{"title":"The Mechanisms of Compound 48/80-Induced Superoxide Generation Mediated by A-Kinase in Rat Peritoneal Mast Cells","authors":"Nobuyuki Fukuishi , Masakiyo Sakaguchi , Shiori Matsuura , Chizuko Nakagawa , Reiko Akagi , Masaaki Akagi","doi":"10.1006/bmme.1997.2594","DOIUrl":null,"url":null,"abstract":"<div><p>This investigation was undertaken to clarify the mechanisms of superoxide anion (O<sub><sub>2</sub></sub><sup>−</sup>) generation in rat peritoneal mast cells. Compound 48/80, a typical histamine liberator mediated by calcium influx, elicited O<sub><sub>2</sub></sub><sup>−</sup>generation 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 O<sub><sub>2</sub></sub><sup>−</sup>generation in the mast cells, but other unsaturated fatty acids had no effect. On the other hand, 48/80-induced O<sub><sub>2</sub></sub><sup>−</sup>generation was inhibited by phospholipase A2 inhibitors, such as arachidonyl trifluoromethyl ketone and manoalide. Forskolin, isoprenaline, and dibutyryl cyclic AMP inhibited the O<sub><sub>2</sub></sub><sup>−</sup>generation, and KT-5720, a cyclic AMP-dependent protein kinase (A-kinase) inhibitor, markedly enhanced the O<sub><sub>2</sub></sub><sup>−</sup>generation. These findings suggest that O<sub><sub>2</sub></sub><sup>−</sup>is 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.</p></div>","PeriodicalId":8837,"journal":{"name":"Biochemical and molecular medicine","volume":"61 1","pages":"Pages 107-113"},"PeriodicalIF":0.0000,"publicationDate":"1997-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1006/bmme.1997.2594","citationCount":"34","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biochemical and molecular medicine","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1077315097925941","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 34
Abstract
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 O2−generation 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 O2−generation in the mast cells, but other unsaturated fatty acids had no effect. On the other hand, 48/80-induced O2−generation was inhibited by phospholipase A2 inhibitors, such as arachidonyl trifluoromethyl ketone and manoalide. Forskolin, isoprenaline, and dibutyryl cyclic AMP inhibited the O2−generation, and KT-5720, a cyclic AMP-dependent protein kinase (A-kinase) inhibitor, markedly enhanced the O2−generation. These findings suggest that O2−is 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.