Mueller H W, O'Flaherty J T, Wykle R L
J Biol Chem. 1984 Dec 10;259(23):14554-9.
In this study, the molecular species distribution of 1-O-alkyl-2-acetyl-sn-glycero-3-phosphocholine (platelet-activating factor) synthesized by rabbit peritoneal and human peripheral neutrophils was examined. Radiolabeled platelet-activating factor synthesized from [3H]acetate by neutrophils stimulated with ionophore A23187, opsonized zymosan, or N-formyl-methionyl-leucyl-phenylalanine was separated into the individual molecular species on the basis of length and degree of unsaturation of the 1-O-alkyl chain using reverse-phase high-performance liquid chromatography. The predominant alkyl chains in the labeled platelet-activating factor synthesized by ionophore- or zymosan-stimulated rabbit cells were 15:0 (4%), 16:0 (43%), 18:0 (11%), and 18:1 (26%). This is in contrast to the alkyl chain distribution of the widely accepted precursor of platelet-activating factor, 1-O-alkyl-2-acyl-sn-glycero-3-phosphocholine, present in the cell. The major alkyl chains contained in the labeled platelet-activating factor synthesized by ionophore-, zymosan-, or N-formyl-methionyl-leucyl-phenylalanine-stimulated human neutrophils were 16:0 (40%), 17:0 (8 and 5%; two isomers), 18:0 (16%), and 18:1 (18%). As found with the rabbit cells, this distribution differs from the alkyl chain content of 1-O-alkyl-2-acyl-sn-glycero-3-phosphocholine in human neutrophils, which contains less than 1% of each 17:0 isomer. We demonstrate here that the platelet-activating factor synthesized by rabbit peritoneal and human peripheral polymorphonuclear neutrophils is heterogeneous and that some selectivity exists in the choice of the 1-O-alkyl-2-acyl-sn-glycero-3-phosphocholine precursor for platelet-activating factor synthesis in these cells. It also appears that the molecular species distribution of platelet-activating factor is independent of the stimulus used to elicit its synthesis.
在本研究中,检测了兔腹膜和人外周血中性粒细胞合成的1-O-烷基-2-乙酰基-sn-甘油-3-磷酸胆碱(血小板活化因子)的分子种类分布。用离子载体A23187、调理酵母聚糖或N-甲酰甲硫氨酰亮氨酰苯丙氨酸刺激中性粒细胞,由[3H]乙酸盐合成的放射性标记血小板活化因子,利用反相高效液相色谱法,根据1-O-烷基链的长度和不饱和度,将其分离为各个分子种类。离子载体或酵母聚糖刺激的兔细胞合成的标记血小板活化因子中,主要的烷基链为15:0(4%)、16:0(43%)、18:0(11%)和18:1(26%)。这与细胞中广泛接受的血小板活化因子前体1-O-烷基-2-酰基-sn-甘油-3-磷酸胆碱的烷基链分布不同。离子载体、酵母聚糖或N-甲酰甲硫氨酰亮氨酰苯丙氨酸刺激的人中性粒细胞合成的标记血小板活化因子中含有的主要烷基链为16:0(40%)、17:0(8%和5%;两种异构体)、18:0(16%)和18:1(18%)。正如在兔细胞中发现的那样,这种分布与人中性粒细胞中1-O-烷基-2-酰基-sn-甘油-3-磷酸胆碱的烷基链含量不同,后者每种17:0异构体的含量均低于1%。我们在此证明,兔腹膜和人外周血多形核中性粒细胞合成的血小板活化因子是异质的,并且在这些细胞中,血小板活化因子合成的1-O-烷基-2-酰基-sn-甘油-3-磷酸胆碱前体的选择存在一些选择性。似乎血小板活化因子的分子种类分布也与引发其合成的刺激无关。