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TNF-α expression in neutrophils and its regulation by glycogen synthase kinase-3: a potentiating role for lithium.
Giambelluca, Miriam S; Bertheau-Mailhot, Geneviève; Laflamme, Cynthia; Rollet-Labelle, Emmanuelle; Servant, Marc J; Pouliot, Marc.
Afiliación
  • Giambelluca MS; Centre de Recherche du Centre Hospitalier Universitaire de Québec and Faculty of Medicine, Université Laval, Quebec City, Quebec, Canada; and.
  • Bertheau-Mailhot G; Centre de Recherche du Centre Hospitalier Universitaire de Québec and Faculty of Medicine, Université Laval, Quebec City, Quebec, Canada; and.
  • Laflamme C; Centre de Recherche du Centre Hospitalier Universitaire de Québec and Faculty of Medicine, Université Laval, Quebec City, Quebec, Canada; and.
  • Rollet-Labelle E; Centre de Recherche du Centre Hospitalier Universitaire de Québec and Faculty of Medicine, Université Laval, Quebec City, Quebec, Canada; and.
  • Servant MJ; Faculty of Pharmacy, Université de Montréal, Montréal, Quebec, Canada.
  • Pouliot M; Centre de Recherche du Centre Hospitalier Universitaire de Québec and Faculty of Medicine, Université Laval, Quebec City, Quebec, Canada; and marc.pouliot@crchul.ulaval.ca.
FASEB J ; 28(8): 3679-90, 2014 Aug.
Article en En | MEDLINE | ID: mdl-24803542
Glycogen synthase kinase 3 (GSK-3) is associated with several cellular systems, including immune response. Lithium, a widely used pharmacological treatment for bipolar disorder, is a GSK-3 inhibitor. GSK-3α is the predominant isoform in human neutrophils. In this study, we examined the effect of GSK-3 inhibition on the production of TNF-α by neutrophils. In the murine air pouch model of inflammation, lithium chloride (LiCl) amplified TNF-α release. In lipopolysaccharide-stimulated human neutrophils, GSK-3 inhibitors mimicked the effect of LiCl, each potentiating TNF-α release after 4 h, in a concentration-dependent fashion, by up to a 3-fold increase (ED50 of 1 mM for lithium). LiCl had no significant effect on cell viability. A positive association was revealed between GSK-3 inhibition and prolonged activation of the p38/MNK1/eIF4E pathway of mRNA translation. Using lysine and arginine labeled with stable heavy isotopes followed by quantitative mass spectrometry, we determined that GSK-3 inhibition markedly increases (by more than 3-fold) de novo TNF-α protein synthesis. Our findings shed light on a novel mechanism of control of TNF-α expression in neutrophils with GSK-3 regulating mRNA translation and raise the possibility that lithium could be having a hitherto unforeseen effect on inflammatory diseases.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Factor de Necrosis Tumoral alfa / Cloruro de Litio / Glucógeno Sintasa Quinasa 3 / Neutrófilos Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: FASEB J Asunto de la revista: BIOLOGIA / FISIOLOGIA Año: 2014 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Factor de Necrosis Tumoral alfa / Cloruro de Litio / Glucógeno Sintasa Quinasa 3 / Neutrófilos Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: FASEB J Asunto de la revista: BIOLOGIA / FISIOLOGIA Año: 2014 Tipo del documento: Article Pais de publicación: Estados Unidos