Feistritzer Clemens, Mosheimer Birgit A, Sturn Daniel H, Bijuklic Klaudija, Patsch Josef R, Wiedermann Christian J
Division of General Internal Medicine, Department of Internal Medicine, Medical University of Innsbruck, Anichstrasse 35, A-6020 Innsbruck, Austria.
J Allergy Clin Immunol. 2004 Nov;114(5):1077-84. doi: 10.1016/j.jaci.2004.06.045.
Increased vascularity of bronchial mucosa is closely related to the expression of angiogenic factors, which contribute to the pathogenesis of diseases such as asthma bronchiale.
Here we examine the effects of the angiogenic growth factors angiopoietin 1 and angiopoietin 2 on eosinophil function in vitro and possible involvement of the angiopoietin receptor Tie-2.
Eosinophil migration was studied by micropore filter assays. Signaling mechanisms required for angiopoietin-dependent migration were tested by using signaling enzyme blockers. Tie-2 mRNA and receptor expression on the cell surface of eosinophils was demonstrated in RT-PCR and by fluorescence-activated cell sorting analysis.
Angiopoietin 1 significantly stimulated eosinophil chemotaxis via activation of phosphodiesterase, phosphatidylinositol 3'-kinase, and tyrosine kinases. The effect on eosinophil migration of angiopoietin 1 was reversed by an antibody against the Tie-2 receptor and by angiopoietin 2. Incubation of eosinophils with angiopoietin 1 abolished the chemotactic effects of vascular endothelial growth factor on human eosinophils via the Tie-2 receptor. Finally, Tie-2 expression by human eosinophils was demonstrated on the transcriptional and protein level.
Data suggest that angiopoietin 1 stimulates directed migration and possibly inhibits vascular endothelial growth factor-induced eosinophil chemotaxis via its Tie-2 receptor, which is expressed by eosinophils. Thus, angiopoietin 1 may play an important role in the modulation of eosinophilic inflammation.
支气管黏膜血管增多与血管生成因子的表达密切相关,这些因子参与了诸如支气管哮喘等疾病的发病机制。
在此我们研究血管生成生长因子血管生成素1和血管生成素2对体外嗜酸性粒细胞功能的影响以及血管生成素受体Tie-2可能的参与情况。
通过微孔滤膜试验研究嗜酸性粒细胞迁移。使用信号酶阻断剂测试血管生成素依赖性迁移所需的信号传导机制。通过逆转录聚合酶链反应(RT-PCR)和荧光激活细胞分选分析证明嗜酸性粒细胞细胞表面的Tie-2 mRNA和受体表达。
血管生成素1通过激活磷酸二酯酶、磷脂酰肌醇3'-激酶和酪氨酸激酶显著刺激嗜酸性粒细胞趋化性。抗Tie-2受体抗体和血管生成素2可逆转血管生成素1对嗜酸性粒细胞迁移的影响。用血管生成素1孵育嗜酸性粒细胞可消除血管内皮生长因子通过Tie-2受体对人嗜酸性粒细胞的趋化作用。最后,在转录和蛋白质水平证明了人嗜酸性粒细胞表达Tie-2。
数据表明血管生成素1通过其嗜酸性粒细胞表达的Tie-2受体刺激定向迁移并可能抑制血管内皮生长因子诱导的嗜酸性粒细胞趋化性。因此,血管生成素1可能在嗜酸性粒细胞炎症的调节中起重要作用。