Nishihara Fuyumi, Nakagome Kazuyuki, Kobayashi Takehito, Noguchi Toru, Araki Ryuichiro, Uchida Yoshitaka, Soma Tomoyuki, Nagata Makoto
Dept of Respiratory Medicine and Allergy Center, Saitama Medical University, Saitama, Japan.
Community Health Science Center, Saitama Medical University, Saitama, Japan.
ERJ Open Res. 2015 Dec 22;1(2). doi: 10.1183/23120541.00003-2015. eCollection 2015 Oct.
In the airways of severe asthmatics, an increase of neutrophils and eosinophils is often observed despite high-dose corticosteroid therapy. We previously reported that interleukin-8-stimulated neutrophils induced trans-basement membrane migration (TBM) of eosinophils, suggesting the link between neutrophils and eosinophils. Concentrations of lipopolysaccharide (LPS) in the airway increase in severe asthma. As neutrophils express Toll-like receptor (TLR)4 and can release chemoattractants for eosinophils, we investigated whether LPS-stimulated neutrophils modify eosinophil TBM. Neutrophils and eosinophils were isolated from peripheral blood of healthy volunteers and severe asthmatics. Eosinophil TBM was examined using a modified Boyden's chamber technique. Eosinophils were added to the upper compartment, and neutrophils and LPS were added to the lower compartment. Migrated eosinophils were measured by eosinophil peroxidase assays. LPS-stimulated neutrophils induced eosinophil TBM (about 10-fold increase), although LPS or neutrophils alone did not. A leukotriene B receptor antagonist, a platelet-activating factor receptor antagonist or an anti-TLR4 antibody decreased eosinophil TBM enhanced by LPS-stimulated neutrophils by almost half. Neutrophils from severe asthmatics induced eosinophil TBM and lower concentrations of LPS augmented neutrophil-induced eosinophil TBM. These results suggest that the combination of neutrophils and LPS leads eosinophils to accumulate in the airways, possibly involved the pathogenesis of severe asthma.
在重度哮喘患者的气道中,尽管采用了高剂量皮质类固醇治疗,但通常仍会观察到中性粒细胞和嗜酸性粒细胞增多。我们之前报道过,白细胞介素-8刺激的中性粒细胞可诱导嗜酸性粒细胞跨基底膜迁移(TBM),这表明中性粒细胞与嗜酸性粒细胞之间存在联系。重度哮喘患者气道中脂多糖(LPS)的浓度会升高。由于中性粒细胞表达Toll样受体(TLR)4并能释放嗜酸性粒细胞趋化因子,我们研究了LPS刺激的中性粒细胞是否会改变嗜酸性粒细胞的TBM。从健康志愿者和重度哮喘患者的外周血中分离出中性粒细胞和嗜酸性粒细胞。使用改良的Boyden室技术检测嗜酸性粒细胞的TBM。将嗜酸性粒细胞加入上室,将中性粒细胞和LPS加入下室。通过嗜酸性粒细胞过氧化物酶测定法测量迁移的嗜酸性粒细胞。LPS刺激的中性粒细胞可诱导嗜酸性粒细胞TBM(增加约10倍),而单独的LPS或中性粒细胞则不会。白三烯B受体拮抗剂、血小板活化因子受体拮抗剂或抗TLR4抗体可使LPS刺激的中性粒细胞增强的嗜酸性粒细胞TBM降低近一半。重度哮喘患者的中性粒细胞可诱导嗜酸性粒细胞TBM,较低浓度的LPS可增强中性粒细胞诱导的嗜酸性粒细胞TBM。这些结果表明,中性粒细胞和LPS的组合会导致嗜酸性粒细胞在气道中积聚,这可能与重度哮喘的发病机制有关。