Elsner J, Höchstetter R, Kimmig D, Kapp A
Hannover Medical School, Department of Dermatology, Germany.
Eur J Immunol. 1996 Aug;26(8):1919-25. doi: 10.1002/eji.1830260837.
Increased numbers of eosinophils are found in parasitic infections, autoimmune diseases and allergic diseases such as allergic asthma. They are activated by distinct cytokines and chemokines leading to the immigration in the inflamed tissue and mediate tissue damage by releasing reactive oxygen species. Here, the effect of the recently cloned CC chemokine human eotaxin was investigated for its ability to affect different eosinophil effector functions and compared to the CC chemokines MCP-3 and RANTES. Human eotaxin induced chemotaxis of human eosinophils in a dose-dependent manner. The range of efficacy of the CC chemokines compared to the well-known chemotaxin C5a was eotaxin = RANTES > MCP-3 = C5a. In addition, eotaxin induced rapid and transient actin polymerization, a prerequisite for cell migration, in eosinophils in the same range of efficacy as observed for chemotaxis. To investigate whether eotaxin was able to activate the respiratory burst of eosinophils, release of reactive oxygen species was measured by lucigenin-dependent chemiluminescence. Eotaxin induced production of significantly high amounts of reactive oxygen species at a concentration between 10 ng/ml and 500 ng/ml. Surprisingly, the effect of eotaxin was comparable to the well-known eosinophil activator C5a. The range of efficacy of the CC chemokines compared to C5a in the activation of the respiratory burst was eotaxin = C5a > MCP-3 > RANTES. Production of reactive oxygen species was inhibited by pertussis toxin, staurosporin, genestein and wortmannin. Furthermore, eotaxin induced transient increases in intracellular calcium concentration ([Ca2+]i) in human eosinophils. Therefore, pertussis toxin-sensitive Gi-proteins, protein kinase C, tyrosine kinase, phosphatidylinositol-3-kinase and transient increases in [Ca2+]i are involved in the signal transduction of eosinophils following stimulation with eotaxin. In summary, this study reveals the importance of the CC chemokine eotaxin as a potent activator of the respiratory burst, actin polymerization and chemotaxis. Eotaxin, therefore, plays an important role not only by attracting eosinophils to the site of inflammation but also by damaging tissue by its capacity to induce the release of reactive oxygen species.
在寄生虫感染、自身免疫性疾病以及过敏性疾病(如过敏性哮喘)中,嗜酸性粒细胞数量会增加。它们被特定的细胞因子和趋化因子激活,从而迁移至炎症组织,并通过释放活性氧介导组织损伤。在此,研究了最近克隆的CC趋化因子人嗜酸性粒细胞趋化因子对不同嗜酸性粒细胞效应功能的影响,并与CC趋化因子MCP - 3和RANTES进行了比较。人嗜酸性粒细胞趋化因子以剂量依赖的方式诱导人嗜酸性粒细胞的趋化作用。与著名的趋化因子C5a相比,CC趋化因子的效力范围为嗜酸性粒细胞趋化因子 = RANTES > MCP - 3 = C5a。此外,嗜酸性粒细胞趋化因子在与趋化作用相同的效力范围内,诱导嗜酸性粒细胞中肌动蛋白快速且短暂的聚合,这是细胞迁移的一个先决条件。为了研究嗜酸性粒细胞趋化因子是否能够激活嗜酸性粒细胞的呼吸爆发,通过光泽精依赖的化学发光法测量活性氧的释放。嗜酸性粒细胞趋化因子在10 ng/ml至500 ng/ml的浓度范围内诱导产生大量显著的活性氧。令人惊讶的是,嗜酸性粒细胞趋化因子的作用与著名的嗜酸性粒细胞激活剂C5a相当。与C5a相比,CC趋化因子在激活呼吸爆发方面的效力范围为嗜酸性粒细胞趋化因子 = C5a > MCP - 3 > RANTES。百日咳毒素、星形孢菌素、染料木黄酮和渥曼青霉素可抑制活性氧的产生。此外,嗜酸性粒细胞趋化因子诱导人嗜酸性粒细胞内细胞钙浓度([Ca2+]i)短暂升高。因此,百日咳毒素敏感的Gi蛋白、蛋白激酶C、酪氨酸激酶、磷脂酰肌醇-3-激酶以及[Ca2+]i的短暂升高参与了嗜酸性粒细胞趋化因子刺激后嗜酸性粒细胞的信号转导。总之,本研究揭示了CC趋化因子嗜酸性粒细胞趋化因子作为呼吸爆发、肌动蛋白聚合和趋化作用的有效激活剂的重要性。因此,嗜酸性粒细胞趋化因子不仅通过将嗜酸性粒细胞吸引至炎症部位发挥重要作用,还通过其诱导活性氧释放的能力对组织造成损伤。