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血小板激活因子从人血单核细胞中的释放。

Release of PAF-acether from human blood monocytes.

作者信息

Arnoux B, Jouvin-Marche E, Arnoux A, Benveniste J

出版信息

Agents Actions. 1982 Dec;12(5-6):713-6. doi: 10.1007/BF01965089.

Abstract

Stimulation of human blood monocytes with ionophore A 23187 induced the release of platelet-activating factor (PAF-acether). Phagocytosis of zymosan, coated or not with complement, bacteria or immune complexes, stimulated the release of PAF-acether whereas that of latex particles was without effect. Such release did not occur at 4 degrees C or in the presence of EDTA. PAF-acether derived from monocytes shared the same characteristics as hog leucocyte PAF-acether or synthetic 1-O-alkyl-2-acetyl-glyceryl-3-phosphorylcholine. In lung physiology, the release of PAF-acether from monocytes and alveolar macrophages could lead, via the platelets, to bronchoconstriction. It could represent a cause for asthma other than the classical IgE-mastocyte interaction.

摘要

用离子载体A 23187刺激人血单核细胞可诱导血小板活化因子(PAF-乙醚)的释放。酵母聚糖(无论是否包被补体)、细菌或免疫复合物的吞噬作用可刺激PAF-乙醚的释放,而乳胶颗粒的吞噬作用则无此效应。这种释放在4℃或存在乙二胺四乙酸(EDTA)时不会发生。源自单核细胞的PAF-乙醚与猪白细胞PAF-乙醚或合成的1-O-烷基-2-乙酰基甘油-3-磷酸胆碱具有相同的特性。在肺生理学中,单核细胞和肺泡巨噬细胞释放的PAF-乙醚可通过血小板导致支气管收缩。它可能代表了除经典的免疫球蛋白E(IgE)-肥大细胞相互作用之外的哮喘病因。

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