Ishimoto T, Akiba S, Sato T
Department of Pathological Biochemistry, Kyoto Pharmaceutical University, Misasagi.
J Biochem. 1996 Sep;120(3):616-23. doi: 10.1093/oxfordjournals.jbchem.a021457.
The association of prostaglandin D2 (PGD2) production as well as arachidonic acid release with the phospholipase D (PLD)-linked mechanism was studied in rat peritoneal mast cells. Stimulation of mast cells with cross-linking of the high-affinity Fc receptor for IgE caused increases in the release of arachidonic acid and PGD2, which are suppressed almost completely by ethanol or RHC 80267, a diacylglycerol lipase inhibitor. Ethanol did not influence inositol phosphate release in response to an antigen. An increase in diacylglycerol, that is inhibited by propranolol, was observed, with a peak within 1 min. Antigen stimulation induced little production of lysophosphatidylcholine, while ionomycin as a control markedly induced the production. However, the phospholipase A2 (PLA2) activity in the cytosol of antigen-stimulated cells increased to the level in ionomycin-stimulated cells. The addition of the ADP-ribosylation factor-containing fraction prepared from bovine brain, that is known to specifically activate PLD, to permeabilized mast cells in the presence of GTP gamma S, apparently increased arachidonic acid and PGD2 release, but not in the presence of ethanol. Furthermore, arachidonic acid release by an antigen was enhanced by melittin, that activates PLA2, but PGD2 production was not. These results suggest that antigen-stimulated PGD2 production as well as arachidonic acid release are strongly associated with the sequential PLD-linked pathway.
在大鼠腹膜肥大细胞中研究了前列腺素D2(PGD2)生成以及花生四烯酸释放与磷脂酶D(PLD)相关机制的关联。用IgE高亲和力Fc受体交联刺激肥大细胞会导致花生四烯酸和PGD2释放增加,而乙醇或二酰基甘油脂肪酶抑制剂RHC 80267几乎可完全抑制这种增加。乙醇不影响抗原刺激引起的肌醇磷酸释放。观察到二酰基甘油增加,其被普萘洛尔抑制,在1分钟内达到峰值。抗原刺激几乎不诱导溶血磷脂酰胆碱的生成,而作为对照的离子霉素则明显诱导其生成。然而,抗原刺激细胞胞质溶胶中的磷脂酶A2(PLA2)活性增加到离子霉素刺激细胞中的水平。在存在GTPγS的情况下,向通透的肥大细胞中添加从牛脑制备的含ADP-核糖基化因子的组分(已知其可特异性激活PLD),明显增加了花生四烯酸和PGD2的释放,但在存在乙醇的情况下则没有。此外,蜂毒肽可增强抗原刺激引起的花生四烯酸释放,蜂毒肽可激活PLA2,但不影响PGD2的生成。这些结果表明,抗原刺激的PGD2生成以及花生四烯酸释放与PLD相关的连续途径密切相关。