Eskildsen-Helmond Y E, Van Heugten H A, Lamers J M
Department of Biochemistry, Cardiovascular Research Institute (COEUR), Faculty of Medicine and Health Sciences, Erasmus University Rotterdam, The Netherlands.
Mol Cell Biochem. 1996;157(1-2):39-48. doi: 10.1007/BF00227879.
There is now clear evidence that receptor-dependent phospholipase D is present in myocardium. This novel signal transduction pathway provides an alternative source of 1,2-diacylglycerol, which activates isoforms of protein kinase C. The members of the protein kinase C family respond differently to various combinations of Ca2+, phosphatidylserine, molecular species of 1,2-diacylglycerol and other membrane phospholipid metabolites including free fatty acids. Protein kinase C isozymes are responsible for phosphorylation of specific cardiac substrate proteins that may be involved in regulation of cardiac contractility, hypertrophic growth, gene expression, ischemic preconditioning and electrophysiological changes. The initial product of phospholipase D, phosphatidic acid, may also have a second messenger role. As in other tissues, the question how the activity of phospholipase D is controlled by agonists in myocardium is controversial. Agonists, such as endothelin-1, atrial natriuretic factor and angiotensin II that are shown to activate phospholipase D, also potently stimulate phospholipase C-beta in myocardium. PMA stimulation of protein kinase C inactivates phospholipase C and strongly activates phospholipase D and this is probably a major mechanism by which agonists that promote phosphatidyl-4,5-bisphosphate hydrolysis secondary activate phosphatidylcholine-hydrolysis. On the other hand, one group has postulated that formation of phosphatidic acid secondary activates phosphatidyl-4,5-bisphosphate hydrolysis in cardiomyocytes. Whether GTP-binding proteins directly control phospholipase D is not clearly established in myocardium. Phospholipase D activation may also be mediated by an increase in cytosolic free Ca2+ or by tyrosine-phosphorylation.
目前已有明确证据表明,受体依赖性磷脂酶D存在于心肌中。这条新的信号转导途径提供了1,2 - 二酰甘油的另一种来源,后者可激活蛋白激酶C的同工型。蛋白激酶C家族成员对Ca2+、磷脂酰丝氨酸、1,2 - 二酰甘油的分子种类以及包括游离脂肪酸在内的其他膜磷脂代谢产物的各种组合反应不同。蛋白激酶C同工酶负责特定心脏底物蛋白的磷酸化,这些底物蛋白可能参与心脏收缩力、肥大生长、基因表达、缺血预处理和电生理变化的调节。磷脂酶D的初始产物磷脂酸可能也具有第二信使的作用。与其他组织一样,心肌中磷脂酶D的活性如何受激动剂控制这一问题存在争议。已证明可激活磷脂酶D的激动剂,如内皮素 - 1、心房利钠因子和血管紧张素II,也能有效刺激心肌中的磷脂酶C - β。佛波酯对蛋白激酶C的刺激会使磷脂酶C失活并强烈激活磷脂酶D,这可能是促进磷脂酰 - 4,5 - 二磷酸水解的激动剂继发激活磷脂酰胆碱水解的主要机制。另一方面,有一组人推测,磷脂酸的形成继发激活心肌细胞中的磷脂酰 - 4,5 - 二磷酸水解。在心肌中尚未明确GTP结合蛋白是否直接控制磷脂酶D。磷脂酶D的激活也可能由胞质游离Ca2+的增加或酪氨酸磷酸化介导。