van Heugten H A, Eskildsen-Helmond Y E, de Jonge H W, Bezstarosti K, Lamers J M
Department of Biochemistry, Cardiovascular Research Institute COEUR, Faculty of Medicine & Health Sciences, Erasmus University Rotterdam, The Netherlands.
Mol Cell Biochem. 1996;157(1-2):5-14. doi: 10.1007/BF00227875.
A multitude of agonists like e.g. endothelin-1, angiotensin-II, serotonin, thrombin, histamine and vasopressin as well as alpha 1-adrenergic and muscarinic stimulation lead to stimulation of the phosphoinositide cycle in the heart. Besides the seven membrane spanning-domain receptor-coupled stimulation of the key enzyme of the phosphoinositide cycle, phospholipase C-beta, another class of hormones, growth factors, also couple to the phosphoinositide cycle, now through receptors with intrinsic tyrosine kinase activity that can phosphorylate and stimulate the phospholipase C-gamma isozyme. In this review we summarize the multitude of receptor (sub)types, G-protein-subunit- and phospholipase C-isozymes that are present in the heart. Furthermore, generation of second messengers and cellular responses are described together with the (patho)physiological implications for the heart of phosphoinositide cycle activation and second messenger accumulation.
许多激动剂,如内皮素-1、血管紧张素-II、血清素、凝血酶、组胺和加压素,以及α1-肾上腺素能和毒蕈碱刺激,都会导致心脏中磷酸肌醇循环的激活。除了通过七跨膜结构域受体偶联刺激磷酸肌醇循环的关键酶磷脂酶C-β外,另一类激素、生长因子也通过具有内在酪氨酸激酶活性的受体偶联到磷酸肌醇循环,这些受体可以磷酸化并刺激磷脂酶C-γ同工酶。在本综述中,我们总结了心脏中存在的多种受体(亚型)、G蛋白亚基和磷脂酶C同工酶。此外,还描述了第二信使的产生和细胞反应,以及磷酸肌醇循环激活和第二信使积累对心脏的(病理)生理影响。