Komabayashi T, Yakata A, Izawa T, Noguchi M, Suda K, Tsuboi M
Department of Physiology and Pharmacology, Tokyo College of Pharmacy, Japan.
Jpn J Pharmacol. 1992 May;59(1):97-103. doi: 10.1254/jjp.59.97.
We investigated the effects of A23187 and phorbol 12,13-dibutyrate (PDBu) on sn-1,2-diacylglycerol (DAG) accumulation and phosphatidylcholine (PC) hydrolysis in rat parotid acinar cells. Both A23187 and PDBu, in concentration ranges of 0.001-0.1 microM, stimulated DAG accumulation and PC hydrolysis in a time- and concentration-dependent manner. Treatment with A23187 and PDBu stimulated the release of [3H]choline and [3H]phosphocholine into the medium, indicating [3H]PC hydrolysis is due to the activation of phospholipases C and D; however, [3H]phosphatidylethanolamine hydrolysis was not indicated. These releases were unaffected by the addition of glucose 6-phosphate, a phosphatase inhibitor. Staurosporine, a protein kinase C inhibitor, significantly inhibited the DAG accumulation and the PC hydrolysis stimulated by these agents. Combinations of A23187 and PDBu potentiated the stimulatory effect which each of these agents alone had on DAG accumulation and PC hydrolysis. This mode of action was additive but not synergistic. These results suggest that DAG accumulation induced by A23187 and PDBu is related to the PC hydrolysis mediated via the activation of phospholipases C and D, and that it is not related to phosphatidylethanolamine hydrolysis.
我们研究了A23187和佛波醇12,13 - 二丁酸酯(PDBu)对大鼠腮腺腺泡细胞中sn-1,2-二酰甘油(DAG)积累和磷脂酰胆碱(PC)水解的影响。在0.001 - 0.1微摩尔浓度范围内,A23187和PDBu均以时间和浓度依赖性方式刺激DAG积累和PC水解。用A23187和PDBu处理刺激了[3H]胆碱和[3H]磷酸胆碱释放到培养基中,表明[3H]PC水解是由于磷脂酶C和D的激活;然而,未观察到[3H]磷脂酰乙醇胺水解。这些释放不受磷酸酶抑制剂6-磷酸葡萄糖添加的影响。蛋白激酶C抑制剂星形孢菌素显著抑制了这些试剂刺激的DAG积累和PC水解。A23187和PDBu的组合增强了这些试剂单独对DAG积累和PC水解的刺激作用。这种作用方式是相加的而非协同的。这些结果表明,A23187和PDBu诱导的DAG积累与通过磷脂酶C和D的激活介导的PC水解有关,而与磷脂酰乙醇胺水解无关。