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HMG-CoA reductase inhibitor simvastatin inhibits proinflammatory cytokine production from murine mast cells.

机译:HMG-CoA还原酶抑制剂辛伐他汀抑制鼠肥大细胞产生促炎性细胞因子。

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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-alpha 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-alpha mRNA, was evaluated. RESULTS: Incubation of BMMCs with simvastatin resulted in the inhibition of LPS-induced TNF-alpha 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-alpha 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.
机译:背景:他汀类药物抑制3-羟-3-甲基戊二酰辅酶A(HMG-CoA)还原酶,它是甲羟戊酸途径中的关键限速酶。越来越多的数据表明,他汀类药物对包括实验性自身免疫性脑脊髓炎和抗原诱导的过敏性气道炎症在内的许多实验模型均具有抗炎作用。但是,他汀类药物的抗炎作用的潜在机制仍是未知之数。在这项研究中,我们检查了代表性的他汀类药物辛伐他汀对鼠肥大细胞促炎细胞因子产生的影响。方法:在存在或不存在辛伐他汀的情况下,用脂多糖(LPS)刺激骨髓源性肥大细胞(BMMC),并评估其在mRNA和蛋白质水平上的分泌。评估了辛伐他汀对Tristetraprolin的表达的影响,Tristetraprolin是一种促进TNF-αmRNA衰变的RNA结合蛋白。结果:辛伐他汀与BMMC一起孵育可抑制LPS诱导的mRNA和蛋白水平上的TNF-α产生。辛伐他汀还抑制LPS刺激的BMMC产生IL-6。然而,辛伐他汀没有增强三四脯氨酸的表达。结论:辛伐他汀部分抑制了转录产物的从头合成,从而抑制了活化的肥大细胞中TNF-α和IL-6的产生,该抑制作用可能是辛伐他汀的抗炎作用。

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