Abstract
Epstein-Barr virus (EBV) is closely associated with nasopharyngeal carcinoma (NPC), a human malignancy notorious for its highly metastatic nature. Among EBV-encoded genes, latent membrane protein 1 (LMP1) is expressed in most NPC tissues and exerts oncogenicity by engaging multiple signaling pathways in a ligand-independent manner. LMP1 expression also results in actin cytoskeleton reorganization, which modulates cell morphology and cell motility— cellular process regulated by RhoGTPases, such as Cdc42. Despite the prominent association of Cdc42 activation with tumorigenesis, the molecular basis of Cdc42 activation by LMP1 in NPC cells remains to be elucidated. Here using GST-CBD (active Cdc42-binding domain) as bait in GST pull-down assays to precipitate active Cdc42 from cell lysates, we demonstrated that LMP1 acts through its transmembrane domains to preferentially induce Cdc42 activation in various types of epithelial cells, including NPC cells. Using RNA interference combined with re-introduction experiments, we identified FGD4 (FYVE, RhoGEF and PH domain containing 4) as the GEF (guanine nucleotide exchange factor) responsible for the activation of Cdc42 by LMP1. Serial deletion experiments and co-immunoprecipitation assays further revealed that ectopically expressed FGD4 modulated LMP1-mediated Cdc42 activation by interacting with LMP1. Moreover, LMP1, through its transmembrane domains, directly bound FGD4 and enhanced FGD4 activity toward Cdc42, leading to actin cytoskeleton rearrangement and increased motility of NPC cells. Depletion of FGD4 or Cdc42 significantly reduced (∼50%) the LMP1-stimulated cell motility, an effect that was partially reversed by expression of a constitutively active mutant of Cdc42. Finally, quantitative RT-PCR and immunohistochemistry analyses showed that FGD4 and LMP1 were expressed in NPC tissues, supporting the potential physiologically relevance of this mechanism in NPC. Collectively, our results not only uncover a novel mechanism underlying LMP1-mediated Cdc42 activation, namely LMP1 interaction with FGD4, but also functionally link FGD4 to NPC tumorigenesis.
Highlights
Epstein–Barr virus (EBV) is a human c-herpesvirus that is closely associated with many human malignancies, including nasopharyngeal carcinoma (NPC), Burkitt’s lymphoma, T-cell lymphoma, and gastric carcinoma [1]
To assess the effect of latent membrane protein 1 (LMP1) on Cdc42 activation in cells, we carried out Glutathione S-transferase (GST)-pull-down assays using GST-CBD as bait to precipitate active Cdc42 in lysates of 293 Tet-On cells, in which the expression of LMP1 was induced by doxycycline (Dox)
Consistent with the results obtained in 293 Tet-On cells, LMP1 expression led to a 3.3-fold increase in active Cdc42 in NP69 cells (Figure 1B), and induced 4.6, 6.7, 10.2, and 10.6-fold increases in active Cdc42 in four tested NPC cell lines (TW02, TW01, TW04, and TW06), respectively (Figure 1C)
Summary
Epstein–Barr virus (EBV) is a human c-herpesvirus that is closely associated with many human malignancies, including nasopharyngeal carcinoma (NPC), Burkitt’s lymphoma, T-cell lymphoma, and gastric carcinoma [1]. In NPC, EBV infection is predominantly latent and viral gene expression is restricted. Among the expressed viral genes, latent membrane protein 1 (LMP1) is detected in most NPC tissues [3]. LMP1 is a 62-kDa integral membrane protein composed of a short N-terminal domain, six transmembrane domains, and a 200-amino-acid (aa) cytoplasmic tail at the C-terminus [7]. By mimicking TNFR (tumor necrosis factor receptor) family members, LMP1 through its cytoplasmic tail engages TRAFs (TNFR-associated factors) and TRADD (TNFR-associated death domain protein) to transduce multiple signaling pathways, including nuclear factor-kappa B (NF-kB)-mediated transcription [8] and the c-Jun amino-terminal kinase (JNK) pathway [9,10]. Unlike TNFR-based signaling, LMP1 appears to signal in a ligand-independent fashion relying on its N-terminus and transmembrane domains to selfassociate in the lipid rafts [11,12,13]. LMP1 is a constitutively active receptor [14,15,16]
Sign-in/Register to view highlights & summary Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
