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血小板活化因子与巨噬细胞。I. 大鼠和小鼠腹腔巨噬细胞而非肥大细胞释放该因子的证据。

Platelet-activating factor and macrophages. I. Evidence for the release from rat and mouse peritoneal macrophages and not from mastocytes.

作者信息

Mencia-Huerta J M, Benveniste J

出版信息

Eur J Immunol. 1979 May;9(5):409-15. doi: 10.1002/eji.1830090512.

Abstract

Platelet-activating factor (PAF) is a phospholipid mediator of anaphylaxis, released from basophils of several mammalian species, that aggregates platelets and releases their vasoactive amines. The ionophore A23 187 induced the release of PAF from rat and mouse peritoneal cells, a mixed cell population that was fractionated using 5--15% Ficoll gradients and adherence to plastic petri dishes. PAF was associated with large, acid phosphatase-containing, adherent mononuclear cells. Mastocytes did not release PAF but released histamine by the action of ionophore or 48/80; they could not be held responsible for inactivation of PAF or inhibition of the PAF-induced platelet aggregation. These data indicate that, besides blood basophils, peritoneal macrophages are a likely source for PAF, a result that adds a new important function to the macrophage:aggregation of platelets and liberation of their inflammatory and vasoactive substances.

摘要

血小板活化因子(PAF)是一种过敏反应的磷脂介质,由几种哺乳动物的嗜碱性粒细胞释放,可使血小板聚集并释放其血管活性胺。离子载体A23187可诱导大鼠和小鼠腹膜细胞释放PAF,腹膜细胞是一种混合细胞群体,使用5%-15%的菲可梯度和贴壁于塑料培养皿的方法进行分离。PAF与大的、含酸性磷酸酶的贴壁单核细胞相关。肥大细胞不释放PAF,但通过离子载体或48/80的作用释放组胺;它们不能对PAF的失活或PAF诱导的血小板聚集的抑制负责。这些数据表明,除了血液中的嗜碱性粒细胞外,腹膜巨噬细胞可能是PAF的来源,这一结果为巨噬细胞增加了一项新的重要功能:血小板聚集及其炎症和血管活性物质的释放。

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