期刊
ANTIVIRAL RESEARCH
卷 96, 期 3, 页码 296-304出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.antiviral.2012.09.021
关键词
Epstein-Barr virus (EBV); Protein kinase inhibitors (PKI); Signal transduction; EBV BGLF4 protein kinase; Viral reactivation
资金
- National Institutes of Health [R21-AI072221]
Signaling pathways mediating Epstein-Barr virus (EBV) reactivation by Ag-bound B-cell receptor (BCR) were analyzed using a panel of 80 protein kinase inhibitors. Broad range protein kinase inhibitors Staurosporine, K252A, and PKC-412 significantly reduced the EBV genome copy numbers measured 48 h after reactivation perhaps due to their higher toxicity. In addition, selected inhibitors of the phosphatidylinositol-3-kinase (PI3K), protein kinase C (PKC), mitogen-activated protein kinase (MAPK) and nuclear factor kappa B (NF-kappa B) pathways, glycogen synthase kinase 3 beta (GSK-3 beta), platelet-derived growth factor receptor-associated tyrosine kinase (PDGFRK), and epidermal growth factor receptor-associated tyrosine kinase (EGFRK) significantly reduced the EBV genome copy numbers. Of those, only U0126 and Erbstatin analog, which inhibit MAPK pathway and EGFRK, respectively, did not inhibit viral reactivation assessed by expression of the EBV early protein, EA-D. None of the tested compounds, except for K252A, affected the activity of the EBV-encoded protein kinase in vitro. These results show that EBV reactivation induced by BCR signaling is mainly mediated through PI3K and PKC, whereas MAPK might be involved in later stages of viral replication. (c) 2012 Elsevier B.V. All rights reserved.
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