| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 9001733 | Biochemical Pharmacology | 2005 | 8 Pages | 
Abstract
												Tristetraprolin (TTP) is a factor that regulates mRNA stability and the expression of certain inflammatory genes. In the present study, we found that TTP expression was increased in macrophages exposed to bacterial lipopolysaccharide (LPS). Dexamethasone and dissociated steroid RU24858 inhibited LPS-induced TTP protein and mRNA expression and the inhibitory effect was reversed by a glucocorticoid receptor antagonist mifepristone. Histone deacetylase inhibitors trichostatin A (TSA) and apicidin reduced the inhibitory effect of dexamethasone and RU24858 on TTP expression, but the glucocorticoids did not alter TTP mRNA half-life. These results suggest that anti-inflammatory steroids reduce TTP expression in activated macrophages by a glucocorticoid response element (GRE)-independent mechanism, possibly through histone deacetylation and transcriptional silencing.
											Keywords
												LPSPD 98059SB 203580PDTCGREGAPDHJnkNF-κBc-Jun N-terminal kinaseERK1/2MAPKGlucocorticoid response elementnuclear factor κBlipopolysaccharidemitogen-activated protein kinasepyrrolidinedithiocarbamateextracellular signal-regulated kinase 1/2glyceraldehyde-3-phosphate dehydrogenaseglucocorticoid receptor
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											Authors
												Ulla Jalonen, Aleksi Lahti, Riku Korhonen, Hannu Kankaanranta, Eeva Moilanen, 
											