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前列腺素D2对调节人嗜碱性粒细胞组胺释放的作用。

Effect of prostaglandin D2 in modulating histamine release from human basophils.

作者信息

Peters S P, Kagey-Sobotka A, MacGlashan D W, Lichtenstein L M

出版信息

J Pharmacol Exp Ther. 1984 Feb;228(2):400-6.

PMID:6198512
Abstract

Prostaglandin (PG) D2 is the major cyclooxygenase metabolite of arachidonic acid released after immunologic stimulation of mast cells. In this report, we demonstrate that this PG is unlike other PGs previously investigated in that it enhances human basophil histamine release at concentrations of 1 to 100 nM. Enhancement is seen when antigen, the phorbol diester, 12-O-tetradecanoylphorbol-13-acetate and ionophore A23187 are used to initiate release and, in preparations of basophils, purified to 51 to 66% of total cell number as well as in preparations of mixed leukocytes. This enhancement is a late or "second stage" phenomenon as defined by the two stages of histamine release and is additive with the enhancement produced by D2O, but not with the enhancement produced by indomethacin or 5-hydroperoxyeicosatetraenoic acid. PGD2 also reverses the inhibition of release produced by drugs and hormones such as dimaprit and PGE2 that activate adenylate cyclase to increase cellular cyclic AMP levels. These data suggest that PGD2 may play an important role in allergic and immunologic reactions and suggest a mechanism by which mast cells and basophils can interact during these reactions.

摘要

前列腺素(PG)D2是肥大细胞受到免疫刺激后释放的花生四烯酸的主要环氧化酶代谢产物。在本报告中,我们证明这种前列腺素与先前研究的其他前列腺素不同,因为它在1至100 nM的浓度下可增强人嗜碱性粒细胞组胺释放。当使用抗原、佛波酯、12-O-十四酰佛波醇-13-乙酸酯和离子载体A23187引发释放时,以及在嗜碱性粒细胞制备物(纯化至占细胞总数的51%至66%)和混合白细胞制备物中,均可观察到增强作用。这种增强是组胺释放两个阶段所定义的晚期或“第二阶段”现象,并且与D2O产生的增强作用相加,但与吲哚美辛或5-氢过氧化二十碳四烯酸产生的增强作用不相加。PGD2还可逆转由药物和激素(如激活腺苷酸环化酶以增加细胞内环磷酸腺苷水平的二甲双胍和PGE2)所产生的释放抑制作用。这些数据表明PGD2可能在过敏和免疫反应中起重要作用,并提示了肥大细胞和嗜碱性粒细胞在这些反应中可能相互作用的机制。

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