Komabayashi T, Yakata A, Izawa T, Suda K, Tsuboi M
Department of Physiology and Pharmacology, Tokyo College of Pharmacy, Japan.
Res Commun Chem Pathol Pharmacol. 1990 Oct;70(1):11-20.
We investigated the atropine-resistant accumulation of sn-1,2-diacylglycerol (DAG) on stimulation of 1 microM carbachol (CCh) in parotid acinar cells. CCh-induced DAG accumulation was biphasic, peaking at 5 and 20 min. Atropine inhibited two peaks in a dose-dependent manner, but the first peak was inhibited much more than the second one. Atropine (10 microM) completely inhibited both DAG accumulation and the breakdown of phosphatidylinositol 4-monophosphate and 4,5-bisphosphate (PIP2) 5 min after stimulation with CCh. In contrast, the breakdown of PIP2 at 20 min was completely inhibited by 10 microM atropine, but DAG accumulation was not. This atropine-resistant component at 20 min is significantly inhibited by staurosporine, a protein kinase C inhibitor. These results suggest that atropine-resistant accumulation of DAG at 20 min derives directly from other lipids rather than phosphoinositides and is regulated by a protein kinase C-dependent mechanism(s).
我们研究了在腮腺腺泡细胞中,1微摩尔卡巴胆碱(CCh)刺激下sn-1,2-二酰甘油(DAG)的阿托品抗性积累。CCh诱导的DAG积累呈双相性,在5分钟和20分钟时达到峰值。阿托品以剂量依赖的方式抑制了这两个峰值,但第一个峰值的抑制程度比第二个峰值大得多。在用CCh刺激5分钟后,10微摩尔阿托品完全抑制了DAG积累以及磷脂酰肌醇4-单磷酸和4,5-双磷酸(PIP2)的分解。相比之下,20分钟时PIP2的分解被10微摩尔阿托品完全抑制,但DAG积累未被抑制。20分钟时这种阿托品抗性成分被蛋白激酶C抑制剂星形孢菌素显著抑制。这些结果表明,20分钟时DAG的阿托品抗性积累直接来源于其他脂质而非磷酸肌醇,并受蛋白激酶C依赖性机制调控。