Yamaguchi Takafumi, Kimura Hirokazu, Kurabayashi Masahiko, Kozawa Kunihisa, Kato Masahiko
Gunma Prefectural Institute of Public Health and Environmental Sciences, Maebashi, Gunma, Japan.
Immunol Lett. 2008 Jun 15;118(1):88-95. doi: 10.1016/j.imlet.2008.03.005. Epub 2008 Apr 10.
T helper (Th) 2-type cytokines play a dominant role in allergic inflammation. Accumulating evidence suggests that Th1-type cytokines antagonize Th2-type cytokine responses; however, recent studies demonstrate that Th1 cytokines might enhance Th2 immune responses. We examined whether interferon (IFN)-gamma, a representative Th1 cytokine, modifies the effector functions of human eosinophils stimulated by granulocyte-macrophage colony-stimulating factor (GM-CSF) and interleukin (IL)-5. GM-CSF and IL-5 have significant functional homology, and contribute to the regulation of Th2 immunity. After the pretreatment of eosinophils with IFN-gamma, GM-CSF- or IL-5-induced eosinophil functions were examined, including superoxide anion generation, degranulation, adhesion, expression of GM-CSF receptor (R), IL-5R, or CD11b, and phosphorylation of intracellular signaling molecules. Superoxide anion generation was measured using the cytochrome c reduction method. Degranulation and cell adhesion were evaluated based on eosinophil-derived neurotoxin (EDN) contents in supernatants or adherent cells. Phosphorylation of signaling molecules was analyzed using a multiplex beads array system. Preincubation with IFN-gamma resulted in enhanced GM-CSF- or IL-5-induced superoxide anion generation and degranulation of human eosinophils, whereas stimulus-induced eosinophil adhesion was unaffected. In addition, IFN-gamma did not influence the expression of GM-CSFR, IL-5R, and CD11b. Furthermore, IFN-gamma upregulated GM-CSF- or IL-5-induced phosphorylation of extracellular signal-regulated kinase (ERK), p38 mitogen-activated protein kinase (MAPK), c-Jun N-terminal kinase (JNK), and activating transcription factor (ATF)-2. Finally, we confirmed that MAPK inhibitors blocked the enhancement of stimuli-induced superoxide anion generation of IFN-gamma treated eosinophils. In conclusion, IFN-gamma might upregulate ERK, p38, or JNK/ATF-2 phosphorylation induced by GM-CSF or IL-5, leading to enhanced cytokine-induced eosinophil superoxide generation and degranulation.
辅助性T细胞(Th)2型细胞因子在过敏性炎症中起主导作用。越来越多的证据表明,Th1型细胞因子可拮抗Th2型细胞因子反应;然而,最近的研究表明,Th1细胞因子可能会增强Th2免疫反应。我们研究了干扰素(IFN)-γ(一种代表性的Th1细胞因子)是否会改变粒细胞-巨噬细胞集落刺激因子(GM-CSF)和白细胞介素(IL)-5刺激的人嗜酸性粒细胞的效应功能。GM-CSF和IL-5具有显著的功能同源性,并有助于调节Th2免疫。在用IFN-γ预处理嗜酸性粒细胞后,检测GM-CSF或IL-5诱导的嗜酸性粒细胞功能,包括超氧阴离子生成、脱颗粒、黏附、GM-CSF受体(R)、IL-5R或CD11b的表达以及细胞内信号分子的磷酸化。使用细胞色素c还原法测量超氧阴离子生成。根据上清液或贴壁细胞中嗜酸性粒细胞衍生神经毒素(EDN)的含量评估脱颗粒和细胞黏附。使用多重微珠阵列系统分析信号分子的磷酸化。用IFN-γ预孵育可增强GM-CSF或IL-5诱导的人嗜酸性粒细胞超氧阴离子生成和脱颗粒,而刺激诱导的嗜酸性粒细胞黏附不受影响。此外,IFN-γ不影响GM-CSFR、IL-5R和CD11b的表达。此外,IFN-γ上调GM-CSF或IL-5诱导的细胞外信号调节激酶(ERK)、p38丝裂原活化蛋白激酶(MAPK)、c-Jun氨基末端激酶(JNK)和激活转录因子(ATF)-2的磷酸化。最后,我们证实MAPK抑制剂可阻断IFN-γ处理的嗜酸性粒细胞刺激诱导的超氧阴离子生成增强。总之,IFN-γ可能上调GM-CSF或IL-5诱导的ERK、p38或JNK/ATF-2磷酸化,导致细胞因子诱导的嗜酸性粒细胞超氧生成和脱颗粒增强。