Swendsen C L, Ellis J M, Chilton F H, O'Flaherty J T, Wykle R L
Biochem Biophys Res Commun. 1983 May 31;113(1):72-9. doi: 10.1016/0006-291x(83)90433-3.
Rabbit peritoneal neutrophils incorporated [14C]arachidonic acid into seven molecular species of choline-containing phosphoglycerides. These 2-[14C]arachidonoyl species differed with respect to the alkyl ether or acyl residue bound at the sn-1 position; four of the seven were ether-linked. Stimulation with calcium ionophore A23187 induced a proportionate release of arachidonate from all seven molecular species: 40% of the released arachidonate came from alkyl ether species. Thus, 1-O-alkyl-2-arachidonoyl-sn-glycero-3-phosphocholine (GPC) is a significant source of metabolizable arachidonic acid. Since 1-O-alkyl-2-lyso-GPC is the metabolic precursor of platelet activating factor, these results further interrelate pathways forming arachidonate metabolites and platelet activating factor; they also supply a rationale for the observation that both classes of stimuli form concomitantly during cell activation.
兔腹膜中性粒细胞将[14C]花生四烯酸掺入七种含胆碱的磷酸甘油酯分子物种中。这些2-[14C]花生四烯酰基物种在sn-1位结合的烷基醚或酰基残基方面有所不同;七种中有四种是醚连接的。用钙离子载体A23187刺激会导致花生四烯酸从所有七种分子物种中按比例释放:释放的花生四烯酸中有40%来自烷基醚物种。因此,1-O-烷基-2-花生四烯酰基-sn-甘油-3-磷酸胆碱(GPC)是可代谢花生四烯酸的重要来源。由于1-O-烷基-2-溶血-GPC是血小板活化因子的代谢前体,这些结果进一步将形成花生四烯酸代谢物和血小板活化因子的途径联系起来;它们还为在细胞活化过程中这两类刺激同时形成的观察结果提供了理论依据。