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嗜酸性粒细胞趋化因子及嗜酸性粒细胞趋化因子受体(CCR3)在葡聚糖颗粒诱导的大鼠肺部炎症中的表达

Eotaxin and eotaxin receptor (CCR3) expression in Sephadex particle-induced rat lung inflammation.

作者信息

Harrington P M, Newton D J, Williams C M, Hunt J A, Dearman R J, Kimber I, Coleman J W, Flanagan B F

机构信息

Department of Immunology, University of Liverpool, Alderley Park, Macclesfield, UK.

出版信息

Int J Exp Pathol. 1999 Jun;80(3):177-85. doi: 10.1046/j.1365-2613.1999.00112.x.

Abstract

The beta chemokine eotaxin is a potent eosinophil activator and chemoattractant. We examined immunohistochemically eotaxin protein expression in a range of normal rat tissues and in rat lung during Sephadex particle-induced pulmonary inflammation. The time course of eotaxin expression in lung at various time points after Sephadex administration was related to the appearance of eosinophils in the bronchoalveolar lavage fluid and tissue distribution of eotaxin receptor (CCR3) positive cells. Results showed that eotaxin protein was constitutively expressed by both lung airway epithelial cells and gut epithelial cells in normal tissues in the absence of inflammation. During Sephadex induced pulmonary inflammation, eotaxin expression increased in alveolar macrophages prior to the major increase in eosinophil numbers which reached a peak at 72 h. The pattern of eotaxin pulmonary expression and the location of CCR3 receptor positive cells suggest a chemoattractant gradient resulting in migration firstly into the tissue and subsequently through the airway epithelium into the airways. Treatment of rats with the glucocorticoid dexamethasone or the immunosuppressant cyclosporin A reduced eosinophil entry into lung tissue and airways but had no apparent effect on eotaxin expression in vivo, indicating that both these drugs inhibit eosinophil recruitment either by an eotaxin-independent mechanism, or by targetting factors that synergise with eotaxin, or an event post eotaxin expression.

摘要

β趋化因子嗜酸性粒细胞趋化因子是一种有效的嗜酸性粒细胞激活剂和趋化剂。我们采用免疫组织化学方法检测了正常大鼠一系列组织以及葡聚糖颗粒诱导的大鼠肺部炎症模型中肺组织内嗜酸性粒细胞趋化因子蛋白的表达情况。葡聚糖给药后不同时间点肺组织中嗜酸性粒细胞趋化因子表达的时间进程与支气管肺泡灌洗液中嗜酸性粒细胞的出现以及嗜酸性粒细胞趋化因子受体(CCR3)阳性细胞的组织分布相关。结果显示,在无炎症的正常组织中,肺气道上皮细胞和肠道上皮细胞均组成性表达嗜酸性粒细胞趋化因子蛋白。在葡聚糖诱导的肺部炎症过程中,嗜酸性粒细胞趋化因子在肺泡巨噬细胞中的表达在嗜酸性粒细胞数量大幅增加之前就开始上升,嗜酸性粒细胞数量在72小时达到峰值。嗜酸性粒细胞趋化因子在肺部的表达模式以及CCR3受体阳性细胞的定位表明存在一种趋化梯度,首先导致细胞迁移至组织中,随后穿过气道上皮进入气道。用糖皮质激素地塞米松或免疫抑制剂环孢素A治疗大鼠可减少嗜酸性粒细胞进入肺组织和气道,但对体内嗜酸性粒细胞趋化因子的表达无明显影响,这表明这两种药物要么通过不依赖嗜酸性粒细胞趋化因子的机制,要么通过靶向与嗜酸性粒细胞趋化因子协同作用的因子,或者在嗜酸性粒细胞趋化因子表达后的某个事件来抑制嗜酸性粒细胞的募集。

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