Pulmonary Research Group, Department of Medicine, University of Alberta, Edmonton, AB, Canada; Department of Paediatrics, University of Alberta, Edmonton, AB, Canada.
Immunology. 2015 Apr;144(4):641-8. doi: 10.1111/imm.12416.
Degranulation from eosinophils in response to secretagogue stimulation is a regulated process that involves exocytosis of granule proteins through specific signalling pathways. One potential pathway is dependent on cyclin-dependent kinase 5 (Cdk5) and its effector molecules, p35 and p39, which play a central role in neuronal cell exocytosis by phosphorylating Munc18, a regulator of SNARE binding. Emerging evidence suggests a role for Cdk5 in exocytosis in immune cells, although its role in eosinophils is not known. We sought to examine the expression of Cdk5 and its activators in human eosinophils, and to assess the role of Cdk5 in eosinophil degranulation. We used freshly isolated human eosinophils and analysed the expression of Cdk5, p35, p39 and Munc18c by Western blot, RT-PCR, flow cytometry and immunoprecipitation. Cdk5 kinase activity was determined following eosinophil activation. Cdk5 inhibitors were used (roscovitine, AT7519 and small interfering RNA) to determine its role in eosinophil peroxidase (EPX) secretion. Cdk5 was expressed in association with Munc18c, p35 and p39, and phosphorylated following human eosinophil activation with eotaxin/CCL11, platelet-activating factor, and secretory IgA-Sepharose. Cdk5 inhibitors (roscovitine, AT7519) reduced EPX release when cells were stimulated by PMA or secretory IgA. In assays using small interfering RNA knock-down of Cdk5 expression in human eosinophils, we observed inhibition of EPX release. Our findings suggest that in activated eosinophils, Cdk5 is phosphorylated and binds to Munc18c, resulting in Munc18c release from syntaxin-4, allowing SNARE binding and vesicle fusion, with subsequent eosinophil degranulation. Our work identifies a novel role for Cdk5 in eosinophil mediator release by agonist-induced degranulation.
嗜酸性粒细胞对刺激物的脱颗粒反应是一个受调控的过程,涉及通过特定的信号通路将颗粒蛋白排出。一种潜在的途径依赖于周期蛋白依赖性激酶 5(Cdk5)及其效应分子 p35 和 p39,它们通过磷酸化 SNARE 结合的调节因子 Munc18,在神经元细胞胞吐作用中发挥核心作用。新出现的证据表明 Cdk5 在免疫细胞的胞吐作用中起作用,尽管其在嗜酸性粒细胞中的作用尚不清楚。我们试图研究 Cdk5 及其激活剂在人嗜酸性粒细胞中的表达,并评估 Cdk5 在嗜酸性粒细胞脱颗粒中的作用。我们使用新鲜分离的人嗜酸性粒细胞,通过 Western blot、RT-PCR、流式细胞术和免疫沉淀分析 Cdk5、p35、p39 和 Munc18c 的表达。在嗜酸性粒细胞活化后测定 Cdk5 激酶活性。使用 Cdk5 抑制剂(罗司维特、AT7519 和小干扰 RNA)来确定其在嗜酸性粒细胞过氧化物酶(EPX)分泌中的作用。Cdk5 与 Munc18c、p35 和 p39 一起表达,并在人嗜酸性粒细胞被 eotaxin/CCL11、血小板激活因子和分泌型 IgA-Sepharose 激活后磷酸化。当细胞被 PMA 或分泌型 IgA 刺激时,Cdk5 抑制剂(罗司维特、AT7519)减少 EPX 释放。在使用小干扰 RNA 敲低人嗜酸性粒细胞中 Cdk5 表达的实验中,我们观察到 EPX 释放被抑制。我们的研究结果表明,在活化的嗜酸性粒细胞中,Cdk5 被磷酸化并与 Munc18c 结合,导致 Munc18c 从突触融合蛋白-4 释放,允许 SNARE 结合和囊泡融合,随后嗜酸性粒细胞脱颗粒。我们的工作确定了 Cdk5 在激动剂诱导的脱颗粒作用中通过嗜酸性粒细胞介质释放的新作用。