Traf Activation Of C/Ebp Beta (Nf-Il6) Via P38 Mapk Induces Hiv-1 Gene Expression In Monocytes/Macrophages

C/EBP beta plays a pivotal role in activation of human immunodeficiency virus type 1 (HIV-1) in monocytes/macrophages. However, mechanisms for functional regulation of C/EBP beta remain uncharacterized. Previous studies indicated that NF-kappa B activation by tumor necrosis factor (TNF) receptor family, which activates TNF receptor associated factor (TRAF), induces HIV-1 expression. We found that TRAF signals activate HIV-1 LTR with mutations of NF-kappa B sites in promonocytic cell line U937, suggesting existence of an alternative HIV-1 activating pathway. In this study, we have characterized the signal transduction pathway of TRAF other than that leading to NF-kappa B, using U937 cell line, and its subline, U1, which is chronically infected by HIV-1. We show that signals downstream of TRAF2 and TRAF5 activate p38 MAPK, which directly phosphorylates C/EBP beta and that activation of p38 MAPK potently activates C/EBP beta-mediated induction of HIV-1 gene expression. We also show TRAF2 and TRAF5 are expressed in monocytes/macrophages of spleen samples from HIV-1 infected patients. Identification of TRAFp38 MAPK-CEBP beta pathway provides a new target for controlling reactivation of latent HIV-1 in monocytes/macrophages. (C) 2007 Elsevier Masson SAS. All rights reserved.