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首页> 外文期刊>The journal of immunology >Cutting Edge: Dexamethasone Negatively Regulates Syk in Mast Cells by Up-Regulating Src-Like Adaptor Protein
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Cutting Edge: Dexamethasone Negatively Regulates Syk in Mast Cells by Up-Regulating Src-Like Adaptor Protein

机译:前沿:地塞米松通过上调Src样衔接蛋白来负调控肥大细胞中的Syk

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We have identified Src-like adaptor protein (SLAP) as one of several dexamethasone-inducible inhibitory regulators in mast cells. SLAP is a known inhibitor of T cell signaling and interacts with the tyrosine kinase, Zap70. Exposure of RBL-2H3 mast cells to dexamethasone markedly increased expression of SLAP. Cells so exposed or made to overexpress SLAP exhibited reduced Ag-stimulated phosphorylation of Syk (a cognate of Zap70), linker for activation of T cells, phospholipase Cγ, and ERK. Ca2+ mobilization, Ca2+-dependent degranulation, and ERK-dependent release of arachidonic acid were suppressed as well. Small interfering RNA directed against SLAP blocked the induction of SLAP and reversed the inhibitory effects of dexamethasone on phosphorylation of Syk, linker for activation of T cells, and phospholipase Cγ, but not downstream events, which are likely suppressed by up-regulation of downstream of tyrosine kinase-1 and MAPK phosphatase-1. The induction of these inhibitory regulators may contribute to the immunosuppressive activity of dexamethasone in mast cells.
机译:我们已经确定Src样衔接蛋白(SLAP)是肥大细胞中几种地塞米松诱导型抑制性调节剂之一。 SLAP是已知的T细胞信号转导抑制剂,并与酪氨酸激酶Zap70相互作用。 RBL-2H3肥大细胞暴露于地塞米松明显增加了SLAP的表达。如此暴露或使其过度表达SLAP的细胞表现出Ag刺激的Syk(Zap70的同源基因)磷酸化,T细胞活化的连接子,磷脂酶Cγ和ERK减少。 Ca2 +动员,Ca2 +依赖性脱粒和花生四烯酸的ERK依赖性释放也受到抑制。针对SLAP的小分子干扰RNA阻断了SLAP的诱导,并逆转了地塞米松对Syk磷酸化,T细胞活化的连接子和磷脂酶Cγ的抑制作用,但对下游事件没有抑制作用,而下游事件可能被下游的上调所抑制酪氨酸激酶1和MAPK磷酸酶1。这些抑制性调节剂的诱导可能有助于地塞米松在肥大细胞中的免疫抑制活性。

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