Hong S L, Levine L
J Biol Chem. 1976 Sep 25;251(18):5814-6.
Transformed mouse fibroblasts, in which [3H]arachidonic acid was incorporated in the cellular lipids, released radioactive materials into the medium when stimulated by bradykinin and thrombin. Most of this released radioactivity was found in the landins; the remainder was present in the arachidonic acid fraction. When the cells stimulated by serum or when they were mechanically manipulated, not only prostaglandins but also high levels of arachidonic acid were released. Anti-inflammatory steroids, which decrease the availability of arachidonic acid, inhibited the stimulated release of prostaglandins caused by the vasoactive agents, suggesting that bradykinin and thrombin stimulated prostaglandin synthesis by increasing deacylation of the phospholipids. The efficiency of the conversion of the released arachidonic acid into prostaglandins appears to reflect the cellular proximity of the phospholipid deacylating activity and prostaglandin synthesizing system.
已将[3H]花生四烯酸掺入细胞脂质中的转化小鼠成纤维细胞,在受到缓激肽和凝血酶刺激时会将放射性物质释放到培养基中。释放出的大部分放射性物质存在于脂类中;其余部分则存在于花生四烯酸部分。当细胞受到血清刺激或进行机械操作时,不仅会释放前列腺素,还会释放高水平的花生四烯酸。降低花生四烯酸可用性的抗炎类固醇抑制了血管活性药物引起的前列腺素刺激释放,这表明缓激肽和凝血酶通过增加磷脂的脱酰作用来刺激前列腺素合成。释放出的花生四烯酸转化为前列腺素的效率似乎反映了磷脂脱酰活性与前列腺素合成系统在细胞内的接近程度。