Ceramide-dependent trafficking of Epstein-Barr virus LMP1 to small extracellular vesicles

Epstein-Barr virus (EBV) is a human herpesvirus that is associated with a multitude of cancers. The primary EBV oncogene latent membrane protein 1 (LMP1) is secreted from infected cancer cells in small extracellular vesicles (EVs). Additionally, the tetraspanin protein CD63 forms a complex with LMP1 and CD63 can be trafficked to EVs through a ceramide-dependent manner. Therefore, we hypothesize that ceramide is required for efficient packaging of LMP1 into small EVs. Following treatment with the neutral sphingomyelinase inhibitor GW4869, LMP1 cellular localization was disrupted and immunoblotting of EV lysates revealed a significant reduction in extracellular LMP1. NTA of EVs from the LCLs treated with GW4869 demonstrated a significant decrease in particle secretion. Additionally, ceramide inhibition resulted in enhanced LMP1-mediated NFkB activation in EV producing cells. Taken together, these data reveal a critical role for the lipid ceramide in LMP1 exosomal traf-ficking and the oncogenic signaling properties of the viral protein.

Automated summary

Epstein-Barr virus (EBV) is associated with various cancers and its oncogene LMP1 is secreted in small extracellular vesicles (EVs). The protein CD63 forms a complex with LMP1 and can be transported to EVs through ceramide. Therefore, we propose that ceramide is necessary for efficient packaging of LMP1 into small EVs.