a激酶介导的化合物48/80诱导大鼠腹膜肥大细胞产生超氧化物的机制

Nobuyuki Fukuishi , Masakiyo Sakaguchi , Shiori Matsuura , Chizuko Nakagawa , Reiko Akagi , Masaaki Akagi
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引用次数: 34

摘要

本研究旨在阐明大鼠腹膜肥大细胞中超氧阴离子(O2−)产生的机制。化合物48/80是一种典型的由钙内流介导的组胺解毒剂,以剂量依赖性的方式诱导肥大细胞产生O2−。免疫组化和Western blot分析表明,肥大细胞含有47-kDa的吞噬细胞氧化酶(p47phox)蛋白,该蛋白是NADPH氧化酶系统的胞质组分之一。花生四烯酸刺激肥大细胞产生O2−,而其他不饱和脂肪酸没有作用。另一方面,48/80诱导的O2 -生成被磷脂酶A2抑制剂(如花生四烯酮三氟甲基酮和manoalide)抑制。Forskolin、异丙肾上腺素和二丁基环AMP均抑制O2 -生成,而环AMP依赖性蛋白激酶(a激酶)抑制剂KT-5720显著增强O2 -生成。这些发现表明,O2−是由肥大细胞中的NADPH氧化酶样酶系统产生的,该酶系统被胞质磷脂酶A2释放的花生四烯酸激活。因此,它受环AMP-A激酶系统的调节。
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The Mechanisms of Compound 48/80-Induced Superoxide Generation Mediated by A-Kinase in Rat Peritoneal Mast Cells

This investigation was undertaken to clarify the mechanisms of superoxide anion (O2) generation in rat peritoneal mast cells. Compound 48/80, a typical histamine liberator mediated by calcium influx, elicited O2generation from the mast cells in a dose-dependent fashion. It was demonstrated by immunohistochemical study and Western blot analysis that the mast cells contained the 47-kDa phagocyte oxidase (p47phox) protein, which was one cytosolic component of the NADPH oxidase system. Arachidonic acid stimulated O2generation in the mast cells, but other unsaturated fatty acids had no effect. On the other hand, 48/80-induced O2generation was inhibited by phospholipase A2 inhibitors, such as arachidonyl trifluoromethyl ketone and manoalide. Forskolin, isoprenaline, and dibutyryl cyclic AMP inhibited the O2generation, and KT-5720, a cyclic AMP-dependent protein kinase (A-kinase) inhibitor, markedly enhanced the O2generation. These findings suggest that O2is generated by a NADPH oxidase-like enzyme system in mast cells and that this enzyme system is activated by arachidonic acid released by cytosolic phospholipase A2. Thus, it is regulated by the cyclic AMP-A kinase system.

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