucial steps in the viral life cycle that are mediated by host cell kinases, these enzymes also represent complementary targets for antiviral therapy. This article is part of a Special Issue entitled: Inhibitors of Protein Kinases.</div>
</front>
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