Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/26096
Title: Differential inhibitory mechanism of cyclic AMP on TNF-alpha and IL-12 synthesis by macrophages exposed to microbial stimuli
Authors: Procópio, Daniela O. [UNIFESP]
Teixeira, Mauro M.
Camargo, Maristela M.
Travassos, Luiz R.
Ferguson, Michael AJ
Almeida, Igor C.
Gazzinelli, Ricardo T.
Universidade Federal de Minas Gerais (UFMG)
FIOCRUZ
Universidade Federal de São Paulo (UNIFESP)
Univ Dundee
Keywords: cyclic AMP
glycosylphosphatidylinositol-mucins
IL-12
IL-10
lipopolysaccharide
macrophage
microbial stimuli
prostaglandins
TNF-alpha
Trypanosoma cruzi
Issue Date: 1-Jul-1999
Publisher: Stockton Press
Citation: British Journal of Pharmacology. Basingstoke: Stockton Press, v. 127, n. 5, p. 1195-1205, 1999.
Abstract: 1 Microbial stimuli such as bacterial lipopolysaccharide (LPS) or glycosylphosphatidylinositol-mucins derived from Trypanosoma cruzi trypomastigotes (tGPI-mucins) are effective stimulators of the synthesis of cytokines by macrophages. Here, we evaluated the ability of cyclic AMP mimetic or elevating agents to modulate TNF-alpha and IL-12 synthesis by murine inflammatory macrophages.2 Cholera Toxin (ChTx) inhibited tGPI-mucins (2.5 nM) or LPS (100 ng ml(-1)) induced TNF-alpha and IL-12(p40) synthesis in a concentration-dependent manner. Similarly, the cyclic AMP mimetics, 8-bromo cyclic AMP or dibutyryl cyclic AMP, or prostaglandin (PG) E-2 inhibited the synthesis of both cytokines by macrophages exposed to microbial stimuli.3 the protein kinase A inhibitor H-89 partially reversed the inhibitory effects of dibutyryl cyclic AMP and PGE(2) on both IL-12(p40) and TNF-alpha synthesis.4 Pretreatment of macrophages with dibutyryl cyclic AMP or ChTx augmented the synthesis of IL-10 triggered by microbial products. Elevation of cyclic AMP inhibited the synthesis of TNF-alpha, but not IL-12(p40), by inflammatory macrophages from IL-10 knockout mice.5 Kinetic studies showed that synthesis of both TNF-alpha and IL-10 peaked at 8 h and IL-12 at 24 h after stimulation with microbial stimuli.6 Together, our findings favour the hypothesis that the cyclic AMP inhibitory activity on IL-12(p40) but not on TNF-alpha synthesis is dependent on de novo protein synthesis, most likely involving IL-10, by macrophages stimulated with microbial products. Accordingly, dibutyryl cyclic AMP inhibited IL-12(p40) synthesis only when added before or at the same time of the stimuli. in contrast, the effect of this cyclic AMP analogue on TNF-alpha synthesis was protracted and observed even 2 h after the addition of the stimuli.
URI: http://repositorio.unifesp.br/handle/11600/26096
ISSN: 0007-1188
Other Identifiers: http://dx.doi.org/10.1038/sj.bjp.0702624
Appears in Collections:Em verificação - Geral

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