Reddy S T, Herschman H R
Departments of Biological Chemistry and Molecular and Medical Pharmacology, and the Molecular Biology Institute, UCLA Center for the Health Sciences, Los Angeles, California 90095, USA.
J Biol Chem. 1997 Feb 7;272(6):3231-7. doi: 10.1074/jbc.272.6.3231.
Aggregation of IgE cell surface receptors on MMC-34 cells, a murine mast cell line, induces the synthesis and secretion of prostaglandin D2 (PGD2). Synthesis and secretion of PGD2 in activated MMC-34 cells occurs in two stages, an early phase that is complete within 30 min after activation and a late phase that reaches a maximum about 6 h after activation. The early and late phases of PGD2 generation are mediated by prostaglandin synthase 1 (PGS1) and prostaglandin synthase 2 (PGS2), respectively. Arachidonic acid, the substrate for both PGS1 and PGS2, is released from membrane phospholipids by the activation of phospholipases. We now demonstrate that in activated mast cells (i) secretory phospholipase A2 (PLA2) mediates the release of arachidonic acid for early, PGS1-dependent synthesis of PGD2; (ii) secretory PLA2 does not play a role in the late, PGS2-dependent synthesis of PGD2; (iii) cytoplasmic PLA2 mediates the release of arachidonic acid for late, PGS2-dependent synthesis of PGD2; and (iv) a cytoplasmic PLA2-dependent step precedes secretory PLA2 activation and is necessary for optimal PGD2 production by the secretory PLA2/PGS1-dependent early pathway.
MMC - 34细胞(一种小鼠肥大细胞系)上IgE细胞表面受体的聚集可诱导前列腺素D2(PGD2)的合成与分泌。活化的MMC - 34细胞中PGD2的合成与分泌分两个阶段进行,早期阶段在活化后30分钟内完成,晚期阶段在活化后约6小时达到最大值。PGD2生成的早期和晚期阶段分别由前列腺素合酶1(PGS1)和前列腺素合酶2(PGS2)介导。花生四烯酸是PGS1和PGS2的底物,通过磷脂酶的激活从膜磷脂中释放出来。我们现在证明,在活化的肥大细胞中:(i)分泌型磷脂酶A2(PLA2)介导花生四烯酸的释放,用于早期依赖PGS1的PGD2合成;(ii)分泌型PLA2在晚期依赖PGS2的PGD2合成中不起作用;(iii)细胞质型PLA2介导花生四烯酸的释放,用于晚期依赖PGS2的PGD2合成;(iv)细胞质型PLA2依赖步骤先于分泌型PLA2激活,并且对于分泌型PLA2/PGS1依赖的早期途径产生最佳PGD2是必需的。