TY - JOUR T1 - Compounds That Increase or Mimic Cyclic Adenosine Monophosphate Enhance Tristetraprolin Degradation in Lipopolysaccharide-Treated Murine J774 Macrophages JF - Journal of Pharmacology and Experimental Therapeutics JO - J Pharmacol Exp Ther SP - 514 LP - 522 DO - 10.1124/jpet.107.133702 VL - 326 IS - 2 AU - Ulla Jalonen AU - Erja-Leena Paukkeri AU - Eeva Moilanen Y1 - 2008/08/01 UR - http://jpet.aspetjournals.org/content/326/2/514.abstract N2 - Tristetraprolin (TTP) is a trans-acting factor that can regulate mRNA stability by binding to the cis-acting AU-rich element (ARE) in the 3′-untranslated region in mRNAs of certain transiently expressed genes. The best-studied target of TTP is tumor necrosis factor (TNF)-α. By binding to ARE, TTP increases the degradation of TNF-α mRNA, thereby reducing the expression of TNF-α. We examined the effects of cAMP analogs and the cAMP-elevating agents forskolin and β2-agonists on lipopolysaccharide (LPS)-induced TTP mRNA and protein expression by quantitative real-time reverse transcriptase-polymerase chain reaction and Western blotting in activated macrophages. All of these agents caused a slight increase in LPS-induced expression of TTP mRNA. However, TTP protein levels were significantly reduced when the cells were treated with the combination of LPS and cAMP-elevating agent compared with LPS alone. Proteasome inhibitors MG132 (N-[(phenylmethoxy)-carbonyl]-l-leucyl-N-[(1S)-1-formyl-3-methylbutyl]-l-leucinamide) and lactacystin increased TTP protein levels and abolished the effects of cAMP-enhancing compounds on TTP protein levels. The results suggest that mediators and drugs that enhance intracellular cAMP reduce TTP expression in macrophages exposed to inflammatory stimuli by increasing TTP degradation through the proteasome pathway. The American Society for Pharmacology and Experimental Therapeutics ER -