Whorton A R, Young S L, Data J L, Barchowsky A, Kent R S
Biochim Biophys Acta. 1982 Jul 20;712(1):79-87. doi: 10.1016/0005-2760(82)90087-x.
Porcine aortic endothelial cells studied at confluence were found to synthesize both prostacyclin and prostaglandin E2. Addition of arachidonic acid, bradykinin, the calcium ionophore A23187 or thrombin stimulated prostaglandin formation, whereas addition of angiotensin II did not. Bradykinin was found to stimulate very potently arachidonic acid release from cells prelabelled with [3H]arachidonate, the response being dose-dependent and half-maximal at 8 ng/ml. The rate of release of label (primarily arachidonate) from cells was increased by bradykinin (100 ng/ml) approximately 8-fold, with a return to control levels by 10 min. The calcium ionophore, A23187, similarly released [3H]arachidonic acid from prelabelled cells; the rate of release was approximately linear for 15 min. Both bradykinin and ionophore A23187 stimulated [3H]arachidonate release from endothelial cell phospholipids, an effect which was abolished in a dose-dependent manner by mepacrine. Release in response to bradykinin was prevented by incubation in Ca2+-free medium. Trifluoperazine, a compound which can inhibit calmodulin-mediated events, blocked the release of label stimulated by bradykinin. These data indicate that the likely mechanism of bradykinin-stimulated prostaglandin production in endothelial cells involves the activation of a phospholipase via a Ca2+-calmodulin-dependent pathway.
对汇合状态下的猪主动脉内皮细胞进行研究时发现,它们能合成前列环素和前列腺素E2。添加花生四烯酸、缓激肽、钙离子载体A23187或凝血酶可刺激前列腺素的形成,而添加血管紧张素II则无此作用。发现缓激肽能非常有效地刺激预先用[3H]花生四烯酸标记的细胞释放花生四烯酸,该反应呈剂量依赖性,在8 ng/ml时达到半数最大效应。缓激肽(100 ng/ml)可使细胞中标记物(主要是花生四烯酸)的释放速率增加约8倍,并在10分钟内恢复到对照水平。钙离子载体A23187同样能使预先标记的细胞释放[3H]花生四烯酸;释放速率在15分钟内大致呈线性。缓激肽和离子载体A23187均能刺激内皮细胞磷脂释放[3H]花生四烯酸,这一效应可被米帕林以剂量依赖性方式消除。在无钙培养基中孵育可阻止缓激肽引起的释放。三氟拉嗪是一种能抑制钙调蛋白介导事件的化合物,它能阻断缓激肽刺激的标记物释放。这些数据表明,缓激肽刺激内皮细胞产生前列腺素的可能机制涉及通过钙-钙调蛋白依赖性途径激活磷脂酶。