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证明血小板活化因子能够激活肥大细胞并诱导趋化反应。

Demonstration that platelet-activating factor is capable of activating mast cells and inducing a chemotactic response.

作者信息

Nilsson G, Metcalfe D D, Taub D D

机构信息

Department of Genetics and Pathology, Uppsala University, Uppsala, Sweden.

出版信息

Immunology. 2000 Feb;99(2):314-9. doi: 10.1046/j.1365-2567.2000.00972.x.

Abstract

Platelet-activating factor (PAF) is generated in a variety of inflammatory conditions in which mast cells accumulate. However, little is known about the ability of PAF to influence mast cell function directly. In this study we examine the ability of PAF to activate mast cells and regulate mast cell chemotaxis. PAF was found to induce intracellular calcium mobilization and chemotactic responses in both murine and human mast cells. PAF induced transient increases in intracellular Ca2+ concentrations with a 50% effective dose of 1 nM and induced significant migratory responses at PAF concentrations of 1 nM to 1 microM in the human leukaemia mast cell line (HMC-1). Using signal transduction inhibitors, both PAF-induced calcium mobilization and migration of mast cells were shown to require activation of pertussis toxin-sensitive G proteins. PAF-induced calcium and chemotactic responses were cross-desensitized by C5a. Together, these data demonstrate that PAF is capable of activating distinct signalling pathways in mast cells associated with calcium mobilization and cell migration; and that PAF may thus contribute to the regulation of mast cell responses and hyperplasia at sites of inflammation.

摘要

血小板活化因子(PAF)在肥大细胞聚集的多种炎症状态下产生。然而,关于PAF直接影响肥大细胞功能的能力知之甚少。在本研究中,我们检测了PAF激活肥大细胞和调节肥大细胞趋化性的能力。发现PAF可诱导小鼠和人肥大细胞的细胞内钙动员和趋化反应。PAF诱导细胞内Ca2+浓度短暂升高,其50%有效剂量为1 nM,并在人白血病肥大细胞系(HMC-1)中,当PAF浓度为1 nM至1 microM时诱导显著的迁移反应。使用信号转导抑制剂,结果显示PAF诱导的钙动员和肥大细胞迁移均需要百日咳毒素敏感的G蛋白激活。PAF诱导的钙和趋化反应可被C5a交叉脱敏。总之,这些数据表明PAF能够激活肥大细胞中与钙动员和细胞迁移相关的不同信号通路;因此PAF可能有助于调节炎症部位的肥大细胞反应和增生。

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