Kennerly D A, Sullivan T J, Sylwester P, Parker C W
J Exp Med. 1979 Oct 1;150(4):1039-44. doi: 10.1084/jem.150.4.1039.
Purified rat peritoneal mast cells stimulated with the polycationic histamine-releasing agent compound 48/80 demonstrated a two- to four-fold increase in cellular levels of 1,2-diacylglycerol (DAG) within 1 min as detected by radioactive labeling and direct quantitation experiments. When 2-[1-14C]arachidonoyl-DAG was incubated in the presence of mast-cell homogenates, a rapid conversion to free arachidonate, and to a lesser extent, to monoacylglycerol, triglyceride, and phospholipid was observed. The release of arachidonate was proportional to the amount of broken-cell preparation added and the time of incubation, was prevented by preheating mast-cell preparations, and did not occur when 1-[1-14C]arachidonoyl-phosphatidylcholine was used as substrate, suggesting that the degradation was mediated by an enzyme with Dag-lipase activity. Although much work remains to be done to clarify the precise role of DAG in mast cells, DAG metabolism may be involved in secretion by generating substances which may faciliate membrane fusion and also in arachidonic acid-derived mediator formation by liberating esterified arachidonic acid from mast-cell lipids. Taken together, these studies indicate that the formation of DAG may play a central role in mast-cell function.
用聚阳离子组胺释放剂化合物48/80刺激纯化的大鼠腹膜肥大细胞,通过放射性标记和直接定量实验检测发现,细胞内1,2 - 二酰甘油(DAG)水平在1分钟内增加了2至4倍。当在肥大细胞匀浆存在的情况下孵育2 - [1 - 14C]花生四烯酰 - DAG时,观察到其迅速转化为游离花生四烯酸,在较小程度上转化为单酰甘油、甘油三酯和磷脂。花生四烯酸的释放与添加的破碎细胞制剂的量和孵育时间成正比,通过预热肥大细胞制剂可阻止其释放,并且当使用1 - [1 - 14C]花生四烯酰 - 磷脂酰胆碱作为底物时不会发生释放,这表明降解是由具有Dag - 脂肪酶活性的酶介导的。尽管要阐明DAG在肥大细胞中的精确作用仍有许多工作要做,但DAG代谢可能通过产生促进膜融合的物质参与分泌过程,并且还通过从肥大细胞脂质中释放酯化的花生四烯酸参与花生四烯酸衍生介质的形成。综上所述,这些研究表明DAG的形成可能在肥大细胞功能中起核心作用。