Okano Y, Ishizuka Y, Nakashima S, Tohmatsu T, Takagi H, Nozawa Y
Biochem Biophys Res Commun. 1985 Mar 29;127(3):726-32. doi: 10.1016/s0006-291x(85)80003-6.
Rat peritoneal mast cells respond to various types of secretagogues, such as antigen (receptor-mediated), A23187 (calcium mobilizing), and compound 48/80 (membrane perturbing), and release arachidonic acid from membrane phospholipids prelabeled with [3H]arachidonate. The rate of arachidonic acid liberation varied from one stimulant to the other. Ionophore A23187 (0.1 micrograms/ml) appeared to be most potent in releasing arachidonate among the three stimulants at which doses each secretagogue caused almost equivalent histamine secretion. However, upon stimulation with these three secretagogues, the radioactivity of phosphatidylcholine (PC) was markedly reduced with a concomitant increase of arachidonate radioactivity. Hydrolysis of PC by phospholipase A2 is likely to be the major route of arachidonic acid liberation in either IgE-mediated or non-IgE activation in mast cells.
大鼠腹膜肥大细胞对多种促分泌剂有反应,如抗原(受体介导)、A23187(钙动员剂)和化合物48/80(膜扰动剂),并从预先用[3H]花生四烯酸标记的膜磷脂中释放花生四烯酸。花生四烯酸的释放速率因刺激剂的不同而有所差异。在三种促分泌剂中,离子载体A23187(0.1微克/毫升)在释放花生四烯酸方面似乎最有效,在这些剂量下,每种促分泌剂引起的组胺分泌几乎相当。然而,在用这三种促分泌剂刺激后,磷脂酰胆碱(PC)的放射性显著降低,同时花生四烯酸放射性增加。磷脂酶A2对PC的水解可能是肥大细胞中IgE介导或非IgE激活时花生四烯酸释放的主要途径。