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首页> 外文期刊>Biochemical and Biophysical Research Communications >Role of Janus kinase-2 in IgE receptor-mediated leukotriene C4 production by mast cells.
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Role of Janus kinase-2 in IgE receptor-mediated leukotriene C4 production by mast cells.

机译:Janus激酶2在肥大细胞IgE受体介导的白三烯C4产生中的作用。

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摘要

We have previously shown that Janus kinase 3, a member of the family of non-receptor protein tyrosine kinases, plays a critical role in the regulation of FcepsilonRI-mediated mast cell responses. In the current study, we investigated the role of another JAK family member, JAK2, in these responses. Our results show that the treatment of IgE-sensitized mouse mast cells with an inhibitor of JAK2 (AG490) blocked the release of leukotriene C(4) in a dose-dependent fashion after antigen challenge. However, prostaglandin PG D(2) production and degranulation were not affected under identical experimental conditions. Transfection of RBL-2H3 mast cells with JAK-2 specific small interfering RNA resulted in a 50% reduction of LTC(4) release in response to FcepsilonRI crosslinking, but did not inhibit mast cell degranulation or calcium ionophore-induced LTC(4) release, indicating involvement of JAK2 in IgE receptor-mediated leukotriene release. Taken together, these data suggest that JAK2 is a critical regulator of IgE/antigen-induced production of LTC(4) in mast cells.
机译:我们以前已经表明,Janus激酶3,非受体蛋白酪氨酸激酶家族的成员,在FcepsilonRI介导的肥大细胞反应的调节中起着关键作用。在当前的研究中,我们调查了另一个JAK家族成员JAK2在这些反应中的作用。我们的结果表明,用JAK2抑制剂(AG490)对IgE致敏小鼠肥大细胞的治疗以抗原依赖后以剂量依赖的方式阻止了白三烯C(4)的释放。但是,在相同的实验条件下,前列腺素PG D(2)的生产和脱粒作用不受影响。 RBL-2H3肥大细胞与JAK-2特异性小干扰RNA的转染导致FcepsilonRI交联反应使LTC(4)释放减少50%,但不抑制肥大细胞脱粒或钙离子载体诱导的LTC(4)释放,表明JAK2参与IgE受体介导的白三烯释放。综上所述,这些数据表明,JAK2是肥大细胞中IgE /抗原诱导的LTC(4)产生的关键调节剂。

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