Hamel-Côté Geneviève, Gendron Daniel, Rola-Pleszczynski Marek, Stankova Jana
Immunology Division, Department of Pediatrics, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Sherbrooke, QC, Canada.
PLoS One. 2017 Jul 7;12(7):e0180336. doi: 10.1371/journal.pone.0180336. eCollection 2017.
Atherosclerosis is a pro-inflammatory condition underlying many cardiovascular diseases. Platelet-activating factor (PAF) and interleukin 6 (IL-6) are actively involved in the onset and progression of atherosclerotic plaques. The involvement of monocyte-derived macrophages is well characterized in the installation of inflammatory conditions in the plaque, but less is known about the contribution of monocyte-derived dendritic cells (Mo-DCs). In the same way, the involvement of calcium, phospholipase C and A2 in PAF-induced IL-6 production, in different cells types, has been shown; however, the importance of the Jak/STAT pathway and its regulation by protein-tyrosine phosphatases in this response have not been addressed. In this study, we report that PAF stimulates PTP1B activity via Jak2, thereby modulating PAF-induced IL-6 production. Using HEK 293 cells stably transfected with the PAF receptor in order to discriminate the pathway components, our results suggest that Jak2 modulates PAF-induced IL-6 production via both positive and negative pathways. Jak2 kinase activity was necessary for maximal transactivation of the IL-6 promoter, as seen by luciferase assays, whereas the same kinase also downregulated this promoter transactivation through the activation of a calcium/calpain/PTP1B pathway. The same pathways were operational in monocyte-derived dendritic cells, since PAF-induced PTP1B activation negatively regulated PAF-induced IL-6 mRNA production and, in addition, Jak2 activated calpain, one of the components involved in PAF-induced PTP1B activation. Results obtained in this study indicate that Jak2 activation is important for maximal IL-6 promoter transactivation by PAF and that PTP1B is involved in the negative regulation of this transactivation. However, PTP1B does not directly regulate Jak2 activation, but rather Jak2 regulates PAF-induced PTP1B activation.
动脉粥样硬化是许多心血管疾病潜在的促炎病症。血小板活化因子(PAF)和白细胞介素6(IL-6)积极参与动脉粥样硬化斑块的发生和发展。单核细胞衍生的巨噬细胞在斑块炎症状态的形成中所起的作用已得到充分表征,但对于单核细胞衍生的树突状细胞(Mo-DC)的作用了解较少。同样,在不同细胞类型中,钙、磷脂酶C和A2参与PAF诱导的IL-6产生已得到证实;然而,Jak/STAT途径及其在该反应中受蛋白酪氨酸磷酸酶调节的重要性尚未得到探讨。在本研究中,我们报告PAF通过Jak2刺激PTP1B活性,从而调节PAF诱导的IL-6产生。为了区分途径成分,我们使用稳定转染了PAF受体的HEK 293细胞,结果表明Jak2通过正向和负向途径调节PAF诱导的IL-6产生。荧光素酶测定显示,Jak2激酶活性对于IL-6启动子的最大反式激活是必需的,而同一激酶也通过激活钙/钙蛋白酶/PTP1B途径下调该启动子的反式激活。相同的途径在单核细胞衍生的树突状细胞中也起作用,因为PAF诱导的PTP1B激活负调节PAF诱导的IL-6 mRNA产生,此外,Jak2激活钙蛋白酶,钙蛋白酶是参与PAF诱导的PTP1B激活的成分之一。本研究获得的结果表明,Jak2激活对于PAF介导的最大IL-6启动子反式激活很重要,并且PTP1B参与该反式激活的负调节。然而,PTP1B并不直接调节Jak2激活,而是Jak2调节PAF诱导的PTP1B激活。