Prostaglandin E2 Reduces Toll-Like Receptor 4 Expression in Alveolar Macrophages by Inhibition of Translation

Alveolar macrophages (AMs) represent the first line of innate immune defense in the lung. AMs use pattern recognition receptors (PRRs) to sense pathogens. The best studied PRR is Toll-like receptor (TLR) 4, which detects LPS from gram-negative bacteria. The lipid mediator prostaglandin (PG)E-2 dampens AM immune responses by inhibiting the signaling events downstream of PRRs. We examined the effect of PGE(2) on TLR4 expression in rat AMs. Although PGE(2) did not reduce the mRNA levels of TLR4, it decreased TLR4 protein levels. The translation inhibitor cycloheximide reduced TLR4 protein levels with similar kinetics as PGE(2), and its effects were not additive with those of the prostanoid, suggesting that PGE(2) inhibits TLR at the translational level. The action of PGE(2) could be mimicked by the direct stimulator of cAMP formation, forskolin, and involved E prostanoid receptor 2 ligation and cAMP-dependent activation of unanchored type I protein kinase A. Cells pretreated with PGE(2) for 24 hours exhibited decreased TNF-alpha mRNA and protein levels in response to LPS stimulation. Knockdown of TLR4 protein by small interfering RNA to the levels achieved by PGE(2) treatment likewise decreased TNF-alpha mRNA and protein in response to LPS, establishing the functional significance of this PGE(2) effect. We provide the first evidence of a lipid mediator acting through its cognate G protein-coupled receptor to affect PRR translation. Because PGE2 is produced in abundance at sites of infection, its inhibitory effects on AM TLR4 expression have important implications for host defense in the lung.