Dexamethasone Differentially Regulates Cytokine Transcription and Translation in Macrophages Responding to Bacteria or Okadaic Acid

• Published in: Cellular signalling Vol. 11; no. 9; pp. 665 - 670
• Main Authors: Gewert, Karin, Svensson, Ulf, Andersson, Karolina, Holst, Elisabet, Sundler, Roger
• Format: Journal Article
• Language: English
• Published: England Elsevier Inc 01-09-1999
• Subjects: Animals; Anti-Inflammatory Agents - pharmacology; Bacteria; Cells, Cultured; Dexamethasone; Dexamethasone - pharmacology; Female; Fusobacterium nucleatum - immunology; Gene Expression Regulation - drug effects; Glucocorticoid; Glucocorticoids - pharmacology; Interleukin-1; Interleukin-1 - genetics; Macrophage; Macrophages, Peritoneal - cytology; Macrophages, Peritoneal - drug effects; Macrophages, Peritoneal - immunology; Mice; Okadaic acid; Okadaic Acid - immunology; Okadaic Acid - pharmacology; Peptostreptococcus - immunology; Propionibacterium acnes - immunology; Protein Biosynthesis - drug effects; Tumor Necrosis Factor-alpha - genetics; Tumour necrosis factor-α; P. anaerobius–Peptostreptococcus anaerobius; Interleukin-1; TNF–tumor necrosis factor; P. acnes–Propionibacterium acnes; Tumour necrosis factor-α; Dexamethasone; IL-1–interleukin-1; Glucocorticoid; LPS–bacterial lipopolysaccharide; Bacteria; Okadaic acid; Macrophage; F. nucleatum–Fusobacterium nucleatum
• ISSN: 0898-6568; 1873-3913
• DOI: 10.1016/S0898-6568(99)00014-5

Many microorganisms and microbial products induce expression of pro-inflammatory cytokines such as interleukin-1 (IL-1α/β) and tumour necrosis factor-α (TNF-α) in macrophages, primarily by transcriptional activation. We show here, by using mouse macrophages in primary culture, that pre-treatment with dexamethasone inhibits bacteria-induced IL-1β expression as mRNA and cellular pro-IL-1β in parallel, consistent with an effect primarily on transcriptional activation. In contrast, the expression of TNF-α mRNA was only partly inhibited despite virtually complete inhibition of TNF-α protein formation. Furthermore, the selective induction of primarily cell-associated 26,000
M
r pro-TNF-α by the protein phosphatase inhibitor okadaic acid also was partly inhibited at the mRNA level by dexamethasone, whereas additional translational inhibition appeared to be lacking. This latter finding is reminiscent of earlier findings regarding signalling to activation of cytosolic phospholipase A
2, which is sensitive to dexamethasone when elicited by bacteria, but not when elicited by okadaic acid. The present results raise the possibility that the inhibitory effect of dexamethasone on TNF-α translation, but not on transcriptional activation, is mediated by one or more okadaic acid-sensitive protein phosphatases.