Kochhar N, Kaul D
Department of Experimental Medicine, PGIMER, Chandigarh, India.
FEBS Lett. 1992 Dec 7;314(1):17-9. doi: 10.1016/0014-5793(92)81450-z.
Since phospholipases exist within a membrane lipid environment, it is not unreasonable to assume that cholesterol capable of changing the lipid environment can effect the coupling relationship among the signal transducing components. Our previous study showed that the 'molecular switch' through which membrane cholesterol modulates cyclic nucleotide levels and Na+/H+ exchange within human platelets is phospholipase A2. We demonstrate here that membrane cholesterol initiates the activation of phosphatidyl choline phospholipase D and phosphatidic acid thus generated promotes the activation of its phospholipase A2 in the presence of extraplatelet calcium. More important, inhibition of phospholipase D by zinc blocks the activation of phosphatidic acid phospholipase A2 in platelets upon cholesterol incorporation. Our result led us to postulate that membrane cholesterol induced initiation promotion coupling of phospholipases D and A2 in human platelets may be responsible for the hypersensitized state of platelets in hypercholesterolemic patients.
由于磷脂酶存在于膜脂环境中,因此可以合理推测,能够改变脂质环境的胆固醇会影响信号转导成分之间的偶联关系。我们之前的研究表明,膜胆固醇调节人血小板内环状核苷酸水平和Na+/H+交换的“分子开关”是磷脂酶A2。我们在此证明,膜胆固醇启动磷脂酰胆碱磷脂酶D的激活,由此产生的磷脂酸在血小板外钙存在的情况下促进其磷脂酶A2的激活。更重要的是,锌对磷脂酶D的抑制作用会阻止胆固醇掺入后血小板中磷脂酸磷脂酶A2的激活。我们的结果使我们推测,膜胆固醇诱导的人血小板中磷脂酶D和A2的起始促进偶联可能是高胆固醇血症患者血小板超敏状态的原因。