Reddy S T, Winstead M V, Tischfield J A, Herschman H R
Department of Biological Chemistry, UCLA Center for the Health Sciences, Los Angeles, California 90095-1570, USA.
J Biol Chem. 1997 May 23;272(21):13591-6. doi: 10.1074/jbc.272.21.13591.
Prostaglandin D2 (PGD2) synthesis in activated mast cells occurs in two phases, an early phase that is dependent on prostaglandin synthase 1 and a delayed phase that is dependent on activation-induced prostaglandin synthase 2 gene expression. Early phase PGD2 synthesis in activated mast cells also requires the activity of a secretory phospholipase A2 (PLA2). It has been thought that the secretory PLA2 expressed in mast cells is group IIa PLA2, encoded by the Pla2 g2a gene. However, activated bone marrow-derived mast cells prepared from Pla2 g2a+/+ mice and mast cells prepared from mice with a mutation in the Pla2 g2a gene both demonstrate early phase PGD2 synthesis. Moreover, mast cells from both murine strains secrete PLA2 activity following activation. Northern and reverse transcriptase/polymerase chain reaction analyses demonstrate that mast cells from Pla2 g2a+/+ and Pla2 g2a-/- mice do not express group IIa PLA2 message. Instead, Northern and reverse transcriptase/polymerase chain reaction analyses demonstrate that both Pla2 g2a+/+ and Pla2 g2a-/- mast cells express mRNA for group V PLA2, encoded by the Pla2gV gene. An antisense oligonucleotide directed against group V PLA2 is also able to inhibit both the early phase of PGD2 production and the secretion of PLA2 activity by activated mast cells. Our data suggest that (i) group IIa PLA2 does not play a significant role in murine mast cell prostaglandin synthesis, (ii) group V PLA2 mediates early mast cell PGD2 production and transcellular PGE2 production in murine mast cells, and (iii) much of the data, based on studies with chemical inhibitors and antibodies, suggesting that group IIa PLA2 is responsible for arachidonic acid mobilization needs to be reevaluated.
活化肥大细胞中前列腺素D2(PGD2)的合成分为两个阶段,早期阶段依赖于前列腺素合酶1,延迟阶段依赖于激活诱导的前列腺素合酶2基因表达。活化肥大细胞中早期阶段的PGD2合成还需要分泌型磷脂酶A2(PLA2)的活性。一直以来人们认为肥大细胞中表达的分泌型PLA2是由Pla2 g2a基因编码的IIa型PLA2。然而,从Pla2 g2a+/+小鼠制备的活化骨髓源肥大细胞和从Pla2 g2a基因突变小鼠制备的肥大细胞均表现出早期阶段的PGD2合成。此外,两种小鼠品系的肥大细胞在激活后均分泌PLA2活性。Northern印迹分析和逆转录酶/聚合酶链反应分析表明,Pla2 g2a+/+和Pla2 g2a-/-小鼠的肥大细胞不表达IIa型PLA2信息。相反,Northern印迹分析和逆转录酶/聚合酶链反应分析表明,Pla2 g2a+/+和Pla2 g2a-/-肥大细胞均表达由Pla2gV基因编码的V型PLA2的mRNA。针对V型PLA2的反义寡核苷酸也能够抑制活化肥大细胞PGD2产生的早期阶段以及PLA2活性的分泌。我们的数据表明:(i)IIa型PLA2在小鼠肥大细胞前列腺素合成中不发挥重要作用;(ii)V型PLA2介导小鼠肥大细胞中早期肥大细胞PGD2的产生和跨细胞PGE2的产生;(iii)基于化学抑制剂和抗体研究得出的表明IIa型PLA2负责花生四烯酸动员的许多数据需要重新评估。