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选择性4型环核苷酸磷酸二酯酶抑制剂咯利普兰对嗜酸性粒细胞趋化因子介导的人嗜酸性粒细胞活化和迁移的抑制作用

Inhibition of eotaxin-mediated human eosinophil activation and migration by the selective cyclic nucleotide phosphodiesterase type 4 inhibitor rolipram.

作者信息

Santamaria L F, Palacios J M, Beleta J

机构信息

Grupo Farmacéutico Almirall, S. A. Research Center, Barcelona, Spain.

出版信息

Br J Pharmacol. 1997 Jul;121(6):1150-4. doi: 10.1038/sj.bjp.0701243.

Abstract
  1. The effect of the selective type 4 phosphodiesterase (PDE 4) inhibitor rolipram on human eosinophil activation and migration mediated by eotaxin was investigated. 2. Studies were performed with human freshly isolated eosinophils from peripheral blood of healthy donors by a magnetic cell separation (MACS) technique to a purity > 99%. To test the effect of rolipram, eosinophils were stimulated with recombinant human eotaxin and the cell surface activation markers CD11b and L-selectin were analysed by flow cytometry. Furthermore, eotaxin mediated eosinophil migration was measured in a transendothelial chemotaxis assay. 3. Our results indicate that rolipram inhibited eotaxin-induced CD11b up-regulation up to 60.6 +/- 7.6% at the highest tested dose (10 microM), whereas transendothelial chemotaxis was partially inhibited reaching a plateau of approx. 30% at a rolipram concentration of 0.1 microM. 4. We conclude that the selective PDE 4 inhibitor rolipram decreases eotaxin mediated eosinophil activation, an observation that may contribute to elucidate the mechanism by which PDE 4 inhibitors reduce antigen-induced eosinophil infiltration in different animal models of allergic inflammation.
摘要
  1. 研究了选择性4型磷酸二酯酶(PDE 4)抑制剂咯利普兰对嗜酸性粒细胞趋化因子介导的人嗜酸性粒细胞活化和迁移的影响。2. 采用磁珠细胞分选(MACS)技术从健康供体的外周血中新鲜分离出人嗜酸性粒细胞,纯度>99%,进行相关研究。为了测试咯利普兰的作用,用重组人嗜酸性粒细胞趋化因子刺激嗜酸性粒细胞,并用流式细胞术分析细胞表面活化标志物CD11b和L-选择素。此外,在跨内皮趋化试验中检测嗜酸性粒细胞趋化因子介导的嗜酸性粒细胞迁移。3. 我们的结果表明,在最高测试剂量(10 microM)下,咯利普兰可将嗜酸性粒细胞趋化因子诱导的CD11b上调抑制高达60.6 +/- 7.6%,而跨内皮趋化在咯利普兰浓度为0.1 microM时受到部分抑制,达到约30%的平台期。4. 我们得出结论,选择性PDE 4抑制剂咯利普兰可降低嗜酸性粒细胞趋化因子介导的嗜酸性粒细胞活化,这一观察结果可能有助于阐明PDE 4抑制剂在不同过敏性炎症动物模型中减少抗原诱导的嗜酸性粒细胞浸润的机制。

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