Daniel L W, Beaudry G A, King L, Waite M
Biochim Biophys Acta. 1984 Jan 17;792(1):33-8. doi: 10.1016/0005-2760(84)90279-0.
Challenge of Madin-Darby canine kidney (MDCK) cells with the divalent cation ionophore A23187 caused a marked increase in the deacylation of [3H]arachidonic acid but not of [14C]palmitic acid. When the cells were treated with 12-O-tetradecanoyl-phorbol-13-acetate (TPA) and A23187, there was an additional increase in the deacylation of [3H]arachidonic acid compared to that observed with either agent alone. In contrast to deacylation, the stimulation of prostaglandin production by A23187 was small compared to the stimulation by TPA. Cycloheximide inhibited synthesis of prostaglandins in TPA-treated cells, but did not block the stimulated deacylation caused by either TPA or A23187. These data indicate that, while both TPA and A23187 stimulated the deacylation of [3H]arachidonic acid, TPA had an additional, cycloheximide-sensitive effect that was required for efficient conversion of the release fatty acids to prostaglandins. Thus, although required, deacylation appeared to be independent of and insufficient to stimulate maximum prostaglandin synthesis in these cells.
用二价阳离子载体A23187刺激犬肾Madin-Darby(MDCK)细胞,导致[3H]花生四烯酸的脱酰作用显著增加,但[14C]棕榈酸的脱酰作用未增加。当细胞用12-O-十四烷酰佛波醇-13-乙酸酯(TPA)和A23187处理时,与单独使用任何一种试剂相比,[3H]花生四烯酸的脱酰作用进一步增加。与脱酰作用相反,A23187对前列腺素生成的刺激作用与TPA相比很小。放线菌酮抑制TPA处理细胞中前列腺素的合成,但不阻断TPA或A23187引起的脱酰作用增强。这些数据表明,虽然TPA和A23187都刺激了[3H]花生四烯酸的脱酰作用,但TPA具有一种额外的、对放线菌酮敏感的效应,这种效应是释放的脂肪酸有效转化为前列腺素所必需的。因此,虽然脱酰作用是必需的,但它似乎独立于这些细胞中最大前列腺素合成的刺激作用,且不足以刺激最大前列腺素合成。