HMG-CoA Reductase Inhibitor Simvastatin Inhibits Proinflammatory Cytokine Production from Murine Mast Cells
Authors:
- Hiroko KanariHKHiroko Kanari
- Akira SutoASAkira Suto
- Michio FujiwaraMFMichio Fujiwara
- Kei IkedaKIKei Ikeda
- Koichi HiroseKHKoichi Hirose
- Norihiko WatanabeNWNorihiko Watanabe
- Itsuo IwamotoIIItsuo Iwamoto
- Hiroshi NakajimaHNHiroshi Nakajima
- 1 May 2008
- journal article
- research article
- Published by S. Karger AG in International Archives of Allergy and Immunology
- Vol. 146 (Suppl. 1) , 61-66
Abstract
Background: Statins inhibit 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase, a key rate-limiting enzyme in the mevalonate pathway. Accumulating data suggest that statins exhibit anti-inflammatory effects on a number of experimental models including experimental autoimmune encephalomyelitis and antigen-induced allergic airway inflammation. However, the mechanism underlying the anti-inflammatory effect of statins is still largely unknown. In this study, we examined the effect of a representative statin, simvastatin, on proinflammatory cytokine production from murine mast cells. Methods: Bone marrow-derived mast cells (BMMCs) were stimulated with lipopolysaccharide (LPS) in the presence or absence of simvastatin, and TNF-α and IL-6 production from BMMCs was evaluated at mRNA and protein levels. The effect of simvastatin on the expression of tristetraprolin, an RNA-binding protein that promotes decay of TNF-α mRNA, was evaluated. Results: Incubation of BMMCs with simvastatin resulted in the inhibition of LPS-induced TNF-α production at both mRNA and protein levels. Simvastatin also inhibited IL-6 production from LPS-stimulated BMMCs. However, simvastatin did not enhance the expression of tristetraprolin. Conclusions: Simvastatin inhibits the production of TNF-α and IL-6 from activated mast cells in part by inhibiting de novo synthesis of their transcripts and the inhibition may account for the anti-inflammatory effect of simvastatin.Keywords
This publication has 10 references indexed in Scilit:
- NADPH oxidase 4 is an oncoprotein localized to mitochondriaCancer Biology & Therapy, 2010
- Nox4 and Nox2 NADPH Oxidases Mediate Distinct Cellular Redox Signaling Responses to Agonist StimulationArteriosclerosis, Thrombosis, and Vascular Biology, 2008
- Molecular evolution of the reactive oxygen-generating NADPH oxidase (Nox/Duox) family of enzymesBMC Ecology and Evolution, 2007
- Suppressing phosphatidylcholine‐specific phospholipase C and elevating ROS level, NADPH oxidase activity and Rb level induced neuronal differentiation in mesenchymal stem cellsJournal of Cellular Biochemistry, 2007
- Cannabidiol-Induced Apoptosis in Human Leukemia Cells: A Novel Role of Cannabidiol in the Regulation of p22 and Nox4 ExpressionMolecular Pharmacology, 2006
- Angiotensin II increases differentiation of dopaminergic neurons from mesencephalic precursors via angiotensin type 2 receptorsEuropean Journal of Neuroscience, 2004
- Role of common cytokine receptor γ chain (γc)– and Jak3-dependent signaling in the proliferation and survival of murine mast cellsBlood, 2000
- Complete and Reversible Inhibition of NADPH Oxidase in Human Neutrophils by Phenylarsine Oxide at a Step Distal to Membrane Translocation of the Enzyme SubunitsJournal of Biological Chemistry, 1995
- Active oxygen species stimulate vascular smooth muscle cell growth and proto-oncogene expression.Circulation Research, 1992
- Establishment and characterization of multipotent neural cell lines using retrovirus vector‐mediated oncogene transferJournal of Neurobiology, 1990