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Roles of Cell Signaling Pathways in Cell-to-Cell Contact-Mediated Epstein-Barr Virus Transmission
| Title: | Roles of Cell Signaling Pathways in Cell-to-Cell Contact-Mediated Epstein-Barr Virus Transmission |
| Authors: | Nanbo, Asuka Browse this author →KAKEN DB | | Terada, Haruna Browse this author | | Kachi, Kunihiro Browse this author | | Takada, Kenzo Browse this author →KAKEN DB | | Matsuda, Tadashi Browse this author →KAKEN DB |
| Issue Date: | Sep-2012 |
| Publisher: | American Society for Microbiology |
| Journal Title: | Journal of Virology |
| Volume: | 86 |
| Issue: | 17 |
| Start Page: | 9285 |
| End Page: | 9296 |
| Publisher DOI: | 10.1128/JVI.00712-12 |
| Abstract: | Epstein-Barr virus (EBV), a human gamma herpesvirus, establishes a life-long latent infection in B lymphocytes and epithelial cells following primary infection. Several lines of evidence indicate that the efficiency of EBV infection in epithelial cells is accelerated up to 10^[4]-fold by co-culturing with EBV-infected Burkitt's lymphoma (BL) cells compared with infection with cell-free virions, indicating that EBV infection into epithelial cells is mainly mediated via cell-to-cell contact. However, the molecular mechanisms involved in this pathway are poorly understood. Here, we establish a novel assay to assess cell-to-cell contact-mediated EBV transmission by co-culturing an EBV-infected BL cell line with an EBV-negative epithelial cell line under the stimulation for lytic cycle induction. By using this assay we confirmed that EBV was transmitted from BL cells to epithelial cells via cell-to-cell contact but not via cell-to-cell fusion. The inhibitor treatments of extracellular signal-regulated kinase (ERK) and nuclear factor (NF)-κB pathways blocked EBV transmission in addition to lytic induction. The blockage of phosphoinositide 3-kinase (PI3K) pathway impaired EBV transmission coupled with inhibition of the lytic induction. Knockdown of the RelA/p65 subunit of NF-κB reduced viral transmission. Moreover these signaling pathways were activated in co-cultured BL cells and in epithelial cells. Finally we observed that the viral replication was induced in co-cultured BL cells. Taken together, our data suggest that cell-to-cell contact induces multiple cell signaling pathways in BL cells and epithelial cells, contributing to the induction of the viral lytic cycle in BL cells and the enhancement of viral transmission to epithelial cells. |
| Rights: | © 2012 American Society for Microbiology |
| Type: | article (author version) |
| URI: | http://hdl.handle.net/2115/52109 |
| Appears in Collections: | 薬学研究院 (Faculty of Pharmaceutical Sciences) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)
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Submitter: 南保 明日香
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