The latent membrane protein 1 (LMP1) oncogene of Epstein-Barr virus can simultaneously induce and inhibit apoptosis in B cells

ZL Pratt, J Zhang, B Sugden - Journal of virology, 2012 - Am Soc Microbiol
Journal of virology, 2012Am Soc Microbiol
The latent membrane protein 1 (LMP1) of Epstein-Barr virus (EBV) regulates its own
expression and the expression of human genes via its two functional moieties; the
transmembrane domains of LMP1 are required to regulate its expression via the unfolded
protein response (UPR) and autophagy in B cells, and the carboxy-terminal domain of LMP1
activates cellular signaling pathways that affect cellular proliferation and survival. An
apparent anomaly in the complex regulation of the UPR and autophagy by LMP1 is that the …
Abstract
The latent membrane protein 1 (LMP1) of Epstein-Barr virus (EBV) regulates its own expression and the expression of human genes via its two functional moieties; the transmembrane domains of LMP1 are required to regulate its expression via the unfolded protein response (UPR) and autophagy in B cells, and the carboxy-terminal domain of LMP1 activates cellular signaling pathways that affect cellular proliferation and survival. An apparent anomaly in the complex regulation of the UPR and autophagy by LMP1 is that the induction of either pathway can lead to cellular death, yet neither EBV-infected B cells nor B cells expressing only LMP1 die. Thus, we sought to understand how B cells that express LMP1 survive. The transmembrane domains of LMP1 activated apoptosis in B cells, the apoptosis required the UPR, and the carboxy-terminal domain of LMP1 blocked this apoptosis. The expression of the mRNA of Bcl2a1, encoding an antiapoptotic homolog of BCL2, correlated directly with the expression of LMP1 in EBV-positive B-cell strains, and its expression inhibited the apoptosis induced by the transmembrane domains of LMP1. These findings illustrate how the carboxy-terminal domain of LMP1 supports survival of B cells in the presence of the deleterious effects of the complex regulation of this viral oncogene.
American Society for Microbiology