کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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3425249 | 1227275 | 2009 | 8 صفحه PDF | دانلود رایگان |
Hepatitis C virus nonstructural protein 4B (NS4B) is an endoplasmic reticulum (ER) membrane associated protein and a potent causative factor of ER stress. Here we reported that unfolded protein response (UPR) can be activated by HCV NS4B through inducing both XBP1 mRNA splicing and ATF6 cleavage in human hepatic cells. Flow cytometric analysis revealed that HCV NS4B stimulates the production of reactive oxygen species (ROS) by perturbing intracellular Ca2+ homeostasis. Luciferase assay showed that HCV NS4B also activates the multifunctional transcription factor, NF-κB, in a dose-dependent manner through Ca2+ signaling and ROS. Further immunoblot analysis showed that HCV NS4B promotes NF-κB translocation into the nucleus via protein-tyrosine kinase (PTK) mediated phosphorylation and subsequent degradation of IκBα. These studies provide an important insight into the implication of NS4B in HCV life cycle and HCV-associated liver disease by affecting host intracellular signal transduction pathways.
Journal: Virology - Volume 391, Issue 2, 1 September 2009, Pages 257–264